The uncritical, blind faith in vaccines is the preeminent sacred cow of modern medicine. (It happens to be its preeminent cash cow as well.) It is a quasi-religious, dogmatic article of conviction, rather than a sound scientific theory or an empirically-based clinical precept.

Vaccines have been controversial since their introduction centuries ago. Only in very recent history has there been a rigidly enforced orthodoxy of belief within the medical establishment that vaccines must be unanimously regarded as “safe and effective,” no questions asked.

Even more recent is the practice of smearing and labeling anyone questioning this doctrine as a heretic: an “anti-vaxxer.” In fact, according to the Merriam-Webster Dictionary, the earliest known use of that now-ubiquitous epithet was only in 2001. 

Religious faith has tremendous potential for good in society, but when it is misrepresented as science, its track record is miserable and deadly. “Safe and effective” is not scientific shorthand, or even an advertising slogan; it is a mantra. “Anti-vaxxer” is not a category of person, it is a charge of heresy. And just as vaccine critics are heretics, so the high priests of vaccines, the Faucis of the world, the people who in their own words “represent science,” are fanatics.

Does that really sound like science to you? Galileo, Semmelweis, and a few others might disagree.

Any honest person who lived through the COVID-19 era in the United States will acknowledge that the Department of Health and Human Services (HHS) with its lengthy “alphabet soup” of agencies (CDC, NIH (with its NIAID), FDA (with its CBER), etc., etc.), promoted and repeated the “safe and effective” mantra regarding the COVID-19 vaccines throughout an era of intense public fear. 

Any honest person will also acknowledge that the mainstream media avidly repeated and amplified the “safe and effective” mantra and stoked the fear, all while ruthlessly attacking anyone questioning that same dogma, labeling them “anti-vaxxers,” or sometimes even “murderers.”

Little to no mention was made – or allowed – of the gigantic financial incentives and other entanglements these powerful entities have with the vaccine manufacturers, nor the trillions of dollars involved. 

Religious dogmas, especially those relentlessly inculcated by powerful forces under extreme conditions, are hard to break free from.

To readers who may know people caught in the rigid, dogmatic belief in the infallibility of vaccines, I offer the following 10 sentences.

Share them with friends, family, and colleagues who cannot seem to reconsider vaccine dogma, especially those with an uncritical view of the current vaccine schedules. Ask them to carefully read each of the 10 sentences below, one at a time, and ask themselves: does this sentence seem true or false to me? If it seems false, on what basis do I think it is false? Then move on to the next one and do the same.

(Some of the sentences are complex, but I am confident an intelligent layperson can understand them all.)

When they are finished with all 10 sentences, encourage your friends to ask themselves: 

• Do they truly believe that every child in the United States should receive 20 or more different vaccines before age 18? 
• Should vaccines ever be mandated? 
• Shouldn’t we, as an educated, free society, systematically review the official vaccine recommendations, and, just as we would do with Grandma’s overflowing pill box, reduce them to the truly necessary minimum?
• Shouldn’t we reassert the autonomy of patients over their own bodies?

Here is the trouble with vaccines, in 10 sentences:

1. Like “antibiotics,” “vaccines” are a large and diverse class of medicines, and as with all large classes of medicines, different products in the class work by different mechanisms, some being quite effective while others are ineffective, some being reasonably safe for appropriate human use while others are fraught with side effects and toxicities, and therefore to assume that any large class of medicines – including vaccines – is categorically “safe and effective,” is naïve, illogical, false, and dangerous.

2. While the full extent of vaccine toxicity is undetermined, it is a historical fact that numerous vaccines have been proven to be highly toxic and even deadly to patients, via multiple pathophysiological mechanisms, including: a) direct contamination of the vaccine (e.g. the Cutter Incident), b) disease caused by unintended, pathological immune response to the vaccine (e.g. Guillain–Barré syndrome caused by the swine flu vaccine), c) unintended contraction and/or transmission of the disease the vaccine was designed to prevent, caused by the vaccine itself (e.g. the current oral polio vaccine), and d) vaccine toxicity of unknown or uncertain cause (e.g. intestinal intussusception with the rotavirus vaccine, and fatal blood clots with the Johnson & Johnson COVID-19 vaccine).

3. In fact, the known toxicity of vaccines is so well-established that a Federal law – the National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was passed to specifically exempt vaccine manufacturers from product liability, based on the legal principle that vaccines are “unavoidably unsafe” products.

4. Since the 1986 NCVIA act protecting vaccine manufacturers from liability, there has been a dramatic increase in the number of vaccines on the market, as well as the number of vaccines added to the CDC vaccine schedules, with the number of vaccines on the CDC Child and Adolescent schedule rising from 7 in 1986 to 21 in 2023. 

5. Of the 21 vaccines on the 2023 CDC Child and Adolescent Immunization Schedule, only a small minority (e.g. measles, mumps, rubella, varicella, and HiB) are capable of providing genuine herd immunity, a fact that negates the common, population-based arguments for mandating the other vaccines, which comprise the sizable majority of the vaccines on the schedule.

6. The pharmaceutical industry has established an almost unimaginable degree of media control, institutional influence, and regulatory capture, via its funding of other entities, as it is a) the largest industry lobby in Washington, DC, b) the second largest industry in TV advertising, c) a major source of personal revenue for high-level HHS “alphabet soup” agency bureaucrats, many of whom hold patent and royalty rights on pharmaceutical products, d) a major funder of influential physician organizations (e.g. the American Academy of Pediatrics and prominent medical journals, and e) involved in payment-based incentivization of practicing physicians, who frequently receive monetary bonuses for high rates of vaccination in their patient panels.

7. The COVID-19 mRNA vaccines were developed and administered to the public a) much faster and with much less testing than any other vaccines on the market, b) under Emergency Use Authorization, c) utilizing a technological platform that had never seen commercial use before, and, despite generating reports of vaccine-related deaths and serious adverse events at much higher rates than traditional vaccines, and despite the fact that they have been removed from the pediatric market in multiple other developed countries, the COVID-19 mRNA vaccines have already been placed on the CDC Child and Adolescent Immunization Schedule, just a little over 2 years after their introduction to the public.

8. There has been no systematic public accounting by the CDC (or any of the HHS agencies) for the more than 35,000 reported COVID-19 vaccine-related deaths and more than 1,500,000 reported COVID-19 vaccine-related adverse events reported as of July 7, 2023, to the CDC’s own Vaccine Adverse Event Reporting System (VAERS), nor for the corresponding numbers of COVID vaccine-related deaths and adverse events reported to Eudravigilance (the European Union’s equivalent to VAERS), even as the CDC continues to strongly promote these vaccines for use, including placing them on the CDC Child and Adolescent Immunization Schedule.

9. By labeling the novel COVID mRNA products as “vaccines,” the definition of the term “vaccine” has become so broadened that essentially any medication that induces an immune response against a disease may now be dubbed a “vaccine,” thereby shielding pharmaceutical companies from liability under the National Childhood Vaccine Injury Act of 1986 to a previously unimagined extent.

10. Vaccine mandates thereby compel citizens to submit to medical treatments a) that are regarded under Federal law to be “unavoidably unsafe,” b) that because they are unavoidably unsafe, their manufacturers are protected by Federal law from liability for harm done to citizens, c) whose manufacturers and government agencies nevertheless promote publicly as “safe and effective,” in direct contradiction to their legal status as “unavoidably unsafe,” and d) that have increased tremendously in number in recent decades, and, with mRNA technology and a broadened definition of the term “vaccine,” stand to multiply at an even greater rate in the future.

I hope these 10 sentences will help the unconvinced to reconsider the central dogma surrounding vaccines. We, as a society, need to reject the article of faith that vaccines are fundamentally “safe and effective.” 

Vaccines, due to their unavoidably unsafe nature, should NEVER be mandated, and a thorough, product-by-product accounting of the individual vaccines needs to be done outside of government agencies.

How can we accomplish this?

Please forgive me if you thought I was done. I have 10 more sentences listing my proposed solutions to the trouble with vaccines. I ask you to trudge through these as well. Most of them are shorter than the first 10. Thank you.

A Proposed Solution to the Trouble with Vaccines in 10 (more) Sentences:

1. The National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) should be repealed, returning vaccines to the same liability status as other drugs. 

2. Federal law should be passed prohibiting the mandating of any and all vaccines at all levels of government.

3. Federal law should be passed prohibiting all direct-to-consumer advertising of prescription drugs.

4. Federal law should be passed prohibiting all collaboration between the Department of Health and Human Services’ “alphabet soup” agencies (FDA, CDC, NIH, etc.) and either the Department of Defense (US Army, DARPA, etc.) or the Federal Intelligence Agencies (CIA, DHS, etc.) with regard to vaccine development or vaccine distribution to the public.

5. Federal law should be passed prohibiting all persons working within the HHS agencies from gaining any personal financial benefit from vaccines, including the gaining and holding of patents or royalties, and civil servants in those agencies should be required to take an oath of office not to profit off  of any products they approve, regulate, or about which they advise the public.

6. A thorough and public investigation, including criminal prosecutions where appropriate, should be made regarding the key players (both public and private) involved in the development, marketing, manufacture, sale, and administration of the COVID-19 mRNA vaccines, and following the investigation, there should be appropriate reform within the HHS agencies.

7. Detailed, independent, Cochrane-style reviews of every vaccine on the CDC vaccine schedules should be undertaken and made public, and no scientists with financial interests within the pharmaceutical industry should conduct these reviews.

8. Detailed, independent reviews of all reports from the Vaccine Adverse Event Reporting System (VAERS) related to the COVID-19 mRNA vaccines should be undertaken and made public, and appropriate reforms to VAERS should be made.

9. A detailed Congressional review of the money trails related to COVID-era programs, including Operation Warp Speed and the Coronavirus Aid, Relief, and Economic Security (CARES) Act, should be conducted, focusing on fraud and abuse at all levels, including how private companies such as Pfizer and Moderna profited so enormously from taxpayer-funded initiatives.

10. A open, public discussion and debate should be undertaken on the appropriate role of vaccines in public health, including, among other issues, a) a critical review of the current medical dogma on vaccines, b) an accounting of the mistakes, abuses, and potential lessons of the COVID-19 era, and c) a thorough discussion of the undeniable conflicts between public health as it is now practiced and the fundamental civil rights of citizens.

The medical establishment’s current dogma on vaccines (“safe and effective,” no questions asked) and its corresponding catechism (the ever-expanding vaccine schedules) are in desperate need of reform. I submit that we begin with the above steps.

Reformers are not heretics, although they are commonly labeled as such by powerful persons resisting reform. I, for one, am not a heretic, nor am I an “anti-vaxxer.” I don’t want to throw the baby out with the bathwater. The problem is, when one looks closely at the vaccine schedules, there turns out to be a lot more bathwater and a lot less baby than advertised.

It is time for the profession of medicine, and society as a whole, to come out of the Dark Ages on this topic. It is time for an open, forthright reevaluation of vaccines and their role in public health.

Clayton J. Baker, MD

C.J. Baker, is an internal medicine physician with a quarter century in clinical practice. He has held numerous academic medical appointments, and his work has appeared in many journals, including the Journal of the American Medical Association and the New England Journal of Medicine. From 2012 to 2018 he was Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester.

Most sane people believe that the burden of proving safety should lie on the party conducting a questionable action, rather than their victim. For example, if a criminal shot someone, the prosecution would not be required to prove that the victim’s sudden death after the gunshot wound was not just a spontaneous coincidence, a result of extreme stress from the situation, or due to a pre-existing medical condition.

Unfortunately, the pharmaceutical industry has been able to establish a special type of privilege within the legal system which has made it very difficult to demonstrate that vaccines (along with many other pharmaceuticals) can ever be at fault for anything. Because of this, we recently had a flood of experimental vaccines mandated upon the population, which were never tested for safety (despite many serious concerns with their design), whose (likely fraudulent) clinical trial data was never made accessible to the public.

We then had, as far as I know, the most aggressive propaganda campaign in history, and I watched the majority of my colleagues lose the ability to recognize any problems related to the vaccines. Instead, they developed an almost surreal religious devotion to the coming salvation of the vaccines becoming available.

Once the vaccines entered the market, a variety of red flags began going off indicating that these vaccines were killing people, and rather than address these concerns, the government—in concert with the media—chose to deny any of this was occurring. Instead they mandated the vaccines upon the entire population. I was understandably worried that the vaccines would cause problems and tried to do my part to head this off in 2020, but I did not expect anything on the scale of what we have encountered since then.

I personally became involved in all of this because soon after the vaccines entered the market, I began to have many friends and patients reach out to ask me if the vaccine could kill as someone they knew had had a tragic sudden death after vaccination. Once the magnitude of the problem dawned on me, I realized that even though my available options were limited, I could at least do my best to document each case sent my way so that someone would bear witness to what had happened. Otherwise, the dead had no voice. Beyond knowing I had a duty to compile this list however, I was not sure what to do with it. Later after someone kindly helped launch this Substack, I decided to post it, it ended up being seen by a lot of people…and that is how I ended up writing here.

Because of how long it took to verify each case, I realized that I had to end it a year in (at which point I knew of 45 individuals who had either critical or fatal injuries of a similar nature in close proximity to vaccination). Since that time, I still continue to hear reports I periodically document and discuss.

