Dr. McCullough Drops the Hammer in the Senate — FDA Concedes with Expanded Myocarditis Warning

“When a product causes death, that demands a black box warning — immediately.”

That was the clear and urgent message from Dr. Peter McCullough, testifying before the Senate Homeland Security and Governmental Affairs Committee this week at a hearing titled: The Corruption of Science and Federal Health Agencies: How Health Officials Downplayed and Hid Myocarditis and Other Adverse Events Associated with the COVID-19 Vaccines.

Dr. McCullough presented data from both his clinical experience and the peer-reviewed literature, exposing the widespread risks of COVID-19 mRNA injections — particularly myocarditis in young men and fatal vaccine outcomes confirmed by autopsy.

“I’ve examined thousands of patients with this problem,” he told the Senate. “Before the pandemic, I had seen just two cases in my entire career.”

Just one day before the hearing, likely for preemptive damage control purposes, the FDA quietly updated its myocarditis warning on Pfizer and Moderna’s COVID-19 vaccines, expanding the risk category to males aged 16 to 25 and citing an incidence of 8 cases per million doses for the 2023–2024 formulations. Unfortunately, no mention of death was added — despite robust, peer-reviewed autopsy evidence confirming fatal vaccine-induced myocarditis.

Dr. McCullough referenced multiple such cases, including the tragic findings of Gill et al, who documented two teenage boys (ages 16 and 17) found dead at home just days after receiving the Pfizer vaccine. Autopsies confirmed unequivocal myocarditis as the cause of death.

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The Century of Evidence Vaccines Cause Sudden Infant Death Syndrome

•Since at least 1933, the medical community has known that vaccines cause infant deaths. To conceal this, those deaths were renamed “crib death” and then “Sudden Infant Death Syndrome” (SIDS), eventually being attributed to infants not sleeping on their backs.

•This revisionism is not supported by the existing evidence nor the historical changes in the frequency of SIDS. Most recently, SIDS rates have had an unprecedented decrease in tandem with the COVID-19 lockdowns reducing vaccination rates.

•The vaccine most strongly associated with SIDS, DPT, was protected for decades by the government despite knowing a large body of evidence around the world showed it killed infants—particularly when an inevitable hot lot was released. Eventually, so many injury lawsuits were filed that in 1986, the government had to give blanket immunity to the vaccine manufacturers.

•This article will concisely review the vast body of evidence showing vaccines cause SIDS and reveal the mechanism modern research has now repeatedly proven causes vaccines to trigger infant death.

We’re always told that vaccines were a medical marvel that safely ended the dark age of infectious disease. However, when the actual records are examined, they often abjectly failed to prevent those diseases, and worse still, frequently caused outbreaks and severely injured many of the recipients.

This in part resulted from the inherent toxicity of vaccines and in part because manufacturing challenges regularly resulted in hot lots being released. Rather than address this, the vaccine industry chose to create a variety of strategies to conceal those issues, such as enshrining the dogma “all vaccines are safe” and giving blanket legal immunity to all the “safe” vaccines.

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Vaccine Side-Effects: Democrats Lied, Thousands Died

So now we learn not only that Joe Biden has Stage Five prostate cancer, but that starting in February 2021, the POC/LGBTQ committee that was operating Biden like a Muppet concealed, then downplayed the risk of heart disease from the COVID vaccines.

It’s funny how we find out all this dirt, within 48 hours after the committee’s announcement about Joe’s cancer.  Because he’s got a few months to live, he’s now officially the “Fall Guy.”

Everything bad can be blamed on him, if it can’t be blamed on Trump.  All the Muppeteer committee members can pretend they’re innocent and resume their White House and Cabinet posts on January 20, 2029 if the Democrat party Deep State (DPDS) steals another presidential election.

From Daily Wire:

According to the report from the Senate Permanent Subcommittee on Investigations, officials knew as early as February 2021 that the vaccines were associated with myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the thin sac surrounding the heart). Still, they waited to warn the public until June as they pushed the vaccine on Americans.

The report concludes that U.S. health officials “knew about the risks of myocarditis,” “downplayed the health concern,” and deliberately “delayed informing the public about the risk.”

Sen. Ron Johnson (R-WI), who chairs the committee and will lead a hearing on it later this afternoon, told The Daily Wire that Biden officials delayed reporting the side effects because they were concerned about “vaccine hesitancy.” 

“But in being concerned about that, they violated the inviolable principle of informed consent,” Johnson said.

