Prominent Canadian physician Dr. Charles Hoffe has spoken out courageously to warn people of the very serious dangers of the Covid mRNA genetic “vaccines”. He now faces trial from the Canadian health authorities aiming to silence him and effectively destroy his medical practice.

What is most disturbing about this unprecedented case is that, if the prosecution gets its way, all the evidence produced by the State claiming the Covid vaccines are “safe and effective” will be deemed indisputable, irrefutable — and Dr. Hoffe would not be able to defend himself or call expert witnesses!

In other words, a totalitarian show trial designed to intimidate all doctors and patients who value medical freedom of choice, the right to a fair trial, freedom of speech, and medical ethics.

The College of Physicians and Surgeons of British Columbia, where Dr. Hoffe practices, had scheduled the disciplinary hearing for March 4th through March 15th. But at the last minute, the College pulled a fast one.

“When [the College] saw the mountain of evidence stacked against them, and against the public health narrative, obviously they panicked because I don’t think they realized how vigorous our opposition was going to be,” explains Hoffe in a March 7th interview.[1]

As a countermeasure, the College dumped a massive trove of documents on Dr. Hoffe’s lawyer AND invoked an almost unheard-of legal trick called Judicial Notice, which means the disciplinary Panel would accept all the College’s basic assertions as uncontestably true. Hoffe’s voluminous evidence — both from his own private practice as a family doctor and from the scientific literature — that the Covid mRNA vaccines cause widespread death, neurological problems, micro-clotting, infertility, immune-system damage, and other severe adverse side effects would be inadmissible.

Given this outrageous legal trick, Dr. Hoffe’s lawyer had no choice but to request an adjournment and hire four more attorneys to sift through the College’s eleventh-hour document-dump.

If the Disciplinary Committee implements Judicial Notice, explains Dr. Hoffe,

“I would have no opportunity to testify in my defense, nor would any of [my eight] expert witnesses….It would render this literally a kangaroo court. This is an astonishing act of injustice, where you literally accuse somebody of something and then remove their ability to defend themselves.”[2]

The government’s objective, he says, is “to try to make an example of me and make sure all the other doctors toe the line and keep quiet and just obey.” Dr. Hoffe, who is widely regarded as a heroic truth-teller across much of Canada, comes across as a down-to-earth man of great integrity, honesty and humility. An outspoken advocate for patient safety, medical ethics, and the Hippocratic oath (“First, do no harm”), he is accused by the medical authorities of spreading “misinformation,” putting people at risk, and encouraging “vaccine hesitancy.” After 31 years as an emergency room physician with not a single patient complaint against him, he was fired from his ER position for telling a nurse that somebody who had natural immunity didn’t need to get the Covid jab.

Exposing the Medical Cartel’s Coverup

In a speech delivered at the site of the College of Physicians and Surgeons in Vancouver in August 2022, Dr. Hoffe declared:

“What we have seen in the last 18 months since the start of the vaccine rollout is the biggest disaster in medical history. Never before in medical history has any medical treatment killed and maimed so many people….You only have to look at the OpenVAERS.com in the USA. 30,000 people dead, 55,000 permanently disabled, 50,000 cases of myocarditis, and 1.3 million vaccine injuries…This is an utterly failed experiment, and the College of Physicians and Surgeons here in B.C. is the one organization who could have and should have said no.”[3]

OpenVAERS.com is an easy-to-access version of the US Centers for Disease Control’s Vaccine Adverse Events Reporting System. VAERS vastly underreports the number of vaccine-induced injuries and deaths, capturing an estimated 1% to 10% of adverse events.

In his March 7, 2024 interview about the upcoming trial, Hoffe notes that OpenVAERS currently reports “almost 70,000 permanently disabled and about 2 million vaccine injuries, and yet Health Canada and the FDA look the other way and continue to tell us it’s safe and effective.” At the time of this writing, OpenVAERS registered 37,231 COVID vaccine reported deaths.

The Covid vaccine manufacturers admit that their poorly tested, highly experimental injections do not prevent infection with Covid and do not stop transmission of the (alleged) SARS-CoV-2 virus.

And yet the charade goes on….in Canada, the United States, most of Europe, Australia and the no-longer “free world.”

Dr. Hoffe has repeatedly pointed out these facts as well as the fact that the more Covid shots you get, the more likely you are to be diagnosed with Covid. This is true of individuals and whole nations. As Hoffe cogently observes, “Every vaccine injury reporting system across the world reports record numbers of deaths and disabilities and vaccine injuries that we’ve never seen the likes of from any medical treatment in history. And yet they completely turn a blind eye and they just carry on recommending that people get vaccinated. It’s absolutely absurd.” [4]

Micro-clots

Dr. Hoffe determined that up to 62% of his patients who got the Covid mRNA vaccine develop micro-blood-clots too small to detect on MRI or CT scan. He was the first medical expert to state publicly that these blood clots are not rare.

According to Hoffe, these micro-clots permeate the capillary network in the vaxxed, resulting in blockage of capillaries (pulmonary arterial hypertension); this condition usually kills people within 3 years, and those who survive may suffer steady deterioration, especially if they take another Covid shot. The only way you can find out if the Covid “vaccine” gave you micro-blood clots is to ask your doctor to give you a D-dimer test, like the one Dr. Hoffe has performed on his patients.[5]

This finding alone should have led to the immediate withdrawal of all the Covid-19 genetic “vaccines.” They are indeed “clot-shots” as the critics have warned repeatedly. But the Pharma-controlled mainstream media lies and assures us that both large and tiny blood clots are “extremely rare,” when the opposite is true.

Most of Dr. Hoffe’s patients developed micro-clots within 7 days after the jab, but others may well experience micro-clotting later on as the genetic cocktail (“vaccine”) wreaks its harmful effects on the body.

Another Canadian doctor, Rochagné Kilian, an emergency medicine specialist in Ontario, sounded the alarm on the astronomical rise in D-dimer levels she observed in patients shortly after they received a Covid-19 vaccine. She links this phenomenon to micro-clotting, disseminated intravascular coagulation, and autoimmune disease in the vaxxed. Dr. Kilian lost her job and had her license to practice medicine suspended for warning the public about the very serious risks of the Covid shots.[6,7]

Support

To voice support for Dr. Charles Hoffe, please write concise, polite, yet strong letters to:
The College of Physicians and Surgeons of BC
300–669 Howe Street
Vancouver BC V6C 0B4
Canada

You could also fax them at 604-733-3503. FaxZero.com lets anyone send up to five free faxes per day to anywhere in the U.S. or Canada. The FaxZero website is easy to use and has no gimmicks or ads. Again, send polite, concise, powerfully worded faxes. The College’s website also has a Message facility (https://www.cpsbc.ca).

Let’s let the College of Physicians and Surgeons of BC know what people think of their outrageous, underhanded ‘lawfare’ tactics and their persecution of an outstanding physician/healer.

The necessity of Dr. Hoffe to hire four additional lawyers will involve significant new legal expenses..

To help Dr. Hoffe with this burden, please go to:

https://www.givesendgo.com/GANZA or

https://www.fundingthefight.ca/donate

*

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Notes

1. Dr. Charles Hoffe Trial Update – March 7, 2024 (video). Interview with Derek Sloan https://rumble.com/v4hvp8x-dr.-charles-hoffe-trial-update-march-7-2024.html

2. Ibid.

3. Covid mRNA Vaccine. Biggest Disaster in Medical History: Dr. Charles Hoffe. Hoffe Gives Riveting Speech In Vancouver, British Columbia, Canada https://www.globalresearch.ca/video-biggest-disaster-medical-history/5790270

4. https://rumble.com/v4hvp8x-dr.-charles-hoffe-trial-update-march-7-2024.html

5. Canadian Doctor: 62% of Patients Vaccinated for COVID Have Permanent Heart Damage. By Brian Shilhavy https://healthimpactnews.com/2021/canadian-doctor-62-of-patients-vaccinated-for-covid-have-permanent-heart-damage

6. Emergency Medicine Doctor shows Micro Blood Clots in D-dimer Tests Following COVID-19 Shots https://www.bitchute.com/video/RwKbDnR8BOzg

7. Government’s Own Data Proves COVID-19 Shots Are Causing Blood Clots, Heart Disease, and DEATH. Brian Shilhavy https://healthimpactnews.com/2021/governments-own-data-proves-covid-19-shots-are-causing-blood-clots-heart-disease-and-death

When I originally made this Substack, I found myself in a very frustrating position—I had something I felt was essential for the world to know (that we were repeating the disastrous smallpox vaccination campaign, its cruel mandates, and the widespread counterprotests against them by the working class). Still, I had no way to get the message out. I tried to find a way to do so for a while, and eventually, Steve Kirsch generously gave me a platform to do so.

Because of this, I have a considerable degree of empathy with people who find themselves in a similar position to mine. Thus one of my goals in building the subscriber base here has been to make that platform available to those in a similar situation to me, and I periodically publish compelling things readers share with me I believe are accurate (e.g., this citizen’s survey of blood clots amongst the vaccinated).

Recently a longtime reader contacted me to share his story. Based on my previous correspondences with him over the last year, I believe he has accurately represented himself here. I also want to note that his story shares many parallels to the treatment of other doctors attempting to do the right thing throughout COVID-19 (e.g., Paul Marik’s experience).

One of the reasons we lack doctors everyone wants to see is because those who try to do the right thing get pushed out of the system. Because there is so much corporate control of medicine, even doctors who want to do the right thing know they have no recourse if the hospital turns against them. Those doctors thus have to choose between toeing the line and doing their best within those circumstances or leaving the system entirely.

Their leaving thus leaves even fewer physicians that patients would want to see available within the corporate medical system. For many things like emergent hospital care, the patients cannot address the issue by simply opting out of the system. These problems worsened during COVID-19, particularly in the blue states, which has created the unfortunate situation where patients often have to travel out of state for the care they need, which is immensely unfair, especially to those who aren’t somewhat wealthy.

Dr. Miller’s Story

My Covid 19 Cancellation Story    April 9, 2023

I am a physician who stood against the false narratives swirling around COVID and for a time, it seemed like I lost.

Before COVID became a public reality, I was working as a successful Trauma Surgeon and Surgical ICU Physician in the hospital that had the first diagnosed COVID case in America. I was working as one of the more senior surgeons of a team of 12 surgeons. The hospital and medical community had already been struggling prior to COVID with various departures from reality with narratives including ‘racism everywhere’ and ‘diversity as long as it supports deviancy,’ but it wasn’t appearing to dramatically affect patient care.

[Dr. Miller’s surgical specialty currently requires 6-7 years of grueling training after completing medical school and thus pays a high salary. Because of the investment required to obtain it, most doctors are reluctant to ever part with it].

In 2018-2019, I stumbled onto a fraud scheme perpetrated by some of the administrative doctors in our hospital that did cause patient harm, so I reported our hospital administration for fraud. I similarly observed and discovered other connected issues that caused patient harm, by various other providers, that I tried to bring to light in our hospital. I was “rewarded” with 12 complaints filed against me over a 2-week period, in retaliation. These complaints accused me of breaches of almost every aspect of professional behavior and ethics. It followed one of the administrators sending out an email asking her colleagues to ‘get rid of Dr. Miller.’ None of these allegations stood (they were all false to begin with), and I continued to do my job to the best of my abilities in this hostile situation, but it became increasingly difficult. Eventually, every single complaint was dismissed as unsubstantiated.

Then, through February and March of 2020, our hospital had a large number of COVID patients including a real upsurge of many sick patients in early March. A couple weeks later, it hit the news, but only AFTER the virus had passed its inflection point in our hospital and AFTER our healthcare system was not in any threat of having inadequate resources. Things then went completely mad with hype and fear- again, this was AFTER the real infectious surge was past.

Suddenly, our hospital outcomes and quality data became hidden and opaque to us. Prior to this, most all data was openly shared and discussed in quality assurance meetings. The hospital forced upon us a narrative that was pure lunacy and contrary to all available observations and previously available data. A chilling example is the following: I was working a shift in the ICU in late April 2020 and had basically nothing to do because greater than half our beds were empty. We were “low censusing” any nurses willing to go home because there were so few sick patients. I was having a cup of coffee, chatting with the staff and another ICU physician, who was in leadership, when the daily newspaper was delivered. Prior to the paper being delivered, we were all relaxed, jocular, and noting how little work we all had. The other ICU physician picked up the local paper where the main headline said, ‘Local ICU Overwhelmed.’ The article was referencing our ICU, as we were the only hospital in the county. He looked at me, started sweating, panicked, and said, “What are we going to do? We may not be able to handle this!” I replied with, “Pour another cup of coffee and laugh at the morons writing the paper.” He became visibly distressed and left to call the hospital administration about the situation, who confirmed they were complicit with the newspaper article. This colleague was one of the medical directors of our ICU. Our hospital and ICU were not overfull at the peak number of infections in March 2020. In fact, the ICU was never overfull, even after the horrible protocols that hurt so many patients were established. I knew we were in serious trouble as a medical community when clinical leaders started believing the words in a newspaper and hospital administrators more than their own eyes and experience.

[Mattias Desmet’s mass formation hypothesis helps explains how people can delude themselves into a reality in stark contrast to the objective evidence in front of them].

Then, I watched as every policy, practice, and quality metric that makes a trauma and surgical program have good patient outcomes be undermined or abandoned by my colleagues and hospital administration. I filed countless complaints to our quality department for disgusting breaches of care that were now becoming commonplace. I could not turn my back on my oaths taken to advocate for patients. Between mid-2020-2021, following a leak of information from the opaque administration, I learned that our unanticipated morbidity and mortality numbers had more than doubled for indexed trauma patients. It was horribly demoralizing to watch.

[This is an excellent example of a society in decline].

After the vaccine was rolled out in late 2020, it became a functional mandate in the broader community, and then definitively mandated by the late summer of 2021. The medical community in the county I was working in (Snohomish, WA) started refusing to care for unvaccinated patients, except in the hospital setting. I couldn’t believe that patients were banned from accessing basic primary care at first, but then I spoke to a man at my church who was denied both refills of his diabetic medications and treatment for a sinus infection by his primary care provider, all because of his COVID vaccination status. This was so inconceivable that I still didn’t believe it! Even when patients did make it to the hospital, I learned that the physicians and staff in the emergency room were directed to provide a lower tier of medicine to this group of patients. It was less than acceptable, and worse, less dignified, than the care given to any other patients pre and post COVID. I had to verify with physician leaders that they approved of this inhumanity. I found out that all the major healthcare systems in the county had agreed to this action, and drove the creation of the policies that demanded physicians act in direct opposition to their oaths. After discovering this, I departed from the medical community in spirit.

[My observation throughout history has been that when a malignant collective ideology takes hold, only 5-10% will be willing to go against it].

Working with my pastor, we turned our church into a free clinic to care for those ostracized from society. I obtained independent malpractice insurance, and we started seeing patients. People were desperate. We didn’t advertise, but there were so many people seeking basic healthcare that we struggled to see everyone. I did my best to see people in their time of need, but it was hard. I was still working in my full-time hospital position. I just didn’t have enough hours in the day. Most of the people I cared for were seen at the church - they were met with maskless smiles, prayer, support, and free medical care. Sometimes, people would be waiting in my driveway for me when I arrived home in the early morning after a night shift or late at night after I finished a day shift. What became obvious as the most important thing about our clinic, is that our patients needed to be treated as valuable people created in God’s image.

Prior to this experience, I was a seasoned/hardened subspecialist with the best reputation one could hope for in the hospitals I worked. When other doctors, health executives, nurses, and local politicians or their families had surgical problems, I was often the one asked to deliver their care even if I wasn’t scheduled to be working. After our health care system abandoned the oaths we took as physicians, I had an identity crisis and pivoted to putting more efforts into the free clinic, caring for the dispossessed patients.

[Throughout my career, I have tried to volunteer in free clinics because I frequently find they are the only place you can focus on helping patients rather than dotting the i’s and crossing the t’s the corporate medical system requires everyone to do].

Eventually, my work at the free clinic treating unvaccinated patients became known, and the hospital administration learned of it. Subsequently, the real pressure against me started. The hospital responded by opening an investigation of me on synthesized charges of ‘micro-aggression.’ There ended up being 2 separate and independent investigations (one by the hospital, one by my physician group leadership who were working in tandem with the hospital) into my conduct. My colleagues, who months earlier asked for my help and guidance about both professional and personal matters, would no longer return my calls, text messages, emails, or speak to me in public, for fear of being labeled as affiliated with me while in my state of political disfavor. The investigations themselves and the repercussions to my reputation were the punishment. I was treated as guilty, even when proven innocent, by the hospital administration and my colleagues. The investigations eventually exonerated me, my behavior, and my healthcare delivery, but left open the possibility for immediate suspension/termination if I committed a ‘micro-aggression’ in the future. Obviously, this was a no-win scenario for me since micro-aggressions are subjective, undefinable, unprovable, and therefore indefensible. I refused to continue working without an independent mediator, so the hospital gladly paid out my contract instead of mediation and restoration.

[One of the things that surprised me about working in hospitals was seeing things I’d previously associated with high school drama transpire inside the facility—something many of my colleagues have also observed].

Separately during this time, I was reported to the State Medical Board by an outpatient pharmacist for prescribing a 2-week course of Fluvoxamine (an anti-depressant) prescription to help a patient recovering after COVID. This prescription had been banned by the Washington State Medical Association as a treatment for COVID or its repercussions. Incidentally, the patient had a positive response and near complete recovery from her illness, but the pharmacist and WSMA didn’t seem to care about that data point but were apparently offended that I violated their protocol.

By March/April of 2022, multiple other clinics in the county began to accept care for most patients, regardless of vaccination status, and so we wound down the free clinic at my church, transitioning people’s care to physicians in established practices who would now agree to deliver appropriate care. As I had been reported to the state (although no formal charges were brought) and I was being pushed out of hospital medicine for practicing ethical medicine, I knew it was time to leave Washington State. The message to me was clear: if I stayed, I would have formal investigations that would prohibit me from obtaining a medical license in another state. My livelihood would be stripped away. So, we sold our homes and boats, liquidated our assets, and moved to South Florida in May 2022. I was, and am, bitter at the establishment of medicine that committed these crimes, so I planned to retire at age 50 with the move and have nothing further to do with the establishment.

[Dr. Miller made the correct decision. Had he not left, he likely would have been permanently barred from practicing medicine in the future. This illustrates a major issue with the current medical board system].

However, after the hurricane came through Florida in the fall of 2022, I started doing volunteer work for hurricane victims. This included some medical relief work. I realized there is still good that can be done in medicine, that people need healthcare providers, and that by nature, I am a healer.

So, in February of 2023, I returned to practicing medicine and started working as a Primary Care Physician at a holistic clinic where no patient is turned away. I discovered that I enjoy being a Family Physician, too. I lost my prestigious career and my social position, but I did not lose my ethics or integrity. I did not violate my oaths of practice. So, ultimately, I have won. And I’m happy.

Conclusion

I applaud Dr. Miller for being willing to share his story publicly. Many physicians over the years have told me that the medical profession's mistake was surrendering too much of each doctor's power to the corporate medical machine. Over the last few years, we have witnessed a direct consequence of this unchecked power grab.

In the future, I believe three concrete steps need to be taken to address this issue:

• The first is that patients living in blue states must create the political will to have their state governments stop pushing these ridiculous actions. Doing so will likely require directly informing the public that most of the laws and policies being enacted are being done to support corporate interests rather than patients—as directly attacking specific violations of medical freedom has been largely unsuccessful thus far due to it being blended into the red vs. blue partisan dichotomy (which is very difficult to shift in either direction) rather than being portrayed as corruption affecting the entire electorate.

• The second is that patients need to financially support services and physicians they believe in and, as much as possible, opt out of ones that don't. We are seeing a miniature version of that with Substack, as the legacy media is rapidly losing viewership (since most of what they publish is garbage). Simultaneously journalists are making more on Substack than they did at their old jobs—both of which are putting pressure on the legacy media to stop publishing garbage and making many journalists want to jump ship to Substack.

• The third is the doctors need to be much more aggressive in taking their power back (they need to band together—potentially with the correct type of union). The corporate medical system cannot function without them, and there is a constant shortage of physicians in the United States, so that position needs to be leveraged to force the corporate medical system to behave rather than perpetuate the current corporate status quo

The following book represents an extraordinary historical achievement in the reporting of events in science and medicine.

It also appears to be a record of a great crime against humanity.

In 2022, the Pfizer documents, a tranche of 55,000 documents, many of them thousands of pages long, were released via a court order. This was due to a successful lawsuit by attorney Aaron Siri. The US Food and Drug Administration had asked the court to keep these documents hidden for 75 years — until after most of us alive now would be dead and gone.

Luckily, the court did not concur.

We at DailyClout.io, a website devoted to civic transparency, realized that the raw documents were impossible to cover in normal journalistic ways. One reason was the massive scope of the documentation. But another reason was that the documents are written for scientists and medical researchers, in language that only specialists in those fields could really understand properly or explain.

We sent out a call for expert volunteers from those fields on our own platforms, and we did so also on the video and podcast platform, War Room Pandemic, hosted by Stephen K. Bannon. A global audience thus recognized how important it was for an informed public — who had been harried, bullied, and “mandated” to receive Pfizer’s and Moderna’s mRNA injections in 2021-2022 — to understand what was really revealed inside of the Pfizer documents.

As a result of our calls for expert help, we received 2000, then 2500, and finally 3500 responses from volunteers, many of whom are experts in their fields. Biostatisticians, lab clinicians, pathologists, anesthesiologists, sports medicine physicians, cardiologists, research scientists, RNs, and many other related disciplines are represented among these decent, highly-skilled people who offered to read through these difficult, technical documents — pro bono, as a service to humanity (and out of respect as well, in many cases, for their own lifelong commitment to real science, real medicine, and truth in general). Many of them were not only published, peer-reviewed academic authors in their fields, but some were peer reviewers themselves. There was no way, with a group this distinguished in science and medicine doing the labor, that the interpretation of these documents could be dismissed as “fringe,” subjective, or as the work of “conspiracy theorists.”

Of course, managing a project in which 3500 highly trained specialists from all over the world work together virtually on unpacking and reporting on such a massive trove of material, would have been impossible for mere mortals.

At first, indeed, we did not know how to organize the thousands of specialists who offered their help.

Enter Amy Kelly, who is also a heroine of this story. She is a talented project manager, and now DailyClout’s COO; and she has a distinguished background in complex organizational projects in various fields.

Ms. Kelly managed, seemingly effortlessly, to organize the volunteers into six working teams, with subcommittees of expert readers. Under her extraordinary leadership, the thousands of specialists around the globe started to communicate with one another, share their findings, and draft their reports. I trained the volunteers in writing for a general audience, and I also trained our DailyClout editors in editing what was often dense medical language, but with extremely important findings, into accessible reports that anyone with any level of education could follow and understand.

For all of us, but mostly for the volunteers and Ms. Kelly, the next year represented a Herculean effort to turn this material, that one of the most powerful companies in the world trusted would never be made public, into fifty readable reports sharing the most urgent headlines of all — the reports that are now in your hands.

You will see that the 46 reports document what may be a massive crime against humanity. You will see that Pfizer knew, as it appears, that the mRNA vaccines did not work. You will see that the ingredients, including lipid nanoparticles, in the mRNA injections bio-distributed throughout the body in a couple of days, accumulating in the liver, adrenals, spleen — and ovaries. You will see that Pfizer and the FDA knew that the injections damaged the hearts of minors — and yet waited months to inform the public. You will see that Pfizer sought to hire over a thousand new staffers simply to manage the flood of “adverse events” reports that they were receiving and that they anticipated receiving. You will see that 61 people died of stroke — half of the stroke adverse events being within a couple of days after injection — and that five people died of liver damage with, again, many of the liver damage adverse events sustained shortly after the injection. You will see neurological events, cardiac events, strokes, brain hemorrhages, and blood clots, lung clots and leg clots at massive scale. You will see that headaches, joint pain, and muscle pain are rampant as adverse events, though these are not disclosed as routine side effect warnings by our agencies.

Most seriously of all, you will see a 360-degree attack on human reproductive capability: with harms to sperm count, testes, sperm motility; harms to ovaries, menstrual cycles, placentas; you will see that over 80 per cent of the pregnancies in one section of the Pfizer documents ended in spontaneous abortion or miscarriage. You will see that 72 per cent of the adverse events in one section of the documents were in women, and that 16 percent of those were “reproductive disorders,” in Pfizer’s own words. You will see a dozen or more names for the ruination of the menstrual cycles of women and teenage girls. You will see that Pfizer defined “exposure” to the mRNA vaccine as including skin contact, inhalation and sexual contact, especially at the point of conception.

History has not yet concluded its assessment of what Pfizer — and the FDA, who were in custody of all of these documents — has done. We are at the very start of that assessment.

But to me it is clear that the following documents, written by impeccably skilled experts, and linked to primary sources, show that a crime has likely been committed against humanity that is unprecedented in its scale.

We owe the War Room/DailyClout Pfizer Documents Research Volunteers — some named, most of them unnamed — who labored for a year, and do so to this day, and for nothing more than the privilege of serving humanity, science, medicine and the actual truth — a tremendous debt. We thank Mr. Bannon and his team for so often supporting our call for experts and for helping us to announce the results in real time, as the reports came in. We thank all of the other news outlets, of all kinds, who risked reprisals from Big Pharma or even from the government — which recent lawsuits have shown allied with Big Pharma — who have also showcased the work of the Volunteers, in an effort truly to inform their viewers.

Please share this document with your loved ones if you also find it to be important.

Everyone by law deserves informed consent when it comes to medical interventions — it is actually a crime to withhold it (really many crimes appear to be represented here, but history will sort that out as well).

It has been a privilege to report on this team’s work, and to do all I can as CEO of DailyClout, to help sustain their, and the remarkable Ms. Kelly’s, work on humanity’s behalf.

Sincerely,

Dr. Naomi Wolf
CEO, DailyClout.io
March 21, 2023
Salem, Massachusetts

Note: This article is primarily a human story. The most important parts of this article are the videos (if you only have time to watch one, watch Maddie’s, below) that were compiled and edited for this article. The written details are just to provide the necessary context for the significance of their testimonies.

In the first part of this series, I discussed how the gross malfeasance observed by many in the COVID-19 vaccine trials did not come out of nowhere. Rather, it is yet one more occurrence in a chronic pattern of egregious conduct by the pharmaceutical industry, which has progressively worsened because there has not been the political will to address the growing corruption within the biomedical establishment.

There, I focused upon the events within the human papillomavirus (HPV) vaccine trials (and the subsequent red flags which emerged after they entered the market), because many at the time had difficulty believing something like that could even happen and it was possible to sweep the issue under the rug, since the vaccines were only targeted on one segment of the population—women. Now, not only has the exact same thing happened (to a very eerie degree) with the COVID vaccines across the globe, but what is happening now is even worse than what happened less than a decade ago.

The best metaphor I have come up with to describe what I’ve observed in the pharmaceutical clinical trial process is that enrolling in one is akin to entering an abusive relationship. The abuser will initially flatter you and promise you one thing after another in return for your consent to enter their web of deception. Then, once they have you, they will break each promise they made, gradually treating you worse and worse, and gaslight ing you into believing that those issues are not really happening. Finally, once they no longer need you, they will discard you and leave you to pick up the pieces (which is often almost impossible if you have a life-changing medical injury).

Thanks for reading The Forgotten Side of Medicine! Subscribe for free to receive new posts and support my work.

In the previous article , I introduced the concept of two different types of scientific fraud:

• Soft fraud is when the data is presented misleadingly to propose a conclusion that's not supported by the data, or some of the data is intentionally omitted (e.g., you do not publish an incriminating study or you find a way to reclassify an adverse event so it does not show up in the final clinical trial report).
• Hard fraud is when the data itself is just fabricated.

While many are comfortable with committing "soft” fraud, very few will commit “hard” fraud (although this cannot necessarily be said of India or China ). Instead, most of the fraud we encounter is soft fraud (e.g., this characterizes many of the studies used to try to debunk hydroxychloroquine in the treatment of COVID-19). This, in turn, makes it possible for outside investigators (e.g., this community) to read between the lines, identify what actually happened, and determine what the results of a given study should have been, had it not been twisted to provide the results desired by its sponsor.

Conversely, I believe that the general reluctance to commit hard fraud exists because it crosses a line that even the fairly corrupt academic and legal systems still stand behind. However, we frequently see things that come quite close to that line, such as dishonest researchers altering a trial midway through so it arrives at the needed results. Fauci, for example, did this repeatedly with remdesivir to get it onto the market, and similarly, the COVID-19 vaccine manufacturers like Pfizer ended their previously promised long-term placebo groups once they got their emergency-use authorizations (which should have required that long-term follow-up), so the long-term side effects of these vaccines could never be assessed.

Note: Although you can conceal most things by manipulating clinical trials, the one thing that is very difficult to hide is the total number of deaths (as they cannot be reclassified to something else). When Pfizer prematurely ended their trial at 6 months, more people had died in the vaccine group than the placebo group (and I suspect that this would have further worsened with time). The report disclosing this inconvenient fact (which destroyed the entire rationale for vaccine mandates) was released over a year ago .

Much of modern (industry-sponsored) science is designed to conceal things that would create problems for those sponsoring the science. Similarly, an ethos has been installed within our culture to doubt our own observations, and instead defer to the evidence-based scientific consensus, as the former, but not the latter is allegedly highly susceptible to biases that invalidate its conclusions. I disagree with this, and would argue that important things can often only be discerned by perceptive anecdotal observations.

Many organized religions throughout history have sought to control their populations by monopolizing the truth, and modern science is no different, monopolizing the evidence so that only a costly industry narrative can constitute "truth.” All of this is why we repeatedly see situations where someone has an undeniable medical injury, and afterwards, every professional they talk to tells them the injury could not have possibly been linked to the medication because there is “ no evidence ” it could have happened (also known as medical gaslighting ).

With the COVID-19 vaccines, we have seen alarming evidence of their harm across the board. For example, so many people are being harmed that VAERS has received more serious adverse events from the COVID vaccines than all other vaccines in history-- 28% of Americans know someone whom they believe the vaccines killedThe life insurance industry shows an unprecedented spike in deaths amongst working-age Americans following workplace-mandated vaccines being forced upon them. However, all of these safety signals are being ignored and dismissed as erroneous products of cognitive biases because they don’t meet the elusive bar for “evidence.”

Our current society has been conditioned to worship “evidence-based” science, and believes that it should be the sole arbiter of truth. One of the core tenets of evidence-based medicine is that the best available evidence should be used to inform clinical decisions. This is now widely interpreted to mean that large randomized controlled trials (RCTs) or clinical guidelines produced by committees of ( often corrupt ) experts are the “best” forms of evidence, and thus are the only things allowed to inform clinical decisions.

One of my largest disagreements with this dogma occurs when a situation arises where observations suggest something inconvenient to commercial interests, but the question at hand has not been formally assessed by large RCTs. The observations are summarily dismissed because “there is no evidence” for them. In these cases, I believe that the more limited data point (e.g., a series of similar clinical cases) constitutes the best available evidence, and should be treated as such until more comprehensive evidence is arrived at through a clinical study.

Much of my success as a clinician has arisen from utilizing more “limited” forms of evidence to inform my clinical decisions rather than waiting for an RCT (which may take years to be done) to settle the question—unfortunately many doctors become paralyzed and cannot act unless they have something like that to back them up. In contrast, if you read medical journals from earlier eras, physicians regularly made remarkable discoveries utilizing inductive reasoning, which is why I frequently study those ancient documents.

Overall, I believe there are three major issues with relying excessively upon RCTs:

• The first, summarized in this essay by Harvey Risch, is that the value of (perfect) RCTs is heavily over-emphasized. In my eyes, most individuals who fixate on RCTs view an investigation being randomized and controlled as a necessary box to check off, rather than (like Risch) actually understanding what it entails from a statistical perspective.

