It’s happening. The manufacturers and regulators knew it was a risk, yet, like numerous aspects of the Covid vaccine mRNA technology, did not test for excretion potential of spike proteins or LNP’s.
Awareness of the Federal Regulators and Vaccine Manufacturers
The data showing the toxicity and lethality of the vaccines started within weeks of the roll-out with hundreds of thousands of adverse events and hundreds of deaths reported to VAERS in January of 2021, far exceeding previous stopping points of any new medical product or vaccine.
Although ignored (to this day), anyone paying unbiased attention could see a further mountain of evidence develop, including a skyrocketing number of newspaper and television reports of healthy athletes and young people arresting and dying while doing normal everyday activities or sports (countered by corporate/government controlled media with a plethora of fact checking articles using cherry picked data to inform the world that what they are seeing is not factually true).
Then life insurance industry data emerged showing historically unprecedented rises in death claims being paid out amongst the healthiest sectors of society temporally associated with the proliferation of Covid mRNA vaccine mandates within schools, corporations, universities, health care institutions, federal contractors etc. Most telling of the deathly impact of mandates was the fact that the largest increases among the sudden, rapid rises in excess deaths occurred among employed white collar workers.
It truly is unimaginable that we now must consider the risks (and reality) of “shedding” of the vaccine products from the vaccinated to the unvaccinated. This now has implications for nearly every human being walking the earth, vaccinated or unvaccinated (including me).
This series will explore the regulatory, scientific, epidemiological, and clinical data indicating that shedding is occurring. The health of who knows how many is now being threatened, with the extent of the risks likely both highly variable and difficult to predict, both in the short term and long term. That is unless we start to seriously study the phenomenon further. So, let’s review what is known.
Within 3 months of the rollout of the global Covid mRNA vaccination campaign, I was consulted by two different unvaccinated women in their late 30’s and early 40’s respectively, who reported that they were suffering acute menstrual abnormalities in the days following close exposure to a recently vaccinated practitioner (one visited a massage therapist and another an acupuncturist). Both had a history of highly regular, uncomplicated menstrual cycles over decades.
Since that time, at least twenty other unvaccinated and vaccinated people, both men and women, have reported to me compelling histories of typical post-mRNA vaccine adverse effects subsequent to close exposure to vaccinated family members, contacts, or friends.
Further, my partner Scott Marsland at our Leading Edge Clinic, who also specializes in treating Long Covid/Long Vax syndromes, has a growing series of detailed case histories of similar “shedding” events occurring. I will revisit this in a later post in this series, but I will briefly say here that our clinical observations conclude that symptomatic shedding events do occur. However, we have little idea of exactly how common it is occurring among the general population.
This is further complicated by the fact that even if it were occurring frequently, the vast majority of people suddenly developing typical vaccine side effects symptoms after exposure to a vaccinated person would never think to relate it to exposure to shed vaccine products. It is my belief that very few people in the general public are aware of the possibility it could occur. You know, because the regulators have assured the country that mRNA technology is “safe and effective.”
However, my general sense is that it occurs largely in people who have increased physiologic sensitivity to environmental exposures, toxins, or pharmaceuticals and that it is generally transmitted by someone recently vaccinated or someone who is producing a lot of spike protein. Note that is my “general sense.” More studies are required to fully understand both the frequency of and physiologic impacts from such events.
My ignorance as to the frequency of symptomatic shedding events is due to the fact that the concept of transmitting spike proteins (or lipid nanoparticles) from a Covid mRNA vaccinated person to another is one of the least studied and published-on aspect of the mRNA vaccine technology.
What is so shocking about that lack of research (actually nothing is shocking anymore) is that shedding has major global implications. Apparently it is not just me who thinks this because, as an expert on several aspects of Covid, I have been lecturing across the U.S, Europe, and South America in conferences, Parliamentary hearings, or invited lectures. Questions about shedding appear everywhere (in the dozens of Q & A’s that I have participated in, it is nearly always the first question. It is also a very common topic in the chat of our FLCCC weekly webinar.
Know that in this tonight’s FLCCC webinar, I will present a 15-20 minute overview of this series along with my private practice partner Scott Marsland. We expect to be deluged with questions after.
Anyway, I believe that by the end of this series on the science, epidemiology, and clinical observations of shedding, you will be convinced that it can and does occur.
What IS The Definition Of Shedding In Regards To The Covid mRNA Vaccines?
From our Federal government, in this FDA document, the term “shedding” is defined as:
“The release of viral or bacterial gene therapy products from the patient by any or all of the following routes: feces (feces); secretions (urine, saliva, nasopharyngeal fluids, etc.); or through the skin (pustules, lesions, sores).”
They forgot to mention “exhaled breath.” More on that later. The “products” they refer to that can be transmitted from a Covid vaccinated person to another include not only the genetically programmed spike protein product, but also the lipid nanoparticle (LNP) containing the mRNA that is in the injections as well as naked mRNA that can be released from the LNP. Even more worrying is the recent shocking discovery that every single Moderna and Pfizer vaccine vial is contaminated with high levels of DNA plasmids potentially capable of integrating into the human genome. Contemplating that last one is disturbing, the implications of which we will not know for some time.
Why Would The Modified mRNA Vaccine Technology Lead To The Possibility of Shedding?
“Gene therapy products are all products that mediate their effects by transcription and/or translation of transferred genetic material and/or by integrating into the host genome and that are administered as nucleic acids, viruses, or genetically engineered microorganisms.
Also note that in this European Medicines Agency (EMA) document, the mRNA vaccines also meet their definition of gene therapy medicinal products (GMTP’s).
Ok, now that we know what a gene therapy product is and that the Covid mRNA injection is actually a form of gene therapy (marketed to the public as a “vaccine”), what does that have to do with “shedding?” Again from the FDA document regarding the evaluation of the safety of gene therapy products, they emphasize the importance of studying shedding:
Shedding is distinct from biodistribution because the latter describes how a product is spread within the patient’s body from the site of administration while the former describes how it is excreted or released from the patient’s body. Shedding raises the possibility of transmission of virus or bacteria based gene therapy products (VBGT) from treated to untreated individuals (e.g., close contacts and health care professionals).
This guidance represents FDA’s current thinking on how and when shedding data should be collected for VBGT and oncolytic products during preclinical and clinical development and how shedding data can be used to assess the potential for transmission to untreated individuals.
So, with these findings in mind, it may be no wonder why the FDA insists on shedding studies:
Further on in the document, the FDA again emphasizes the importance of shedding studies:
Note that the FDA emphasizes the importance of doing human shedding studies and not just relying on animal studies:
To inform the design of human shedding studies, shedding data may be collected in animals following administration of the VBGT or oncolytic product. These data can help estimate the likelihood and potential shedding profile in humans, particularly when there is concern about transmission to untreated individuals. However, such data cannot substitute for human shedding studies for several reasons.