For example, a good friend is a nurse in a cardiac unit and has told me many of the patients she sees now with heart failure are much younger than they were a few years ago. I previously advised her against getting the vaccine due to her history of rheumatic fever (a condition where the immune system attacks and damages part of the heart). This was because I had noticed both COVID-19 and especially its vaccine seemed to cause inflammatory flares at previous sites of injuries or inflammation (Lyme is also known for doing this). The vaccine also has a remarkably high rate of exacerbating pre-existing autoimmune conditions—such as the 24.2% rate found in a recent Israeli survey which is comparable to what a few colleagues have observed, and I suspect exacerbation of preexisting inflammation within the circulatory system, like what this study of 566 patients found, is a key mechanism behind vaccine deaths.

A month ago, the nurse informed me that she had decided to vaccinate and had subsequently developed a heart condition. Additionally, she shared that the same had also happened to her mother following vaccination and that her sibling's partner is suffering longterm complication from a large stroke that immediately followed receiving a booster.

Looking back on it, the thing I found the most disappointing about my own documentation project was that once it went viral, it should have triggered the drug regulators evaluating the vaccines to take preventative action. Instead, due to the meticulously planned campaign of mass censorship that we all found ourselves in, more red flags than I can count were ignored by the “very rigorous” vaccination surveillance systems that were allegedly ensuring there were no safety issues with these vaccines.

Because of the immense power behind the medical-industrial complex, those debating this program have been stuck fighting an uphill battle. However, despite the immense degree of corruption, withholding of critical data, and censorship, these vaccines are dangerous enough that more and more evidence is nonetheless emerging of their danger, and the public is beginning to recognize it (e.g., consider how resistant the public has been to get COVID boosters). The previous article here discusses polling that shows this appears to be happening:

We Now Have A Clear Estimate Of The Rate Of Vaccine Injuries
Throughout my entire life, I’ve always found that trying to argue against Big Business is like fighting with one or both hands tied behind your back because large industries can always co-opt and buy out every authoritative source on the subject, and then censor any inconvenient facts that still persist. This is an immensely challenging situation.

Immediately after it was published, I was informed by a reader that possibly the most important dataset over the last two years was released today. For those interested, much of the context for today’s article can be found in the article above.

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

German Data

One of the depressing realizations one gains from studying the evidence-based literature is discovering how many issues exist within it and how difficult it is to know which data sources can be trusted. One of my favorite authors, Dr. Malcom Kendrick, devoted a book to addressing this subject and shared a pertinent anecdote for today’s events:

“In truth, the figures on vaccine damage are exceedingly difficult to analyse, because causality is very difficult to prove on a case by case basis. However, when it comes to negative findings I always like to go to Germany. It has been demonstrated many times that the Germans are the most likely to report negative findings accurately. Yes I know, terrible racial stereotyping, but a fact is a fact. What do the Germans have to say on the matter?

“Between 1978 and 1993 approx. 13,500 cases of undesired effects resulting from medications for vaccinations was reported to the Paul Ehrlich-Institute [PEI]…the majority was reported by the pharmaceutical industry. In 40% [5,400] of these cases the complications were severe, 10% [1,350] pertained to fatalities on account of effects.”

Additionally, as I learned from Kendrick, since early 2001, the federal infection protection law has mandated that specific severe vaccine injuries be immediately reported directly to the PEI (Germany’s equivalent of the FDA for vaccines and biologics). The German’s list of reportable injuries is much broader than what I have seen acknowledged by many other countries (e.g., those which are possible to receive compensation for within the United States) and includes the previously discussed complications of DPT along with many of the reactions typically associated with the COVID-19 vaccines. However, while that historical trend exists, Germany has not been one of the best countries for reporting COVID vaccine injuries (which I suspect is due to the political direction their government has moved in).

(The above graph illustrates why many of my German friends are not happy with their government)

Because of their tradition of reporting adverse reactions to vaccination, Germans (or at least some of them) have been more resistant to toeing the party line on concealing the dangers of the COVID-19 vaccines than citizens of many other countries (my friends there are enraged by the egregious concealment of critical safety data by the German government). In turn, some of the most critical vaccine data available comes from the German people as many of them have retained their intellectual integrity throughout the pandemic.

For instance, although autopsies should always be conducted on those who died suspiciously after vaccination, due to the global climate of intimidation against conducting any type of research that challenges the COVID vaccine program, it is rarely done. Instead, almost every autopsy has been performed by a few brave pathologists in Germany, and I have tried to detail the pathologist’s work throughout my postings (e.g., see here).

Some of the most important contributions of these autopsies include:

• Demonstrating that there is highly unusual tissue inflammation in those who died after vaccination. Pathologists had not observed this phenomena before the COVID-19 vaccines, and stated the inflammation they observed would likely be fatal.
• Demonstrating that the COVID spike protein could also be found in the tissues of those who died.
• Demonstrating that another key part of the SARS-CoV-2 virus was not present, meaning that the only possible source of the spike protein was the vaccine.

The most definitive study on this subject was recently completed. It examined 35 individuals who died within 20 days of vaccination, and after a lengthy examination excluded 10 who had a potential cause of death other than vaccination. Of the remaining 25, most had causes of death that frequently been linked to vaccination, and of those, 5 were found to have myocarditis potentially linked to the vaccine, and in 3 cases the vaccine was determined to be the definitive cause of their myocarditis and death. These results are very important for convicting the vaccines if it can also be proven that a large number of unexpected deaths are occurring following vaccination.

The Religion of Data

Every group needs to have some type of ideology to unite behind. Presently, one of the fixations within the Western world is on more and more data being the solution to everything. In turn, there are many concerns with this approach (e.g., it dehumanizes people, its “necessity” is used to justify violating citizen’s right to privacy while collecting it and it is being used to build an infrastructure that controls every aspect of our lives).

Although data is often claimed to be our salvation, and I will admit sometimes is quite helpful, in many other cases, it fails abysmally to address our problems. A major reason for this failure is that no one wants to critically analyze data this is gathered if that data suggests we should stop supporting an entrenched financial interest.

I am most aware of this in healthcare, as I know of numerous systems which were designed to analyze electronic medical records and either identify which pharmaceutical worked best for a condition, or if a pharmaceutical (or vaccine) was unsafe. Not surprisingly, all of these systems were never adopted, and the endless data we collect in healthcare (e.g., all the diagnostic coding data which medical insurance providers provide as a condition of reimbursement to healthcare providers) is rarely utilized to improve the public good. However, while prevailing biases frequently produces flawed analyses of data, data itself does not lie and has immense potential to expose dangerous health care practices if people are willing to look at it.

The largest insurance provider in Germany, BKK, provides coverage to approximately 10.9 million Germans. A board member, Andreas Schöfbeck, observed some very concerning signs in their data, and unlike everyone else, had the courage to disclose it in a letter to the German government (e.g. he addressed the PEI), after which, he was dismissed from his position. The BKK dataset (discussed by Jessica Rose) was the one which showed 2.05% of vaccine recipients subsequently sought medical care with a healthcare provider (others estimated it demonstrated 3.5% were struggling with persistent vaccine side effects).

This concerning safety signal prompted one German Political Party, the AFD (a controversial right wing party that has gained appeal through opposing the mandates) to file the German equivalent of FOIA for the rest of the insurance data (note: a few friends in Germany who are lifelong liberals joined AFD told me they believe “conservative” is a more appropriate label for AFD). Recently AFD obtained AOK Sachsen-Anhalt’s data, which once analyzed, demonstrated that many of the conditions we associate with COVID-19 injuries noticeably increased when the vaccination campaign initiated. According to this interview and Google translate, the conditions which rose five-fold or more were:

AFD’s FOIA Request

AFD also submitted a FOIA request to KBV, the association which represents all physicians who receive insurance in Germany and thus the largest insurance dataset available. The official response to their FOIA request reads as follows (this was my attempted translation):

”Dear Mr. Sichert,

With an e-mail dated October 27th, 2022 you have submitted an application to the KBV after the Freedom of Information Act (IFG) on access to data of the diagnostic codes by law health-insured patients.

You have asked for the following data packages to be sent by email:

Package 1: Filtering of all insured persons who will have an ICD coding in 2021 had vaccine side effects. You have applied for the codes T88.1, T88.0, U12.9 and Y59.9 apply.

Package 2: You request the transmission of a list of the frequency of all ICD codes of the insured persons from package 1 for the period 2016 to 2021, if proportionately available also for 2022, by quarter. The data query should after your request with V and G.

Package 3: You request the transmission of a listing of the frequency of all ICD codes of all insured persons - without the number of insured persons from package 1 - for the period from 2016 to 2021, if proportionately available also for 2022 quarters. The data query should be done with V and G.

The KBV corresponds to your application and includes a tabular overview as an attachment with the desired information about the frequency of at.

The abbreviations used in the table have the following meaning:

nw= number of patients with “vaccination side effects” (defined according to requested Filtering 1 in 2021)
onws= patient numbers "without vaccination side effects" (defined according to requested Filtering 2 in 2021)

Quarters of the reporting period are set as YYYYQ (e.g. 20214=Q4 2021).

The small font size in the printout is again unavoidable, since we want to make it easier to compare wanted to show all quarters of the two comparison groups on one sheet (the pdf document). However, like last time, it can be enlarged.

Today, the AFD hosted a press conference to unveil the data of those 72 million patients (the 90% of Germans with statutory health insurance) AFD had obtained from KBV. This data summarizes the number of times all ICD-10 (an international standard) diagnostic codes were used by German healthcare providers for these patients (outside of hospitals) from the first quarter of 2016 to the first quarter of 2022.

Tom Lausen is a data activist who had previously revealed the PEI and the RKI (the German equivalent of the CDC) were concealing concerning vaccine safety data and was allowed to analyze both BKK and AOK’s data. For this presentation, Lausen was able to provide a preliminary summary of the KBV data a few days after it was released:

A rough translation of this presentation can be found here (additionally YouTube now will translate the subtitles). If this video is deleted it can also be found here.

A few of the points emphasized in this presentation include:

• The [PEI](http://Paul Ehrlich Institute), the RKI and the German government have failed in their duty by federal law to evaluate COVID-19 vaccine injuries. Many of my friends and readers likewise believe they have done an atrocious job by attempting to conceal the vaccine injuries, and these agencies are frequently chastised by the German people for their conduct. Many of the arguments against the validity of this data must be viewed in the context of the fact it would be very easy to the government agencies to access and analyze this data, but despite many requests to over the last two years, they have all adamantly refused to, which is why AFD had to force them to act with its FOIA.
• It is estimated that 90% of the suspicious deaths that occur after vaccination are not reported to the PEI, and approximately 90% of those reported come from the patient themselves or their relative (which again demonstrates that German healthcare providers are failing in their duty to report vaccine injuries).
• The PEI has nonetheless received over 3,000 reports of suspicious deaths following vaccination, but has refused to perform any autopsies on those deaths. The excuse the PEI has used for their inaction is not having the explicit authority to order the autopsies (which is a spurious excuse). Fortunately as noted above, other groups without any official authority to order autopsies have nonetheless taken the initiative to perform them.

For this press conference, a presentation was put together detailing Lausen’s preliminary findings and the correspondences with the regulatory agencies, all of which can be found here. To the best of my ability, I translated and slightly modified the key portions of the presentation so that they could be accessible to English speakers, but I am certain more will be translated in the upcoming days.

The KBV Data

All of the KBV data can be reviewed with a simple search tool here, although it does not seem to work for certain ICD-10 codes. Due to the importance of this data, for data preservation purposes, I am also providing a copy of the raw data the AFD received:

Germany Total Icd 10 Code Submissions 2016 2022 1.87MB ∙ PDF File

This PDF file was supplied in a manner that makes the data quite difficult to analyze. Fortunately, one of my readers was able to move the above file into an easily sortable spreadsheet and thereby address some of the challenges with the PDF:

German Data Sortable Sheet 3.06MB ∙ XLSX File

Finally, the above sheet was sorted by that reader into a smart spreadsheet which allows you to easily observe which codes had the greatest increase in 2021-2022 (e.g. to sort them or create graphs). For those of you who are data inclined, you will likely want to create this sheet yourself, but for everyone else this is an excellent reference to start with). They were also able to use a script to put about one third of the names for the ICD-10 codes, but since there are fifteen thousand of them, it wasn’t practical for us to manually add in the rest and you will frequently need to directly look up the codes themselves (if a group wants to add the other codes in, I will be happy to repost that).

When Lausen presented the data, for each time period (e.g., 2016 quarter 1), he chose to add two different values together (code_20161 and nocode_20161). As best as I can tell from reviewing the FOIA request and the provided data, these categories represent those who also received a vaccine injury code and those who did not (as a result the majority of Germans belong to the “nocode” category).

I believe Lausen’s rationale for presenting the data in this manner was that a large number of vaccine injuries will go unreported and many vaccine injured patients are thus within the “nocode” category. Conversely, the total number of medical conditions observed in the country is not dependent upon accurate recognition of vaccine injuries.

Separating the patients by (the somewhat inaccurately classified) vaccine injury status is nonetheless a helpful means for evaluating vaccine injuries (I saw a variety of interesting trends in my preliminary examination). However, for the reasons outlined in this article, for the initial spreadsheet presented below, those result are combined.

Additionally, some of the extreme outliers exist because new ICD-10 codes are added each year and thus did not exist prior to 2021/2022. Finally, some of the codes you would expect to have large changes may not show in this dataset if they are codes typically used in a hospital setting as this dataset does not include hospital code submissions.