• Secondly, if the magnitude of an effect is small (e.g., this drug might reduce your risk of a heart attack years down the road by 5%), it takes an elaborate and costly trial to detect that faint effect, and it is very likely that you will have a greater chance of being harmed by a side effect than benefiting from the drug. Conversely, if the effect is large (e.g., shooting someone with a gun typically kills them), you don’t need an elaborate trial to detect the effect; a very small one will suffice to identify it. I subscribe to the belief that many useful medical interventions have a large enough magnitude of effect that it is not necessary to do complex testing to tease out their benefits.

• The third point is that large RCTs are extremely expensive to conduct (meaning that only industry and occasionally vested interests within the government can fund them, which is why many therapies I stand behind have never been able to achieve this gold standard in research performed for them). The rarely considered cost of doing an RCT frequently invalidates the entire RCT model, because study after study has shown that the financial interests of a study’s sponsor heavily influence its conclusion, and that influence is much greater than any benefit that can be obtained through randomization or controlling for the placebo effect.

Because of the “sponsor bias”, large studies need to have a way to arrive at a sponsor’s desired conclusion without committing hard scientific fraud. Over the years, a relatively consistent toolbox has evolved for committing soft scientific fraud, and those familiar with it were able to immediately recognize it being applied throughout the COVID-19 clinical trials

The COVID-19 Vaccine Trials

The essential purpose of the COVID-19 vaccine trials was to do the following:

• Be completed in a much shorter time frame than normal so that the vaccines could make it to the market before the pandemic ended on its own (which is essentially what has happened in Africa where vaccines were never used ).

  Note: The FDA also understood the urgency to open this long-term marketplace and waived a variety of oversights that would normally be required using the present “emergency” as the justification for doing so.

• Come up with something that could be used to justify that the vaccines were “effective” so that the medical profession would wholeheartedly support and promote them.

• Conceal any adverse reactions from the vaccines that would make the medical profession reluctant to recommend the vaccines, and, more importantly, ensure doctors would deny any harms they observed in patients during the rollout could be linked to the vaccine (as doctors acknowledging widespread injuries would destroy the public’s willingness to continue vaccinating).

Long before the vaccines entered the market, I started to see the signs that an elaborate publicity campaign was being put together to frame the vaccines as the miraculous “ solution ” to the horrific pandemic situation we were experiencing (which was largely self-inflicted). Once the vaccines became available, that publicity campaign kicked into high gear and became the most aggressive propaganda campaign we had ever witnessed in our lifetimes. I tried to cover some of the most insane examples here:

Not surprisingly, this scheme also led to the vaccine manufacturers having the audacity to use titles like “ Safety and Efficacy of the BNT162b2 [Pfizer] mRNA Covid-19 Vaccine ” for the publications of their trials . Simultaneously, we were hit with the same soundbite over and over “ well we had hoped the vaccines would be effective, but we never imagined they would be this effective .” My colleagues ate that up, and it became nearly impossible to provide any piece of evidence with which to challenge this modern-day miracle.

Problems With Pfizer’s Trials

_Note: I mostly critique Pfizer. This is not because Pfizer is the only bad actor. It’s because I’ve spent the majority of my time reviewing their work (I can’t read everything), and because Pfizer received full approval for their vaccine, it was possible to view many of their regulatory submissions through FOIAs (and their equivalents)_

When I read through the Pfizer trial , a few red flags jumped out at me:

• The vaccines were never tested for preventing transmission, and based on their design and my knowledge of precisely how previous vaccines failed to prevent transmission , I did not believe you could take it on faith that the vaccine's efficacy in reducing symptoms translated to the benefit all my colleagues ultimately cared about (reducing the transmission of COVID-19).

• The actual benefits provided by the vaccine were very small. You had to vaccinate 119 people to prevent one minor case of COVID-19 (e.g., a sore throat + a positive test), 2711 people to prevent one “severe” case of COVID-19, and since no deaths were prevented in the trial, well over 21,720 people needed to be vaccinated (21,720 is the total number who were vaccinated in the trial) to prevent a single death from COVID-19.

• Most of the suspected adverse reactions to these vaccines did not appear to have been amongst the adverse events that were monitored (they were also unlikely to appear in the brief timespan of symptoms being monitored within this trial).

• The adverse events that were reported were much higher than what has typically been reported in trials for other vaccines [e.g., 59% experienced fatigue after Pfizer's vaccine, whereas around 10-15% experience fatigue after an influenza vaccine].

• The actual benefit that the vaccines provided was much less than these adverse events that were acknowledged within the trial report. Arkmedic did an excellent breakdown of it here .

• The noteworthy adverse events about which I remembered reading in the online support groups I had joined in 2020 for vaccine trial participants were not accounted for in any of the trial reports I read (Pfizer included). I had joined these online groups because I was suspicious of the vaccines and felt that doing this would be the only way to find out what the pharmaceutical companies had actually done.

From looking at all of this, my immediate thought was “if this was the best they could do using every possible trick at their disposal to rearrange their data to paint a positive picture of the vaccines, just how bad was the actual trial data ?”

Unfortunately, my physician colleagues (who frequently lectured us on how to skeptically dissect scientific publications) were so enraptured by the “the vaccine is even more safe and effective than we imagined” meme, that all these points fell on deaf ears. Fortunately, some did notice these issues, and Peter Doshi published a series of editorials (summarized here ) in the British Medical Journal (BMJ - considered to be one of the top 5 medical journals in the world ) that explained why the design of the vaccine trials and the evidence for Pfizer’s vaccines was very poor, and could not justify an FDA approval. Sadly, his experience with his colleagues mirrored my own, and his points were almost entirely ignored by the medical profession.

One of Doshi’s many observations was that there were signs in the data that the trial was not blinded, and the entire benefit of the vaccine may have been due to a failure to test vaccinated individuals for COVID-19 (thus creating the illusion that vaccinated individuals were less likely to have laboratory-confirmed COVID-19).

Subsequently, a whistleblower, Brook Jackson , who helped run one of Pfizer’s clinical trials, came forward and testified to the following:

• The COVID-19 vaccine trial she participated in was run in a much more haphazard way than any others she had worked on throughout her career.

•The trial was not blinded, and protocols that should have been followed to ensure blinding were flagrantly violated.

• Vaccinated individuals with COVID-19 were not being tested for COVID-19.

• Adverse reactions in vaccinated individuals were not adequately recorded.

Due to a concern that this conduct would violate the FDA’s requirements for clinical trial sites, Brook alerted her superiors about what was happening so that these issues could be addressed. After her pleas repeatedly fell on deaf ears, she eventually notified the FDA directly. Although the FDA did not investigate her concerns, they appeared to have informed her employer, as Brook was terminated the same day.
Note: As detailed by Doshi , there has been a longstanding issue with the FDA providing insufficient oversight for clinical trial sites, and as a separate investigation into vaccine oversight revealed, it was suspected that their laxity in oversight would dramatically worsen during Operation Warp Speed, which was the partnership between the Departments of Health and Human Services (HHS) and Defense(DOD) aimed at helping to accelerate the development of a COVID-19 vaccine.

After these events transpired, Brook submitted her story to the BMJ who corroborated her allegations through documents she provided, and through other employees at the trial site. I would strongly recommend reading the BMJ’s investigation to understand exactly what happened there. Since her termination, Brook filed a whistleblower lawsuit against Pfizer which is presently in the federal courts.

Later, when I reviewed the events with Brook, one of the most interesting things I learned is that most of the data which is collected at clinical trial sites never even makes it to the FDA. Instead the FDA only receive a very small sample of it that is trusted to be representative of everything that occurs. I suspect this is one of the many reasons why the FDA could truthfully claim they had no knowledge any of this happened, although as this article shows they are clearly also culpable since they did not choose to pursue getting the reports for adverse events (like Maddie’s) they knew were happening.

In summary, as you can see from the above information, there was a real risk that soft fraud would occur during the clinical trials. However, unlike the many cases in which this has happened in the past, for the COVID-19 vaccine, we also had the unique opportunity to have numerous whistleblowers come forward and corroborate that this happened for the COVID-19 vaccines.

[

A Midwestern Doctor @MidwesternDoc

Whistleblowers are critical for righting the wrongs in government and healthcare. They always pay a steep price, but still would choose to do it again. Gøtzsche's presentation provides the best explanation I have ever seen on what drives the heroes we need now more than ever.

](https://twitter.com/MidwesternDoc/status/1609225914885476353)

The COVID-19 Vaccine Trial Strategy

Pfizer and Moderna knew quite early on (although exactly how early is a matter of speculation) that there were serious risks involved in using the mRNA spike protein platform for vaccination (this was also most likely the case for AstraZeneca and Johnson & Johnson with their spike protein vaccine). This left them in a bit of a bind; how could the vaccines they were committed to making for Operation Warp Speed be “safe” enough to win the vaccine race and get the market share they wanted?

As far as I can tell from reading the preclinical documents (e.g., this one ), this was initially accomplished by opting out of much of the safety testing on non-human subjects, which would normally be required before proceeding to human studies (e.g., Pfizer was allowed by regulators to exempt itself from testing for autoimmunity or cancer risks). I took this as a tacit admission that it was known that there were serious issues here (given that there were major concerns with these issues and they have since become some of the most common serious complications of the vaccines). In turn, they concluded that their best option was to never formally test for them so they could plausibly deny knowing that the issue existed (this is a common industry tactic) and claim that there was no evidence that the issue exists.

Once the human trials began, the goal shifted to doing everything possible to minimize the number of inevitable adverse events which occurred. This was essentially accomplished by:

• Making it very difficult for trial subjects to report any complications from the vaccines except for a very narrow subset of symptoms that were not a major publicity issue for the vaccine manufacturers. This characterizes both the limited V-safe data (which was still incriminating enough that a lawsuit was needed to get it from the CDC) and the even more limited list of adverse reactions found within the main section of Pfizer’s clinical trial report [fever, headache, fatigue, chills, vomiting, diarrhea, muscle pain, joint pain, or use of a fever medication along with pain, redness, or swelling at the vaccination site]. Furthermore, all of these symptoms were only monitored for 7 days post- vaccination (many vaccine injuries do not occur within this brief window, which was a well known fact prior to the COVID-19 vaccines).

  _Note: the more severe injuries in Pfizer’s study were reported in an extremely vague manner ( see page 9 ), which made it impossible to determine anything._

• Aggressively reclassifying each serious complication as unrelated to the vaccines (typically by claiming it was in fact due to a pre-existing psychiatric condition or COVID-19).

• Avoiding any type of long-term followup on patients which could provide incriminating safety data, regardless of prior commitments to do so.

Because of this strategy, the vaccine manufacturers could not acknowledge any complications that research participants experienced as being related to the vaccines. Instead, all they could do was gaslight the patients into believing that the injury was unrelated to the vaccine, and have healthcare providers collude to create the narrative that the injury was not related to vaccination.

One of the cruel complications of this approach was that it required reneging on the promises that were given to the trial subjects at the start of the research study—any medical complications they received would be covered (because providing any type of help would require acknowledging that there were potential complications from the vaccine). The one, possibly unanticipated, downside of choosing not to help with medical expenses accrued in the trial is that it could solicit the outrage necessary for trial participants to speak out publicly about what happened to them, and for the public to listen…which to some extent has now happened.

All of these potential issues were why the BMJ has repeatedly called for the raw data for the COVID-19 vaccine trials to be released. It is almost certain that the scant clinical trial data we have been provided by the pharmaceutical companies is highly misleading, and that lack of information makes it completely unethical to mandate the vaccines on the population. This is especially true because the lack of data acknowledging the injuries makes it impossible for those who are injured to receive any type of medical care or support (hence, why many providers are now labeling vaccine injuries as long-covid, because it represents the best shot they have of getting help).

The COVID-19 Vaccine Trial Participants

When you review these cases, it does appear that they were all coordinated as a very similar playbook was used on each participant. However, I believe this was more of an emergent phenomenon because very similar things to the approaches used here have occurred in the past. Much of what follows is déjà vu from Merck’s HPV vaccine trials, and to a lesser extent these examples also match what friends of mine experienced with complications from other pharmaceuticals that were already FDA approved (as doctors are often very resistant to believing drugs they prescribed could cause harm).

For example, many of the adverse events shown below were reclassified as being a complication of pre-existing psychiatric conditions, and this has been the default strategy for gaslighting patients throughout the history of medicine . I believe the new emphasis on reclassifying injuries as COVID-19 resulted from a climate of hysteria, where anything could be labeled as COVID-19 and there is enough of an overlap between spike protein injuries from COVID-19 to the vaccine itself, that it could be rationalized that many vaccine injuries were actually due to the virus.

Maddie’s story

To expand the market for the COVID-19 vaccines, a case needed to be made that they were safe and effective for children (who had for all practical purposes a 0% chance of dying from COVID-19). For this reason, we saw a variety of predatory advertisements such as this one from Pfizer:

An individual who was severely injured in the above trial has dedicated her life to making her story known around the world:

Much of the time that went into this article came from editing Maddie de Garay’s story on the Highwire into a shorter version (as I recognize that while the entire presentation is extremely compelling, far fewer people will watch a full episode—as you’d guess it was extremely challenging to decide which parts to cut out of it).

Because of how important I felt this story was for the world to see, I emailed it to Pierre Kory for him to share it (he has a lot more followers), and I would request that you both watch this and consider sharing it as well, because it has a really powerful message:

[

Pierre Kory, MD MPA @PierreKory

Pfizer's trial only vaccinated 1,131 children so a single serious injury would have made the vaccine too dangerous. Maddie's story shows just how far medicine will go to betray and gaslight patients who threaten its narrative. We may never know who else was swept under the rug.

](https://twitter.com/PierreKory/status/1613319015178330113)

Most of what is in this video should speak for itself. A few additional things I’d add though:

• Maddie’s attitude is remarkable. I am genuinely amazed that she is not more bitter about her situation, especially given how healthy and active she was before her injury (it is incredibly difficult for people who have serious injuries to come to terms with what has happened to them, and accept that they can no longer do what they had previously been able to do). Instead, she is almost entirely focused on preventing others from also experiencing her nightmare.

• One of the issues highlighted in the Real Anthony Fauci is that Fauci has developed a network of principal investigators (PIs) to conduct questionable research trials for his drugs.

• There is absolutely no question that Maddie’s PI, Dr. Frenck, knew what her injury was the moment it started (as it had previously been reported in many adults), knew what it meant for Pfizer if the injury was acknowledged by the trial (given how few people were in the trial), and that he had enough influence to shape the medical process which Maddie received so that it would not be something that had to go in the clinical trial report. His choice to initiate this coverup resulted in necessary care (which could have prevented her paralysis) being delayed until it was too late, and he is directly responsible for what happened to Maddie.

• The allergist that Maddie worked with who diagnosed her with a faux condition, Functional Neurological Disorder (FND) to conceal the adverse event, according to Open Payments (a required database for pharmaceutical payments to physicians), from 2015-2021, had received $652,650.65 for associated research funding (with the amount increasing year by year).

• FND is an extremely disingenuous disease that is frequently used to gaslight patients who have received severe neurological injuries. I wrote much more about it here , including how neurologists lack the insight to recognize what they are doing when they authoritatively throw this diagnosis around.

• The experience Maddie had at the hospital was awful, and to some extent surreal, but for length considerations, I cut it from the presentation. Amongst other things, Maddie became much worse after she was at the hospital (e.g., she lost her ability to walk), and believes it was due to her MRI. I periodically encounter people with complex issues who get much worse from MRIs (especially the COVID-19 vaccine injuries). I’ve seen a few explanations for this, and of those, the most likely (but not only) explanation is it being due to the MRI’s contrast agent. Gadolinium is quite toxic for some, but this toxicity is rarely considered in medicine.

• Maddie was very fortunate to have a parent who was a nurse. Similar situations are even worse for those who have no direct experience in health care.

• They also provided the information at the end of the episode for Maddie’s lifefunder .

Brianne’s story

[

A Midwestern Doctor @MidwesternDoc

Exactly what happened in the clinical trials is critical to uncover as they are the basis for the lie the vaccines are safe and all other evidence is "anecdotal." Dressen (and others she's found) were erased and left to fend for themselves once their reactions raised red flags.](https://twitter.com/MidwesternDoc/status/1613370463958212608)

Many of the key points that needed to be made are contained within the above clip (I put two different presentations together). The key points I had to edit out to shorten it were:

• Brianne was actively communicating with the National Institute of Health (NIH) as part of a study for treating COVID-19 neurological injuries, which were repeatedly delayed by the NIH for political reasons (but was eventually published). In that study, they eventually settled on using intravenous immunoglobulin to treat the injury (which interestingly, also sometimes helps HPV vaccine injuries, but is also an expensive treatment requiring a large donor pool, and thus has limits to its scalability ). I wrote more about Brianne’s experience with the NIH and their study here .

• Brianne founded an organization dedicated to helping COVID-19 vaccine injury victims. According to their organization (this was in response to Maddie’s story):

In the longer version of the above presentation, she mentions she and three other individuals injured in the clinical trials (each detailed in this article) all had their injuries classified as something innocuous to conceal them (e.g., Maddie’s injury was functional abdominal pain, Olivia’s T-cell lymphoma was lymphadenopathy). If I find out who the other 3 participants were, I will update the article to include them.

Note: The reason I now post tweets with videos throughout these articles is because Substack only allows videos from a few platforms to be embedded in articles (this matters because most people understandably won’t click through to outside videos). Of those platforms, Twitter is the only one that does not censor or delete controversial videos (I thought Vimeo worked as well, but a month and a half ago Vimeo deleted my entire channel).

Olivia’s story

Olivia’s story is the video at the top of this article (presented in that way due to its length) and in the Rumble video below:

Although her story is very similar to the others, there are a few important takeaway points from Olivia’s story which may not be immediately apparent.

First, for a variety of reasons detailed here, it’s often difficult for doctors to recognize subtle medical injuries unless they have been specifically trained to look for them . Instead, doctors tend to rationalize all of them as being due to psychiatric issues . What is unique about Olivia’s situation is that because everything that happened to her was so unusual, and most importantly, could be directly observed visually (so you could not deny it was happening), outside doctors were actually willing to acknowledge her injuries. Despite that, this is how Moderna’s PI treated her (clipped from the above video):

[

A Midwestern Doctor @MidwesternDoc

If you are injured in a vaccine clinical trial, they will deny your injury, not help you as promised, and not report it. This story is remarkable because Olivia had such strong evidence linking her injury to Moderna, outside doctors agreed, but even then, this is what happened](https://twitter.com/MidwesternDoc/status/1612625075022491648)

Nonetheless, despite it being unambiguous that her injury was due to the vaccine, Moderna did not pay for her medical care as promised, and did not report her injury. Additionally, the clinical trial site director said she would only be able to acknowledge that the cancer Olivia had was linked to the vaccine if “ more research emerged in the future linking it ” even though this happened at the trial that was supposed to determine if this could happen ( note: this example illustrates a common deficit in critical thinking that exists throughout my profession ).

Although her shoulder injury is alarming (and like Maddie, the physical therapy Olivia was forced to go through to “address” it should never have been conducted), the cancer she has is much worse. Based on her history, there is a very strong case that it was linked to her vaccination, and had this been presented in Moderna’s trial report, would have had huge implications for the many patients now developing cancers who are told they cannot possibly be related to the vaccine, and thus these victims are denied the support they need.

Unnamed Moderna Trial Participant’s Story

A while back, I was requested to review 865 vaccine injuries that were submitted in a survey to assess the plausibility thatthe deaths described were due to the vaccine. One of the reports caught my eye since it represented a critical incident that was not reported within Moderna’s trial report (see page 40 ), so I reached out to the doctor (who will remain unnamed) who submitted the report and had good reason to be knowledgeable of this patient’s history.

According to the doctor, the gentleman who passed away was part of the clinical trial at Research Atlanta that was paid for by Moderna. He developed atrial fibrillation after the vaccine, and approximately 3 months after vaccination, he was hospitalized (but never vented or sent to the ICU) at Grady Memorial Hospital (which is very close to the CDC).

At the hospital, he received a CT scan, which revealed blood clots in his lungs. At the time, no one was aware that the vaccine could cause blood clots (both Moderna and the CDC had insisted that the vaccine was safe, and had not revealed it was associated with blood clots). The blood clots were then assessed to have been due to metastatic cancer, as there was no other explanation for them, despite the fact that a full cancer workup was conducted which could not detect any signs of cancer in the patient. The doctor I corresponded with (who I deemed competent to assess this question) is certain that the patient did not have metastatic cancer.

The patient was then assessed to be terminally ill, discharged to hospice, and then died in hospice care (which may have been partly due to respiratory difficulties resulting from the opioids he was given for hospice). As you might expect, the clinical trial contacts were notified of what happened to this patient, but they ignored the report.

Augusto’s Story

Augusto was another clinical trial participant who was abused by Pfizer. Fortunately, he was a lawyer and did everything he could to hold them accountable.

The only direct summary I have found of Augusto’s experience can be found within this (shortened) interview (an article was also written documenting his experience here ):

Although Augusto had the same experience as everyone else (e.g., they tried to say his issues were due to psychological problems and his adverse event never ended up in Pfizer’s final clinical trial report), there were also some remarkable aspects of his case:

• His hospitalization was initially documented by a senior specialist as an adverse reaction to a coronavirus vaccine (although as the previous examples have shown, this did not ultimately change the course of things).

• In addition to the team erroneously reporting the hospitalization which Augusto had directly told them about, the PI who was supervising his case fabricated a medical record to claim Augusto had an anxiety disorder. His injury (a pericardial effusion suggestive of pericarditis) was attributed to COVID-19 (even though Augusto had a negative test) and anxiety (even though anxiety cannot to my knowledge cause a pericardial effusion).

• The PI who was supervising his clinical trial site was also the lead author of Pfizer’s New England Journal of Medicine (NEJM) study . Augusto’s experience and the documentation he had to support the lead author's misconduct is most likely the strongest argument for NEJM retracting Pfizer’s pivotal vaccine study ( note: in addition to the erroneous COVID-19 studies mentioned here, the NEJM also previously published Merck’s highly questionable HPV vaccine study ).

• Augusto obtained the record of another participant who died from a heart attack at the same hospital to which he was admitted, but was not registered in the final Pfizer clinical trial report.

• Augusto formally complained to the Department of Justice about this clinical trial conduct, but the government decided to avoid addressing it, despite their conduct being unlawful.

Pfizer vs. Moderna

Although many things could be said about these cases (which I suspect also holds true for the other ones I am not yet familiar with), one of the things that stands out to me from these reports is the differences in how Pfizer and Moderna conducted their trials.

In Pfizer’s case, they had a robust apparatus in place to have a team of physicians immediately neutralize any claims that the vaccine could be harmful. However, in Moderna’s case, they just told the doctors involved that the events could not be related to the vaccine and most doctors took those claims at face value (as they did not want to believe the vaccine could be harmful). Moderna, in effect, succeeded through inaction (by not documenting injuries or paying compensation for medical care they were obligated to).

I suspect this difference in strategies was due to Moderna being a fledging pharmaceutical company without an apparatus like the one Pfizer had developed over decades. Fortunately for Moderna, their laid-back approach ended up working out just as well since the FDA just rubber-stamped both of their vaccines.

Regardless of the approach that was followed though, I hope this examination into their mutual research misconduct helps to explain how these “impossible to predict” side effects that were never detected in the “robust” clinical trials could have suddenly emerged once the vaccines entered the market.

Conclusion:

Typically, it is nearly impossible to identify clinical trial participants and attempt to re-create what happened within a clinical trial. Due to the diligent work of leaders in this area like Del Bigtree , Aaron Siri , and a few clinical trial participants being brave enough to speak out publicly, we have been able to establish that serious adverse events occurred in all of the spike protein-producing vaccine trials.

More importantly, it should be apparent by now that the FDA has deliberately ignored this misconduct and tried to sweep the known adverse events under the rug. Based on all of this, I can state with near certainty there are other significant adverse reactions that did not make it to the final clinical trial reports.

Note: The fact that news stories like the above (the HPV vaccine trial malfeasance was the focus of the previous article ) received mainstream coverage (e.g., ABC news ) a mere decade ago goes to show just how rapidly the censorship of the media has increased in recent years. It also highlights how consequential failing to report the adverse events from a clinical trial can be for everyone injured after the fact .

Although exactly what degree of underreporting research fraud has occurred will probably never be known unless a legal investigation interviews each participant, as the examples in this article demonstrate, what is already known demonstrates that the vaccines are both ineffective and too dangerous to have on the market. On a more human level, what was done to these trial participants was appalling and needs to be prosecuted, and in the future may even happen if it becomes necessary to restore the public’s willingness to participate in the clinical trials which our medical system depends upon.

A major challenge of politics is catering a message to different political tribes, as each one will support certain messages and vehemently reject others. Most of the work we have done on the vaccine issue has been targeted to further convince those who already have doubts about the vaccines or sway those in the middle (which now represents a large portion of America ). Very little work however has been directed to those who are already committed to the vaccines (since it is largely a lost cause to try to change their minds).

For a variety of reasons detailed in a recent article , I believe the message that has the best shot at reaching those already committed to the vaccines (and motivating congress and the courts to do something) is to prove that fraud was committed by the manufacturers. This is why I attempted to present some of the best evidence we have currently for that assertion here (that Pfizer did not report what is actually in their vaccines). An even more important part of proving that case is showing exactly what actually happened in the clinical trials.

My sincere hope is that this article will inspire others who participated in the trials to come forward, and it is something that can be cited when people (especially doctors) try to argue that the clinical trials proved that the vaccines were “ safe .” I also faintly hope that awareness of this issue can inspire congressional hearings (which did happen previously with the disastrous anthrax vaccines that were forced on the military ). Although I doubt it would ever happen, I believe that the best solution to all the issues outlined in this article is to give trial participants the legal right to sue pharmaceutical companies for compensation if the severe adverse reactions they experience are not included in the final trial report.

Because of the videos, this article was an enormous amount of work to put together. I sincerely believe these stories need to be heard, so if you take the time to listen to them and share the ones that speak to you with others, many would sincerely appreciate that.

Lastly, on a lighter note, one of the practices I occasionally do to calibrate my medical intuition is to guess which fortune cookie best fits each member of a group I am with and then see how accurate the pairings were once they are opened. Sometimes I also go a step further and guess what specific subject the future fortune will address. The one I got today tested as being directed at the readers of this article:

”A dose of adversity is often as needful as a dose of medicine.”

I asked the AI Chat Bot “What was the role of the DoD in covid-countermeasures?” Here is what it wrote:

“The Department of Defense (DoD) played a significant role in the development of countermeasures against COVID-19, the disease caused by the novel coronavirus. The DoD worked closely with other federal agencies, such as the Department of Health and Human Services (HHS), to respond to the pandemic.

One of the main roles of the DoD in the COVID-19 response was to provide logistical support and medical resources to help healthcare workers and first responders on the front lines of the pandemic. The DoD also worked to develop and distribute personal protective equipment (PPE) and other supplies to support the response efforts.

In addition, the DoD provided funding and resources to support the development of vaccines and treatments for COVID-19. The Defense Advanced Research Projects Agency (DARPA), a research arm of the DoD, played a key role in this effort by funding and supporting the development of treatments and vaccines through its "Rapid Response Research" program.

Overall, the DoD played a vital role in the response to the COVID-19 pandemic by providing logistical support, medical resources, and funding for research and development efforts to combat the disease.”

AI Chat Bot gets a “F” - for a highly controlled narrative answer, which was fed to all MSM sources, while the “alternative” media did not examine it very much, with some exceptions. It wasn't just logistics or even just lots of funding, and certainly nobody was “combatting disease”.

The truth is much more interesting than fiction:

All Covid countermeasures, including the biological warfare agents marketed as “Covid-19 vaccines”, were ordered by the US DoD as a “large scale manufacturing demonstration” via Other Transactions Authority contracts.

Hundreds of Covid countermeasures contracts became available via FOIA and SEC disclosures in redacted form.  Review of these contracts indicates a high degree of control by the US Government (DoD/BARDA) and specifies the scope of deliverables as “demonstrations” and “prototypes” only.  In other words, the US Government and DOD specifically ordered a fake theatrical performance from the pharmaceutical manufacturers. Just to make extra certain that the pharmas are free to conduct the fakery, the contracts include the removal of all liability for the manufacturers and any contractors along the supply and distribution chain under the 2005 PREP Act and related federal legislation.

The contracts are structured under Other Transactions Authority (OTA) - OTA method of contracting allows federal agencies to order otherwise-regulated products bypassing any such regulations, as well as financial accountability mechanisms that cover standard government contracting, and other laws that regulate disclosure and Intellectual Property (IP) derived from publicly funded research.

“Other” is a catchall category that is not a contract, not a research grant, not a procurement, etc.: not any normally regulated/accountable government contracting. 

Here is a typical contract scope for “vaccines”:

While the DOD/BARDA countermeasure contracts refer to safety and efficacy requirements for vaccines and mention current Good Manufacturing Practices (cGMP) compliance, these items are explicitly carved out as not being paid for nor ordered by the US Government. 

This gets even more interesting when we examine some of the redactions in contracts:

I know what is in the redacted part of the above paragraph and it was not hard to figure out. The first redaction under 1.1.1 BACKGROUND is “Fosun Pharmaceuticals”, so the sentence reads “Fosun Pharmaceuticals”, Pfizer and BioNTech entered into an agreement for the co-development\u2026”

Note: the only journalist I am aware of in either “mainstream” or “resistance” who mentioned Fosun was Naomi Wolf, kudos to her. I was in touch with The Epoch Times to try to publish this information, and even they decided to bury the story (but they published my other materials). I did discuss this on Dr. Jane Ruby's show, and kudos to her as well for not being afraid to cover the truth.

Pfizer-BioNTech is really a 3-party R&D alliance: Fosun-Pfizer-BioNTech, and by “party” I mean that one of the three is the Chinese Communist Party. Fosun is a huge Chinese conglomerate that owns a large number of global companies, and its chairman Guo Guangchang is a very high ranking member of the CCP. It is curious that the US DoD awarded $10 billion (Pfizer's Operation Warp Speed/DoD/BARDA contract) to a venture whose substantial equity (and IP) holder is the the Chinese Communist Party. For avoidance of doubt:

Below is the timeline of some of the key investments and R&D deals I was able to identify from public SEC shareholder disclosures, immediately preceding and following the “pandemic”:

Just to make sure, we are talking about the exact technology in the mRNA shots. Here is the definition from March 17, 2020 agreement between Pfizer and BioNTech (p. 4):

The same document describes a data sharing agreement, “pharmacovigilance” globally among the 3 parties. They will count the bodies and share the data with each other:

On the “pharmacovigilance” aspect, there is a 4th participant in this arrangement - the Israeli Ministry of Health, which entered into a data sharing agreement with Pfizer on January 6, 2021 and gave Pfizer (and by extension, US DoD and anyone who controls it, BioNTech and anyone who controls it, Fosun and anyone who controls it, i.e. CCP) access to all their citizens' centralized electronic health records. But don't worry, Benjamin Netanyahu promised to keep the data de-identified. Right.

Side note - Israeli government recently “misplaced” the Manufacturing and Supply Agreement with Pfizer mentioned in the data sharing agreement above (so we know for sure it exists). The government sadly cannot find it for some reason\u2026

This gets even larger and more interesting when looking at the sources of “R&D” financing. Turns out, there were numerous financial backers and co-investors in the BioNTech “venture” in the years preceding the global fraud and mass murder exercise. According to Crunchbase, BioNTech, a tiny company with just a handful of employees and NO PRODUCTS or scale manufacturing, raised $1.7B in 9 rounds of investments since around 2008. Large portion of the money, $1B+ was raised before 2020. What was it for, since no big clinical trials or scale manufacturing was happening then? That's a good question, worth examining at some point. Cursory review of some of the investment rounds indicates wide and very international involvement of a variety investors from US, Europe, UK, Australia, South Africa, mainland China, Hong Kong and Singapore among others. These likely included many government actors: “sovereign” funds, pension funds and the like who often do these investments by allocating money to “private venture funds” (limited partners in a private venture funds are confidential). Maybe I will do a separate article on this at a later date.

