HHS/CDC Fund Online Game ‘Bad Vaxx’ to ‘Psychologically Inoculate’ Vaccine Resistance
Ironically, the game uses the very techniques it claims to train users to detect.
By Jon Fleetwood | December 27, 2025
U.S. taxpayer funds are being used by federal health agencies to develop and test online psychological games designed to condition how people—especially younger audiences—interpret and respond to vaccine skepticism.
An August Nature Scientific Reports study reveals that the project was funded by the Centers for Disease Control and Prevention (CDC) under the U.S. Department of Health and Human Services, through a CDC award administered by the American Psychological Association.
The paper states that the funding totaled “$2,000,000 with 100% funded by CDC/HHS.”
The grant supporting the project is titled “COVID—INOCULATING AGAINST VACCINE MISINFORMATION,” award number 6NU87PS004366-03–02.
That award has already handed out over $4.3 million in taxpayer funds since its activation in 2018.
The project language mirrors the study’s conceptual framework: dissent is treated as exposure to a pathogen, and resistance to dissent is treated as immunity.
The government-funded study centers on the creation and evaluation of an online game called Bad Vaxx.
According to the authors, the purpose of the game is not to examine disputed vaccine claims or to compare competing evidence, but to reduce what they define as “vaccine misinformation” by shaping how players cognitively process vaccine-critical content.
This is despite the CDC’s own VAERS data confirming over 2.7 million injuries, hospitalizations, and deaths linked to vaccines since 1990.
The study authors explain their premise at the outset:
“Vaccine misinformation endangers public health by contributing to reduced vaccine uptake.”
From this premise, the study moves directly to intervention design.
“We developed a short online game to reduce people’s susceptibility to vaccine misinformation.”
The paper frames this approach as a form of psychological prevention, borrowing language from immunology rather than education or debate.
“Psychological inoculation posits that exposure to a weakened form of a deceptive attack… protects against future exposure to persuasive misinformation.”
The Bad Vaxx game operationalizes this concept by training players to recognize four specific “manipulation techniques”: what it refers to as emotional storytelling, fake expertise, the naturalistic fallacy, and conspiracy theories.
These techniques are treated as characteristic of vaccine misinformation as a category.
“The game trains people to spot four manipulation techniques, which previous studies have identified as being commonly used in the area of vaccine misinformation.”
The study does not include a corresponding examination of whether similar persuasive techniques may be used in vaccine-promoting messaging, government communications, or pharmaceutical advertising.
Ironically, the Bad Vaxx project itself relies on the same persuasive architecture it claims to neutralize—emotional framing, authority cues, and repetition—embedded in a gamified format designed to shape intuition rather than invite scrutiny.
The classification of “vaccine misinformation” is established in advance and applied only to information critical of injectable pharmaceutical products.
Throughout the paper, vaccine skepticism is framed as a behavioral and social risk rather than as a possible response to uncertainty, evolving evidence, or institutional error.
The taxpayer-funded authors write:
“Susceptibility to misinformation about COVID-19 predicts lower compliance with public health regulations and lower willingness to get vaccinated.”
The choice of a game as the delivery mechanism is emphasized as a strength of the intervention.
The authors repeatedly describe the format as “entertaining,” “immers[ive],” and scalable, highlighting its ability to shape intuition rather than deliberation.
“A practical, entertaining intervention in the form of an online game can induce broad-scale resilience against manipulation techniques commonly used to spread false and misleading information about vaccines.”
Games function by rewarding correct pattern recognition, reinforcing desired responses, and reducing analytical friction.
The study’s outcome measures reflect this design: discernment scores, confidence ratings, and willingness to share content, rather than independent evaluation of claims or evidence comparison.
The researchers also emphasize the potential reach of such interventions.
“The Bad Vaxx game has the potential for adoption at scale.”
This matters because the funding source is not an academic foundation with no policy stake.
The CDC is the primary federal agency responsible for vaccine schedules, promotion, and uptake.
Yet the study does not address how this institutional role shapes the definition of misinformation used in the intervention, nor does it acknowledge the conflict inherent in a public health authority funding psychological tools aimed at managing disagreement with its own policies.
The dystopian nature of the project emerges from the structure itself: state funding, psychological conditioning, asymmetric definitions, and a delivery system designed to bypass debate in favor of intuition.
What the paper documents, in concrete terms, is the use of taxpayer funds to develop and validate a behavioral intervention—delivered through a medium optimized for psychological conditioning—that trains users to reflexively distrust a predefined category of speech, while exempting vaccine-promoting institutions from equivalent scrutiny.
Bill Gates, Pfizer CEO Albert Bourla Ordered to Testify in Dutch COVID Vaccine Injury Lawsuit
By Michael Nevradakis, Ph.D. | The Defender | December 23, 2025
Bill Gates and Pfizer CEO Albert Bourla will have to appear in person in the Netherlands to testify at a hearing in a COVID-19 vaccine injury lawsuit, a Dutch court ruled late last month.
The court order relates to a lawsuit filed in 2023 by seven people injured by COVID-19 vaccines. One of the victims has since died.
The lawsuit centers around the question “of whether the COVID-19 injections are a bioweapon,” Dutch newspaper De Andere Krant reported. In addition to Gates and Bourla, the suit names 15 other defendants, including former Dutch prime minister and current NATO Secretary General Mark Rutte, the Dutch state, and several Dutch public health officials and journalists.
De Andere Krant said last month’s ruling “is a significant setback for the defendants, who are accused of misleading victims about the ‘safety and effectiveness’ of the vaccines.” However, it “remains to be seen” whether the defendants will comply with the court’s order and appear at next year’s hearing.
The defendants may face additional legal challenges in Dutch courts in the new year. A second lawsuit, filed in March by three COVID-19 vaccine injury victims in the Netherlands, presents a similar set of allegations and names the same defendants.
At a press conference last week, Dutch attorney Peter Stassen, who represents the vaccine-injured plaintiffs in both cases, earlier this month petitioned the courts in both cases to hear in-person testimony by five expert witnesses regarding the safety and efficacy of the mRNA COVID-19 vaccines.
According to Stassen, oral hearings will be held in both cases next year, but hearing dates have not yet been scheduled. Stassen seeks to consolidate the cases.
The expert witnesses include:
- Catherine Austin Fitts, founder and publisher of the Solari Report and former assistant secretary of the U.S. Department of Housing and Urban Development.
- Sasha Latypova, a former pharmaceutical research and development executive.
- Joseph Sansone, Ph.D., a psychotherapist who is litigating to prohibit mRNA vaccines in Florida.
- Katherine Watt, a researcher and paralegal.
- Mike Yeadon, Ph.D., a pharmacologist and former vice president of Pfizer’s allergy and respiratory research unit.
Earlier this month, Stassen and the expert witnesses released a series of YouTube videos presenting their evidence and proposed testimony.
Plaintiffs ‘victims of people who unjustly suppress the truth’
Both lawsuits have taken a circuitous path in the Dutch court system.
In October 2024, the District Court of Leeuwarden rejected Gates’ motion to dismiss the case, ruling that it has jurisdiction over Gates and ordering Gates to pay the defendants’ legal fees.
In June 2025, the plaintiffs increased their claims against the defendants and petitioned the court to accept the expert witnesses’ testimony.
On Dec. 7, Stassen submitted written statements and the recorded video statements by the expert witnesses to the District Court of Leeuwarden.
The second lawsuit kicked off in March with an application for preliminary evidence proceedings. In August, the District Court of Leeuwarden denied the application, finding that the plaintiffs lacked standing to seek a preliminary hearing while attempting to join the 2023 lawsuit.
In September, Stassen filed an appeal, alleging that the court did not afford the plaintiffs a fair trial, in violation of the European Convention on Human Rights, and calling upon the court to allow the expert witnesses to testify in court.
During last week’s press conference, Stassen said the plaintiffs — and the broader public — “are victims of people who unjustly suppress the truth.”
“By suppressing the truth, my clients were misled. Had they not been misled, they would not have gotten the COVID-19 shot, a shot that the suppressors of the truth still tout as a safe and effective vaccine to this day,” Stassen said.
Expert witnesses: COVID shots ‘indistinguishable from bioweapons’
During the press conference, Stassen also noted his efforts to have the Dutch courts accept his expert witnesses’ in-person testimony. He said the witnesses intend to present evidence showing that the COVID-19 shots:
- Are “indistinguishable from bioweapons.”