Kbv Data Sorted Into Accessible Excel Sheet - 9.46MB ∙ XLSX File

In the coming days, I know many will use this data to verify our work identifying which codes in 2021-2022 had the greatest increase (you can also do that piece by piece with the already available tool), and then cross reference those to the increases reported in VAERS or other datasets. There is an immense amount to be ascertained here, and I believe it represents the credible evidence we have been looking for since the start of the pandemic to have an objective metric for quantifying the impact of vaccine injury. However, it is also critical we determine which of the observed trends are not due to artifacts within the data.

Lausen’s Presentation of the KBV Data

This is probably the most important graph of Lausen’s presentation. We have all heard stories of individuals dying suddenly after vaccination (I’ve even read a report of an individual who appeared to be in good health making a thump in another room and being found dead shortly after by their spouse).

This issue was recently brought to the public’s attention with Died Suddenly, a documentary that effectively brought attention to this issue, but also had factual errors which were counterproductive for persuading the public that this issue is real. However, while some of the proof that Died Suddenly provided to assert the existence of the sudden death phenomenon could not stand up to outside scrutiny, the same cannot be said of the KBV data.

Additionally, one way that individuals have analyzed the unusual changes in health following the vaccination campaigns has been to assess how far they fall outside of the expected range of variation (this was also done for the final spreadsheet). I did a quick calculation for the above graph and found that 2021’s increase from 2016-2020 was 37.7σ, while 2022’s was 41.0σ. This is quite a big deal (the rarity of an event happening by chance increases exponentially as the σ increases). For context, a 7σ event has a 1/390,632,286,180 chance of spontaneously occurring (it is thought to occur once in a billion years), a 10σ event happens spontaneously once every 5.249e+020 years, and a 25σ event happens by chance every 1.309e+135 years (I was not able to find a reference on the probabilities for the even higher σ events observed here).

Given these numbers, it is very difficult to argue that these events were not caused by something. In this regard, we are also quite fortunate that while the vaccines were rushed to the market over a period of time far too short to establish safety, that process still took a year. Because of this lag, it is possible to refute the reflexively cited counterargument that these changes were due to COVID-19 or the lockdowns, as these only occurred in 2020 (the only possible exception I can think of is that Delta emerged near the end of 2020, but the spike started well before Delta became prevalent in Europe later in 2021).

This is a similar graph to the previous one, but include sudden cardiac death, which as many of you know also “unexpectedly” increased. Many authoritative sources have argued Lausen made a mistake to correlate vaccine injuries with the spike in sudden death because very few vaccines were given at the start of 2021 and thus if a correlation was there, it should have been not emerged until the second quarter.

For context, this was the rate of COVID vaccination in Germany:

As you can see, many vaccines were given in the first quarter of 2021.

COVID-19 is not the only vaccination regularly received. For example in Germany in 2019, it was estimated that 39% of those 65 and older received an influenza vaccination. However, unlike previous vaccines, the introduction of the COVID-19 vaccine caused far more people to require medical care for a vaccine side effect.

Given that Germany has a longstanding practice of evaluating vaccine injuries, this graph makes a very important point. An actual increase in vaccine injuries is occurring and it is not a result of a bias leading to over-reporting; it is a result of the vaccines being dangerous and patients needing medical care for the injuries.

Additionally, an outside team which looked at this data concluded approximately 5% of vaccine recipients subsequently required medical care, which is in line with the 7.7% discovered in V-Safe’s data and required a court order to be released as the CDC understandably did not wish to disclose this information. Note: I believe this discrepancy could be partially explained by the undercounting of vaccine codes highlighted in this article.

The general correlation between these two datasets is important. V-safe monitored 10 million vaccine recipients for a few specific things and was arguably the best surveillance system in place for tracking the side effects of these vaccines as it had a large but defined sample who were provided an easy way to report the chosen side effects. Since one of its key metrics matches the KBV data, this argues that at least some of the KBV data is valid.

Note: I am not sure if this specific dataset is referring to the total number of patients who sought care or the total number of times codes were submitted for vaccine injuries (which would mean a smaller number in total were injured).

Given that there are thousands of ICD codes that I could search the database for (many other increases, such as those of certain cancers, were highlighted in Lausen’s presentation), I had to put some thought into which of those many increases would be the best to show for this article (there were a lot of compelling candidates).

Previously, I proposed a model for the unusual fibrous clots observed in Died Suddenly that revolved around spike proteins causing protein misfolding. In support of this model, I highlighted an observed increase of an extremely rare protein misfolding disease which continues to be reported in VAERS.

Creutzfeldt-Jakob disease typically develop over years and occurs in approximately one in a million people annually, making its occurrence immediately after vaccination rare to the point that suggests causation (and as Jessica Rose noted, new reports are continuing to arrive in VAERS). The increase I proposed was a key point of contention for those who did not agree with my misfolded clot hypothesis, so I was eager to see if a current dataset could evaluate what was occurring.

This increase is also quite large, and for all practical purposes impossible to have occurred by chance (although I will mention the authors who published the original case series linking COVID vaccination to 26 cases of CJD also determined that Delta appeared to have an increased capacity to trigger protein misfolding but I do not believe that can explain the above trend).

Since this article was published, one reader has now attempted to present a longer analysis of this data which shows multiple interesting trends (e.g., many of the side effects commonly attributed to COVID vaccination appeared to have increased) along with raising additional questions about this data. It is my hope others will also do so!

Citizen’s Substack
Analysis of the recently published German insurance data
A dataset listing ICD-10 disease codes for all insurance claims filed by German doctors (outside of hospitals) for publicly insured Germans from 2016–1Q22 was recently published (more information). I’ll start with the obvious charts: chest pain, myocarditis and pericarditis increased by 17.8%, 48.5% and 25%, respectively, in 1Q22 compared to 1Q19…

Finally, the presentation on the KBV data proposes a fatality rate for the COVID vaccines. This chart was compiled by Lausen from the officially reported adverse events to the vaccines and likely are significantly undercounting the vaccine fatality rate.

Is This Data Valid?

Following the AFD’s press conference, the leading medical research institute in Germany, ZI, acted as a third party to present a rebuttal of how AFD interpreted KBV’s data. I did not agree with their argument (that there results were an artifact of AFD also requesting for everyone who specifically died in 2021), but did note that their response acknowledged the authenticity of this data.

The primary argument presented by ZI was that since the FOIA request selected for all patients who were vaccine injured in 2021-2022, the rise in deaths observed in 2021-2022 was simply due to the fact anyone who was vaccinated in 2021-2022 could not have died prior to 2021-2022 and thus the increase in deaths observed in 2021-2022 compared to what occurred prior to this time was due to the cohort effect.

On the surface this seems like a credible way to dismiss anyone who would make such an elementary mistake and believe in this data. However, the German authorities have a long track record of attempting to cover up evidence of COVID vaccine harm (in addition to the points discussed above, the German government has been perpetually delaying releasing the death statistics for 2021), so these arguments require a critical evaluation. In turn, there is a few major issue with it:

First, the “nocode” group should not suffer from the cohort effect and it was this group that comprised the majority of the increase in sudden deaths (review the wording of the FOIA request shown above). If the “code” group were to be removed (which potentially suffers from the cohort effect), an almost identical trend would still be present. Lausen presented his data by merging the code and nocode groups together which invalidated this counterargument, and I cannot see how a “cohort effect” is present in the combined data unless KBV failed to fulfill the FIOA in the manner that was requested (Lausen also subsequently provided an interview addressing the government criticisms of his analysis).

An outside analyst also looked at this data and demonstrated that other fatal conditions (which should be vulnerable to same the cohort effect ZI is asserting) did not have the same 2021 spike:

Second, the large σ found for many, (but by no means all) non-fatal conditions in the dataset indicates that something besides artifacts relating to time of death is causing the changes observed. I acknowledge that it is very possible some of the discrepancies present are due to not yet identified artifacts within the data, but at this point in time I have not been able to identify them. I believe that since KBV was focused on debunking the rise in sudden death codes, they did not focus on the rise in other codes for conditions associated with COVID vaccine injuries that were also observed. However, while this was not their focus, this point must nonetheless be considered since it does negate their counterargument.

Additionally, The death argument ZI made was also inconsistent with the death codes in question nonetheless being reported prior to 2021, which they attributed to “coding errors or unaddressed billing fraud.” To some extent this is hand-waving that many others have contested (and something any type of auditing algorithm should have caught years before), but I do not believe it is as important as the first two points.

Conversely, the strongest argument ZI put forward to establish that a cohort effect was occurring for the reported deaths was this spreadsheet. I have not yet been able to discern how the data in it was derived as it does not match the other things I looked at, so I cannot comment on if this is correct (an independent analyst arrived at the same conclusion I did). This spreadsheet is the one source of data that could refute AFD’s argument so I would greatly appreciate any additional thoughts on this one). However, I must also note that if this data is actually correct, it still does not negate the non-fatal complications of vaccination being observed.

A German rebuttal of ZI’s arguments was posted here. AFD also discussed the above rebuttal in a thread here stating:

"Hello all. The death-numbers that we have published are being hotly debated right now. Now the Central Institute for the KBV has joined in has said that the data we presented were quite easy to explain: 'The data is only for people who have accessed a medical service in 2021 and only such people had been billed and therefore would be in the data and everything in the years before are statistical runaways. There are also different causes of death that were significantly higher in the years before such as I46.9 (heart attack without successful reanimation). ' All together 104 000 people have been coded as deaths in the years 2016-2020 of whom the Central Institute of the KBV now says that they were billed medical services in 2021. Now we have a question: If this is really true, we demand an explanation from the Central Institute of the KBV how 104 000 persons that have died in the years 2016-2020 have been billed medical services in 2021.” [Translated courtesy of a reader]

The following was also written in the tweet: “Allegedly, the figures from the KBV are only for patients with health insurance, for whom services were billed in 2021. However, the causes of death were coded for 104,000 patients in previous years. Do we have a data scandal or a billing scandal?”

This table also refutes ZI’s argument that only those who were able to see a doctor and thus were alive in 2021 comprised the cohort of the insurance data.

Many of the German commentators I saw online were also skeptical of the official rebuttals to this data. I was recently sent a detailed summary of the events after the press conference which demonstrated that the rationale for debunking the data changed as time went forward. As best as I can tell, no clear reason was presented for why Lausen’s analysis was flawed given. Instead it was insinuated either that Lausen incorrectly filtered the data (my team and others however arrived at the same results Lausen did) or that there was a data transmission error from the KBV (which is possible but would have had to have been deliberate or inconceivable incompetence).

KBV also issued an astonishing statement refuting AFD’s presentation:

The KBV board clarifies: Based on the billing data transmitted by the KBV to the AfD or. ICD-10 codes cannot be used to establish causal relationships between COVID-19 vaccinations and deaths. From the KBV's point of view, the increase in deaths shown in quarters I-IV 2021 and quarter I 2022 is largely pandemic-related mortality. This once again illustrates the importance of COVID 19 vaccination as an effective measure to prevent serious forms of progress up to deaths. Without the vaccination, mortality would probably have been much higher.

This statement also cited the previously referenced ZI letter and another one which noted:

• The codes in this database do not include codes entered on death certificates and thus cannot be assigned as the cause of death [however all of these codes cannot be entered unless the patient died; also as the statement above shows KBV is admitting an increase in deaths did occur].

• The codes in this database cannot be correlated with vaccination status because many people received the COVID vaccines in settings that did not result in codes being submitted and coding for COVID vaccination has not yet been included in the dataset due to special regulations [I agree with this point, but it fails to refute this dataset since Lausen chose to combine the code and nocode groups; instead, it simply argues that vaccine injuries are underreported in this dataset].

• This database was not created for the purpose of conducting medical research and therefore no conclusion can be drawn from it [I don’t believe this is a valid argument; a lot can be inferred from it and it is the best available database we have, so until the government chooses to make a better database available, it is “the evidence.” Additionally, this is a very similar argument to what is said for VAERS, but unlike VAERS there is not an over or underreporting issue present with this dataset].

I do not believe any of the above points refute the sudden increases in submitted billing codes (hypothesized to correlate with vaccine injuries) that occurred a year after the pandemic started at the exact same time the vaccination campaign began. However, I also believe some type of not yet identified artifact could account for at least some of what was observed and I have spent the last week revising this article to account for the additional information I come across. If anyone can provider a stronger refutation of the data presented here (preferably, at the pinned comment), I would greatly appreciate it. We need to help each other stay honest and I will gladly retract this article if a critical mistake was made.

Note: An independent analyst who reviewed the entire dataset found that it showed many other signs of being plausible.

Conclusion

Given the extremely concerning implications of the German data, it is not surprising that governments around the world and healthcare systems or insurance providers have been reluctant to release their own data. It is my sincere hope that this release will open the flood gates to additional disclosures and I am in complete agreement with the conclusion of this presentation:

I wish we had an American political party stating the same. There are signs of hope however; today Ron DeSantis did something incredible and requested a grand jury against Pfizer and Moderna, an essential step a few leaders in our movement have been working to lay the groundwork for over the last two years. I am also hopeful that this grand jury will compel the state of Florida to release similar data that can be used to assess the safety of these vaccines.

I strongly encourage those of you who who are able to begin looking through the KBV dataset and identifying important trends that can be correlated to other observations we have made over the last two years. I believe there are many excellent articles that could be written on them. I sincerely thank all of you for your continued support!