Note, many people ask me “what about China and Russia?” when I talk about our own government and DoD engaged in mass genocide of Americans. I answered about China - they are allied with the US DoD on this. The CCP is profiting from the financial windfall of the US government printing dollars and throwing them into the mRNA furnaces where they are driving masses of the brainwashed citizens to suicide themselves. China claims to use “traditional vaccines” - if you believe what the Chinese say, I have a bridge to sell you.

I have not seen evidence of any similar alliance with Russia. This makes sense, because ultimately this boils down to the war of US vs Russia using proxies and alliances (as it always does). This does not mean that Russia are “the good guys”. Simply that the owners of Russia (whoever they are, not necessarily based in Russia) disagree with the owners of the US (whoever they are, not necessarily based in the US). Russia is running the same “covid script”, using knock off RNA/DNA injections, probably buying materials from the same suppliers, and also using war to kill off their own younger population. It's just that they are doing it for THEIR OWN interests, not that of the US and their allies.

Back to this western continent - we have already established that “Covid-19 vaccines” are biowarfare agents, legally not medicines, not pharmaceuticals, and not regulated as such.

Use of Emergency Use Authorized (EUA) covered countermeasures under a declared Public Health Emergency cannot constitute a clinical investigation (21 USC 360bbb-3(k)), therefore these countermeasures could not be tested for safety or efficacy in accordance with US law (21 CFR 312 and 21 CFR 601), nor could compliance with current Good Manufacturing Practices (cGMP) or Good Distribution Practices (GxP in general) be enforced by the FDA. 

This legal fact was known to the US Government, DOD, BARDA, FDA, CDC, HHS officials signing the contracts, involved in the OWS, and it was also known to Pfizer, Moderna and other pharma companies. mRNA technology has always been designated dual-use, a category of bioweapons:

From the start, “covid pandemic” was treated by the US Government as a national security matter (i.e. war) and covid policy was set by the National Security Council (assemblage of Defense and Intelligence heads), not HHS.

March 13, 2020: “PanCAP Adapted U.S. Government COVID-19 Response Plan” (PanCAP-A) states that United States policy in response to SARS-CoV-2 is set not by the public health agencies designated in pandemic preparedness protocols (Pandemic and All Hazards Preparedness Act , PPD-44 , BIA), but rather by the National Security Council, or NSC.  NSC does not have regular attendees from public health agencies and its focus is national security and foreign policy matters.\" 

Below is the organization chart from the PanCAP-A document, p.9:

When a known weaponizable tech is given a liability-free, extrajudicial status shielded from all regulations, it's not hard to put 2 and 2 together. The national security, DoD and Intelligence officials absolutely knew all of this. They went ahead and authorized a $10 billion purchase order of this weaponizable tech from the Fosun-Pfizer-BioNTech enterprise (backed by numerous foreign governments including the Chinese), to deliver and deploy it onto Americans, during the time of war.

I think by now it should become clear that the “5th gen warfare” is not just the use of psyops and total control of social media by the FBI and CIA (that's so last century!) It's also not “profits over safety”, “bad FDA overlooked myocarditis” or “big pharma pays politicians for election campaigns”. We are way, way past that. I keep pointing out that if the motive were JUST PROFIT, then the most profitable strategy would have been to ship placebo. They would not be violating any laws by doing so, there would be no adverse events and deaths, the product would look perfectly cGMP compliant, while covid would have gone away quickly by itself. Yet, the governments (plural)-pharma cartel insists on killing and injuring millions of people, obviously limiting the profit potential by doing so.

The current war is the war of the global governments (plural), that only pretend to be at odds with each other, marketing themselves as “left”, “right”, “communists”, “green”, “capitalists”, “socialists”, “populists”, “conservatives”, etc. etc. in a never ending clown show of the political theater. Behind the scenes, the “official enemies” are partners and co-investors into “joint ventures” against us, people of the world. They use taxpayers' money to fund, develop, then “approve”, purchase and deploy prohibited biowarfare agents for killing and injuring their own civilian population, their own armed forces, first responders, healthcare workers, pregnant women and children . To stop this every one of us must start using correct precise language, start calling things what they really are.

This is the fourth part of a series in which Paula Jardine examines how the Covid vaccine programme was conceived by US defence planners nearly 20 years ago as a 21st century ‘Manhattan Project’ for biodefence. You can read Part 1 here, Part 2 here and Part 3 here.

BILL Frist was the 2003-2007 US Senate majority leader who championed the USA’s biodefence projects and promoted the concept of a ‘Manhattan Project’ against a pandemic, described in Parts 1, 2 and 3 of this series. He was also the politician who sponsored the Public Readiness and Emergency Preparedness Act (PREP) Act of December 2005 as soon as the World Health Organisation’s International Health Regulations had been amended to include a provision enabling WHO to declare Public Health Emergencies of International Concern (PHEIC). Critically it was this Act that established indemnity for the manufacturers of therapeutics, vaccines or diagnostics released during the course of a public health emergency against any and all harm caused.

Also working to influence US national biosecurity policy was Dr Robert Kadlec, described in Part 3. Working with him, and principally under the auspices of the Johns Hopkins Centre for Health Security (founded by Dr Tara O’Toole in 1998) were other participants in Operation Dark Winter, the code name for a senior-level situational simulation conducted on June 22-23, 2001, designed to wargame a covert and widespread smallpox bio-terrorist attack on the United States. These biosecurity hawks included O’Toole and Tom Inglesby of the Johns Hopkins Center for Civilian Biodefense Strategies (CCBS).

When O’Toole was nominated some years later to serve in the Department of Homeland Security in 2009, critics warned of her paranoia. Microbiologist Dr Richard Ebright, one of the scientists who, in May 2021, called for a full and unrestricted international forensic investigation into the origins of Covid-19, said it was a disastrous nomination: ‘O’Toole supported every flawed decision and counterproductive policy on biodefense, biosafety, and biosecurity during the Bush Administration. [She] is as out of touch with reality, and as paranoiac, as former Vice President Cheney . . . It would be hard to think of a person less well suited for the position . . . She was the single most extreme person, either in or out of government, advocating for a massive biodefense expansion and relaxation of provisions for safety and security’. Dr Ebright concluded: ‘She makes Dr Strangelove look sane.’

It was Kadlec who formed the Bipartisan Commission on Biodefense in 2014 and began the planning his Manhattan Project in earnest. Those involved with him in this commission included Tom Ridge, the first Homeland Security Secretary, Donna Shalala, a former Health and Human Services (HHS) Secretary, Dr Margaret Hamburg, a former Food and Drug Administration (FDA) commissioner, Scooter Libby,  formerly of Project for a New American Century (PNAC), William Karesh, the vice president of EcoHealth Alliance and an adviser to the WHO on reforms to the International Health Regulations (IHR), and Kenneth Wainstein, now the Under Secretary of Homeland Security for Intelligence and Analysis.

The Commission’s National Blueprint for Biodefense published in2015 called for major ‘reform’. Consider it the blueprint for Kadlec’s Manhattan Project, for the CEPI (Coalition for Epidemic Preparedness Innovations) strategy and for the subsequent changes to the WHO IHR required to make the plan work.

The list of the BioDefense Commissions ‘we must’ demands follows:

·         revolutionise the development of Medical Countermeasures (MCM, which are vaccines and therapeutics) for emerging infectious diseases; 

·         fully fund and incentivise the MCM enterprise; 

·         remove bureaucratic hurdles to MCM innovation; 

·         develop a system for environmental detection that leverages the ingenuity of industry and meets the growing threat; 

·         overhaul the Select Agent Program (which oversees the possession, use and transfer of risky biological agents and toxins) to enable a secure system that simultaneously encourages participation by the scientific community; 

·         help lead the international community toward the establishment of a fully functional and agile global public health response apparatus.

Three years later in May 2018 when Johns Hopkins ran Clade X, a table top simulation around a novel parainfluenza virus, O’Toole was involved once again. Johns Hopkins CHS also co-hosted with the Bill and Melinda Gates Foundation the better-known coronavirus simulation Event 201 in October 2019.

It was during a Clade X discussion on manufacturing capacity sufficient to end the fictitious pandemic through vaccination that O’Toole said: ‘Industry are more than willing to help but vaccines are very specific creatures that are difficult to turn to new purposes. We’re going to have to go to innovative manufacturing methods that will require a lot of leniency from the FDA and the understanding of the American people that we’re doing things on an emergency basis so every box in terms of safety and risk assessment may not be checked. But the vaccine is the only way forward.’ [My emphasis]

This was clear advocacy for vaccines as the exit strategy for the Clade X novel parainfluenza virus pandemic, and later once the Covid pandemic was underway, was to be the only exit offered to lockdown.

Today, O’Toole is an executive vice-president of the CIA spin-off venture capital firm In-Q-Tel in charge of a strategic initiative called BiologyNext. In April 2020 in a presentation to the Centre for Strategic and International Studies (CSIS) she said: ‘The bio-revolution is really founded on several core technologies that I’m going to simplify greatly. But it is all about being able to read, write, and edit the code of life. One of the most important recognitions of the past century in science, at least, is that life is written in code. And as Jason Kelly of Ginkgo Bioworks has put it: Biology is essentially programmable . . .

‘Ron Weiss, who is a synthetic biologist, predicted in 2014 that an RNA-based delivery method that allowed you to use RNA as a kind of platform to deliver new bits and pieces inside the cell would be a game-changing inflection point in synthetic biology. And the Covid-19 pandemic is giving us a chance to test that out. You may know that one of the vaccines that is coming on very quickly is made by Moderna. And it is a messenger RNA-based vaccine. So if that works, Ron Weiss’s prediction may come true.’ [My emphasis]

In August 2019 Kadlec’s department ran yet another table-top simulation, the Crimson Contagion. It simulated the impact of and response to the arrival in the US of an avian flu from China. It was a scoping exercise to identify legal authorities, US federal government funding resources and manufacturing capabilities for vaccines. It concluded that $10billion would be required to respond to a novel pandemic influenza strain.

A month later on September 19, 2019, President Trump signed the Executive Order on Modernizing Influenza Vaccines which launched the Manhattan Project by directing various US government departments and the US Department of Defense to propose a plan and a budget within 120 days – by January 17, 2020, to be precise. 

Anthony Fauci’s diary, released following a freedom of information request, notes a teleconference concerning the ‘Global pandemic’ taking place on January 15, 2020, a date at which a global pandemic existed only in some people’s imaginations.

On January 23, 2020, after the Moderna vaccine announcement in Davos, Fauci had a conference call with Dr Richard Hatchett, CEPI’s CEO, and the following day, a Saturday, he had a senior leadership update with Dr Kadlec in advance of a meeting with Stephane Bancel of Moderna on Monday January 27. Perhaps Kadlec, Hatchett and Bancel were amongst the unnamed people on Fauci’s January 15conference call.

On January 30, 2020, when the WHO declared a SARS CoV2 Public Health Emergency of International Concern, just 7,818 patients were said to be sick with Covid, of whom only 82 were outside China. As far as Kadlec was concerned, this was now a shooting war.

Following CEPI’s announcement in Davos on January 23, US-based manufacturers Innovio Pharmaceuticals were miraculously ready to begin developing a Covid vaccine, and Moderna already had its funding to begin manufacturing the first batch of the vaccine co-owned and co-developed with Anthony Fauci’s National Institute of Allergy and Infectious Diseases (NIAID) for use in a human clinical trial. 

The legislation that he and Frist had shepherded through Congress between 2003 and 2005 had concentrated power in the hands of the US Health and Human Services Secretary (and the US Administration for Strategic Preparedness and Response) during public health emergencies. 

The basic goals of the architects had been achieved. These, the American investigative paralegal Katherine Watt has argued, were to set up legal conditions in which all governing power in the United States would be automatically transferred from the citizens and the three constitutional branches into the hands of one person, the Health and Human Services Secretary, ‘effective at the moment the HHS Secretary himself declared a public health emergency, legally transforming free citizens into enslaved subjects’.

The HHS Secretary Alex Azar, to whom ASPR’s Kadlec reported, was the senior legal counsel at HHS when the PREP Act was passed in 2005. Azar co-operatively declared a public health emergency on January 30, 2020, backdating it to January 27.

He then made a PREP Act declaration on February 4, enhancing liability protection for any person or firm involved in developing countermeasures, including Innovio and Moderna.

The announcement said: ‘The world is facing an unprecedented pandemic. To effectively respond, there must be a more consistent pathway for Covered Persons to manufacture, distribute, administer or use Covered Countermeasures across the nation and the world.’

HHS Secretary determinations are unreviewable by the US courts.

Further research by Katherine Watt into another PREP Act declaration for medical countermeasures by Azar in March 2020 shows it effectively sidestepped the Nuremberg Code by stipulating that the ‘use’ of any counter measures ‘shall not be considered to constitute a clinical investigation’ while also removing the right to informed consent. As there is, by decree, no clinical trial, there are no stopping conditions for the use of said countermeasures.

It is startling how Dr Kadlec and his few associates have, over a period of more than 20 years, managed to orchestrate an undemocratic and unethical bio-security coup with global reach. 

The Manhattan Project was renamed Operation WarpSpeed when it was launched in May 2020. The involvement of the US Federal Government which through the NIAID owns the patent for the spike protein used in the vaccines, and its Department of Defense that ran and financed Operation WarpSpeed, arguably elevates this War on Microbes Manhattan Project to an unprecedented bioweapon attack on humanity using an under-tested novel injectable pharmaceutical.

This is the third part of a series in which Paula Jardine examines how the Covid vaccine programme was conceived by US defence planners nearly 20 years ago as a 21st century ‘Manhattan Project’ for biodefence. You can read Part 1 here and Part 2 here. 

WHEN it comes to the business of vaccines and biosecurity, the land of free enterprise is all up for large-scale state intervention to create and prop up markets.  Some of the generals behind the biosecurity ‘Manhattan Project’ believe the War on Microbes is too important to leave to politicians or Adam Smith’s invisible hand.

In June 2020, former Senator Bill Frist appeared before the Senate Health, Education, Labor and Pensions (HELP) Committee, reminding them he’d argued the need for this project fifteen years earlier. 

‘I called for and had outlined “a greater than Manhattan Project for the 21st century” with no less than “the creation, with war-like concentration, of the ability to detect, identify and model any emerging or newly emerging infection, natural or otherwise; for the ability to engineer the immunization and cure, and to manufacture, distribute and administer whatever may be required to get it done and to get it done in time”,’ Frist told the Senate in his testimony.

‘We have a dangerously inadequate vaccine manufacturing base in the United States. This must be rectified. Bottom line: there’s so little profit and so much uncertainty in vaccine manufacturing today. We must establish longstanding public-private partnerships with industry that are sustained and are not at risk of disappearing with each [Congressional] appropriations cycle.  We cannot expect the private sector to independently invest billions of dollars developing antivirals and vaccines for novel viruses that we hope we’ll never need to use. That’s not a sustainable business model.’ 

For some years to come, Frist asserted, this should be the chief work of the nation, ‘for the good reason that failing to make it so would be to risk the life of the nation’.

Whether this idea originated from Senator Frist is another matter. Dr Robert Kadlec, the ‘General Ripper’ behind this new Manhattan Project, was at that time the leading biosecurity official in President George W Bush’s administration. He was at the April 2005 National Academy of Sciences Pandemic Influenza Symposium where an unidentified participant called for funding for a Manhattan-like Project to protect against a pandemic, calling it an insurance policy. 

But the groundwork for this Manhattan Project was being laid even earlier. In June 2001, two months before the 9/11 atrocity, the Johns Hopkins Center for Health Security (CHS) held a table-top exercise it called Dark Winter, simulating a smallpox bioterrorism attack on the US orchestrated by Osama bin Laden’s Al Qaeda. Dr Tara O’Toole, who founded the CHS in 1998, was the principal designer of the exercise, butKadlec is credited with giving it its name. AColonel Randall Larsen, who’d hired Kadlec to work at the Air War College in the mid-1990s, was another designer of the exercise along with Tom Inglesby, the CHS’s current director. 

Kadlec became the Homeland Security Director of Biosecurity Policy in January 2002 and soonafter attempted to restart the smallpox vaccination programme. In 2004, he launched Project Bioshield, a $5.6billion ten-year programme which created BARDA, the Biomedical Advanced Research and Development Authority. This was intended to motivate US pharmaceutical companies to start developing biodefence products (medical countermeasures which are principally vaccines) ‘by providing a substantial guaranteed market, expediting governmental contracting practices and clarifying FDA regulatory requirements for products used in a public health emergency’. 

Project Bioshield funding enabled the US government to stockpile smallpox and anthrax vaccines manufactured by the companies Bavarian Nordic and Emergent BioSolutions. Both companies and the industry lobby group Biotechnology Innovation Organization were amongst the funders of Kadlec’s Bipartisan Commission on Biodefense he founded ten years later, in 2014, when he was working as a paid consultant to Emergent BioSolutions.The company, founded by Fuad El-Hibri and originally known as BioPort Inc, purchased a vaccine factory and the rights to manufacture anthrax vaccine for the US military in 1998.

On his appointment as Assistant Secretary for Preparedness and Response (ASPR) in 2017, Kadlec failed to declare a conflict of interests on his ethics forms, that in 2012 he and El-Hibri had co-founded an international biodefence company called East West Solutions LLC or that he had been employed by Emergent BioSolutions as a consultant. https://www.help.senate.gov/imo/media/doc/05062020%20Kadlec%20Ethics%20Letter%20Updated%20signed%20pdf.pdf  In September 2019, when Kadlec was ASPR and in control of the US national stockpile, Emergent BioSolutions was awarded a ten-year $2billion contract to replenish the US national stockpile of smallpox vaccine.

Emergent BioSolutions was later subcontracted to manufacture Covid vaccines for AstraZeneca and Johnson & Johnson in the US. However the company’s poor manufacturing standards led to a Congressional investigation being launched in 2021. 

Since Covid, the ‘war on microbes’ has not let up: attention simply moved on to the next opportunity to promote a vaccine. Each outbreak seems to follow the oft-repeated pattern of having been preceded by a Strangelove-like situational simulation based on a fictional scenario. Outbreaks of disease, requiring the WHO to declare a public health emergency of international concern (PHEIC) and public health authorities to announce a vaccination campaign, have a strange knack of occurring soon after the simulation exercises, ensuring the public health community is well prepared in advance.

In December 2020, the Nuclear Threat Initiative (NTI), whose interim vice president is the former US Department of Health and Human Services Secretary Margaret Hamburg, conducted a consultation with experts for a table top exercise on ‘reducing high-consequence biological threats’ in preparation for the exercise to run at the Munich Security Conference in March 2021. The scenario involved a fictitious monkeypox outbreak. Hamburg was herself a player in the June 2001 Dark Winter smallpox table top exercise and is a member of the Biodefense Commission. At the 2021 Munich monkeypox simulation she was joined by a familiar roster of biosecurity figures including the ubiquitous Sir Jeremy Farrar, his old friend George Gao, the then head of the China CDC, Dr Chris Elias of the Bill & Melinda Gates Foundation, US Senator Sam Nunn who played the President in Dark Winter, Luc Debruyne, Vice President of CEPI, Dr Michael Ryan, Director of the WHO Emergencies Programme, with whom Anthony Fauci was in weekly contact in early 2020 during the time that Covid was escalated to a pandemic, and Arnaud Bernaert the WEF’s Head of Shaping the Future of Health and Health Care.

Bernaert, Gao and Elias were involved in Event 201, the coronavirus table top exercise co-sponsored by the Johns Hopkins Centre for Health Security, the Gates Foundation and the WEF in October 2019. In the WEF press release for Event 201 Bernaert said, ‘We are in a new era of epidemic risk, where essential public-private cooperation remains challenged, despite being necessary to mitigate risk and impact. Now is the time to scale up cooperation between national governments, key international institutions and critical industries, to enhance global capacity for preparedness and response.’

In May 2022, the WHO declared a monkeypox outbreak which was escalated to a full-scale Public Health Emergency of International Concern in July 2022. Bavarian Nordic, the Danish headquartered vaccine manufacturer belonging to a Washington-based consortium called the Alliance for Biosecurity, signed a contract with an unnamed European country to supply smallpox vaccines for use as a monkeypox vaccine. The company is a sponsor of Kadlec’s Biodefense Commission, and its largest shareholder is ATP, Denmark’s national pension fund. Other notable entities amongst its top five shareholders include Vanguard Asset Management and Norway’s sovereign wealth fund Norge Bank.

In Part 4 I will examine how Kadlec began preparations for his Manhattan Project two years before the 2016 US Presidential election.

This is the second part of a series in which Paula Jardine examines how the Covid vaccine programme was conceived by US defence planners nearly 20 years ago as a 21st century ‘Manhattan Project’ for biodefence. You can read Part 1 here. 

THE name Robert Kadlec may mean nothing to you, but anyone who has watched Stanley Kubrick’s Cold War era satirical masterpiece Dr Strangelove will quickly get the idea of who this man is. 

Colonel Kadlec is the General Ripper of the War on Microbes. It is no small irony that the Biodefense Commission that Kadlec set up in 2014 is funded by the Hudson Institute, which was co-founded by Herman Kahn, the Rand Corporation war gamer. Kahn’s theory that nuclear war could be deterred if the Soviet Union believed the United States had second strike capability was the inspiration for Kubrick’s Dr Strangelove character and the film.

Kadlecbegan his career as an Air Force physician before he diverted into the world of biological weapons during the first Gulf War of 1990-91. He became an intelligence analyst for the US Joint Special Operations Command (JSOC) on chemical and biological weapons. He subsequently became a member of the UN Weapons Inspection team in Iraq led by Dr David Kelly, who was found dead in 2003.

Kadlec was later (2014) to tell the House of Representatives Committee on Homeland Security that ‘while the United States was victorious in 1991, the scale and scope of Iraq’s biological weapons programme remained elusive despite the most intrusive inspection and monitoring regime ever conceived and implemented by the United Nations Special Commission (UNSCOM).’ 

No conclusive proof was ever found that Iraq had biological weapons, but testimony in 1995 from a defector, Saddam Hussein’s son-in-law Colonel General Hussein Kamel Hassan al-Majid, intelligence which was later assessed as being of limited content and value, maintained the belief of Kadlec and others that they did exist, providing the pretext for the 2003 Iraq War which removed Hussein from power. This belief was no doubt bolstered in part because in the 1980s the Iraqi Technical and Scientific Import Division had (quitelegally) bought samples of an anthrax strain developed by US germ warfare researchers at Fort Detrick, from the American Type Culture Collection, a non-profit organisation in Manassas, Virginia, that provides samples of bacteria and viruses for scientific study. (Arguably the absence of concrete evidence reinforced rather than diminished this belief in the graveness of the threat.)

Between 1993-96 Kadlec served on the US Delegation to the Biological Weapons Convention. His thinking on biowarfare is set out in his contribution to a 1995 Air War College book called Battlefield of the Future. 

In it he argued that biological weapons are the poor nations’ nuclear bombs: they could be made cheaply and easily in facilities with other legitimate purposes, are invisible and, if aerosolised, could be spread over wide areas using an agricultural crop duster. His contention was that they uniquely offered the possibility of ‘plausible deniability’ to the perpetrators because pathogenic agents could be mistaken for naturally occurring epidemics. His particular concern was that vaccines, which are highly specific in what they protect against, take ten to 15 years to develop. 

Wired magazine reported on the US military’s desire for genetic vaccines to make soldiers ‘immune to all known pathogens’ in 1996. As if that wasn’t enough of an aspirational Pandora’s Box, it also reported the military’s desire for the capability of targeting enemy leaders using genetically engineered super pathogens ‘so selective in their behaviour they’re capable of targeting specific individuals, verifying their identities by means of their DNA sequences’. 

It was immediately after 9/11 in 2001 thatKadlec became a special adviser to Defense Secretary Donald Rumsfeld and subsequently appointed Director of Biosecurity Policy in the Homeland Security Department of President George W Bush, where he drafted a document calledNational Biodefense Policy for the 21st Century. This, in April 2004, became the Homeland Security Presidential Policy Directive 10. Kadlec wrote that theUnited States ‘will continue to use all means necessary to prevent, protect against, and mitigate biological weapons attacks perpetrated against our homeland and our global interests’. 

Speaking about the need for a Homeland Biosecurity Policy,President G W Bush said: ‘Armed with a single vial of a biological agent, small groups of fanatics, or failing states, could gain the power to threaten great nations, threaten world peace. America, and the entire civilized world, will face this threat for decades to come. We must confront the danger with open eyes, and unbending purpose.’

Notably Kadlec’s 2018 update of this policy went much further. It declared the extraordinary intent to apply the US approach to countering weapons of mass destruction to all infectious disease outbreaks, naturally occurring or otherwise.

Returning to 2005, this was the year that saw Kadlec attending a National Academy of Sciences Symposium on Pandemic Influenza. This centred on the belief of American public health authorities thatthe recurrence of an influenza pandemic with high mortality was both inevitable and posed a grave threat to humanity. Becauseinfluenza rapidly mutates and is not usually particularly lethal it provideda good research model for biosecurity purposes, not to mention a useful tool for advancing policy objectives. The ubiquitous Imperial College London modeller Neil Ferguson told the symposium that disease containment required ‘a concerted international response – probably with teams on the ground chasing cases’, effectively laying the groundwork for ‘all means necessary’ not to stop at the US border.

Though the 1918 influenza pandemic was originally said to have been caused by H1N1 swine flu, today the US Centers for Disease Control (CDC) says it was caused by ‘H1N1 with genes of avian origin’. This is based onUS Army researchers who claimed in 1999 to have fully sequenced ‘Spanish Influenza’ (using PCR) from autopsy samples taken in 1918 and a sample retrieved from a victim buried in permafrost since 1918. They said the illness was more closely related to avian flu than any mammalian species.

Ferguson’s modelling on avian flu was published in August 2005, claiming that ‘if targeted action is taken within a critical three-week window, then an outbreak could be limited to fewer than 100 individuals within two months’, but if unchecked up to 200million could die. This was just one of his wildly improbable and spectacularly wrong forecasts.

It was claimed that if bird flu mutated to more readily infect humans, the mortality rate would be more than 50 per cent. Bird flu, which first appeared in Thailand’s huge commercial poultry flocks, serendipitously appeared just as an eight-year marathon effort to have the World Health Assembly of the WHO agree key amendments to the International Health Regulations was coming to a close. The significance of these amendments, finally adopted in 2005, is that they included a new provision toenable the Director General to declare Public Health Emergencies of International Concern (PHEIC) on the recommendation of the WHO Emergency Committee. This mirrored the Public Health Emergency provision added to American public health law in 1983. Covid was declared a PHIEC by the WHO on January 30, 2020. 

From 2003 to 2007, only 216 people died from bird flu. The threat and the headline fatality rate appear to have been overstated. Dr Nguyen Tuong Van of Hanoi’s Institute for Clinical Research, who treated some bird flu victims during the 2004 outbreak said, ‘Most people who die of bird flu are poor and not in the best physical condition in the first place.’  

Jeremy Farrar’s 2004 paper on the Vietnamese outbreaks says rapid antigen testing was ‘less sensitive than PCR for diagnosis of influenza H5N1.’ Patients were given anti-viral drugs, mainly Tamiflu, which was developed by Gilead Sciences, a company chaired by Donald Rumsfeld, and almost all were mechanically ventilated, which itself elevates the mortality rate. Tamiflu may have been part of the problem. As a recent review of Tamiflu concludes: ‘A cocktail of pandemic panic, publicity propaganda, and scientific misconduct turned a new medicine with only modest efficacy into a blockbuster. It appears that the multiple regulatory checks and balances gave way as science lost its primacy and pharmaceutical enterprise lost no time in making the most of it.’ 

The 2005 WHO report Avian Influenza: Assessing the pandemic threat  itself makes curious, and occasionally implausible, reading. According to this account, the ‘highly pathogenic’ bird flu, as it was usually described, was being spread asymptomatically by wild waterfowl (airborne bioterrorists to Kadlec’s way of thinking) to the small domestic free-range flocks kept by rural families in Asia, and that these birds were transmitting it to people. The real problem according to the business end of the report was that H5N1 bird flu was so ‘highly pathogenic’ that it was killing the chicken embryos used for flu vaccine manufacture. This made finding new methods of manufacturing them all the more desirable. Even better if these new methods could produce more vaccines, faster. 

Another conundrum, Dr Jesse Goodman of the FDA told the NAS symposium, was the markets.   ‘Markets – that is demand and sales – are the main drivers of manufacturing. No one is going to build factories just for a possible pandemic,’ he said. 

The WHO had convened a meeting in November 2004 with all the major vaccine manufacturers to explore ways in which industry, regulatory authorities, governments, and WHO could collectively speed up the development of pandemic vaccines that could be made rapidly and in as large a quantity as possible. It was argued that wider use of seasonal vaccines would make the vaccines more commercially viable and the resulting increased production capacity would enable manufacturers to pivot production to pandemic strains whenever they should be needed. 

Senator Bill Frist, the Republican Senate Majority leader at the time Kadlec was the leading bioterrorism expert in the Bush Jr Administration, full-throatedly echoed Kadlec’s thinking at the 2005 WEF at Davos, saying: ‘The greatest existential threat we have in the world today is biological. Why? Because unlike any other threat it has the power of panic and paralysis to be global.’  He also asserted: ‘We need to do something that even dwarfs the Manhattan Project,’ the codename for the US effort to devise an atomic weapon during the Second World War. 

Next: Kadlec’s simulation exercises and his conflicts of interest.

In this series, Paula Jardine examines how the Covid vaccine programme was conceived by US defence planners nearly 20 years ago as a 21st century ‘Manhattan Project’ for biodefence.

WHEN Dominic Cummings testified before Parliament in June 2021 and he was asked about the UK Covid Vaccine taskforce, he said: ‘What Bill Gates and people like that said to me and others at No 10 was, “You need to think of this much more like some of the classic programmes of the past – the Manhattan Project in World War Two or the Apollo programme – and build it all in parallel. In normal Government accounting terms, that is completely crazy, because if nothing works out you have spent literally billions building all these things up, and the end result is nothing – you get zero for it, it’s all waste.’

Gates is the promoter, facilitator and profiteer-in-chief of the great vaccine Manhattan Project but he certainly isn’t the originator of it. The call for a biosecurity Manhattan Project dates back to the George W Bush administration.

On July 11, 2019, a think tank called the Biodefence Commission held a panel discussion entitled A Manhattan Project for Biodefence: Taking Biological Threats off the Table. The objective was to ‘create a national, public-private research and development undertaking to defend the United States against biological threats’.

Dr Robert Kadlec, the Assistant Secretary for Preparedness and Response (ASPR) in the US Department of Health and Human Services (HSS) was a panellist. During the discussion Kadlec said, ‘It’s time to say “Go big, or go home” on this issue.’ Covid-19 gave him just the opportunity to implement this Manhattan Project as appears to have been intended. 

Kadlec founded the Biodefense Commission in 2014 when he was a consultant to one of its donors, the vaccine manufacturer Emergent Biosolutions. The Hudson Institute, a think tank co-founded by Herman Kahn of the Rand Corporation, the pioneer of war gaming who was satirised as Dr Strangelove in Stanley Kubrick’s film of the same name, is the Commission’s fiscal sponsor. 