Here is the full subcommittee report.  This report never would have been prepared if Democrats had kept control of the Senate last fall.  The Subcommittee on Investigations would have been launching new bogus investigations into Team Trump instead.

Spearheaded by Dr. Anthony Fauci, the official diktat of the DPDS was that the vaccines were “safe and effective.”  They knew better.  The Israelis had started distributing Pfizer vaccines several weeks before we did.  So they knew that vaccinated patients were getting myocarditis with alarming frequency, months before we did.
They were warning Joe’s Muppeteer committee, but that committee wasn’t passing on this warning to the American people.

This is another one of Fauci’s many crimes against humanity, the most evil being his funding of gain-of-function research at the Wuhan Institute of Virology, using our tax dollars.  That’s how COVID was unleashed upon the world, causing the deaths of 2 million people worldwide, including a million Americans.

Very few government figures in recent history — Hitler, Stalin, Chairman Mao and Pol Pot, for example — have killed more of their own countries’ people.

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COVID Vaccine “Safe and Effective” Narrative Collapses on Camera

The “safe and effective” narrative collapsed on camera during Senator Ron Johnson’s explosive Senate hearing on COVID-19 vaccine injuries Wednesday afternoon.

Senator Ron Johnson brought the receipts, exposing how the Biden administration DELIBERATELY hid vaccine harms from the public.

Then Dr. James Thorp (OB-GYN) revealed miscarriage data so disturbing, it left the room silent.

This is the Senate hearing they never wanted you to see. I turned three hours of footage into a five-minute read.

Senator Ron Johnson opened the hearing with a bombshell: the Biden administration knew about deadly heart risks tied to the COVID shots, and deliberately kept it from the public.

Johnson released newly subpoenaed records exposing a detailed timeline of what officials knew and when. While Pfizer and Moderna received insider updates, doctors and citizens who raised concerns were silenced.

In February 2021, Israeli health officials warned the CDC of “large reports of myocarditis, particularly in young people” following Pfizer injections, just two and a half months after the vaccine received emergency use authorization.

By April, the CDC was already reviewing myocarditis data from Israel and the Department of Defense. But instead of alerting the public, they stayed quiet.

By the end of that month, VAERS had recorded 2,926 deaths, nearly half of which occurred within three days of injection. “Somebody ought to be looking at it,” Johnson said.

In May, the CDC considered issuing a formal health alert—but scrapped it. They replaced it with watered-down guidance that removed a key warning for doctors to restrict physical activity in myocarditis patients.

Francis Collins, then director of the NIH, brushed it all off. “Senator, people die,” he told Johnson.

In just six months, the toll was staggering: 384,270 reports of adverse events, 4,812 deaths, and 1,736 of those occurred within just 48 hours of injection.

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FDA Directs COVID-19 Vaccine Makers to Expand Heart Inflammation Warning

The Food and Drug Administration (FDA) has directed COVID-19 vaccine manufacturers to expand the warning for two forms of inflammation, according to letters made public on May 21.

The FDA told BioNTech, which produces a vaccine with Pfizer, and Moderna to update warnings regarding myocarditis—or heart inflammation—and the related condition pericarditis.

Richard Forshee, acting director of the FDA’s Office of Biostatistics and Pharmacovigilance, said that new information has emerged, including a 2024 FDA study that found that some myocarditis patients had signs of heart scarring months after vaccination.

The companies must update labels to state that following administration of the 2023–2024 versions of the vaccines, “the highest estimated incidence of myocarditis and/or pericarditis was in males 16 through 25 years of age,” Forshee said. The highest estimated incidence of the post-vaccination inflammation is about 38 cases per million doses for both vaccines, according to the proposed update.

The current warnings say that the highest observed risk after Moderna vaccination is in males aged 18 to 24 and that the highest risk after Pfizer-BioNTech vaccination is in males aged 12 to 17.

The companies were also directed to add new information summarizing the FDA study, including that “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 updates should also state that “it is not known if these heart MRI findings might predict long-term heart effects of myocarditis,” according to the letters.

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Another “Conspiracy Theory” PROVEN TRUE about mRNA CLOT SHOTS reveals tricked human cells keep producing DEADLY SPIKE PRIONS indefinitely

We called it at the beginning, when Big Pharma and the CDC were lying through their teeth, claiming that the mRNA “technology” would only have your cells create spike proteins for a short amount of time, just long enough for your immune system to create antibodies, and then end the production of the virus-mimicking prions. Big fat lie.