- Offer “no health benefits whatsoever.”
- Are “neither safe nor effective.”
- Were released in the U.S. under emergency use authorization, “a legal status that removes the enforcement of the pharmaceutical law and consumer safeguards by the FDA,” or the U.S. Food and Drug Administration.
- Are “by design, intended to cause the damage described in the package insert and reports as ‘side effects’” — including, “sudden death, heart failure, cancer, and the most horrific diseases.”
- Are a “key component” of the “Great Reset,” “a military project in which NATO plays a significant role.”
In their video statements, the experts questioned the safety of the COVID-19 shots and the global response to the COVID-19 pandemic.
Sansone told The Defender that he and the other expert witnesses are advocating to testify in court, as this “can be more influential” than written testimony.
Sansone said he intends to provide evidence that the COVID-19 vaccines are bioweapons that violate the Biological Weapons Convention and the Biological Weapons and Anti-Terrorism Act of 1989 — the latter authored by late University of Illinois law professor Francis Boyle, Ph.D., an expert witness in the original lawsuit who died in January.
“Governments, healthcare facilities and the media deliberately concealed this information from the public, showing clear criminal intent,” Sansone said in his video.
Latypova told The Defender the lawsuits are the only ones worldwide alleging that “COVID was not a public health event but a government ‘project’ that resulted in mass casualty that can be characterized as ‘genocide,’ or more broadly, ‘democide’ of the population.”
In her statement, Latypova alleged that “military governance and contracting were used to develop, procure, deliver, distribute these shots all over the world” — and to bypass standard regulatory oversight procedures for pharmaceutical products.
“There is substantial evidence of non-compliance with good manufacturing practices, which is the law that governs pharmaceutical purity and honesty in labeling all over the world,” Latypova said.
Watt said the vaccines were a component of a broader effort by political, military and pharmaceutical actors to deceive the public, using the pandemic as a pretext.
“Communicable disease and pandemic threats are political fabrications based on widespread use of intentionally deceptive diagnostic testing devices for the purposes of instilling public fear and justifying vaccination and biodefense programs,” she said.
According to Fitts, global central banks and financial institutions were involved in these efforts. She said the pandemic represented an “egregious misuse of healthcare policies to implement economic and political agendas” with the goal of engineering a “Great Reset” of the global financial system.
Yeadon said that since 2020, he has attempted to warn the public that the COVID-19 vaccines are designed to “lower the fertility [rate] and [people’s health] and reduce population.”
He said that even though he was censored on social media for making such comments, “this is what I have watched happen all around me for five years.”
Pfizer CEO sought to block expert witnesses, dismiss lawsuits
Stassen said that several of the defendants, including Bourla, Rutte and the Dutch state, sought to block the testimony of the plaintiffs’ expert witnesses. Gates was the only defendant who “deferred to the court’s judgment on this point,” Stassen said.
In September, Gates and Bourla submitted written statements of defense.
In his statement, Gates said he does not have any connection to or influence over the policies of international bodies such as the World Health Organization, either personally or through the Bill & Melinda Gates Foundation.
Bourla said the court “has been sufficiently informed and can dismiss the claims without the need to order an oral hearing.”
In a previous statement submitted to the District Court of Leeuwarden last year, Bourla denied that he was liable for the injuries and damages the plaintiffs sustained and maintained that Pfizer’s COVID-19 vaccine is “safe and effective.”
In June, another attorney for the plaintiffs, Arno van Kessel, was arrested “with considerable force,” as part of a nationwide sweep by Dutch police against alleged members of a “sovereign citizen” movement with a “potential intent to use violence” against the Dutch state. He remains confined in a high-security prison.
De Andere Krant reported that earlier this month, van Kessel’s pre-trial detention was extended until February, despite “a complete lack of convincing evidence.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
The vindication (and brutal punishment) of Dr. Reiner Fuellmich
By Stephen Karganovic | Strategic Culture Foundation | December 23, 2025
Alongside the powers that be everywhere, Google’s still anonymous AI is also a pious believer in the virtues of free expression. It proclaims boldly and for all the right reasons that free speech is vital to democracy, in which it also claims to believe. It reminds us also, which is good to know, that freedom of expression promotes an informed citizenry and self-governance and ensures government accountability. Furthermore, that open dialogue and debate facilitate the “marketplace of ideas,” which is a vital condition for social progress and provides society with a much-needed “safety valve.” And finally, that the unhindered right to express one’s thoughts, beliefs, and values without fear is a fundamental aspect of human dignity and self-fulfilment. Amen, amen, amen.
In theory, all would heartily salute those noble sentiments. And that includes even some of their most ruthless violators, such as the German government.
For over a year after kidnapping him abroad, the German government kept prominent German lawyer Dr. Reiner Fuellmich in prison on contrived charges and under extraordinarily harsh and inhuman conditions, which were seemingly designed just to torment him. In Germany, for Dr. Fuellmich at least, the right to express one’s thoughts with dignity (never mind self-fulfilment) in the manner so movingly preached by Google’s AI avatar went out the window many moons ago.
How many are there who still remember who Dr. Fuellmich is and what he stands for, let alone are aware of his current plight?
For those who do not, a brief note is in order. Shortly after the sudden appearance of the Covid affair in 2019, Dr. Fuellmich, a prominent trial attorney from Gottingen, gained public attention by raising sensible questions about the nature and origin of the commotion which was becoming global in scope. Identical questions were on the minds of many, but few were capable of articulating them in legal terms as effectively as he was. Initially, his questions were formulated rather timidly, barely overstepping the unspoken bounds of permissible inquiry. There was nigh a suggestion of any “conspiracy theory” or frontal challenge to the integrity of the system that in a matter of weeks had improvised, for purposes then still unknown, a global health emergency which was the pretext for unprecedentedly comprehensive social disruptions and the imposition of hitherto inconceivable restrictions on elementary human liberties.
As prominent professionals in the medical and other fields began also to sound the alarm and to raise questions from their respective areas of expertise, it became obvious to those who followed Reiner Fuellmich’s public pronouncements that both the direction and tone of the Covid inquiry he and his associates were pursuing were beginning to change. The issues he was now beginning to raise were no longer merely technical. Increasingly, as he dug deeper he was calling into question the bona fides of the political, media, and pharmaceutical intimidation machine that was invoking a supposed pandemic to implement a global lock-down regime, with compulsory mass injection of untested “therapeutic” substances.
Dr. Fuellmich’s basic questions about the “pandemic” are well worth recapitulating:
- “One: is there a corona pandemic, or is there only a PCR test pandemic, specifically, does a positive PCR test result mean that the person tested is infected with COVID-19, or does it mean absolutely nothing, in connection with the COVID-19 infection;
- “Two, do the so-called anti-corona measures, such as the lockdowns, facemasks, social distancing, and quarantine regulations serve to protect the world’s population from corona, or do they serve only to make people panic, so they believe, without asking any questions, that their lives are in danger, so that in the end, the pharmaceutical and technology companies can generate huge profits from the sale of PCR tests, antigen and antibody tests and vaccines, as well as the harvesting of our genetic fingerprints; and
- “Three, is it true that the German government was extensively lobbied, more so than any other government, by the chief protagonists of the so-called corona pandemic? Germany is known as a particularly disciplined country and was therefore to become a role model for the rest of the world, for its strict, and therefore, successful adherence to the corona measures.”
When, compelling as they evidently were, those interrogatories remained ignored in the public arena (whilst Dr. Fuellmich himself was being ridiculed and vilified just for asking) there began a perceptible shift in the scope and focus of his inquiry. His razor sharp legal mind was activated in the highest degree. The Establishment’s stonewalling on mostly softball issues gradually led him to undertake an unsparing in-depth scrutiny of the systemic background of the global Covid affair, fully intending to go to the root of it and leaving no stone unturned. Dr. Fuellmich threw the gauntlet when he announced that he was assembling evidence of crimes against humanity on a massive scale and of sufficient weight to convene a Medical Nuremberg II, with parallel criminal and class action proceedings that he intended to initiate in the judicial system of the United States and also before the European Court of Human Rights.