On Wednesday December 4, 2019, the House Committee on Energy and Commerce held its annual hearing on US public health preparedness and response for seasonal and pandemic influenza. Testifying before it were Dr Anthony Fauci of the National Institute of Allergy and Infectious Diseases, Dr Nancy Messonnier from the Centers for Disease Control (CDC), Dr Peter Marks from the Food and Drug Administration (FDA) and Kadlec. 

Seventy-six days earlier,on September 19, 2019, an Executive Order on Modernizing Influenza Vaccines in the United States to Promote National Security and Public Health had been signed by President Trump, directing the National Institutes of Health (NIH), the Biomedical Advanced Research and Development Authority (BARDA), the CDC and the FDA to ‘accelerate the adoption of improved influenza vaccine technologies’. The Departments of Health and Human Services and the Department of Defense were to propose a plan and a budget for this effort within 120 days,  in other words, before January 17, 2020. 

The White House said: ‘Unfortunately, many of the vaccines we use today are produced overseas, using time-consuming, egg-based technology, which limits their effectiveness and makes production too slow to effectively combat a potential deadly influenza pandemic.’ 

Fauci may be the best known of the four witnesses but Kadlec is by far the most consequential. Kadlec, a retired US Air Force Colonel, and former Director of Biosecurity Policy in the George W Bush Administration, is the principal architect of 21st century US biosecurity policy. He said in his testimony: ‘ASPR’s mission is to save lives and protect Americans from 21st century health security threats.’ 

As a member of Bush’s Homeland Security Council he drafted the 2004 National Biodefense Policy for the 21st Century. He was the instigator behind the 2004 Project Bioshield Act that created a strategic national stockpile of anthrax and smallpox vaccines (manufactured by his Biodefense Commission’s funders). In 2005, as staff director to Senator Richard Burr’s Subcommittee on Bioterrorism, hedrafted the 2006 Pandemics and All-Hazards Preparedness Act (PAHPA, pronounced ‘Papa’). This act created the Biomedical Advanced Research and Development Authority (BARDA) and the Assistant Secretary of Preparedness and Response (ASPR) position. The ASPR controls the national stockpile of smallpox and anthrax vaccines and otherpublic health emergency medical equipment such as ventilators. During emergencies this Assistant Secretary has expansive powers enabling him or her to act as the single point of control co-ordinating national response. Kadlec was confirmed as ASPRin August 2017 after being recommended to President Trump by Senator Burr. 

At the December 4, 2019 meeting of the House Committee on Energy and Commerce, Kadlec was asked what his department was doing to enhance American manufacturing capacity. He said: ‘On the issue of vaccines alone, I think the key thing is, I can’t go into the particulars but we’re going to have an announcement here shortly that will indicate some investments domestically to expand some of our newer technologies for vaccine manufacturing and I think the key thing there is, we are actively pursuing this in accordance with the executive order.’ 

Fauci testified that pursuant to Trump’s executive order his agency, the National Institute for Allergy and Infectious Disease (NIAID), was conducting and supporting research into new platform technologies including mRNA. Fauci said: ‘State-of-the-art technologies could be used to develop universal influenza vaccines as well as improve the speed and agility of influenza vaccine manufacturing.’ 

When Kadlec wasasked what the benefits were to the American people of investing in platform technologies such as mRNA he said: ‘The availability of such platform-based approaches would transform national preparedness against currently known threats as well as newly emerging threats in the future.’ Citing theASPR/BARDA funded development of a Zika vaccine made using mRNA technology he went on: ‘This technology has promise as a rapid platform for a number of infectious diseases, including influenza and novel diseases that may emerge in the future. 

The Zika vaccine he referred to was being developed by Moderna, the US-based mRNA gene-therapy biotech. It didn’t have an influenza vaccine in development but it was actively working with Fauci’s NIAID to develop a ‘jointly owned coronavirus vaccine’. A prototype of this vaccine was sent to Dr Ralph Baric, the leading coronavirus expert who has worked collaboratively with Dr Shi Zhenghli of the Wuhan Institute of Virology, for animal testing on December 17, 2019. 

Moderna’s European rival BioNTechannounced in August 2018 that it was in collaboration with Pfizer todevelop an mRNA flu vaccine. It was aiming to move this from the preclinical stage to phase 1 trials by the end of 2020. Professor Dr Ugur Sahin, co-founder and CEO of BioNTech said: ‘A significant presence in infectious disease supports our goal of building a global immunotherapy company that provides more effective and precise immune-mediated approaches for the prevention and treatment of serious illnesses, such as the prevention of flu and the treatment of cancer.’ 

BioNTech diversified from developing cancer therapies – none of which was successfully licensed – into vaccines after a provision in a 2009EU directive intended to enable genetic engineered viruses to be used in vaccines was identified in 2016 and interpreted by them and others as a regulatory loophole enabling gene therapies directed at infectious diseases to circumvent the more stringent and onerous Advance Medicines Clinical Trials protocols. In 2020, this flu vaccine research was pivoted to Covid vaccine research.

Using this regulatory back door, both the UK Medicines and Healthcare Regulatory Agency (MHRA) and the European Medicines Agency (EMA) evaluated BioNTech’s mRNA Covid gene therapies as run-of-the-mill vaccines. The mRNA gene therapies contain no viruses; instead they genetically modify the recipient, reprogramming their cells to produce a protein from the virus that will stimulate their immune system to create a response against the virus, meaning the EU directive should not have been applicable.

During the launch of Coalition for Epidemic Preparedness Innovations (CEPI) at Davos in January 2017, Gates enthusiastically promoted mRNA vaccines. ‘Now there’s a new class of vaccine, DNA / RNA vaccine that we hope we can just change a small part of it, and so the manufacturing facility would already be there, the trials you would go through would be very quick. You would understand what end point, what correlate you want and so in an emergency, the regulators would understand what sort of protocol we’re going to use,’ said Gates.  

‘With Ebola we had a scientific challenge that these platforms weren’t ready, we didn’t understand which country, what type of indemnity, and so there was a lot of fumbling around. It’s only by fixing those regulatory uncertainties and using these new platforms that we have a chance of getting that time to be less than a year.’ 

Gates’s foundation took an equity stake in BioNTech ahead of its October 2019 US stock market launch. When he was asked in 2017 about the danger of these platform vaccines making people less well, he said: ‘You are right that the safety threshold is really, really extremely high because we have to maintain the reputations of all the vaccines, convince parents in all these countries that these shots are really there to help your child out. Anything that you do to healthy people is going to have a tougher standard than, say, a new cancer drug, where if you don’t have the new drug, the outcome is going to be quite negative.’

This tougher standard was soon forgotten. The Pfizer/BioNTech product was pushed into use by the UK Medicines and Healthcare Regulatory Authority (MHRA) on December 2, 2020 using a ‘compassionate use’ mechanism called a Temporary Use Authorisation to bypass the European regulator during the last month that the UK was under European Union law. MHRA reviewed only a few hundred pages of summary data, not the full dossier.

The FDA has a pathway for accelerated approval of ‘vaccines licensed in other countries with competent regulatory authorities.’  p21 Emergency Use Authorisation of the Pfizer/BioNTech vaccine as provided for under the 2004 Project Bioshield Act quickly followed in the US on December 11, 2020 and the European Medicines Authority (EMA) fell into line on December 21.  Kadlec’s long-desired Manhattan Project was now detonating. 

Part 2 of this series will focus on Dr Robert Kadlec, the principal planner of the US’s War on Microbes and of this biosecurity ‘Manhattan Project’.

Multiple people have sent me the same story, on various blogs, in the last 48 hours. Just released medical studies show that mRNA COVID "vaccines" teach the human immune system to ignore and tolerate coronavirus-spike-protein, and also cancer-cells.

 We have multiple kinds of immunoglobulins ("antibodies") that we make to help us maintain health.

• IgM is the rapid-response immunoglobulin, like EMS.
• IgG comes in just before 2 weeks, and is the long-term learned antibody response. There are 4 kinds of IgG examined here, IgG1-4.
• IgG 1-3 antibodies bind to foreign proteins, like viral membranes, coat them, prevent them from working, and prepare them to be chewed-up by certain types of white blood cells. 
• IgG4 is different, a tolerance-antibody, which tags a thing in the body as "Don't-Destroy".

IgG4 responses are appropriate when the body is repeatedly exposed to non-harmful things like ragweed-pollen, which should not be ferociously attacked, because that causes more harm than ignoring them. When a person gets "Allergy Shots" of small amounts of what they are allergic to over a long time, and slowly increasing the amount, they are training this kind of immune response to ignore the allergen.

The Pfizer/Biontech mRNA product is what has been primarily tested, and it is assumed that the Moderna product, being so very similar, has the same effect of inducing IgG4 antibodies to the spike-protein of SARS-CoV2, as well as IgG3 antibodies, "blocking antibodies" early-on. The graphs show that after the first and second shot, the blocking antibodies increase and predominate, but as the months go by, following the second shot, the IgG3 blocking antibodies wane, and the IgG4 tolerance-antibodies increase. 

This is the same time frame that we have seen for the transition from "vaccines" inhibiting the coronavirus initially, but seeming to make infection with the coronavirus more-likely after 5-6 months. The world is now 3 years into this pandemic, and should be over it for the most part, but cases of infection are increasing across the world, notably in the more "vaccinated" countries and cities. The coronavirus levels in city sewage are the highest that they have ever been. in highly-"vaccinated" cities.

After a third "booster" injection of mRNA "vaccine", there is essentially no measurable IgG3, just high levels of IgG4. The immune system has been taught to ignore the SARS-CoV2 spike protein from January 2020. There is more to the virus than the 20% which is the spike-protein. People who caught COVID before getting mRNA "vaccine products" will still have their natural antibodies to the other 80% of the virus, but those who were mRNA "vaccinated" first, will probably have little to no antibodies other than those induced by the injection. Most of the human population has a gaping hole, the very same gaping hole in its immunologic defenses. 

Igor s Newsletter - Booster-Caused IgG4 Immune Tolerance Explains Excess Mortality and "Chronic Covid"

The world is therefore extremely susceptible to an infection which will breach that hole in the defenses of the "vaccinated". An engineered military coronavirus could be designed specifically to exploit that vulnerability, but coronaviruses will naturally mutate to whatever works, and exploit it without laboratory assistance. The current strains of coronavirus in circulation are very contagious, especially to the "vaccinated" and "boosted", but not often fatal, since they do not bind to ACE-2 receptors in the lungs and blood-vessels, as the pre-Omicron strains all did. The Omicron and later strains bind to the upper airways, like a "normal cold".

Arkmedic's blog - Two papers have appeared in quick succession that just need to be put together

Unacceptable Jessica - The immunological mechanism of action for lost immunity, a shift to tolerance and autoimmunity from the shots

Alex Berenson - Do Covid mRNA vaccines damage our ability to control the coronavirus after a booster shot?

The same NK-cells ("natural killer cells") that destroy viral-infected-human-cells also destroy mutated cells which become cancers if they multiply unchecked.

The suppression of this cancer-surveillance function leads to rapid growth of existing cancers. This is seen with people who have been undergoing treatment for cancer, and suddenly worsen after "vaccination" and "boosting". It would also allow new cancers to develop from mutated cells, which would take a little longer to notice, but would present as "suddenly developed cancer". This is happening, too. I recently posted this story below.

Academic Medical Oncologist Angus Dalgleish in the UK has been trying to get government agencies to evaluate the sudden rash of cancer recurrences, new diagnoses and deaths among the "vaccinated". Other cancer specialists agree with me about vaccine harm, but the authorities still won't listen

To summarize the timeline of adverse events we can say that some people get severe reactions like anaphylaxis and heart-inflammation quickly, which may kill them within hours to days. Other clotting disorders may kill them from bleeding, perhaps into their brains, within the first 2-4 weeks following the first or second injection. Production of large blood clots that block the lungs, major arteries, coronary arteries, or arteries feeding the brain, eyes or other vital organs may cause severe disability or death. Autoimmune disease, caused by similarities between parts of the spike protein, and normal proteins in the body, can cause chronic inflammation of organs like the liver and heart. Spike-protein in the bloodstream can cross into the brain, and cause it to be inflamed from autoimmune disease.

The function of the mRNA "vaccine products" is to get into human cells and induce them to produce and release January 2020 COVID spike-protein, which process continues for half a year, based upon spike-protein being found in the blood of "fully-vaccinated" 2-shot recipients at 6 months following the second injection. mRNA usually is degraded by enzymes in human cells after a few minutes, but the mRNA in these "vaccine products" has been modified so that it is not  ever broken down by those enzymes. 

What we see happening is analogous to the person getting "allergy shots" to become tolerant to pollen allergies. There is a long-term presence of January 2020 COVID spike-protein in the bodies of mRNA COVID "vaccine product" recipients. 

It stands to reason that this is what induces the IgG4 "tolerance antibody" response by the immune system. That has not yet been "proven", but it is a useful way to look at what has now been revealed, and it fits well with our understanding. It provides a working hypothesis, unless that hypothesis must later be revised for new information about the mechanisms of action of these experimental products in human immune systems.

Regrets:

Professor Shmuel Shapira, who headed the Israel Institute for Biological Research from 2013 to 2021, and led Israel's domestic coronavirus vaccine development program, has castigated the Health Ministry both over its push to impose lockdowns in 2020 and 2021, as well its support for the mass-vaccination campaign beginning in December 2020.

In a series of tweets, Professor Shapira criticized the Health Ministry for deeming Pfizer s mRNA vaccines safe and effective, and lamented having received three doses of the vaccine himself. "I am telling the unpleasant truth out the vaccine that is neither effective nor safe, " Shapira wrote. "I was wrong 3 times: In the first shot, in the second shot, and in the third shot."

Who said that those who are injected do not admit that they were wrong? People keep forgetting Israel was volunteered as the Lab of the World. There was hardly any data but very brief and minimal size clinical studies.

Global Disaster. Govt. Database Shows 10,000% Increase In Cancer Reports Due To Covid Vaccines. The damage caused by the coronavirus and the halting of studies in Israel (second place in the world) reveal a wave of problems in reading comprehension. So we will explain to you slowly and in easy Hebrew. _Hello First Grade: Those who are opponents and victims of injecting what is ineffective and unsafe are not opponents of vaccines, and certainly not vaccine deniers.

Jessica Rose Ph.D. has more on the cover-up of deaths and adverse events from COVID "vaccination". Information, already released, is "disappeared". Unacceptable Jessica - The lost myocarditis, death, neuropathy and pulmonary embolism safety signals as part of the free text purge from the VAERS Foreign data set

Questions about fertility issues, stillbirths, and neonatal deaths began to be raised last winter when Scotland experienced a month of higher infant mortality than at any time over the past three decades. Then in the spring of 2022, roughly nine months after most young adults were jabbed with the COVID shots, COVID data analysts began noticing unusual drops in birth rates. The hope was that these numbers were just short-term aberrations due to some unknown transient cause. But months later, the evidence is growing too strong to ignore, suggesting a much longer-term problem, which bizarrely has garnered little concern from policymakers, governments, the medical establishment, or the media. It ranks alongside died suddenly both in terms of its magnitude to humanity and the shocking degree of silence in response.

In fact, some media outlets were even celebrating the low birth rates without expressing any curiosity as to the sudden cause.

Sweden is a perfect country to study because it never locked down and should not have been affected socially by the lockdowns. Yet not only did the Swedes experience a sharp decline in births nine months after their vaccination program, the numbers are further deteriorating over time.

Furthermore, any hypothesis as to the cause of the plummeting birth rates would also have to logically account for the rise in neonatal deaths. For example, lockdowns would not explain why the babies being born are experiencing more health problems. The spike protein embedded in the babies blood, however, would.

Israeli researcher Josh Guetzkow obtained neonatal death data from Israeli health insurance fund Maccabi, which covers 25% of Israelis. He found a tripling of neonatal deaths in two of the quarters post-vaccination.

What if the  world is "sane" but the owners want to quietly kill half of us? In a sane world, the makers of these therapies would be behind bars, but instead they are getting a promotion to concoct even more products with this same dangerous technology.

Typically, failure of a corporate partner is an impetus for a government to break the partnership. In the case of vaccines, however, the more they fail, the more they are elevated, subsidized, and even mandated. Unless their definition of failure is the opposite of how humanity would define it.

Biomedicine (Taipei). 2022; 12(3): 1–4.

• Published online 2022 Sep 1. doi: 10.37796/2211-8039.1371
• PMCID: PMC9629406
• PMID: 36381188

Covid 19 vaccines and the misinterpretation of perceived side effects clarity on the safety of vaccines

Raymond D. Palmera,b

Raymond D. Palmer

• Full Spectrum Biologics, South Perth, WA, 6151, Australia
• Full Spectrum Biologics, WA, 6102, Australia
• Find articles by Raymond D. Palmer
• [E-mail address: moc.em@remlap.yar.
• Received 2022 Mar 12; Revised 2022 Apr 20; Accepted 2022 May 4.
• Copyright © the Author(s)

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

Abstract

In the era of Covid 19 and mass vaccination programs, the anti-vaccination movement across the world is currently at an all-time high. Much of this anti-vaccination sentiment could be attributed to the alleged side effects that are perpetuated across social media from anti-vaccination groups.

Fear mongering and misinformation being peddled by people with no scientific training to terrorise people into staying unvaccinated is not just causing people to remain susceptible to viral outbreaks, but could also be causing more side effects seen in the vaccination process. This brief review will offer data that may demonstrate that misinformation perpetuated by the anti-vaccination movement may be causing more deaths and side effects from any vaccine.

A mini review of published literature has been conducted and found that mental stress clearly causes vasoconstriction and arterial constriction of the blood vessels. Therefore, if subjects are panicked, concerned, stressed or scared of the vaccination, their arteries will constrict and become smaller in and around the time of receiving the vaccine. This biological mechanism (the constriction of veins, arteries and vessels under mental stress) is the most likely cause for where there has been blood clots, strokes, heart attacks, dizziness, fainting, blurred vision, loss of smell and taste that may have been experienced shortly after vaccine administration. The extreme mental stress of the patient could most likely be attributed to the fear mongering and scare tactics used by various anti-vaccination groups.

This paper does not aim to rule in or out every side effect seen, but it is highly likely that many apparent side effects seen shortly after a subject has received a vaccine could be the result of restricted or congested blood flow from blood vessel or arterial constriction caused by emotional distress or placebo based on fear around vaccines.

Keywords: Covid 19, Vaccines, Side effects, Misinterpretation, Ischemia, Stress, Cardiovascular

Introduction

Vaccines introduced in late 2020 or early 2021 were closely watched, scrutinised, and monitored by the world’s mainstream population due to their fast to market delivery. Subsequent health concerns were quickly made public across social media and news outlets driving further vaccine hesitancy. One of the most common health concerns was that various types of Covid 19 vaccines were causing strokes or blood clots. The science for the vaccines causing blood clots has not been found, but other causes for this cascade from vaccines to blood clotting events may be found in existing medical literature.

Covid 19 vaccines use many of the same ingredients that have been safely used for many years, with the only major difference being the mRNA [1,2]. However, anti-vaccination sentiment and side effects are at an all time high, and this may point to a statistical significance.

Vaccines include antigens that produce an immune response which is adept at providing protection from disease [3]. However, reactogenicity from vaccines is very rare according to Herve et al. and mostly associated with mild irritations or other discomfort at the site of injection. Once vaccine antigens enter the body, they are distinguished as pathogens by the body’s immune system, the pathogen-associated molecular patterns (PAMPs) or damage-associated molecular patterns (DAMPs), pattern-recognition receptors (PRRs), including Toll-like receptors (TLR) that are located on peripheral circulating immune cells [3,4].

Even though the likelihood of mental stress causing strokes, heart attacks or blood clots may at first appear unlikely, a brief investigation of current medical literature clearly shows that simple tasks under clinical observing conditions such as public speaking can induce serious adverse outcomes [5]. Krantz et al. demonstrated that subjects with ischemia from mental stress experienced cardiac episodes more frequently than subjects without mental stress ischemia (8 of 34; 23%; p = 0.048).

Mental stress-induced myocardial ischemia (MSIMI) is a condition where blood flow to the heart is restricted due to emotional distress. MSIMI has been found to be more severe in females when peripheral blood vessels are constricted [6]. If MSIMI results in ischemia, it can also double the chance of a heart attack or death in subjects where heart disease is present [7]. Jiang et al. found a significant increase in nonfatal and fatal cardiac events in subjects with MSIMI.

It has been found that the level of microvascular constriction but not the angiographic burden of coronary artery disease (CAD) is correlated with MSIMI [8]. Patients with CAD and exercise induced ischemia (EII) with the existence of MSIMI were highly predicted to undergo a loss of life event [9].

Visceral arteries are also implicated in constriction from mental stress. Notably the renal artery showed decreased blood flow during mental stress testing [10]. The superior mesenteric artery (SMA) did not display any significant difference according to Hayashi et al. The findings of renal artery constriction also may lead into serious downstream kidney events. This data clearly indicates that mental stress can prevent blood flow far beyond the cardiovascular system inducing many other aberrations.

Adverse cardiovascular events that were reported from Covid 19 vaccines have been monitored closely by The World Health Organisation (WHO) [11]. Of those events, palpitations (717(14.74)), increased heart rate (439 (9,03), flushing (592(12.17) and tachycardia (798 (16.41)) were all reported as having the highest rate of incidence. However, Kaur et al. does not find any causality from the vaccines listed. Furthermore, restricted blood flow or blockages caused by MSIMI inducing vasoconstriction could be the smoking gun in all the aforementioned conditions such as palpitations, increased heart rate, flushing and tachycardia [12,13].

Vaccines monitored by Kaur et al. were Comirnaty (BNT162b2), Moderna COVID-19 Vaccine (mRNA1273), COVID-19 Vaccine AstraZeneca (AZD1222); also known as Covishield, Sputnik V, COVID-19 Vaccine Janssen (JNJ-78436735; Ad26.COV2.S), CoronaVac, BBIBP-CorV, Epi-VacCorona, Convidicea (Ad5-nCoV), Covaxin, CoviVac, ZF2001.

Moreover, vasoconstriction could also result in hyperpnea, postural faint, light headedness or dizziness which have all been included as possible side effects from the Covid 19 vaccines [14,15]. Post vaccine smell and taste disorders have also been implicated as side effects of Covid 19 vaccines, however both these disorders may be attributed to blood flow disorders from mental stress induced vasoconstriction [16].

The litany of suspected or perceived side effects discussed here from Covid 19 vaccines correlates firmly with well-established vasoconstriction disorders where blood flow is reduced or blocked completely. MSIMI is found in 70% of people with CAD [17], and it is predicted that approximately 16.3 million Americans above the age of twenty have CAD. Notably The American Heart Association (AHA) reports that approximately 82.6 million people in the United States have some form of cardiovascular disease [18]. When MSIMI is combined with these conditions, it presents a further aggravated risk for mortality.

The data presented herein, poses an interesting question, is the fear mongering around vaccines causing many of these perceived side effects by inducing unnecessary stress in vulnerable people? Is the movement and character of anti-vaccination information that may strike fear into the general population causing anxiety and vascular constriction resulting in pathologies such as dizziness, hypernea, fainting, blood clotting, stroke and heart attack? The science discussed here clearly establishes that anxiety and fear causes vasoconstriction disorders, and that a particular movement that is trying to save people with a profound lack of scientific and medical training (the anti-vaccination movement) from vaccine side effects may actually be the entity causing the majority of side effects.

Sullivan et al. had demonstrated that MSIMI was found to be more dangerous in females when peripheral blood vessels were constricted. When females underwent a tonometry exam the average ratio was associated at 0.11–0.35, just over a threefold ratio [6]. The Centre for Disease Control (CDC) also found that there was approximately between a three and fourfold increase in females reporting adverse side effects than men from the Covid 19 vaccine [19]. The numbers reported from the CDC were 4296 adverse side effects from females, and 1056 from men. The parallel in this data is quite clear, and may profoundly exonerate Covid 19 vaccines as ground zero for the perceived side effects and implicate the well established and studied condition of MSIMI and other blood flow conditions as the smoking gun.

Apart from MSIMI and other cardiac impairments discussed here, the placebo effect is also a strong marker in potential side effects, as the belief in detrimental side effects (the nocebo effect) can cause detrimental side effects [20]. It has also been shown that the placebo effect can be so powerful that it can affect end-organ functions that are controlled by the autonomic nervous system [21]. Both the placebo and nocebo effect are both noted here due to MSIMI being caused by mental stress, that is the connection between mental state and biological disorder which is already well established across the literature. This shows major cause for concern where fear mongering around vaccines is being perpetuated, as those with expectations of getting adverse side effects may increase their risk of experiencing adverse side effects [22].

Obesity may also play a role in poor outcomes for Covid 19 vaccines [23]. Obese subjects also appear to be at higher risk of MSIMI [24] which is consistent with this paper’s findings. An increase in adverse reactions was also found in obese subjects when using the Pfizer vaccine [25]. Obesity or poor arterial health may heighten the chances of a vaccine side effect.

Conclusion

This mini review finds that subjects with a history of heart disease, obesity, poor health combined with extreme stress or fear of vaccines should visit their medical practitioner and discuss the use of therapies or medications such as vaso or arterial dilators or possibly anticoagulants prior to their vaccines, as these measures under professional guidance may assist in maintaining healthy blood flow through a subject’s system and may offer benefits to ensure adverse reactions from underlying health conditions are not confused with adverse reactions from vaccines.

All data or claims of adverse reactions from vaccines should first be weighed against a subject’s health history with a focus on their vascular and arterial systems, cardiologic fitness and propensity for mental stress induced ischemia.

This brief review is not exhaustive but finds that it is highly probable that many adverse reports from recent vaccines are associated with vasoconstriction in conjunction with MSIMI or CAD.

This paper also presents the opportunity for governments to peer back into the claims of adverse vaccine side effects and weigh up the volume of existing health conditions that many of those subjects may have had. If it can be established in a high volume of cases of apparent side effects that CAD, HD, MSIMI or EII were present, then the adverse reactions can be laid against emotional distress or anxiety as opposed to the vaccines. The cause or source of that emotional distress and fear must then be investigated, recognised, and managed for future vaccination programs. Humanity on average has experienced a viral outbreak every two years for the last decade. So, managing this alarmism over perceived vaccine side effects is paramount in delivering fast to market solutions for future vaccination programs.

Limitations of study

This review is limited by primarily focusing on vasoconstriction conditions caused by a stress response, and also by a lack of large-scale clinical trial studies to determine whether using novel combinations of vasodilators or anticoagulants with vaccines could reduce vaccine side effects, which may also assist in clarifying whether side effects were emanating from vaccines or conditions such as MSIMI. Further investigation into whether side effects could be attributed as a stress response is required.

Footnotes

• Dates Written - Monday, 22 November 2021.
• Contributors - Raymond D Palmer.
• Conflict of interest - Raymond D Palmer is Chief Science Officer of Full Spectrum Biologics.

References

1. Polack FP, Thomas SJ, Kitchin N, Absalon J, Gurtman A, Lockhart S, et al. Safety and efficacy of the BNT162b2 mRNA covid-19 vaccine. N Engl J Med. 2020;383(27):26032615. doi: 10.1056/NEJMOA2034577. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

2. Kaur SP, Gupta V. COVID-19 Vaccine: a comprehensive status report. Virus Res. 2020;288:198114. doi: 10.1016/J.VIRUSRES.2020.198114. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

3. Hervé C, Laupèze B, Del Giudice G, Didierlaurent AM, Da Silva FT. The how’s and what’s of vaccine reactogenicity. NPJ Vaccines. 2019;4(1):1–11. doi: 10.1038/s41541-0190132-6. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

4. Beutler B. Microbe sensing, positive feedback loops, and the pathogenesis of inflammatory diseases. Immunol Rev. 2009;227(1):248–63. doi: 10.1111/J.1600-065X.2008.00733.X. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

5. Krantz DS, Santiago HT, Kop WJ, Merz CNB, Rozanski A, Gottdiener JS. Prognostic value of mental stress testing in coronary artery disease. Am J Cardiol. 1999;84(11):1292–7. doi: 10.1016/S0002-9149(99)00560-3. [PubMed] [CrossRef] [Google Scholar]

6. Sullivan S, Hammadah M, Al Mheid I, Wilmot K, Ramadan R, Alkhoder A, et al. Sex differences in hemodynamic and microvascular mechanisms of myocardial ischemia induced by mental stress. Arterioscler Thromb Vasc Biol. 2018;38(2):473–80. doi: 10.1161/ATVBAHA.117.309535. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

7. Vaccarino V, Sullivan S, Hammadah M, Wilmot K, Al Mheid I, Ramadan R, et al. Mental stress induced-myocardial ischemia in young patients with recent myocardial infarction: sex differences and mechanisms. Circulation. 2018;137(8):794. doi: 10.1161/CIRCULATIONAHA.117.030849. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

8. Ramadan R, Sheps D, Esteves F, Zafari AM, Bremner JD, Vaccarino V, et al. Myocardial ischemia during mental stress: role of coronary artery disease burden and vasomotion. J Am Hear Assoc Cerebrovasc Dis. 2013;2(5) doi: 10.1161/JAHA.113.000321. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

9. Sheps DS, McMahon RP, Becker L, Carney RM, Freedland KE, Cohen JD, et al. Mental stress-induced ischemia and all-cause mortality in patients with coronary artery disease: results from the Psychophysiological Investigations of Myocardial Ischemia study. Circulation. 2002;105(15):1780–4. doi: 10.1161/01.CIR.0000014491.90666.06. [PubMed] [CrossRef] [Google Scholar]

10. Hayashi N, Someya N, Endo MY, Miura A, Fukuba Y. Vasoconstriction and blood flow responses in visceral arteries to mental task in humans. Exp Physiol. 2006;91(1):215–20. doi: 10.1113/EXPPHYSIOL.2005.031971. [PubMed] [CrossRef] [Google Scholar]

11. Kaur RJ, Dutta S, Charan J, Bhardwaj P, Tandon A, Yadav D, et al. Cardiovascular adverse events reported from COVID-19 vaccines: a study based on WHO database. Int J Gen Med. 2021;14:3909. doi: 10.2147/IJGM.S324349. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

12. Clementy N, Fourquet A, Andre C, Bisson A, Pierre B, Fauchier L, et al. Benefits of an early management of palpitations. Medicine (Baltim) 2018;97(28) doi: 10.1097/MD.0000000000011466. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

13. Heusch G. Heart rate in the pathophysiology of coronary blood flow and myocardial ischaemia: benefit from selective bradycardic agents. Br J Pharmacol. 2008;153(8):1589. doi: 10.1038/SJ.BJP.0707673. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

14. Taylor S, Asmundson GJG. Immunization stress-related responses: implications for vaccination hesitancy and vaccination processes during the COVID-19 pandemic. J Anxiet Disord. 2021;84:102489. doi: 10.1016/J.JANXDIS.2021.102489. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

15. Taneja I, Medow MS, Glover JL, Raghunath NK, Stewart JM. Increased vasoconstriction predisposes to hyperpnea and postural faint. Am J Physiol Heart Circ Physiol. 2008;295(1):H372. doi: 10.1152/AJPHEART.00101.2008. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

16. Lechien JR, Diallo AO, Dachy B, Le Bon SD, Maniaci A, Vaira LA, et al.COVID-19: postvaccine smell and taste disorders: report of 6 cases. Ear Nose Throat J. 2021. Published online. [PubMed] [CrossRef]

17. Mental stress-induced myocardial ischemia: an under-recognized cardiac risk factor? American college of cardiology; [Accessed 1 December 2021]. https://www.acc.org/latest-in-cardiology/articles/2014/07/18/18/35/mental-stress-inducedmyocardial-ischemia-an-underrecognized-cardiac-risk-factor . [Google Scholar]

18. Roger VL, Go AS, Lloyd-Jones DM, Adams RJ, Berry JD, Brown TM, et al. Heart disease and stroke statistics–2011 update: a report from the American Heart Association. Circulation. 2011;123(4) doi: 10.1161/CIR.0B013E3182009701. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

19. Gee J, Marquez P, Su J, Liu R, Myers T, Nair N, et al. First month of COVID-19 vaccine safety monitoring — United States, December 14, 2020–January 13, 2021. MMWR Morb Mortal Wkly Rep. 2021;70(8):283–8. doi: 10.15585/MMWR.MM7008E3. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

20. Wager TD, Atlas LY. The neuroscience of placebo effects: connecting context, learning and health. Nat Rev Neurosci. 2015;16(7):403. doi: 10.1038/NRN3976. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

21. Meissner K. The placebo effect and the autonomic nervous system: evidence for an intimate relationship. Philos Trans R Soc Lond B Biol Sci. 2011;366(1572):1808–17. doi: 10.1098/RSTB.2010.0403. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

22. Benedetti F, Carlino E, Pollo A. How placebos change the patient’s brain. Neuropsychopharmacology. 2011;36(1):339–54. doi: 10.1038/NPP.2010.81. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

23. Kipshidze N, Kipshidze N, Fried M. COVID-19 vaccines: special considerations for the obese population. Obes Surg. 2021;31(8):1. doi: 10.1007/S11695-021-05404-Y. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

24. Soufer R, Fernandez AB, Meadows J, Collins D, Burg MM. Body mass index and risk for mental stress-induced ischemia in coronary artery disease. Mol Med. 2016;22:286. doi: 10.2119/MOLMED.2016.00128. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

25. Menni C, Klaser K, May A, Polidori L, Capdevila J, Louca P, et al. Vaccine side-effects and SARS-CoV-2 infection after vaccination in users of the COVID Symptom Study app in the UK: a prospective observational study. Lancet Infect Dis. 2021;21(7):939–49. doi: 10.1016/S1473-3099(21)00224-3/ATTACHMENT/05D885CC-88B3-43A5-BE70912E3DD2F3A6/MMC1.PDF. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

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One of the patterns you observe at every level in nature is that there are niches: Roles to play in an ecosystem that allow you to survive for an extended period of time. As you enter a niche and begin to dominate it, your environment will polish you like a raw gem, until eventually you perform your role in an optimal manner.

