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.

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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).

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…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.

Read More ...

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.

• The Problem with Gene-Based Injections | Academia Catches Up
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• How The WHO Captured Your Constitution.
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• Roche Pharma | The Tamiflu Fraud
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• Trojan Horse | The Problem with Gene-based Injections - Part 2
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• First Principles | The Problem with Gene-based Injections - Part 1
  The cellular environment is incredibly complex and dynamic. To understand the concerns with gene-based injections, we need to go back to basics.

• International Grand Jury | Day 3: The PCR Test
  An international grand jury investigating crimes against humanity has kicked off.

• International Grand Jury | Day 2: Historical Background
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• Lessons from History | 3. Pellagra & Misinformation
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• Geert Vanden Bossche was mocked as an anti-vaxxer. But, were his predictions accurate?
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• Lessons from History | 1. The 15-Year S.M.O.N. Epidemic of Japan
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• Community-Acquired Pneumonia: What to Know, and Why it Matters
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• Mass Formation Psychosis - Theory, Implications & Jon Stewart
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• Pandemic Hydra: Paralyzed by Fear or Confusion?
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• Where Have All The Experts Gone?
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• WTF Happened to Influenza in 2020-2021?
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• How We Got Here Part 2: Medical Tower of Babel
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• How We Got Here.
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Introduction

This one is BIG (roughly 7000 words, 50 minute read) and is probably my most important post to date. I have been collecting information for this post for over a year. When you are done reading it, I need your help to share it.

Herein I pull together the totality of scientific evidence to date — as well as other clues of which I am aware — that demonstrate the covid vaccines to be reproductively toxic, and that this effect may well be intentional.

One does not need to prove these hypotheses beyond a shadow of a doubt in order to act on them personally. We are equipped by nature to make observations and act on our intuition. Personally, I’ve always trusted mine as it has generally served me well in life. There are many things we cannot prove without a shadow of a doubt using randomized double-blind clinical trials. Yet we do (or don’t do them) anyway.

This is generally how hypothesis formation starts and sometimes it is impossible to move beyond hypotheses while data are still being gathered. I suspect the adversaries of humanity are hoping we’ll move forward with their plan for us, while they stonewall exactly the sort of data gathering we desire.

To offer you an outline for this essay at the outset:

How the New Normal Set a Precedent for Unparalleled Restrictions Since WWII

• Denial of Early Treatment Drugs
• Vaccine Passports/Digital ID
• Narrative Control and Censorship
• The Extreme Breadth and Length of Covid Vaccination Campaigns Were Pre-Planned

Population Control: a Motive for Vaccination Beyond Digital ID and CBDCs

• Popular Sentiments of Professionals
• Institutional Players
• Medical Literature and History of Anti-Fertility Vaccination
• Vaccination Against Placental Proteins
• Vaccination Against Fertility Hormones

Covid Vaccines: Anti-Fertility Bioweapons?

• Vaccination Against Syncitin Through Vaccination Against Spike Protein
• Toxic LNP Delivery Systems
• Other Toxic Components
• Covertly Added Mutant Aromatase Gene

Evidence for Reproductive Toxicity

• Re-Analysis of 2021 NEJM Analysis of V Safe Data

• DMED data

• Independent Physician Reports

• Funeral Director Reports

• Public Comments on CDC Analysis of V Safe Data

• VAERS Data

• Public Comments on Female Reproductive Problems

Discussion

• Thoughts of Christopher Langan, The World’s Smartest Man
• Insights from 20 Year-Old Science Fiction: The Aschen Agenda

Conclusion

Grab a drink and join me for the first section (a brief tour of the past two years) so I can set the stage for what may be a much more insidious agenda than you ever imagined, and the elites’ potential endgame(s).

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How the New Normal Set a Precedent for Unparalleled Restrictions Since WWII

• misuse of PCR tests
• misuse of masks
• exaggerations about the importance of asymptomatic spread
• misconceptions about the importance of lockdowns
• a level of censorship more suited to China than a liberal democracy
• denial of early treatment drugs
• religious dogma that the gene-based covid injections are safe and effective
• lies that vaccine passports increase safety

I want to focus on the latter half of that list.

Denial of Early Treatment Drugs

This was the major tipoff to me in 2020 that something was wrong. It was never actually required to prove that early treatment drugs work: the two primary drugs which shall not be named are among the safest and most common drugs in world history, with decades of safe use and billions of doses.

On that basis alone, there was therefore no reason to deny these drugs to patients during an emergency and a pandemic, even if they were useless. Off-label drug prescriptions are common and legal in the US, a country awash with and addicted to pharmaceuticals!

Those two drugs were relentlessly demonized as not just useless, but dangerous. It was a flat-out lie that demonstrated to me an underhanded motive. In late 2020, I thought this ulterior motive was just about obscene profits, since I’d already witnessed similar underhandedness for decades in the cancer treatment industry. It was not until early 2021 during the vaccine rollout that I began to be much more disturbed.

Vaccine Passports/Digital ID

That governments and mass media around the world have continued with propagandistic techniques about the vaccines for so long is another huge red flag. The denial of early treatment set the stage for vaccine dogma. The population was brainwashed to believe that vaccines were our only way out of the pandemic.

While there has been some letup in the northern hemisphere on this dogma in recent weeks, the grip is much stronger down under, where people must still show a vaccine pass everywhere to have access to a basic life, i.e. to go anywhere except a grocery store and often required to work, rent a place to live, or even get a haircut (such as in New Zealand). Australia and Canada are similarly draconian. These countries are the testing grounds for World Economic Forum (WEF) digital tyranny.

Last year it was thought by “conspiracy theorists” that the vaccine passports (or digital Health ID) would lead to more sweeping Digital ID, which would then lead to the installment of central bank digital currencies (so-called programmable money that operates like a voucher instead of money), the elimination of cash, and so on.

CBDCs and the elimination of cash would give central planners unprecedented levels of control over the amount and type of resources a population is allowed to consume. They would operate like vouchers rather than money. They would expire after a certain time and only be useful on certain categories of items. In this way, political authorities will be able to control every aspect about your life: what you consume, and where you go.

For a glimpse into how these will work, the Ukraine government announced emergency payments to those impacted by war. But only if you are vaccinated… and only through the digital system.

This is how the other shoe of “covid” could drop. You’ll get CBDCs (food stamps, vouchers for other things) but only if you have a vaccine pass.

Note that this process of digital IDs and central bank digital currencies is most accelerated in New Zealand, Canada, and Australia – three countries where uptake of vaccines has been quite high by a trusting and compliant population.

Here’s New Zealand’s Ministry of Health “digital ID” page. Note the interesting color choices since the onset of the Ukraine conflict.

And listen to this nice message with tinkly music from the Canadian Bankers Association referencing the World Economic Forum, regarding the rollout of CBDCs.

[Chicken Gate 🇨🇦 @ChickenGate

A message from the Canadian Bankers Assoc referencing the World Economic Forum. The state wants to own you in the name of convenience.](https://twitter.com/ChickenGate/status/1496272056178159619)

February 22nd 2022
2,177 Retweets2,978 Likes

Prior to the covid era, virtually no one except the most ardent Marxist would go willingly into a food stamp-like system for virtually everything they consume. Nobody.

The government response to Covid-19 conditioned people to have their movement and rights dramatically restricted to levels not seen since WWII.

These wartime-like restrictions — and indeed, the almost seamless transition to actual war propaganda in the Ukraine crisis, which is sucking yet more people into the mass psychosis, some of whom were not taken in by covid hysteria — may be sufficient to usher in a complete transformation of the banking system. If you want a conspiracy theory about how subliminal messaging is being used for this purpose, the Good Citizen has an interesting piece.

Narrative Control and Censorship

Since early 2020, information control has become very important, and, as Glenn Greenwald has just written, we are already seeing that it will get much worse in a traditional land war.

First, there was the relentless lying and use of psychological operations to frighten and subdue the population. The British government even acknowledged their own use of such tactics.

Inquiring journalists are now a nearly extinct species. Mass media reads like blatant propaganda. Jingoism is everywhere and the Ukraine crisis has made that even more apparent than ever, especially for those of us without central lines installed like port-a-caths to infuse a constant drip of BBC, CNN, etc. for hours each day.

Then there is the relentless demonization, canceling, and deactivation of anyone on social medial platforms who is pointing out the absurdities.

Fact-checking labels on social media posts and YouTube in 2020 escalated exponentially in 2021 to the complete digital cancellation of almost anyone who deviates from the “safe and effective” slogan.

The receptivity of the masses is very limited, their intelligence is small, but their power of forgetting is enormous. In consequence of these facts, all effective propaganda must be limited to a very few points and must harp on these in slogans until the last member of the public understands what you want him to understand by your slogan.

Adolf Hitler

The pattern is eerily consistent with previous totalitarian and authoritarian systems of the 20th century. Independent thought will not be tolerated, and you will be gaslighted by the government, the media, and a majority of your fellow citizens who cannot face their own terror, so they pretend you’re still living in a free society and the censorship you are experiencing is not censorship at all, but merely the actions of a private company acting completely independent of government instruction and protecting the public from you, a dangerous person who, from their perspective, is shouting “Fire!” in a crowded theater.