Dr. Fuellmich had stepped on some very sensitive and hostile toes. Clearly no such lunacy as he was contemplating could possibly be allowed. Plans were laid immediately to derail him by means of one of those shabby, low life operations in which secret services excel. Informants were planted in the target’s immediate circle to snitch on him and under false witness to furnish compromising evidence. A secret indictment (lettre de cachet, as this practice was known under the ancien regime in France and which recently was revived by the Hague Tribunal) for a purported money laundering scheme was duly prepared and German authorities waited for the convenient opportunity to catch their unsuspecting prey. That opportunity presented itself two years ago when Dr. Fuellmich, as a German citizen, appeared on the premises of the German consulate in Mexico (technically German territory, of course) to solicit a routine consular service. There, he was apprehended and promptly packed off to Germany to be disposed of as the German authorities saw fit. The only saving grace is that he was not snuffed and chopped up like the dissident journalist at the Saudi consulate in Istanbul.
Following an unprecedented, almost two-year, pre-trial incarceration under medieval conditions that was seemingly devised especially for him (the old “flight risk” ruse was cited as the official rationale for this harsh measure) in April 2025 Dr. Fuellmich was finally sentenced to three years and nine months in prison on the bogus charges filed against him. On the surface, everything appears neat and proper. Technically, he was condemned for a crime of moral turpitude. His real “offence” against the vindictive globalist Establishment, the irrefutable public exposure of its totalitarian and population-reduction agenda and its corrupt liaison with the nefarious pharmacological mafia and compulsory promotion of its lethal products, was not even alluded to in the course of those proceedings. Yet, while Dr. Fuellmich is rotting in prison, every one of the principal claims for which he actually was imprisoned is now being scientifically corroborated.
The so-called “covid vaccines” are now known to be associated with heart damage, exactly as Dr. Fuellmich and numerous other researchers insistently warned during the “pandemic” (also here). As predicted by Dr. Fuellmich and his research team, a surge of life threatening blood clots has been correlated with the mass injection of untested “vaccines.” There has also been a marked acceleration of deadly cancer conditions. As further evidence of the fraudulence of the “pandemic emergency,” a peer reviewed study has demonstrated that 86% of allegedly PCR-positive “Covid cases” were not even real infections. That had originally been stated by Dr. Fuellmich, to widespread derision at the time. It is a fact that dismantles the scientific foundation used to justify lockdowns, social distancing, and vaccine mandates. And perhaps the most damning fact of all, Japanese scientists have demonstrated that contrary to disinformation about infected bats and unsanitary Chinese markets when the pandemic broke out, all known Covid variants are in fact of laboratory origin. That raises obvious and legitimate questions about criminal intent both on the level of the proposed “cures” and of the fabricated health emergency itself that those cures presumably were developed to resolve.
The vicious treatment allotted to the distinguished German lawyer Dr. Reiner Fuellmich is comparable to the persecution of figures like Giordano Bruno. It gives the lie to the collective West’s pharisaical pretence of freedom of expression. The dark stain it leaves will be indelibly recorded as a shameful episode in the history of German jurisprudence.
Hepatitis B Vaccination of Newborns: Seriously Misleading Media Reports
By Peter C. Gøtzsche | Brownstone Institute | December 19, 2025
Fiction or faith. It is a major failure to give equal prominence to people presenting scientific facts and people talking about their feelings or beliefs with no evidence in their support, or to allow them to contradict unchallenged the most reliable evidence we have.
However, virtually every time I know something about a healthcare issue considered controversial, this is what I see in the news, and the hepatitis B vaccine controversy illustrates this abundantly.
On 5 December 2025, with a vote of 8 versus 3, the Advisory Committee on Immunization Practices (ACIP) at the Centers for Disease Control and Prevention (CDC) ended the recommendation that all newborns in the United States receive a hepatitis B shot at birth. The birth dose was recommended only if the mother had tested positive for the virus or if her infection status was unknown.
The change was very rational, and as in Western Europe, only Portugal recommends a universal birth dose, it would seem difficult to argue against it. But the media did and failed us badly. Two days after the vote, I downloaded news stories from 14 major media outlets, and they were all very negative. The media used three main tactics to support their beliefs:
They denigrated the Secretary of Health, Robert F. Kennedy, Jr., the members of ACIP he had selected, and some of the presenters at the meeting.
They gave undue prominence and praise to the three dissenting ACIP voices and outsiders, who were depicted as experts or scientists, as if to say that they must be right, and they were widely quoted for their remarks, which were rarely rational or evidence-based.
They didn’t check if what the critics of the policy change claimed was correct.
The Denigration of Kennedy
Of the 14 news outlets, only Nature did not denigrate Kennedy.
Reuters started its press release by saying it was “a major policy win” for Kennedy that vaccine advisers named by him reversed a decades-long recommendation “that disease experts say will reverse decades of public health gains.” So, Kennedy’s advisers were not experts, and as the critics were experts, they must be correct, right?
Reuters noted that the CDC is “now run by a Kennedy-appointed acting head, Jim O’Neill, who is not a scientist;” that Kennedy founded the anti-vaccine group Children’s Health Defense; fired ACIP’s previous 17 “independent” experts and replaced them with a group that largely supports his views; dropped broad recommendations for the Covid vaccine and cut funding for mRNA vaccines.
The facts are that several of the previous experts at the ACIP were not independent but had conflicts of interest in relation to vaccine manufacturers and other drug companies; that recommending Covid vaccines only to high-risk groups brought the US on par with Europe; and that cutting funding for mRNA vaccine research was well motivated. Kennedy said that his team had reviewed the science and found that these vaccines fail to protect effectively against upper respiratory infections like Covid and flu. His department was therefore shifting the funding toward “safer, broader vaccine platforms that remain effective even as viruses mutate.”
Reuters misrepresented the ACIP meeting entirely, claiming that “many of Kennedy’s committee members criticized the vaccine as unsafe.” What they said was that safety had not been adequately studied, which was correct.
The other media called Kennedy a vaccine sceptic (The Hill, Health Policy Watch, CBC), a vaccine activist (CNN, the Guardian), or an anti-vaccine advocate (PBS), who fired all 17 previous members of the ACIP, replacing them with people who largely shared his scepticism (New York Times, Washington Post, National Public Radio, CNN, PBS, CBS News, Time, Health Policy Watch, CBC, BBC, Guardian ) with a “goal of upending vaccine policy” (New York Times ), and the vote fulfilled a long-held goal of the anti-vaccine movement (The Hill ).
The CBC, the largest news broadcaster in Canada, noted that Kennedy had promoted debunked theories linking vaccines to autism. It is correct that studies of the MMR vaccine and aluminium adjuvants did not find a link, but the aluminium study is seriously flawed, some studies have claimed a link, and as it has not been studied if the extensive US childhood vaccine program might cause autism, the CDC has suggested additional research projects.
The Washington Post said that aluminium had become a focal point for anti-vaccine groups that claim cumulative exposure may harm neurological development and that vaccine researchers note that aluminium is present naturally in breast milk, food, and water at far higher levels than in vaccines and is rapidly cleared from the body. It is highly misleading to compare dietary intake with injections, as very little aluminium is absorbed from the gut and the rest is effectively eliminated via the kidneys, and as aluminium adjuvants in vaccines are harmful.
The Hill and CNN noted that aluminium adjuvants in vaccines have been proven to be safe (which is false), but that vaccine sceptics like Kennedy have long said they are linked to allergies and other health conditions (which is correct). Natural infection protects against allergies, and studies comparing vaccinated with unvaccinated children have shown vaccines increase the occurrence of asthma and other atopic diseases.
The Denigration of ACIP Members and Meeting Presenters
Nature noted that several panel members continued to express broad criticism of vaccines.
The New York Times lamented that most of the new ACIP members and some of the presenters have no experience in vaccine research or clinical practice and that the divisiveness and dysfunction of the committee in making the decision raised questions about the reliability of the advisory process.
This is terribly misleading. People who have learned to read can assess the merits of vaccines, and scientific debate is what furthers science. Acting ACIP chair Robert Malone said that the committee’s work must be guided by evidence, transparency, and a willingness to scrutinise assumptions rather than protect them.
Health Policy Watch wrote that Malone has been criticised for vaccine misinformation, which is a meaningless comment without any mention of what the issues were. Some of the most outstanding vaccine researchers in the world, professors Peter Aaby and Christine Stabell Benn from Copenhagen, have been criticised for misinformation and have had lectures and interviews removed from YouTube even though everything they said was correct.
CBS News noted that ACIP member Retsef Levi, a mathematician with no medical training (so what?), had falsely claimed that experts had never tested the vaccines appropriately, and the New York Times called it incorrect when lawyer Aaron Siri, a presenter, said that “not one” of the shots administered to children had been compared against a placebo or an inert substance. But Levi and Siri were correct. No childhood vaccine on CDC’s schedule was studied in placebo-controlled trials or relied upon before licensure.