There’s this example, of Fortune 500 multinational corporations, which signal the pride flag in Western nations, but not in the Middle East or Africa. Institutions don’t really hold beliefs. Rather, they attempt to fit into their local niche through mutation. In the West that means the Catholic church for example will pretend to be OK with homosexuality. Corporations can go a step further, unbound by tradition they can proclaim they’re all in favor of all sorts of stuff.

Natural selection operates on institutions along with organisms. The Catholic church has survived for 2000 years, because it always sought to maintain appeal to wide sections of society. And so although it technically teaches you can go to hell for masturbation, it can simultaneously uphold an impression of having no real qualms with homosexuality anymore. The truth is that it will teach whatever its environment requires it to teach.

Religions are like viruses that infect the mind, they can be benign or virulent, depending on the environment they find themselves in. They also compete for hosts. Virulent versions like Salafism or Mormon fundamentalism can destroy lives, as patriarchs will end up marrying teenage girls and raping their own sons. These religions suffer from interference however. A more benign version like Hinduism, Buddhism, Evangelical Christianity or Catholicism will prevent such a highly virulent version from finding a host for itself.

As the population’s immune system develops, as people begin to recognize the damage caused to their society by virulent expressions of a religion, it becomes forced to evolve towards more benign forms, as its alternative is extinction through aggressive rejection. The Catholic church became more tolerant over time, as its alternative was to go extinct. Dutch priests who spend their days bemoaning unmarried couples living together, or homosexuality, or emphasizing other such doctrines tend to alienate what little flock they have left. Survival thus only happens insofar as the system purges more virulent variants of itself.

Once a religion becomes too benign however, once it ceases to control its followers lives, it risks moving towards extinction. If it’s benign enough to tolerate birth control, it becomes harder to produce new adherents. If it’s benign enough to cease warning people of hell, it’s benign enough for people to stop bothering with proselytizing. If a society’s immune system has grown sufficiently intolerant of the religion, it can drive it into extinction, but its myopic focus on its target can lead it to be blindsided by more virulent primitive versions that move into its host.

LGBTQI+ can be thought of as a competing religion that the immune system doesn’t recognize as a danger. It has its own theological doctrines reminiscent of neoplatonism, with people who have pre-existent “male” or “female” essences, that can be born into the “wrong body”, which can be solved through surgical and hormonal alterations to produce the “right body”, congruent with the pre-existing “gender identity”. It’s a religion shrouded in mystery that takes hold in societies that have eliminated competing religions.

Organisms tend to manipulate their environment to favor their own proliferation. If you have lactic acid bacteria and yeast in dough, they create the kind of PH and other environmental conditions that make it impossible for other organisms to conquer the bread. Similarly, religions try to create the kind of environment in which they can sustain themselves. For Catholicism this means abortion is eliminated, along with Internet porn. This then leads people to seek out sex with others, which leads to pregnancy, often unplanned, which then forces young people into the nuclear family framework that is compatible with Christian culture.

LGBTQI+ similarly creates an environment compatible with its own proliferation. You bombard social media with beautiful girls, so that the other girls start feeling insecure, they dissociate from their gender, feel unattractive to men and consider lesbianism or “non-binary” gender and associated solutions to their situation. Similarly, proliferation of Internet porn creates perverse sexual fetishes in men, which also helps proliferate the religion. Islam does similar things: By encouraging polygamy, the religion creates a deficit of women that men can have marital relations with. Those men are then encouraged to go out and conquer other communities.

This is basically the mob principle. You have different mobs to which you can pay protection money. The benign mob shatters your store’s window, the more virulent variants leave a horse’s head in your bed. If you pay the benign mob, it will help you avoid having to deal with the virulent mob, as they don’t wish to lose their milk cow.

But if you zoom in deep enough, at the level of self-replicating genetic material, you also encounter this principle. Before SARS-COV-2, there were four known corona viruses that regularly occupy our body. Those viruses are a product of natural selection. Their ancestors would have been relatively virulent, they would have injured or killed quite a few people they infected.

People who were infected with virulent variants of these viruses, would develop immunity that is relatively long-lasting and aggressive. People who were infected with more benign variants on the other hand, would develop less aggressive immunity. This would open them up to tolerance of the virus, or it would enable reinfection. Over time, the population would develop immunity against epitopes associated with virulence. And thus over time the four corona viruses known to infect our species became relatively benign, as is generally the case for all respiratory viruses capable of reinfection.

You don’t need the whole population to have immunity against every single epitope associated with virulence. In fact, a homogeneous immune response against anything is quite dangerous. Rather, you just need to make sure that every epitope associated with virulence, invokes a sufficiently aggressive immune response in a portion of the population, that more benign alternative varieties end up with a fitness advantage. When one in every ten shopkeepers shoots a mob guy who threatens him with a gun, variations of the mob that simply break your window will have a selective advantage.

The four known hCov viruses need to be thought of as benign domesticated versions of religion. You could think of a version of LGBTQIA+ that ceased believing in making fake penises out of forearm skin but now simply encourages girls to have boyish haircuts, or a version of Mormonism that ceased believing in polygamy. Through interference, these benign versions prohibit more virulent versions from spreading themselves. When you create a vacuum on the other hand, when you leave the niche unoccupied, it’s conquered by whatever shows up first, which tends to be something that aggressively replicated itself without consideration for its host.

The hCov viruses are capable of causing asymptomatic SARS-COV-2 infections, or preventing infection altogether. They are benign versions of the mob, that prevent SARS-COV-2 from spreading itself. Other viruses like rhinovirus also show such an effect. The social distancing experiment could be thought of as an attempt at State Atheism, that basically sought to ban all religions. Then once the experiment ended, Salafist extremism rapidly became the new form of Islam.

Rather than eliminating SARS-COV-2 through its social distancing experiments, Germany appears to have succeeded at almost eliminating the hCov viruses. The social distancing experiments would have caused a genetic bottleneck for these viruses. Whatever versions then survived were no match for the rapidly expanding genetic diversity and increasing ACE2 affinity of novel SARS-COV-2 variants. Just as the hCov’s interfere with SARS-COV-2, SARS-COV-2 interferes with its four cousins. And so the result could be a virological state shift: Just as a jellyfish dominated ocean creates the kind of conditions in which fish can’t replenish themselves, SARS-COV-2 can prevent the hCov’s from reestablishing themselves.

And so now you’re dealing with a situation where you chased the old mob out of town, only to be met with a new mob that is far more cruel. And when it comes to the process of viral domestication, people have been far too optimistic. You can go back a year and see how everyone hailed the arrival of Omicron as the end of the pandemic, yet today your excess mortality in the EU is higher than it was in 2021 and 2020 for the same period. The virus became less virulent but better capable of spreading itself. It is now readily returning to higher levels of virulence, as there is simply no proper discrimination against virulence-associated factors yet due to the mass vaccination program.

Medieval Europeans had wolf bounties, you could be paid for exterminating wolves, as they were recognized as dangerous animals that kill people and livestock. This is how wolves were exterminated in multiple countries. The same thing was done to bears, people received bounties for killing bears, which drove Norwegian bears into near extinction by the 1920’s. To such people, the idea that we would eventually regret extermination bears or wolves, that we would come to recognize them as vital elements of our ecosystem, would have been unthinkable.

In a similar manner, I’m quite convinced that as the global SARS-COV-2 experiment continues, along with the LGBTQI+ experiment, people will eventually start to look for ways to reign in the effect that these virulent viruses have on our population. There is a live vaccine against SARS-COV-2, that naturally spreads through populations. It’s called an hCov virus. How much genetic diversity of these viruses have we already lost? There may be rare variants out there, now lost to time, that would have infected people who were now infected with SARS-COV-2.

With every new virus that infects a population, it remains to be seen whether it is capable of losing its virulent characteristics. We’ve seen with Islam numerous times throughout history that virulent forms resurface. We’re biased by the anthropic principle: Viruses that don’t lose virulence would have wiped us out, so we wouldn’t be around to observe them today.

It could be that LGBTQI+ can’t lose its virulence, that installing fake penises on insecure teenage girls or making surgical wounds in porn-addicted nerds is a kind of fundamental pillar of this religion that no mutation can eliminate. LGBdroptheT was an attempt at producing a less virulent version of the religion, but it doesn’t get far.

Similarly, there’s no strict guarantee that SARS-COV-2 can lose its virulence. We fundamentally just don’t know. If virulence enables reinfection by killing or damaging T-cells, or if the virulence is tied to the furin cleavage site and losing that site creates a massive transmission disadvantage, then it’s possible to see a scenario in which this is just a permanent burden on our population that reduces life expectancy and accelerates the aging process for the rest of human history.

In that case, your best option may be something akin to rewilding of European nature. Rather than continuing the catastrophic social distancing experiments which attempt to artificially maintain a vacuum, you could become witness to intentional seeding of the hCov viruses. For those viruses to receive a helping hand in their natural role of functioning as a benign version of the mob against more cruel corona viruses that jump into our species from other animals could then enable them to move SARS-COV-2 towards extinction, aided by our own buildup of immunity against virulence associated epitopes over time.

Does this sound strange to you? Well then I would ask you: What do you think the polio virus vaccines are? They are an attempt to reduce the health impact of polio, by spreading more benign versions of the polio virus. Instead of 5000 cases of paralysis per million infections, these benign versions cause 3 cases per million. And similarly, the hCov’s are benign corona viruses that have withstood the test of time: We know they won’t spontaneously revert to some malignant form.

Attempts to eliminate the benign respiratory viruses need to be thought of as the insistence that the left has to kill off the vestiges of religion in the West. More virulent forms will just invade the niche: Salafism, LGBTQ, tradcats etc.

And just as the benign respiratory viruses train and strengthen the body so that it can deal with more malignant viruses, the benign religions train and strengthen the mind, so that it learns to be critical of authority. The absurdities and cruelties that happen within the religious system teaches you that all power has to be examined skeptically, even when it appeals to absolute unquestionable truths.

Without this kind of provoked immune response against authority, people stand no real chance when they are faced with a far more a malignant form, like a wealthy surgeon who proclaims in the name of “Science” that their LGBTQIA+ adhering daughter should have her breasts amputated.

And so perhaps we shouldn’t just be seeding the hCov’s. Perhaps we should start seeding the old religions again too.

The Vilification of Healthy People; Especially Children

Throughout the past several years apparently healthy people have been re-defined as being potential asymptomatic spreaders of a disease that can be lethal in high-risk individuals. The disease is known as the novel coronavirus disease that was first identified in 2019 (COVID-19). People around the world have been instilled with near-paralyzing fear that their family member, friend, neighbour and/or colleague who has no signs or symptoms can kill them by spreading severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), which is the causative agent of COVID-19.

This paradigm that a person has no way of knowing who is safe to be around has formed the rationale for mass lockdowns, masking, and mandating ‘vaccines’ for which the initial clinical experiments are still ongoing. This has caused massive fracturing of relationships around the globe. Nobody has been spared. Families have split, best friendships that lasted decades ended abruptly, and colleagues lashed out.

We were told that everyone had to do their part to prevent hospitals from being overwhelmed. Those who felt healthy could not be trusted. Unbeknown to them they might have a wicked pathogen oozing out of their body. Healthy children who were at a statistical risk equivalent to zero of dying from COVID-19 would almost certainly kill their grandparents if they were not locked down, masked and ‘vaccinated’. Those who resisted lockdowns, masking, and mandating of so-called vaccines that could neither prevent the disease nor transmission of its causative agent have been treated like uncaring villains that are deserving of segregation. Remember this front page of one of Canada’s best-known newspapers that was published on August 26, 2021?…

The Prime Minister of Canada, Justin Trudeau, has been a classic example of a leader who has vigorously promoted this kind of hatred and division within his own country.

So, how did we get so far off-track with our response to COVID-19?

Why will future history books, if accurate, document this as the most mismanaged crisis of our time?

Most of the blame rests on the scientific and medical community allowing a very elegant scientific test to be chronically misused. This test is known as the ‘reverse transcriptase-polymerase chain reaction’ (RT-PCR).

Did we follow the science?

In court, I have often seen judges puzzled by the apparent contradictions in the scientific evidence being put forward by various experts. These judges often question how scientists can interpret the same data so differently. When it comes to the science underpinning COVID-19, published papers can be placed into two bins:

1. Those that are trustworthy because they are based on sound scientific methods.

2. Those that are untrustworthy because they are based on flawed scientific methods.

In the past several years science in bin 2 has become voluminous and has contributed excessively to the rationale for the so-called prevailing ‘COVID-19 narrative’. The problem is that the science in bin 2 cannot be properly interpreted because it is built on a fundamentally flawed foundation. Too many scientists failed to critically assess the methods used to generate the early COVID-19 data. This has resulted in this junk science to snowball out of control. The RT-PCR test is at the heart of this problem.

The House Built on Sand Must be Dismantled

If one goes back to the birth of COVID-19 science and critically assesses it, misusing the RT-PCR test jumps out as a key fundamental flaw that caused substantial overestimation of the number of cases of COVID-19 and erroneous labeling of healthy people as asymptomatic spreaders of a deadly disease. The only way to correct course and stop the avalanche of faulty COVID-19 science is to establish which papers can and cannot be trusted. Importantly, editors of scientific journals cannot allow any more COVID-19 ‘facts’ to be published unless the authors unequivocally demonstrate that their data are based on methods that have been implemented properly. Most notably, authors must demonstrate that their research methodologies have been appropriately calibrated such that their conclusions are justified.

Misuse of An Elegant Scientific Technique Has Plagued COVID-19 Science From the Very Beginning

To properly gauge the scope of an outbreak of an infectious disease, one first needs to accurately diagnose it. Diseases are diagnosed primarily based on two things:

1. Accurately detecting the presence of a pathogen using a laboratory-based test.

2. Detection of signs and/or symptoms consistent with the disease, which is usually done by a physician.

Symptoms are aspects of a disease that a person experiences but cannot be assessed easily by an observer. Examples include general malaise, pain, and a loss of appetite. In contrast, signs of illness can be objectively observed and documented by others, and include coughing, sneezing, or a fever that can measured with a thermometer. Often, symptoms precede the onset of signs of illness.

When it comes to defining what it means to be ‘asymptomatic’, there are three relevant scenarios:

1. A person who is not infected with a pathogen will never be at risk of developing the disease associated with that pathogen. These are healthy individuals who are asymptomatic by virtue of not having been infected. They cannot infect others.

2. A person can be infected with a potential pathogen but never develop symptoms of a disease because the causative agent fails to cause substantial harm in the body. In many cases, this might be because the immune system can respond rapidly and effectively. There have also been examples of people getting infected with SARS-CoV-2 but never apparently experiencing symptoms nor developing signs of COVID-19. Infection does not always result in disease. For example, billions of microbes, including many bacteria and viruses, live on and in our bodies without causing us harm. They have invaded our bodies but do not cause disease, even though some of them can cause serious disease in other people or even ourselves should they get into an inappropriate physiological location (e.g., some fecal bacteria entering a body via the oral route). Infected but asymptomatic (disease-free) people are also healthy (i.e., there is no impairment to their ability to function in their daily activities).

3. People who get infected and then progress to a diseased state always have a period in between when they are ‘asymptomatic’. Technically, these individuals that do eventually get sick are referred to as being ‘pre-symptomatic’. One does not know if a person is truly asymptomatic or pre-symptomatic until the typical incubation period for a pathogen has passed; this is the expected time from infection to the onset of symptoms in a susceptible person. A person who is infected and symptomatic can spread the causative agent of the disease to others.

When people have COVID-19, they experience obvious symptoms and signs also usually become apparent. This is the scenario that has been easy to manage throughout the declared COVID-19 pandemic. People who are sick have been asked to stay home. From a social hygiene perspective, it is my expert opinion that this should be encouraged for all the infectious diseases we live with. This would reduce infectious disease-related morbidities and mortalities.

In the context of COVID-19, most masking, isolation and vaccination policies around the world are predicated on the assumption that transmission of SARS-CoV-2 can be efficiently mediated by asymptomatic people who are transiently infected but never get COVID-19 and/or pre-symptomatic individuals. This is based on the assumption that SARS-CoV-2 can replicate to the point where a person who is not coughing or sneezing can expel a threshold dose required to potentially infect another person. Although this is theoretically possible and likely occurs rarely, it is incorrect to conclude that this is commonplace and a significant driver of the spread of COVID-19. This incorrect concept is based on an array of scientific studies that relied on RT-PCR testing that was inappropriately calibrated.

How to Define a Case of COVID-19

Cases of COVID-19 should only be determined as follows:

1. It should be a physician making the diagnosis.

2. It should be based on the presence of signs and symptoms that are consistent with the clinical definition of COVID-19.

3. The presence of symptoms and/or signs should be supported by laboratory results derived from properly calibrated tests that demonstrate the presence of SARS-CoV-2 virions. A virion is a single virus particle. Virions can be replication-competent; these are the only ones that can potentially infect another person and cause disease. Or they can be replication-incompetent; these ones can never spread to others and cause COVID-19.

Throughout the declared pandemic many so-called ‘cases’ of COVID-19 were incorrectly ‘diagnosed’. Cases, especially early in the declared pandemic, have been defined by individuals other than physicians, assumed based on signs and symptoms only, or exclusively based on a positive laboratory test result. The latter has been extremely common. This contradicts the World Health Organization, which noted that “Most PCR assays are indicated as an aid for diagnosis, therefore, health care providers must consider any result in combination with timing of sampling, specimen type, assay specifics, clinical observations, patient history, confirmed status of any contacts, and epidemiological information”.

The core definition, and all-too-often the sole definition of ‘cases’ of COVID-19 has been based on the use of a laboratory testing method referred to as ‘RT-PCR’. To understand how asymptomatic people were mislabeled as significant sources of transmission of SARS-CoV-2, one must first understand how RT-PCR testing should have been properly calibrated around the world.

A polymerase is a protein that can copy DNA, which is a genetic blueprint. So, the PCR method requires this genetic blueprint known as DNA to be present in order to work. If DNA is in a sample, when a scientist adds a polymerase, a few other ingredients, and then varies the temperature, new copies of tiny portions of the DNA will be made. With each ‘cycle’ that the PCR test is run, more copies of these fragments of the genetic blueprint will be made. Once a threshold number of copies appear in the sample, they can be detected. Think of it like a photocopier. From a great distance, you might not be able to tell if a single copy of a page has been made. However, once you have a stack of five hundred pages sitting on the output tray, you know for sure that the photocopier is churning out copies. In short, PCR is a method that scientists can use to determine whether a particular genetic blueprint is present in a sample.

The genetic blueprint for SARS-CoV-2 is not made of DNA. Instead, it is made of a related structure called ‘RNA’. Therefore, to use the PCR test to determine whether an RNA-based virus is present in a sample requires one additional step at the beginning. Specifically, a ‘reverse transcriptase’ is used to convert the RNA from SARS-CoV-2 into DNA, portions of which can then be detected with the PCR test. This is how the RT-PCR test is used to detect the presence of small pieces of the genetic material from SARS-CoV-2.

The Inappropriate Use of RT-PCR Testing Caused a Disconnect Between Laboratory Studies and ‘Real World’ Data

Laboratory studies suggested that asymptomatic individuals could potentially shed infectious SARS-CoV-2 one to two days before the onset of symptoms of COVID-19. However, the largest ‘real world’ study done to date looked at the prevalence of SARS-CoV-2 in ~10 million people in Wuhan, China and found no evidence of asymptomatic transmission. This typical disconnect in the results of laboratory-based studies and ‘real world’ data is due to the former types of experiments having relied on the use of uncalibrated or incorrectly calibrated RT-PCR tests. An RT-PCR test can only determine if tiny fragments of the genetic material from a virus is present in a sample. It can never indicate, on its own, whether that material is from virus particles that have the potential to infect and cause disease, or from replication-incompetent virions or even portions thereof that cannot cause disease.

Flawed RT-PCR Testing Caused Over-Diagnosis of COVID-19

On its own, a positive result on a RT-PCR test to detect SARS-CoV-2 is insufficient to diagnose COVID-19, yet this became routine in most parts of the world. In addition to the potential for false positive tests, true positive results can also be obtained from genomes of SARS-CoV-2 particles that are no longer infectious. An example of the latter would be an individual who has mounted an effective immune response and may have remnant replication-incompetent viral particles or partially degraded viral genetic material inside relatively long-lived white blood cells that have killed the virus. These cells are known as ‘phagocytes’ and are part of our immune system. Indeed, following clearance of SARS-CoV-2 from the body, full and/or partial genomes of SARS-CoV-2 can remain for up to several weeks. Phagocytosis (or ‘eating’) of SARS-CoV-2 is a mechanism to kill and remove the virus from the body. These phagocytic cells tend to hang on to these ‘killed’ virions so that they can activate other immunological effector cells, including B cells that produce the antibodies we have heard so much about. As such, these phagocytes can be a source of SARS-CoV-2 genomes that could be amplified by a PCR test. However, these genomes would not have the potential to cause COVID-19. Instead it would evidence that the infection has resolved or is resolving. Persistence of whole or partial genomes that are not associated with infectious particles is well-documented for a variety of other viruses, including measles, Middle East respiratory syndrome-coronavirus, and other coronaviruses. A positive RT-PCR test for the presence of SARS-CoV-2 should never be used, on its own, to define cases of COVID-19; and definitely should not be used to claim that someone has the potential to infect another person.

Building a Rock-Solid Foundation for COVID-19 Science:

The Gold Standard Functional Virology Assay that Should Always be Used to Calibrate RT-PCR Tests

A gold standard test for infectivity of a virus is a cell-based functional assay that determines the potential to replicate and cause cell death. The assay works like this: Cells that are stripped of their anti-viral properties are put into a dish and allowed to adhere to the bottom. The cells would typically cover the entire bottom of the dish. A scientist can look under a microscope to confirm the cells are healthy. A sample then gets added to the cells. If the sample contains replication-competent (i.e., potentially disease-causing) virions, these will infect and kill the cells. A day or two later, the scientist can check the cells under a microscope again. If they see what is called a ‘cytopathic effect’, which means the cells have died, this indicates that replication-competent virions were present. If there was no cytopathic effect, there were no replication-competent virions. Here are pictures from my research team that show how this virology test works…

…the cells on the left were not exposed to a replication-competent (infectious) virus. They remain happily adhered to the bottom of the dish. There was no cytopathic effect. The cells on the right were exposed to a replication-competent virus that infected and killed them. As the cells died, they rounded up and lost their ability to remain stuck to the bottom of the plate. This is a classic example of cytopathic effect. You can see how easy it is to use this test to determine whether a sample contains any infectious virions.

To calibrate a RT-PCR test for SARS-Cov-2, samples from nasopharyngeal swabs of a large array of people would be split into two; one for RT-PCR testing and the other for testing in the gold standard virology assay. Scientists would note the cycle threshold values from the RT-PCR test that are associated with evidence of replication-competent virions from the cellular virology assay versus those that did not cause a cytopathic effect. This allows a cycle threshold cut-off to be determined. Above this threshold, there is no evidence of replication-competent virions in samples from the nasopharyngeal swabs. This is the objective and proper way to calibrate a RT-PCR test when studying transmission of a virus. Without doing this, RT-PCR test results cannot be interpreted in a meaningful way, and they would lead to inappropriate conclusions, like asymptomatic people being spreaders of COVID-19.

Early in the declared COVID-19 pandemic the Public Health Agency of Canada appropriately performed this calibration of their RT-PCR test. For the test they were using, they identified a cycle threshold cut-off of 24 for declaring people to have the potential to infect others. If they had subsequently offered this service to support studies of the spread of COVID-19, only samples yielding a signal at 24 or fewer cycles would be declared to have evidence of potentially infectious SARS-CoV-2. However, with no explanation provided, this initial and appropriate way of calibrating the RT-PCR assay was not required for labs around the world that were studying transmission of SARS-CoV-2. In fact, cycle threshold cut-offs were arbitrarily assigned. As such, RT-PCR data used to determine global cases of COVID-19 have been highly unreliable.

Even so-called ‘fact-checkers’ of people who criticized the inappropriate designation of the RT-PCR as a stand-alone gold standard diagnostic test have had to admit that it cannot possibly distinguish between infectious and non-infectious virions or parts thereof. For example, a ‘fact check’ from Reuters concluded “PCR tests are being used widely in England to show that SARS-CoV-2 viral genetic material is present in the patient”. I bolded the relevant text. Indeed, RT-PCR tests are a valuable tool for determining whether portions of a virus’s genetic material are present in a sample. They cannot determine whether that genetic material is from a replication-competent virion that would have the potential to infect someone.

Positive RT-PCR tests for SARS-CoV-2 in asymptomatic people are almost universally based on high cycle threshold values, which raises the question of whether these individuals harbor infectious viral particles. The absence of a functional cell-based assay to prove infectivity renders results of asymptomatic testing impossible to interpret accurately. Indeed, the World Health Organization, agreeing with many health professionals around the world, has emphasized that spreading of SARS-CoV-2 by asymptomatic individuals is rare and an emphasis should be placed, therefore, on testing people with signs or symptoms of illness, not those who are apparently healthy.

In addition to the Canadian study that identified a cycle threshold of 24 as an appropriate cut-off for declaring samples positive for infectious SARS-CoV-2, other studies reported results of similar calibrations of other RT-PCR assays for SARS-CoV-2. They identified cycle threshold cut-offs of 22-27 and 30. Altogether, this suggests that tests with cycle threshold values above 22-30 are likely not indicative of the presence of replication-competent SARS-CoV-2.

The logical conclusion is that it is erroneous to declare samples with high cycle threshold values, especially those above 30, as being positive for infectious SARS-CoV-2. However, in many countries people were assumed to be infectious when their samples were declared positive using RT-PCR assays with cycle threshold cut-offs as high as 45 cycles. Such an unjustifiably high cut-off would have resulted in a substantial overestimation of cases of COVID-19 and would have led to erroneous labeling of asymptomatic people as potential spreaders of COVID-19.

Failure to Calibrate the RT-PCR Test Shows How a Representative Influential Scientific Study Incorrectly Concluded that Asymptomatic People Might be a Risk for Spreading COVID-19

The figure below shows results of a published study that claimed to depict the frequency at which asymptomatic people tested positive for SARS-CoV-2 relative to that observed for people with symptomatic infections. Specifically, graphs are shown from figure 2 of a paper published in the influential Journal of the American Medical Association - Internal Medicine. The argument being made was that the frequency at which asymptomatic people tested positive for SARS-CoV-2 was like that observed for people with symptomatic infections. However, the authors failed to calibrate their RT-PCR assay.

Following is the description the authors of the study provided in the methods section of their paper. The most important portion of this text is the last sentence, which is bolded.

“Specimen Collection and RT-PCR for SARS-CoV-2

The URT specimens were collected from both nasopharyngeal and oropharyngeal swabs obtained by trained medical staffs (physicians and nurses). For LRT specimens, participants were given instructions the night before to collect a first morning sputum (after gargling) in a specimen cup; RT-PCR assays for SARS-CoV-2 were performed using Allplex 2020-nCoV assay (Seegene, Seoul, ROK) to determine the presence of virus through the identification of 3 genetic markers: envelope (env) gene, RNA-dependent RNA polymerase (RdRp) gene, and nucleocapsid protein (N) gene. The cycle threshold (Ct) during RT-PCR testing refers to when the detection of viral amplicons occurs, it is inversely correlated with the amount of RNA present. A lower Ct value indicates large quantities of viral RNA. It was considered positive when the Ct values of all genes were less than 40 cycles.”

Remarkably, the authors applied an arbitrary cycle threshold of 40 to define a positive test result. Proper calibration of the test was not performed. I applied a new cycle threshold cut-off of 24, based on the published results of the Canadian study for calibrating a RT-PCR test for SARS-CoV-2. This is shown as a red dotted line on the graphs in the figure above. Symbols appearing in the light red rectangle above this line would be considered negative, in contrast to the positive designation that the authors had assigned. Remarkably, 99.7% of the people the authors declared to be harbouring infectious SARS-CoV-2 likely had no evidence of potentially infectious SARS-CoV-2 virions, had the test been properly calibrated. This represents a fatal flaw in this paper; one that negates its conclusion that “Isolation of asymptomatic patients may be necessary to control the spread of SARS-CoV-2”. It should also precipitate its retraction. Such a paper should never have been allowed to be published in the first place.

This highlights a fatal flaw that has been extremely common in publications throughout the declared pandemic that claimed asymptomatic people could be a significant source of transmission of SARS-CoV-2 that could cause COVID-19 in other people. Every paper making this claim should have the materials and methods section carefully evaluated to determine whether the cycle threshold cut-off for the RT-PCR assay was based on the appropriate calibration method or was selected arbitrarily.

Here is a list of other influential publications of original research studies that erroneously concluded that asymptomatic people might be significant sources of replication-competent SARS-CoV-2 virions. Most are based on fatally flawed RT-PCR testing and the remaining papers fail to disclose how they defined an ‘infection’. All of them should be retracted. None of their conclusions can be trusted…

1. Bai, Y. et al. Presumed Asymptomatic Carrier Transmission of COVID-19. Jama 323, 1406-1407 (2020).

2. Arons, M.M. et al. Presymptomatic SARS-CoV-2 Infections and Transmission in a Skilled Nursing Facility. The New England journal of medicine 382, 2081-2090 (2020).

3. Stock, A.D. et al. COVID-19 Infection Among Healthcare Workers: Serological Findings Supporting Routine Testing. Front Med (Lausanne) 7, 471 (2020).

4. Bi, Q. et al. Epidemiology and transmission of COVID-19 in 391 cases and 1286 of their close contacts in Shenzhen, China: a retrospective cohort study. The Lancet. Infectious diseases 20, 911-919 (2020).