We have watched as many people we knew have become full-fledged totalitarians. Their brains have been cracked by relentless propaganda and fear-mongering and they have turned their backs on you, doing the dirty work of their own oppressors as they weave themselves into pretzels trying to justify why the greatest restrictions on human liberty since WWII are necessary over an illness that has morphed from a severe influenza in 2020 to a cold in 2022.

We also saw that “ misinformation” became a widely accepted fact when authorities wanted to steer the population in a completely different direction. At first, in 2020, “conspiracy theories” took about 6 months to turn into facts. In 2022, they turn into facts in less than 24 hours.

Because the population has become a super-organism with a hive mind that can be directed at will, be prepared that when the science “changes” again (for instance, in autumn 2022), the public will accept new “covid” or “flu” or “climate” restrictions unquestioningly as part of the “New Normal” especially if they are somehow tied to nationalistic propaganda campaigns in the new Ukraine crisis.

This is why few people questioned obviously alarming things, such as pregnant women receiving the vaccines without having studied them in pregnant women, let alone studying them in a Phase III trial.

Or the vaccine being pushed onto ever younger age groups to protect the elderly, even though the risks to children from covid-19 are vanishingly small.

And this is now why many still don’t question the need for endless booster shots, not just for the elderly, but for every human being on earth.

James Hill, MD, has a comprehensive 43 point list of other contradictions and tip-offs.

The drive on the part of pharmaceutical companies and governments to suppress information about the vaccines was relentless. I particularly liked this short video by Nick Hudson, released in November 2021, chairman of PANDA: What is the FDA Hiding?

And now with the initial release of Pfizer documents as forced by the judicial system, we are beginning to learn just a small part of what the FDA has been hiding.

Big Pharma is a cutthroat industry depending on constant rollouts of blockbuster drugs, but I do not believe that even they would ordinarily take the risk of rolling out a brand new technology on a global population (when it has only completed Phase II trials), unless it were under duress.

It’s hard not to see the potential for a conspiracy here.

I suspect that the powers that be have ordered these CEOs — and governments and regulatory agencies, for that matter — to deliver. Or else.

Others disagree, of course. They think covid-19 is a serious enough disease to warrant rapid rollouts of insufficiently tested novel technology on the entire global population – not just one or twice, but multiple times. Of course, a similar but slightly less hysterical situation has existed for many years with influenza vaccines, especially in the United States, so this fact alone is insufficient to demonstrate ulterior motives beyond profit-seeking that is driven by regulatory incentives surrounding their manufacture.

This is not entirely unprecedented as influenza vaccines don’t work either, but 50% of the US population rolls up their sleeves for one each year.

The difference between covid and influenza vaccines is that the former are associated with unprecedented levels of adverse events that are being systematically suppressed by governments, legacy media, and Big Tech. (If you have been living under a rock for a year and you want to delve into it, check Drs. Robert Malone and Jessica Rose, Mathew Crawford, Steve Kirsch, eugyppius, and bad cattitude.)

And it’s certainly all consistent with hushing those in the insurance industry that would ordinarily be able to hold abusive corporations and negligent policymakers to account in a court of law. A board member of a large German insurance company blew the whistle on covid vaccines, and was suspended from the board.

Authorities continue to insist on their necessity, so messengers like that will continue to be shot on sight.

Those lower down in the hierarchy are likely brainwashed. Don’t underestimate the power of a couple of decades working for WHO to accomplish this: the field of public health already self-selects for personalities with controlling, Good Nazi tendencies.

Many other healthcare workers who are not so bullish on the covid vaccines have been threatened. Loss of employment is generally censure enough in itself, as we’ve often seen with vaccine mandates. Most people don’t have the independent wealth to break free from their employer in the face of such a massive onslaught of propaganda.

So, the presence of a conspiracy does not require large numbers of people to be “in on the plan” any more than hundreds of thousands of NSA workers and private contractors were “in on the plan.” They were doing what they were told, and they were told that it was essential for public health national security. That only a few like Bill Binney or Edward Snowden arise out of such a morass to blow whistles should surprise no one.

The Breadth and Length of Covid Vaccination Campaigns Were Pre-Planned

Let’s turn now to the frequency and amount of covid-19 injections planned. Germany backs covid vaccines for another 7 years and purchases enough vaccine to last until 2029.

The injections are very important to authorities and, as we have just learned with the announcement of potential approval of a fourth dose in the US, continue to occupy a central role in the drama. This is despite the fact that many scientists (including even Fauci and Hotez — plausible deniability perhaps? or just grooming the public for patience?) doubted quite early on that the vaccines would work.

While the most apocalyptic of the predictions regarding Antibody Dependent Enhancement (ADE) did not come true, the vaccines very obviously do not stop spread and there is some reason to believe that they are causing antigenic fixation (see Dr. Geert Vanden Bossche). So in a sane world, no one would continue to use coercion to get people vaccinated. They would leave it as a private choice, as it is with influenza vaccines.

Yet coercion continues in the worst jurisdictions, and mandates have probably only temporarily dropped in many places, and may return in autumn, particularly in exchange for your new vouchers for existence (CBDCs), the 2022 version of wartime food stamps.

I’ve pointed out the apparent uniformity of this vaccination scheme in western countries in a previous post, but it bears repeating here.

Listen to the zeal with which Kerry Chant, Chief Public Health Office of New South Wales, Australia, talks in August 2021 about cycles of vaccination, re-vaccination, and the purchase of “large doses of vaccine” into 2022 (1.3 minutes):

In a similar vein, here’s Justin Trudeau, in July 2021, discussing booster shots. Canada has purchased 30 million doses of Pfizer alone in 2022 and 2023, with 60 million in 2024. At a population of roughly 38 million, this means very broad coverage of the eligible population four more times after 2021. (less than 1 minute)

Here’s Jacinda Ardern, New Zealand’s PM, admitting there will be no endpoint to the covid vaccination program:

How did they know how well the shots would work back then? They didn’t.

And finally, here’s Sajid Javid, UK Health Minister, discussing the reduced interval between shots as a minimum of 3 months rather than 6 months. A similar policy is now in place in New Zealand.

I highly recommend listening to these short videos for the general body language and tone. If you can listen to them without getting the heebie jeebies, you are made of stronger stuff than I.

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Population Control: a Motive for Vaccination Beyond Digital ID and CBDCs

So, what might be some additional motivations for endless injections every three to six months, for at least several billion people in the western world, that may have nothing to do with covid or Digital ID?

Put on your tinfoil hat, or… just use some common sense and think like a control freak or a villain would.

There are massive unfunded liabilities in the welfare and pension systems due to an aging population and the theft of personal wealth from the 2008 financial crisis. For another, a higher use of fossil fuels per capita than in the developing world.

None of this is a secret. It’s just that people do not want to consider that authorities would take draconian steps to limit human population, even though it’s been talked about openly in the past.

Popular Sentiments of Professionals

Consider the following sentiments which have been echoed for 5 decades now by highly educated westerners.

"A cancer is an uncontrolled multiplication of cells, the population explosion is an uncontrolled multiplication of people. We must shift our efforts from the treatment of the symptoms to the cutting out of the cancer. The operation will demand many apparently brutal and heartless decisions."

Prof. Paul Ehrlich, The Population Bomb, 1968

"A reasonable estimate for an industrialized world society at the present North American material standard of living would be 1 billion. At the more frugal European standard of living, 2 to 3 billion would be possible."

United Nations, Global Biodiversity Assessment

"Current lifestyles and consumption patterns of the affluent middle class involving high meat intake, use of fossil fuels, appliances, air-conditioning, and suburban housing are not sustainable."

Maurice Strong, Rio Earth Summit, 1992

“If I were reincarnated I would wish to be returned to Earth as a killer virus to lower human population levels.”

Prince Philip

“There are too many people, that’s why we have global warming. We have global warming because too many people are using too much stuff.”

Ted Turner, billionaire, founder of CNN, major UN donor (and large CO2 producer)

Institutional Players

In 1995 (a reminder for those of us who feel as if it’s yesterday that this is over 25 years ago!), a peer reviewed paper entitled “Immunization to regulate fertility: biological and cultural frameworks” was published in Social Science and Medicine. An excerpt of the abstract reads (my emphasis added):

"Many scholars and government officials subscribe to the following logic: the global environmental crisis is due to over-population which necessitates population control programs; thus pregnancy can be considered a disease subject to state control. But pregnancy is not a disease nor is over-population the single major cause of environmental degradation. However, as governments grapple with the economic, social, and ecological consequences of population growth, draconian measures to control fertility will be ever more tempting.”

The urge of elites and central planners to control human reproduction pre-dates publication by a half century at least and has multiple drivers. It began in eugenicist institutional and governmental programs in the 1920s. Eugenics was discredited and forced underground for awhile after the Nazi atrocities, but it resurfaced under new auspices with John D. Rockefeller III who “organized the Population Council in 1953, predicting a “Malthusian crisis” in the developing world and financing extensive experiments in population control.”