The CBC also described Levi as a person with no medical degree who had questioned the safety of the Covid-19 vaccines and called for Covid vaccine programs to be halted. Well, I have observed repeatedly that Levi’s arguments were far more persuasive than those offered by people with medical degrees, e.g. by ACIP member Cody Meissner, a paediatric infectious-disease specialist (see below).
And Covid vaccines are definitely not safe; they have killed children who developed myocarditis and adults who developed blood clots. It was very prudent to change the “all-inclusive” US Covid vaccine programs when by far most people have been infected, whether vaccinated or not, and because repeated boosters can weaken the immune system and increase the risk of respiratory infections, also for flu shots. Healthcare workers themselves have already delivered a verdict. According to the CDC’s own data, fewer than 10% received a booster in the past year.
National Public Radio denigrated Siri: an anti-vaccine lawyer with no medical or scientific training, and the Washington Post failed their readers, too: “Aaron Siri, a Kennedy ally and lawyer for the anti-vaccine movement, delivered a presentation for more than 90 minutes. Siri said clinical trials for vaccines have not been properly performed, that safety surveillance after vaccines are licensed is lacking and that the efficacy of vaccines in reducing deaths and spread of disease has been overstated. Siri and Kennedy-aligned activists argue that the cumulative number of shots places an undue burden on child immune systems. Scientists counter that… the immune system can safely handle far more antigens than vaccines contain.”
Siri is correct and the reason why he was given so much time is that he is evidence-based and very knowledgeable. His book about vaccines is outstanding. And “scientists” have no evidence that the immune system can safely handle many vaccine antigens injected simultaneously. This is unknown and needs studying.
The Washington Post also noted that “Siri petitioned the government in 2022 on behalf of the anti-vaccine group Informed Consent Action Network, which is run by Kennedy’s former communications director, to reconsider its approval of Sanofi’s stand-alone polio vaccine. Siri argued that the government had relied on inadequate data, a claim regulators rejected.”
However, the petition notes that “the clinical trials relied upon to license this product did not include a control group and only assessed safety for up to three days after injection. These trials therefore did not comply with the applicable federal statutory and regulatory requirements necessary to prove the product was ‘safe’ prior to licensure.” As live, attenuated polio vaccines can mutate and cause polio, I agree with Siri that this drug had not been adequately studied before licensure.
The New York Times and National Public Radio wrongly implied that Siri wanted to remove all polio vaccines (“polio vaccines” or “the polio vaccine”).
Praising “Experts” and Giving Them Undue Prominence
Safety was a major issue. Dissenting ACIP member Cody Meissner said at the meeting that we know that the vaccine is safe, and his reassurances were quoted by the New York Times, the Washington Post, National Public Radio, Nature, the BBC, and Time.
However, when the Institute of Medicine in 2013 was commissioned to review the safety of the CDC childhood vaccine schedule, they could not find a single study that had compared health outcomes in vaccinated children with those in children who had not received any vaccines and they concluded: “There is no evidence that the schedule is not safe.” Similarly, Time wrote about the hepatitis B vaccine that there is “no evidence in regard to lack of safety.” My comment on this kind of reasoning was: “If the brakes in a new car model have never been tested, the reassuring conclusion would be: ‘There is no evidence that the brakes don’t work.’”
At the ACIP meeting, Meissner accused Siri of presenting “a terrible, terrible distortion of all the facts” (New York Times, National Public Radio, The Hill, CNN, Time ) and of making “absolutely outrageous statements about safety.” This was totally false and Meissner should know better. ACIP members were shown that the clinical trials underpinning approval of the hepatitis B vaccine were small, lacked a placebo group, and followed infants for no more than seven days after vaccination, which would not detect any long-term adverse outcomes. Normally, such findings would have shocked people and prompted caution, but Meissner insisted that “There is no evidence of harm.” Well, if you don’t look, you won’t find.
Levi hit the nail on the head: “What is the number needed to vaccinate – among babies born to hepatitis B-negative mothers – to prevent one case of chronic hepatitis B?” No one supplied an answer. But if the true number was “in the millions,” then any credible harm-benefit analysis would require showing a number-needed-to-harm one infant seriously even higher.
Meissner, however, opined that the move was rooted in baseless scepticism and that we will see more hepatitis B infections (Washington Post, Nature ). He was also against possibly using fewer than three doses of the vaccine (New York Times, The Hill ), arguing that antibody titres are not a good correlate of protection and did not have scientific backing (Nature ). The inconsistency was unmistakable. Antibodies are embraced as proof of vaccine efficacy when convenient, e.g. in drug regulation, otherwise not.
Another dissenting ACIP member, psychiatrist Joseph Hibbeln, was quoted a great deal although he said nothing of substance: The revised guidance was “unconscionable” (Washington Post ), “the decisions should be based on data” (The Hill ), “Those are all speculations” (Time ), “Is there any specific evidence of harm of giving this vaccination before 30 days?” (Guardian ). Not a single journalist wondered why a psychiatrist sat in a vaccine committee.
Dr Tracy Beth Høeg, a presenter at the meeting, noted that the US was an outlier recommending around 72 childhood vaccine doses, while countries like Denmark use fewer than 30. PBS and Time argued that the US is not an outlier in recommending hepatitis B vaccines for newborns because 116 of the 194 WHO member states did the same. This is not a proper comparison, and, as noted above, in Western Europe, only Portugal recommends a universal birth dose.
Levi noted that “The policy in the US is completely misaligned with many countries that… care about their children just as much as we do,” and when Meissner viewed the growth of the childhood vaccine schedule as an achievement for child health, Siri countered correctly that the US “has the worst health outcomes amongst all developed countries.”
The media quoted three previous CDC directors. Rochelle Walensky said that over the past few months, she had observed “a systematic undermining of the nation’s vaccine program” (National Public Radio) and that the “US vaccine-safety monitoring system can detect very, very rare safety events“ (Nature ). Maybe, but she ignored them. In April 2021, cases of myocarditis after Covid-19 vaccination, particularly among young male vaccine recipients, had been reported to the Vaccine Adverse Event Reporting System at the CDC, but Walensky said by the end of the same month: “We have not seen a signal and we’ve actually looked intentionally for the signal in the over 200 million doses we’ve given.”
Tom Frieden provided a doomsday statement: “The ACIP recommendation… puts millions of American children at greater risk of liver damage, cancer and early death.” He advised everyone to “stand up for fact-based care” and “not accept this misguided and dangerous recommendation” (Time).
Demetre Daskalakis had a weird argument: “This will signal to clinicians that there is something wrong with the vaccine – there is not” (Reuters, CNN). It could also signal greater responsibility at the CDC than under previous directors. But the BBC and the Washington Post joined the folly arguing that public health experts, representatives of medical organisations, and some ACIP members worried the vote could raise unfounded safety concerns about the vaccine and undermine hard-won trust in vaccines leading to more sickness.
The media gave organisations undue prominence without ever considering if they were impartial. They urged people to look to “independent recommendations,” e.g. from the American Medical Association and the American Academy of Pediatrics, for “science-based advice” (National Public Radio).
I would call it advice based on money. The Academy would continue to support the birth dose of the vaccine (Reuters, CBS News, Health Policy Watch, CNN, Time, CBC) but all journalists forgot to say that it receives many millions of dollars from vaccine manufacturers and other drug companies. Unsurprisingly, hepatitis B vaccine makers Merck, Sanofi, and GSK defended their products as safe, and Merck was “deeply concerned by the vote” (Reuters ). Perhaps because Merck’s shares dropped?
“Don’t listen to ACIP at all… listen to the American Academy of Pediatrics” (CNN), which said that the “irresponsible and purposely misleading” guidance would harm children; called it a “deliberate strategy to sow fear and distrust among families” (CBC); and delivered a gigantic falsehood: “Vaccine recommendations are largely similar across developed countries” (CBS News).
Reuters noted that ACIP members had said that the birth dose “was out of step with peer countries, particularly Denmark,” but then quoted “a CDC disease expert” for saying that the US is not comparable to Denmark with its universal healthcare and more thorough screening for the virus. The Washington Post said that “public health experts” had noted that European countries recommending fewer shots for children were smaller and had better health care systems, and that medical associations had argued that the US schedule had been thoroughly studied (which is blatantly false). None of the media quoted Levi, who mentioned that the US and Denmark have the same background rate of hepatitis B despite different policies on the birth dose.
