Questioning Your Doctor Is Now Considered A Psychological Problem (Seriously)
By Dr. Roger McFillin | Radically Genuine | October 31, 2026
I want to give you a warning before we go any further.
If you have ever questioned your doctor, pushed back on a prescription, or asked to slow down on a vaccine, the medical establishment now has a framework for you. And it isn’t “careful,” or “informed,” or “engaged.”
Your resistance will be seen as a psychological problem to be managed.
I’m not exaggerating. Let me show you.
On October 19th, Medscape, one of the most widely read publications among physicians in this country, ran a piece called “Why Your Patient Trusts Unsupported Claims but Not You.” It’s part of a series titled Healing a Broken Trust.
Read it carefully, and notice who is never asked to change.
It opens with a survey. More than a thousand physicians with 99.9 percent of them admitting they encountered patients influenced by “misinformation” in the past year.
What’s the definition of “misinformation?” Anything that disagrees with their standard of care. Quite bold for the same group that brought you the every increasing vaccine schedule for children, Covid Vaccinations, Acetaminophen, Statins, SSRI’s, a low fat diet, Opioids for pain and others as “evidence based medicine”.
Sit with that number. Essentially every doctor surveyed believes the problem in the exam room is what the patient has been reading.
Then it borrows a research term: “selective skepticism.” The idea is that you dismiss evidence from experts while uncritically swallowing pseudoscience. Isn’t that the pot calling the kettle black?
That’s how your questions are being categorized.
And the solution? It isn’t “let’s re-examine our evidence.” It isn’t “let’s ask why trust collapsed.” The solution is a persuasion technique. They call it inoculation. The doctor warns you ahead of time that you may see posts online saying a medication is about pharmaceutical profits, so that when you run into that idea, you’ve already been primed to dismiss it.
Think about what that means. The answer to your question has been scripted before you ever ask it. Your doubt is treated like a pathogen, and the doctor administers a dose of messaging to build immunity against it.
Now, in fairness, the article talks about listening more and seeing the patient as a whole person. Good. But listening as a technique to move you toward a predetermined conclusion isn’t listening. As a psychologist, I’d call that compliance work.
I’ve spent my entire career inside this system. Psychiatric hospitals, juvenile justice, community mental health, private practice. And I’ve studied how high-control groups operate.
Here’s what they do.
Doubt is reframed as a defect in the person doubting.
Outside information is labeled dangerous before you’ve even seen it.
Members are pre-warned about what critics will say, so they reject it on contact.
And the authority is self-referencing. It’s true because the institution says it’s true.
Now hold that list up against what I just read you. I’m not saying your doctor is a cult leader. Most physicians are sincere people working inside a system they were trained never to question. That’s exactly what makes it so powerful. The people enforcing the belief system are the ones most captured by it.
Here’s the question that article never asks. Has this system earned the trust it’s demanding?
Look around. We are living through a chronic disease epidemic. Autoimmune disease, allergies, obesity, diabetes, anxiety, depression, kids on prescriptions before they can drive. Never in history has a population been more medicated, more screened, more vaccinated, and more chronically ill at the same time.
That’s not a healthcare system it is a sick care system. It is extraordinarily good at managing illness for life and remarkably uninterested in why people got sick in the first place.
And it didn’t happen by accident. In 1910, the Flexner Report, commissioned by the Carnegie Foundation and followed by enormous Rockefeller philanthropy, remade American medical education. Many schools closed and traditions of healing were pushed to the margins. What survived was a paradigm: the body as a machine, disease as a chemical problem, and a pharmaceutical answer for every symptom.
We are living inside that paradigm more than a century later. And when people start to notice it isn’t working, the response isn’t humility. It’s a communication strategy.
In Case You Have Not Been Following
Now let me bring this close to home, here in Pennsylvania.
At Children’s Hospital of Philadelphia, there’s a program called “Close Your Eyes, We’ll Immunize.” Since 2023, children who are already going under sedation or anesthesia for another procedure are offered flu shots while they’re unconscious. Last season, over two thousand doses. And they’re exploring adding RSV and COVID shots, plus catch-up vaccines for kids who are “behind.”
I want to be clear here: parents consent. But think about when that consent is being requested. In pre-op. Your child is scared, about to be put under. You’re anxious, you trust the people in scrubs, and someone asks if you’d like to “take care of” the flu shot while they’re at it. That is the most vulnerable moment a parent has. That isn’t a calm, informed decision. In fact, they are having you put your digital name on a screen scrolling past words you would never have the time to read.
And it isn’t just Philadelphia. Children’s Hospital Colorado has vaccinated more than 18,000 kids under deep sedation or general anesthesia.
Here’s what should concern you clinically. A 2007 review in Pediatric Anaesthesia suggested spacing vaccines and anesthesia apart by days, specifically so a vaccine reaction isn’t mistaken for a surgical complication. So if your child spikes a fever after the procedure, what caused it? The anesthetic? The antibiotic? The surgery? The shot? Nobody will be able to tell you.
And look at the name of the program. It celebrates the fact that the child isn’t awake.
Dark.
So here’s what I want you to take from this.
Questioning is not a disorder. It’s the foundation of informed consent. A system confident in its evidence welcomes questions. A system that needs to “inoculate” you against questions is telling you something about itself.
Ask for the evidence. Ask what the risks are. Ask what happens if you wait. Ask who benefits. And if your questions are treated as a psychological problem, that tells you everything you need to know about whether that relationship deserves your trust.
You are not a compliance metric. Your children are not a vaccination rate.
Gates, Bourla on Trial in Netherlands Accused of ‘Great Reset’ Scheme at Vaccine Injury Hearing
By Michael Nevradakis, Ph.D. | The Defender | October 23, 2026
An attorney for seven Dutch plaintiffs in a COVID-19 vaccine injury lawsuit against Bill Gates and Pfizer CEO Albert Bourla accused Gates and others of
orchestrating the pandemic to help usher in the “Great Reset,” a global economic, political and social system promoted by the World Economic Forum.
During oral arguments Thursday, attorney Peter Stassen told a packed courtroom that the COVID-19 vaccines were akin to a bioweapon, developed as part of a broader global effort to strip democratic and individual rights.