But again, no studies testing whether excretion of mRNA-containing LNPs, modified spike-encoding mRNA, or spike produced by vaccinated people have been done. Well, I shouldn’t say none, because in this paper the author cites a Pfizer document obtained by FOIA which apparently revealed that shedding was studied in the urine and feces of intra-muscular injected rats. Unfortunately, that document is no longer at the website referenced.
To summarize from the above, the FDA’s position is that:
the mRNA vaccines are gene therapy products
Gene therapy products require shedding studies in both animals and humans
Gene therapy product shedding raises the possibility of transmission from treated to untreated individuals
Note that much of the rest of this series of posts on shedding is guided by a masterful comprehensive review of the topic of gene therapy product shedding by independent researcher (by definition) Helene Banoun inInfectious Diseases Research. Hers is one of the only papers I could find that attempted to meticulously explore what is known about shedding of the mRNA gene therapy vaccines.
As already stated, an important point Banoun makes is:
There was no regulation of mRNA clinical trials prior to RNA vaccines, yet there is strict regulation of gene therapy products. It is difficult to justify that mRNA vaccines are not considered in the same way as gene therapies regarding this regulation; indeed the only difference is that they are (historically) supposed to protect against a disease and not cure it. Gene therapies are intended for a small number of people in poor health, whereas vaccines are used on a large scale on healthy people: it would therefore be wise to apply stricter rules to them.
She further points out another omission of the regulatory process:
Any experiment involving the deliberate transfer of a nucleic acid to a human must be preceded by Institutional Biosafety Committee approval (document on the regulatory standards is here), but approval was not given because of the emergency clearance given to mRNA vaccines.
Therefore, according to both the American and European agencies, mRNA vaccines are gene therapy products and should have been subjected to excretion studies of all secreted fluids (urine, exhaled droplets, saliva, sputum, nasopharyngeal fluids, semen, breast milk, feces, and sweat). Again, these studies were not done for mRNA vaccines nor for the DNA adenovirus vaccine (J&J).
So, where are the clinical human shedding studies? Well, I just learned of one that is about to be published (next ten days?) where the research team exposed a population of unvaccinated women to vaccinated individuals and their assessment outcome was the development of menstrual abnormalities. I know the results but want to respect the research teams right to present their original work. They have promised to share their manuscript with me and Paul Marik as soon as the peer-review and acceptance process is complete. I have no idea what journal they submitted to but I can be highly confident it is not the New England Journal of Medicine.
The entire reason why I did a “deep dive” into shedding science is because shedding was not studied when it absolutely should have been and I believe with near certainty that it occurs. Note my use of “near certain” is only to seem objective but it really is too late for that – both my partner Scott and I have diagnosed and successfully treated a number of shedding “victims.”
The lack of shedding studies prior to the mRNA rollout was, in my opinion, an insanely reckless and irresponsible omission (or willfully criminal, take your pick). As an evolving expert in the evaluation and treatment of Covid mRNA vaccine injury syndromes, I and others have identified thespike protein as the main component responsible for not only the pathogenicity of Covid but also of the vaccines, with this review paper proposing a new field named “spikeopathy” (study of the disease processes triggered by the spike protein).
If vaccine transcribed spike protein can be transmitted in sufficient quantity from vaccinated folks to unvaccinated ones, it stands to reason that adverse effects of the vaccine can develop in some unvaccinated people who came into contact (or close proximity) with vaccinated people.How did they get away with not studying this possibility?
An easy answer is they were doing science at “warp speed.” The more uncomfortable answer is that the “vaccines”, although meeting the definition of a gene therapy product, were actually not even legally considered a medical product at all and thus did not require a diverse range of safety studies (like on genotoxicity, reproductive risks, excretion potential etc). What? Why? How?
The reality is that the Covid vaccines, as a result of successive federal legislative actions which evolved over decades, was legally categorized as a “countermeasure” under a “public health emergency.” Such “countermeasures” require no specific regulatory approval process prior to dissemination. All a countermeasure needs is the recommendation of the Secretary of Health and Human Services that “it may be effective.”
This is the conclusion derived from the legal investigatory work of various independent and legal experts and researchers like Catherine Watts, Todd Callender, and Sasha Latypova. If interested in learning more, I would watch this lecture by Sasha Latypova (scroll down the page to find her lecture). As they have uncovered, “countermeasures” (even gene therapy ones) do not legally require studies of excretion potential, bio-distribution, pharmacokinetics, genotoxicity, insertional mutagenesis etc.
They don’t even require FDA regulated clinical trials of efficacy or safety.
So why did Pfizer and Moderna even do the efficacy trials? Latypova maintains that they did this not only to satisfy the public’s confidence to increase vaccine uptake, but also to “fool” the public into thinking these vaccines were medical products subject to standard (albeit accelerated) pharmaceutical product regulatory processes.
This obscured the reality that they were instead classified as military “countermeasures” against a perceived (if not actual) bioweapon. To wit, the COO of Operation Warp Speed was a General from the Department of Defense (DOD) and the vaccine manufacturers were under contract with the DOD to produce the countermeasure, sometimes referred to as a “demonstration (demo)” and/or a “prototype” in numerous legal documents they uncovered.
Anyway, as a result of this lack of a legal requirement to fully study these products in a public health emergency, the list and types of studies that should have been conducted (but were not) is long. Researchers and clinicians have been screaming about this since they were rolled out. These cries were met with a deafening silence by governmental health agencies across the world.
I know, it is a lot to take in.
But the latest “word on the street” is that the finance and insurance industries may finally be waking up to this fraud and its devastating impacts on U.S disability and death rates. Knowledge of these society-wide impacts largely results from the work of two different research teams led by former Blackrock portfolio manager Ed Dowd and insurance industry consultant Josh Stirling).
This article describes the reasons why Pfizer and Moderna stock are crashing of late. Put more succinctly, from what I hear it is due to the hedge fund guys shorting their stock. I believe Pfizer is in even deeper trouble now that this “forensic” paper just got published finding that they hid vaccine trial deaths which obscured a 3.7 fold increased risk of cardiac death in the vaccinated arm of their trial.
“Shedding” Part 1– Shedding of Covid mRNA Vaccine Components and Products From The Vaccinated to the Unvaccinated – Part 1
“Shedding” Part 2 – The Bio-Distribution and Excretion Potential of Covid mRNA Vaccine Products
“Shedding” Part 3 – Can You Absorb Lipid Nanoparticles From Being Exposed To a Vaccinated Person?