5. Böhmer, M.M. et al. Investigation of a COVID-19 outbreak in Germany resulting from a single travel-associated primary case: a case series. The Lancet. Infectious diseases 20, 920-928 (2020).

6. Chan, J.F. et al. A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. Lancet (London, England) 395, 514-523 (2020).

7. Van Vinh Chau, N. et al. The Natural History and Transmission Potential of Asymptomatic Severe Acute Respiratory Syndrome Coronavirus 2 Infection. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 71, 2679-2687 (2020).

8. Chaw, L. et al. Analysis of SARS-CoV-2 Transmission in Different Settings, Brunei. Emerging infectious diseases 26, 2598-2606 (2020).

9. Cheng, H.Y. et al. Contact Tracing Assessment of COVID-19 Transmission Dynamics in Taiwan and Risk at Different Exposure Periods Before and After Symptom Onset. JAMA internal medicine 180, 1156-1163 (2020).

10. Gao, M. et al. A study on infectivity of asymptomatic SARS-CoV-2 carriers. Respiratory medicine 169, 106026 (2020).

11. Gao, Y. et al. A cluster of the Corona Virus Disease 2019 caused by incubation period transmission in Wuxi, China. The Journal of infection 80, 666-670 (2020).

12. Guan, W.J. et al. Clinical Characteristics of Coronavirus Disease 2019 in China. The New England journal of medicine 382, 1708-1720 (2020).

13. He, X. et al. Temporal dynamics in viral shedding and transmissibility of COVID-19. Nat Med 26, 672-675 (2020).

14. Hodcroft, E.B. Preliminary case report on the SARS-CoV-2 cluster in the UK, France, and Spain. Swiss medical weekly 150 (2020).

15. Hoehl, S. et al. Evidence of SARS-CoV-2 Infection in Returning Travelers from Wuhan, China. The New England journal of medicine 382, 1278-1280 (2020).

16. Lauer, S.A. et al. The Incubation Period of Coronavirus Disease 2019 (COVID-19) From Publicly Reported Confirmed Cases: Estimation and Application. Annals of internal medicine 172, 577-582 (2020).

17. Li, R. et al. Substantial undocumented infection facilitates the rapid dissemination of novel coronavirus (SARS-CoV-2). Science (New York, N.Y.) 368, 489-493 (2020).

18. Li, C. et al. Asymptomatic and Human-to-Human Transmission of SARS-CoV-2 in a 2-Family Cluster, Xuzhou, China. Emerging infectious diseases 26, 1626-1628 (2020).

19. Liu, Y., Funk, S. & Flasche, S. The contribution of pre-symptomatic infection to the transmission dynamics of COVID-2019. Wellcome open research 5, 58 (2020).

20. Lu, X. et al. SARS-CoV-2 Infection in Children. The New England journal of medicine 382, 1663-1665 (2020).

21. Lu, S. et al. Alert for non-respiratory symptoms of coronavirus disease 2019 patients in epidemic period: A case report of familial cluster with three asymptomatic COVID-19 patients. Journal of medical virology 93, 518-521 (2021).

22. Luo, S.H. et al. A confirmed asymptomatic carrier of 2019 novel coronavirus. Chinese medical journal 133, 1123-1125 (2020).

23. Mizumoto, K., Kagaya, K., Zarebski, A. & Chowell, G. Estimating the asymptomatic proportion of coronavirus disease 2019 (COVID-19) cases on board the Diamond Princess cruise ship, Yokohama, Japan, 2020. Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin 25 (2020).

24. Sun, K. et al. Transmission heterogeneities, kinetics, and controllability of SARS-CoV-2. Science (New York, N.Y.) 371 (2021).

25. Nishiura, H. et al. Estimation of the asymptomatic ratio of novel coronavirus infections (COVID-19). Int J Infect Dis 94, 154-155 (2020).

26. Nishiura, H., Linton, N.M. & Akhmetzhanov, A.R. Serial interval of novel coronavirus (COVID-19) infections. Int J Infect Dis 93, 284-286 (2020).

27. Pan, Y., Zhang, D., Yang, P., Poon, L.L.M. & Wang, Q. Viral load of SARS-CoV-2 in clinical samples. The Lancet. Infectious diseases 20, 411-412 (2020).

28. Pan, X. et al. Asymptomatic cases in a family cluster with SARS-CoV-2 infection. The Lancet. Infectious diseases 20, 410-411 (2020).

29. Park, S.Y. et al. Coronavirus Disease Outbreak in Call Center, South Korea. Emerging infectious diseases 26, 1666-1670 (2020).

30. Payne, D.C. et al. SARS-CoV-2 Infections and Serologic Responses from a Sample of U.S. Navy Service Members - USS Theodore Roosevelt, April 2020. MMWR. Morbidity and mortality weekly report 69, 714-721 (2020).

31. Kimball, A. et al. Asymptomatic and Presymptomatic SARS-CoV-2 Infections in Residents of a Long-Term Care Skilled Nursing Facility - King County, Washington, March 2020. MMWR. Morbidity and mortality weekly report 69, 377-381 (2020).

32. Qian, G. et al. COVID-19 Transmission Within a Family Cluster by Presymptomatic Carriers in China. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 71, 861-862 (2020).

33. Ran, L. et al. Risk Factors of Healthcare Workers With Coronavirus Disease 2019: A Retrospective Cohort Study in a Designated Hospital of Wuhan in China. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 71, 2218-2221 (2020).

34. Rosenberg, E.S. et al. COVID-19 Testing, Epidemic Features, Hospital Outcomes, and Household Prevalence, New York State-March 2020. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 71, 1953-1959 (2020).

35. Sakurai, A. et al. Natural History of Asymptomatic SARS-CoV-2 Infection. The New England journal of medicine 383, 885-886 (2020).

36. Samsami, M., Zebarjadi Bagherpour, J., Nematihonar, B. & Tahmasbi, H. COVID-19 Pneumonia in Asymptomatic Trauma Patients; Report of 8 Cases. Archives of academic emergency medicine 8, e46 (2020).

37. Tabata, S. et al. Clinical characteristics of COVID-19 in 104 people with SARS-CoV-2 infection on the Diamond Princess cruise ship: a retrospective analysis. The Lancet. Infectious diseases 20, 1043-1050 (2020).

38. Tong, Z.D. et al. Potential Presymptomatic Transmission of SARS-CoV-2, Zhejiang Province, China, 2020. Emerging infectious diseases 26, 1052-1054 (2020).

39. Treibel, T.A. et al. COVID-19: PCR screening of asymptomatic health-care workers at London hospital. Lancet (London, England) 395, 1608-1610 (2020).

40. Wei, W.E. et al. Presymptomatic Transmission of SARS-CoV-2 - Singapore, January 23-March 16, 2020. MMWR. Morbidity and mortality weekly report 69, 411-415 (2020).

41. Xu, J., Li, Y., Gan, F., Du, Y. & Yao, Y. Salivary Glands: Potential Reservoirs for COVID-19 Asymptomatic Infection. Journal of dental research 99, 989 (2020).

42. Yang, R., Gui, X. & Xiong, Y. Comparison of Clinical Characteristics of Patients with Asymptomatic vs Symptomatic Coronavirus Disease 2019 in Wuhan, China. JAMA network open 3, e2010182 (2020).

43. Yang, N. et al. In-flight transmission cluster of COVID-19: a retrospective case series. Infectious diseases (London, England) 52, 891-901 (2020).

44. Ye, F. et al. Delivery of infection from asymptomatic carriers of COVID-19 in a familial cluster. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 94, 133-138 (2020).

45. Yu, P., Zhu, J., Zhang, Z. & Han, Y. A Familial Cluster of Infection Associated With the 2019 Novel Coronavirus Indicating Possible Person-to-Person Transmission During the Incubation Period. The Journal of infectious diseases 221, 1757-1761 (2020).

46. Zhang, J., Tian, S., Lou, J. & Chen, Y. Familial cluster of COVID-19 infection from an asymptomatic. Critical care (London, England) 24, 119 (2020).

47. Almadhi, M.A. et al. The high prevalence of asymptomatic SARS-CoV-2 infection reveals the silent spread of COVID-19. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 105, 656-661 (2021).

48. Choi, A. et al. Symptomatic and Asymptomatic Transmission of SARS-CoV-2 in K-12 Schools, British Columbia, Canada April to June 2021. Microbiology spectrum, e0062222 (2022).

…these 48 papers represent most, if not all, of the peer-reviewed scientific evidence that has been used by most public health officials to mislabel asymptomatic people as sources of COVID-19-causing SARS-CoV-2. All of it is fatally flawed.

It was even concluded in a study that patients testing ‘positive’ with cycle threshold values above 33 could likely be discharged from hospitals. Such a recommendation would never be made if there was any evidence that these people harboured SARS-CoV-2 virions with the potential to infect others. So one must wonder why testing labs were allowed to arbitrarily pick cycle thresholds ranging from 38 to 45 as upper limits for defining the presence of infectious SARS-CoV-2.

Exclusive reliance on improperly calibrated RT-PCR testing as an indication of ‘infection’ has also led to the erroneous conclusion that post-symptomatic people may also need to be masked and/or isolated.

I have yet to see appropriate scientific evidence to justify the unusually high cycle threshold values being used in studies that label people as asymptomatic sources of COVID-19. In the absence of such data, there is no justification for masking, isolating or mandating experimental vaccine technologies for asymptomatic people.

Others have also criticized the exclusive use of RT-PCR tests in diagnosing COVID-19 and drawing conclusions about transmission in the absence of infectivity testing.

How RT-PCR Testing Should Have Been Used to Support Diagnoses of COVID-19

All labs should have been required to calibrate their RT-PCR test prior to providing any ‘real world’ data to public health officials that would be used to study the transmission of SARS-CoV-2. Use of the gold standard functional virology assay to do this calibration would have provided each lab with a strong objective rationale for their specific cycle threshold cut-off value when determining whether a person could have the potential to infect others. And this should have always been married to a clinical diagnosis rendered by a physician. As mentioned earlier, if this standard is applied retroactively to the COVID-19 scientific literature, it becomes obvious that much of it is untrustworthy.

Much of the Foundational COVID-19 Science is Fundamentally Flawed

RT-PCR testing has generally been misused during the declared COVID-19 pandemic due to failures to calibrate it properly. The result has been mislabeling asymptomatic people as significant potential sources for transmission of COVID-19. This, in turn, has resulted in inappropriate mandating of masking, isolation, and ‘vaccines’ for people who do not represent a genuine health risk to others. It has also taken the diagnostic expertise away from physicians and placed it in the hands of anonymous laboratory technicians.

Now, we are left with a mountain of COVID-19 science that cannot be interpreted properly. Scientists with integrity and the relevant expertise know that a substantial but undefined number of people that tested ‘positive for COVID-19’ never had the potential to spread SARS-CoV-2 to others and many of these also did not actually have the disease known as COVID-19.

Resolving the Apparent Conflicts in Evidence Presented by ‘Experts’

To judges who are puzzled by the differing interpretations of experts in their courts, the explanation is fairly simple. If you remove the fundamentally flawed science from expert reports, you will be left with trustworthy data that generally do not support what has been the prevailing narrative over the past several years. When scientists talk about following the overall weight of the scientific evidence, what we really mean is to follow the weight of the trustworthy scientific evidence. Do not get bedazzled by the numerous reports that have accumulated, often in ‘prestigious’ journals, that were based on flawed scientific methods. Don’t get distracted by the number of health ‘authorities’ that have blindly propagated this flawed science. Truth is not a democracy. It is not defined by a majority vote.

Harm to Public Trust in Science

The global propagation of poorly conducted science over the past several years has caused massive and irreparable harm. Children and teenagers took the brunt of this damage. They were given no choice. They had no voice. They became shields used in a conflict waged by adults who wielded faulty science like it was the gospel truth.

As a scientist with deep expertise in viral immunology, I am incredibly disheartened by the state of my scientific disciplines. My colleagues that sat in their ivory towers allowing junk science to justify crushing constitutional freedoms should be ashamed of themselves. I am proud of the relatively few who stood tall on a foundation of integrity and endured brutal treatment for the past couple of years. I can only hope that the harm done to public trust in the health sciences can be remedied.

Full paper - PDF 50 Pages Posted: 12 Sep 2022

• Kevin Bardosh
  University of Washington; University of Edinburgh - Edinburgh Medical School
• Allison Krug
  Artemis Biomedical Communications LLC
• Euzebiusz Jamrozik
  University of Oxford
• Trudo Lemmens
  University of Toronto - Faculty of Law
• Salmaan Keshavjee
  Harvard University - Harvard Medical School
• Vinay Prasad
  University of California, San Francisco (UCSF)
• Martin A. Makary
  Johns Hopkins University - Department of Surgery
• Stefan Baral
  John Hopkins University
• Tracy Beth Høeg
  Florida Department of Health; Sierra Nevada Memorial Hospital

Date Written: August 31, 2022

Abstract

Students at North American universities risk disenrollment due to third dose COVID-19 vaccine mandates. We present a risk-benefit assessment of boosters in this age group and provide five ethical arguments against mandates. We estimate that 22,000 - 30,000 previously uninfected adults aged 18-29 must be boosted with an mRNA vaccine to prevent one COVID-19 hospitalisation. Using CDC and sponsor-reported adverse event data, we find that booster mandates may cause a net expected harm: per COVID-19 hospitalisation prevented in previously uninfected young adults, we anticipate 18 to 98 serious adverse events, including 1.7 to 3.0 booster-associated myocarditis cases in males, and 1,373 to 3,234 cases of grade ≥3 reactogenicity which interferes with daily activities. Given the high prevalence of post-infection immunity, this risk-benefit profile is even less favourable. University booster mandates are unethical because: 1) no formal risk-benefit assessment exists for this age group; 2) vaccine mandates may result in a net expected harm to individual young people; 3) mandates are not proportionate: expected harms are not outweighed by public health benefits given the modest and transient effectiveness of vaccines against transmission; 4) US mandates violate the reciprocity principle because rare serious vaccine-related harms will not be reliably compensated due to gaps in current vaccine injury schemes; and 5) mandates create wider social harms. We consider counter-arguments such as a desire for socialisation and safety and show that such arguments lack scientific and/or ethical support. Finally, we discuss the relevance of our analysis for current 2-dose CCOVIDovid-19 vaccine mandates in North America.

Note: Funding: This paper was partially supported by a Wellcome Trust Society and Ethics fellowship awarded to KB (10892/B/15/ZE) and Wellcome Trust grants to EJ (216355, 221719, 203132).
Competing Interest Statement: We do not have any competing interests to declare.

Keywords: COVID-19 vaccines, mandates, ethics, young adults, risk-benefit analysis

Both COVID-19 illness, caused by infection with the SARS-CoV-2 virus, and COVID-19 vaccination, ostensibly to prevent SARS-CoV-2 infection and serious COVID-19 morbidity, have been associated with the development of myopericarditis, i.e., inflammation of the heart muscle itself (myocarditis) or its suspending sack (pericarditis). This brief review demonstrates, first, the dubious association between SARS-CoV-2 infection and myopericarditis, and second, the robust association between COVID-19 vaccination, especially with mRNA vaccines, and myopericarditis, including, in particular, the study of fatal cases upon autopsy.

The direct relationship between SARS-CoV-2 infection and myocarditis remains tenuous at best. Recent ecological, controlled retrospective cohort and autopsy data do not support an association. The overall absence of support for a specific ‘SARS-CoV-2 myocarditis syndrome’ from focused autopsy studies of presumed myocarditis deaths is consistent with findings from general necropsy studies of COVID-19 deaths. These investigations have established SARS-CoV-2 infection leading to fatal COVID-19 is indeed, as the name implies, a respiratory illness. Wong et al., for example, described how, “No overt pathological findings attributable to SARS-CoV-2 infection could be recognised outside of the lung… [B]eyond the respiratory tract [SARS-CoV-2 infection] does not induce any major pathology… in fatal cases.”

A systematic review of primarily spontaneously reported data from the U.K., USA and European Union/European Economic Area (EU/EEA), beginning with vaccine launch through mid-March 2022, found 0.22% (n=30) of 13,571 Covid vaccine-associated myocarditis or pericarditis events were fatal. These data are complemented by a much smaller, but growing autopsy literature. The limited necropsy data characterising COVID-19 vaccine-associated deceased persons with myocarditis and myopericarditis repeatedly affirm heart-related pathologies directly attributable to very recent vaccination. Such findings contrast with the lack of definitive epidemiologic or autopsy evidence for a unique SARS-CoV-2 infection myocarditis, as Caforio et al. note:

Strong evidence for a SARS-CoV-2 role in direct infection of cardiac myocytes leading to virus induced myocarditis in patients is missing… [T]here is not yet definitive EMB [endomyocardial biopsy]/autopsy proof that SARS-CoV-2 causes direct cardiomyocyte damage in association with histological myocarditis.

Tables 1-3 detail the published autopsy findings from six fatal cases of post-Covid mRNA vaccine-associated myocarditis. The etiologies for cases 1 and 2 were most consistent with an epinephrine-mediated ‘toxic myocarditis’, whereas cases 3-6 evidenced hyperinflammatory myocarditis. Ultimately, after extensive investigation, each case was deemed a Covid vaccine-caused fatal myocarditis.

Two new clinical studies – one peer-reviewed by researchers in Turkey, and one pre-print by researchers in France – have begun to establish an alarming link between an incurable, degenerative brain disease called Creutzfeldt-Jakob disease (CJD) and the experimental Covid-19 vaccine.

CJD is a “rare” disease that is caused by abnormal infectious proteins in the brain called “prions,” according to NHS. Although the presence of prions is not necessarily dangerous or deadly, the proteins will cause degenerative brain damage if they become diseased or misfolded. Once this process begins, the malfunctioning prions will continue to corrupt other cells, leading to a prognosis that is always fatal.

As of right now, CJD is uncurable. There are zero treatment options available. The diagnosis is essentially a death sentence, but symptoms are traditionally dormant for several years before manifesting into a deadly complication.

Unfortunately, with the new cases of CJD that have been linked to the vaccine, that doesn’t seem to be the case. The disease is progressing at an alarming and unprecedented rate. So much so that the team of French researchers highlighted their concerns of the experimental mRNA vaccines contributing directly to creating a new, more aggressive type of CJD.

According to the French study, a total of 26 cases of vaccine-linked CJD were included in the research.

At the time of the study’s publication, a whopping 20 out of the 26 CJD patients had already passed away from the disease. Additionally, researchers found that there were “more than 50 cases” of the fatal disease that appeared after taking the experimental vaccines.

Despite traditionally taking as much as a decade to manifest with symptoms, the study found symptoms in these new cases began appearing just 11.38 days post-vaccination. In these cases, the disease is killing the affected individuals in under 5 months’ time (4.76 months).

From the French pre-print:

“…we are analyzing the concomitance of cases, which occurred in various European countries, between the first doses of Pfizer or Moderna mRNA vaccine and the sudden and rapid onset of the first symptoms of Creutzfeldt-Jakob disease, which usually requires several years before observing its first symptoms…

…We subsequently recall the usual history of this dreadfull subacute disease, and compare it with this new, extremely acute, prion disease, following closely vaccinations. In a few weeks, more 50 cases of almost spontaneous emergence of Creutzfeldt-Jakob disease have appeared in France and Europe very soon after the injection of the first or second dose of Pfizer, Moderna or AstraZeneka vaccines.”

Researchers were also able to identify the probable cause of the sudden-onset CJD post-vaccination. When the vaccines were first synthesized, the genetic makeup was based on the original strain of the virus that came out of the Wuhan Institute of Virology – which had a prion region on its spike protein.

This spike protein and prion region in the experimental mRNA has been shown to interact with human cells and is the likely culprit for the more aggressive version of CJD, according to the French pre-print.

From The Epoch Times:

“…when the Wuhan variant’s spike protein gene information was made into a vaccine as part of the mRNA and adenovirus vaccines, the prion region was also incorporated.

As part of the natural cellular process, once the mRNA is incorporated into the cells, the cell will turn the mRNA instructions into a COVID-19 spike protein, tricking the cells into believing that it has been infected so that they create an immunological memory against a component of the virus…

…A U.S. study has speculated that a misfolded spike protein could in turn create a misfolded prion region that may be able to interact with healthy prions to cause damage, leading to CJD disease.”

Published just before the French study, the peer-reviewed paper out of Turkey also identified sudden CJD cases appearing after getting any of the experimental Pfizer, Moderna, and AstraZeneca vaccines. However, instead of taking over 11 days on average for symptoms to appear, the researchers found the disease is showing up 10x quicker – a single day after vaccination.

From the peer-reviewed study:

Reports of neurological problems are increasing for the clinical presentation of COVID19…

…Creutzfeldt–Jakob disease, a spongiform encephalopathy caused by prions, is characterized by a severe neurological destruction, which has an extremely high mortality. In this publication, we presented a patient who was admitted to the Pamukkale University Anesthesiology Intensive Care Units with the neurological findings that developed after the COVID-19 vaccine (CoronaVac, Sinovac Life Sciences, Beijing, China). The patient died due to the progressive neurological disorders…

…The onset of acute neurological symptoms after Covid19 vaccination suggested that there might be an adverse effect related to the vaccine. Suppression of immunity after vaccination may have accelerated the emergence of prion disease or the onset of the disease may be coincidental. In order for CJD diagnosis to be associated with the vaccine, the cause-effect relationship between them must be revealed. Therefore, further studies are needed in this area.”

In the end, researchers (rightfully) called for more research to be conducted into this issue – Well that’s exactly what the team of French researchers did, and according to one of the main authors of that study – Dr. Jean-Claude Perez – the new findings confirm the worst – there is a new, more aggressive form of CJD.

From Dr. Perez:

“This confirms the radically different nature of this new form of CJD, whereas the classic form requires several decades.”

Add CJD to the list of mRNA vaccine horrors. We are really running out of room.

We need to understand not only that the vaccinators are wrong, and how they are wrong, but also why they are wrong. If we misdiagnose the source of their error, we’ll go looking for evidence against them in the wrong places, and oppose them in the wrong ways.

Consider a story I’ve been following since last week, about an epidemiologist at Berlin Charité named Harald Matthes. It’s nothing special, merely the most recent occurrence of an obnoxious media dynamic:

Last year, Matthes set up a simple online survey for vaccine side-effects. Volunteers could sign up to fill out questionnaires at regular intervals about their post-vaccination experience. About 0.8% of those surveyed reported what Matthes classified as serious adverse reactions, a number 40 times higher than the official Paul-Ehrlich-Institut rate of 0.02%. Matthes has yet to release his data, but last week he appeared in the German media to announce his preliminary results and demand outpatient clinics for victims of vaccination.

Then the fact-checkers descended. One of the most influential attacks appeared in [Die Zeit](http://Much claimed, nothing proven The doctor Harald Matthes says that severe side effects after the Corona vaccination are much more frequent than known. Research shows that his figures are untenable.), under the headline “Much claimed, nothing proven.” The article dismantles Matthes’s study piece-by-piece: He’s wrong because he defines “severe reaction” differently from the Paul-Ehrlich-Institut; he’s wrong because his survey data comes from volunteers rather than a representative sample; and, above all, he’s wrong because he failed to establish a background rate of severe events in the unvaccinated:

It’s completely normal for people to fall ill, sometimes seriously, during the observation period of a study. Every day, almost 1,000 people in Germany suffer a heart attack … It’s important to take this background noise into account, especially when looking for rare vaccine side effects.

There’s a reason I haven’t written about Matthes’s study: These are serious criticisms.

The point, though, is that when it comes to Long Covid, Die Zeit forgets all of this methodological rigour.

In article after article after histrionic article, their journalists demonstrate a total lack of regard for definitions. Everything and anything is Long Covid, so long as it’s preceded by at least the suspicion of SARS-2 infection. All kinds of methodologically dubious Long Covid studies receive the breathless endorsement of Die Zeit, a paper that has never really bothered about the background rate of brain fog or sleep disturbances or joint pain in the population of Germany. Throw it all into the Long Covid bucket, says Die Zeit; after all, SARS-2 is extremely dangerous. Any scary thing anybody says about it must be true.

If you want to know how millions of people can so relentlessly defend the vaccines as “safe and effective,” regardless of what harm they inflict, while simultaneously fearing SARS-2 as a killer virus even after the emergence of Omicron, wonder no more: It is precisely this tendency to uncritically accept every scary poorly-sourced study about SARS-2 risk, while subjecting every last finding to the disadvantage of the vaccines to exacting, isolated demands for rigour. Masks benefit from a similar dynamic, as did lockdowns before them, and mass testing, and contact tracing and other things besides.

If vaccine injuries and deaths were counted in the same way as Long Covid cases and Corona deaths, the vaccines would all be pulled from shelves tomorrow. Alternatively, if we minimised SARS-2 risk in the same way we whitewash the vaccines, nobody would care about mass vaccination at all.

There is very little overt, deliberate deception driving this mass delusion. This is why, as Alex Berenson points out, there’s just not very much in the Pfizer documents that we didn’t already know, and why there’s never going to be very much in them.

The present insanity arises not from the plans of genocidal masterminds in the WHO, but from two years of mass media panic propaganda bordering on psychological abuse, in response to which a great many people find themselves confined in their own self-fashioned moral prisons, having decided that they are not good people unless they mask and self-isolate until SARS-2 vanishes from the earth. They want the vaccines to work, and they find it uncomfortable to contemplate the risks and imperfections of these pharmaceutical products.

Scientists aren’t immune to these emotions. The vaccine developers at Moderna and Pfizer, together with their government regulators, designed trials that would help the vaccines succeed, because they’d spent months awash in Corona panic porn like the rest of us. They made the trials shorter, lest waning efficacy grab too many headlines; they did their best to recruit as few old and vulnerable participants as possible, to keep the efficacy numbers up. This is not to say that there are no liars and malicious actors in the halls of public health, merely that the influence of the insane, panicking hordes is greater.

Orchestrated lying by specific parties very clearly did play an important role in establishing lockdowns and other mass containment policies. The vaccines are a different matter. Hundreds of thousands of scientists and journalists across the world have been wrong about them, in the very same simple and predictable ways, from the very beginning.

A few liars and grifters would be easier – you could expose them and end all of this tomorrow. We’re instead facing the much more intractable problem of pervasive self-deception and motivated reasoning. We need to stop looking for the reveal, and start thinking about how we can ease people out of their madness.

That’s not going to be easy.

The COVID-19 pandemic is one of the most manipulated infectious disease events in history, characterized by official lies in an unending stream lead by government bureaucracies, medical associations, medical boards, the media, and international agencies.[3,6,57] We have witnessed a long list of unprecedented intrusions into medical practice, including attacks on medical experts, destruction of medical careers among doctors refusing to participate in killing their patients and a massive regimentation of health care, led by non-qualified individuals with enormous wealth, power and influence.

For the first time in American history a president, governors, mayors, hospital administrators and federal bureaucrats are determining medical treatments based not on accurate scientifically based or even experience based information, but rather to force the acceptance of special forms of care and “prevention”—including remdesivir, use of respirators and ultimately a series of essentially untested messenger RNA vaccines. For the first time in history medical treatment, protocols are not being formulated based on the experience of the physicians treating the largest number of patients successfully, but rather individuals and bureaucracies that have never treated a single patient—including Anthony Fauci, Bill Gates, EcoHealth Alliance, the CDC, WHO, state public health officers and hospital administrators.[23,38]

The media (TV, newspapers, magazines, etc), medical societies, state medical boards and the owners of social media have appointed themselves to be the sole source of information concerning this so-called “pandemic”. Websites have been removed, highly credentialed and experienced clinical doctors and scientific experts in the field of infectious diseases have been demonized, careers have been destroyed and all dissenting information has been labeled “misinformation” and “dangerous lies”, even when sourced from top experts in the fields of virology, infectious diseases, pulmonary critical care, and epidemiology. These blackouts of truth occur even when this information is backed by extensive scientific citations from some of the most qualified medical specialists in the world.[23] Incredibly, even individuals, such as Dr. Michael Yeadon, a retired ex-Chief Scientist, and vice-president for the science division of Pfizer Pharmaceutical company in the UK, who charged the company with making an extremely dangerous vaccine, is ignored and demonized. Further, he, along with other highly qualified scientists have stated that no one should take this vaccine.

Dr. Peter McCullough, one of the most cited experts in his field, who has successfully treated over 2000 COVID patients by using a protocol of early treatment (which the so-called experts completely ignored), has been the victim of a particularly vicious assault by those benefiting financially from the vaccines. He has published his results in peer reviewed journals, reporting an 80% reduction in hospitalizations and a 75% reduction in deaths by using early treatment.[44] Despite this, he is under an unrelenting series of attacks by the information controllers, none of which have treated a single patient.

Neither Anthony Fauci, the CDC, WHO nor any medical governmental establishment has ever offered any early treatment other than Tylenol, hydration and call an ambulance once you have difficulty breathing. This is unprecedented in the entire history of medical care as early treatment of infections is critical to saving lives and preventing severe complications. Not only have these medical organizations and federal lapdogs not even suggested early treatment, they attacked anyone who attempted to initiate such treatment with all the weapons at their disposal—loss of license, removal of hospital privileges, shaming, destruction of reputations and even arrest.[2]

A good example of this outrage against freedom of speech and providing informed consent information is the recent suspension by the medical board in Maine of Dr. Meryl Nass’ medical license and the ordering of her to undergo a psychiatric evaluation for prescribing Ivermectin and sharing her expertise in this field.[9,65] I know Dr, Nass personally and can vouch for her integrity, brilliance and dedication to truth. Her scientific credentials are impeccable. This behavior by a medical licensing board is reminiscent of the methodology of the Soviet KGB during the period when dissidents were incarcerated in psychiatric gulags to silence their dissent.

OTHER UNPRECEDENTED ATTACKS

Another unprecedented tactic is to remove dissenting doctors from their positions as journal editors, reviewers and retracting of their scientific papers from journals, even after these papers have been in print. Until this pandemic event, I have never seen so many journal papers being retracted— the vast majority promoting alternatives to official dogma, especially if the papers question vaccine safety. Normally a submitted paper or study is reviewed by experts in the field, called peer review. These reviews can be quite intense and nit picking in detail, insisting that all errors within the paper be corrected before publication. So, unless fraud or some other major hidden problem is discovered after the paper is in print, the paper remains in the scientific literature.

We are now witnessing a growing number of excellent scientific papers, written by top experts in the field, being retracted from major medical and scientific journals weeks, months and even years after publication. A careful review indicates that in far too many instances the authors dared question accepted dogma by the controllers of scientific publications—especially concerning the safety, alternative treatments or efficacy of vaccines.[12,63] These journals rely on extensive adverting by pharmaceutical companies for their revenue. Several instances have occurred where powerful pharmaceutical companies exerted their influence on owners of these journals to remove articles that in any way question these companies’ products.[13,34,35]

Worse still is the actual designing of medical articles for promoting drugs and pharmaceutical products that involve fake studies, so-called ghostwritten articles.[49,64] Richard Horton is quoted by the Guardian as saying “journals have devolved into information laundering operations for the pharmaceutical industry.”[13,63] Proven fraudulent “ghostwritten” articles sponsored by pharmaceutical giants have appeared regularly in top clinical journals, such as JAMA, and New England Journal of Medicine—never to be removed despite proven scientific abuse and manipulation of data.[49,63]

Ghostwritten articles involve using planning companies whose job it is to design articles containing manipulated data to support a pharmaceutical product and then have these articles accepted by high-impact clinical journals, that is, the journals most likely to affect clinical decision making of doctors. Further, they supply doctors in clinical practice with free reprints of these manipulated articles. The Guardian found 250 companies engaged in this ghostwriting business. The final step in designing these articles for publication in the most prestigious journals is to recruit well recognized medical experts from prestigious institutions, to add their name to these articles. These recruited medical authors are either paid upon agreeing to add their name to these pre- written articles or they do so for the prestige of having their name on an article in a prestigious medical journal.[11]

Of vital importance is the observation by experts in the field of medical publishing that nothing has been done to stop this abuse. Medical ethicists have lamented that because of this widespread practice “you can’t trust anything.” While some journals insist on disclosure information, most doctors reading these articles ignore this information or excuse it and several journals make disclosure more difficult by requiring the reader to find the disclosure statements at another location. Many journals do not police such statements and omissions by authors are common and without punishment.