Speaking outside the courthouse in Leeuwarden, Netherlands, Stassen said Thursday’s hearing “was about publicly telling what is happening in this courtroom and what is the real case. The real case is that COVID-19 was not a disease but was a project.”
He accused Gates and Bourla of participating in that project, which he said was coordinated and undemocratic. He also accused the defendants of using censorship and propaganda to hide their intentions while promoting the COVID-19 vaccines as “safe and effective.”
COVID-19 vaccines were developed and procured as military countermeasures, bypassing the standard development and approval pipeline for such products. By developing the shots as military countermeasures, they bypassed traditional safety regulations, leading to widespread injury, Stassen said.
Stassen said that while this is a civil case, he believes the defendants’ actions constitute serious criminal offenses that violate global treaties and the Nuremberg Code.
For their part, attorneys for the defendants “claimed the shots saved millions of lives and that they were safe and effective,” said Joseph Sansone, Ph.D., a psychotherapist, critic of the mRNA shots and one of the expert witnesses for the plaintiffs.
“They basically said, like a parrot, that all of Stassen’s accusations were either conspiracy theory or based on medical reports that are from people who are not neutral in this case,” said Ido Dijkstra, a Dutch journalist and the editor-in-chief of De Andere Krant, who attended the hearing.
Dutch attorney Meike Terhorst said the defense did not respond to Stassen’s assertions that COVID-19 was a project. “There was no response to that at all, nothing.”
Journalist Penny Marie, who has reported on the case, told The Defender that Stassen’s arguments “mirror what so many people worldwide say and have experienced and investigated.”
The defendants’ legal team did acknowledge that they were “touched” by the suffering of the vaccine-injured plaintiffs. Terhorst said the five living plaintiffs face “immense problems” with their health.
Dijkstra said the presiding judge on the three-judge panel appeared to “support the mainstream narrative,” but “gave the impression that she wanted to understand Stassen’s reasoning.”
Thursday’s hearing stemmed from a lawsuit filed in 2023 by seven people injured by COVID-19 vaccines — including two who have since died — against Gates, Bourla and 15 other defendants, including former Dutch prime minister and NATO Secretary General Mark Rutte, the Dutch state, and several Dutch public health officials and journalists.
According to Dutch attorney Meike Terhorst, who is not connected to the case but attended the hearing, none of the defendants appeared in court.
A ruling is expected as early as December but may be delayed until February 2027.
Expert witnesses barred from testifying in person
During oral arguments, Stassen addressed the court’s refusal to allow his team’s expert witnesses to testify in person. Earlier this week, the court limited the witnesses to video statements presenting their arguments.
Defense attorneys attacked the credentials of some of the witnesses. For instance, they claimed that Sasha Latypova — a former pharmaceutical research and development executive — has only a bachelor’s degree and is unqualified to provide testimony on scientific and medical matters.
Latypova disputed the claims, telling those gathered outside the courthouse that she has a “graduate degree from Dartmouth College and 25 years of pharmaceutical R&D and regulatory experience” — including interacting with the U.S. Food and Drug Administration, European Medicines Agency and Japanese regulators “on behalf of my clients.”
Catherine Austin Fitts, founder and publisher of the Solari Report and another of the expert witnesses for the plaintiffs, told The Defender that Bourla’s attorneys questioned the credentials of another witness — Mike Yeadon, Ph.D. Fitts said she was “surprised” by their claims.
“Yeadon served as vice-president of Pfizer’s allergy and respiratory research unit and worked for many years at Pfizer. Does Pfizer make it a practice to staff the company with unqualified people in senior positions? Does this explain why Pfizer appointed a veterinarian to be the CEO?” Fitts asked, referring to Bourla.
Terhorst said it is “very strange” for Dutch courts to not allow oral testimony by plaintiffs’ witnesses, as otherwise, “it is not easy to substantiate your claims.”
Despite the limitation, Terhorst said the witnesses bolstered the plaintiffs’ case. “The case is important based on the evidence provided by key witnesses,” she said.
“I think we [gave] a very clear sign to the court that there can be not justice if the court is not willing to look further at this expert evidence, because you can come to a judgment based on truth and a real discussion between the parties,” Stassen said during the press conference.
Vaccine-injured were ‘misled’ about safety of COVID shots
In an interview with journalist Fiona Rose Diamond earlier this week, Stassen said the plaintiffs “felt misled” by the Dutch government and by those who promoted the COVID-19 shots in the media.
“They felt misled by the whole system … And they were misled because they were told that this was a safe and effective vaccine, and in fact, the only way out of [the] crisis,” Stassen said.
At Thursday’s press conference, Stassen added that the plaintiffs sued not just because of their injuries, but because “they want the truth.”
Fitts highlighted the significance of the case, noting that under the Dutch legal system, the vaccine-injured can file lawsuits in response to their injuries — contrasting this with legal restrictions the injured face in the U.S.
“The PREP Act has made it impossible for such lawsuits to be brought in the United States,” Fitts said, referring to the Public Readiness and Emergency Preparedness Act of 2005. Under the PREP Act, anyone who produces or administers emergency countermeasures, such as the COVID-19 shots, is shielded from legal liability.
Terhorst noted that the vaccine-injured in the Netherlands face other obstacles.
“Vaccine injury is not even recognized in the Netherlands,” she said. She noted that some vaccine-injured people briefly received treatment under public health programs that the Dutch state earmarked for long COVID patients. However, this treatment was later “terminated.”
Terhorst said lawyers for the Dutch state “said nothing” during the hearing about offering compensation to these victims, including the plaintiffs and their families.
This is one of several obstacles the plaintiffs have faced as this case has progressed. Last year, 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.
Terhorst said van Kessel spent seven months imprisoned in a high-security prison, lost his license to practice law, is not allowed to leave the country and was fitted with an ankle monitor — which was removed Thursday, in parallel with the hearing.
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.
She Followed the Actual Data on COVID Vaccines and Masks — Her Career Took a Huge Hit
By Jill Erzen | The Defender | October 2, 2026
Tracy Beth Høeg, M.D., Ph.D., an epidemiologist and sports physician, said her decision to follow the data during the COVID-19 pandemic came at a steep professional price.