“Shedding” Part 4 – Evidence of Placental and Breast Milk Transmission of Covid mRNA Vaccine Components
In the early hours of Monday, October 23rd, the 20-year-old Dutch cyclist Mark Groeneveld passed away, apparently of a heart attack, after having dropped out of a race in Hong Kong earlier in the day. Several reports (here, for instance, in Dutch) claim that he dropped out of the race for mechanical reasons and that his subsequent collapse was “unrelated”.
In a statement on Facebook, his team X-Speed United writes: “While the circumstances of Mark’s passing are currently under investigation, we have received preliminary information that suggests it may have been due to a heart attack.”
This would make Groeneveld the fifth Dutch or Flemish cyclist to be stricken by serious heart problems this year. Groeneveld’s death comes just one month after the Flemish cyclist Nathan Van Hooydonck got into a car crash after suffering what the Belgian paper De Morgenhas described as “cardiac arrest” while driving. The incident happened on September 12th, just two days after the conclusion of the Tour of Great Britain, in which Van Hooydonck helped his teammate Wout van Aert of Team Jumbo Vista to victory.
Van Hooydonck, who was 27 years old at the time of the incident, would have to be placed in an artificial coma. He would subsequently undergo surgery to have a defibrillator implanted. He has retired from professional racing.
Just two weeks before the Van Hooydonck incident, in the early hours of August 29th, the 32-year-old Dutch cyclist Wesley Kreder of the French Cofidis team suffered what he himself has described as “cardiac arrest” while sleeping. “I’m happy to be alive,” Kreder told the Dutch public broadcaster NOS. Kreder has also announced his retirement from competitive racing.
Two other professional cyclists, the 35-year-old Flemish cyclist Sep Vanmarcke and the 25-year-old Dutch cyclist Jarno Mobach, announced their retirements this summer after they were both discovered to have heart tissue scarring. Mobach is a former winner of the junior version of the prestigious Paris-Roubaix race. Vanmarcke announced his retirement in July and Mobach in late September, just a couple of days after Van Hooydonck’s announcement.
As previously reported on the Daily Sceptichere, Flemish cycling already had a serious scare in the summer of 2021, when three members of just one Flemish cycling team developed cardiac problems and would be diagnosed with myocarditis shortly after being vaccinated against COVID-19.
Robert Kogon is the pen name of a widely-published journalist covering European affairs. Subscribe to his Substack and follow him on X.
Federal Health Minister Karl Lauterbach has again called on people to get a booster vaccination. “Despite the pandemic and awareness campaigns, the importance of the Covid booster is apparently greatly underestimated,” he tells Spiegel. “So far, unfortunately, only a fraction of those for whom it is recommended have had a booster vaccination.” He calls on all at-risk groups and older people to catch up and ideally combine it with a flu vaccination.
According to the vaccine uptake statistics of the Robert Koch Institute, only about 2.5 million people have received three or more boosters. This means that only a fraction of those over 60 are likely to have sufficient protection against Covid …
They let Lauterbach flap his gums a little more about population immunity, Long Covid, secondary infections and how the vaccines can make all this better because reasons, before sticking the knife in him:
Lauterbach urgently needs to boost vaccine uptake. The pharmaceutical contracts concluded under his predecessor Jens Spahn have secured much larger quantities of vaccine than are currently being used. Between September and November, about 14.1 million vaccine doses of monovalent vaccine targeted at XBB 1.5. will be delivered. An additional 10.6 million vaccine doses of Novavax XBB 1.5. vaccines will also become available, as soon as they are approved by the European Commission.
Our dissolute snake oil salesmen – who is either so stupid or so desperate that he actually tweeted a link to this not-so-subtle takedown – is currently sitting on 11.5 million Pfizer/BioNTech doses, trembling at the prospect of Novavax dropping another 10 million on his head, with no hope at all that more than 5 million Germans will ever line up for these worthless products. This is despite the best efforts of the regional press, who have been trying to gaslight their elderly readers into getting yet another jab since September. Today the Main Postpublished a typical piece, claiming that vaccine demand is starting to creep up now, really it is; while yesterday it was the turn of Münchner Merkur to claim that everyone is talking about the shiny new vaccines and to drag in some pulmonologist to talk about the “predominantly positive reception” they’ve enjoyed.
In a precedent-setting victory last month, a New York State Supreme Court judge ruled that 10 New York City school teachers fired for refusing the COVID-19 vaccine on religious grounds must be reinstated with back pay, benefits, seniority and attorney fees.
But the city immediately appealed the decision, so none of those teachers have returned to their jobs or received any payments.
“These workers absolutely did win reinstatement and back-pay,” Sujata Gibson, the teachers’ attorney told The Defender. “Unfortunately, in New York State courts, the government is entitled to an ‘automatic stay’ of any such relief pending resolution of the appeal.”
Gibson also said:
“CHD [Children’s Health Defense] is supporting us in our fight to defend these wins on appeal, and we are pursuing additional options to try to speed this process up and secure relief for additional plaintiffs. But the fight is not over yet.”
Nearly 7,000 New York City Department of Education (DOE) workers who sought religious accommodation from the COVID-19 vaccine mandate in 2021 were denied based on standards that a federal court later ruled unconstitutional.
The suit also sought class-action certification for all DOE workers who were denied religious exemptions. Judge Ralph Porzio denied the motion to grant class status, a ruling the plaintiffs are appealing.
Regardless, Gibson said the decision was “a precedent-setting victory, and a watershed moment in the teachers’ fight.”
Thousands of workers were subjected to the very same processes the judge ruled were “arbitrary and capricious,” and they could sue individually based on that precedent, if it is upheld by the appeals court, Gibson said.
Michael Kane, one of the plaintiffs and a member of Teachers For Choice, told The Defender that after filing the appeal, the city has six months to take the next step in the case — so even though they won with the last ruling, the fired teachers will have to continue to fight for their rights and the relief they are entitled to.
The struggle continues, despite confusion on social media
Last week, a Fox News story from Oct. 25, 2022, “New York Supreme Court reinstates all employees fired for being unvaccinated, orders backpay” was picked up and celebrated on social media by influential figures and their followers. It circulated on X, formerly Twitter, and Instagram, where hundreds of thousands of social media users “liked” the posts, Kane said.
The story itself was vague — it did not cite the actual case that had been ruled on and it gave the impression that all New York City workers fired for refusing vaccination would be returning to work with back pay.
In fact, the story was posted after the state’s Supreme Court ruled in favor of plaintiffs George Garvey and 15 other New York City Department of Sanitation employees who were fired by the city for non-compliance with the mandate.
That historic ruling was applicable not only to the 16 workers who sued but also to all public employees in New York City, including the police and fire department.
But in that case, the city also appealed the ruling and the appeals process is ongoing.
New York City workers, with substantial public support, continue to fight, Kane said.
He added:
“This isn’t just for us, it’s for our kids and our grandkids. This is laying the groundwork. It took over 50 years for Plessy v. Ferguson to be overturned by Brown v. Board of Education. Civil rights battles are long, protracted struggles, and that’s what we’re in. It’s not fun, but that’s what we’re in.”