As for the more recent involvement of wealthy individuals in population control, Bobby Rajesh Malhotra tackles the legacy of the Bill and Melinda Gates Foundation in a dryly humorous and artistic way. For those who want to read more, I also recommend Andreas Oehler’s article Going for the Jugular Take 2 — All Ducks in a Row.

Medical Literature and History of Anti-Fertility Vaccination

Vaccination Against Placental Proteins

As most are aware, the Bill and Melinda Gates Foundation (BMGF) is inextricably linked with World Health Organization (WHO) efforts. What may be less well known is that since the 1970s, the WHO has had a Task Force on Fertility Regulation -- i.e. development of birth control vaccines targeting either gametes or developing embryos:

From the same publication above, another screencap:

Hold the thought of vaccination against placental antigens in your mind for now. We’ll come back to it later.

Vaccination Against Fertility Hormones

While research into anti-fertility vaccines is longstanding, in 2017 there was a new revelation. A peer-reviewed paper was published that detailed the highly unethical vaccination of Kenyan women in the early 1990s on the false pretext of protecting them from tetanus, while actually aiming to sterilize them.

This paper is entitled HCG Found in WHO Tetanus Vaccine in Kenya Raises Concern in the Developing World and the abstract reads, in part, as follows (my emphasis added):

"In 1993, WHO announced a “birth-control vaccine” for “family planning”. Published research shows that by 1976 WHO researchers had conjugated tetanus toxoid (TT) with human chorionic gonadotropin (hCG) producing a “birth-control” vaccine. Conjugating TT with hCG causes pregnancy hormones to be attacked by the immune system. Expected results are abortions in females already pregnant and/or infertility in recipients not yet impregnated. Repeated inoculations prolong infertility. Currently WHO researchers are working on more potent anti-fertility vaccines using recombinant DNA. WHO publications show a long-range purpose to reduce population growth in unstable “less developed countries”. By November 1993 Catholic publications appeared saying an abortifacient vaccine was being used as a tetanus prophylactic. In November 2014, the Catholic Church asserted that such a program was underway in Kenya. Three independent Nairobi accredited biochemistry laboratories tested samples from vials of the WHO tetanus vaccine being used in March 2014 and found hCG where none should be present. In October 2014, 6 additional vials were obtained by Catholic doctors and were tested in 6 accredited laboratories. Again, hCG was found in half the samples. Subsequently, Nairobi’s AgriQ Quest laboratory, in two sets of analyses, again found hCG in the same vaccine vials that tested positive earlier but found no hCG in 52 samples alleged by the WHO to be vials of the vaccine used in the Kenya campaign 40 with the same identifying batch numbers as the vials that tested positive for hCG. Given that hCG was found in at least half the WHO vaccine samples known by the doctors involved in administering the vaccines to have been used in Kenya, our opinion is that the Kenya “anti-tetanus” campaign was reasonably called into question by the Kenya Catholic Doctors Association as a front for population growth reduction."

Such draconian methods are not limited to African countries:

"I recall Sanjay, son of Indian PM Indira Gandhi, awarding villagers transistor radios in exchange for undergoing sterilisation in the mid 1970s. He combined a state of emergency, eugenics, sterilisation passports, and radio news propaganda in the same fell swoop. Sound familiar? India was and remains the elite’s testing ground.”

We have now established completely unethical means of attempted sterilization through vaccination on false pretenses in developing countries, sponsored and developed by WHO. And this is not a very recent development.

Many in the “developed” western world, in all its naiveté, probably assumed that such techniques would never be deployed inward.

Covid Vaccines: Anti-Fertility Bioweapons?

Vaccination Against Syncytin Through Vaccination Against Spike Protein

Let’s return to the concept of vaccination against placental proteins. Note that vaccination against the placental protein of syncitin was the mechanism that was proposed by Drs. Mike Yeadon and Wolfgang Wodarg when, on December 1, 2020, they wrote to the European Medicines Agency, firmly demanding that they delay their emergency approval of covid vaccines. You can find a copy of that petition at this link.

Their concerns included inadequate safety testing of new technology agents and the pretense that there was an emergency warranting ‘emergency use authorisation’. They pointed out the risk of acute allergic reactions which might be life-threatening (which were, in fact, observed on the first day of public dosing) and potential impacts on fertility, because of the weak, but very clear similarity of coronavirus spike protein & syncytin-1, the latter of which is an essential protein to human fertility.

Other letters warning against blood clots were subsequently written and may be found at this link.

In a study of 15 females that were vaccinated with the Pfizer / BioNTech vaccine, antibodies to syncytin-1 were detected very early in every single female. The authors said it was below a threshold of concern, but there is no way to know what that threshold is, because it’s not been studied.

Dr. Mike Yeadon discussed this problem at some length here.

And this is an interesting and similar summary of concerns, written by a PhD in immunology in December 2020.

American scientists also voiced these concerns in early 2021. Here is a public comment from Dr. Janci Chunn Lindsay at an ACIP (CDC) meeting on April 23, 2021.

"Hi, my name is Dr Janci Chunn Lindsay. I hold a doctorate in biochemistry and molecular biology from the University of Texas and have over 30 years of scientific experience primarily in toxicology and mechanistic biology.

"In the mid 1990s, I aided in the development of a temporary human contraceptive vaccine, which ended up causing unintended autoimmune ovarian destruction and sterility in animal test models despite efforts against this and sequence analyses that did not predict this.

"I strongly feel that all the gene therapy vaccines must be halted immediately due to safety concerns on several fronts.

"First there is credible reason to believe that the GTs will cross react with ... and reproductive proteins in sperm, ova and placenta and lead to impaired fertility and reproductive outcomes.

"Respected virologist Bill Gallaher made excellent arguments as to why you would expect cross reaction due to beta sheet confirmation similarities between spike protein and SIN-1 and -2.

"I have yet to see a single immunological study which disproves this despite the fact that it would literally take the manufacturers a single day to do these ... studies to ascertain this. It's been over a year since the assertions were first made that this could occur.

"We have seen 100 pregnancy losses reported in VAERS as of April 9th and there have been reports of impaired spermatogenesis and placental findings from both a natural infection, vaccinated, and ... knock out animal models that have similar placental pathology implicating a ... mediated role in these outcomes.

"Additionally, we have heard multiple reports of menses irregularities in those vaccinated. These must be investigated. We simply cannot put these GTs in our children who are at .002 risk for COVID mortality if infected or any more of the child-bearing age population without thoroughly investigating this matter, as we could potentially sterilize an entire generation.

"Speculation that this will not occur and a few anecdotal reports of pregnancies in the new trials are not sufficient proof that this is not impacting on a population-wide scale.

"Secondly, all of the gene therapies are causing coagulopathy. This is not isolated to one manufacturer, and this is not isolated to one age group, as we are seeing coagulopathy deaths in healthy young adults with no secondary comorbidities.

"There have been 795 reports related to blood clotting disorder as of April 9th in the VAERS reporting system, 338 of these being due to thrombocytopenia. There are forward and backward mechanistic proofs for why this is happening. The natural infection is known to cause coagulopathies due to the spike proteins. All GTs direct the body to make the spike protein.

"... in September of 2020 showed that if you infuse spike protein into mice that have humanizing tumor ... and blood platelets that you also get disseminated thrombosis. Spike protein incubated with human blood in vitro also caused blood clot development which was resistant to fibrolysis. The spike protein that's causing thrombocytic events, which cannot be resolved through natural means, and all vaccines must be halted until they can be reformulated to guard against this diverse effect."

These comments of Dr. Lindsay’s are completely consistent with those of Drs. Yeadon and Wodarg. I’d also note that her comment at the end about immune escape has also been vindicated at this point, but this is beyond the scope of this essay.

Toxic LNP Delivery Systems

But there may be other mechanisms by which covid-19 vaccines contribute to infertility in both women and men, including reproductively toxic lipid nanoparticle delivery systems or the possibility for the intentional direction of LNPs to the gonads in order to deliver the mRNA payload there.

The Japanese biodistribution study amplifies this concern. Dr. Byram Bridle was the force bringing this to light last year by requesting the study from the Japanese, and the data showed that the lipid nanoparticles of the Pfizer vaccine concentrated in the ovaries. The precautionary principle requires that we assume this is happening in women administered the vaccine.

From the Japanese biodistribution study, here is the table of tissue concentrations of vaccine lipid nanoparticles after administration to mice.

This concern was also voiced in July 2021 by Doctors For Covid Ethics:

"Of particularly grave concern is the very slow elimination of the toxic cationic lipids. In persons repeatedly injected with mRNA vaccines containing these lipids— be they directed against COVID, or any other pathogen or disease—this would result in cumulative toxicity. There is a real possibility that cationic lipids will accumulate in the ovaries. The implied grave risk to female fertility demands the most urgent attention of the public and of the health authorities."

The document also states:

It is noteworthy that the level of radioactivity in the liver rises very fast within the first eight hours but then stagnates, whereas in the ovaries and the adrenal glands the rise continues even two full days after the injection. This suggests that the radioactivity may be redistributed from the liver to these glands.