Her research challenged policies on school closures, masking and COVID-19 vaccines. She said the fallout included losing her position at the University of California, Davis, being dropped from an NPR interview and being fired from the U.S. Food and Drug Administration (FDA).
Høeg said her experience exposed the unwillingness of universities, media and public health institutions to adapt when research conflicted with their accepted narratives.
In an interview this week with investigative journalist Paul D. Thacker on The DisInformation Chronicle, Høeg said institutions too often treated the accepted narrative as settled and then dismissed or attacked people who questioned it.
That approach did more than distort the public discussion about COVID-19, Høeg said. It also created a scientific and institutional culture that could affect how other medical questions are handled long after the pandemic.
For Høeg, the solution is simple: Scientists should follow the evidence wherever it leads.
“It’s a core belief of mine that you have to be objective when you’re doing scientific studies,” she said. “Otherwise, you just shouldn’t do them. It’s pointless if you’re not willing to be objective.”
‘I … didn’t realize the jeopardy that I was putting myself in’
During the pandemic, Høeg published 30 to 40 papers on COVID-19 transmission, masking, youth sports, vaccine risk-benefit, pregnancy, long COVID, visitor restrictions and testing.
Some of her research challenged widely accepted claims.
One study found little evidence of COVID-19 transmission among children in Wisconsin schools, which was consistent with data from Europe. Another examined myocarditis risk in boys after their second Pfizer COVID-19 vaccine dose and found the risks outweighed the benefits in boys who didn’t have underlying health conditions.
Høeg said she didn’t initially understand the professional risks she was taking by challenging the prevailing narrative.
“There was sort of a hesitancy to do this sort of research because I think people were afraid for their careers,” she said. “I actually was blessed with having recently moved from Denmark and didn’t realize the jeopardy that I was putting myself in by doing these sorts of studies.”
At the time, Høeg was conducting research at the University of California, Davis.
She said the university received calls, including from Nature magazine, complaining about her studies on pandemic policies. Eventually, the university asked her not to use her affiliation with the school.
Høeg said the university refused to renew her voluntary position in 2022, after the European Journal of Clinical Investigation published her study on myocarditis risks in boys who received the COVID-19 vaccine.
NPR also dropped an interview with Høeg for “All Things Considered” after she raised concerns about masking children during outdoor sports.
In a pre-interview discussion with NPR, she told the outlet, “We don’t have evidence that these masks work to prevent transmission. … Bottom line is, we shouldn’t be doing these unproven things to children that are harmful.”
Soon after, NPR told Høeg she was no longer needed for the interview.
“It does say a lot about our universities and institutions because it’s like they had been brainwashed to an extent to believe what the media was saying rather than actually look at the data,” Høeg said.
‘They repeated the same wording … even when the data didn’t back it up’
In 2022, Høeg and her colleagues conducted a follow-up analysis of a Centers for Disease Control and Prevention (CDC) study on school mask mandates.
Høeg said their analysis used a larger dataset and a longer time period and reached the opposite conclusion about the relationship between mask mandates and COVID-19 transmission among children.
The team’s submission to the CDC’s Morbidity and Mortality Weekly Report (MMWR) was rejected. Høeg said reviewers described the submission as “rife with polemics.”
“Well, maybe it’s polarizing if you disagree with it,” Høeg said.
The rejection unearthed an underlying problem at the CDC, according to Høeg.
“They have a scientific agenda,” she said. “And so as soon as you have a scientific agenda, science has been thrown out the window. Science doesn’t have an agenda other than to find the truth.”
A 2024 analysis by Høeg and colleagues examined 77 mask studies published in the MMWR beginning in 2020. According to Høeg, 75% of the studies said masks were effective, while only 14% reported statistically significant results and none were randomized studies.
One finding especially stood out to her: She said 5% of the studies found masks were connected to higher infection rates, yet “they still concluded that masks worked.”
“They repeated the same wording over and over again in each of the studies, that ‘masks are necessary to decrease the spread’ and ‘masks are critical in controlling the case rates of COVID-19,’” she said. “They use the same sort of wording even when the data didn’t back it up at all.”
‘Why are we demonizing people for looking into this?’
Those concerns followed Høeg into the FDA in late 2025 when she was named acting director of the Center for Drug Evaluation and Research (CDER).
A leaked memo from then-FDA official Dr. Vinay Prasad said career staff had linked at least 10 child deaths to the COVID-19 vaccine between 2021 and 2024.
Høeg said she reviewed the Vaccine Adverse Event Reporting System (VAERS) reports and found that investigations involving medical records and autopsies had already been conducted.
“My question at the time was … why are these not being made public?” Høeg told Thacker.
Høeg said news leaked that she would present information about the deaths and their possible association with COVID-19 vaccines. She said the media response focused on portraying her as an “anti-vaxxer” rather than asking why the deaths had been investigated but not publicly disclosed.
“If we have these sorts of deaths happening in children due to medical products of any kind, why are we sitting on them for years?” she asked. “That’s the take-home I want people to have from this.”
She also questioned why people who investigate potential safety problems are attacked for trying to expose the dangers.
“Why are we demonizing people for looking into this? … Isn’t that what the public wants?” she asked.
‘The deep state really is a thing’
In May, just days after FDA Commissioner Marty Makary resigned, Høeg said she arrived at work to find media reports claiming she had resigned — something she said she knew nothing about.
FDA lawyers later asked her to resign, but she refused to sign the letter. She was subsequently locked out of the agency’s systems and escorted from the building.
Høeg said she never received a performance-based explanation for her termination. She also said the person identified as the author of her termination memo later denied writing or seeing it.
According to Høeg, agency lawyers told her the order came from “way above their pay grade.”
The experience changed how she viewed other departures from the agency. “It opened my eyes to the fact that maybe a number of the people who I thought had resigned really had not resigned,” she said.
“The deep state really is a thing,” she added.
‘Women who want to get pregnant … should be told about these risks’
For Høeg, the concerns she encountered during the COVID-19 era are not limited to COVID-19.
In 2025, she helped organize an FDA panel examining potential risks associated with selective serotonin reuptake inhibitors, or SSRIs, during pregnancy.