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
What is “shedding” and what are the implications for our health? Tonight, host Betsy Ashton will be joined by Dr. Pierre Kory and Scott Marsland, FNP-C for this important discussion.
My clinical practice is loaded with patients who took one or two vaccines early in 2021 and realized like most of us that the the mRNA products were not safe. A common question is: “doctor when does this shot get out of my body?”
Acevedo-Whitehouse and Bruno raise this point in a recent peer reviewed publication concerning the entire mRNA vaccine product pipeline.
Therapeutic applications of synthetic mRNA were proposed more than 30 years ago, and are currently the basis of one of the vaccine platforms used at a massive scale as part of the public health strategy to get COVID-19 under control. To date, there are no published studies on the biodistribution, cellular uptake, endosomal escape, translation rates, functional half-life and inactivation kinetics of synthetic mRNA, rates and duration of vaccine-induced antigen expression in different cell types. Furthermore, despite the assumption that there is no possibility of genomic integration of therapeutic synthetic mRNA, only one recent study has examined interactions between vaccine mRNA and the genome of transfected cells, and reported that an endogenous retrotransposon, LINE-1 is unsilenced following mRNA entry to the cell, leading to reverse transcription of full length vaccine mRNA sequences, and nuclear entry. This finding should be a major safety concern, given the possibility of synthetic mRNA-driven epigenetic and genomic modifications arising.
These are stunning revelations. I have called for a halt on mRNA research development until these fundamental questions can be answered. If synthetic mRNA cannot be broken down by the human body, there were be no way to shut off potentially dangerous antigens such as the Spike protein of SARS-CoV-2, Influenza virus hemagglutinin (HA), or any other toxin produced from the genetic code. To make matters worse, it appears that all of these proteins will be expressed on the cell surface and cause auto-immunity with any new mRNA vaccine. This alone is a show stopper for me in my practice. I am advising NO mRNA vaccines for my patients.
The following fictional story may or may not bear resemblance to events in real life.
Imagine, if you will, that you are a first-generation high tech gazillionaire. In fact, at one time you were said to be the richest man on earth, although that is no longer the case. Nevertheless, you remain unimaginably wealthy, with all the responsibilities and burdens that such wealth brings. (Given the extremely unusual circumstances of this tale, to make it more relatable, we will assign you a fictional name.) Your birth certificate reads Gilbert Harvey Bates III, but the world knows you as Gil Bates.
Gil Bates’s erstwhile net-worth preeminence (stolen as it was by an upstart online retailer named Biff Jezos) is not the only important loss he has suffered. Also in the rearview mirror is his youth, his marriage, and his position as CEO of the behemoth tech company he created, MacroHardTM.
After Gil Bates stepped down as CEO of MacroHardTM, he focused on his philanthropic work. The centerpiece of this work is the immensely well-funded (and therefore immensely influential) Bates Foundation. The Foundation’s scope may be mind-bogglingly broad, but one problem especially consumed Bates: there are far too many people on the planet.
In his youth, Gil Bates read a controversial book called The Overpopulation Bomb, written by a visionary scientist named Saul Derelicht. That alarming book, a huge bestseller in its day, described a neo-Malthusian hell on earth resulting from human overpopulation, and proposed mass sterilization and other aggressive population reduction techniques as the solution.
Gil Bates became convinced, and remains convinced – especially as the worldwide human population has soared beyond 8 billion units – that Homo sapiens have obscenely overpopulated the planet. Once Bates had sold software packages to the great majority of them, he vowed that this existential threat to the planet must be addressed.
But what was to be done? How could this great affront to Gaia be reconciled? When it comes to a responsibility so great, a task so immense, no single man – not even Gil Bates – could hope to accomplish it alone.
Fortunately for the future of Earth, Bates knew a host of like-minded, enlightened elites, pre-eminent individuals of great wealth, power, and worldwide influence. Among the most important:
A dour Teutonic economist named Kraut Schlob. The son of an ambitious industrialist who built flamethrowers for the Third Reich, Schlob is the founder and chairman of the World Enslavement Forum. The Forum has become the premier worldwide gathering of hyper-elites who wish to discuss globalist policies, and enjoy the company of high-end prostitutes, free from the prying eyes of commoners.
An immensely powerful – if embarrassingly vertically challenged – American health bureaucrat named Dr. Fantoni Auci. For decades, Dr. Auci controlled the overwhelming majority of US Government medical research funding. As such, no one in the vast American network of hospitals, research institutes, or universities dares to cross Dr. Auci, and he wields similar influence internationally. In fact, he oversees funding for multiple secret virology research laboratories, as far away as China.
A mysterious veterinarian named Adalbert Ghoula. Ghoula is the CEO of Kaiser, Inc., the world’s largest and most rapacious pharmaceutical company, which Ghoula has grown into a veritable modern day IG Farben. In his earlier days, Ghoula oversaw the development of a vaccine that successfully induces the chemical castration and sterilization of swine.
The consensus, reached after lengthy consultations with these men and other luminaries, was that the worldwide human population must be reduced from 8 billion to 500 million units.
But how? Several possible avenues were proposed.
War has been used for millennia to reduce populations, and while highly effective locally or regionally, it would be entirely ineffective at removing the necessary fifteen-sixteenths of people on Earth. After all, the deadliest war in history, World War II, resulted in a mere 80 million deaths, just 3 percent of the world’s population at the time.
The use of a bomb was considered a special kind of bomb, reminiscent of the “neutron bomb” of yore, which would supposedly reduce populations while sparing infrastructure. This seemed closer to the mark than all-out war, but ultimately it was determined that setting off bombs would be both impractical and far too obvious. After all, even herd animals will not consent to being openly and massively slaughtered, no matter how necessary the culling may be. The herd must be kept forever in the dark.
A plague, a pestilence, a pandemic seemed more promising. Past naturally occurring pandemics had reduced human populations much more successfully than wars. The Black Death of 1346-53 may have reduced the world population by as much as 25 percent, a much more encouraging number than the measly 3 percent from World War II. As an added economic bonus, the Black Death served as a very effective concentrator of wealth for the survivors, as it caused minimal collateral property loss.
However, a more detailed review of historical worldwide population estimates demonstrated that a pandemic alone could only serve as a temporizing measure at best. Most estimates show that by 1400, the worldwide population had unfortunately returned to its pre-plague total.
Clearly, the necessary 94 percent reduction in population could not be achieved by culling the herd alone. Sterilization would be needed as well. But how to achieve such mass sterilization? Many H. sapiens possess an intense desire to procreate – that’s the source of the problem, after all. Unfortunately, prior historical initiatives for mandatory sterilization – even those of limited scale and scope, such as those targeting the mentally deficient – have met great opposition, at least in the so-called “free” nations.