As concerns the information made available to the public, virtually all the media is under the control of these pharmaceutical giants or others who are benefitting from this “pandemic”. Their stories are all the same, both in content and even wording. Orchestrated coverups occur daily and massive data exposing the lies being generated by these information controllers are hidden from the public. All data coming over the national media (TV, newspaper and magazines), as well as the local news you watch every day, comes only from “official” sources—most of which are lies, distortions or completely manufactured out of whole cloth—all aimed to deceive the public.

Television media receives the majority of its advertising budget from the international pharmaceutical companies—this creates an irresistible influence to report all concocted studies supporting their vaccines and other so-called treatments.[14] In 2020 alone the pharmaceutical industries spent 6.56 billion dollars on such advertising.[13,14] Pharma TV advertising amounted to 4.58 billion, an incredible 75% of their budget. That buys a lot of influence and control over the media. World famous experts within all fields of infectious diseases are excluded from media exposure and from social media should they in any way deviate against the concocted lies and distortions by the makers of these vaccines. In addition, these pharmaceutical companies spend tens of millions on social media advertising, with Pfizer leading the pack with $55 million in 2020.[14]

While these attacks on free speech are terrifying enough, even worse is the virtually universal control hospital administrators have exercised over the details of medical care in hospitals. These hirelings are now instructing doctors which treatment protocols they will adhere to and which treatments they will not use, no matter how harmful the “approved” treatments are or how beneficial the “unapproved” treatments are.[33,57]

Never in the history of American medicine have hospital administrators dictated to its physicians how they will practice medicine and what medications they can use. The CDC has no authority to dictate to hospitals or doctors concerning medical treatments. Yet, most physicians complied without the slightest resistance.

The federal Care Act encouraged this human disaster by offering all US hospitals up to 39,000 dollars for each ICU patient they put on respirators, despite the fact that early on it was obvious that the respirators were a major cause of death among these unsuspecting, trusting patients. In addition, the hospitals received 12,000 dollars for each patient that was admitted to the ICU—explaining, in my opinion and others, why all federal medical bureaucracies (CDC, FDA, NIAID, NIH, etc) did all in their power to prevent life- saving early treatments.[46] Letting patients deteriorate to the point they needed hospitalization, meant big money for all hospitals. A growing number of hospitals are in danger of bankruptcy, and many have closed their doors, even before this “pandemic”.[50] Most of these hospitals are now owned by national or international corporations, including teaching hospitals.[10]

It is also interesting to note that with the arrival of this “pandemic” we have witnessed a surge in hospital corporate chains buying up a number of these financially at-risk hospitals.[1,54] It has been noted that billions in Federal Covid aid is being used by these hospital giants to acquire these financially endangered hospitals, further increasing the power of corporate medicine over physician independence. Physicians expelled from their hospitals are finding it difficult to find other hospitals staffs to join since they too may be owned by the same corporate giant. As a result, vaccine mandate policies include far larger numbers of hospital employees. For example, Mayo Clinic fired 700 employees for exercising their right to refuse a dangerous, essentially untested experimental vaccine.[51,57] Mayo Clinic did this despite the fact that many of these employees worked during the worst of the epidemic and are being fired when the Omicron variant is the dominant strain of the virus, has the pathogenicity of a common cold for most and the vaccines are ineffective in preventing the infection.

In addition, it has been proven that the vaccinated asymptomatic person has a nasopharyngeal titer of the virus as high as an infected unvaccinated person. If the purpose of the vaccine mandate is to prevent viral spread among the hospital staff and patients, then it is the vaccinated who present the greatest risk of transmission, not the unvaccinated. The difference is that a sick unvaccinated person would not go to work, the asymptomatic vaccinated spreader will.

What we do know is that major medical centers, such as Mayo Clinic, receive tens of millions of dollars in NIH grants each year as well as monies from the pharmaceutical makers of these experimental “vaccines”. In my view, that is the real consideration driving these policies. If this could be proven in a court of law the administrators making these mandates should be prosecuted to the fullest extent of the law and sued by all injured parties.

The hospital bankruptcy problem has grown increasingly acute due to hospitals vaccine mandates and resulting large number of hospitals staff, especially nurses, refusing to be forcibly vaccinated.[17,51] This is all unprecedented in the history of medical care. Doctors within hospitals are responsible for the treatment of their individual patients and work directly with these patients and their families to initiate these treatments. Outside organizations, such as the CDC, have no authority to intervene in these treatments and to do so exposes the patients to grave errors by an organization that has never treated a single COVID-19 patient.

When this pandemic started, hospitals were ordered by the CDC to follow a treatment protocol that resulted in the deaths of hundreds of thousands of patients, most of whom would have recovered had proper treatments been allowed.[43,44] The majority of these deaths could have been prevented had doctors been allowed to use early treatment with such products as Ivermectin, hydroxy-chloroquine and a number of other safe drugs and natural compounds. It has been estimated, based on results by physicians treating the most covid patients successfully, that of the 800,000 people that we are told died from Covid, 640,000 could have not only been saved, but could have, in many cases, returned to their pre-infection health status had mandated early treatment with these proven methods been used. This neglect of early treatment constitutes mass murder. That means 160,000 would have actually died, far less than the number dying at the hands of bureaucracies, medical associations and medical boards that refused to stand up for their patients. According to studies of early treatment of thousands of patients by brave, caring doctors, seventy-five to eighty percent of the deaths could have been prevented.[43,44]

Incredibly, these knowledgeable doctors were prevented from saving these Covid-19 infected people. It should be an embarrassment to the medical profession that so many doctors mindlessly followed the deadly protocols established by the controllers of medicine.

One must also keep in mind that this event never satisfied the criteria for a pandemic. The World Health Organization changed the criteria to make this a pandemic. To qualify for a pandemic status the virus must have a high mortality rate for the vast majority of people, which it didn’t (with a 99.98% survival rate), and it must have no known existing treatments—which this virus had—in fact, a growing number of very successful treatments.

The draconian measures established to contain this contrived “pandemic” have never been shown to be successful, such as masking the public, lockdowns, and social distancing. A number of carefully done studies during previous flu seasons demonstrated that masks, of any kind, had never prevented the spread of the virus among the public.[60]

In fact, some very good studies suggested that the masks actually spread the virus by giving people a false sense of security and other factors, such as the observation that people were constantly breaking sterile technique by touching their mask, improper removal and by leakage of infectious aerosols around the edges of the mask. In addition masks were being disposed of in parking lots, walking trails, laid on tabletops in restaurants and placed in pockets and purses.

Within a few minutes of putting on the mask, a number of pathogenic bacteria can be cultured from the masks, putting the immune suppressed person at a high risk of bacterial pneumonia and children at a higher risk of meningitis.[16] A study by researchers at the University of Florida cultured over 11 pathogenic bacteria from the inside of the mask worn by children in schools.[40]

It was also known that children were at essentially no risk of either getting sick from the virus or transmitting it.

In addition, it was also known that wearing a mask for over 4 hours (as occurs in all schools) results in significant hypoxia (low blood oxygen levels) and hypercapnia (high CO2 levels), which have a number of deleterious effects on health, including impairing the development of the child’s brain.[4,72,52]

We have known that brain development continues long after the grade school years. A recent study found that children born during the “pandemic” have significantly lower IQs—yet school boards, school principals and other educational bureaucrats are obviously unconcerned.[18]

TOOLS OF THE INDOCTRINATION TRADE

The designers of this pandemic anticipated a pushback by the public and that major embarrassing questions would be asked. To prevent this, the controllers fed the media a number of tactics, one of the most commonly used was and is the “fact check” scam. With each confrontation with carefully documented evidence, the media “fact checkers” countered with the charge of “misinformation”, and an unfounded “conspiracy theory” charge that was, in their lexicon, “debunked”. Never were we told who the fact checkers were or the source of their “debunking” information—we were just to believe the “fact checkers”. A recent court case established under oath that facebook “fact checkers” used their own staff opinion and not real experts to check “facts”.[59] When sources are in fact revealed they are invariably the corrupt CDC, WHO or Anthony Fauci or just their opinion. Here is a list of things that were labeled as “myths” and “misinformation” that were later proven to be true.

• The asymptomatic vaccinated are spreading the virus equally as with unvaccinated symptomatic infected.

• The vaccines cannot protect adequately against new variants, such as Delta and Omicron.

• Natural immunity is far superior to vaccine immunity and is most likely lifelong.

• Vaccine immunity not only wanes after several months, but all immune cells are impaired for prolonged periods, putting the vaccinated at a high risk of all infections and cancer.

• COVID vaccines can cause a significant incidence of blood clots and other serious side effects

• The vaccine proponents will demand numerous boosters as each variant appears on the scene.

• Fauci will insist on the covid vaccine for small children and even babies.

• Vaccine passports will be required to enter a business, fly in a plane, and use public transportation

• There will be internment camps for the unvaccinated (as in Australia, Austria and Canada)

• The unvaccinated will be denied employment.

• There are secret agreements between the government, elitist institutions, and vaccine makers

• Many hospitals were either empty or had low occupancy during the pandemic.

• The spike protein from the vaccine enters the nucleus of the cell, altering cell DNA repair function.

• Hundreds of thousands have been killed by the vaccines and many times more have been permanently damaged.

• Early treatment could have saved the lives of most of the 700,000 who died.

• Vaccine-induced myocarditis (which was denied initially) is a significant problem and clears over a short period.

• Special deadly lots (batches) of these vaccines are mixed with the mass of other Covid-19 vaccines

Several of these claims by those opposing these vaccines now appear on the CDC website—most still identified as “myths”. Today, extensive evidence has confirmed that each of these so-called “myths” were in fact true. Many are even admitted by the “saint of vaccines”, Anthony Fauci. For example, we were told, even by our cognitively impaired President, that once the vaccine was released all the vaccinated people could take off their masks. Oops! We were told shortly afterward— the vaccinated have high concentrations (titers) of the virus in their noses and mouths (nasopharynx) and can transmit the virus to others in which they come into contact—especially their own family members. On go the masks once again— in fact double masking is recommended. The vaccinated are now known to be the main superspreaders of the virus and hospitals are filled with the sick vaccinated and people suffering from serious vaccine complications.[27,42,45]

Another tactic by the vaccine proponents is to demonize those who reject being vaccinated for a variety of reasons. The media refers to these critically thinking individuals as “anti-vaxxers”, “vaccine deniers”, “Vaccine resisters”, “murders”, “enemies of the greater good” and as being the ones prolonging the pandemic. I have been appalled by the vicious, often heartless attacks by some of the people on social media when a parent or loved one relates a story of the terrible suffering and eventual death, they or their loved one suffered as a result of the vaccines. Some psychopaths tweet that they are glad that the loved one died or that the dead vaccinated person was an enemy of good for telling of the event and should be banned. This is hard to conceptualize. This level of cruelty is terrifying, and signifies the collapse of a moral, decent, and compassionate society.

It is bad enough for the public to sink this low, but the media, political leaders, hospital administrators, medical associations and medical licensing boards are acting in a similar morally dysfunctional and cruel way.

LOGIC, REASONING, AND SCIENTIFIC EVIDENCE HAS DISAPPEARED IN THIS EVENT

Has scientific evidence, carefully done studies, clinical experience and medical logic had any effect on stopping these ineffective and dangerous vaccines? Absolutely not! The draconian efforts to vaccinate everyone on the planet continues (except the elite, postal workers, members of Congress and other insiders).[31,62]

In the case of all other drugs and previous conventional vaccines under review by the FDA, the otherwise unexplained deaths of 50 or less individuals would result in a halt in further distribution of the product, as happened on 1976 with the swine flu vaccine. With over 18,000 deaths being reported by the VAERS system for the period December 14, 2020 and December 31st, 2021 as well as 139,126 serious injuries (including deaths) for the same period there is still no interest in stopping this deadly vaccine program.[61] Worse, there is no serious investigation by any government agency to determine why these people are dying and being seriously and permanently injured by these vaccines.[15,67] What we do see is a continuous series of coverups and evasions by the vaccine makers and their promoters.

The war against effective cheap and very safe repurposed drugs and natural compounds, that have proven beyond all doubt to have saved millions of lives all over the world, has not only continued but has stepped up in intensity.[32,34,43]

Doctors are told they cannot provide these life-saving compounds for their patients and if they do, they will be removed from the hospital, have their medical license removed or be punished in many other ways. A great many pharmacies have refused to fill prescriptions for lvermectin or hydroxy- chloroquine, despite the fact that millions of people have taken these drugs safely for over 60 years in the case of hydroxy chloroquine and decades for Ivermectin.[33,36] This refusal to fill prescriptions is unprecedented and has been engineered by those wanting to prevent alternative methods of treatment, all based on protecting vaccine expansion to all. Several companies that make hydroxy chloroquine agreed to empty their stocks of the drug by donating them to the Strategic National Stockpile, making this drug far more difficult to get.[33] Why would the government do that when over 30 well-done studies have shown that this drug reduced deaths anywhere from 66% to 92% in other countries, such as India, Egypt, Argentina, France, Nigeria, Spain, Peru, Mexico, and others?[23]

The critics of these two life-saving drugs are most often funded by Bill Gates and Anthony Fauci, both of which are making millions from these vaccines.[48,15]

To further stop the use of these drugs, the pharmaceutical industry and Bill Gates/Anthony Fauci funded fake research to make the case that hydroxy chloroquine was a dangerous drug and could damage the heart.[34] To make this fraudulent case the researchers administered the sickest of covid patients a near lethal dose of the drug, in a dose far higher than used on any covid patient by Dr. Kory, McCullough and other “real”, and compassionate doctors, physicians who were actually treating covid patients.[23]

The controlled, lap-dog media, of course, hammered the public with stories of the deadly effect of hydroxy- chloroquine, all with a terrified look of fake panic. All these stories of ivermectin dangers were shown to be untrue and some of the stories were incredibly preposterous.[37,43]

The attack on Ivermectin was even more vicious than against hydroxy-chloroquine. All of this, and a great deal more is meticulously chronicled in Robert Kennedy, Jr’s excellent new book—The Real Anthony Fauci. Bill Gates, Big Pharma, and the Global War on Democracy and Public Health.[32] If you are truly concerned with the truth and with all that has occurred since this atrocity started, you must not only read, but study this book carefully. It is fully referenced and covers all topics in great detail. This is a designed human tragedy of Biblical proportions by some of the most vile, heartless, psychopaths in history.

Millions have been deliberately killed and crippled, not only by this engineered virus, but by the vaccine itself and by the draconian measures used by these governments to “control the pandemic spread”. We must not ignore the “deaths by despair” caused by these draconian measures, which can exceed hundreds of thousands. Millions have starved in third world countries as a result. In the United States alone, of the 800,000 who died, claimed by the medical bureaucracies, well over 600,000 of these deaths were the result of the purposeful neglect of early treatment, blocking the use of highly effective and safe repurposed drugs, such as hydroxy-chloroquine and Ivermectin, and the forced use of deadly treatments such as remdesivir and use of ventilators. This does not count the deaths of despair and neglected medical care caused by the lockdown and hospital measures forced on healthcare systems.

To compound all this, because of vaccine mandates among all hospital personnel, thousands of nurses and other hospital workers have resigned or been fired.[17,30,51] This has resulted in critical shortages of these vital healthcare workers and dangerous reductions of ICU beds in many hospitals. In addition, as occurred in the Lewis County Healthcare System, a specialty-hospital system in Lowville, N.Y., closed its maternity unit following the resignation of 30 hospital staff over the state’s disastrous vaccine mandate orders. The irony in all these cases of resignations is that the administrators unhesitatingly accepted these mass staffing losses despite rantings about suffering from short staffing during a “crisis”. This is especially puzzling when we learned that the vaccines did not prevent viral transmission and the present predominant variant is of extremely low pathogenicity.

DANGERS OF THE VACCINES ARE INCREASINGLY REVEALED BY SCIENCE

While most researchers, virologists, infectious disease researchers and epidemiologists have been intimidated into silence, a growing number of high integrity individuals with tremendous expertise have come forward to tell the truth—that is, that these vaccines are deadly.

Most new vaccines must go through extensive safety testing for years before they are approved. New technologies, such as the mRNA and DNA vaccines, require a minimum of 10 years of careful testing and extensive follow-up. These new so-called vaccines were “tested” for only 2 months and then the results of these safety test were and continue to be kept secret. Testimony before Senator Ron Johnson by several who participated in the 2 months study indicates that virtually no follow-up of the participants of the pre-release study was ever done.[67] Complains of complications were ignored and despite promises by Pfizer that all medical expenses caused by the “vaccines” would be paid by Pfizer, these individuals stated that none were paid.[66] Some medical expenses exceed 100,000 dollars.

As an example of the deception by Pfizer, and the other makers of mRNA vaccines, is the case of 12-year-old Maddie de Garay, who participated in the Pfizer vaccine pre-release safety study. At Sen. Johnson’s presentation with the families of the vaccine injured, her mother told of her child’s recurrent seizures, that she is now confined to a wheelchair, must be tube fed and suffers permanent brain damage. On the Pfizer safety evaluation submitted to the FDA her only side effect is listed as having a “stomachache”. Each person submitted similar horrifying stories.

The Japanese resorted to a FOIA (Freedom of Information Act) lawsuit to force Pfizer to release its secret biodistribution study. The reason Pfizer wanted it kept secret is that it demonstrated that Pfizer lied to the public and the regulatory agencies about the fate of the injected vaccine contents (the mRNA enclosed nano-lipid carrier). They claimed that it remained at the site of the injection (the shoulder), when in fact their own study found that it rapidly spread throughout the entire body by the bloodstream within 48 hours.

The study also found that these deadly nano-lipid carriers collected in very high concentrations in several organs, including the reproductive organs of males and females, the heart, the liver, the bone marrow, and the spleen (a major immune organ). The highest concentration was in the ovaries and the bone marrow. These nano-lipid carriers also were deposited in the brain.

Dr. Ryan Cole, a pathologist from Idaho reported a dramatic spike in highly aggressive cancers among vaccinated individuals, (not reported in the Media). He found a frighteningly high incidence of highly aggressive cancers in vaccinated individuals, especially highly invasive melanomas in young people and uterine cancers in women.[26] Other reports of activation of previously controlled cancers are also appearing among vaccinated cancer patients.[47] Thus far, no studies have been done to confirm these reports, but it is unlikely such studies will be done, at least studies funded by grants from the NIH.

The high concentration of spike proteins found in the ovaries in the biodistribution study could very well impair fertility in young women, alter menstruation, and could put them at an increased risk of ovarian cancer. The high concentration in the bone marrow, could also put the vaccinated at a high risk of leukemia and lymphoma. The leukemia risk is very worrisome now that they have started vaccinating children as young as 5 years of age. No long-term studies have been conducted by any of these makers of Covid-19 vaccines, especially as regards the risk of cancer induction. Chronic inflammation is intimately linked to cancer induction, growth and invasion and vaccines stimulate inflammation.

Cancer patients are being told they should get vaccinated with these deadly vaccines. This, in my opinion, is insane. Newer studies have shown that this type of vaccine inserts the spike protein within the nucleus of the immune cells (and most likely many cell types) and once there, inhibits two very important DNA repair enzymes, BRCA1 and 53BP1, whose duty it is to repair damage to the cell’s DNA.[29] Unrepaired DNA damage plays a major role in cancer.

There is a hereditary disease called xeroderma pigmentosum in which the DNA repair enzymes are defective. These ill-fated individuals develop multiple skin cancers and a very high incidence of organ cancer as a result. Here we have a vaccine that does the same thing, but to a less extensive degree.

One of the defective repair enzymes caused by these vaccines is called BRCA1, which is associated with a significantly higher incidence of breast cancer in women and prostate cancer in men.

It should be noted that no studies were ever done on several critical aspects of this type of vaccine.

• They have never been tested for long term effects

• They have never been tested for induction of autoimmunity

• They have never been properly tested for safety during any stage of pregnancy

• No follow-up studies have been done on the babies of vaccinated women

• There are no long-term studies on the children of vaccinated pregnant women after their birth (Especially as neurodevelopmental milestone occur).

• It has never been tested for effects on a long list of medical conditions:

  • Diabetes

  • Heart disease

  • Atherosclerosis

  • Neurodegenerative diseases

  • Neuropsychiatric effects

  • Induction of autism spectrum disorders and schizophrenia

  • Long term immune function

  • Vertical transmission of defects and disorders

  • Cancer

  • Autoimmune disorders

Previous experience with the flu vaccines clearly demonstrates that the safety studies done by researchers and clinical doctors with ties to pharmaceutical companies were essentially all either poorly done or purposefully designed to falsely show safety and coverup side effects and complications. This was dramatically demonstrated with the previously mentioned phony studies designed to indicate that hydroxy Chloroquine and Ivermectin were ineffective and too dangerous to use.[34,36,37] These fake studies resulted in millions of deaths and severe health disasters worldwide. As stated, 80% of all deaths were unnecessary and could have been prevented with inexpensive, safe repurposed medications with a very long safety history among millions who have taken them for decades or even a lifetime.[43,44]

It is beyond ironic that those claiming that they are responsible for protecting our health approved a poorly tested set of vaccines that has resulted in more deaths in less than a year of use than all the other vaccines combined given over the past 30 years. Their excuse when confronted was—“we had to overlook some safety measures because this was a deadly pandemic”.[28,46]

In 1986 President Reagan signed the National Childhood Vaccine Injury Act, which gave blanket protection to pharmaceutical makers of vaccines against injury litigation by families of vaccine injured individuals. The Supreme Court, in a 57-page opinion, ruled in favor of the vaccine companies, effectively allowing vaccine makers to manufacture and distribute dangerous, often ineffective vaccines to the population without fear of legal consequences. The court did insist on a vaccine injury compensation system which has paid out only a very small number of rewards to a large number of severely injured individuals. It is known that it is very difficult to receive these awards. According to the Health Resources and Services Administration, since 1988 the Vaccine Injury Compensation Program (VICP) has agreed to pay 3,597 awards among 19,098 vaccine injured individuals applying amounting to a total sum of $3.8 billion. This was prior to the introduction of the Covid-19 vaccines, in which the deaths alone exceed all deaths related to all the vaccines combined over a thirty-year period.

In 2018 President Trump signed into law the “right-to-try” law which allowed the use of experimental drugs and all unconventional treatments to be used in cases of extreme medical conditions. As we have seen with the refusal of many hospitals and even blanket refusal by states to allow Ivermectin, hydroxy-chloroquine or any other unapproved “official” methods to treat even terminal Covid-19 cases, these nefarious individuals have ignored this law.

Strangely, they did not use this same logic or the law when it came to Ivermectin and Hydroxy Chloroquine, both of which had undergone extensive safety testing by over 30 clinical studies of a high quality and given glowing reports on both efficacy and safety in numerous countries. In addition, we had a record of use for up to 60 years by millions of people, using these drugs worldwide, with an excellent safety record. It was obvious that a group of very powerful people in conjunction with pharmaceutical conglomerates didn’t want the pandemic to end and wanted vaccines as the only treatment option. Kennedy’s book makes this case using extensive evidence and citations.[14,32]

Dr. James Thorpe, an expert in maternal-fetal medicine, demonstrates that these covoid-19 vaccines given during pregnancy have resulted in a 50-fold higher incidence of miscarriage than reported with all other vaccines combined.[28] When we examine his graph on fetal malformations there was a 144-fold higher incidence of fetal malformation with the Covid-19 vaccines given during pregnancy as compared to all other vaccines combined. Yet, the American Academy of Obstetrics and Gynecology and the American College of Obstetrics and Gynecology endorse the safety of these vaccines for all stages of pregnancy and among women breast feeding their babies.

It is noteworthy that these medical specialty groups have received significant funding from Pfizer pharmaceutical company. The American College of Obstetrics and Gynecology, just in the 4th quarter of 2010, received a total of $11,000 from Pfizer Pharmaceutical company alone.[70] Funding from NIH grants are much higher.[20] The best way to lose these grants is to criticize the source of the funds, their products or pet programs. Peter Duesberg, because of his daring to question Fauci’s pet theory of AIDS caused by HIV virus, was no longer awarded any of the 30 grant applications he submitted after going public. Prior to this episode, as the leading authority on retroviruses in the world, he had never been turned down for an NIH grant.[39] This is how the “corrupted” system works, even though much of the grant money comes from our taxes.

HOT LOTS—DEADLY BATCHES OF THE VACCINES

A new study has now surfaced, the results of which are terrifying.[25] A researcher at Kingston University in London, has completed an extensive analysis of the VAERs data (a subdepartment of the CDC which collects voluntary vaccine complication data), in which he grouped reported deaths following the vaccines according to the manufacturer’s lot numbers of the vaccines. Vaccines are manufactured in large batches called lots. What he discovered was that the vaccines are divided into over 20,000 lots and that one out of every 200 of these batches (lots) is demonstrably deadly to anyone who receives a vaccine from that lot, which includes thousands of vaccine doses.

He examined all manufactured vaccines—Pfizer, Moderna, Johnson and Johnson (Janssen), etc. He found that among every 200 batches of the vaccine from Pfizer and other makers, one batch of the 200 was found to be over 50x more deadly than vaccines batches from other lots. The other vaccine lots (batches) were also causing deaths and disabilities, but nowhere near to this extent. These deadly batches should have appeared randomly among all “vaccines” if it was an unintentional event. However, he found that 5% of the vaccines were responsible for 90% of the serious adverse events, including deaths. The incidence of deaths and serious complications among these “hot lots” varied from over 1000% to several thousand percent higher than comparable safer lots. If you think this was by accident—think again. This is not the first time “hot lots” were, in my opinion, purposefully manufactured and sent across the nation—usually vaccines designed for children. In one such scandal, “hot lots” of a vaccine ended up all in one state and the damage immediately became evident. What was the manufacture’s response? It wasn’t to remove the deadly batches of the vaccine. He ordered his company to scatter the hot lots across the nation so that authorities would not see the obvious deadly effect.

All lots of a vaccine are numbered—for example Modera labels them with such codes as 013M20A. It was noted that the batch numbers ended in either 20A or 21A. Batches ending in 20A were much more toxic than the ones ending in 21A. The batches ending in 20A had about 1700 adverse events, versus a few hundred to twenty or thirty events for the 21A batches. This example explains why some people had few or no adverse events after taking the vaccine while others are either killed or severely and permanently harmed. To see the researcher’s explanation, go to https://www.bitchute.com/video/6xIYPZBkydsu/ In my opinion these examples strongly suggest an intentional alteration of the production of the “vaccine” to include deadly batches.

I have met and worked with a number of people concerned with vaccine safety and I can tell you they are not the evil anti-vaxxers you are told they are. They are highly principled, moral, compassionate people, many of which are top researchers and people who have studied the issue extensively. Robert Kennedy, Jr, Barbara Lou Fisher, Dr. Meryl Nass, Professor Christopher Shaw, Megan Redshaw, Dr. Sherri Tenpenny, Dr. Joseph Mercola, Neil Z. Miller, Dr. Lucija Tomjinovic, Dr. Stephanie Seneff, Dr. Steve Kirsch and Dr. Peter McCullough just to name a few. These people have nothing to gain and a lot to lose. They are attacked viciously by the media, government agencies, and elite billionaires who think they should control the world and everyone in it.

WHY DID FAUCI WANT NO AUTOPSIES OF THOSE WHO DIED AFTER VACCINATION?

There are many things about this “pandemic” that are unprecedented in medical history. One of the most startling is that at the height of the pandemic so few autopsies, especially total autopsies, were being done. A mysterious virus was rapidly spreading around the world, a selected group of people with weakened immune systems were getting seriously ill and many were dying and the one way we could rapidly gain the most knowledge about this virus—an autopsy, was being discouraged.

Guerriero noted that by the end of April, 2020 approximately 150,000 people had died, yet there were only 16 autopsies performed and reported in the medical literature.[24] Among these, only seven were complete autopsies, the remaining 9 being partial or by needle biopsy or incisional biopsy. Only after 170,000 deaths by Covid-19 and four months into the pandemic were the first series of autopsies actually done, that is, more than ten. And only after 280,000 deaths and another month, were the first large series of autopsies performed, some 80 in number.[22] Sperhake, in a call for autopsies to be done without question, noted that the first full autopsy reported in the literature along with photomicrographs appeared in a medico-legal journal from China in February 2020.[41,68] Sperhake expressed confusion as to why there was a reluctance to perform autopsies during the crisis, but he knew it was not coming from the pathologists. The medical literature was littered with appeals by pathologist for more autopsies to be performed.[58] Sperhake further noted that the Robert Koch Institute (The German health monitoring system) at least initially advised against doing autopsies. He also knew that at the time 200 participating autopsy institutions in the United States had done at least 225 autopsies among 14 states.

Some have claimed that this dearth of autopsies was based on the government’s fear of infection among the pathologists, but a study of 225 autopsies on Covid-19 cases demonstrated only one case of infection among the pathologist and this was concluded to have been an infection contracted elsewhere.[19] Guerriero ends his article calling for more autopsies with this observation: “Shoulder to shoulder, clinical and forensic pathologists overcame the obstructions of autopsy studies in Covid-19 victims and hereby generated valuable knowledge on the pathophysiology of the interaction between the SARS-CoV-2 and the human body, thus contributing to our understanding of the disease.”[24]

Suspicion concerning the worldwide reluctance of nations to allow full post mortem studies of Covid-19 victims may be based on the idea that it was more than by chance. There are at least two possibilities that stand out. First, those leading the progression of this “non-pandemic” event into a perceived worldwide “deadly pandemic”, were hiding an important secret that autopsies could document. Namely, just how many of the deaths were actually caused by the virus? To implement draconian measures, such as mandated mask wearing, lockdowns, destruction of businesses, and eventually mandated forced vaccination, they needed very large numbers of covid-19 infected dead. Fear would be the driving force for all these destructive pandemic control programs.

Elder et al in his study classified the autopsy findings into four groups.[22]

1. Certain Covid-19 death
2. Probably Covid-19 death
3. Possible Covid-19 death
4. Not associated with Covid-19, despite the positive test.

What possibly concerned or even terrified the engineers of this pandemic was that autopsies just might, and did, show that a number of these so-called Covid-19 deaths in truth died of their comorbid diseases. In the vast majority of autopsy studies reported, pathologists noted multiple comorbid conditions, most of which at the extremes of life could alone be fatal. Previously it was known that common cold viruses had an 8% mortality in nursing homes.

In addition, valuable evidence could be obtained from the autopsies that would improve clinical treatments and could possibly demonstrate the deadly effect of the CDC mandated protocols all hospitals were required to follow, such as the use of respirators and the deadly, kidney-destroying drug remdesivir. The autopsies also demonstrated accumulating medical errors and poor-quality care, as the shielding of doctors in intensive care units from the eyes of family members inevitably leads to poorer quality care as reported by several nurses working in these areas.[53-55]

As bad as all this was, the very same thing is being done in the case of Covid vaccine deaths—very few complete autopsies have been done to understand why these people died, that is, until recently. Two highly qualified researchers, Dr. Sucharit Bhakdi a microbiologist and highly qualified expert in infectious disease and Dr. Arne Burkhardt, a pathologist who is a widely published authority having been a professor of pathology at several prestigious institutions, recently performed autopsies on 15 people having died after vaccination. What they found explains why so many are dying and experiencing organ damage and deadly blood clots.[5]

They determined that 14 of the fifteen people died as a result of the vaccines and not of other causes. Dr. Burkhardt, the pathologist, observed widespread evidence of an immune attack on the autopsied individuals’ organs and tissues— especially their heart. This evidence included extensive invasion of small blood vessels with massive numbers of lymphocytes, which cause extensive cell destruction when unleashed. Other organs, such as the lungs and liver, were observed to have extensive damage as well. These findings indicate the vaccines were causing the body to attack itself with deadly consequences. One can easily see why Anthony Fauci, as well as public health officers and all who are heavily promoting these vaccines, publicly discouraged autopsies on the vaccinated who subsequently died. One can also see that in the case of vaccines, that were essentially untested prior to being approved for the general public, at least the regulatory agencies should have been required to carefully monitor and analyze all serious complications, and certainly deaths, linked to these vaccines. The best way to do that is with complete autopsies.