The American Psychiatric Association criticized the panel for what it called “misinterpretation and unbalanced viewpoints.” Høeg said the media also portrayed any discussion of potential risks as “misinformation about SSRI use” and a signal that depression wasn’t being taken seriously.
According to Høeg, the panel discussed risks already addressed in FDA labeling and scientific research, including miscarriage, premature birth, postpartum hemorrhage, congenital heart defects and neonatal adaptation syndrome.
“This should not be controversial that women who want to get pregnant and who are pregnant should be told about these risks,” she said.
She also warned about the lack of ongoing monitoring of drug safety.
“The FDA is not actively investigating the safety of these products in pregnancy or at all after the initial trials are done,” she said.
Høeg said the discussion should not be interpreted as an argument against treating depression. “I don’t think that any of this should be synonymous with not taking depression seriously,” she said. “That’s just nonsense.”
‘There’s just no reporting on this. … People have died taking this drug’
Høeg also discussed Tavneos, the Amgen-manufactured brand name for avacopan, a drug approved to treat a type of blood-vessel inflammation.
While at CDER, Høeg said she raised concerns that the pivotal clinical trial used to approve the drug had included manipulated data.
According to Høeg, at least eight deaths had been attributed to the drug because of liver injury.
The New England Journal of Medicine later retracted the paper detailing the trial, and European regulators withdrew the drug’s authorization. While the FDA has proposed withdrawing Tavneos’ approval, it remains available in the U.S.
Yet, the media barely covered it.
“There’s just no reporting on this,” Høeg said. “People have died taking this drug. … We asked for them to withdraw it from the market, and the media is just totally silent.”
Thacker: ‘There was no real learning in the end. … If anything, we became dumber’
Høeg said it is troubling that some of the most disputed COVID-19 policies are still treated as settled questions.
“How is this still part of our collective conversation that people … are still saying school closures were necessary and mask mandates were necessary?” she asked.
Thacker said the failure to learn from those policies could have consequences during the next pandemic. People who developed a “false sense of safety from masks” during COVID-19 could mistakenly assume masks will protect them from a more dangerous virus in the future, he said.
Thacker also questioned whether the country understands anything about the COVID-19 vaccines. “There was no real learning in the end. … If anything, we became dumber,” he said.
Høeg said the problem stems from the widespread failure to reconsider policies when the evidence changed.
“Once the government decided this is what we have to do, they just kept digging in, even though the data didn’t support it,” she said.
“This is why I keep doing these interviews, because it’s important for people to know the truth.”
Watch Høeg on ‘The DisInformation Chronicle’ podcast here:
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.
Florida AG Sues Pfizer, Bourla Over Deceptive Marketing of COVID Vaccines
By Michael Nevradakis, Ph.D. | The Defender | October 2, 2026
Florida Attorney General James Uthmeier on Thursday sued Pfizer and its CEO, Albert Bourla, alleging that the drugmaker misled the public by marketing its COVID-19 vaccine as safe and effective while not disclosing the vaccine’s potential risks to pregnant women, children and teenagers.
The 49-page lawsuit alleges Pfizer violated Florida’s Deceptive and Unfair Trade Practices Act by deceptively marketing its vaccine to the public in turn for making billions of dollars in profit.
According to the complaint, Pfizer’s COVID-19 vaccine marketing campaign focused on two principal themes: that the shot “posed no material safety risks” and that “mass vaccination was necessary to stop the transmission of COVID-19” — even though Pfizer never tested the vaccine’s ability to stop the virus from spreading.
Pfizer possessed extensive evidence that its vaccine caused serious adverse events — including 1,223 reported deaths following vaccination as of February 2021 and 52 miscarriages among vaccinated pregnant women. However, the company assured the public the vaccine was safe.
“Today we sued Pfizer for deceptively marketing the products as safe — making billions — while pregnant women were miscarrying their babies and teenagers were having heart attacks,” Uthmeier said in a statement.
Florida AG says state has track record of success with similar lawsuits
In a statement, Pfizer said the allegations are baseless, and that the “representations made by Pfizer about its COVID-19 vaccine have been accurate and science-based” and that it “stands behind the safety and efficacy” of the product.
But Forrest B. Saunders, communications director for Uthmeier’s office, told The Defender “the complaint and comments by Florida Attorney General James Uthmeier speak for themselves.”
Saunders said Florida has a track record of success with such lawsuits, having “recovered millions for Floridians through consumer protection efforts.”
Naomi Wolf, CEO of Daily Clout and author of “The Pfizer Papers: Pfizer’s Crimes Against Humanity,” helped release documents in 2023 and 2024 revealing serious adverse events among pregnant women and irreversible harms to reproductive health. She called the lawsuit “a glimmer of potential justice long overdue.”
Florida resident Haley Schwartz, who was seriously injured following her COVID-19 vaccination in 2021, also welcomed the suit. She said injuries caused by the vaccine “have received inadequate attention” for years.
“Finally seeing these issues examined through a formal legal process feels significant and creates an important opportunity for greater scrutiny, transparency, and accountability regarding what was communicated to the public,” Schwartz said.
The lawsuit seeks civil penalties of $10,000 for each violation of the state’s consumer protection law — and $15,000 for each violation involving an elderly or disabled person.
Florida seeks to force Pfizer to return some of its profits and is asking for a permanent injunction against further deceptive practices.
Pfizer’s deceptive marketing sought to ‘ensure windfall profits’
According to the complaint, Pfizer engaged in a deceptive and “wide-ranging marketing campaign” to “drive consumer demand” for its COVID-19 vaccine, overcome widespread public skepticism and “ensure windfall profits.”
“This emphasis on the purported safety of the vaccine directly responded to widespread public concerns about a pharmaceutical product that had been developed on an unusually accelerated timeline, with uniquely limited testing and oversight, and employing novel mRNA technology,” the complaint states.
Pfizer’s campaign included public statements by Bourla claiming the COVID-19 vaccine was safe. The complaint cites a January 2023 interview in which Bourla claimed that Pfizer had not detected “a single [safety] signal” linked to the vaccine.