My primary goal is to draw attention to this data so numerous independent parties can objectively analyze it and independently verify if the trends it shows correlate to “controversial” increases observed in other datasets like VAERS. This data is extremely important as it is the only access we have ever been given to observe the changes in illness that follow the COVID vaccination campaigns. I also suspect the most important use of this data **will be to establish causality for specific vaccine injuries.

**This matters because typically when someone suffers a pharmaceutical injury, it is not acknowledged by the the government and the courts because “there is no evidence the product is associated with that injury,” and as you might expect, the pharmaceutical industry work tirelessly to make sure the evidence that could implicate their product never emerges.

At this point I’ve lost track of how many sad instances I’ve seen where this happened to a medically injured patient (in some cases to the point the gaslighted victim gives up and ends their lives), so I greatly support having an independent means to assess causality for vaccine injuries. Those injured by the COVID-19 vaccines are profoundly suffering and they really need help (on the bright side however, recently Senator Johnson and shortly after Governor DeSantis gave a voice to these victims).

Postscript: It appears a similar rise in unexplained deaths is occurring in Canada.

Now that my piece on Exogenous Moral Orientation has accumulated many views and comments, I want to respond in a general way to the objections raised by my readership.

When you write an essay putting forth a Broad Theory of How Things Are, nobody will read it unless it has a lede that speaks to contemporary interests and a concrete focus on current events. That’s the only reason I opened with Bill Gates and his rumoured ambition to depopulate the earth. I ought to have anticipated that this would prove as much a distraction as an enticement. In answer to the many emails and comments taking issue with my statements here, I would observe that theories of Gates and the vaccines must be brought into alignment with several basic facts: Vaccination rates across Africa and the third world are truly dismal, Gates himself has repeatedly criticised the mRNA vaccines for their inability to stop transmission, and the earth’s population has continued to increase since the pandemic began, undaunted by all public health policies. 1 If the plan is indeed depopulation via the mass administration of shitty pharmaceuticals, we can take some solace in the boundless idiocy of our shadowy overlords.

Beyond those specifics, it is incredibly important to realise that the political order of the West is marked by affinities and proclivities; it tends in specific directions. In an attempt to make sense of pandemic policy, many try to find the single point of manipulation – the PCR test fraud, the false study that sabotaged hydroxychloroquine, or the key vaccinator responsible for steering early funding to BioNTech. You must widen your view to see that these are single plots in a much broader nexus of policies and scheming that all strive in the same direction, while lacking any single point of control or direction.

What is Bill Gates trying to do? Many will doubt that he really wishes “ to create a world where every person has the opportunity to live a healthy, productive life ,” but the inverse image of the man as an aspiring global depopulator will not convince very many people beyond our circles either. Like other philanthropists, Gates has very mundane and self-interested aims:

By attaching his name to initiatives that are already highly regarded – that the cultural system already prefers – he hopes to achieve broader relevance and transform his personal wealth into a form of cultural and political influence. This doesn’t mean that Gates isn’t bad or that he shouldn’t be stopped. It just means that he is a follower more than he is a leader, and that we shouldn’t expect this sad, weak, bloated man to explain very much.

I was pleased to see that some left-leaning readers of the plague chronicle happily identified with the exogenous moral orientation, more or less as I described it. They objected, however, that they didn’t recognise their own political preferences in the decisions of our elite at all.

It’s an old and extremely interesting political illusion, that for those on the left, something akin to a “corporate right” appears to be steering the world, while those on the right see the establishment as primarily leftward tending. Aware of this strange fact, both sides will often use words like “neoliberal” to characterise elite political orientation as something separate from or beyond the conventional political spectrum. The problem is that leftism is not well understood. It is actually a kind of ideological technology, optimised to displace a prior ruling aristocracy and seize control of institutions via alliances of opportunity with disadvantaged social groups. Appeals to economic justice and redistributive policies are simply a means of forming these alliances, which are then used to empower a new managerial elite. This doesn’t mean that many leftists aren’t totally sincere and committed to their vision of equality, but as in all political movements, it is the opportunists and the cynics who run the show. These kinds of people have no interest in any egalitarian utopia, were that even possible, and this gives rise to our optical illusion: From the left, the new elite, which consolidates power for its own purposes, seems to have an aura of “the right” about it, while those on the right are most sensitive to the leftist ideological tactics that brought this new elite to power.

But, that’s just leftism as an ideology. The EMO is a moral instinct prior to ideology, and it can fit any number of different ideological systems. The EMO operates as a taste or a preference, which returns specific answers to specific policy questions. These answers change easily depending upon the scope and the framing of a given problem, leading to a wealth of inconsistencies. If the choice is between the native population of a Western country and third-world immigrants, the EMO will demand that the third-worlders be favoured. If the choice is between reliable power generation in the third world and the environment, the EMO will demand that the environment be favoured. What is apparently very difficult to squeeze past the EMO, are things which look like pragmatic compromises, such as endeavouring to improve third-world conditions via conventional power plants. This path, even though it is the most promising both for the environment and for real people in the world, fails to satisfy the operative moral demands and is eschewed. 2 Contradictions like these are clues, which reveal that we’re dealing here not with any coherent agenda, but rather with moral instincts and unexamined preferences.

Various commenters insist on the reality, the urgency and even the existential crisis posed by climate change. In fact, I formulated these thoughts while reading climate change literature, and I think nothing reveals the reality of the EMO so clearly as this subject. Even if, for the sake of argument, we posit that all of the climate models are correct and that the earth is steadily warming as a result of human CO2 emissions, we still lack a good explanation for Western climate policies, which are only secondarily interested in reducing emissions, and which deploy CO2 primarily as a pretence to circumscribe human impact on the environment. German emissions would be substantially lower, had we invested the billions we put into wind and solar into nuclear power generation instead. In that case, we would have the capacity to scale heat pumps and electric vehicles without threatening to break the grid, confining emissions still further. Instead, Green policies effectively demand an indefinite, continued reliance on natural gas and coal, which is acceptable, because the danger of nuclear power in their minds is not so much the overhyped threat of another Chernobyl, as it is the very real prospect of enabling further civilisational and industrial expansion at the expense of “nature,” which the EMO cannot countenance.

Another clue that something is not quite right with climate change, is that, as an area of cultural and political anxiety, it exists only in the EMO thought-world. This is in contrast to other issues, which prompt varying responses in those with endogenous and exogenous moral inclinations. Consider the war in Ukraine. Those with a pronounced endogenous moral orientation will be sceptical of the conflict and demand that military resources be conserved for national defence. Those with a pronounced exogenous moral orientation will be more likely to appeal to abstract universals like democracy and demand empathy with out-group Ukrainians. 3 We would expect climate change, as an objective problem, to provoke endogenously oriented solutions, and we would expect these to be very extreme, given the alleged immediacy and gravity of the threat. If we are indeed on the brink of triggering a climate “tipping point” (the concept is far more controversial even within the halls of Science than you have been led to believe), limpwristed Paris Agreements would be the least of it. Major powers would be imposing industrial limits on their rivals via sanctions and threats, to reserve the remaining CO2 capacity of the atmosphere for themselves. But, we see nothing like this at all, which suggests that the cluster of prognostications, beliefs and prescriptions around climate change are themselves the exogenously oriented moral response to a totally separate issue, which I will leave my readers to ponder. 4

Finally, because many objected that I overestimate Gates’s sincerity, I’d like to emphasise that I’m not making any claims about the subjective, inner life of anybody. I’m merely trying to articulate the moral system that explains the actions and professed beliefs of philanthropists, policymakers and many ordinary people in the West. By encouraging elites to ally themselves with immigrants or other more endogenously oriented outsiders against their native populations, the EMO definitely has malicious effects. The depressing truth is that people will be inclined to buy into moral systems which benefit them in other ways, and it is very hard to know where sincerity ends and cynicism begins, or to what degree sincerity can ever be an excuse.

Footnotes:

1. The growth rate – which has been in long-term decline – decreased by a barely-perceptible 0.1% since 2020 . 1

2. Third-worlders are typically favoured only when this redounds to the disadvantage of westerners; they are generally disfavoured on environmental and human-impact questions. Pragmatic environmentalists who subscribe to the theory of demographic transition ought to support any means of improving third-world conditions, as even relatively modest environmental impacts here promise to lower the birth rate. Instead, they favour hugely increasing the environmental impact of millions of third-worlders via mass immigration to the developed West, while they perpetuate third-world poverty via things like unworkable energy leapfrogging schemes, thus (at least in their framework) ensuring that birth rates and mortality remain elevated.
   Note that that the moral dynamic surrounding Covid – rooted particularly in a kind of hygiene purity mania – prevented pragmatic solutions to the pandemic in much the same way. The authors of the Great Barrington Declaration tried to sell their alternative to mass containment under the rubric of “focused protection,” but in fact it is better to say that their plan hinged on building natural immunity in the youngest and least vulnerable demographics via “focused exposure.” The moral instincts governing pandemic policy made accepting any infections impossible, even at the cost of higher mortality. 2

3. These are of course only two of various possible constellations. More endogenously oriented Americans, who want to expand American influence in the world or who hold specific anti-Russian animosities, may well find themselves on the Ukrainian side. The same goes some endogenously oriented Eastern Europeans, who perceive the war as a national threat. 3

4. This is true whatever you think about the empirical reality of claims that atmospheric CO2 from human industrial activity is responsible for some portion of industrial-age warming – a proposition I tend to accept in broad terms. 4

One of the things that the plague chronicle aims to do, is draw back the curtain on the institutional or cultural roots of particular malignancies, which seem at first to be contingent on specific bad actors. While I understand that some of you find this irritating, it’s not my purpose to let anybody off the hook. It’s rather to point out that the very real villains we’re all concerned about are mere expressions of much deeper forces, and that fixing things will involve a lot more than rounding up all the Anthony Faucis of the world and trying them for crimes against humanity.

One vein of Corona analysis sees the entire pandemic as the plot of globalist conspirators who are interested in reducing the world population. There are many variations on this theory, but the most basic would hold that lockdowns and the rest were a means of driving us to accept harmful vaccination, which will cause a massive die-off among the vaccinated in the coming years and prepare the way for whatever netzero sustainable future Klaus Schwab has planned for the survivors.

My readers often send me links to podcasts, videos and other media providing proofs of this Global Depopulation Agenda. Clip compilations like this one constitute an important genre in this area. They generally feature globalist goons – in this case, Bill Gates – saying ominous things about the overabundance of humans at different interviews and panel discussions.

I have a look at almost everything you send me, and by now I’ve seen enough to note that the internet case against Gates rests heavily on the same dozen or so video statements. Some of these items, for example the third one in that link (where Gates is talking about reducing childhood mortality), are deliberately deceptive, and it’s an important question, why this area is so awash in clearly manipulated media . The rest of the clips are more or less accurate representations of Gates’s arguments, the only problem being that they’re presented too narrowly.

The fourth at that link, for example, is from a TED talk, where Gates opines that

The world today … is headed up to about nine billion [people]. Now if we do a really great job on new vaccines, healthcare, reproductive health services, we could lower that by perhaps ten or fifteen percent.

The fifth is very similar. Here, Gates pleads:

The problem is that the population is growing the fastest where the people are the least able to deal with it, so it’s in the very poorest places that you’re going to have a tripling in population by 2050. And so their ability to feed, educate, provide jobs, stability, protect the environment, in those locations means they’re facing an almost impossible problem.

If you read these statements carefully, you’ll see they don’t actually support the idea that Gates wants to reduce the world population by vaccinating people to death. First, he could hardly be expected to air such plots in a public forum; and second, Gates almost always pairs his remarks about population with other concerns about healthcare, food and education. These are strange scruples for a homicidal maniac bent on killing billions.

These statements only begin to make sense, when you realise that they’re rooted in the sociological theory of demographic transition . This theory observes that, as societies advance technologically and economically, they shift from an order of high birth rates and high death rates, to an order of low birth rates and low death rates. Gates, who like all globalist elites is worried about environmental impacts from there being too many humans, believes that he can reduce the total peak population in places like Africa by introducing medical interventions to lower mortality and thereby guide populations to a low-birthrate, post-transition demographic pattern. Whether this theory is right, or whether this makes Gates’s interventions morally defensible, are separate questions. What is beyond dispute, is that this is what Gates is arguing and what everybody in his audience understands him to be arguing.

The banal truth is that Gates is an unoriginal flabby Western liberal. He’s worried about the environment, about population and about disadvantaged brown people, and he thinks he can solve all these problems by improving healthcare. This isn’t a defence of him. I happen to think he’s a malign influence and that if we can’t rein in the Gates’s of the world we’re finished, but that’s not because he’s bent on using mRNA vaccines to decimate humanity.

Those concerned about the Global Depopulation Agenda will not be appeased by these clarifications, of course. They’ll point to anti-natalist messaging and policy in Western nations, and also to organisations like the Club of Rome and establishment intellectuals like Paul Ehrlich , who have openly railed against the spectre of overpopulation. They’ll argue – rightly – that our entire political culture is in thrall to a green movement which opposes any technology that might further human flourishing via reliable energy, regardless of its carbon impact. They’ll say I myself have frequently complained that countries like Germany are doing permanent damage to their economies by pursuing an energy transition which will make no difference in the longer term, because future carbon emissions are almost entirely a function of increasing prosperity and population growth in the developing South and East.

If there isn’t a Global Depopulation Agenda, what’s going on, and how are all these ominous developments to be explained?