However, a vaccine could be used for mass sterilization. Ghoula’s earlier work at Kaiser was proof of this. But a fundamental problem remained: how to get the unsuspecting population – specifically, its children and young adults – to take the stealth-sterilizing inoculation?
The solution, when it came, was a thing of beauty, sublimely subtle and symmetrical. The answer was a two-step process: a pandemic and a vaccine. One population reduction device would be released, presented as a worldwide plague. It would be followed by a second population reduction device, presented as the cure.
And the technology was already in place to make it happen. It merely had to be perfected, then enacted.
Employing the Black Magic of gain-of-function virology research, an animal respiratory virus, previously never infecting humans, was genetically engineered to readily infect and spread amongst humans. At a key moment in political history, when a particularly bothersome populist American President named T. Ronald Dump was running for reelection, the virus was released from a Chinese laboratory into the human population.
As the new virus spread, reports of the death and devastation it wrought were spread as well. In actuality, the virus had been engineered so that it was deadly only to the frail, chronically ill, and very old. It was cleverly propagandized, however, as a threat to persons of all ages, a modern day Black Death of sorts.
The US deep state, desperate to disrupt the Dump presidency and remove him from office, were willing partners to manage the control and manipulation of the population through propaganda, and to enforce unprecedented, prolonged lockdowns of society. Remarkably, they even convinced President Dump to sanction the lockdowns, and to fund the development of the vaccine. Most other countries followed suit.
The new virus rapidly killed off many of the oldest and sickest members of society, as would be expected of a novel respiratory virus. However, the locked-down and isolated populations were barraged with media messages that stirred up mass terror of the virus. Businesses were closed, save for those deemed “essential.” Schools were closed, though children were already known to be at statistically zero risk of death. Dissenters were harassed, scapegoated, and punished.
Then, a solution to the pandemic was presented: the vaccine. The vaccine was the savior, the only way out of this crisis.
A few irritating, contrarian dissenters fought back. They protested for civil rights. They stressed the near impossibility of producing an effective vaccine against a rapidly mutating respiratory virus. They identified numerous “safety signals” found in the vaccine trials, and tried to expose these as best they could. But the mainstream media drowned them out, the social media companies (controlled by the deep state) censored them ruthlessly, and after all, once the vaccines were mandated, most people took at least a couple of doses.
And the joke was on the dissenters in another, more important respect. These meddlesome do-gooders were indeed intelligent enough to identify the toxicities inherent in the vaccines. But they decried them as “safety signals.” The fatal toxicities they identified still seemed to them to be flaws, mistakes, and the unfortunate results of a hasty and mad rush to make money off of the pandemic.
Imagine the naïvete.
Early in the vaccine “rollout,” young women reported abnormal vaginal bleeding and other menstrual problems after receiving the vaccines, raising concerns about potential unintended consequences to female reproduction. Pathologists found ovaries infiltrated with multiple toxins from the vaccines, both the dreaded “spoke” protein of the virus and “lucid nanoparticles” from the vaccine’s delivery system. Even occluded Fallopian tubes were identified.
Soon thereafter, reports appeared in the alternative media of dramatically increased numbers of sudden deaths, primarily in young men, after receiving the vaccine. It often visibly occurred in athletes while on the playing field. This caused considerable alarm, impossible as it was to hide.
In a masterful demonstration of the “limited hangout,” officials acknowledged the sudden death phenomenon, but would not even allow mention of the vaccine as a possible cause within the mainstream medical community. Instead, protocols and clinics for this sudden epidemic of heart disease in the young were established, but strangely without any official curiosity as to the cause. All they knew for sure was that it couldn’t be the vaccine.
Of course, the infamous “spoke” protein, the same viral antigen chosen by the vaccine’s designers to induce the vaccinated patient’s body to produce in quantity, just happens to be the most toxic part of the virus. The “spoke” protein deposits itself in tissues throughout the body, wreaking havoc wherever it goes. It has a particular affinity for the heart muscle, causing the inflammatory process known as myocarditis that leads to cardiac arrests.
“Spoke” doesn’t stop with the heart, however. It is a remarkably versatile toxin, a sort of Swiss Army monkey wrench in the human body. It causes gigantic, gruesome, rubbery blood clots in the vasculature, seizures in the central nervous system, the aforementioned deposits in ovaries and Fallopian tubes (and testes, for that matter), etcetera, etcetera. What a stroke of genius to choose “spoke” as the antigen the vaccines induce replication of!
The vaccines held another nasty little secret, which even the pathetic, naïve resistance only recognized much later. The vaccines were “contaminated” with plasmids containing MV-40 and MV-40-like DNA sequences. Yes, that MV-40, the monkey virus known to cause cancer in multiple animal species.
Could the appearance of so-called “turbo cancers” in vaccinated persons somehow be related to this “contamination?” Well, another limited hangout, this time courtesy of Healthcare Canada, took care of that.
Excess death rates rose dramatically after the vaccine rollout. Birth rates plummeted. To the do-gooders, refuseniks, and dissidents, this was a scandal.
But what did they know? To use a phrase all-too-familiar to the seasoned software developer, these toxicities were not bugs, but features. The vaccines were working exactly as they were supposed to work.
Silly plebes! The “vaccines” were actually a deliberate, multi-pronged, population reduction device. They were designed to kill a percentage of young people – mostly male – outright, to poison and disable the female reproductive system at multiple points, and to insert teratogenic plasmids into recipients’ cells, to pick off others at undisclosed, later dates. They were merely packaged and marketed as a vaccine against a (lab-manufactured) flu-like illness.
As successful as they have been, there remains so much more work yet to be done.
A definite lull occurred in the population’s acceptance of repeated injections of the vaccine. The dissidents may be naïve, but they are persistent, and sometimes effective to a degree. But ultimately they will fail.
The general population is lazy, uneducated, and easily terrified. (Some say they are being done a favor by being culled.) They are accustomed to the precedents set by other vaccines. Their reluctance will be worn down with time. Of course respiratory viruses are imperfect targets for vaccines. Once again, that’s not a bug, it’s a feature! It only means that a new booster of the vaccine will be needed every year – at least.
With each new round of boosters, a new population of girls and young women will be rendered infertile. A new group of boys and young men will suffer cardiac arrest – a very quick and painless way to die, really.
Countless others will contract cancers – turbo cancer, to use the current term for these rapidly progressing and deadly malignancies, often of unusual types – bone cancers, muscle cancers, and other former rarities. Not an easy way to die, admittedly. But these tumors mercifully progress to end stage very swiftly, and their value as a population reduction device is undeniable.