The complaint suggests public skepticism was warranted:
“Pfizer knew that data showed its COVID-19 vaccine was connected to myocarditis and pericarditis among minors; had reason to believe its COVID-19 vaccine would cause adverse events for pregnant women and their unborn babies in the first trimester, including miscarriage [and] thousands of reports of other adverse events including stroke and even death, especially among the elderly.”
By Feb. 28, 2021, Pfizer’s internal adverse event database already contained 158,893 adverse event reports and reports of 1,223 deaths linked to its COVID-19 shot, according to the complaint.
Pfizer by then also “possessed reports for 458 pregnant women exposed to its COVID-19 vaccine during pregnancy” — over half of whom sustained at least one adverse event. Of 52 miscarriages, most occurred during the first trimester, “many within days of vaccination.”
Pfizer ended its COVID-19 vaccine trial involving pregnant women early, due to low participation, particularly among women in the early stages of pregnancy. But the drugmaker didn’t disclose “material facts already in its possession showing the risks associated with its COVID-19 vaccine during pregnancy.”
Pfizer official admitted vaccine not tested for stopping transmission
Pfizer promoted its COVID-19 vaccine as a means of “protecting … loved ones” through a “wide-ranging marketing campaign” which suggested that the vaccine would stop the spread of COVID-19, the suit alleges.
But Janine Small, Pfizer’s president of international developed markets, said the vaccine was not tested on stopping the virus, according to a 2021 statement cited in the lawsuit.
Karl Jablonowski, Ph.D., senior research scientist for Children’s Health Defense (CHD), said the “assurances of safety the company gave required knowledge Pfizer simply did not have.”
He cited a February 2021 Pfizer “nonclinical overview” document listing an extensive range of safety studies Pfizer did not conduct.
“Pfizer’s COVID-19 vaccine may actually have been the least-studied approved product it has made this century,” Jablonowski said.
The lawsuit alleges that Pfizer’s misleading marketing claims translated into a financial windfall for Pfizer and Bourla. Between 2020 and 2023, Pfizer’s COVID-19 vaccine revenue exceeded $80 billion, and Bourla received nearly $102 million in compensation.
Legal liability shield may not protect Pfizer in Florida lawsuit
COVID-19 countermeasures, including vaccines, are protected by a legal liability shield under the Public Readiness and Emergency Preparedness Act (PREP Act) of 2005.
Attorney Ray Flores, CHD’s senior outside counsel, said these protections may not extend to state-level consumer protection cases.
“All states have consumer protection statutes that normally would allow individual consumers to bring suit for fraudulent practices. Under the PREP Act, however, only states have the potential for successful suits,” Flores said.
Kansas and Texas have active lawsuits against Pfizer in the 10th and 5th U.S. Circuit Courts of Appeals, respectively. The suits make similar claims to Florida’s — namely, that Pfizer violated state consumer protection laws by marketing its COVID-19 vaccine as safe and effective.
“All three cases are remarkably similar, as they are brought under parens patriae,” a legal principle that allows states to file lawsuits to protect state residents, Flores said.
However, he said Florida’s lawsuit may face obstacles, as Pfizer may seek to move the case from state to federal court “to invoke PREP Act protection” — similar to what the company did in the Kansas and Texas lawsuits.
Flores said other states may be waiting on the sidelines for the outcomes of the Texas and Kansas cases.
“I wish more attorneys general would take such legal action,” Flores said. “There was a rumor back in 2024 that Utah, Mississippi and Louisiana were also suing Pfizer. It sounded good, and got lots of press, but it was never true.”
Flores also said he would like to see state attorneys general pressure U.S. Health Secretary Robert F. Kennedy Jr. to “flex his muscles” by ending the PREP Act’s liability shield for COVID-19 vaccines.
Bourla defended the liability shield for vaccine makers in an interview last year.
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.
Elmo Sold mRNA Jabs to Your Toddler. Now They Are “Off-Label.”
How Sesame Street, CNN, and federal health officials turned a children’s vaccine campaign into a one-way lesson in trust.
By Sayer Ji | September 30, 2026
How a $240 million messaging machine put a three-year-old puppet to work selling an mRNA shot to parents of infants — and what the government has quietly admitted since.
On June 28, 2022, Sesame Street posted a 60-second video to its YouTube channel titled “Elmo Gets the COVID-19 Vaccine | PSA.”
It’s a well-made piece of persuasion. Elmo, who has been three and a half years old since 1984, shows off his “super duper” bandage. There “was a little pinch. But it was okay.” Then his father, Louie, looks into the camera and speaks to every hesitant parent in America:
“I had a lot of questions about Elmo getting the COVID vaccine. Was it safe? Was it the right decision?”
Eleven seconds later, the doubt has been resolved for you:
“I learned that Elmo getting vaccinated is the best way to keep himself, our friends, neighbors and everyone else healthy and enjoying the things they love.”
A hug follows. Then an announcer: “It’s okay to have questions about COVID vaccines for your kids.”
That’s the move worth studying. The ad takes the parent’s instinct to ask questions, gives it to a beloved puppet, and answers it before the parent has a chance to. It presents doubt so it can close it down.
This was not a whimsical one-off from a children’s television workshop. It was one output of what its own organizers called the largest communications program in our nation’s history, built with federal public-health agencies, a major medical trade association, and tens of millions of corporate dollars.
Four years later, Pfizer-BioNTech’s product is no longer authorized for children ages six months through four years. Federal guidance and product labeling have also narrowed which pediatric uses are on-label, a shift sharply at odds with the PSA’s broad, categorical reassurance. Nobody made a puppet video about that.
This is the story of who built the campaign, what it cost, and what came after.
Part I: Who Was Behind It
Sesame Workshop’s own press release is candid about who was in the room. The PSA was released “in collaboration with the Ad Council and COVID Collaborative’s COVID-19 Vaccine Education Initiative,” and it was “produced in partnership with the Centers for Disease Control and Prevention (CDC) and American Academy of Pediatrics (AAP).”
Five institutions. Each one deserves a name and a face.
Sesame Workshop
The nonprofit behind Sesame Street produced and released the spot. Its campaign lead was Dr. Jeanette Betancourt, Senior Vice President of US Social Impact. Its president at the time, Sherrie Westin, was named CEO in July 2024.
