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We Now Know How The Government Lied About the COVID Vaccines

For more than 250 years, the same playbook has been used to prop up toxic vaccines. At long last, we have a chance to end it.

Story at a Glance:

Since the dawn of vaccination, authorities have habitually doubled down on unsafe and ineffective vaccines, regardless of the pushback they received or the evidence against them.

Sustaining this has required increasingly brazen methods to censor and conceal the deluge of “extremely rare” injuries caused by an ever-expanding vaccination schedule.

Senator Ron Johnson, who has worked tirelessly to expose this coverup, recently held a Senate hearing whose title says it all: “Unmasked: How Biden Health Officials Purposely Turned a Blind Eye Toward COVID-19 Vaccine Safety Signals.”

Faced with a tsunami of vaccine injuries too large for anyone to ignore, the FDA and CDC searched for a way to statistically dismiss it, eventually settling on comparing Moderna’s injury rate to Pfizer’s and declaring the vaccines “safe” because there was no major difference between the two.

When a senior FDA analyst pointed out this obvious flaw and suggested comparing them to less toxic vaccines instead, documents show the entire FDA turned against her to suppress her findings. As a result, dozens of conditions we have all seen the COVID vaccines cause were never officially linked to them—despite the data clearly showing they were.

The unprecedented damage caused by the COVID-19 vaccines has created a historic loss of trust in the parties who covered it up, giving us a once-in-a-lifetime opportunity to force them to start telling the truth and end an immunization experiment that has profoundly damaged the health of our society.

COVID Vaccine Hearing Exposes Deliberate Blind Eye to ‘Overwhelming Evidence of Harm’

This is not a fringe “conspiracy theory.” It was revealed by the government’s own investigation—and it’s a story they don’t want you to read.

According to VAERS, the US’s vaccine adverse event reporting system, more adverse events and deaths have been reported following COVID vaccines than from all other vaccines combined over the system’s 30+ year history.

More dangerous than ivermectin. More dangerous than hydroxychloroquine (which turned out not to be so dangerous after all).

It was 55 times more deadly than the flu vaccine (0.46 deaths vs 25.5 deaths per million doses).

And even more dangerous than Remdesivir, which earned the nickname “Run Death Is Near” after it wreaked havoc on the kidneys and livers of tens of thousands of COVID patients in the hospital.

But still the question remains. How did US health officials miss a safety signal this big?

Dr. Szarfman went on to retire from the FDA in 2025 after more than 35 years of service.

She raised concerns about safety signal masking. The FDA essentially told her to shut up.

Because in their eyes, “49 examples of extreme masking” could create “erroneous conflicts” and fuel “vaccine hesitancy.”

So, health officials decided to let people die from devastating side effects and bury the data because it was too inconvenient to take head-on.

People should be going to jail for this.

BREAKING: Senate Investigation Finds FDA Officials Covered-Up 25 COVID Shot Safety Signals

FDA’s own data flagged sudden cardiac death, heart attacks, blood clots, neurological damage, and dementia… and the FDA analyst uncovering it was ordered to “cease and desist.”

Their new method (Regression-Adjusted Gamma Poisson Shrinker — RGPS) fixed a known flaw called “masking” — where signals for one COVID vaccine get drowned out by the sheer volume of reports from the others.

What they found was explosive:

49 examples of extreme masking
~25 new statistically significant safety signals that FDA’s standard MGPS method completely missed
Signals included: sudden cardiac death, acute myocardial infarction, pulmonary infarction, Bell’s palsy, non-site specific embolism/thrombosis, dementia, and “Death and sudden death” — for Pfizer, Moderna, and J&J shots
Dr. Szarfman repeatedly shared these findings with senior CBER officials (the very people in charge of vaccine safety), including Dr. Peter Marks, in March, April, May, and July 2021.

Their response?

Told her to “hold off” on creating and sending any more data mining reports
Called her work a “major distraction”
Worried it would “create erroneous conflicts that feed into anti-vaccination rhetoric”
Eventually ordered her to “cease and desist”
Later, FDA quietly locked down distribution of its own weekly data mining reports to CDC — right around the time FOIA requests and Sen. Johnson’s letters started coming in. One CDC official even admitted they may have asked FDA to stop sending them “because of the FOIAs.”

Even after Dr. Szarfman and DuMouchel published their findings in Drug Safety (2022) showing masking was eight times more likely with COVID vaccines, and Dr. Robert Califf replied “Thanks. These are good,” no changes were made to the methodology.

This is documented, internal FDA communication showing deliberate suppression of safety signals at the exact moment millions of Americans were being told the shots were “safe and effective.”