As well as:

Pfizer tested its vaccine for reproductive toxicity on only one species (rats) and on only small numbers of animals (21 litters). A greater than twofold increase in pre-implantation loss of embryos was noted, with a rate of 9.77% in the vaccine group, compared to 4.09% in the control group. The EMA report merely states that the higher value was “within historical control data range” [5, p. 50]. EMA should of course have obligated Pfizer to state unambiguously whether or not the observed 14 difference was statistically significant; and if it was not, to increase sample sizes so as to ensure the required statistical power. The same criticism applies to the reported observations of “very low incidence of gastroschisis, mouth/jaw malformations, right sided aortic arch, and cervical vertebrae abnormalities.” Overall, Pfizer’s studies are inadequately described and apparently were also inadequately carried out. The observed pre-implantation loss indicates toxicity at a very early stage of development, either to the embryo or the nascent placenta. It might be caused by a high level of spike protein expression, but also by toxic lipids; and it might occur already within the ovaries, but also affect the fertilized egg or subsequent developmental stages within the Fallopian tubes or the uterus. This also applies to malformations, although these would more likely be caused by damage later on in embryonic development, suggesting transfer of toxicity across the placenta.

Both the information about syncitin as well as the LNP accumulation in animal models should clearly have caused medicines regulators to halt vaccination in women of childbearing potential early last year. But it didn’t.

Other Toxic Components

As a brief note, a toxic substance (SM-102) is also listed as a component of Moderna’s covid vaccine. A report in the EU Times details that an official OSHA safety data sheet for this substance clearly states: “For research use only, not for human or veterinary use” and indicates that it may be carcinogenic and teratogenic, and with prolonged and repeated use it attacks the respiratory functions, the central nervous system, kidneys and liver.

As discovered by a study commissioned by Tess Lawrie’s ebmcsquared, there is also the potential for graphene in the vaccines, which is known to be cytotoxic. (The potential for reproductive toxicity of graphene is beyond the scope of this article.)

Covertly Added Mutant Aromatase Gene

The information above that emerged in early 2021 becomes much more chilling in the context of a highly predictive statement by two anonymous whistleblowers from Moderna on 4chan, dated 9 Dec 2020.

According to this statement, which I transcribed and wrote about in a preliminary post here, there are alleged to be at least two extra mRNA sequences in the covid vaccines coding for mutant proteins.

First is a mutant version of aromatase, CYP19A1. The purpose of this is allegedly to diminish estrogen and therefore fertility in children of recipients of the covid vaccine by causing premature ovarian failure.

The second gene is alleged to be a mutant cyclin dependent kinase inhibitor, CDKN1B, designed to sabotage the cell cycle, thus giving rise to more cancer in the population.

Eerily, they also mention the addition of “up-regulating LINE-1” to integrate the mRNA into the genome. This is of course the opposite of what we have been told by authorities.

If this is true, the full effect of these alterations may not be fully realized yet for decades.

Although I think the integration of these sequences into the genome is likely more complex than pure recessive/dominant characteristics, depending on whether the original genes are knocked out or where the sequences integrate, these predictions by the Moderna whistleblowers are fairly precise and were made prior to covid vaccine rollouts. So, over a year later, we can make preliminary evaluations of their allegations.

How did these predictions age? Eerily well. In Lasting Legacy of Trojan Horses, Andreas Oehler writes:

• 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” (Aldén 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 Aldén 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 prossess 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.

How about cancer rates? Dr. Ryan Cole has been recording highly elevated rates of cancer in his practice and the preliminary raw data released by three whistleblower physicians from the Defense Medical Epidemiological Database on the incidence of various diseases, before and after the onset of COVID-19 vaccination of military forces, show the following [according to Robert Malone](http://* https://rwmalonemd.substack.com/p/regarding-the-defense-medical-epidemiological?s=r):

• Total Number of Malignant Neuroendocrine Tumor Reports By Year up 276%
• Total Number of Neoplasms for All Cancers By Year up 218%
• Total Number of Malignant Neoplasms for Digestive Organs By Year up 477%
• Total Number of Neoplasms for Breast Cancer By Year up 469%
• Total Number of Neoplasms for Testicular Cancer By Year up 298%

There are many anecdotal reports of rapid cancer onset or aggressive resurgence of previous cancers after covid vaccination, as well as reports in VAERS. These are beyond the scope of this piece, but are also cause for concern and point toward the potential veracity of the Moderna whistleblowers’ statements.

IMPORTANT NOTE TO RESEARCHERS: All brands of covid vaccines should be independently analyzed for the presence of the mutant aromatase and cyclin dependent kinase inhibitor mRNAs mentioned.

Evidence for Reproductive Toxicity

Review of Shimabukuro et al.’s 2021 NEJM Analysis of V Safe Data

Focusing on the reproductive aspects, there are several lines of evidence we can follow to determine what the preliminary effect on reproduction may be.

First, in a peer-reviewed paper entitled Spontaneous Abortions and Policies on COVID-19 mRNA Vaccine Use During Pregnancy, authors Aleisha Brock and Simon Thornley from New Zealand point out errors in the New England Journal of Medicine Shimabukuro et al. (2021) analysis of V Safe Registry data. By breaking out the data for pregnancies under 20 weeks, they show an alarmingly high rate of pregnancy loss in this group, 7-8 times higher than the original results and the background average, at 82%-91%.

Of the misleading conclusions in the NEJM piece by Shimabukuro et al. (20210, they note:

“The study indicates that at least 81.9% (≥ 104/127) experienced spontaneous abortion following mRNA exposure before 20 weeks, and 92.3% (96/104) of spontaneous abortions occurred before 13 weeks’ gestation (Table 4, footnotes).[4] This is a very high proportion of pregnancy loss observed in those exposed to the mRNA vaccination before 20 weeks’ gestation, ranging from 81.9–91.2% (n = 114–127), which is significantly different to baseline estimates from other studies (11.3%, n = 79,978 [6]; p < 0.001), being 7- to 8-fold higher than expected (p < 0.001). The authors’ interpretation of no difference in the observed incidence of pregnancy loss in those who received their first mRNA vaccine before 20 weeks’ gestation compared to baseline must be questioned.

At face value, the study presented indicates that exposure to mRNA vaccination in the third trimester is safe and supported by another study exploring exposure from 29 weeks.[9] However, as highlighted by McCullough and colleagues,[5] 12.6% of this group reported ‘Grade 3’ adverse events (i.e. severe or medically significant but not immediately life-threatening)[10] and 8% reported a temperature above 38°C after the second mRNA dose (which can induce miscarriage or premature labor). The study follow-up concluded 28 days after birth, with long-term effects of prenatal exposure to infants unknown.

Note: the morning-after abortion pill, RU-486, has an efficacy rate of 80% to 90%.

It would appear at first glance that the “morning after pill”, and mRNA vaccines deployed prior to 20 weeks gestation, have comparable abortion potential.

Note the unusual Editor’s notes at the end of the Brock/Thornley article. Was this paper targeted for potential retraction, similar to the Rose/McCullough myocarditis paper?

DMED data

What other evidence is there for reproductive toxicity?

Second is the DMED military data, which [according to Robert Malone, shows](http://* https://rwmalonemd.substack.com/p/regarding-the-defense-medical-epidemiological?s=r)

• Total Number of Congenital Malformations Reports By Year up 87%
• Total Number of Female Infertility Reports By Year up 419%
• Total Number of Dysmenorrhea Reports By Year up 221.5%
• Total Number of Ovarian Dysfunction Reports By Year up 299%
• Total Number of Spontaneous Abortion Reports By Year DOWN by 10%
• Total Number of Male Infertility Reports By Year up 320%

The spontaneous abortion rate is in contrast to Brock and Thornley’s re-analysis of the NEJM paper. However, using the DMED data, Dr. Jessica Rose estimates that there could be as many as over 700,000 spontaneous abortions as a result of the covid vaccines in the general population.

[Unacceptable Jessica

Spontaneous abortion URF in DoD database adjustment based on 'updated' data.

First off, please go to this article written by Daniel Horowitz. It presents a serious dilemma to the thinking individual. I have personally refrained from writing anything up on this data set since it ‘arrived’ to me pre-analyzed and I don’t jibe with that. I need raw data to be satisfied. And even more strange are the differences between the original …
](https://jessicar.substack.com/p/spontaneous-abortion-urf-in-department?utm_source=substack&utm_campaign=post_embed&utm_medium=web)

Israeli Hospital Data

Another scientist who is an associate of Dr. Rose produced an analysis of aborted pregnancies in two Israeli hospitals and found cause for concern.