The clearest statement of what Sesame thought it was offering came from its own chief marketing officer. Launching an earlier round of vaccine PSAs, Samantha Maltin, EVP and CMO, said the goal was to:
“… harness the power of Sesame Workshop and the reach of the Ad Council…”
Harness the power. The asset being put to use was fifty years of trust that parents and children have placed in these characters.
The Ad Council
The Ad Council turns corporate media budgets into “public service” messaging. Its president and CEO, Lisa Sherman, was the campaign’s public face. On the Elmo spot:
“It’s important that parents feel informed and confident about what the COVID-19 vaccines mean for their families, and we are proud to work with our partners, medical experts – and of course Elmo – to spread that message.”
She also named the urgency: this was “an important decision many need to make in advance of the upcoming school season.”
COVID Collaborative
The COVID Collaborative is a bipartisan assembly of former officials, and it convened the vaccine education initiative with the Ad Council. Its CEO is John Bridgeland, former Director of the White House Domestic Policy Council. Its president is Gary Edson, and its co-chairs are former Idaho Gov. and Sen. Dirk Kempthorne (R) and former Massachusetts Gov. Deval Patrick (D). The Collaborative is a project of UNITE, chaired by Tim Shriver.
The CDC
The CDC was a named production partner, and it wasn’t a passive one. According to the campaign’s organizers, the CDC provided scientific guidance on all aspects of the campaign, and its brand appeared on select creative assets.
The American Academy of Pediatrics
The AAP, the pediatricians’ professional association, was the other named production partner. Its president in 2022 was Dr. Moira Szilagyi. Looking back later, she said: “Somewhere what got lost in our country, I think, was what a miracle these vaccines were.”
Keep the AAP in mind. It comes back in Part IV.
Part II: Follow the Money
The Elmo spot was built on a large funding structure, and its size helps explain how thoroughly this message saturated American media.
The corporate fund. On November 23, 2020, before any vaccine was authorized, the Ad Council announced a $50 million fund for the COVID-19 Vaccine Education Initiative, created with the COVID Collaborative. By February 2021 it had exceeded that goal.
The COVID Collaborative reports more than $52 million raised. The leading contributors it names are Amazon, Apple, Bank of America, Cisco, CVS Health, Facebook, General Motors, Google and YouTube, the Humana Foundation, NBCUniversal/Comcast, Salesforce, Verizon, Walgreens, and Walmart.
Two of those names stand out. CVS Health and Walgreens both gave the shots the campaign was promoting in their own pharmacies.
The donated media. The money was only the seed. By October 26, 2021, the initiative had surpassed its goal of $240 million in donated media and related publicity. Donors of airtime and ad inventory included Disney (ABC, ESPN, Hulu), FOX, NBCUniversal and Telemundo, ViacomCBS, WarnerMedia, Facebook and Instagram, Google and YouTube, TikTok, Snapchat, Spotify, Pinterest, LinkedIn, and The Weather Channel.
Several of the same platforms that donated airtime and advertising inventory to the vaccine-education campaign were simultaneously under public and private pressure to enforce COVID-19 misinformation rules against specifically identified individuals, including people named in CCDH’s ‘Disinformation Dozen’ report. YouTube later [restored] my channels and stated that, after review, they did not violate its Community Guidelines.
The taxpayer layer. Alongside the private effort, HHS ran its own $265 million COVID public-education campaign starting in summer 2020. That included a $250 million NIH award to the Fors Marsh Group, which created the “We Can Do This” brand, all paid for through a $300 million interagency agreement drawing on CDC’s CARES Act funds. Under its “Vaccinate with Confidence” framework, the CDC funded more than 200 partners. Across the March 2021–December 2022 rollout, it funded 110 primary and 1,051 subrecipient partners at the national, state, and community level.
A note on accuracy. I have not found documentation that Pfizer or Moderna directly paid for the Elmo spot, and the campaign materials don’t list them as partners. Pfizer does appear as a Sesame Workshop donor in later years, in the $100,000–$249,999 band of its 2024 impact report. That’s worth knowing, but it’s a separate fact. The documented structure is damning on its own: corporate money, federal science guidance, and a medical trade association, all speaking through a puppet.
Part III: It Wasn’t One Ad
The Elmo spot was the youngest-audience edge of a sustained effort to put Sesame Street characters to work for vaccine messaging.
- November 2021: CNN and Sesame Street co-produced a family town hall, “The ABCs of COVID Vaccines.” That same month, Big Bird delivered his own pro-vaccine message to young viewers, which drew public criticism from Sen. Ted Cruz.
- June 2022: Elmo’s PSA, released days after the FDA’s emergency authorization for children as young as six months.
- Later: Sesame Workshop, the Ad Council, COVID Collaborative, and CDC launched a further series of PSAs with Elmo, Louie and other Muppets, “created in close partnership with the CDC.”
The criticism started right away. Cruz accused Sesame Street of having Elmo “aggressively advocate” for shots in young children and noted that the spot cited no scientific evidence. The comedian Russell Brand put it more sharply:
“When it starts getting into complex territory that involves the power of the state, the influence of pharmaceutical companies, the impact of coronavirus on young children — these are not issues I want resolved by members of Elmo’s family.”
The critics were dismissed as cranks at the time. Here is what the government has said since.
Part IV: The Walk-Back Nobody Advertised
There was no $240 million campaign for any of what follows. No Muppets and no hug at the end. It came out as label changes, regulatory memos, and footnotes in clinical guidance.
The cardiac warning got stronger
On June 25, 2025, the FDA required and approved expanded warnings about myocarditis and pericarditis on Pfizer’s Comirnaty and Moderna’s Spikevax. The new label estimates about 8 cases per million doses in people aged 6 months through 64 years, and about 27 per million in males aged 12 through 24, in the week after vaccination.
The most important sentence isn’t about frequency, though. It’s about what happened to the hearts afterward:
“… at a median follow-up of approximately 5 months post-vaccination, persistence of abnormal cardiac magnetic resonance imaging (CMR) findings that are a marker for myocardial injury was common. The clinical and prognostic significance of these CMR findings is not known.”