While we learned important information from these autopsies what is really needed are special studies of the tissues of those who have died after vaccination for the presence of spike protein infiltration throughout the organs and tissues. This would be critical information, as such infiltration would result in severe damage to all tissues and organs involved—especially the heart, the brain, and the immune system. Animal studies have demonstrated this. In these vaccinated individuals the source of these spike proteins would be the injected nanolipid carriers of the spike protein producing mRNA. It is obvious that the government health authorities and pharmaceutical manufacturers of these “vaccines” do not want these critical studies done as the public would be outraged and demand an end to the vaccination program and prosecution of the involved individuals who covered this up.

CONCLUSIONS

We are all living through one of the most drastic changes in our culture, economic system, as well as political system in our nation’s history as well as the rest of the world. We have been told that we will never return to “normal” and that a great reset has been designed to create a “new world order”. This has all been outlined by Klaus Schwab, head of the World Economic Forum, in his book on the “Great Reset”.[66] This book gives a great deal of insight as to the thinking of the utopians who are proud to claim this pandemic “crisis” as their way to usher in a new world. This new world order has been on the drawing boards of the elite manipulators for over a century.[73,74] In this paper I have concentrated on the devastating effects this has had on the medical care system in the United States, but also includes much of the Western world. In past papers I have discussed the slow erosion of traditional medical care in the United States and how this system has become increasingly bureaucratized and regimented.[7,8] This process was rapidly accelerating, but the appearance of this, in my opinion, manufactured “pandemic” has transformed our health care system over night.

As you have seen, an unprecedented series of events have taken place within this system. Hospital administrators, for example, assumed the position of medical dictators, ordering doctors to follow protocols derived not from those having extensive experience in treating this virus, but rather from a medical bureaucracy that has never treated a single COVID-19 patient. The mandated use of respirators on ICU Covid-19 patients, for example, was imposed in all medical systems and dissenting physicians were rapidly removed from their positions as caregivers, despite their demonstration of markedly improved treatment methods. Further, doctors were told to use the drug remdesivir despite its proven toxicity, lack of effectiveness and high complication rate. They were told to use drugs that impaired respiration and mask every patient, despite the patient’s impaired breathing. In each case, those who refused to abuse their patients were removed from the hospital and even faced a loss of license—or worse.

For the first time in modern medical history, early medical treatment of these infected patients was ignored nationwide. Studies have shown that early medical treatment was saving 80% of higher number of these infected people when initiated by independent doctors.[43,44] Early treatment could have saved over 640,000 lives over the course of this “pandemic”. Despite the demonstration of the power of these early treatments, the forces controlling medical care continued this destructive policy.

Families were not allowed to see their loved ones, forcing these very sick individuals in the hospitals to face their deaths alone. To add insult to injury, funerals were limited to a few grieving family members, who were not allowed to even sit together. All the while large stores, such as Walmart and Cosco were allowed to operate with minimal restrictions. Nursing home patients were also not allowed to have family visitations, again being forced to die a lonely death. All the while, in a number of states, the most transparent being in New York state, infected elderly were purposefully transferred from hospitals into nursing homes, resulting in a very high death rates of these nursing home residents. At the beginning of this “pandemic” over 50% of all death were occurring in nursing homes.

Throughout this “pandemic” we have been fed an unending series of lies, distortions and disinformation by the media, the public health officials, medical bureaucracies (CDC, FDA and WHO) and medical associations. Physicians, scientists, and experts in infectious treatments who formed associations designed to develop more effective and safer treatments, were regularly demonized, harassed, shamed, humiliated, and experience a loss of licensure, loss of hospital privileges and, in at least one case, ordered to have a psychiatric examination.[2,65,71]

Anthony Fauci was given essentially absolute control of all forms of medical care during this event, including insisting that drugs he profited from be used by all treating physicians. He ordered the use of masks, despite at first laughing at the use of masks to filter a virus. Governors, mayors, and many businesses followed his orders without question.

The draconian measures being used, masking, lockdowns, testing of the uninfected, use of the inaccurate PCR test, social distancing, and contact tracing had been shown previously to be of little or no use during previous pandemics, yet all attempts to reject these methods were to no avail. Some states ignored these draconian orders and had either the same or fewer cases, as well as deaths, as the states with the most strictly enforced measures. Again, no amount of evidence or obvious demonstration along these lines had any effect on ending these socially destructive measures. Even when entire countries, such as Sweden, which avoided all these measures, demonstrated equal rates of infections and hospitalization as nations with the strictest, very draconian measures, no policy change by the controlling institutions occurred. No amount of evidence changed anything.

Experts in the psychology of destructive events, such as economic collapses, major disasters and previous pandemics demonstrated that draconian measures come with an enormous cost in the form of “deaths of despair” and in a dramatic increase in serious psychological disorders. The effects of these pandemic measures on children’s neurodevelopment is catastrophic and to a large extent irreversible.

Over time tens of thousands could die as a result of this damage. Even when these predictions began to appear, the controllers of this “pandemic” continued full steam ahead. Drastic increases in suicides, a rise in obesity, a rise in drug and alcohol use, a worsening of many health measures and a terrifying rise in psychiatric disorders, especially depression and anxiety, were ignored by the officials controlling this event.

We eventually learned that many of the deaths were a result of medical neglect. Individuals with chronic medical conditions, diabetes, cancer, cardiovascular disease, and neurological diseases were no longer being followed properly in their clinics and doctor’s offices. Non-emergency surgeries were put on hold. Many of these patients chose to die at home rather than risk going to the hospitals and many considered hospitals “death houses”.

Records of deaths have shown that there was a rise in deaths among those aged 75 and older, mostly explained by Covid-19 infections, but for those between the ages of 65 to 74, deaths had been increasing well before the pandemic onset.[69] Between ages of 18 and aged 65 years, records demonstrate a shocking hike in non-Covid-19 deaths. Some of these deaths were explained by a dramatic increase in drug-related deaths, some 20,000 more than 2019. Alcohol related deaths also increased substantially, and homicides increased almost 30% in the 18 to 65-year group.

The head of the insurance company OneAmerica stated that their data indicated that the death rate for individuals aged 18 to 64 had increased 40% over the pre-pandemic period.[21] Scott Davidson, the company’s CEO, stated that this represented the highest death rate in the history of insurance records, which does extensive data collections on death rates each year. Davidson also noted that this high of a death rate increase has never been seen in the history of death data collection. Previous catastrophes of monumental extent increased death rates no more than 10 percent, 40% is unprecedented.

Dr. Lindsay Weaver, Indiana’s chief medical officer, stated that hospitalizations in Indiana are higher than at any point in the past five years. This is of critical importance since the vaccines were supposed to significantly reduce deaths, but the opposite has happened. Hospitals are being flooded with vaccine complications and people in critical condition from medical neglect caused by the lockdowns and other pandemic measures.[46,56]

A dramatic number of these people are now dying, with the spike occurring after the vaccines were introduced. The lies flowing from those who have appointed themselves as medical dictators are endless. First, we were told that the lockdown would last only two weeks, they lasted over a year. Then we were told that masks were ineffective and did not need to be worn. Quickly that was reversed. Then we were told the cloth mask was very effective, now it’s not and everyone should be wearing an N95 mask and before that that they should double mask. We were told there was a severe shortage of respirators, then we discover they are sitting unused in warehouses and in city dumps, still in their packing crates. We were informed that the hospitals were filled mostly with the unvaccinated and later found the exact opposite was true the world over. We were told that the vaccine was 95% effective, only to learn that in fact the vaccines cause a progressive erosion of innate immunity.

Upon release of the vaccines, women were told the vaccines were safe during all states of pregnancy, only to find out no studies had been done on safety during pregnancy during the “safety tests” prior to release of the vaccine. We were told that careful testing on volunteers before the EUA approval for public use demonstrated extreme safety of the vaccines, only to learn that these unfortunate subjects were not followed, medical complications caused by the vaccines were not paid for and the media covered this all up.[67] We also learned that the pharmaceutical makers of the vaccines were told by the FDA that further animal testing was unnecessary (the general public would be the Guinea pigs.) Incredibly, we were told that the Pfizer’s new mRNA vaccines had been approved by the FDA, which was a cleaver deception, in that another vaccine had approval (comirnaty) and not the one being used, the BioNTech vaccine. The approved comirnaty vaccine was not available in the United States. The national media told the public that the Pfizer vaccine had been approved and was no longer classed as experimental, a blatant lie. These deadly lies continue. It is time to stop this insanity and bring these people to justice.

Footnotes

How to cite this article: Blaylock RL. COVID UPDATE: What is the truth? Surg Neurol Int 2022;13:167.

Disclaimer

The views and opinions expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Journal or its management.

REFERENCES

1. Abelson R. Buoyed by federal Covid aid, big hospital chains buy up competitors. The New York Times Mat 21, 2021 (updated Oct 22, 2022) https://www.nytimes.com/2021/05/21/health/covid-bailout-hospital-merger.html .

2. Albright L. Medical nonconformity and its persecution. Brownstone Institute. https://brownstone.org/articles/medical-nonconformaity-and-its-persecution [Last accessed on 2022 Feb 06]

3. Ausman JI, Blaylock RL. What is the truth? United States: James I. and Carolyn R. Ausman Education Foundation (AEF); 2021. The China Virus. [Google Scholar]

4. Beder A, Buyukkocak U, Sabuncuoglu H, Keskil ZA, Keskil S. Preliminary report on surgical mask induced deoxygenation during major surgery. Neurocirugia. 2008;19 [Google Scholar]

5. Bhakdi S. Presentation of autopsy findings. https://www.brighteon.com/4b6cc929-f559-4577-b4f8-3b40f0cd2f77 Pathology presentation on findings https://pathologie-konferenz.de/en [Last accessed on 2022 Feb 06]

6. Blaylock RL. Covid-19 pandemic: What is the truth? Surg Neurol Inter. 2021;12(151) [Google Scholar]

7. Blaylock RL. National Health Insurance (Part 1): the socialist nightmare. Aug 19, 2009 https://haciendapublishing.com/national-health-insurance-part-i-the-socialist-nightmare-by-russell-l-blaylock-md [Last accessed on 2022 Feb 06]

8. Blaylock RL. Regimentation in medicine and its human price (part 1 & 2) Hacienda publishing. March 20, 2015 https://haciendapublishing.com/regimentation-in-medicine-and-its-human-price-part-2-by-russell-l-blaylock-md [Last accessed on 2022 Feb 06] [Google Scholar]

9. Blaylock RL. Haciendia Publishing; When rejecting orthodoxy becomes a mental illness. Aug 15, 2013 https://haciendapublishing.com/when-rejecting-orthodoxy-becomes-a-mental-illness-by-russell-l-blaylock-m-d [Last accessed on 2022 Feb 06] [Google Scholar]

10. Bloche MG. Corporate takeover of Teaching Hospitals. Georgetown Univ Law Center. 1992. https://scholarship.law.georgetown.edu/cgi/viewcontent.cgi?referer=https://www.google.com/&httpsredir=1&article=1731&context=facpub [Last accessed on 2022 Feb 06]

11. Bosh X, Ross JS. Ghostwriting: Research misconduct, plagiarism, or Fool’s gold. Amer J Med. 2012;125(4):324–6. [PubMed] [Google Scholar]

12. Breggin PR, Breggin GR. Breggin PR, Breggin GR. Covid-19 and the Global Predators: We are the Prey. Ithaca, NY: Lake Edge Press; 2021. Top Medical Journals Sell their Souls; pp. 285–292. [Google Scholar]

13. Breggin, p133 [Last accessed on 2022 Feb 06]

14. Bulik BS. The top 10 ad spenders in Big Pharma for 2020. Fierce Pharma Apr 19, 2021 https://www.fiercepharma.com/special-report/top-10-ad-spenders-big-pharma-for-2020 [Last accessed on 2022 Feb 06]

15. Children’s Health Defense Team Harvard experts critique cozy FDA-Pharma relationship. The Defender. Jan 28, 29020.

16. Chughtai AA, Stelzer-Braid S, Rawlinson W, Pontivivi G, Wang Q, Pan Y, et al. Contamination by respiratory viruses on outer surface of medical mask used by hospital healthcare workers. BMC Infect Dis. 2019. Article number 491.

17. Coleman-Lochner L. U.S. Hospitals pushed to financial ruin as nurses quit during pandemic. Bloomberg. Dec 21, 2021 https://www.bloomberg.com/news/articles/2021-12-21/u-s-hospitals-pushed-to-financial-ruin-as-nurses-quit-en-masse [Last accessed on 2022 Feb 06]

18. D’Souza K. Pandemic effects may have lowered baby’s IQs, study says EdSource. https://edsource.org/2021/pandemic-may-have-lowered-baby-iq-study-says/661285. [Last accessed on 2022 Feb 06]

19. Davis GG, Williamson AK. Risk of covid-19 transmission during autopsy. Arch Path Lab Med. 2020;144(12):1445a–1445. [Google Scholar]

20. Department of Health and Human Services: Part 1. Overview Information. https://grants.nih.gov/grants/guide/rfa-files/RFA-HD-20-013.html [Last accessed on 2022 Feb 06]

21. Durden T. Life Insurance CEO says deaths up 40% among those aged 18 to 64. Tyler Durden Report. 2022. Jan 3,

22. Elder C, Schroder AS, Aepfelbacher M, Fitzek A, Heinemann A, Heinrich F, et al. Dying with SARS-CoV-2 infection an autopsy study of the first consecutive 80 cases in Hamberg, Germany. Inter J Legal Med. 2020;134:1275–84. [Google Scholar]

23. Front Line Covid Critical Care Alliance. https://covid19criticalcare.com [Last accessed on 2022 Feb 06]

24. Gueriero M. Restriction of autopsies during the Covid-19 epidemic in Italy. Prudence or fear? Pathologica. 2020;112:172–3. [PMC free article] [PubMed] [Google Scholar]

25. Hope JR. Sudden death by “hot lot”—Dr. Michael Yeadon sounds the alarm. The Desert review. 2022. Jan 24,

26. Huff E. Idaho doctor reports “20 times increase” in cancer among those “vaccinated” for covid. Natural News. 2021. Sept 14, https://www.naturalnews.com/2021-09-14-idaho-doctor-20times-increase-cancer-vaccinated-covid.html [Last accessed on 2022 Feb 06]

27. Ioannou P, Karakonstantis S, Astrinaki E, Saplamidou S, Vitsaxaki E, Hamilos G, et al. Transmission of SARS-C0V-2 variant B1.1.7 among vaccinated health care workers. Infect Dis. 2021:1–4. [Google Scholar]

28. James Thorpe interview by Dr. Steve Kirsch. Rumble https://rumble.com/vru732-dr.-james-thorp-on-medical-censorship.html [Last accessed on 2022 Feb 06]

29. Jiang H, Mei Y-F. SARS-CoV-2 spike protein impairs DNA damage repair and inhibits V(D)J recombination in vitro. Viruses. 2021;13:2056. doi: 10.3390/10.3390/v13102056. [PMC free article] [PubMed] [CrossRef] [Google Scholar] Retracted

30. Jimenez J, Vigdor N. Covid-19 news: Over 150 Texas hospital workers are fired or resign over vaccine mandates. The New York Times. 2021. Jun 22, https://www.nytimes.com/live/2021/06/22/world/covid-vaccine-coronavirus-mask [Last accessed on 2022 Feb 06]

31. Katz E. Postal service seeks temporary exemption from Biden’s vaccine-or-test mandate. Government Executive. 2022. Jan 22, https://www.govexec.com/workforce/2022/01/postal-service-seeks-temporary-exemption-bidens-vaccine-or-test-mandate/360376 [Last accessed on 2022 Feb 06]

32. Kennedy R., Jr . Skyhorse Publishing; 2021. The Real Anthony Fauci. Bill Gates, Big Pharma, and the Global War on Democracy and Public Health; pp. 24–29. [Google Scholar]

33. Kennedy RF., Jr pp. 24–25.

34. Kennedy RF., Jr pp. 26–30.

35. Kennedy RF., Jr p. 32.

36. Kennedy RF., Jr pp. 35–56.

37. Kennedy RF., Jr pp. 47–56.

38. Kennedy RF., Jr p. 135.

39. Kennedy RF., Jr p. 217.

40. Lee M. University of Florida finds dangerous pathogens on children’s face mask. NTD https://www.ntd.com/university-of-florida-lab-finds-dangerous-pathogens-on-childrens-face-masks_630275.html [Last accessed on 2022 Feb 06]

41. Liu Q, Wang RS, Qu GQ, Wang YY, Liu P, Zhu YZ, et al. Gross examination report of a Covid-19 death autopsy. Fa Yi Xue Za Zhi. 2020;36:21–23. [PubMed] [Google Scholar]

42. Loffredo J. Fully vaccinated are Covid ‘Superspreaders’ Says inventor of mRNA technology. https://childrenshealthdefernce.org/defender/justin-Williams-Robert-Malone-fully-vaccinated-covid-super-spreaders [Last accessed on 2022 Feb 06]

43. Marik PE, Kory P, Varon J, Iglesias J, Meduri GU. MATH+ protocol for the treatment oof SARS-CoV-2 infection: the scientific rationale. Exp rev Ant-infective Ther. 2020 doi: 10.1080/14787210.2020.1808462. [CrossRef] [Google Scholar]

44. McCullough P, Kelly R, Ruocco G, Lerma E, Tumlin J, Wheeland KR, et al. Pathophysiological basis and rationale for early outpatient treatment of SARS-CoV-2 (COVID-19) Infection. Amer J Med. 2021;134:16–22. [PMC free article] [PubMed] [Google Scholar]

45. McCullough P. Study: Fully vaccinated healthcare workers carry 251 times viral load, pose threat to unvaccinated patients, Co-workers. The Defender 08/23/21. [Google Scholar]

46. McCullough P. “We’re in the middle of a major biological catastrophe”: Covid expert Dr. Peter McCullough. 2021. Oct 6, https://www.lifesitenews.com/news/were-in-the-middle-of-a-major-biological-catastrophe-top-covid-doc-mccullough/?_kx=9EtupqemhhFXJ1kgCo9W3xUNfwrkqB5nT7V2H15fUnA%3D.WXNMR7 [Last accessed on 2022 Feb 06]

47. McGovern C. Thousands report developing abnormal tumors following Covid shots. LifeSite News. Nov 1, 2021 https://www.lifesitenews.com/news/thousands-report-developing-abnormal-tumors-following-covid-shots [Last accessed on 2022 Feb 06]

48. Mercola J. Bill Gates and Anthony Fauci: a ‘formidable, nefarious’ partnership. Mercola.com. https://childrenshealthdefense.org/defender/rfk-jr-the-real-anthony-fauci-bill-gates [Last accessed on 2022 Feb 06]

49. Moffatt B, Elliott C. Ghost Marketing: Pharmaceutical companies and ghostwritten journal articles. Persp Biol Med. 2007;50(1):18–31. [Google Scholar]

50. Mulvany C. Covid-19 exacerbates bankruptcy for at-risk hospitals. Health Care Financial Management Association. 2020. Nov 9,

51. Muoio D. How many employees have hospitals lost to vaccine mandates? Here are the numbers so far. Fierce Healthcare. 2022. Jan 13, https://www.fiercehealthcare.com/hospitals/how-many-employees-have-hospitals-lost-to-vaccine-mandates-numbers-so-far [Last accessed on 2022 Feb 06]

52. Nalivaeva NN, Turner AJ, Zhuravin IA. Role of prenatal hypoxia in brain development, cognitive functions, and neurodegeneration. Front Neurosci. 2018 doi: 10.3389/fnins.2018.00825. [CrossRef] [Google Scholar]

53. Nicole Sirotek shares what she saw on the front lines in NYC. # Murder. https://rumble.com/vt7tnf-registered-nurse-nicole-sirotek-shares-what-she-saw-on-the-front-lines-in-n.html [Last accessed on 2022 Feb 06]

54. Noether M, Mat S. Hospital merger benefits: Views from hospital leaders and econometric analysis. Amer Hospital Assoc. Charles Rivers Associates. Jan, 2017 https://www.aha.org/guidesreports/2017-01-24-hospital-merger-benefits-views-hospital-leaders-and-econometric-analysis [Last accessed on 2022 Feb 06]

55. Nurse Colette Martin testimony to Louisiana House of Representatives. https://www.youtube.com/watch?v=cBwnIRUav5I [Last accessed on 2022 Feb 06]

56. Nurse Dani: It’s the Covid-19 hospital protocols are killing people. https://rumble.com/vqs1v6-nurse-dani-its-the-covid-19-hospital-protocols-are-killing-people.html [Last accessed on 2022 Feb 06]

57. Parpia R. Mayo Clinic fires 700 employees for refusing to get Covid-19 vaccinations. The Vaccine Reaction. https://thevaccinereaction.org/2022/01/mayo-clinic-fires-700-employees-for-refusing-to-get-covid-19-vaccinations [Last accessed on 2022 Feb 06]

58. Pomara C, Li Volti G, Cappello F. Covid-19 deaths: are we sure it is pneumonia? Please, autopsy, autopsy, autopsy! J Clin Med. 2020 doi: 10.3390/jcm9051259. [CrossRef] [Google Scholar]

59. New York Post. Post Editorial Board Facebook admits the truth: “Fact checks” are just (lefty) opinion. Dec 14,2021. https://nypost.com/2021/12/14/facebook-admits-the-truth-fact-checks-are-really-just-lefty-opinion [Last accessed on 2022 Feb 06] [Google Scholar]

60. Rancourt DG. Mask don’t work. A review of science relevant to the covid-19 social policy. https://archive.org/details/covid-censorship-at-research-gate-2 [Last accessed on 2022 Feb 06]

61. Redshaw M. As reports of injuries after Covid vaccines near 1 million mark. CDC, FDA clear Pfizer, Moderna boosters for all adults. The Defender 11/19/21.

62. Roche D. Boston Herald. 2021. Sept 14, Members of Congress and their staff are exempt from Biden’s vaccine mandate, Newsweek 9/10/21 Boston Herald Editorial Staff. Editorial: Political elites exempt from vax mandates. [Google Scholar]

63. Ross E. How drug companies’ PR tactics skew the presentation of medical research. The Guardian. https://www.theguardian.com/science/2011/may/20/drug-companies-ghost-writing-journalism [Last accessed on 2022 Feb 06]

64. Saul S. Ghostwriters used in Vioxx studies, article says. New York Times. April 15, 2008 https://www.fpparchive.org/media/documents/public_policy/Ghostwriters%20Used%20in%20Vioxx%20studies_Stephanie%20Saul_Apr%2015,%202008_The%20New%20Times.pdf [Last accessed on 2022 Feb 06]

65. Saxena V. Doctors loses medical license. Ordered to have Psych Eval for Ivermectin Scrits, Sharing Covid “misinformation” BRP News. Available from: https://bizpacreview.com/2022/01/16/doctor-loses-license-orderedto-have-psych-eval-for-prescribing-ivermectin-sharining-covid-falsehoods-1189313. [Last accessed on 2022 Feb 06]

66. Schwab K, Malleret T. Cologny/Geneva: The Covid-19 Pandemic and the Great Reset. Forum Publishing 2020 World Economic Forum. [Google Scholar]

67. Sen. Ron Johnson on Covid-19 vaccine injuries to test subjects. https://www.youtube.com/watch?v=6mxqC9SiRh8 [Last accessed on 2022 Feb 06]

68. Sperhake J-P. Autopsies of Covid-19 deceased? Absolutely! Legal Med. 2020 doi: 10.1016/j.legalmed.2020.101769. [CrossRef] [Google Scholar]

69. Svab P. Non-Covid death spike in Americans aged 18-49. The Epoch Times. Jan 26-Feb 1 2022.

70. US Medical, Scientific, Patient and Civic Organization Funding Report: Pfizer: Fourth Quarter 2010. https://cdn.pfizer.com/pfizercom/responsibility/grants_contributions/pfizer_us_grants_cc_q4_2010.pdf [Last accessed on 2022 Feb 06]

71. Vivek Saxena. Doctors loses license, ordered to have psych eval for Ivermectin scrits, sharing Covid ‘misinformation’ BPR News. https://www.bizpacreview.com/2022/01/16/doctor-loses-license-ordered-to-have-psych-eval-for-prescribing-ivermectin-sharing-covid-falsehoods-1189313 .

72. Westendorf AM, et al. Hypoxia enhances immunosuppression by inhibiting CD4+ effector T cell function and promoting Treg activity. Cell Physiol Biochem. 2017;41:1271–84. [PubMed] [Google Scholar]

73. Wood PM. Coherent Publishing; 2018. Technocracy: The Hard Road to World Order. [Google Scholar]

74. Wood PM. Coherent Publishing; 2015. Technocracy Rising: The Trojan Horse of Global Transformation. [Google Scholar]

Articles from Surgical Neurology International are provided here courtesy of Scientific Scholar

In commenting on the many absurdities of the Corona regime, and asking what their purpose could possibly be, I’m often told that “it’s about power” or “it’s about control.”

I confess that I don’t find these explanations convincing. I think they’re grounded in a mistaken view of how western states exercise power and the constraints they face in this. The idea seems to be, that states accumulate the potential to act, which potential is however constrained by the law or popular opinion; and that they are forever striving to escape these artificial constraints through subterfuge and deception, in order to transmute more of their accumulated potential into real-world prerogatives.

I see it otherwise. As far as I can tell, neither laws nor popular opinion limit the action of modern states in any serious way. There are constraints, but these lie elsewhere, mostly in the area of coordination. As I’ve written several times now, our governments have become profoundly demobilised. Political power has accumulated at ever lower levels, with the press, academia and in the bureaucratic institutions. This process represents a kind of political decay, and yet it has distinct advantages for the senescent elite: It ensures broad consensus across all major corporate, government and media factions, shielding them precisely from things like popular opinion and judicial review.

The monstrous institutional apparatus can only act effectively if enough of its widely distributed nodes are activated and aligned behind the same agenda. This requires some kind of (in most cases external) stimulus. Corona has revealed how powerful modern states can be, if only they can get enough of their decentralised distributed substance to back a given programme. Laws become totally meaningless in the face of such coordination; the ensuing propaganda campaign overcomes popular resistance easily.

(The problem of coordination is also why I think the lockdowners and the vaccinators had a much harder time in the United States than in Europe. American [unlike German] federalism is a real force, which fragments the various parties to power still further. Coordination for the American government is thus much harder than it is in Europe, or New Zealand.)

Even in a condition of high coordination, though, the exercise of power or control by the state represents exertion. It’s like running, or lifting a weight. Modern states, with their multitude of international adventures and national initiatives, are fully committed here. The more the various arms of the state have been stirred to action, the more power it has to act in the moment; for a time, the stimulation of SARS-2 provided enough surplus energy to bring vaccine mandates within the realm of possibility. With Omicron, though, the enthusiasm and with it the coordination faded, and the exertion was no longer worth it. They could have still done it, but it would have meant redirecting resources from someplace else and not doing some other thing.

Anyway, that’s my basic model of how state power functions. It’s like the Eye of Sauron: It can’t look everywhere at once, it can’t do everything. And when it’s looking at you, the purpose isn’t just to control your life for the thrill of it. If that’s all the state wanted, it could look anywhere.

States act with purpose, towards specific goals. Their constituent pieces function like a distributed intelligence, which is always striving for something, and – especially when policies become bizarre, clearly unattainable, or circular – it’s worth trying to figure out what that something might be. It might not always be obvious; we shouldn’t assume that states will have goals or aims that make all that much sense to humans.

In fact, while they’re made up of people, western states often behave towards bizarre and alien ends, like an extraterrestrial or a sentient machine: They insist on human uniformity, they’re indifferent to children, they’re hostile to traditional cultures, they hate pathogens, they’re wary of real-life social interaction, they’re mildly wary of the natural world, they like buildings made of glass, steel and concrete, they abhor death, they like to count things, they dislike the rural environment, they prefer the highest possible degree of networking and interconnection.

Mike Yeadon

In this comprehensive review, Dr. Yeadon argues that all the main narratives about SARS-CoV-2 and imposed “measures” are lies.

Given the foregoing, it is no longer possible to view the last two years as well- intentioned errors. Instead, the objectives of the perpetrators are most likely to be totalitarian control over the population by means of mandatory digital IDs and cashless central bank digital currencies (CBDCs).

Download The-Covid-Lies-updated

In the first part of the article (The Covid Lies), Dr. Yeadon counters the 12 widespread Covid narratives with the following arguments:

1. The infection fatality rate of SARS-CoV-2 is 0.1 – 0.3%, which is not significantly different from some seasonal influenza epidemics.
2. Based on the peer-reviewed articles, at least 30 to 50% of the population has prior cross-immunity.
3. SARS-CoV-2 does discriminate. “_The lethality of this virus, as is common with respiratory viruses, is 1000X less in young, healthy people than in elderly people wi_th multiple comorbidities.”
4. Asymptomatic transmission is the “central conceptual deceit” used to “underscore almost every intrusion: masking, mass testing, lockdowns, border restrictions, school closures, even vaccine passports.”
5. PCR test is “the central operational deceit.”
6. Neither cloth nor surgical masks prevent respiratory virus transmission.
7. Lockdown is “epidemiologically irrelevant” and never works. “Only “stay home if you’re sick” works.“
8. “Covid-19 is the most treatable respiratory viral illness ever”. Safe and effective early treatments are available.
9. Based on the peer-reviewed articles, very few clinically significant reinfections of SARS-Cov-2 have ever been confirmed.
10. SARS-CoV-2 mutates slowly, and no variant is even close to escaping naturally-acquired immunity. However, there is the possibility that the so-called vaccines prevent the establishment of immune memory, leading to the repeated infections, which would be a form of acquired immune deficiency.
11. Safety is the top priority in a public health mass intervention, even more than effectiveness. “It was NEVER appropriate to attempt to “end the pandemic” with a novel technology vaccine.”
12. The four gene-based “vaccines” are toxic. The basic rules of selecting vaccine candidates are: 1) the agent has no inherent biological action (non-toxic); 2) the agent should be the genetically most stable part of the virus; 3) the agent should be most different from human proteins. Spike protein as the vaccine does not fit any of the above criteria.

In the second part of the article (How Much of the Covid-19 Narrative Was True? Additional Reflections), Dr. Yeadon further stresses his contention on the Covid-19 narratives on:

• Unprecedented Pronouncements by the senior scientific and medical advisers, such as “Everyone is vulnerable.”
• Instigating Fear
• Using Mass Testing to Promote Fear
• One Dominant Narrative
• More Vaccine Lies
• The Question of Motive

At the end of the article, Dr. Yeadon also provides a list of extra supplemental points to support his conclusions.

About the author:

Dr. Michael YEADON PhD was Formerly Vice President & Chief Scientific Officer Allergy & Respiratory at Pfizer Global R&D. He holds Joint Honours in Biochemistry and Toxicology and a PhD in Respiratory Pharmacology. He is an Independent Consultant and Co-founder & CEO of Ziarco Pharma Ltd.