[Jackanapes Junction

Stillbirths, Miscarriages and Abortions in Vaccinated vs. Unvaccinated Women

Data from Rambam hospital in Haifa reveal a stillbirth, miscarriage and abortion (SBMA) rate of 6% among women who never received a COVID-19 vaccine, compared to 8% among women who were vaccinated with at least one dose (and never had a SARS-Cov-2 infection…](https://jackanapes.substack.com/p/still-births-miscarriages-and-abortions?utm_source=substack&utm_campaign=post_embed&utm_medium=web)

Independent Physician Reports

Are there any other suspicious reports? Yes. Two doctors in Canada, Drs. Mel Bruchet and Nagase, have reported an alarmingly high rate of stillbirths. I also learned about this news from Dr. Rose’s Substack, but wanted to link directly to the two primary sources.

Dr. Rose discusses the harassment of these doctors on her newsletter.

Funeral Director Reports

A funeral director in the UK speaks about his experience, and what he's been seeing in the morgues in recent times. In his work, he sees that infant morgues are so full that dead babies are being stored in the adult morgues instead. “I just see the dead babies in the fridges” (Under 9 minutes)

Public Comments on CDC Analysis of V Safe Data

Finally, another analysis of V Safe registry data, this time from the CDC, was also published in August 2021, with similar conclusions to the Shimabakuro NEJM study.

Receipt of mRNA COVID-19 vaccines preconception and during pregnancy and risk of self-reported spontaneous abortions, CDC v-safe COVID-19 Vaccine Pregnancy Registry 2020-21

The conclusion of this paper is that rate of spontaneous abortion is the same as the background rate.

What I found interesting was the overwhelming dissent in the comment section (57 comments) and the large number of suppressed comments (22) awaiting moderation. See for yourself the nature of some of the comments. Were these women included in this analysis?

VAERS Data

The above lines of evidence deal largely directly with pregnancy loss rather than the possibilities for future conception, but Dr. Jessica Rose also produced a general summary of female reproductive problems in the VAERS data:

[Unacceptable Jessica

The female reproductive issues in VAERS - why is this even a thing?

As promised. The Female Reproductive Issues reported to VAERS. This is so important for our bloody species. I still cannot believe that this is what I am doing with my time - trying to convince humans why it’s a good idea to consider what is contained in a syringe that has been connected to an unprecedented number of adverse events in every adverse even…](https://jessicar.substack.com/p/the-female-reproductive-issues-in?utm_source=substack&utm_campaign=post_embed&utm_medium=web)

Public Comments on Female Reproductive Problems

These mirror a flood of anecdotal reports from women around the world in 2021, particularly at the peak of the vaccination campaign. Dr. Naomi Wolf had her Twitter account terminated around the time that she was writing heavily about this issue, probably because her posts were attracting even more comments from the general public corroborating these concerns. Reports about irregular menstruation were strongly denied and labeled as conspiracy theories by authorities, with women around the world feeling as if they were thrown into a Victorian era, gaslighted and labeled with “female hysteria.”

As with many other aspects of the pandemic, these “conspiracy theories” were later acknowledged in the media as actual phenomena. Here are two examples:

https://www.spectator.co.uk/article/The-Covid-vaccines-may-affect-periods.-Are-we-allowed-to-talk-about-this/amp

https://thegrayzone.com/2021/08/13/cdc-fda-women-covid-19-vaccines-menstrual-disruption/

As for male fertility, Canadian Pathologist Dr. Roger Hodgkinson warned that mRNA vaccines may damage men's reproductive organs.

Discussion

Thoughts of Christopher Langan, The World’s Smartest Man

It is here that I’d like to turn to Christopher Langan, a guy with a rather interesting life story who is alleged to be the world’s smartest man as judged by IQ tests (up to 210). I do not agree with everything in the following statements he has made. Nevertheless, it is interesting to follow his train of thought. Here is what he had to say about what he believes is the true purpose of the covid vaccines. These statements were screen capped from Facebook in June 2021.

Insights from 20 Year-Old Science Fiction: The Aschen Agenda

Last year, as I saw much of this information rolling in, I was strongly reminded of two episodes in a favorite Sci Fi TV series, Stargate SG1. I posted YouTube videos of these episodes to Facebook.

“Predictive programming is a subtle form of psychological conditioning provided by the media to acquaint the public with planned societal changes to be implemented by our leaders. If and when these changes are put through, the public will already be familiarized with them and will accept them as natural progressions, thus lessening possible public resistance and commotion.”

- Alan Watt

Stargate SG1 is a small Air Force unit that roams the galaxy through an ancient alien device called a stargate. They visit other worlds to discover and neutralize potential threats to Earth.

On their adventures, they encounter an alien race called the Aschen that are the epitome of a Trojan horse: this race allies itself with other worlds, offering them advanced technologies and medicines, which are used to subtly wipe out their populations. The depopulated planets are then terraformed into farmland. “Orphaned” children are raised and re-educated by Aschen families to serve as subsistence agricultural workers. Dwarf stars are changed on these planets to lengthen the growing season, and the surplus food is sent through the Stargate to feed the Aschen.

Their conquest is not a crime of passion. It is well-planned. Systematic. And takes hundreds of years. These are cold and calculating villains.

Here’s a partial transcript to tempt you to watch the videos below. Read carefully if you don’t watch the videos.

INT—IN A CAVERN UNDERNEATH THE RUINS OF A ANCIENT CITY ON THE VOLIAN HOME WORLD

DANIEL
Here's something. The headline says something about pandemic, some sort of—I can't translate that—maybe fever. Now, assuming the Aschen are the newcomers in this article, they provided a—can't translate that word either—but it appears to have been some sort of vaccine. And the Volian people were immensely grateful.

The Aschen vaccine had a side effect. I don't know what. It might be an Aschen word, but I know it was big news around here.

TEAL'C
How would you know this Daniel Jackson?

DANIEL
Well, it's in big, black letters "Aschen vaccine causes—something". I don't know what it is, but I don't think it's a good thing.

TEAL'C
These pictures appear to be much like those we saw of people celebrating.

DANIEL
Ah, I don't think they're celebrating. I think they're rioting.

INT—SGC BRIEFING ROOM

DANIEL
Okay, here's what we know. Around two hundred years ago, the Volians were a thriving urban civilisation approximating turn of the century north America in terms of technology.

CARTER
That wasn't very long ago.

DANIEL
No, it wasn't.

HAMMOND
What happened to them?

DANIEL
Well, all we know is that there was a 'flu pandemic similar to the one on Earth in 1918, that killed over twenty million people. Now, that is when the Aschen came.

O'NEILL
Through the Stargate?

DANIEL
Actually in ships. You see the Volian Gate wasn't discovered until years later. They befriended the Volians, offered them a vaccine for their epidemic, and saved their world. Now, by all accounts, the Aschen were heroes to the Volians, and their friendship lasted for years. But, then, something happened.

O'NEILL
What?

DANIEL
I don't know.

TEAL'C
We found no evidence of a battle.

DANIEL
I found one clue—here.

[Daniel indicates a newspaper cutting shown on the projector.]

DANIEL
Um—this word loosely translates as medicine, vaccine, drug, followed by "from the newcomers" followed by "causes", followed by—some word I can't translate. Now, this was the latest issue of the paper we could find, which most likely indicates the paper shut down or was shut down the very next day.

CARTER
Vaccine causes—what?

DANIEL
I don't know. But it caused something. Because in the span of two hundred years, the Volians went from an urban civilisation of millions to an agrarian civilisation of thousands after they were “saved” by the Aschen.

Here’s the ending of the episode showing how the Aschen respond when their true plan is discovered:

Stargate SG1 was full of alternate timelines. In an alternate timeline the Aschen were actually able to establish a treaty with Earth and deploy their anti-aging vaccine. Ten years after that deployment, SG1 discovers the true nature of the Aschen program, by which time the Aschen had managed to sterilize 90% of Earth’s population.

Jack, an original member of the SG1 team, smelled something “off” about the Aschen. But nobody listened to him.

O'NEILL
Let me tell you something, Carter. You want to erase your mistakes? That's your business. My conscience is clear. I warned everybody, I threw up the red flag and everybody—including you—shut me down.

CARTER
I'm asking you to put that behind us.

O'NEILL
You're not happy with the way things turned out…I'm sorry to hear that. Personally, I like things the way they are. No more saving the world, just a nice pond with no pesky fish in it, and the single most pressing issue in my life is whether or not to get a dog…There're a lot of pros and cons to consider.

CARTER
Jack. I'm talking about the future of the human race.

O'NEILL
So was I.

Eventually, he gets over his bitterness, and he joins up with the team again to save the world. The only answer in this alternative timeline is time travel to prevent it from happening in the first place. In 2010, the team agree to send a note through the Stargate to stop the contact with the Aschen from ever happening:

There’s an interesting personal story juxtaposed in this alternate timeline. The human heroine scientist in the drama, Samantha Carter, discovers she, too, is a victim of the Aschen’s sterilization program, which has been disguised as an anti-aging vaccine.

She tells her husband Joe, a diplomat to the Aschen, about her discovery:

JOE
The Aschen doctors said you were fine.

CARTER
This isn't just about me. I read this right from an Aschen terminal. Mollem gave me access to work on something else. The birth rate has been cut over ninety percent.

JOE
Oh my God. It was supposed to be a third of that.

CARTER
You KNEW!?

JOE
The Aschen insisted on it.