Read it twice. Five months out, markers of heart-muscle injury were “common,” and the agency says their long-term significance is “not known.” This isn’t a critic’s claim. It comes from an FDA-funded, FDA-co-authored study, and it’s now printed on the label.
The spot told parents “there was a little pinch. But it was okay.” Nobody in the ad said “unknown long-term cardiac significance.”
The authorization for the youngest children was pulled
On August 27, 2025, Pfizer-BioNTech’s COVID vaccine was no longer authorized for children under 5. CDC’s current clinical guidance puts it plainly: “Pfizer-BioNTech COVID-19 Vaccine is no longer authorized in the United States for children ages 6 months–4 years.”
That is the age group the Elmo spot was released to reach. It went out days after emergency authorization opened the shots to children as young as six months. Four years later, one of the two products it promoted to parents of those children can’t legally be given to them.
Healthy children are now “off-label”
The broad “everyone six months and older” recommendation is gone. In May 2025, HHS dropped the routine recommendation for healthy children, and the CDC moved to what it calls shared clinical decision-making.
CDC’s current guidance, updated September 23, 2026, limits Moderna’s approval for the youngest children to those with “at least one condition that places them at increased risk for severe COVID-19.” Then it states the conclusion outright:
“Vaccination of children 5-11 years of age with any product other than Spikevax or Comirnaty and vaccination of children in this age group without high-risk conditions is off-label use.”
“Vaccination of persons 12-64 years of age without high-risk conditions is off-label use.”
In 2022, the message was that vaccinating Elmo was “the best way to keep himself, our friends, neighbors and everyone else healthy.” In 2026, the CDC’s own wording is that giving the shot to a healthy child is off-label.
The deaths question
On November 28, 2025, Dr. Vinay Prasad, then director of the FDA’s Center for Biologics Evaluation and Research, sent staff a memo headed “Deaths in children due to COVID-19 vaccines and CBER’s path forward.” He wrote that career staff “have found that at least 10 children have died after and because of receiving COVID-19 vaccination,” based on an initial review of 96 child deaths reported to VAERS between 2021 and 2024.
The FDA’s formal analysis, made public in May 2026, came back more cautious. Of the 96 reports reviewed, none were classified as “certain.” Five were classified “possible” and two “probable,” mostly involving myocarditis, with an average age of 13. The agency stressed that these classifications don’t prove causation.
Media coverage framed that result as a debunking. Set the headline aside, though. The FDA’s own conservative review, using WHO causality criteria, still found seven child deaths it could not rule out as vaccine-related, and it called two of them probable.
And yet, still being promoted
This is where the irony stops being subtle.
Visit the FDA’s parent-facing page today, Vaccines for Children – A Guide for Parents and Caregivers. The COVID-19 vaccine is still listed alongside measles and polio among “the most commonly administered vaccines.” And parents are still told:
“Getting a COVID-19 vaccine is the best way to prevent COVID-19, including the potential consequences of hospitalization and death.”
That’s Louie’s line almost word for word, four years later, from the same agency whose label now carries the cardiac warning, whose authorization for under-5s was pulled, and whose own reviewers flagged seven child deaths.
The American Academy of Pediatrics, a production partner on the Elmo spot, hasn’t backed off either. As of September 2026, the AAP recommends COVID-19 vaccination for “all infants and children ages 6 months through 23 months,” and for “anyone ages 2 to 18 who isn’t at risk but whose parents or guardian wants them to get a shot.”
So we have two different postures at once. The regulator has narrowed approval, expanded the warning, and reclassified healthy-child use as off-label. The professional association that helped make the puppet ad still recommends the shot for every baby. And the FDA’s own parent guide still uses the 2022 talking points.
Part V: What They’ll Say — and Why It Doesn’t Save Them
Serious readers deserve the strongest counterargument, so here it is.
CDC’s guidance cites a retrospective cohort of more than 4 million people aged 16–25 from 2020 to 2025. It found myocarditis incidence of 0.05% after COVID illness versus 0.005% after vaccination. In other words, the infection carries a higher myocarditis risk than the shot.
That’s a legitimate data point and I’m not going to pretend it doesn’t exist. It doesn’t answer the question this piece is asking, for three reasons.
First, the comparison is an average over a population of teenagers and young adults. It says nothing about a healthy toddler with near-zero risk of severe disease. That’s the child this campaign targeted, and the child for whom the CDC now calls the shot off-label.
Second, it doesn’t address the finding printed on the label: persistent markers of heart-muscle injury at five months, of “not known” significance. The open letter discussed below says there are “no studies demonstrating prevention of hospitalization or death” in children. If that’s right, an unknown cardiac risk is being weighed against a benefit that was never shown.
Third, and most importantly, the argument here doesn’t depend on any contested injury number. It depends on an asymmetry. When the product was being promoted, it got a puppet, $50 million, a quarter-billion in donated airtime, the CDC’s logo, and the pediatricians’ endorsement. When the regulator narrowed the product, it got a label revision and a footnote. The public was sold a certainty the evidence never supported, and was never told when that certainty was withdrawn.
That isn’t public health communication. It’s a marketing campaign that never issued a correction.
Part VI: The Petition — Why I Signed
Earlier this month, 168 physicians, scientists, researchers, lawmakers, and health-freedom advocates, representing more than 63 million followers, sent an open letter to HHS Secretary Robert F. Kennedy Jr. and President Trump demanding removal of the mRNA platform. The effort was coordinated by Dr. Mary Talley Bowden. The signatories include Rep. Thomas Massie, former Rep. Marjorie Taylor Greene, Louisiana Deputy Surgeon General Dr. Sean Troxclair, Dr. Peter McCullough, Dr. Robert Malone, Dr. Aseem Malhotra, Tucker Carlson, and others.
I’m one of them, and I want to explain why.
The letter’s first demand is to “ban mRNA/gene therapy-derived technologies for all vaccines.” That includes the products still being given to children. Its other demands are to end the PREP Act declaration and its “ironclad liability shield for manufacturers and administrators,” ask Congress to repeal the PREP Act, ban direct-to-consumer pharmaceutical advertising, end the incentive structures that push providers toward medical coercion, and end conflicts of interest at the CDC, FDA, NIH, and NIAID.