The American Medical Association is also heavily corrupted by industry money and said that ACIP’s decision was “reckless and undermines decades of public confidence in a proven, lifesaving vaccine. Today’s action is not based on scientific evidence” (CNN).
The American College of Physicians said that “This vote… will only endanger children and increase risk of death for millions,” and a hepatitis researcher urged people to “go back to our true experts… our CDC colleagues” (Health Policy Watch).
Time noted that “A group of several dozen professional medical organizations and health advocacy groups, including the American Medical Association” expressed alarm over the committee’s decisions: “Previously, we could expect science to drive decisions.”
Some panellists and media noted that universal hepatitis B vaccination at birth had helped to nearly eliminate cases among newborns in the United States, and that there was no evidence of harm (New York Times, Washington Post, The Hill, Guardian ). However, absence of evidence is not evidence of absence. When Levi countered that the risk for a child of getting infected was extremely low, supporters of the birth dose noted that the virus can be spread by household objects like toothbrushes, razors, or combs used by an infected person. This is a fake argument and the CDC website is explicit: “Although HBV can be found in saliva, it is not spread through kissing or sharing utensils. It is also not spread through sneezing, coughing, hugging, breastfeeding, or food or water.”
Levi also said that the decline in hepatitis B cases occurred long before the birth-dose policy was introduced and was concentrated in older age groups, not among infants, which supported a risk-based policy, focused on infants born to hepatitis B-positive mothers and on high-risk adult populations. When ACIP liaison Dr Flor Muñoz of the Infectious Diseases Society of America claimed that much of the discussion amounted to “misinformation,” Levi responded: “It’s not misinformation… this is CDC data.” When Muñoz pushed back, presenting her disagreement as established fact, Levi replied: “I appreciate your beliefs and feelings about this, but these beliefs and feelings are not supported by the data that were presented.”
Levi also pointed to ACIP’s prior recommendation of Covid-19 vaccination for healthy, extremely low-risk children, which he described as “one of the most outrageous” examples of framework failure.
ACIP’s decision sparked anger from Republican Senator Bill Cassidy (R-LA), a doctor, who said the vaccine is safe and effective (BBC, CBS News, Time, Health Policy Watch). He wrote on X that “Siri, a prominent anti-vaccine lawyer, makes his living suing vaccine manufacturers and is presenting as if an expert on childhood vaccines. The ACIP is totally discredited” (Washington Post, The Hill ).
The Hill was particularly critical. It wrote about an ardent objection from major medical organisations, internal spats among ACIP members, and a stark lack of data to support altering decades-long vaccine guidance, in fact, “There’s been great data and studies done on these vaccines, and they are safe and effective.” The Hill quoted top figures from Illinois, Massachusetts, and New York City for their rants, which included that they would not abide by ACIP’s “irresponsible attacks on clear, evidence-based science.”
When journalists “dial-a-quote,” they call organisations or people whom they know will respond in a way that mirrors their own bias pretending they have asked an “independent expert.”
The media were full of evidence-free, derogatory comments that were meaningless because they could not be contested:
- “We can no longer trust federal health authorities when it comes to vaccines,” “heartbreaking to see this science-driven agency turn into an ideological machine” (New York Times );
- “Medical experts have argued that it’s important to vaccinate all newborns for hepatitis B” (Washington Post );
- “The vaccine is incredibly safe,” experts decried the move (Reuters );
- the American Association of Immunologists is “extremely disappointed” in the decision;
- the American College of Physicians called the meeting “completely inappropriate” (CBS News); “many experts expressed dismay at today’s decision” (CNN);
- “A long lineup of medical experts…strongly urged against changing the vaccination schedule” (Health Policy Watch);
- “Public health experts decried the move,” CDC and the ACIP are no longer trustworthy sources and are becoming increasingly irrelevant (CBC);
- “a forum for the discussion of falsehoods,” ACIP members promoted their own sceptical views on vaccines, looking for a bogeyman, and you’re not going to find something if it doesn’t exist (Time );
- “Experts say any change to the current hepatitis B vaccination recommended schedule could have significant and far-reaching consequences for childhood health in the US” (Guardian ).
When the media presented statements that could be contested, they were usually wrong or seriously misleading, e.g. “Siri’s presentation was replete with ‘falsehoods and misrepresentation of the data,’ and he conflated informed consent with mandates” (New York Times ); “fierce objections from medical groups that said the recommendation had proved a successful public health strategy, nearly eradicating the dangerous virus among U.S. children” (Washington Post); a “Minority of members argue the change is not supported by data” (Reuters ).
Persuasion by Big Numbers
Like the drug industry does, the media used big numbers in their propaganda.
Globally, the vaccine has prevented millions of infections (Health Policy Watch). Before the vaccine, around 200,000 to 300,000 people were infected each year; since the vaccines began being universally administered to babies, overall cases are down to around 14,000 annually (PBS).
After a birth dose was recommended in 1991, the shots have prevented an estimated 90,000 deaths in the US (BBC) and reduced hepatitis B infections among infants and children by 99% (CBS News, Time, Health Policy Watch, Nature ).
All these claims are false or seriously misleading. Data presented at the meeting showed that much of the decline in hepatitis B infections over past decades occurred before the birth dose was recommended and it was largely driven by behaviour change, screening, and targeted vaccination of high-risk groups.
Senator Cassidy wrote on X that “Before the birth dose was recommended, 20,000 newborns a year were infected with hepatitis B. Now, it’s fewer than 20” (CBS News, CNN, Health Policy Watch). This was an error of 133 times. CDC data show that in 1990, only around 150 children below one year of age became infected.
Vaccinologist Paul Offit Lied on CNN
The most high-profile vaccinologist in the world, after vaccine “Godfather” Stanley Plotkin, is Paul Offit, but that may be a thing of the past after Siri’s recent revelations and his self-destructing appearance on CNN on the second day of the ACIP meeting.
Offit told viewers he had not been invited to speak at the meeting but internal documents show his claim is false. CDC officials had contacted him repeatedly – via emails, phone calls and a speaker-request form – inviting him to present.
Offit warned viewers that “50% of people in this country have chronic hepatitis B and don’t know it” (only about 0.3% have chronic disease) and suggested newborns were at risk through everyday contact with nannies, daycare workers, and family members because of sharing toothbrushes, towels, or simply being held by an infected adult, which the CDC denied could happen.
Offit described ACIP as a “clown show,” an “anti-vaccine advisory committee” that “puts children in harm’s way.” He lied monstrously saying that before universal infant vaccination, “30,000 children under the age of 10” contracted hepatitis B each year. CDC data presented at the ACIP meeting showed that new hepatitis B cases in children under the age of 10 were around 400 per year before the universal birth dose was introduced.
I am very indebted to journalist Maryanne Demasi, PhD, who wrote many of the articles I quoted above. She gave Offit the opportunity to clarify his remarks but he did not respond. This silence contrasts sharply with the certainty he brings to national television, where his claims are delivered without scrutiny and his financial ties to vaccine manufacturers are almost never mentioned.
Offit is not an impartial commentator. He earned millions from the sale of his stake in Merck’s rotavirus vaccine, RotaTeq, and has long been aligned with the pharmaceutical industry whose products he routinely defends. Yet major news outlets present him as a neutral authority and take his statements at face value.
Conclusions
The media’s reporting on the hepatitis B issue was seriously misleading and their advice that we should trust the “experts” who condemned the ACIP committee’s wise decision is horribly misguided.
The new ACIP’s first chair was biostatistician Martin Kulldorff. He developed the monitoring system the CDC uses for quick detection of vaccine harms, considered the best in the world. On 1 December, Kennedy announced that Kulldorff was appointed to a senior role at the Department of Health and Human Services after he had “transformed ACIP from a rubber stamp into a committee that delivers gold-standard science for the American people.” NIH director Jay Bhattacharya said that “Five years ago, Martin Kulldorff and I co-authored the Great Barrington Declaration calling for an end to pandemic lockdowns. That evidence-based approach to public health now permeates HHS.”
What the media presented was what we call eminence-based medicine, and the medical journals’ reporting on vaccine issues is also a disaster. I shall end with the abstract of an article I published on 10 November:
The reactions to Robert F. Kennedy Jr.’s initiatives to improve vaccine safety have been almost uniformly negative. I studied how the narratives were framed in a cohort of 33 articles in the BMJ of which 30 were written by journalists or the editor. I focused on whether the reporting was balanced and informative, and whether the articles saw any merit in Kennedy’s reforms in his role as Secretary of Health and Human Services or supported the status quo.