The cover-up continues to unravel. Accountability is urgently warranted.

Taxpayer-Funded Scientists Create Human Bird Flu Virus in Georgia BSL-3 Lab That Successfully Crosses Species
USDA, NIAID, and NIH finance genetic experiment generating human avian influenza pathogen from scratch that can infect cows.

Congress Introduces Billion-Dollar Child Vaccine Control Grid: H.R. 8425

Rep. Schrier's bill funnels taxpayer cash into Big Pharma, state propaganda, and pediatric surveillance expansion

Gates-Funded ‘Big Catch-Up’ Delivers 100 Million Vaccine Doses — Including High-Risk DTP Vaccine Not Used in U.S.

The WHO, UNICEF and Gavi, the Vaccine Alliance — backed by the Gates Foundation — said last week that they vaccinated more than 18 million African and Asian children in 36 countries.

BREAKING: Top Fauci Advisor Indicted in First Criminal Prosecution Against a Senior COVID Official

David Morens criminally charged with hiding emails, destroying records, and evading transparency laws to shape the COVID “natural origins” narrative

New York Proposes an Additional Layer of Legal Protection to Those Profiting From Injecting Vaccines
“shall not be liable for any injury caused..."

While assuring you that childhood vaccines are safe, New York is proposing yet another layer of legal protection to prevent anyone from suing doctors and pharma for the injuries these products supposedly won’t cause to children.

They can’t have it both ways—either it’s safe or it’s not safe and thus needs legal protection that no other product enjoys.

This proposed New York law would make it so those profiting from injecting vaccines “shall not be liable for any injury caused by an act or omission in prescribing, dispending, ordering, furnishing, or in the administration of vaccines…to a minor…, including the residual effects…” You get the drift.

It requires suspending reason and reality to believe a product that is safe would need this type of law as a shield… If you want to lodge your opposition to this bill with the members of the NY legislature, you can do so here.

Moderna’s Bets on Bird Flu Pandemic

Moderna’s press release confirms the jab is for a coming avian influenza pandemic:

“H5 influenza, or bird flu, remains a pandemic threat. The start of our Phase 3 trial for an H5 influenza vaccine marks a significant milestone in our ongoing efforts to strengthen global pandemic preparedness,” said Stéphane Bancel, Chief Executive Officer of Moderna. “Our platform technology’s efficiency and scalability are critical to supporting global health security and responding to potential future threats.”

“The first-of-its-kind pivotal trial of an mRNA-based pandemic influenza vaccine underscores the potential of this technology to reshape how we confront emerging pathogens,” said Dr. Richard Hatchett, CEO of CEPI. “If successful, these efforts could transform our ability to respond swiftly and equitably to one of the world’s most enduring threats.”

…

“Although the current risk to the human population of avian influenza remains low, the virus continues to evolve and spread in birds and various animal hosts in the UK and elsewhere,” said Dr. Richard Pebody, Director of Epidemic and Emerging Infections at the UK Health Security Agency (UKHSA). “UKHSA remains alert to the potential that this pathogen could adapt to spread from person to person, and will continue to monitor all available data. This important initiative to trial a new mRNA pandemic influenza vaccine is a key step towards further strengthening our ability to protect people against future influenza pandemics.”

Moderna Begins Injecting 4,000 Adults with modRNA Bird Flu Pandemic Vaccine

New avian influenza jab funded with $54 million from Bill Gates' vaccine cartel CEPI.

In a major acceleration of bird flu pandemic orchestration and mass vaccination infrastructure, Moderna, Inc. yesterday announced that “the first participants in the U.S. and UK have been dosed in a Phase 3 study of the Company’s investigational mRNA-based H5 pandemic influenza vaccine candidate, mRNA-1018.”

This is the first mRNA-based pandemic influenza (H5 bird flu) vaccine to reach Phase 3 clinical trials anywhere in the world.

The move comes after President Donald Trump selected a military influenza pandemic policy architect—Dr. Erica Schwartz, who built and enforced surveillance, vaccination, and compliance systems—to take control of the CDC.

Signalling its high confidence that there will be future demand for influenza vaccines, Moderna announced on the same day that another of its influenza jabs, mCOMBRIAX® (mRNA-1083), has been granted marketing authorization by the European Commission (EC).

Moreover, the Trump administration is currently funding gain-of-function experiments on influenza pathogens.

Just as coronavirus gain-of-function experiments and vaccine development (the problem and the solution) were simultaneously carried out before the COVID-19 pandemic, the same dual-track approach is now being applied to influenza—advancing high-risk pathogen work in parallel with the rapid rollout of mRNA vaccine platforms designed to respond to it.