CARTER
Oh, my God…

JOE
Honey, they see farther ahead than we do. They knew that if we didn't limit growth…

CARTER
Is that what you call this?

JOE
This obviously isn't what we agreed to!

CARTER
I can't believe this…

JOE
We didn't have a choice, Sam.

CARTER
You sold us out!

JOE
You think this was my decision?

CARTER
You could have told me!

JOE
Oh, come on, you know how it works! Before the Alliance you spent most of your adult life in secrecy.

CARTER
Please, that was different!

JOE
Sam, it's the same.

CARTER
No!

JOE
It's exactly the same. Our population was unsustainable. Without drastic measures, the Aschen didn't think we were worth investing in. Obviously they went too far, but I can't believe they did this deliberately. There must be some sort of reverse medical procedure they have…

CARTER
You still don't get it.

JOE
Sooner or later the Goa'uld would have wiped us out. Would you prefer that?

CARTER
The Aschen way is slower. That's all.

Conclusion

Such is the nature of the complicity theorist.

The unexamined acceptance of advanced technology as an obvious boon to humanity was the naive belief that the Aschen ultimately used against the worlds they conquered.

Have we just fallen into the same trap?

I can’t prove this what they’re up to. But it sure is fishy.

If so, it’s a good thing uptake isn’t as high in the younger age groups as they wanted. And also if so, hopefully the billionaires in charge of planet Earth aren’t as technically competent as the Aschen. (After all, they want us all to take many more of these injections.) Because this time we don’t have a time machine.

‘Needle Points,’ Tablet’s exploration into the sources and nature of vaccine hesitancy, is presented in four parts. Chapter I begins below. To download a free, printer-friendly version of the complete article, click here.

Since my days in medical school, I have had a fascination with the kernel insight behind vaccination: that one could successfully expose a person to an attenuated version of a microbe that would prepare and protect them for a potentially lethal encounter with the actual microbe. I marveled at how it tutors an immune system that, like the brain, has memory and a kind of intelligence, and even something akin to “foresight.” But I loved it for a broader reason too. At times modern science and modern medicine seem based on a fantasy that imagines the role of medicine is to conquer nature, as though we can wage a war against all microbes with “antimicrobials” to create a world where we will no longer suffer from infectious disease. Vaccination is not based on that sterile vision but its opposite; it works with our educable immune system, which evolved millions of years ago to deal with the fact that we must always coexist with microbes; it helps us to use our own resources to protect ourselves. Doing so is in accord with the essential insight of Hippocrates, who understood that the major part of healing comes from within, that it is best to work with nature and not against it.

And yet, ever since they were made available, vaccines have been controversial, and it has almost always been difficult to have a nonemotionally charged discussion about them. One reason is that in humans (and other animals), any infection can trigger an archaic brain circuit in most of us called the behavioral immune system (BIS). It’s a circuit that is triggered when we sense we may be near a potential carrier of disease, causing disgust, fear, and avoidance. It is involuntary, and not easy to shut off once it’s been turned on.

The BIS is best understood in contrast to the regular immune system. The “regular immune system” consists of antibodies and T-cells and so on, and it evolved to protect us once a problematic microbe gets inside us. The BIS is different; it evolved to prevent us from getting infected in the first place, by making us hypersensitive to hygiene, hints of disease in other people, even signs that they are from another tribe—since, in ancient times, encounters with different tribes could wipe out one’s own tribe with an infectious disease they carried. Often the “foreign” tribe had its own long history of exposure to pathogens, some of which it still carried, but to which it had developed immunity in some way. Members of the tribe were themselves healthy, but dangerous to others. And so we developed a system whereby anything or anyone that seems like it might bear significant illness can trigger an ancient brain circuit of fear, disgust, and avoidance.

It can also trigger rage, but rage is complex, because it is normally expressed by getting close to the object, and attacking it. But with contagion, one fears getting too close, so generally the anger is expressed by isolating the plague-bearer. The BIS is thus an alarm system specific to contagion (and, I should add, to the fear of being poisoned, which before the development of modern chemistry often came from exposure to living things and their dangerous byproducts, such as venoms). Thus it can also be triggered by nonanimate things, like body fluids of some kinds, surfaces others may have touched, or even more abstract ideas like “going to the grocery store.” There is one exception: The BIS doesn’t get or stay activated in people who don’t feel vulnerable, perhaps because they have good PPE, or because their youth gives them strong innate immunity, or because they know they’re already immune, or because they’re seriously misled or delusional about the reality of the disease. For everyone else, though, what might trigger the system is rather plastic; but once triggered, the system is involuntary.
Anti-vaccine protesters outside the San Diego Unified School District office, ahead of a debate over forced vaccination mandate for students, San Diego, Sept. 28, 2021

The BIS is, I would argue, one of the instinctual reactions that missed appearing in medical textbooks perhaps because we’ve not had a pandemic on this scale for 100 years. Because it focuses on potential bearers of disease, the BIS triggers many false alarms, since an infected person may at first show only the mildest and nonspecific symptoms, such as a cough or sniffle, before they become deathly ill; that’s why even a small exhalation or a surface touched by a stranger could trigger the BIS. Were it a medical test of danger, we would say this system tends to err on the “false positive” side. We see it firing every day now, when someone drives alone wearing a mask, or goes for a walk by themselves in an empty forest masked, or when someone—say with good health and no previous known adverse reactions to vaccines—hears that a vaccine can in one in 500,000 cases cause death, but can’t take any comfort that they have a 99.999% chance of it not happening because it potentially can. Before advanced brain areas are turned on and probabilities are factored in, the BIS is off and running.

One of the reasons our discussions of vaccination are so emotionally radioactive, inconsistent, and harsh, is that the BIS is turned on in people on both sides of the debate. Those who favor vaccination are focused on the danger of the virus, and that triggers their system. Those who don’t are focused on the fact that the vaccines inject into them a virus or a virus surrogate or even a chemical they think may be poisonous, and that turns on their system. Thus both sides are firing alarms (including many false-positive alarms) that put them in a state of panic, fear, loathing, and disgust of the other.

And now these two sides of the vaccination debate are tearing America apart, at many levels: families, friendships, states, and the federal government. It’s even affecting the country’s ability to deal with the pandemic, splitting hospital staffs and sundering relations between the scientists studying it.

As of this writing, in the United States about 85% of people over 65—the age group most at risk—are fully vaccinated against COVID (more if you include those who had one shot). Fifty-seven percent of the overall population is fully vaccinated. But around June, the rate of vaccination slowed drastically—down to less than 1 million a day from 3.4 million daily in April, even though many more people (age 12 and up) were now eligible. Five million people who got the first shot had not gone to their follow-up appointment. States started sending vaccines back, while some vaccination sites were empty. In response, U.S. public health officials appeared to believe that the number of people who would voluntarily take the vaccine had reached a ceiling. The change could be seen from the top of the messaging system, with President Joe Biden switching from persuasion to coercion—of the armed services, federal employees, and, as of Sept. 9, of everyone working for companies with 100 employees or more, a category that includes about 100 million Americans.

In a way, this should be the least likely time in history for vaccine hesitancy. For years, vaccinologists explained vaccine skepticism by noting that it largely existed because few had lived through a large-scale pandemic, and because vaccines had already eradicated so many serious diseases that it gave rise to complacency about the threat. But today’s vaccine hesitancy is happening in the midst of a pandemic, in which over 700,000 Americans have died. And a recent Rasmussen poll found that a staggering one-third of Americans “believe officials are lying about vaccine safety.”

It seems to me especially vital that we broaden our understanding of the history and current state of vaccines because, over the summer, many who chose vaccination for themselves concluded that it is acceptable to mandate vaccines for others, including those who are reluctant to get them. That majority entered a state of “crystallization”—a term I borrow from the French novelist Stendhal, who applied it to the moment when a person first falls in love: Feelings that may have been fluid become solid, clear, and absolute, leading to all-or-nothing thinking, such that even the beloved’s blemishes become signs of their perfection.

Crystallization, as I’m using it here, happens within a group that has been involved in a major dispute. For a while there is an awareness that some disagreement is in play, and people are free to have different opinions. But at a certain point—often hard to predict and impossible to measure because it is happening in the wider culture and not necessarily at the ballot box—both sides of the dispute become aware that, within this mass of human beings, there is now a winner. One might say that a consensus arises that there is now a majority consensus. Suddenly, certain ideas and actions must be applauded, voiced, obeyed, and acted on, while others are off limits.
Courtesy the author

One person who understood how this works intuitively was Alexis de Tocqueville. In democracies, as long as there is not yet a majority opinion, a range of views can be expressed, and it appears there is a great “liberty of opinion,” to use his phrase. But once a majority opinion forms, it acquires a sudden social power, and it brings with it pressure to end dissent. A powerful new kind of censorship and coercion begins in everyday life (at work, school, choir, church, hospitals, in all institutions) as the majority turns on the minority, demanding it comply. Tocqueville, like James Madison, was concerned about this “the tyranny of the majority,” which he saw as the Achilles’ heel of democracy. It isn’t only because divisiveness created a minority faction steeped in lingering resentment; it’s also because minorities can sometimes be more right than majorities (indeed, emerging ideas are, by definition, minority ideas to start with). The majority overtaking the minority could mean stamping out thoughts and actions that would otherwise generate progress and forward movement.