The reporting in the BMJ was highly biased. Much of the information provided in Kennedy’s disfavour was misleading, and some was wrong. All initiatives at improving vaccine safety were condemned, without any analysis of their merits in an evidence-based fashion. Instead, the BMJ cited people who had their own agendas and who condemned Kennedy without providing any evidence in their favour while expressing faith in vaccines, with the industry mantra that they are safe and effective, although all drugs will harm some people.
The BMJ did not take any interest in the widespread and lethal corruption in US healthcare institutions – one of Kennedy’s focus points – but toned it down.
Despite the constant ad hominem attacks, Kennedy has succeeded to introduce important changes and plans related to vaccine safety, guidance about how vaccines are used, and about avoiding neurotoxic metals in vaccine adjuvants.
Dr. Peter Gøtzsche co-founded the Cochrane Collaboration, once considered the world’s preeminent independent medical research organization. In 2010 Gøtzsche was named Professor of Clinical Research Design and Analysis at the University of Copenhagen. Gøtzsche has published over 100 papers in the “big five” medical journals (JAMA, Lancet, New England Journal of Medicine, British Medical Journal, and Annals of Internal Medicine). Gøtzsche has also authored books on medical issues including Deadly Medicines and Organized Crime.
Flawed Study Downplays Children’s Risk of Myocarditis From COVID Vaccine
By Josh Mitteldorf, Ph.D. | The Defender | December 3, 2025
Readers of The Defender are familiar with the fact that the COVID-19 mRNA shots pose a risk of myocarditis, especially in children. But they may not know that myocarditis is usually permanently disabling, and in adults, it is often fatal within five years.
Tragically, we are now also learning what the trajectory of myocarditis in vaccinated children actually looks like.
This has been a public relations setback for industry and governments that have been advocating, and sometimes mandating, that children as young as 6 months get the vaccines — even though COVID-19 is almost always mild or symptom-free in young people.
This month, 22 British scientists from prestigious universities published a study intended to ease parents’ minds about risks of the vaccine, and simultaneously scare them about the dangers of getting COVID-19.
The message is that yes, there are rare cases — they always use the word “rare” — in which children get myocarditis after vaccination, but hey, no product can be perfect. And it’s better to risk the vaccine than risk getting COVID-19. Also, they claim, kids are more likely to get myocarditis if they get the virus than they are to get myocarditis from the vaccine.
That’s the message — and the authors and publisher have the clout to widely broadcast that message in a press release and in news headlines in Britain and America.
But what does the study actually say? In short, it asks the wrong question — and even so, the answer they get must be buried in the appendix, because it’s inconsistent with the message they want to promote.
Article summary omitted evidence of vaccine risk
The study design is deeply compromised because the 22 authors constructed a complicated model to avoid doing a straightforward comparison (vaccine only versus disease only).
And even after they cooked the books, even after they took data from almost 14 million children and teens under age 18 in England, they got a result that is barely statistically significant, with overlapping error bars for the risk from COVID-19 and the risk from vaccination.
It gets worse.
The results, which marginally favored the vaccination, were trumpeted in a summary at the top of the paper and announced to the press.
But buried in the appendix, published separately online, is a table that shows a more relevant version of the comparison.
The version in the summary is from an early time frame when the vaccine was not available. The appendix shows comparable data for the time frame in which the vaccine was available, limited to the ages for which the vaccine was offered.
In the appendix, the risk of myocarditis from the disease is half that of the risk from the vaccine. This blatantly contradicts the summary and the headlines generated by the article — and this was a response to the deceptive version of the question, not the more straightforward one that the researchers chose not to answer.
Study authors asked the wrong question
The most pertinent question is the simple one: Did vaccinated children have a higher incidence of myocarditis than unvaccinated children?
This is an easy question to answer, given the data that these authors (but not the public) had access to. In a few minutes, they could have calculated a rate of myocarditis among vaccinated and unvaccinated children.
However, if they did the calculation, they didn’t report the results. My guess is that they did the calculation, didn’t like what they saw, so they didn’t include it in the published article.
As I stated above, I believe the study authors “asked the wrong question.” What I mean is that the article compares the risk of myocarditis from COVID to the risk from vaccination.
But this is not the most relevant question. Why?
Because many people got the vaccine and then got COVID anyway, so they were unnecessarily exposed to both risks.
Conversely, many children who didn’t get the vaccine, didn’t get COVID. Or, they get such a mild case that they don’t even notice it. These children avoided both risks.
This is why comparing the risk of myocarditis from COVID to the risk from the COVID vaccine is not really the pertinent question. It’s not a question of “either or.”
Authors ‘muddied the waters’ by analyzing myocarditis in kids who got vaccine and the virus
The message the authors wanted to imply was that, even though the vaccine increased the risk of myocarditis, it decreased the risk of COVID — and since COVID itself can cause myocarditis, the total risk is actually lower with vaccination than without.
If that is their claim, it’s easy to determine if it is true. The simplest calculation they could have done with the data available to them was also the calculation most pertinent to what parents want to know: Is my child better off with or without the vaccine?
The authors chose not to offer us the simple answer to that straightforward question.
But — given that they asked the wrong question — they might have derived a clean answer just by comparing the subset of children who were vaccinated but never got COVID to the subset who got COVID but were never vaccinated.
Because the study included data spanning two years from all over the U.K., there were hundreds of thousands of children in these subcategories — more than enough to do a clean statistical comparison.
But again, the authors chose not to do this. Or, my guess, they did the comparison and didn’t like the result, so they didn’t include it in the publication.
Instead, the authors analyzed myocarditis in the large group of children who got both the vaccine and the disease. This muddied the waters because there is no clear way to determine whether it was the disease or the vaccine that damaged the child’s heart.
Hence, the complicated model, based on timing.
The possibility that seems likely is that children who got COVID after the vaccination had the highest heart risk of all. Of course, there is the logical possibility that children who got COVID after vaccination had a milder case, with a lower risk of myocarditis.
However, if that had been the result, I would think the authors would not only have included that result, but also headlined it.
One more thing — the study looked only at the Pfizer vaccine. Myocarditis risk from the Moderna vaccine is estimated to be three times higher than Pfizer. They had the Moderna data and chose not to look at it.
Or they looked at it, decided they didn’t like what they saw, and decided not to report it.
‘This is public relations masquerading as science’
So, to summarize:
- The authors asked a complicated question when a simple one was more relevant.
- Given this wrong question, they did not do the most straightforward analysis to answer it.
- Even so, they found that the vaccine held almost twice the risk of myocarditis compared to the disease. This result was only in Table S16 of the Supplementary Appendix — but mentioned nowhere in the body of the paper, let alone in the summary at the top.
- And still they made prominent announcements to the public, claiming that their study confirms that children are better off with the vaccine than without.
This is public relations masquerading as science. For an article like this to be peer reviewed and featured prominently in Britain’s most prestigious medical journal tells us just how deeply the ecosystem of medical research has been corrupted.
And this is the “science” that our U.S. Food and Drug Administration relies on when they approve dangerous vaccines for healthy children who are at almost no risk from the disease itself.
In most statistical articles, the raw data used for a study are published online and linked in an appendix to the article. However, in this case, the U.K. National Health Service (NHS) granted access to the data exclusively to this prestigious group of scientists.
Personally, I would like to see the raw data and perform the analysis that the 22 scientists should have done from the beginning. Children’s Health Defense is in the process of requesting access from the NHS. Stay tuned …
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
5 yrs later: The Largest Vaccine Experiment and Weakest Ever Safety Monitoring
By Sharyl Attkisson | November 19, 2025
The largest vaccination campaign in history has been accompanied by the weakest safety monitoring ever attempted.
The world conducted the largest medical intervention in history when billions of people received Covid-19 vaccines beginning in late 2020. Yet, five years later, no comprehensive, mandatory system exists in the U.S. or anywhere else to track down adverse events the vaccine may be causing on a massive scale.
No government health agency, medical association, or hospital system has required doctors, clinics, or hospitals to routinely ask every patient about new symptoms, cross-reference their Covid and vaccination history, and systematically report that information to a central database capable of detecting possible patterns.