Have no fear. It is only a matter of time; only a matter of lather, rinse, repeat. As long as the herd allows itself to be sent through the sheep dip whenever and however often the shepherds proclaim is necessary, H. sapiens will get to 500 million. All courtesy of a type of bomb after all, but in this case a microscopic bomb that is released in each person via a tiny little injection: The Depopulation Bomb.
Happy Halloween!
C.J. Baker, M.D. is an internal medicine physician with a quarter century in clinical practice. He has held numerous academic medical appointments, and his work has appeared in many journals, including the Journal of the American Medical Association and the New England Journal of Medicine. From 2012 to 2018 he was Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester.
Dr Keith Berkowitz is a founding member, with Dr Pierre Kory, of the Front Line Covid-19 Critical Care Alliance (FLCCC). He is treating a lot of vaccine-injured patients at his practice in midtown Manhattan. Dr Berkowitz was kind enough to answer a few questions on the Covid vaccine and the vaccine injured.
***
Who is most at risk for vaccine injury?
One thought is that if someone had Covid first, and then got the vaccine after being sick, the rates of vaccine injury were higher because they already had an antibody response, their immune system was already revved up, and then they got an injection of another antigen. Another group I see is people with autoimmune disease, they seem to be more triggered. I have several cases of people who had dormant autoimmune disease, such as ulcerative colitis and rheumatoid arthritis, and post vaccine it got retriggered. What people forget about vaccines is that they have an immunosuppressive effect. So in that two- to three-week period, the immune system takes a hit, which makes the body vulnerable to other illnesses. The third group I see that are most at risk of vaccine injury are people with high histamine levels.
What are the most common symptoms of vaccine injury?
Mildest is probably loss of taste and smell, mild digestive issues, or a cough. More severe are the autoimmune responses, the neurological symptoms, like brain fog, and tinnitus (which is one of the toughest to treat), myocarditis and pericarditis (inflammation of the heart), cancer, which I would call the most severe.
Is that new cancers, or cancers that have returned?
I’m seeing both.
Which autoimmune diseases are you seeing?
First, autoimmune disease is what I’m seeing most in vaccine injury. Specifically thyroid disease, more than anything else. What’s interesting is that I’m seeing normal thyroid function, and positive thyroid antibodies. So typically we wouldn’t check for thyroid antibodies if thyroid function was normal. So that group is often missed for that reason.
Would you say any vaccine was worse than the others?
It seems to be batch-related. That’s the question. There’s a theory that 10 per cent of the batches, roughly, caused 90 per cent of the issues. If you look at the original technology, the mRNA was created at a 70 per cent purity. There’s speculation that, because of manufacturing issues, they weren’t able to create that level of purity, and achieved only 50-55 per cent purity. So does one really know if that level of purity works? Especially being that it was never tested.
Why is there so much denial around vaccine injury?
I think there was a blind trust of the government and the pharmaceutical companies, coupled with a fear aspect of Covid (remember people thought that 50 per cent of hospitalised Covid patients died, when it was more like less than 1 per cent). Fear made people not think any more, and now they’re in denial about the choice they made. Another thing I can’t figure out: If you’re vaccinated, how does an unvaccinated person put you at risk? Also, why did doctors not do their own research? It was blind faith. Medications all have side effects – why was this one different?
How do you respond to the proponents of the vaccine who say, regarding vaccine injury, correlation is not causation?
That’s true, but why are they not even looking into it? If they are so confident, then just study it. What do they have to lose? Why not disprove it? Why is disproving it a major issue for them? If you don’t agree with me, prove me wrong.
Traditionally, vaccines take 10-15 years to get approval, because all that time they are studying long-term effects. The Covid vaccine, which was administered as soon as it was created, is still only about three years old. Therefore, have we yet to see the potential damage it can cause?
Absolutely. Do you know what percentage of drugs approved by the US Food and Drug Administration are withdrawn within five years? 31 per cent. One out of three drugs are taken off the market within five years. That’s incredibly high. That tells me we’re not checking properly. Now with this vaccine, one of my biggest questions is why did we decide to use new technology? Is a pandemic the right time to test new technology? I would argue probably not. And why did some countries around the world, like China and Russia, not use this technology? And at the end of the day we have to ask, was the treatment worse than the problem? And should medical products be tied to financial incentives? That creates a huge conflict. There were incentives to use the vaccine. If a drug or a treatment was really that good, would you need to push it like that?
Any final comments?
This is going to take years to figure out. It isn’t going away any time soon. I feel bad for the people who took something which they thought they were doing for the right reason, and now they are suffering. And they’re not being helped. Why does the government create a long Covid initiative, but not a vaccine-injured initiative? Why are we ignoring these patients? And why are we [in the US] approving a product for over six-month-olds when other countries are saying over 65 years? Another thing that doesn’t make sense is a study on teenagers showed that we have to vaccinate a million young men to prevent one hospitalisation. And the potential in a million doses is 1,000 with side effects. So the hospital to side effect rate is one to a thousand. It doesn’t make any sense! My worry is the trust in the medical system may never come back. And I’m not sure that it’s not deserved.
Sen. Ron Johnson (R-Wis.) accused federal public health agencies of displaying an “appalling” lack of transparency with the American public during the pandemic, depriving them of “the benefit of informed consent.”
In a letter sent Oct. 25 to the heads of the U.S. Department of Health and Human Services, the U.S. Food and Drug Administration (FDA), the Centers for Disease Control and Prevention (CDC) and the National Institutes of Health, Johnson said that even now, “As new and alarming information continues to come to light, federal health agencies continue to stonewall and gaslight Congress and the public.”
The lawmaker pointed to an FDA-funded study published this month that identified a potential safety signal linking mRNA COVID-19 vaccines to seizures in children ages 2-5.
Johnson questioned whether the CDC was aware of these findings last month when it recommended everyone 6 months of age and older be vaccinated to protect against COVID-19 this fall and winter.
As a result, they “have not even come close to ensuring that doctors can provide informed consent on a new gene therapy masquerading as a ‘vaccine’ that was rushed to market without adequate safety or efficacy testing,” he said.
In his letter, the lawmaker wrote that the agencies’ refusal to respond to the “vast majority” of his questions and information requests “only heightens [his] level of suspicion.”
He listed over a dozen letters he sent requesting information on the COVID-19 vaccines that the agencies “have failed to adequately address.”
These included requests for data about vaccine lots linked to high rates of adverse events, information suppression on social media and the Countermeasures Injury Compensation Program.
Johnson listed 11 other outstanding requests he made regarding the other aspects of the pandemic.
But these make up only a partial list of over 60 public letters Johnson said he has sent to government agencies concerning various aspects of the pandemic.
“It is well past time for U.S public health agencies to be transparent,” he said.
Johnson requested the agencies respond by Nov. 8 to questions about what they knew about the risks COVID-19 vaccines posed to children, when they knew it and how they plan to address those issues.