It is a fascinating moment when this sort of crystallization happens in a mass culture like America’s, because seemingly overnight even the definition of legitimate speech (or thought or action) also changes. Tocqueville observed that quite abruptly a person can no longer express opinions or raise questions that only days before were acceptable, even though no facts of the matter have changed. At an individual level, people who were within the bounds can be surprised to find themselves “tormented by the slights and persecutions of daily obloquy.” Once this occurs, he wrote, “your fellow-creatures will shun you like an impure being, and those who are most persuaded of your innocence will abandon you too, lest they should be shunned in their turn.”

In the midst of a pandemic, seeing the unvaccinated as “impure” is no surprise, because of course they could carry contagion. But as Tocqueville pointed out, this also occurs when there is no contagion, and we begin to experience those who are on the wrong side as “impure”—as in failing the purity test—and react to them as though they are dangerous. That we do this even when there is no pandemic suggests that there is, along with realistic fear of infection, something else going on here—a sense that those with whom we may disagree are impurities in the body politic, bad people who need to be taught a lesson, even punished.

A June 2021 Gallup poll found that, among the vaccinated, 53% now worry most about those choosing not to get vaccinated, “surpassing concerns about lack of social distancing in their area (27%), availability of local hospital resources and supplies (11%), and availability of coronavirus tests in their area (5%).” True to the BIS’s impulses, this fear is metastasizing into disgust, even hatred, of those who—because they believe or act differently—are now perceived as threats: On Aug. 26, in a front-page story in the Toronto Star, my local newspaper, a resident was quoted as saying: “I have no empathy left for the willfully unvaccinated. Let them die.”

In the midst of such a death wish for fellow human beings, even the person quoted understood that an important mental capacity has been lost: empathy, or the ability to model other people’s minds. When we lose that en masse, the results can be tragic, not least because getting through this must be a group effort.

As I understand it, there are two main approaches to public health in liberal democracies, and both have been tried historically in different places. One begins voluntarily, out of respect for civil liberties, but switches to coercion when some voluntary ceiling, deemed insufficient, is reached. Ideally, this intervention is based on the principle of least-necessary coercion. The benefit to this is that it may work to get more people vaccinated in shorter order. But it also conveys that the government does not trust its citizens to make good decisions on their own, a condescension that in turn—this is human nature 101—eventually generates resentment, even revolt, and the disengagement of significant segments of the population. The other approach, participatory public health, sees the need for coercion as a sign that something in the public health outreach itself has failed; if a ceiling is reached, society’s leaders should not simply resort to force but rather confront the flaws in their own leadership—that they should double-down on their responsibility to generate trust in the public. The goal of participatory public health is not to crush, but to better engage.

It’s not about COVID-deniers or anti-vaxxers, but about the vaccine hesitant—those who are concerned and anxious about COVID but also anxious about these new vaccines.
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In that spirit, what follows is an attempt by a physician and neuroscience writer and someone who got vaccinated, early and voluntarily, to understand those who have not made this choice. This essay is not about COVID-deniers or anti-vaxxers, who oppose vaccines on ideological grounds. Nor is it about the activists or political figures who feed off and benefit from the corrosive discourse around vaccines. It is instead about the vaccine hesitant—those who are concerned and anxious about COVID but also anxious about these new vaccines. These are the people who are not yet vaccinated for reasons that the majority may not understand—and which are often more anchored in history and experience than the majority would suspect. They are the Tocquevillian minority that the majority is threatening with job loss and other restrictions.

One needn’t agree with the decisions or actions of the vaccine hesitant in order to learn something from them and about them, and about society as a whole. They pay attention to, and are vigilant about, different issues than the vaccinated, and have strong feelings about the people and institutions involved in our public health—particularly politicians, the drug regulatory process, and pharmaceutical companies. For many, vaccine hesitancy is not simply about the vaccines; it’s about the absence of faith in the wider systems that brought us the vaccines. “Public health moves at the speed of trust,” notes physician and author Rishi Manchanda. If we want our public health system to function better—safer, swifter, in ways that more effectively safeguard the lives and livelihoods of all citizens—it must be rooted not in coercion but in confidence, and not only among the majority.

Vaccine spike antigen and mRNA persist for two months in lymph node germinal centers... protein production of spike is higher than those of severely ill COVID-19 patients!

Immune imprinting, breadth of variant recognition and germinal center response in human SARS-CoV-2 infection and vaccination Cell. Published:January 24, 2022DOI:https://doi.org/10.1016/j.cell.2022.01.018

Highlights (per the journal)

• Vaccination confers broader IgG binding of variant RBDs than SARS-CoV-2 infection
• Imprinting from initial antigen exposures alters IgG responses to viral variants
• Histology of mRNA vaccinee lymph nodes shows abundant germinal centers
• Vaccine spike antigen and mRNA persist for weeks in lymph node germinal centers

The hidden highlight (lede) buried in this peer reviewed paper is that protein production of spike in people vaccinated with the Moderna or Pfizer vaccine is higher than those of severely ill COVID-19 patients! A person might ask, “How could that be?” In order to understand this, we must carefully analyze what the study shows.

This study asserts that the mRNA and the spike protein produced persists for weeks in lymph node germinal centers in human patients. Having worked with mRNA for decades, I can attest that this is highly unusual.

One very real hypothesis is that the substitution of pseudouridine for uridine to avoid the immune response is working so well that the mRNA is completely evading the normal clearance/degradation pathways. Hence, mRNA that is not being incorporated into cells at the injection site, is migrating to the lymph nodes (and throughout the body as the non-clinical Pfizer data suggest?) and continuing to express protein there. In this case, the cytotoxic protein antigen is spike. Spike protein can be detected for at least 60 days after administration of dose. Note that the duration of the protein expression was only tested for 60 days.

The spike protein, let’s review what it is and how it is being used (from the Daily Skeptic):

These new gene-based ‘vaccines’ are working in a completely novel way – nothing remotely resembling that of traditional vaccines. Given that pharmaceutical companies work competitively it was also somewhat of a surprise they took the same approach of targeting what has been termed the ‘spike protein’ of the SARS-CoV-2 virus.

This (spike) protein is nasty – sometimes being referred to as a ‘pathogenic protein’ – and is recognised as causing many of the awful pathologies associated with the disease of COVID-19. Logically you would inactivate or at least attenuate this nasty spike protein and develop a vaccine around the attenuated virus. But that’s not what was done. These ‘vaccines’ do not contain any of the offending virus at all but rather the gene sequence that causes the nasty spike protein to be made in the body. We have little idea how much of this nasty protein is produced or for how long it lasts after an injection of the gene sequence. Furthermore, stimulating the body’s own complex biological systems to produce the spike protein will mean that the amount of protein produced will vary from person to person. The idea is that the spike protein produced by the gene encoding it elicits a response by our immune system to produce antibodies directed against the spike. When the wild virus comes along and infects us the antibodies recognise the spike protein and attack it thus preventing its nasty effects. And it does, though as we have since learnt this approach isn’t very good at preventing infection or stopping its transmission. Are we perhaps clutching at straws too in claiming that these ‘vaccines’ are preventing serious disease and death? Have we not learnt anything over the past two years in treating Covid symptoms with conventional therapeutic drugs?

Knowing what we know about the spike protein in these vaccines, the study quantitatively measured spike protein levels in plasma after vaccination. Which, it turns out, are higher than the levels observed in a person with a severe COVID-19 infection. Just to write it, the fact that this only now being discovered or it it was known, released to the public is criminal in my opinion. This should have been characterized long ago, including prior to beginning human clinical trials.

That this has not been published or investigated more demonstrates the gross regulatory dereliction of duty by Pfizer, Biointech, Moderna, NIAID VRC and that whole crew. Using these vaccines, which include pseudouridine without fully understanding the implications and without the FDA requiring a complete pre-clinical toxicology regulatory package, including long-term follow-up, as is done with any other unique chemical or adjuvant additive is shocking. Then there is the novel use of the unique nano particles being used in these vaccines, which also were only marginally assessed, as shown by the Japanese Pfizer data.

Protein expression is not being turned off, because the immune response against the mRNA/pseudouridine complex is either not happening or is ineffective. It may also be that the mRNA/pseudouridine complex has a longer half-life than normal mRNA. The In either case, this is regulatory nightmare.

I do not know how to write this more strongly. This technology is immature. The WHO has approved six, more traditional vaccines, all of which the US government could license. These genetic vaccines are not the only option.

To note: The use of pseudouridine in these mRNA vaccines is not the only option. It has often been hypothesized that the reason Dr. Kariko added pseudouridine to the mRNA vaccine was to make an improvement to the original mRNA patents that I was an inventor on. An improvement to an existing patent allows commercialization of that patent. It is an old trick. Remember, that Curevac does not use pseudouridine in its formulation and it is not required or necessary for a significant immune response. In the next generation of mRNA vaccine experiments (hopefully done in an animal model), it is clear that the issues of adding pseudouridine need to be addressed prior to any more of these vaccines going into humans.