Today, untold millions of patients with mysterious or debilitating new conditions are said to be routinely told their symptoms are due to anxiety, depression, unexplained “long Covid,” or simply treated without regard to what could be the cause, without any effort to collect the data that could prove or disprove a vaccine connection.
The federal Vaccine Adverse Event Reporting System (VAERS), co-managed by the CDC and FDA since 1990, remains the primary U.S. tool for identifying previously unknown adverse events from vaccines, and their frequency.
By law, healthcare providers must report certain serious events after any vaccination, including hospitalization, permanent disability, or death, to the VAERS database. But during the Covid-19 vaccine rollout, compliance was extremely low, and — shockingly — neither the government nor medical organizations enforced the requirement at perhaps the most critical time in our history in terms of sheer number being exposed to experiments both in terms of the specific vaccines and novel form of delivery.
A major reason for underreporting to VAERS: many physicians believe — incorrectly — that they should only submit a report if they are personally convinced the vaccine caused the problem. This misunderstanding defeats the entire purpose of a passive reporting system, which is to collect reports of all health issues following vaccination, regardless of suspected cause, so that unexpected patterns can emerge over time.
This is exactly how previously unrecognized serious side effects were discovered with other medications. In the late 1990s, as a CBS News investigative correspondent, I reported on Rezulin (troglitazone), a diabetes drug withdrawn in 2000 after reports of liver failure began appearing in the FDA adverse event reporting system.
What started as a small number of reported liver deaths after Rezulin signaled a much larger problem once standard underreporting multipliers are understood: experts say for each adverse event reported, there are likely 10,000 to 100,000 more that don’t get reported. That’s why a handful of fatalities was so alarming and prompted the FDA to pull the drug from the market.
Similarly, as I also broke news on at CBS, the erectile dysfunction drug Viagra was linked to a form of sudden blindness (non-arteritic anterior ischemic optic neuropathy) years after approval. But it was only because clusters of blindness cases happened to get reported to the FDA’s adverse-event system, and a few intrepid eye doctors noticed a pattern in their patients. The actual doctors prescribing Viagra failed to recognize and report the blindness as a possible adverse event. The side effect was originally denied by the drugmaker, but is now added into warnings on the label.
A third example among many I investigated is cholesterol lowering statins. At first, statin makers denied that potentially fatal muscle problems and brain issues could be related to their medicine. But after enough reports made it into the federal database, it became undeniable— and those adverse events were ultimately added to the label.
VAERS data for Covid vaccines now exceed 1.6 million reports in the U.S. alone, including more than 36,000 deaths and 200,000 hospitalizations reported after vaccination. Experts across the spectrum agree these figures represent massive underreporting because most physicians are not filing reports or even asking their sick patients about their vaccine status, and many adverse events are never recognized as possibly vaccine-related.
What should have happened from day one — and still has not — is a simple, mandatory protocol: at every medical encounter (office visit, ER, hospital admission, or routine checkup), patients should be asked a few standardized questions about new or worsening conditions since their last Covid vaccination or infection, and the answers should be forwarded to a central analytical database. In an era of electronic health records and artificial intelligence, this could be inexpensive and straightforward.
Yet no such program exists.
The National Institutes of Health spent more than $1.15 billion tax dollars on the RECOVER (Researching COVID to Enhance Recovery) initiative to study “long Covid.”
RECOVER has collected detailed longitudinal data on tens of thousands of patients. This includes data that could be valuable, if not vital, to the pursuit of finding out about and helping treat Covid vaccine injuries.
Yet the study’s public protocols and publications to date lump all patients together as Covid injuries— even though the majority of studied patients were also vaccinated.
When I contacted RECOVER representatives in 2024 to ask how they distinguished potential vaccine-related injury from post-viral “long Covid,” they refused to answer and then ceased communications with me.
It begins to look like RECOVER is more about finding and promoting money making pharmaceutical treatments for “long Covid” without really getting at the heart of what Covid vaccines might be doing to our population on a massive scale.
Confirmed serious adverse events now acknowledged by the FDA and CDC to be caused by Covid-19 vaccines include myocarditis and pericarditis (especially in young men after mRNA doses), anaphylaxis, and immune thrombocytopenia.
Other conditions under continuing investigation include tinnitus, Guillain-Barré paralysis syndrome, and various serious neurological disorders.
Rates of certain cancers in people under 50 have risen sharply since 2021, as have reports of aggressive “turbo cancers” and unusual neurological diagnoses.
Without systematic, mandatory post-vaccination surveillance that includes everyone — vaccinated or not — it is impossible to determine whether any of these increases are related to the vaccines, to the virus, to both, or to unrelated factors.
Untold millions of patients are suffering mysterious or debilitating new conditions with doctors potentially misunderstanding or misinterpreting causes, which impacts success of treatment plans. Physicians are rarely if ever asking sick patients about Covid vaccine status. Often, patients report doctors are treating them without even bothering to identify potential causes of their maladies at all, let alone collecting data that could prove or disprove a Covid vaccine connection.
The largest vaccination campaign in history was accompanied by the weakest long-term safety monitoring ever attempted. Five years in, that failure has still not been corrected.
‘Formal, Unequivocal Apologies’ Needed to Restore Public Trust After COVID Vaccine Mandates
By Jill Erzen | The Defender | October 15, 2025
The public deserves “formal, unequivocal apologies from governments and medical bodies” for COVID-19 vaccine mandates and for “silencing truth seekers,” according to a paper published Oct. 9 in the journal Science, Public Health Policy and the Law.
Vaccine mandates and lack of transparency during the COVID-19 pandemic eroded public trust, which deepened the divide between health authorities and the people they serve, according to authors Dr. Aseem Malhotra and Andrea Lamont Nazarenko, Ph.D.
“The pandemic demonstrated that when scientific integrity is lacking and dissent is suppressed, unethical decision-making can become legitimized,” they wrote. “When this happens, public confidence in health authorities erodes.”
Trust in public health agencies plummeted during the pandemic. Confidence in decision-making at the Centers for Disease Control and Prevention (CDC) fell from 73% in 2020 to 61% in 2025, according to polling firm KFF.
Public opinion on physicians and hospitals also suffered, with trust dropping from 71.5% in April 2020 to 40.1% in January 2024, according to a study in JAMA Network Open.
Restoring faith in public health agencies requires “long overdue” apologies, as well as “full transparency of data, independent evaluation of evidence, and accountability through both policy change and public acknowledgment of harm,” the paper’s authors said.
‘Pandemic of the vaccine injured’
The “safe and effective” narrative surrounding the COVID-19 vaccine shifted over the years toward “unsafe and defective,” according to the authors.
Policymakers’ unwillingness to acknowledge the vaccine’s emerging safety signals may be “the most egregious failure” of all. “We are currently facing what some call a ‘pandemic of the vaccine injured,’” the authors said.
In 2022, a study in the journal Vaccine found that the risk of serious harms from the COVID-19 vaccine was two to four times greater than the risk of being hospitalized with COVID-19. That same year, researchers surveyed 40,000 Germans and found a high rate of severe side effects from the COVID-19 vaccine that persisted for months or longer.
Studies from 2025 suggest the risks may not decrease over time.
- A preprint study found that genetic material contained within mRNA COVID-19 vaccines can integrate into the human genome, potentially contributing to the onset of aggressive cancer.
- An analysis of a Japanese database of 18 million people showed that people who received COVID-19 vaccines had a significantly higher risk of death in the first year after vaccination compared to the unvaccinated, and the risk increased with each additional dose.
- A peer-reviewed study published in EXCLI Journal was the first to uncover statistically significant evidence of increased cancer risk following COVID-19 vaccination in Italy.
In public health, policymakers must anchor their decisions in cumulative evidence that evolves with new knowledge, according to Malhotra and Nazarenko. “It is a profound failure of scientific and ethical responsibility to overlook these safety concerns,” they wrote.
Health systems must adjust to manage ‘psychological fallout’ of pandemic
The authors said the health risks revealed by the emerging COVID-19 vaccine studies illustrate one of the central lessons of the pandemic: evidence evolves. Policies must be adjusted as new evidence comes to light, but that didn’t happen, they wrote.
“If the full body of research ultimately shows a net harm from COVID-19 vaccination and pandemic-era policies, the greater barrier will be psychological, not scientific,” Malhotra and Nazarenko said. “Our social systems must therefore be prepared to manage the psychological fallout, responding with clarity and compassion.”
To rebuild legitimacy, institutions must actively uphold ethical principles that prioritize the public over political or corporate interests, they said. The U.S. Department of Health and Human Services (HHS) is taking steps in this direction, according to the authors.