The answer is very important, and it lies in the peculiarities of postwar political ideology and the moral instincts which this ideology expresses.

There are many ways to illustrate this, but the most efficient is probably this classic Nature paper on Ideological differences in the expanse of the moral circle .

Among other things, the authors asked study participants identifying as “conservatives” and “liberals” (in the American sense) to indicate their spheres of primary moral concern. “Conservatives” tended to emphasise those spheres nearest to themselves – their immediate family, their more extended relatives, their friends – as bearing the greatest moral weight. “Liberals,” meanwhile, expressed the greatest moral interest in those spheres furthest from themselves – “all people on all continents,” for example, or “all mammals.”

Plotted as heat-maps on 16 concentric circles, where the first circle is “immediate family” and the sixteenth is “all things in existence”, the comparative results look like this:

Because the future survival of humanity is at stake here, we should drop the dumb “conservative” and “liberal” labels.

The heatmap on the left is not “conservative.” It reflects the ordinary, unremarkable moral orientation of almost all human beings who have ever lived, and almost all currently living humans across the entire world. Without a moral orientation that somehow prioritises your progeny and your relatives (however widely understood), your genes will get nowhere.

The heatmap on the right, meanwhile, represents the anomalous exogenous moral orientation (EMO) of politicial and cultural elites in the developed West, which “liberal” cannot even begin to describe, and which applies primary moral emphasis to circles 13 and 14. These are “all animals in the universe, including alien lifeforms” and “all living things in the universe including plants and trees.” Substantial moral value is also attached to things in the twelfth circle, “all animals on earth including paramecia and amoebae,” and in the fifteenth circle, “all natural things in the universe including inert entities such as rocks.” These are people who, strictly speaking, claim to feel morally bound to family, friends and relatives primarily to the extent that these fall within the “living things” or “things in existence” categories.

While we aren’t exactly governed by shape-shifting lizards , we are governed by completely insane ideologues who would do the bidding of shape-shifting lizards – if necessary at our dire expense – were these ever to be discovered.

Now, it’s not quite as bad as it seems. Remember above all that these are moral aspirations and ideals; they are how study respondents claim to feel. Revealed preferences show that most of these people, in their personal lives, still attach substantial moral weight to their immediate friends, family and community. They probably feel qualms about this, however, and when the context is not so immediate – when, for example, they’re making policy decisions for millions of citizens – they’ll compensate by caving to their idealised EMO wherever possible. Put another way: Bill Gates likes the convenience of his private jet , even as he hopes to discourage people from flying.

Remember also that it is the dose which makes the poison. Some degree of EMO isn’t bad. It’s one reason that we look down on littering, for example. An important expression of growing Western EMO would be the European interest in other peoples and cultures, including much-maligned colonialism and the less-maligned British campaign to abolish the slave trade after the later eighteenth century. Particularly since 1900, however, the EMO of Western governing elites has grown ever more extreme, to the point that it has begun to constitute an existential threat for human civilisation.

How this radical and historically unprecedented EMO came to be so ingrained is a complex question. Putting it down to the media or to propaganda is not fully satisfying, because we’d have to ask where the media and the propagandists got these ideas in the first place.

A prerequisite is technology and our growing alienation from nature. Anyone who has spent a rough week or two on the face of a mountain will come away from the experience personally enriched, but perhaps also doubtful that unmanaged unmitigated nature is every bit as friendly, good and deserving of moral concern as his immediate family. Tropes which locate wisdom in distant indigenous peoples and on foreign continents likewise betray a naivete about the realities of hunter-gatherer existence and a lack of experience with life beyond the prosperous West.

A more important, immediate causal factor, is the upset in established social orders since the Industrial Revolution, which has coincided with the rise of liberal democracy, and the replacement of the traditional aristocracy with new managerial elites. The latter have frequently pursued tactical alliances with outsiders or the lower classes to displace prior establishments – including, as the quiet revolution continues, prior managerial establishments. This is the primary function of Diversity, Inclusion and Equity initiatives in America today, and it obviously encourages and depends upon both orchestraters and beneficiaries to engage in radical EMO rituals.

As the problem seems to be growing worse over time, self-reinforcing selection effects probably also play an important part. The more pronounced EMO is favoured by the governing elite, the more all politicians and persons of prominence in the West are specifically selected for this trait, or at least for their willingness to pantomime it. While people with these moral tendencies have always existed, they’ve never been so heavily concentrated in positions of influence before, and the more concentrated they become, the more aggressively they filter for like-minded radicals like themselves, even in the absence (and in excess) of any specific objective.

Once you have seen this simple dynamic at work, you cannot unsee it.

It explains the increasing prominence of animal (and even alien) protagonists in entertainment media, the overt preference for fringe sexual minorities, the predilection for supranational global political bodies and non-governmental organisations which transcend borders and national institutions.

It explains, in particular, why governing elites are so open to insane unprecedented policies like mass immigration. They no longer have particular national moral categories at all, and so they reluctantly embrace all of humanity, and preferentially all living things everywhere. Similarly, it explains why mainstream liberal policies happily enlarge the carbon footprints of millions of third-world immigrants by welcoming them into the industrialised West, while simultaneously waging war on all aspects industrial society for their supposed negative impacts on nature.

Less obviously, the radical EMO of our leaders and their supporters explains the increasing willingness of elites to tolerate suboptimal and actively harmful policies at home. The moral world of the people who run our countries has grown enormously in size, leaving the spheres of their direct jurisdiction almost microscopic in comparison. Why not shut down all of society in an effort to kill (a likely man-made) virus? Why not inject poorly tested mRNA novelty vaccines in billions and suppress all evidence of negative population-wide effects? That elites increasingly treat their populations like cattle is a direct expression of their expanded moral universe. They have so many other things to care about.

It took a while for these moral sentiments to find their proper ideological articulation. In the early 1970s, people with radical EMO signalled, for a brief time, about the dangers of human overpopulation, and there ensued a moment of moral hysteria in which people like Paul Ehrlich wrote books like The Population Bomb . The years since have seen the emergence of a more differentiated ideological system, which extends lesser but still privileged consideration to third-world populations. Thus antinatalist systems are confined mostly to the West, where the most zealous environmental policies are also implemented. That Europe could disappear tomorrow with minimal effects on long-term global population projections or the future composition of the atmosphere is irrelevant. It is the fact that this is the circle of least moral concern, which is determinative.

In the nineteenth century, somebody like Bill Gates would be far more likely to run domestic charities, but in our present hyper-EMO world, he spends every waking moment thinking about Africa, and how he can help Africans, and in the process also save nature by hastening the African transition towards lower birthrates and bringing the netzero ideal closer to reality. All the policy documents and aspirational statements produced by the World Economic Forum, the United Nations and other bodies are animated by a similar spirit.

A globalist cabal plotting the depopulation of the world would be a grave problem, but one with a clear enough solution. We’re facing, instead, an entire moral and ideological system, with very deep roots in prosperous Western culture. This isn’t a universe where everybody wakes up tomorrow, elects to put Bill Gates on trial for his crimes against humanity, and returns thereafter to sensible public health policy. It’s a world where millions of people share the ideological anxieties of eccentric children like Greta Thunberg, manifest escalating indifference to adverse policy outcomes in their own countries, and dream of a future earth devoid of humans like themselves. Because the driving forces operate at the level of moral instinct and emotion, no amount of evidence or appeals to reason that can stop this. Probably the best hope lies in its naivete and idealism. Worsening conditions will ultimately deprive these ideologies of their cultural appeal; how bad things have to get before this happens, is the terrifying question.

UPDATE: A lot of comments are querying Gates’s sincerity, suggesting ulterior motives, and so forth. I have no direct insight into the man, but I suggest that his interior state is a peripheral matter here. The problem is to understand under what moral orientation he is claiming to operate, and why that moral orientation resonates so broadly with elite Western culture.

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

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.

An anonymous tip from December of 2020 aged exceptionally well, with bad repercussions for the female fertility in girls born to both Covid-19 vaccinee parents.

Although it has been reported on by Igor Chudov a few days ago, I would like to add a bit more beef to this uncorroborated (so far) information, as it is the news no one wants to believe, but it deserves further investigation for the reasons outlined below.

The original Moderna insider tip from Dec. 2020, from two anonymous engineers working there, goes like this:

I'm an industrial engineer at Moderna and the other one of us is a process development engineer. I'm sure the same thing is happening with Pfizer-BioNTech. It was hard to put things together based on the small quantities of additions happening in manual step (highly unorthodox for a continuous process production). The explanation we got was highly sensitive trade secret adjuvants being added. Digging in deeper showed how sensitive it actually was. Most people's understanding of this novel vaccine type is that it works as follows:`

1. Make mRNA coding for S protein
2. Make lipid nanoparticle delivery system
3. Profit

How it actually works from what we've uncovered:

1. Make mRNA coding for S protein
2. Make mRNA coding for mutant versions of CYP19A1 and CDKN1B in smaller amounts
3. Make sure that while delivery system for (1) mostly ends up in liver, most of (2) ends up in the gonads
4. Make sure form and quantity of additive upregulating LINE-1 reverse transcription activity makes it hard to detect among legit adjuvants
5. Effects from (2) integrated by (4) are recessive; mildly oncogenic effects in vaccine recipients unlikely to be noticed for many years
6. (5) recessive but since most of population vaccinated, in next generation female offspring have premature ovarian failure

The beef of this tip is that, in addition to the mRNA code for S spike, the vaccine vials will contain additional mRNA that codes both for a mutant version of CYP19A1 and a mutant version of CDKN1B. Both these mutant proteins are implicated in the female infertility issues. From the advantage of hindsight in March 2022, this information is credible for the following reasons:

• The pharmacokinetics information of the LNPs in mRNA vaccines has been spilled by the Japanese only in May 2021. As it turned out, the LNPs with the mRNA in them do not stay at the injection site, as CDC and other agencies postulated. Instead, they accumulate in the liver and the gonads of the vaccinees in high concentrations. Surprise! So, the tipsters have been confirmed correct in this regard.

• The studies regarding LINE-1 enzymes being able to reverse transcribe the vaccine mRNA back into human DNA appeared much later as well:

  1. Reverse-transcribed SARS-CoV-2 RNA can integrate into the genome of cultured human cells and can be expressed in patient-derived tissues ( Jaenisch et al., 2021.05.21)
  2. Coronavirus gene findings are no cause for alarm, says leading scientist (ABS-CBN, 2021.01.30): The discovery by Professor Rudolf Jaenisch and researchers at the Massachusetts Institute of Technology, stirs up a hornet's nest because mRNA vaccines, including those made by Pfizer/ BioNTech and Moderna, operate in similar ways to the virus to trigger an immune response.
  3. Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line (Aldn et al., 2022.02.25).
  4. Moderna finally cracks into gene editing with Metagenomi pact thanks to 'irresistible' data (Fierce Biotech, 2021.11.02): We finally know who Moderna has been courting behind the scenes to make the big jump into gene editing. The famed biotech has signed a research partnership with CRISPR gene editing company Metagenomi. Metagenomi will offer up access to its gene editing tools. The company recent unveiled data on its CRISPR-associated transposases system that can be used to "precisely integrate large DNA fragments into genomes", allowing for new editing techniques beyond the currently available technology.
  5. Metagenomi Presents New Findings on CRISPR-associated Transposases (CAST) that Allow for Targetable Genomic Integration of Large DNA Fragments (Metagenomi.co, 2021.05.14): Our research presented at ASGCT describes how our first-in-class programmable CAST gene editing system can be used to precisely integrate large fragments of DNA into target genomes and the potential of these systems in the development of both ex vivo and in vivo gene therapies. CRISPR-associated transposases can be reprogrammed to integrate at specific genomic sites using guide RNAs. Target genomes, eh? Transhumans, anyone? A.k.a. mutants?

  Another solid confirmation that the tipsters knew what they were talking about way before this information went public.

• As the reader Jeff C pointed out (and I quote verbatim from here on), the tipsters not only said that LINE-1 could facilitate reverse transcription but that the vaxx has a hidden additive that specifically upregulates LINE-1 (point #4)). The Aldn et al. paper using the BioNTech vaxx clearly showed a high presence of LINE-1 when the vaxx was added that was not there in the control. So something about the vaxx significantly increases LINE-1 just like the tipster said. The fact that the tipster knew this before any of this was publicly known is pretty impressive. If you look back at the Covid virus reverse transcription study (Jaenisch et al - looked at Covid itself, not the vaxx) they artificially increased LINE-1 in the cells via transfection [To increase the likelihood of detecting rare integration events, we transfected HEK293T cells with LINE1 expression plasmids prior to infection with SARS-CoV-2]. That was a key criticism of the study in that it wasn't a real world case. This is in stark contrast to the vaxx study where LINE-1 increased solely due to the vaxx itself. Wasn't that the role of one of the "highly sensitive trade secret adjuvants being added", as hinted by the tipster?

• In Oct. 2021, a former Pfizer quality control manager and a whistleblower, Melissa Strickler, spilled beans on the unusual manufacturing process at the Pfizer Covid-19 vaccine plant in a series of interviews. Pfizer's processes for its vaccine are strangely deviating from usual norms. The compounding room has no idea what are the components they are mixing into the product. This secrecy about what goes into the vials is unprecedented. Furthermore, the vaccine manufacturers are not controlled by any independent bodies as to the quality control, the vials being shipped directly to the vaccine administration locations. This lends credence to the assertion that the mRNA vaccines may contain undisclosed constituents.