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
Dr. Kulvinder Kaur Gill is a pediatric allergist in Toronto. She condemned COVID rules as irrational, political, harmful, and inconsistent with scientific data. In the eyes of the College of Physicians and Surgeons of Ontario (CPSO), Gill was dangerous.
In 2021, the CPSO issued three “cautions” (formal warnings) against her. In 2022 it began disciplinary proceedings. The College alleged that she was undermining confidence in public health measures. Its senior counsel wrote that her communications were unprofessional and unbalanced. In its persecution of Gill, the CPSO has made the case for its own demise. Self-regulated monopolies do not work. The CPSO and other professional regulators need competition.
Gill’s inquisition was not an isolated case. Like other medical regulators in North America, the CPSO forbade its doctors from publicly contradicting COVID orders and recommendations. Its Discipline Tribunal revoked the licence of Patrick Phillips, one of several Ontario doctors pursued for their COVID dissent.
The Nova Scotia medical college investigated Dr. Chris Milburn for writing an op-ed on the death of personal responsibility in the criminal justice system. The Ontario College of Psychologists ordered Jordan Peterson to undergo re-education on the use of social media for tweeting about politics. The BC College of Nurses seeks to discipline Amy Hamm for believing in the biology of two sexes.
The Law Society of Ontario compelled its members to state their concurrence with the ideology of “equity, diversity, and inclusion” until a group of rebel lawyers (of whom I was one) managed to repeal it, although the agenda remains. In British Columbia and Alberta, law societies are instituting politically laden “cultural competency” requirements. Teachers, occupational therapists, engineers, and accountants cannot safely voice doubts about transgenderism or “anti-racist” agendas.
This regulatory bullying is occurring within self-regulated professions. Like “ordinary” regulation, self-regulation is coercive. The state delegates authority to their governing bodies. Some doctors rule over other doctors. A licence from the CPSO is voluntary only in the sense that a driver’s licence is voluntary. You don’t get fines or prison time if you don’t get one, but then you can’t drive or practice medicine. Gill’s livelihood was on the line.
Civil servants do not run self-governing professional bodies, but they are part of the executive branch of government nonetheless. Legislation creates them and they are subject to the constitution. Self-regulation exists only for as long as the legislature says that it does.
Legislatures delegate authority, the theory goes, because professionals have the expertise to ensure competence and ethical practice in the public interest. Your surgeon should know how to cut. Your corporate lawyer should be able to draft articles of incorporation and not skim funds off your trust account. But focusing on technical competence and honest conduct no longer satisfies professional regulatory bodies.
We live in a managerial age. As C.S. Lewis wrote:
“The greatest evil is not now done in those sordid ‘dens of crime’ that Dickens loved to paint. It is not done even in concentration camps and labour camps. In those we see its final result. But it is conceived and ordered (moved, seconded, carried, and minuted) in clean, carpeted, warmed, and well-lighted offices, by quiet men with white collars and cut fingernails and smooth-shaven cheeks who do not need to raise their voices.”
Professions have become managerial cartels. Governing bodies are their godfathers, permitting only proper people and perspectives. Their purpose is not to ensure public access to a variety of professional opinions. Instead, they seek to herd people into “correct” attitudes and behaviors. Propaganda is not evil, but merely a tool to facilitate right results.
Ironically, managerial cartels turn out to be terrible managers. They excel at exercising control but not at producing good outcomes. During COVID, even propaganda was patently incoherent. Yet Gill was one of a scant few doctors and scientists to decry the public health debacle unfolding in front of them. As her lawyer Lisa Bildy wrote in response to the College’s accusations, Gill provided the public with substantiated facts on lockdowns, masking, and COVID vaccines, relying on credible and respected scientific sources and opinions.
The College had scheduled a two-week disciplinary hearing for early 2024. But in September 2023, it abruptly cancelled the hearing with no explanation. Gill’s disciplinary ordeal had come to an end, although her formal warnings remain. Bildy will challenge their validity by judicial review in spring 2024.
Self-regulation protects professions from government interference. That is ironic, given the CPSO’s insistence that their members toe the government line. But self-regulation does not protect individual professionals from the oppression of their peers. A different model beckons: multiple, private regulators competing for members, credibility, and public trust.
Professional cartels benefit the bullies who run them. There’s no reason to grant them the power of monopoly.
Bruce Pardy is executive director of Rights Probe and professor of law at Queen’s University.
Dr. Malik writes:
My name is Ahmad Malik and I am an honest surgeon passionate about free speech and medical ethics.
I have been suspended without pay and cancelled because I dare to challenge the Government narrative, defend informed consent, oppose mandates and lockdowns, question experimental jabs and insist that there are only two biological sexes.
I am raising funds to take legal action against the hospital to lift my suspension and stop the attempts by organisations to censor me.
It will set a precedent that organisations cannot bully, harass and censor those that speak up for medical ethics, and encourage others to speak out.
I am up against large organisations and my case is complex. Legal costs will easily run into the thousands. I need a decent fighting fund which will give me the best chance of being successful.
Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product.
The vaccine makers also failed to account for a large number of subjects who dropped out of the trial.
The authors of the paper described it as a “forensic analysis,” defined by the U.S. National Institute for Standards and Technology as “the use of scientific methods or expertise to investigate crimes or examine evidence that might be presented in a court of law.”
What the analysis shows
Corinne Michels, Ph.D., retired distinguished professor of biology at Queens College, New York, led the DailyClout Pfizer/BioNTech Documents Investigations Team on what the authors claim was the first independent examination of original data from the Pfizer-BioNTech COVID-19 mRNA vaccine (BNT162b2) clinical trial.
Investigators looked at each of the 38 deaths occurring between July 27, 2020, the start of phase 2/3 of the Pfizer-BioNTech vaccine trial, and March 13, 2020, the end date culminating in Pfizer-BioNTech’s 6-month interim report.
This trial phase involved 44,060 subjects. Half received a dose of BNT162b2, half got a placebo consisting of an inactive sterile salt solution.
The trial was unusual because at week 20 after the FDA issued the EUA for the vaccine, trial subjects in the placebo group were allowed to switch to the vaccinated group and receive their first BNT162b2 shot.
Switching from the placebo to the vaccinated group — or “unblinding” — normally occurs when the benefit of the drug is so great that not treating subjects becomes unethical. For example, investigators might consider unblinding a cancer trial if at some point all untreated patients deteriorated or died but all treated patients improved.
Unblinding conditions may be specified in the study design, but they usually involve input or review from medical ethicists.
Of 20,794 unblinded placebo subjects in the Pfizer trial, 19,685 received at least one dose of BNT162b2.
Normally the decision to unblind a vaccine trial would be based on the product’s safety and effectiveness in reaching certain endpoints or objectives. Endpoints for a drug to prevent viral infections might be a positive test or self-reported COVID-19 illness (the “case” numbers that drove much of COVID-19 policy), illness requiring hospitalization or death.