In September, U.S. Health Secretary Robert F. Kennedy Jr. led two roundtable discussions on long COVID that included doctors, researchers and patients. The talks were, in part, in response to “the calls that I get almost every day from people who are suffering from long COVID across the country and don’t know where to go and feel that their voices aren’t being listened to,” Kennedy said.
In August, Kennedy canceled nearly $500 million in contracts and grants intended to develop mRNA vaccines. “We reviewed the science, listened to the experts, and acted,” Kennedy said in announcing the move.
Restoring public trust hinges on informed consent and shared decision-making, according to the authors.
“A contributing factor to the prevalence of injury has been the extent to which government officials and public health authorities overrode the doctor-patient relationship, taking precedence over the ethics of individualized medicine,” they wrote.
Earlier this month, the CDC handed supporters of informed consent a win by updating its childhood immunization schedule to emphasize individual-based decision-making for COVID-19 vaccination in children 6 months and older.
‘Suppression may quiet critics, but it suffocates science’
In 2024, the journal Cureus retracted the first peer-reviewed paper to provide an extensive analysis of COVID-19 mRNA vaccine trial data and post-injection injuries.
“Silencing contestation is not a neutral choice; it is contrary to the methods by which science corrects itself,” Malhotra and Nazarenko said.
“Voices that push the mainstream should be encouraged, not silenced. Yet, contemporary public health often substitutes condemnation for curiosity, marginalizing dissent even when data warrant debate,” they wrote.
According to the authors, Kennedy’s critics provide “the most striking example of silencing opposition.”
Vaccine lobbyists at a leading biotech industry trade group purportedly criticized Kennedy’s “anti-vaccine stance” during an April meeting, calling him a “direct threat to public health.” A spokesperson for the organization denied the statements.
Kennedy’s policies at the HHS have sparked similar claims from six former U.S. surgeons general, who said he is “endangering the health of the nation.” Several senators have made similar assertions and called for Kennedy’s resignation.
Corporations and regulatory bodies commonly use character assassination to weaken their opposition, according to the paper’s authors. Those in power silence dissent by discrediting critics with smear campaigns and labels like “anti-vaxxer,” shifting focus from evidence to identity.
“Suppression may quiet critics, but it suffocates science,” Malhotra and Nazarenko wrote. “The remedy for disagreement is better evidence and open debate — not censorship or character assassination. Robust science requires robust dissent.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
Houston Hospital Denies Refusing Organ Transplants to Unvaccinated Patients
By Brenda Baletti, Ph.D. | The Defender | October 15, 2025
A Houston hospital accused of denying organ transplants to patients who haven’t been vaccinated against COVID-19 today told The Defender it “does not have a policy requiring transplant patients to be vaccinated against COVID-19, or any other disease, and does not deny care based on vaccination status.”
“We abide by all state laws and, as one of the largest transplant programs in the country, the safety of our patients always comes first,” Houston Methodist Hospital said in a statement.
The allegations stem from Texas Attorney General Ken Paxton, who stated in a letter that his office may investigate Houston Methodist Hospital for allegedly denying organ transplants to patients who refused the COVID-19 vaccine, according to a letter his office sent the hospital.
The letter to Houston Methodist Hospital’s President and CEO Marc L. Boom cited a July 24 X post by Texas doctor Mary Tally Bowden. The post included a screenshot of the hospital’s transplant policy showing that patients seeking a kidney transplant must receive the COVID-19 shot.
Monday, Bowden posted Paxton’s press release on X, claiming she had “written and oral proof (recorded conversation)” that the hospital required transplant patients to get the shots. “To my knowledge, their policy has not changed,” she added.
Bowden previously worked at Houston Methodist Hospital. The hospital suspended her privileges after she prescribed ivermectin to prevent and treat COVID-19. The hospital also accused her of spreading “misinformation.”
Bowden sued Houston Methodist after hospital officials refused to provide public information about the institution’s finances during the pandemic.
In the press release issued Monday, Paxton said, “Texans looking to receive medical care should never be turned away due to arbitrary COVID-19 vaccine mandates imposed by woke medical providers.”
He added:
“Vaccine mandates as a precondition for certain life-saving treatments may not only violate new state laws that became effective on September 1, but they also violate human dignity and run contrary to foundational principles of medical ethics. That’s why I’ve requested that Houston Methodist Hospital clarify its compliance with Texas’s new laws and position on vaccine mandates.”
The hospital has 14 days to notify the Texas Office of the Attorney General (OAG) about the steps it has taken to comply with the recently passed provision in the Texas Health and Safety Code, which prohibits denying organ transplants based on vaccination status.
The OAG said it will open a formal investigation if the hospital fails to respond.
Paxton’s office said its letter to the hospital “reaffirms Attorney General Paxton’s stance against COVID-19 vaccine mandates and reflects his commitment to protecting the rights and freedoms of Texans by challenging unlawful vaccine mandates.”
In recent years, Paxton’s office has challenged Big Pharma’s actions related to COVID-19 shots and weight-loss drugs, and has investigated toothpaste companies for deceptive marketing geared toward children.
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
New Book: Covid Through Our Eyes
Review by Maryanne Demasi, PhD | September 28, 2025
When Covid hit, governments, health agencies and the media marched in lockstep. Their united front was sold as “consensus.”
In reality, it was compliance by coercion. Dissenters were punished, questions suppressed, and the public was fed slogans instead of science.
Covid Through Our Eyes tears away that façade.
This collection of essays—written by doctors, scientists, lawyers, journalists, economists and ordinary Australians whose lives were upended—restores the voices silenced during the pandemic.
Each chapter forms part of a collective testimony. And in a final act of principle, not a cent of the book’s sales goes to the authors; all proceeds support Australia’s vaccine injury class action.
A chorus of voices
Editors Robert Clancy, an immunologist, and Melissa McCann, a physician, have gathered an extraordinary range of perspectives.
Among them, British oncologist Angus Dalgleish describes patients relapsing into aggressive cancers after years in remission. He argues that repeated boosters and chronic spike protein exposure created a “pro-cancer milieu.”
Vaccinologist Nikolai Petrovsky recounts how his homegrown vaccine, built on decades of expertise, was cast aside in favour of untested mRNA technology.
Statistician Andrew Madry lays out devastating evidence of excess mortality and the government’s refusal to investigate the causes.
Other contributors highlight phenomena dismissed at the time: immune system imprinting, shifts in antibody subclasses, and persistence of mRNA in the body.
Regulatory expert Philip Altman details how the Therapeutic Goods Administration ignored clear safety signals, choosing convenience over caution.
Lawyers and doctors tell of their battles in the courts and on the streets against vaccine mandates—small victories, bitter defeats, and governments that seemed more determined to silence critics than to defend their policies with evidence.
Clancy himself turns a sharp eye on Australia. Once a nation of independent scientists—from Burnet to Fenner, with pandemic plans crafted at the Commonwealth Serum Laboratories—by 2020 it had surrendered to bureaucracy.
He argues that recovery depends on restoring the doctor–patient relationship and returning vaccine development to proven antigen platforms, not experimental technologies rushed to market.
The media that failed
My own chapter in the book examines how mainstream media collapsed.
Newsrooms abandoned their adversarial role and parroted government lines. Contradictory evidence was buried. Scientists who asked questions were branded fringe. Patients who reported harm were cast as public health risks.
The press did not simply fail; it became an enforcer. That betrayal corroded trust, and the damage persists today.
Stories of loss
The most haunting chapters are personal.
Antonio DeRose, left in a wheelchair after transverse myelitis, describes doctors who refused to acknowledge the cause.
Queenslander Caitlin Gotze died six weeks after her second Pfizer dose, with her myocarditis misdiagnosed as asthma.
Actor and writer Katie Lees collapsed from clotting linked to AstraZeneca; her death was reduced to a single line on a regulator’s website.
These are stories of grief, stark reminders of what happens when agencies, designed to protect, instead deny responsibility.
This book matters
Covid may have slipped from the headlines, but its consequences have not.
Excess deaths remain unexplained. Injured families still fight for recognition. Trust has been squandered. And this nation has yet to hold a Royal Commission into Covid.
Covid Through Our Eyes is essential reading for anyone who wants to understand what really happened to Australians—a nation of people once known for their laid-back spirit, now grappling with a legacy of coercion and injury.
Buy it, read it, and judge for yourself.