• The leak of EMA-Pfizer correspondence in Nov.-Dec. 2020, when EMA was working on Pfizer's vaccine authorization, revealed that EMA was concerned that the mRNA in the vaccine vials contains only 55% of the intended S spike code, the rest being truncated species blamed on the faults in the manufacturing process. Pfizer placated these concerns by pushing the S spike code proportion up to 75%, at least for the time being. After that, EMA stopped looking and declared the jabs kosher. More on this in my post Zeroing in on Gifts from Science to Humanity from Nov. 2021. So, another score for the tipsters - the jabs do contain some exogenous mRNA code that no one analyses or scrutinizes.

• If that is not enough, BigPharma, in collaboration with WHO and NIH, has a long tradition of adding undisclosed ingredients harming female fertility into the vaccines going all the way back to 1970s:

2017: HCG Found in WHO Tetanus Vaccine in Kenya Raises Concern in the Developing World. Baby-Killing Vaccine: Is It Being Stealth Tested?: During the early 1990s, the World Health Organization (WHO) has been overseeing massive vaccination campaigns against tetanus in a number of countries, among them Nicaragua, Mexico, and the Philippines. In October 1994, Human Life International (HLI) received a communication from its Mexican affiliate, the Comite Pro Vida de Mexico, regarding that country's anti-tetanus campaign. Suspicious of the campaign protocols, the Comite obtained several vials of the vaccine and had them analyzed by chemists. Some of the vials were found to contain human chorionic gonadotrophin (hCG), a naturally occurring hormone essential for maintaining a pregnancy. Here are the known facts concerning the tetanus vaccination campaigns in Mexico and the Philippines:

• Only women are vaccinated, and only the women between the ages of 15 and 45. (In Nicaragua the age range was 12-49).
• Human chorionic gonadotrophin (hCG) hormone has been found in the vaccines.
• The vaccination protocols call for multiple injections-three within three months and a total of five altogether. But, since tetanus vaccinations provide protection for ten years or more, why are multiple inoculations called for?

Allied with the WHO in the development of an anti-fertility vaccine (AFV) using hCG with tetanus and other carriers have been UNFPA, the UN Development Programme (UNDP), the World Bank, the Population Council, the Rockefeller Foundation, the All India Institute of Medical Sciences, and a number of universities, including Uppsala, Helsinki, and Ohio State.[5] The U.S. National Institute of Child Health and Human Development (part of NIH) was the supplier of the hCG hormone in some of the AFV experiments.

Again, a corroboration of the thrust of the allegations by the Moderna insiders.

• The strange, irrational drive to vaccinate every last person on Earth, especially children and pregrant women, with the untested and clearly dangerous injections is another huge red flag as to the true goals of the Covid-19 vaccination of the world population. Especially that the population control has been a holy grail for the eugenicist cabal since the 19th century, and in the form of vaccines, no less. Read my post Going for Jugular Take 2 - All Ducks in Row (Dec. 2021) for complete, more or less, disclosure.

• The new plant-based Canada-made non-mRNA vaccine still contains LNP material, for some inexplicable reason. Or should we suspect that it will also contain fertility-harming mRNA?

So, lots of indirect evidence that the Moderna insiders are trustworthy and that their whistle blowing deserves all the attention it can garner. In the form of vial analysis and vaccinee testing, for starters.

In the meantime, this post should serve as a fair warning and one of the elements on which to base your informed decision as to whether to accept any vaccine in 2022 and going onward. Or any injection, for that matter, from your caring health authorities and governments.

Continued in How Will We Know?

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

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Proceedings were paused at the public inquiry looking into the federal government's use of the Emergencies Act on Thursday afternoon after a medical incident.

A lawyer representing the Public Order Emergency Commission collapsed while he was questioning Ontario's deputy solicitor general, the second witness of the day.

Peter Aaby at the Symposium about Scientific Freedom, Copenhagen, 9 March 2019.

Lecture: "WHO is the brain in the system - The sound of silence? A case study of how public health vaccinology deals with fundamental contradictions of current policy."

Anthropologist, Dr Peter Aaby is credited for the discovery of non-specific effects of vaccines, leading the World Health Organization, WHO, to change its measles vaccine programme in the early 1990s.
For almost 40 years, he has run the Bandim Health Project, a health and demographic surveillance system site that he established in Guinea-Bissau in 1978.

This lecture is part of the Symposium about Scientific Freedom and the inauguration of the Institute for Scientific Freedom, which took place in Copenhagen, Denmark, 9 March 2019.

World renowned Danish scientist Peter C Gøtzsche is the founder of the institute. The Institute’s primary area of focus is healthcare and the institute has three main visions:

• All science should strive to be free from financial conflicts of interest.
• All science should be published as soon as possible, and made freely accessible.
• All scientific data, including study protocols, should be freely accessible, allowing others to do their own analyses.

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

Abstract

Introduction

In 2020, prior to COVID-19 vaccine rollout, the Brighton Collaboration created a priority list, endorsed by the World Health Organization, of potential adverse events relevant to COVID-19 vaccines. We adapted the Brighton Collaboration list to evaluate serious adverse events of special interest observed in mRNA COVID-19 vaccine trials.

Methods

Secondary analysis of serious adverse events reported in the placebo-controlled, phase III randomized clinical trials of Pfizer and Moderna mRNA COVID-19 vaccines in adults (NCT04368728 and NCT04470427), focusing analysis on Brighton Collaboration adverse events of special interest.

Results

Pfizer and Moderna mRNA COVID-19 vaccines were associated with an excess risk of serious adverse events of special interest of 10.1 and 15.1 per 10,000 vaccinated over placebo baselines of 17.6 and 42.2 (95 % CI −0.4 to 20.6 and −3.6 to 33.8), respectively. Combined, the mRNA vaccines were associated with an excess risk of serious adverse events of special interest of 12.5 per 10,000 vaccinated (95 % CI 2.1 to 22.9); risk ratio 1.43 (95 % CI 1.07 to 1.92). The Pfizer trial exhibited a 36 % higher risk of serious adverse events in the vaccine group; risk difference 18.0 per 10,000 vaccinated (95 % CI 1.2 to 34.9); risk ratio 1.36 (95 % CI 1.02 to 1.83). The Moderna trial exhibited a 6 % higher risk of serious adverse events in the vaccine group: risk difference 7.1 per 10,000 (95 % CI –23.2 to 37.4); risk ratio 1.06 (95 % CI 0.84 to 1.33). Combined, there was a 16 % higher risk of serious adverse events in mRNA vaccine recipients: risk difference 13.2 (95 % CI −3.2 to 29.6); risk ratio 1.16 (95 % CI 0.97 to 1.39).

Discussion

The excess risk of serious adverse events found in our study points to the need for formal harm-benefit analyses, particularly those that are stratified according to risk of serious COVID-19 outcomes. These analyses will require public release of participant level datasets.

Keywords

SARS-CoV-2COVID-19VaccinesCOVID-19 vaccinesmRNA vaccinesPfizer-BioNTech COVID-19 vaccine BNT162b2Moderna COVID-19 vaccine mRNA-1273NCT04368728NCT04470427Serious adverse eventsAdverse events of special interestBrighton CollaborationCoalition for Epidemic Preparedness InnovationsSafety Platform for Emergency vACcines

1. Introduction

In March 2020, the Brighton Collaboration and the Coalition for Epidemic Preparedness Innovations partnership, Safety Platform for Emergency vACcines (SPEAC), created and subsequently updated a “priority list of potential adverse events of special interest relevant to COVID-19 vaccine trials.” [1] The list comprises adverse events of special interest (AESIs) based on the specific vaccine platform, adverse events associated with prior vaccines in general, theoretical associations based on animal models, and COVID-19 specific immunopathogenesis. [1] The Brighton Collaboration is a global authority on the topic of vaccine safety and in May 2020, the World Health Organization’s Global Advisory Committee on Vaccine Safety endorsed and recommended the reporting of AESIs based on this priority list. To our knowledge, however, the list has not been applied to serious adverse events in randomized trial data.

We sought to investigate the association between FDA-authorized mRNA COVID-19 vaccines and serious adverse events identified by the Brighton Collaboration, using data from the phase III randomized, placebo-controlled clinical trials on which authorization was based. We consider these trial data against findings from post-authorization observational safety data. Our study was not designed to evaluate the overall harm-benefit of vaccination programs so far. To put our safety results in context, we conducted a simple comparison of harms with benefits to illustrate the need for formal harm-benefit analyses of the vaccines that are stratified according to risk of serious COVID-19 outcomes. Our analysis is restricted to the randomized trial data, and does not consider data on post-authorization vaccination program impact. It does however show the need for public release of participant level trial datasets.

2. Methods

Pfizer and Moderna each submitted the results of one phase III randomized trial in support of the FDA’s emergency use authorization of their vaccines in adults. Two reviewers (PD and RK) searched journal publications and trial data on the FDA’s and Health Canada’s websites to locate serious adverse event results tables for these trials. The Pfizer and Moderna trials are expected to follow participants for two years. Within weeks of the emergency authorization, however, the sponsors began a process of unblinding all participants who elected to be unblinded. In addition, those who received placebo were offered the vaccine. These self-selection processes may have introduced nonrandom differences between vaccinated and unvaccinated participants, thus rendering the post-authorization data less reliable. Therefore, to preserve randomization, we used the interim datasets that were the basis for emergency authorization in December 2020, approximately 4 months after trials commenced.

The definition of a serious adverse event (SAE) was provided in each trial’s study protocol and included in the supplemental material of the trial’s publication. [2], [3], [4] Pfizer and Moderna used nearly identical definitions, consistent with regulatory expectations. An SAE was defined as an adverse event that results in any of the following conditions: death; life-threatening at the time of the event; inpatient hospitalization or prolongation of existing hospitalization; persistent or significant disability/incapacity; a congenital anomaly/birth defect; medically important event, based on medical judgment.

In addition to journal publications, we searched the websites of the FDA (for advisory committee meeting materials) and Health Canada (for sections of the dossier submitted by sponsors to the regulator). [5] For the FDA website, we considered presentations by both the FDA and the sponsors. [6] Within each of these sources, we searched for SAE results tables that presented information by specific SAE type; we chose the most recent SAE table corresponding to the FDA’s requirement for a safety median follow-up time of at least 2 months after dose 2.

For each trial, we prepared blinded SAE tables (containing SAE types without results data). Using these blinded SAE tables, two clinician reviewers (JF and JE) independently judged whether each SAE type was an AESI. SAE types that matched an AESI term verbatim, or were an alternative diagnostic name for an AESI term, were included as an AESI. For all other SAE types, the reviewers independently judged whether that SAE type was likely to have been caused by a vaccine-induced AESI, based on a judgment considering the disease course, causative mechanism, and likelihood of the AESI to cause the SAE type. Disagreements were resolved through consensus; if consensus could not be reached, a third clinician reviewer (PW) was used to create a majority opinion. For each included SAE, we recorded the corresponding Brighton Collaboration AESI category and organ system. When multiple AESIs could potentially cause the same SAE, the reviewers selected the AESI that they judged to be the most likely cause based on classical clinical presentation of the AESI.

We used an AESI list derived from the work of Brighton Collaboration’s Safety Platform for Emergency vACcines (SPEAC) Project. This project created an AESI list which categorizes AESIs into three categories: those included because they are seen with COVID-19, those with a proven or theoretical association with vaccines in general, and those with proven or theoretical associations with specific vaccine platforms. The first version was produced in March 2020 based on experience from China. Following the second update (May 2020), the WHO Global Advisory Committee on Vaccine Safety (GACVS) adopted the list, and Brighton commenced a systematic review process “to ensure an ongoing understanding of the full spectrum of COVID-19 disease and modification of the AESI list accordingly.” [7] This resulted in three additional AESIs being added to the list in December 2020. The subsequent (and most recent fourth) update did not result in any additional AESIs being added to the list. [1].

We matched SAEs recorded in the trial against an expanded list of AESIs created by combining Brighton’s SPEAC COVID-19 AESI list with a list of 29 clinical diagnoses Brighton identified as “known to have been reported but not in sufficient numbers to merit inclusion on the AESI list.” [7] Sensitivity analysis was used to determine whether use of the original versus expanded list altered our results.

Risk ratios and risk differences between vaccine and placebo groups were calculated for the incidence of AESIs and SAEs. We excluded SAEs that were known efficacy outcomes (i.e. COVID-19), consistent with the approach Pfizer (but not Moderna) used in recording SAE data. The Pfizer study trial protocol states that COVID-19 illnesses and their sequelae consistent with the clinical endpoint definition were not to be reported as adverse events, “even though the event may meet the definition of an SAE.” [8] For unspecified reasons, Moderna included efficacy outcomes in their SAE tables, effectively reporting an all-cause SAE result. Because we did not have access to individual participant data, to account for the occasional multiple SAEs within single participants, we reduced the effective sample size by multiplying standard errors in the combined SAE analyses by the square root of the ratio of the number of SAEs to the number of patients with an SAE. This adjustment increased standard errors by 10 % (Pfizer) and 18 % (Moderna), thus expanding the interval estimates. We estimated combined risk ratios and risk differences for the two mRNA vaccines by averaging over the risks using logistic regression models which included indicators for trial and treatment group.

We used a simple harm-benefit framework to place our results in context, comparing risks of excess serious AESIs against reductions in COVID-19 hospitalization.