But, perhaps unexpectedly, after 33 weeks the data revealed no significant difference between deaths in the vaccinated and placebo groups for the initial 20-week placebo-controlled portion of the trial.
After week 20, after most former placebo subjects had received the vaccine, deaths among those in the vaccine group continued unabated.
The authors revealed “inconsistencies” between data presented in Pfizer-BioNTech’s 6-month interim report and subsequent publications by Pfizer-BioNTech trial site administrators:
“Most importantly, we found evidence of an over 3.7-fold increase in the number of deaths due to cardiac events in the BNT162b2 vaccinated individuals compared to those who received only the placebo.”
This means that 79% of relevant deaths were not recorded in time to be included in Pfizer’s regulatory paperwork.
By not including relevant subject deaths in the case report, Pfizer obscured cardiac adverse event signals, allowing the EUA to proceed unchallenged.
How did Pfizer get around legal, ethical obligations?
The Pfizer-BioNTech data, obtained through a Freedom of Information Act lawsuit, uncovered four additional deaths in the vaccine group and one more in the placebo group — but Pfizer failed to include these data in their FDA submission despite an explicit study design requirement to do so.
These data, and how they differ from what Pfizer-BioNTech reported in their applications, are summarized in Table 3 of Michels’ study.
One case involved a 63-year-old woman who died 41 days after receiving the shot, but whose death only entered the data pool 37 days later. Another was a 58-year-old woman whose death 72 days after vaccination went unreported for 26 days.
Had Pfizer-BioNTech met their legal and ethical obligation to report all serious adverse events their data would have shown equal deaths in placebo and vaccine groups — which would have shown no clear benefit for the vaccine.
How were they able to skirt those obligations?
For one, they were able to hide behind the the 2005 Public Readiness and Emergency Preparedness (PREP) Act, which provided an almost impenetrable liability shield for vaccine manufacturers for “medical countermeasures” in response to any “public health emergency.”
Second, because COVID-19 was viewed as a national health emergency, regulators abandoned the established, patient-centered, safety-based approval process requiring years of preclinical animal testing — and Pfizer-BioNTech unsurprisingly went along.
Timing of death reports raises questions
Michels also raised issues regarding total death reports and their timing.
Since the death total from both study groups, 38, appeared “surprisingly low” to study authors — particularly during a pandemic — they undertook their own analysis based on population mortality expectations at the time.
Assuming that age-adjusted death rates for the study subjects were similar to those of the general population, they estimated that 222 subjects should have died from July 27, 2020, to March 13, 2021. The reported number, 38, is just 18% of the expected number.
Michels explained this by the large number, 4.2% of “discontinued subjects.” The most concerning of these were subjects “lost to follow-up,” which means missing scheduled visits or other required activities.
Pfizer-BioNTech tried to reach these subjects via phone, certified mail or through their emergency contact but despite their efforts could not account for 395 subjects who had dropped out.
The authors wrote:
“These are not insignificant numbers and could easily account for the low number of deaths reported in this safety period of the trial. Given the importance of knowing the status of each trial subject, there should have been greater effort to locate these individuals.
“Additionally, Pfizer/BioNTech was responsible for oversight of the trial sites. Sites with excessive numbers of lost to follow-up should have been evaluated for performance.”
Michels was also concerned over how certain trial centers had many dropped-out subjects while others had none or just a few.
Ninety-six of 153 trial sites (63%) reported 0 or 1 subjects lost to follow-up and 34 (22%) reported 2-5 dropouts. But four sites reported more than 20 subjects lost to follow-up, amounting to about 5% of all trial subjects.
Since the vaccine makers were responsible for trial site oversight, the authors wrote, “Sites with excessive numbers of lost to follow-up should have been evaluated for performance.”
Finally, based on the data, it appears Pfizer-BioNTech was in no hurry to enter death reports before the EUA submission deadline, particularly for the BNT162b2 group.
Of the 38 reported deaths only one case was added on the day the subject died. Delays of 20+ and 30+ days were common.
One death took 72 days to find its way into the database, and all were entered as occurring on the reporting day, not on the actual date of death.
Of the eight subjects in the vaccine group that should have been reported by Dec. 10, 2020, the EUA application cutoff, the average reporting delay was 17.5 days for subjects in the vaccine group, but just 5.9 days for deaths among subjects in the placebo group.
Angelo DePalma, Ph.D., is a science reporter/editor for The Defender.
Many COVID vaccine skeptics reported an unusual number of “sudden deaths” happening lately.
Such reports are always dismissed as “biased.” And, perhaps, they are biased. I have to admit that I am biased, too, and that keeps me from blaming Covid vaccines for various isolated incidents that I know of.
However, we now have Peter Hotez, one of the most rabid Covid vaccine promoters, unwittingly join the “reporting unusual sudden deaths” club.
Professor Hotez’s today’s tweet laments the sudden passing of his “close colleagues and friends.” Peter mentions that they were “still active when they passed,” so he means sudden deaths.
His suddenly deceased friends were “champions of global health”; tireless Covid vaccine advocates like himself. Professor Hotez is not sure what to blame. Overwork? Exhaustion? – he asks.
I am also not sure; perhaps it is climate change or stress his friends experienced from seeing vaccine misinformation online.
The following translation was performed free of charge to protest an injustice: the destruction by the ADL of Ariel Toaff’s Blood Passover on Jewish ritual murder. The author is the son of the Chief Rabbi of Rome, and a professor of Jewish Renaissance and Medieval History at Bar-Ilan University in Israel, just outside Tel Aviv.
Dr. Toaff is uniquely qualified to write this book, being thoroughly familiar with the derivative literature in English, French, German and Italian, as well as the original documentary sources in Latin, Medieval Italian, Hebrew and Yiddish. This is not something he worked on in secret. On the contrary, he worked on it openly with his university students and colleagues in Israel for several years; one of his students was even going to publish a paper on the subject. The author is extremely careful about what he says, and his conclusions must be taken seriously. It reads like a detective story.
If it had been published in Israel, in Hebrew, no one would have cared. There are large bodies of literature in Hebrew that Jews do not wish Gentiles to know about. But Dr. Toaff’s announcement of its publication in Italy, in Italian, raised a worldwide firestorm of fury.
Under unbearable pressure, the book was withdrawn from publication. Come in out of the darkness, and strike a blow for the light.
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The following translation was performed free of charge to protest an injustice: the destruction by the ADL of Ariel Toaff’s Blood Passover on Jewish ritual murder. The author is the son of the Chief Rabbi of Rome, and a professor of Jewish Renaissance and Medieval History at Bar-Ilan University in Israel, just outside Tel Aviv.
Aletho News 