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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WHO’s Pandemic Agreement is adopted despite concerns about unelected institutions imposing global policies

Members of the World Health Organisation (“WHO”) adopted a global pandemic accord on Tuesday, 20 May 2025; 124 countries voted in favour, no countries voted against, while 11 countries abstained and 46 countries were not present.  The total votes cast don’t add up, but those are the numbers WHO has declared.

For the countries that abstained – of which, shamefully, the UK was not one – their concerns included loss of national sovereignty, lack of legal clarity and the risk of unelected institutions imposing policy.

Please note: The Pandemic Agreement has been called various names over the years.  It has also been referred to as the Pandemic TreatyPandemic Accord and WHO Convention Agreement + (“WHO CA+”). 

To ensure the Pandemic Agreement was adopted by the easiest possible route, WHO had determined that a vote need not take place, and instead it would be adopted by “consensus.”

Surprised that a “democratic institution” did not want to have a vote, Slovakia requested that a vote on the draft Pandemic Agreement take place, which Tedros the Terrorist attempted to stop hours before the vote was scheduled.

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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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Tulsi On Fauci’s Role In Funding COVID Pandemic: “Is It Any Wonder He Sought A Preemptive Pardon?”

Director of National Intelligence Tulsi Gabbard told Megyn Kelly that one reason Dr. Anthony Fauci sought a preemptive pardon before Joe Biden left the White House is because he lied under oath about helping fund the Covid-19 pandemic.

Gabbard recounted the numerous times that Fauci denied providing funding for gain-of-function research at the Wuhan Institute of Virology (WIV) while being questioned under oath by Sen. Rand Paul (R-KY).

“So is it any wonder that he sought a preemptive pardon for anything during a certain period of time by President Biden before he left office,” Gabbard asked.

In the five years since the pandemic first began, the official story that the SARS-CoV-2 virus originated in a Wuhan wet market has been gradually walked back by members of the media, the intelligence community and the government.

The most likely origin of the virus, according to Kelly, is from a lab leak at the WIV where research was being performed on bat coronaviruses.

Earlier this month, the State Council Information Office of the People’s Republic of China released a white paper claiming that the U.S. was trying to “shift the blame” for the virus to China, even as Chinese officials accused the U.S. of potentially being the origin point of the virus.

Gabbard said she has not yet read the white paper but maintains that the postmortem on the Covid-19 pandemic is far from over.

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Justice Department Opens Criminal Investigation Into Andrew Cuomo

The Justice Department opened a criminal investigation into former New York governor – and current NYC Mayoral front-runner – Andrew Cuomo over his testimony on nursing home deaths during the Covid pandemic.

Last month House Oversight Chairman James Comer (R-KY) sent a resubmitted criminal referral to Attorney General Pam Bondi, demanding the Department of Justice pursue charges against disgraced former New York Governor Andrew Cuomo for lying under oath during pandemic-era investigations.

The letter, addressed directly to AG Pam Bondi, accused Cuomo of violating 18 U.S.C. §1001, a federal statute prohibiting false statements to Congress:

On October 30, 2024, the Select Subcommittee on the Coronavirus Pandemic (Select Subcommittee) referred former Governor of the State of New York, Andrew M. Cuomo, for making criminally false statements in violation 18 U.S.C. §1001.1

To our knowledge, the Biden Administration ignored this referral despite clear facts and evidence. Accordingly, we request you review this referral and take appropriate action. For your reference, the referral is attached to this letter.

The Committee on Oversight and Government Reform is the principal oversight committee of the U.S. House of Representatives and has broad authority to investigate “any matter” at “any time” under House Rule X.

TGP reported multiple times in 2020 how Governor Cuomo in New York implemented programs that ordered sick COVID patients back into elderly homes in the state. As a result, thousands of elderly people needlessly died in the state.

Then when the official counts of deaths in state nursing homes were requested from the DOJ, the numbers were fudged. The numbers reported were about 50% less than the real counts.

An investigation into Cuomo’s actions was put in place and Cuomo resigned as governor of the state. However, the investigation into illegal actions by Cuomo related to the huge number of nursing home deaths was dropped by both the Biden DOJ and the Manhattan DA.

“Andrew Cuomo is a man with a history of corruption and deceit, now caught red-handed lying to Congress during the Select Subcommittee’s investigation into the COVID-19 nursing home tragedy in New York,” said Chairman Comer.

Read to the letter to Attorney General Pam Bondi here. The full criminal referral can be found here and an additional supporting transcript can be found here. Review former New York Governor Andrew Cuomo’s transcribed interview transcript here.

Cuomo is under investigation by the DC US Attorney’s Office, according to The New York Times.

The investigation was launched last month when Ed Martin was Acting DC US Attorney. Jeanine Pirro is currently the interim DC US Attorney.

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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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World Health Organization Approves Pandemic Agreement

The World Health Organization (WHO) on May 20 approved a pandemic agreement that is aimed at preventing, preparing for, and responding to future health emergencies.

The treaty says countries shall adopt a “One Health approach” by taking measures to identify and address factors that start pandemics. It says that countries must train workers to prepare for and respond to health emergencies and take steps to strengthen health systems, including improving vaccine coverage.

One section outlines how pharmaceutical companies that volunteer will provide the WHO with 20 percent of their vaccines, medicines, and tests. The WHO will then distribute the products “on the basis of public health risk and need, with particular attention to the needs of developing countries.”

The exact process will be laid out in a future agreement that will be considered at the 2026 World Health Assembly.

The consensus vote took place during the assembly on Tuesday, a day after a committee meeting in which 124 countries voted in favor, zero objected, and 11 abstained.

The approval of the agreement followed three years of negotiations.

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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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