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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.

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

Highlights

• mRNA vaccines promote sustained synthesis of the SARS-CoV-2 spike protein.
• The spike protein is neurotoxic, and it impairs DNA repair mechanisms.
• Suppression of type I interferon responses results in impaired innate immunity.
• The mRNA vaccines potentially cause increased risk to infectious diseases and cancer.
• Codon optimization results in G-rich mRNA that has unpredictable complex effects.

Abstract

The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health.

Graphical abstract

This article is written for all readers, Year 9 students through elder adults. Methods and reasoning herein are pedestrian. Doctors and scientists may opt to skip to “BEGIN HERE TO VIEW DATA”. If you really want to cheat, skip to the bottom and look for yellow highlighted cells in spreadsheets. Understand what they represent. They represent significant, proven, excess death in the circulatory system matching what the pharmaceutical companies and governments call “rare”, another word seemingly redefined in 2021.

The official Massachusetts database of death certificates contains proof that C19 “vaccines” killed thousands of people in Massachusetts in 2021.

This article details a forensic journey in a one-of-a-kind, brute-force, pedestrian, forensic analysis of the official Massachusetts government data to discover what happened and is happening in a population of ~ 6.9 million people at the fore of C19 “science.” Massachusetts is a leading medical and pharmaceutical technology exporter to the world. Some leaders say it is a model for C19 response planning. The truth is that Massachusetts is a model for fraud on the people.

As demonstrated in particularity below, there was a short pandemic of respiratory deaths in 2020. Then, in the year of injections en masse, deaths switched to mainly circulatory system deaths. Something is attacking the circulatory systems of citizens of Massachusetts.

Three main events are initially depicted: a pandemic, an extremely attenuated second wave of disease no longer a pandemic, and a nearly steady-state excess death anomaly in the second half of 2021 (likely began around February 2021, but was obscured by lower than normal deaths of 85+yo’s due to culling from C19 in spring 2020).

Investigation of the anomaly indicates that excess deaths are circulatory system involved, also known and documented in the C19 vaccine trial data. Though myocarditis gets the most notoriety, the entire circulatory system is under attack.

Hereinafter, the C19 “vaccine” will be called “gene modification” because it is a more accurate descriptor of the biological injectable product. Industry and government chose “vaccine” because it is more psychologically acceptable to consumers. “Vaccine” has product-class recognition and reputation. Ergo, the definition of “vaccine” was changed in 2020 to accommodate the inclusion of C19 gene modification into this product-class. Lawsuits based on this issue of “definition” are pending.

EUA WARNING

It is an undeniable fact that the Emergency Use Authorization (EUA) for the C19 gene modification circumvented the normal course of years-long clinical trials that ensure safety and effectiveness of oral and injectable biological and pharmaceutical products.

Through the EUA, which granted immunity from tort to the manufacturers, the burden of precautions (clinical trials) was shifted from the least cost avoider (the manufacturer) to the most cost avoider (the consumer). Though the burden of precautions is pecuniary to the manufacturer, it entails loss of life to the consumer. Id est, pharmaceutical manufacturers avoid costs and increase profits, while consumers die or are maimed after assuming the burden of precautions as lab rats.

INTRODUCTION

Scientists disagree whether the C19 gene modification's spike protein or its lipid nanoparticle is the root cause of injury or death in a minority of people (a death lottery). Either or both theories are in harmony with this article’s conclusion.

To preemptively assuage decriers of “correlation does not equal causation,” this poignant allegory is offered. If five strong swimmers died in one month in a busy lake, would you: A) close the lake to swimmers pending results of investigation, or B) leave the lake open as a small percentage of swimmers continue to die during investigation? Regarding C19 gene modification, governments chose “B”.

While others start at the lowest level of abstraction (cellular & molecular) and then look upward to localized and systemic injuries in an effort to establish a causal chain, this article starts at the highest level of abstraction (all-cause deaths), then investigates downward into anomalies. 1) Is there an anomaly in all-cause deaths? If so, 2) Whom did the anomaly affect, and when? 3) How did the anomaly manifest in immediate and underlying causes? 4) Are the underlying causes traced to the C19 gene modification as a root cause?

. . .

Read the whole article

. . .

CONCLUSION

Three of the four questions posed have been answered:

1. There is an anomaly in all-cause deaths beyond the obvious 8 to 10-week spring 2020 pandemic. The anomaly lasted nearly all of 2021, but manifests visually only from July 2021 through the end of the year and continues into 2022. The first half of 2021, the anomaly was negated by the lack of 85+yo deaths evident by the vertical light blue stripe on the right of the 2021 heat map

2. The people affected in 2021 may be considered old, but they are younger on average than in the 2020 C19 pandemic as seen in the vertical pink alley in 2021 heat map.

3. In order to achieve an all-cause excess mortality of 10% to 20% during 2021, any single or few multiple cause increase would have to be higher in order to affect the all-cause full population denominator. Indeed circulatory system issues are much higher and account for many excess deaths in the order of thousands, but are likely masked by the numerous bleeds and deposits of clots yielding a smattering of different “I” and “D” and “R” codes.

4. No effort is made in this article to tie the C19 gene modification biological injectable product to a mechanism for the circulatory system deaths. Any doctor, scientist, or pedestrian reader can make that inference from the overwhelming correlative data herein. There are tens of thousands of life years lost in 2021 in excess of what was expected by any mathematical formula. These are not from C19. The math does not work out.

Again, the official Massachusetts database of death certificates contains proof that C19 gene modification biological injectable products killed thousands of people in Massachusetts in 2021.

Pandemics do not switch from respiratory to circulatory causes of death in one year. [add sarcasm now] Perhaps it can be done this way. Take the deadly part of the virus and change the mode of entry from aerosols entering lungs to direct injection into the blood stream [lottery win if it gets into a blood vessel].

NOTES

There is a table of eight (8) deaths mentioning “vaccin” or “immuniz” as string searches. Of the 8, only one has ICD-10 codes referring to the injection as a possible cause. The omission of ICD-10 codes is civilly negligent at the very least, and is likely a criminal act of intentional omission leading to fraud on a public record. This will be addressed in the next article. Massachusetts is rife with fraud throughout the entire medical establishment. They do not see it as fraud or as a crime. They see it as the normal course of business for the biggest industry in their little state of 6.9 million people. To those who are injecting children and pushing these death lottery shots, how can you get through another day knowing you were, are, or will be responsible for taking the lives of young children? Or leaving families without a mother or father?

Oh, let this article finally end. Please notice the two tables at the very end. Notice the change in average age by year for both “I” and “J” codes, but more importantly for all-cause total deaths each year in Massachusetts. The average age was lower in 2021 than any of the prior 6 years. That might be expected after a pandemic year that took the old people. However, the total deaths are 3,000 to 4,000 higher in 2021 than any other year except 2020. The average ages of those excess 3,000 to 4,000 who died in 2021 had to have been much younger to change the average as much as they did.

URGENT PLEA

There is not another dataset out there like that one that definitely proves prolonged excess death in causes specific to the circulatory system and in numbers in the thousands of lives and in younger people than expected. C19 was over in Massachusetts in June 2020. What has happened since then has been a hidden disaster of biological injectable product madness.
God bless you all and thank you for reading.

"If the radiance of a thousand suns were to burst at once into the sky, that would be like the splendor of the mighty one." "Now I am become Death, the destroyer of worlds”.

J. Robert Oppenheimer, Scientific director of the Manhattan Project (quoting from the Bhagavad Gita)

by Robert W. Malone MD, MS

Last January, Stew Peters decided to roll out the thesis that I have personal responsibility for the morbidity and mortality associated with the COVID-19 mRNA vaccines consequent to my pioneering work in developing the ideas and reduction to practice of using synthetic mRNA as a transient “gene therapy” method, with the entry level application being for vaccine purposes. This has been echoed by many angry social media detractors seeking to find someone to blame for the lies and adverse events that have been associated with these mRNA vaccines. Mindful of those critics, this Substack essay focuses on some of the differences between what was originally envisioned and the current molecules that are being injected into our bodies. The first section of the essay sets the stage by summarizing (for a general readership) how the whole idea of gene therapy was developed, and then describing how and why this lead to the idea of mRNA as a drug and as a method of generating a vaccine response. The second section gets quite technical, and provides detailed information intended for a scientific audience. The conclusion is written for a general audience.

Gene Therapy, Transhumanism, and the origins of mRNA as a drug or vaccine

The core idea captured in the original nine patents which stem from my work between 1987 and 1989 was that there are multiple key problems with the idea of permanent “gene therapy” as originally envisioned by Richard Roblin, PhD and academic Pediatrician Dr. Theodore Friedman in 1972. The modern embodiment of this concept can be found in the many writings from the WEF and others concerning “Transhumanism” and use of CRISPR/Cas9 gene editing technology. To really understand all of this requires a brief journey through the history and logic of “gene therapy”.

The January 2015 UC San Diego News center piece entitled “Friedman Recognized for Pioneering Gene Therapy Research: School of Medicine professor receives prestigious Japan Prize” nicely summarizes the underlying logic of “Gene Therapy” as envisioned by Friedman and Roblin.

“Though posed as a question, Friedmann and Roblin firmly believed the answer was yes, citing emergent thinking, new studies and growing data that suggested “good DNA” could be used to replace defective DNA in people with inherited conditions.

“In our view,” they wrote, “gene therapy may ameliorate some human genetic diseases in the future. For this reason, we believe that research directed at the development of techniques for gene therapy should continue.”

Though Friedmann said initial response to the paper was “not overwhelming,” it’s now commonly cited as a major milestone in the scientific beginnings of gene therapy research, though Friedmann said it was the Asilomar conference three years later (scientists set safety standards for recombinant DNA technology) where interest really “exploded.”

The idea of gene therapy, which quickly captured the public imagination, was fueled by its appealingly straightforward approach and what Friedmann has described as “obvious correctness”: Disarm a potentially pathogenic virus to make it benign. Stuff these viral particles with normal DNA. Then inject them into patients carrying abnormal genes, where they will deliver their therapeutic cargoes inside the defective target cells. In theory, the good DNA replaces or corrects the abnormal function of the defective genes, rendering previously impaired cells whole, normal and healthy. End of disease.”

Nice theory, what could possibly go wrong? The article continues-

“In 1968, Friedmann, working at the National Institutes of Health in Bethesda, Maryland with the late Jay Seegmiller (a founding faculty member of the School of Medicine) and others, showed that by adding foreign DNA to cultured cells from patients with Lesch-Nyhan syndrome, they could correct genetic defects that caused the rare but devastating neurological disorder. The condition was first described by William Nyhan, MD, a UC San Diego professor of pediatrics, and medical student Michael Lesch in 1964.

The feat was a powerful proof-of-concept, but subsequent efforts to advance the work to human clinical trials stalled. “We began to realize that it would be very complicated to take this idea and make it work in people,” Friedmann said, who joined the School of Medicine faculty in 1969.

In 1990, a 4-year-old girl with a congenital disease called adenoside deaminase (ADA) deficiency, which severely affects immunity and the ability to fight infections, became the first patient treated by gene therapy. White blood cells were taken from her, the normal ADA gene was inserted into them using an engineered and disabled virus and the cells re-injected. Despite initial claims of success, Friedmann said the experiment was eventually deemed a failure. The girl’s condition was not cured, and the research was found wanting.

A report commissioned by National Institutes of Health director Harold Varmus, MD, was highly critical of the entire gene therapy field and the ADA effort in particular, chiding investigators for creating a “mistaken and widespread perception of success.” Friedmann says he took the Varmus report “personally. I felt awful. It almost made me feel like I had been deceiving myself and my colleagues for more than two decades about the promise of gene therapy.” But he also knew there were “many more good people doing gene therapy research than rogues” and continued diligently and conscientiously to pursue his own research.

Nonetheless, media attention and hype about gene therapy continued to be rampant, fueled in part by over-enthusiastic opinions by some scientists. Things crashed in 1999 when an 18-year-old patient named Jesse Gelsinger, who suffered from a genetic disease of the liver, died during a clinical trial at the University of Pennsylvania. Gelsinger’s death was the first directly attributed to gene therapy. Subsequent investigations revealed numerous problems in the experimental design.”

The history of the Varmus report provides an early glimpse of the way things work at NIH and the US HHS. The Scientist appointed to head up the commission to review the science of “Gene Therapy” was none other than my graduate mentor Dr. Inder Verma, who had long been one of the leading proponents of gene therapy, and was subsequently forced to resign from the Salk Institute over a decades long record of what might most gently be called ethical lapses. But this was the scientist appointed by the overall Director of the NIH to “independently” investigate the scientific rigor and merits of the field. One hand washes the other.

What is awry with the original “gene therapy” concept? There are multiple issues, and here are a few-

1) Can you efficiently get genetic material (“polynucleotides”) into the nucleus of the majority of cells in the human body so that any genetic defects (or transhuman genetic improvements) can be made? In short, no. Human cells (and the immune system) have evolved many, many different mechanisms to resist modification by external polynucleotides. Otherwise we would already be overrun by various forms of parasitic DNA and RNA- viral and otherwise. This remains a major technical barrier, one which the “transhumanists” continue to overlook in their enthusiastic but naïve rush to play god with the human species. What are polynucleotides? Basically, the long chain polymers composed of four nucleotide bases (ATGC in the case of DNA, AUGC in the case of RNA) which carry all genetic information (that we know of) across time.