First off, the prions don’t just remain at the site of injection. That was a lie. The spike protein prions spread throughout the vascular system, invade the cleansing organs, the brain and the ovaries, and use light to join together to form white, rubbery clots that drive all-cause mortality rates to skyrocket.

Clot shots altered the injected humanoids to be walking prion factories who are dying of all-cause mortality that all boils back to the mRNA Trojan Horse “technology”

Millions of nanoparticles are created by tricked cells for indefinite periods of time, possibly forever, and the injected humanoids around the globe are suffering mass health detriment. That’s right, Moderna and Pfizer clot shots hijack the immune cells, rewrite your DNA and RNA, and prolong spike protein prion production POSSIBLY FOREVER, in the shortened life of the billions of gene-altered humans who succumbed to the plandemic scam. What a shame.

A groundbreaking study published in Nature has upended long-standing assurances from health authorities that mRNA COVID-19 vaccines quickly degrade in the body. Instead, the research reveals that Pfizer and Moderna shots reprogram immune cells to extend their genetic instructions, forcing prolonged spike protein production — contrary to official claims that effects would last only “a few weeks.” The findings, led by Polish researchers (Krawczyk et al., 2025), expose a hidden mechanism that could have serious long-term health implications, raising urgent questions about safety, transparency, and regulatory oversight.

The study found that immune cells, particularly macrophages, activate an enzyme called TENT5A in response to mRNA vaccines. This enzyme rewrites the vaccine’s genetic code, doubling the length of its poly(A) tail — a molecular timer that determines how long mRNA survives. In some cases, Moderna’s mRNA tail extended from 100 to 200 nucleotides, drastically prolonging spike protein production.

“This wasn’t just persistence—it was amplification,” said Dr. Peter McCullough, a cardiologist and vaccine safety advocate. “The body is essentially tricked into editing the shot’s instructions to make it last longer. This was never part of the clinical trials.”

Public health officials, including CDC advisor Dr. Paul Offit, previously asserted that spike protein production would last only “a couple of weeks.” Yet studies have since detected spike protein in blood samples for up to 709 days post-injection. Moderna’s own 2024 internal documents acknowledged “unacceptable toxicity” risks, yet regulators fast-tracked the shots without addressing these concerns.

Molecular biologist Dr. Jessica Rose likened the process to “giving someone a self-replicating memo. The memo was supposed to be read once and discarded. Instead, the recipient photocopies it endlessly.”

Unlike mRNA vaccines, Novavax’s protein-based shot — which delivers pre-made spike protein — does not trigger TENT5A activity. Immunologist Dr. Byram Bridle explained, “The lipid nanoparticles in Pfizer and Moderna’s shots are the Trojan horse. They smuggle synthetic mRNA into cells, but the payload doesn’t just fade away — it gets enhanced by the immune system.”

The Nature study challenges the foundational safety claims of mRNA vaccines, revealing a mechanism that could lead to prolonged spike protein exposure and unknown health risks. With mounting evidence of regulatory oversights and undisclosed dangers, the findings demand urgent scrutiny. As the scientific community grapples with these revelations, millions who received the shots now face unanswered questions about their long-term well-being. The era of blind trust in rushed medical interventions may be over—but for many, the consequences are just beginning.

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US officials delayed warning public about heart inflammation risk from COVID shot: report

U.S. health officials knew about the risks of myocarditis from COVID-19 vaccines but downplayed the concern and delayed informing the public about the risks of taking the jab — that is according to a new Senate report released by Sen. Ron Johnson Wednesday.  

Johnson, R-Wis., chairman of the Senate Permanent Subcommittee on Investigations, has been investigating the safety and efficacy of the COVID-19 vaccines. Earlier this year, he subpoenaed the Department of Health and Human Services (HHS) for records relating to COVID-19 vaccine safety data and communications about the pandemic. 

The interim report, spanning 55 pages, obtained and reviewed by Fox News Digital, revealed that Biden administration officials “withheld crucial health information from the Subcommittee and the public.” 

Since 2021, Johnson has sent more than 70 oversight letters, which he says were “either completely ignored or inadequately addressed.” 

The report highlights the records Johnson has obtained pursuant to the subpoena from the new, Trump administration-led health agency. Specifically, the report focuses on HHS’ awareness of and response to cases of myocarditis—a type of heart inflammation—following COVID-19 vaccination.