I know the following from the paper is long, but it is very important.

Prolonged detection of vaccine mRNA in LN GCs, and spike antigen in LN GCs and blood following SARS-CoV-2 mRNA vaccination

The biodistribution, quantity and persistence of vaccine mRNA and spike antigen after vaccination (with the Pfizer vaccine), and viral antigens after SARS-CoV-2 infection, are incompletely understood but are likely to be major determinants of immune responses. We performed in situ hybridization with control and SARS-CoV-2 vaccine mRNA-specific RNAScope probes in the core needle biopsies of the ipsilateral axillary LNs that were collected 7-60 days after 2nd dose of mRNA-1273 or BNT162b2 vaccination, and detected vaccine mRNA collected in the GCs of LNs on day 7, 16, and 37 post vaccination, with lower but still appreciable specific signal at day 60 (Figures 7A -7E). Only rare foci of vaccine mRNA were seen outside of GCs. Axillary LN core needle biopsie of non-vaccinees (n = 3) and COVID-19 patient specimens were negative for vaccine probe hybridization. Immunohistochemical staining for spike antigen in mRNA vaccinated patient LNs varied between individuals, but showed abundant spike protein in GCs 16 days post-2nd dose, with spike antigen still present as late as 60 days post-2nd dose. Spike antigen localized in a reticular pattern around the GC cells, similar to staining for follicular dendritic cell processes (Figure 7B). COVID-19 patient LNs showed lower quantities of spike antigen, but a rare GC had positive staining (Figure 7F). Immunohistochemical staining for N antigen in peribronchial LN secondary and primary follicles of COVID-19 patients (Figures 7F - 7I) was positive in 5 of the 7 patients, with a mean percentage of nucleocapsid-positive follicles of more than 25%.

Discussion One of the positive developments amid the global calamity of the SARS-CoV-2 pandemic has been the rapid design, production and deployment of a variety of vaccines, including remarkably effective mRNA vaccines encoding the viral spike (Baden et al., 2021; Polack et al., 2020). We find that BNT162b2 vaccination produces IgG responses to spike and RBD at concentrations as high as those of severely ill COVID-19 patients and follows a similar time course. Unlike infection, which stimulates robust but short-lived IgM and IgA responses, vaccination shows a pronounced bias for IgG production even at early time point

Read that again: Protein production of spike is higher than those of severely ill COVID-19 patients!

The paper also notes that the antibody response is IgG, not IgA or IgM. IgA and IgM antibodies produce a strong mucosal immune response needed for respiratory diseases, unlike IgG.

This Substack article has only skimmed the surface of the implications of this paper in terms of both the science and the malfeasance on the part of our government and pharmaceutical corporations. There is more to come on this issue.

To get to the full paper to download, click here.

Why Weren’t These Vaccines Put Through the Proper Safety Trials For Gene Technology, Asks a Former Pharmaceutical Research Scientist The Daily Skeptic 7 February 2022 by Dr. John D. Flack

This article by the daily skeptic does a great job at documenting that appropriate studies have not been done and even attempts to answer the question why:

Are we perhaps clutching at straws too in claiming that these ‘vaccines’ are preventing serious disease and death? Have we not learnt anything over the past two years in treating Covid symptoms with conventional therapeutic drugs?

Perhaps this has driven Big Pharma to pursue a new more profitable model based on protecting the healthy rather than treating the sick? Enter the era of the gene-based ‘vaccines’. The new technologies have had a long and difficult gestation period with several stillbirths. But perhaps their time had come with the ‘unprecedented’ virus from the East. A declared worldwide health emergency demanded a technological response, and it was there in waiting. But have we been blinded and duped by technology and lost sight of the end game of providing safe and effective medicines? Was it a judicious use of the PCR, rapid antigen test technology and information APP technology to drive the test and trace fiasco?

Was the gene technology ready to be used in a mass world-wide vaccination programme without a thorough examination of the potential problems of short- and long-term safety of this previously untested technology?

In my view, technocracy has trumped the sound principles, established over decades and centuries, of basic medical practice, immunology, virology, pharmaceutical sciences and public health generally. In the process, political democracy, personal freedoms, free speech and choice have been dangerously sidelined and even censored.

No vulgar harassment of police — no “All cops are bastards” signs.

No rocks for every Starbucks window and those of small businesses. No blizzard of break-ins, no store owners standing guard on their shops. No arson or looting.

Jan. 6 insurrection Canadian edition? Ha! It is to laugh. I’ve seen more threatening picnics thrown by a few nuns.

Yet if you listened to much of the established press predictions, Ottawa over the weekend was supposed to be like Rome waiting for the Visigoths. Ooooh — the end of cottage government as we’ve come to know it. A full-scale assault on our Zoom Parliament.

Plain, straight reportage uninflected by the personal dispositions or ideological pre-sets of the reporters or the corporations they work for was hard to come by. Our stern reporters, always ready to squeak agreement to power, worked to set a context. I’ve seen more threatening picnics thrown by a few nuns

They perspired with eagerness that an almost completely incident-free protest might turn into a gathering of “yahoos.” That an angry diesel mob fired up by Boston creams and cold coffee would storm the House of Cottage and end democracy in Canada, such as we know it. They leaped at trivial individual mischiefs and tried to brand the entire protest as negative and even hateful.

The bottom line — they did not cover this protest in the gentle, generally approving manner they have covered so many others, from the Summit of the Americas demonstrations in Quebec City in 2001 to Black Lives Matter in 2020. I believe that Justin Trudeau joined that one.

The contributions over the course of this protest from the prime minister and the NDP’s Jagmeet Singh were viciously demeaning.

Trudeau was extremely derogatory, to the point of calculated insult, concerning all who were not in line with his view of things. And he acted as a woke Pope in assuming the right to make the judgment on which views of Canadians were “unacceptable.” And to declare the protesters a band of racists and misogynists.

Does he not know the meaning of the words he recklessly threw out to brand Canadian citizens? “Racist” is the dynamite word of our time. Throwing the word “racists” at a collection of Canadians is mean, nasty, and false.

It must be remarked that a quadruple black-face prime minister is not the best centurion to stand guard against racism, or to accuse others, who incidentally are not so addicted to facial cosmetics as he plainly is.

You know what the saddest part in all of this is? A walk down to the protest, an easy talk with random truckers, with Trudeau saying his piece, and the drivers theirs — that would have been a Canadian moment. The civilized, respectful thing to do.

It was never to be however. Hard politics is better than harmony. Sunny Days has morphed into Mr. Thunder-cloud.

Then there was the other party leader, Jagmeet Singh, the scaffold and support of Trudeau’s stay as prime minister. Of Mr. Singh let us say it must be very hard to have the instincts of a demagogue without the talent to carry it off. But to give him credit, he does try.

First, just to set the stage, is it really that hard to believe that after two years of a pandemic regime some Canadians are not “on-board” with current policies? Hard to believe that people living and working (or trying these days to get work) far from Ottawa and power, feel left out and frustrated?

Sunny Days has morphed into Mr. Thunder-cloud

More to the point, is it also that hard for a Canadian political leader to believe that some Canadians act on principle, and out of concern for their personal autonomy?

Was not the NDP once, of all parties, populist in a positive sense, more tuned to the “working man and woman” than any other? Those days are obviously long gone and the dimmest memory. Instead what we got from the current and most-urban NDP leader was a smearing of the protest, citing a comment from one individual who claimed “the superiority of the white bloodline” as an index of the thinking of the other leaders, and by insinuation, the whole convoy. A crumb is not the whole cake. Let me put it to the reader: Is this tweet a fair description of the convoy:

Mr. Singh: “Conservative MPs have endorsed a convoy led by those that claim the superiority of the white bloodline and equate Islam to a disease .” (Italics mine.)

The convoy of Canadian truckers, of multiple ethnicities, may be many things. But it is not composed of men and women who subscribe to, use, or think in such crapulous terms. In my judgment Singh’s comments were the lowest of the whole weekend — and he had some stiff competition in that department.

Singh is either desperate to out-Trudeau Trudeau in demonizing the truckers, or there is a serious wobble in the runners on his cushioned rocking chair.

Singh's comments were the lowest of the whole weekend

Final point: Is it really that hard for Trudeau and Singh not to acknowledge that the full majority of people who went all the way to Ottawa are just decent people? Not racists. Not women haters? Not orcs. That these protesters may be as at least as fair-minded and decent as the politicians who govern them.

A talk with a dozen or more of these folk may not have changed minds, on either side, but would have had a touch of Canadian respect and politeness, and taken the charge of sheer politics out of this whole episode.

Far too much to ask I suppose when politics is a cynical game, the press are an essential part of the same game, and some guys in a truck, on the edge of making a living, travel across the country to say a few things to their government. After all … who are they?

PS. As I was writing this, the Conservatives, with their superb sense of political timing, were behind closed doors busily disembowelling themselves. More on that in the next column.