2) What about the immune system? Well, this was one of my breakthroughs way back in the late 1980s. What Ted (Friedman) originally envisioned was the simple idea that if a child had a genetic birth defect causing the body to produce a defective or not produce a critical protein (such as Lesch-Nyhan syndrome or Adenosine Deaminase Deficiency), this could be simply corrected by providing the “good gene” to complement the defect. What was not appreciated was that the immune systems of these children were “educated” during development to either recognize the “bad protein” as normal/self, or to not recognize the absent protein as normal/self. So, introduction of the “go od gene” into a person’s body would cause production of what was essentially a “foreign protein”, resulting in immunologic attack and killing of the cells which now have the ‘good gene”.

3) What happens when things go wrong and the “good gene/protein” is toxic? Well, in the current vaccine situation this is essentially the “Spike protein” problem. I get asked all the time “what can I do to eliminate the RNA vaccines from my body”, to which I have to answer – nothing. There is no technology that I know of which can eliminate these synthetic “mRNA-like” molecules from your body. The same is true for any of the many “gene therapy” methods currently being used. You just have to hope that your immune system will attack the cells that have taken up the polynucleotides and degrade (chew up) the offending large molecule that causes your cells to manufacture the toxic protein. Since virtually all current “gene therapy” methods are inefficient, and essentially deliver the genetic material randomly to a small subset of cells, there is no practical way to surgically remove the scattered, relatively rare transgenic cells. Clearance of genetically modified cells by the cellular immune system (T cells) is the only currently viable method to remove cells that have taken up the foreign genetic information (“transfection” in the case of mRNA or DNA, or “transduction” in the case of a viral vectored gene).

4) What happens if the “good gene” lands in a “bad place” in your genome? It turns out that the structure of our genome is highly evolved, and we are still relative neophytes in our current level of understanding. Despite having sequenced the human genome. The method of “insertional mutagenesis” (sticking genetic information in the form of viral DNA or other ways) has long been one of the leading methods to generate new insights into genetics – from fruit flies to frogs to fish to mice. When new DNA is inserted into chromosomes it can cause many unexpected things to happen. Like development of cancers, for example. This is why there is so much concern about the possibility that the mRNA-like polynucleotides used in the “RNA vaccines” may travel into the nucleus (where the DNA chromosomes reside) and insert or recombine with a cellular genome after reverse transcription (RNA-> DNA). Normally, with DNA-based gene therapy technologies, the FDA requires genotoxicity studies for this reason, but the FDA did not treat the “mRNA vaccine” technology as a gene therapy product.

Based on these risk considerations, the original idea behind using mRNA as a drug (for genetic therapeutic or vaccine purposes) was that mRNA is typically degraded quite rapidly once manufactured or released into a cell. mRNA stability is regulated by a number of genetic elements including the length of the “poly A tail”, but typically ranges from ½ to a couple of hours. Therefore, if natural or synthetic mRNA which is degraded by the usual enzymes is introduced into your body, it should only last for a very short time. And this has been the answer which Pfizer, BioNTech and Moderna have provided to physicians when asked “how long does the injected mRNA last after injection”.

But now we know that the “mRNA” from the Pfizer/BioNTech and Moderna vaccines which incorporates the synthetic nucleotide pseudouridine can persist in lymph nodes for at least 60 days after injection. This is not natural, and this is not really mRNA. These molecules have genetic elements similar to those of natural mRNA, but they are clearly far more resistant to the enzymes which normally degrade natural mRNA, seem to be capable of producing high levels of protein for extended periods, and seem to evade normal immunologic mechanisms for eliminating cells which produce foreign proteins which are not normally observed in the body.

Key findings from this seminal work by Katharina Röltgen et al include the following:

Regarding pseudouridine and mRNA

What is pseudouridine (shorthand symbol Ψ)? Pseudouridine is a modified nucleotide mRNA subunit that is prevalent in natural human mRNAs, and the biologic significance and regulation of the modification process is still being determined and understood. This modification occurs naturally in the cells of our body, in a highly regulated manner. This is in sharp contrast to the random incorporation of synthetic pseudouridine which occurs with the manufacturing process used for producing the Moderna and Pfizer/BioNTech (but not CureVac) COVID-19 “mRNA” vaccines. The “state of the art” of understanding of the biology of natural pseudouridine modifications is summarized circa late 2020 in this excellent review published in the journal Annual Review of Genetics by Erin K Borchardt et al. The open source version (not paywall protected) can be found here. Hang on, because we are about to dive into some serious immunology, molecular and cell biology.

Abstract as follows:

“Recent advances in pseudouridine detection reveal a complex pseudouridine landscape that includes messenger RNA and diverse classes of noncoding RNA in human cells. The known molecular functions of pseudouridine, which include stabilizing RNA conformations and destabilizing interactions with varied RNA-binding proteins, suggest that RNA pseudouridylation could have widespread effects on RNA metabolism and gene expression. Here, we emphasize how much remains to be learned about the RNA targets of human pseudouridine synthases, their basis for recognizing distinct RNA sequences, and the mechanisms responsible for regulated RNA pseudouridylation. We also examine the roles of noncoding RNA pseudouridylation in splicing and translation and point out the potential effects of mRNA pseudouridylation on protein production, including in the context of therapeutic mRNAs.”

A more recent (peer reviewed) publication in the journal Molecular Cell has shed light on some of the mechanisms of action associated with natural pseudouridine modification. It appears that, in the natural context, various highly regulated cellular enzymes (for example PUS1, PUS7, and RPUSD4) act on specific mRNAs and specific locations within those mRNAs while they are being made in the cell to modify the normal uridine nucleotide subunit to form pseudouridine. These modifications occur at locations associated with alternatively spliced RNA regions, are enriched near splice sites, and overlap with hundreds of binding sites for RNA-binding proteins. Latest data indicate that pre-mRNA pseudouridylation is used by human cells to regulate human gene expression via alternative pre-mRNA processing.

Relevant to the “mRNA” vaccines, the Borchardt review makes the following surprising statement, which is consistent with the Cell paper cited above which demonstrates that the synthetic “mRNA” being used for these vaccines persists in patient lymph node tissue for 60 days or longer-

“An exciting possibility is that regulated mRNA pseudouridylation controls mRNA metabolism in response to changing cellular conditions.”

That is a technically precise way of saying that incorporation of pseudouridine is one factor that controls how long an mRNA stays around in your body.

The review proceeds with the following alarming (from the context of the unregulated incorporation of Ψ into the molecules used for vaccine purposes) statement:

“The biological effects of Ψ must originate in chemical differences between U and Ψ, which primarily affect RNA backbone conformation and the stability of base pairs. Because Ψ can form stable pairs with G, C and U in addition to A, it has been proposed as a “universal” base pairing partner. Despite intensive study of the structural effects of Ψ on short, synthetic RNA oligos, it is currently impossible to predict the structural outcome of site-specific RNA pseudouridylation in longer RNAs. The systematic investigation of sequence-context effects on the stability of Ψ-containing duplexes is an important step towards accurate predictions. It will be important to determine the structural consequences of RNA pseudouridylation in cells, which is possible using improved methods to probe RNA structure in vivo.”

Furthermore,

“The effect of Ψ on the yield of functional protein depends strongly on the specific codons used. The mechanisms underlying this sequence dependence are unknown, highlighting how much remains to be understood about the translational consequences of mRNA pseudouridylation in cells.”

Finally, relevant to the immunosuppression being observed after multiple mRNA vaccine boosters (which is increasingly referred to as an acquired immunodeficiency syndrome or AIDS disease), Borchardt et al teach the following:

“Innate Immunity

Cells are equipped with innate immune sensors, including various Toll-like receptors (TLRs), retinoic acid inducible protein (RIG-I), and protein kinase R (PKR), which detect foreign nucleic acid. RNA modifications have been thought to provide a mechanism for discerning “self” RNA from non-self RNA, and indeed, incorporating RNA modifications, including pseudouridine, in foreign RNA allows for escape from innate immune detection. This makes RNA modification a powerful tool in the field of RNA therapeutics where RNAs must make it into cells without triggering an immune response, and remain stable long enough to achieve therapeutic goals. In addition, the presence of modified nucleosides in viral genomic RNA could contribute to immune evasion during infection.

TLRs Toll-Like Receptors (TLRs) are membrane-associated proteins which detect various pathogen associated molecular patterns (PAMPS) and subsequently stimulate production of proinflammatory cytokines. The RNA-sensing TLRs, TLR3, TLR7 and TLR8 reside within endosomal membranes. TLR3 recognizes dsRNA, while TLR7 and TLR8 recognize ssRNA. Upon target recognition, TLRs activate a signaling cascade that results in the expression of proinflammatory cytokines and interferon. In vitro transcribed RNA is immunostimulatory when transfected into HEK293 cells engineered to express either TLRs and inclusion of Ψ in the RNA suppressed this response (most pronounced for TLR7 and TLR8).

RIG-I Retinoic Acid Inducible Protein (RIG-I) is a cytosolic innate immune sensor responsible for detecting short stretches of dsRNA or ssRNA with either a 5′-triphosphate or 5′-disphosphate group (a feature common to various RNA viruses). Activation of RIG-I relieves its autoinhibition, releasing its CARD domains to interact with MAVS and set off a signaling cascade that ultimately results in expression of immune factors. Inclusion of Ψ in a 5′-triphosphate capped RNA abolishes activation of RIG-I, providing another mechanism for pseudouridine-mediated suppression of innate immune activation. Further, the polyU/UC region of the HCV genome is also potent activator of RIG-I and complete replacement of U with Ψ in this RNA fully abrogates downstream IFN-beta induction, despite RIG-I still binding to the modified RNA, but with reduced affinity. Durbin et al present biochemical evidence that RIG-I bound to pseudouridylated polyU/UC RNA fails to undergo the conformational changes necessary to activate downstream signaling.

PKR RNA-dependent Protein Kinase (PKR) is a cytosolic resident innate immune sensor. Upon detection of foreign RNA, PKR represses translation through phosphorylation of translation initiation factor eIF-2alpha. Molecules which activate PKR are varied, but include dsRNA formed intra- or inter-molecularly, and 5′ triphosphate groups. Inclusion of Ψ in various PKR substrates reduces PKR activation and downstream translation repression relative to unmodified RNAs. For example, a short 47-nt ssRNA potently activates PKR when synthesized with U but not with Ψ (~30-fold reduction with Ψ). Ψ also modestly reduced PKR activity when this short RNA was annealed to a complementary unmodified RNA 170. Likewise, in vitro transcribed, unmodified tRNA acted as much more potent activator of PKR than tRNAs transcribed with pseudouridine. It should be noted that it is unclear whether a fully pseudouridylated tRNA adopts canonical folding and what impact this may have on PKR recognition of this substrate. Finally, transfection of an unmodified mRNA caused a greater reduction in overall cellular protein synthesis in cell culture compared to the same mRNA fully pseudouridylated. Consistent with this result, fully pseudouridylated mRNA reduced PKR activation and subsequent phosphorylation of eIF-2alpha.”

Regarding the consequences for the use of mRNA as a drug for therapeutic or vaccine purposes, Borchardt et al conclude that

“Pseudouridine likely affects multiple facets of mRNA function, including reduced immune stimulation by several mechanisms, prolonged half-life of pseudouridine-containing RNA, as well as potentially deleterious effects of Ψ on translation fidelity and efficiency.”

Conclusion

Based on this information, it appears to me that the extensive random incorporation of pseudouridine into the synthetic mRNA-like molecules used for the Pfizer/BioNTech and Moderna SARS-CoV-2 vaccines may well account for much or all of the observed immunosuppression, DNA virus reactivation, and remarkable persistence of the synthetic “mRNA” molecules observed in lymph node biopsy tissues by Katharina Röltgen et al. Many of these adverse effects were reported by Kariko, Weissman et al in their 2008 paper “Incorporation of pseudouridine into mRNA yields superior nonimmunogenic vector with increased translational capacity and biological stability” and could have been anticipated by regulatory and toxicology professionals if they had bothered to consider these findings prior to allowing emergency use authorization and widespread (global) deployment of what is truly an immature and previously untested technology. Therefore, neither the FDA, NIH, CDC, nor BioNTech (which employs Dr. Kariko as a Vice President) nor Moderna can claim true ignorance. To my eyes, what we have seen is more appropriately classified as “willful ignorance”.

In conclusion, based on these data it is my opinion that the random and uncontrolled insertion of pseudouridine into the manufactured “mRNA”-like molecules administered to so many of us creates a population of polymers which may resemble natural mRNA, but which have a variety of properties which distinguish them in a variety of aspects which are clinically relevant. These characteristics and activities may account for many of the unusual effects, unusual stability, and striking adverse events associated with this new class of vaccines. These molecules are not natural mRNA, and they do not behave like natural mRNA.

The question that most troubles and perplexes me at this point is why the biological consequences of these modifications and associated clinical adverse effects were not thoroughly investigated before widespread administration of random pseudouridine-incorporating “mRNA”-like molecules to a global population. Biology, and particularly molecular biology, is highly complex and matrix-interrelated. Change one thing over here, and it is really hard to predict what might happen over there. That is why one must do rigorously controlled non-clinical and clinical research. Once again, it appears to me that the hubris of “elite” high status scientists, physicians and governmental “public health” bureaucrats has overcome common sense, well established regulatory norms have been disregarded, and patients have unnecessarily suffered as a consequence.

When will we ever learn.