On children specifically, the letter makes the point this whole piece has been building toward:
“Parental choice is not realistic when parents are not getting informed consent on the true risks of these products.”
It also takes on the “shared clinical decision-making” framework directly:
“By treating the decision to inject a child with mRNA as a ‘shared decision,’ while treating routine injections as the default, a dangerous legal precedent is being set that assigns powers to the federal government that have historically belonged solely to parents.”
According to the letter, more than 50 million Americans received mRNA COVID shots this year, including about 7 million children, and HHS has awarded $1.24 billion in contracts to Pfizer for future mRNA shots, “including for children.”
The Elmo spot is exactly why that line about informed consent matters. You can’t give informed consent to a hug from a puppet. A one-minute ad that turns a parent’s hesitation into a script and then answers it in eleven seconds isn’t informing anyone. It’s persuasion aimed at the people least able to push back: parents who trust Sesame Street and children who love Elmo.
The letter isn’t the only pressure. Children’s Health Defense’s citizen petition, asking the FDA to revoke the Pfizer and Moderna licenses, has been pending since December 8, 2025 and has drawn more than 104,000 public comments in support. On September 25, the Independent Medical Alliance called on the CDC to immediately withdraw its “off-label” recommendation for healthy infants, children, and adults.
HHS’s response to the open letter, through press secretary Emily Hilliard, was that Secretary Kennedy “believes mRNA products warrant heightened scientific scrutiny,” and that HHS had “wound down investments in mRNA vaccines for upper respiratory viruses because the technology does not effectively protect against infection from rapidly mutating viruses such as COVID-19 and flu.”
Think about that sentence next to the Elmo spot. The federal health department now says the technology “does not effectively protect against infection” from COVID. In 2022, a puppet told America it was “the best way to keep himself, our friends, neighbors and everyone else healthy.”
Heightened scrutiny isn’t enough. A product that federal officials now concede doesn’t reliably prevent infection, that carries a cardiac warning with unknown long-term significance, whose own regulator calls it off-label for healthy children, and whose makers are protected from liability should not be given to children at all.
Conclusion: The Correction That Never Aired
Every institution in the Elmo spot is still operating. Sesame Workshop is still making children’s programming. The Ad Council is still running “public service” campaigns. The CDC’s logo is still on its creative. The AAP still recommends the shot for every infant. The FDA’s parent guide still repeats Louie’s line.
None of them has produced a PSA that says: We told you this was the best way to protect your baby. Since then the label has been changed to warn about heart injury. The authorization for the youngest children was withdrawn. The government now calls this use off-label for healthy kids. We’re sorry we used Elmo to tell you otherwise.
That’s the one-minute spot this country is owed. Until it airs, the original belongs where I’ve put it: in the Hall of Fame of the Covid-era Mockingbird Media, as a case study in what happens when institutions that are supposed to earn a parent’s trust decide to manufacture it instead.
Watch it again. Listen for the moment Louie asks, “Was it safe?”
It was a good question. It still is. They just never let him wait for the answer.
DEATH SPIKES & RISING CANCER IN OUR YOUTH EXPLAINED
The HighWire with Del Bigtree | September 24, 2026
Fresh off testifying at Canada’s Allison Inquiry, physicist Denis Rancourt joins Del to examine mortality and cancer data among 5- to 24-year-olds—and what could be behind their striking, lockstep rise.
HE SAVED LIVES. NOW HE FACES PRISON.
The HighWire with Del Bigtree | September 17, 2026
Emergency medicine physician Ron Elfenbein M.D. went from running federally supported monoclonal antibody clinics to facing federal health care fraud charges after challenging the government’s handling of COVID therapeutics.
THE RISE IN CANCER THEY CAN’T EXPLAIN AWAY
The HighWire with Del Bigtree| September 10, 2026
A mouse study, a wave of new global cancer data, and disturbing testimony out of Canada are all pointing in the same direction. Jefferey digs into what the lipid nanoparticle from the COVID-19 vaccine might be doing to your immune system, and why some researchers think this issue is only getting started.
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New Book
The Garlic Book — 2026
Lies are Unbekoming | November 5, 2026
What The Garlic Book shows
The book is in four parts.
Part One, The Record, treats the history of garlic as evidence. From the clay garlic bulb placed in an Egyptian grave nearly six thousand years ago, through the Ebers Papyrus, through Hippocrates, Dioscorides, Pliny and Galen, the Arab physicians under Avicenna, the medieval herbals, Culpeper, and the plague years, to the last era in which Western physicians prescribed garlic as a matter of course, which ran from 1850 to 1945. It closes with the living traditions that never stopped using it, and with the folklore of charms, vampires and the evil eye.
Part Two, The Chemistry and the Evidence, sets out what is known about why a clove has no smell until it is cut, and why the order of crush, rest and heat changes the medicine. It then reads the clinical evidence against the historical record — bacteria, blood and vessels, cancer epidemiology, metals and fatigue — and names the trials that went against garlic as directly as the trials that went for it, including the 2007 Stanford trial funded by the US National Institutes of Health which found that raw garlic, garlic powder and aged garlic extract moved LDL cholesterol no more than placebo did. It then turns to onion, garlic’s closest relative, and reads the newer evidence published since 2015, before closing with the whole of the record through the terrain lens.
Part Three, Why Medicine Set It Aside, asks the question directly. One chapter contrasts the pharmaceutical model of isolating a single active compound with the folk model of combining whole plants, and reports what the garlic evidence says about which model works better. One chapter examines the economics of research on a plant that cannot be patented. One chapter — Fire Cider — tells the story of a folk preparation whose name was taken into a United States trademark by a Massachusetts company in 2012, and won back by three herbalists in 2014 who documented forty years of prior use through Rosemary Gladstar and her students into the older tradition.
Part Four, Garlic in Practice, is the working manual — the kitchen pharmacy, traditional uses by body system, a full chapter on safety and interactions, and a complaint-by-complaint practical guide. The book closes with The Trial That Was Never Run — a one-chapter reading of the whole evidential architecture.
At the back: two appendices (a traditional list of uses, and a preparation quick-reference), a full bibliography, and a live index.
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