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The First Step on the Covid Shots

The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) is holding a very important meeting on May 22, 2025. Under consideration at this meeting is the fate of the Covid booster shots. There has been considerable anticipation as well as media claims that current recommendations and authorization for these products’ use, particularly in children and pregnant women, may be discontinued. 

Public comments are currently being solicited for the meeting, and wide public interest surrounds this event. Unfortunately, I have received reports from colleagues that some comments submitted to the committee calling for discontinuation of these vaccines have disappeared from the FDA website.

Furthermore, an important article from the FDA published today in the New England Journal of Medicine acknowledges the huge discrepancies in Covid vaccine recommendations in the US vs. other countries – as I describe in detail below. The article hints yet again at possible changes in official recommendations regarding the Covid vaccines. In terms of actual changes, however, none have yet been made official 

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FDA plans to require clinical trials before approving annual COVID vax boosters for healthy people

Food and Drug Administration plans to require new clinical trials before approving annual COVID-19 vaccine boosters for healthy Americans under 65 years old.

The plan appears in a paper published Tuesday in the New England Journal of Medicine, in which FDA Commissioner Dr. Marty Makary and Dr. Vinay Prasad, the FDA’s vaccine chief, wrote any new COVID shot must undergo placebo-controlled clinical trials, NBC News reported

This means that the release of updated COVID vaccines for healthy children and adults this fall will likely be delayed.

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The Covid-19 Crisis: How Political Meddling Threatens Your Health and Medical Freedom.

Doctors who successfully used early COVID-19 treatments like ivermectin faced severe backlash and censorship from medical and government authorities

Hospitals repeatedly blocked effective interventions, putting patients at unnecessary risk by ignoring treatments that could have prevented severe illness

Over 38,000 deaths linked to COVID shots were reported in the Vaccine Adverse Event Reporting System (VAERS), yet health authorities downplayed these numbers

Health care professionals experienced threats to their medical licenses simply for advocating patient-centered treatments and sharing honest clinical results

Taking control of your medical freedom means knowing your rights, documenting your decisions, and actively choosing doctors who prioritize your health over politics

Trust in hospitals and health institutions is sharply declining because of how the health care industry has handled the COVID-19 pandemic. From forced treatments to draconic lockdown mandates, people all over the world suffered greatly. Even doctors who figured out effective treatments that helped save lives were vilified for spreading “misinformation.”

One such case is Dr. Mary Talley Bowden, a Texas-based physician who has treated COVID-19 patients during the height of the pandemic. During her time working in a hospital setting, she observed firsthand how patients recovered quickly using treatments such as ivermectin and monoclonal antibodies. All of this, and more, was discussed in her interview with Tucker Carlson featured above.

Why Vaccine Safety Suddenly Became a Political Battlefield

Getting vaccinated was once viewed as a straightforward part of health care. You’d go your doctor, get your shot, and move on with life, confident you’d done the right thing for your health. While many have criticized vaccinations and their adverse effects on human health, the arrival of the SARS-CoV-2 virus put the entire field under the watchful eyes of the public.

Now, getting the shot isn’t just a health care choice — it’s deeply entwined with politics. Doctors who tried treating their patients with methods outside the official rules faced intense backlash. Bowden shares her side of the story:

• Early treatment is crucial — Using drugs like ivermectin and monoclonal antibodies, she successfully helped thousands of patients recover quickly and fully. Recounting her experience in 2021:

“[M]onoclonal antibodies came about, and those worked great. I mean, I could get as many doses I wanted. I’d get them the next day. I’d just contact the manufacturer, say, I need 200 doses to be at my doorstep. Great. They worked wonderfully. People turned around very quickly.”

• Authorities pushed back against treatments that worked — One reason is that these early treatments undermined the vaccine-focused public health strategy. Powerful organizations insisted vaccines were the only real solution, dismissing alternatives. If patients could recover fully without the vaccine, fewer people would rush to get vaccinated, and Big Pharma wouldn’t like that.

“So this is following the rollout of the COVID shots. The government is upset because people are not buying it. People are not getting them. There’s very low uptake, very low interest. There’s suspicion of these shots,” Bowden says.

“So in March, they started their PR campaign. The government, they went after ivermectin. The FDA put something on their website about, you can’t use ivermectin for COVID. Biden doled out $11.5 billion to groups around the country. Initially, it started with 275.

It went up to 17,000 influencers, church groups, sports leagues, all sorts of people just funneling out taxpayer money to go after doctors like myself that were spreading ‘misinformation’ and to push people to get these COVID shots.”

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