Key points:
- The Trump administration is considering phasing out COVID-19 vaccines, with insiders citing a 2022 peer-reviewed study showing a 16% higher risk of serious adverse events in vaccinated individuals compared to placebo.
- BARDA (Biomedical Advanced Research and Development Authority) has already begun canceling mRNA vaccine contracts, signaling a dramatic shift in federal vaccine policy.
- VAERS data reveals 38,742 reported deaths and 1.6 million adverse events linked to COVID vaccines—figures that dwarf the risks of nearly every other vaccine in history.
- European regulators admitted a "clear link" between AstraZeneca’s jab and deadly blood clots, yet the U.S. never issued comparable warnings.
- Natural immunity and early treatments (like ivermectin and monoclonal antibodies) were suppressed in favor of mass vaccination, despite evidence they could have saved lives.
- The pharmaceutical industry’s capture of the FDA and CDC allowed dangerous products to be fast-tracked without proper long-term safety studies.
How a "safe and effective" narrative collapsed under its own lies
When the first COVID-19 vaccines were rolled out in December 2020, the messaging was absolute: Safe. Effective. The only way back to normal. Politicians, celebrities, and even religious leaders lined up to take their shots on camera, framing hesitation as a moral failing. But behind the PR blitz, the cracks were already forming.
A 2022 study published in Vaccine, led by physicians and researchers, tore apart the foundation of the "safe and effective" myth. By reanalyzing Pfizer and Moderna’s own clinical trial data, they found that mRNA vaccines carried a 16% higher risk of serious adverse events than placebos. For Pfizer, that meant 36% more severe reactions; for Moderna, 6% more. These weren’t mild headaches or sore arms—these were hospitalizations, neurological disorders, and life-altering injuries.
Yet, instead of sounding the alarm, regulators buried the findings. The FDA, which had fast-tracked these vaccines under Emergency Use Authorization (EUA), never demanded the long-term safety studies that should have been mandatory for a product injected into billions of people. Why? Because the system was rigged from the start.
The Biomedical Advanced Research and Development Authority (BARDA), a division of HHS, had already poured billions into mRNA vaccine development. But now, under Robert F. Kennedy Jr.’s leadership, BARDA is canceling those contracts, signaling that even the government can no longer ignore the damage. Dr. Aseem Malhotra, a cardiologist and close associate of Kennedy, told The Daily Beast that the decision to pull the jab could come "within months"—either in stages or as a "clean break" from the failed experiment.
This isn’t just about bad science. It’s about betrayal.
Real people, real injuries, and a system that looked the other way
Wyatt McGlaun was a healthy 17-year-old from Texas when he got his first COVID shot. Weeks later, he was paralyzed from the waist down, diagnosed with Guillain-Barré syndrome—a brutal neurological disorder where the immune system attacks the nerves. His story isn’t unique. Hundreds of thousands of Americans have reported similar horrors: blood clots, heart inflammation, neurological damage, and sudden deaths in otherwise young, healthy individuals. Military servicemembers were under duress to comply with the COVID jab depopulation program, with countless young men and women injured with myocarditis following vaccination.
Yet, when these victims sought answers, they were gaslit.
- The CDC dismissed reports of menstrual irregularities in women post-vaccination as "anecdotal."
- The FDA ignored warnings from its own scientists about myocarditis risks in young men.
- The NIH suppressed research on natural immunity, even though studies showed it was far more robust than vaccine-induced protection.
And then there’s VAERS—the Vaccine Adverse Event Reporting System—where 38,742 deaths and 1.6 million injuries have been logged. These aren’t just numbers. They’re husbands, wives, children, and parents whose lives were destroyed by a product they were told was safer than Tylenol.
Even European regulators—hardly known for their skepticism—admitted a "clear link" between AstraZeneca’s jab and deadly blood clots. Yet in America, the same warnings were never issued. Why? Because the pharmaceutical industry owns the regulators.
Pfizer, Moderna, and Johnson & Johnson raked in billions while their products maimed and killed. And when Emergent BioSolutions—a company with a long history of quality control failures—contaminated 15 million J&J doses, government officials knew about the risks for months and did nothing.
This isn’t incompetence. It’s criminal negligence.
Will the truth finally set us free?
The Trump administration’s potential phase-out of COVID vaccines is a stunning reversal—but it’s only the first step. The real question is: Will there be accountability?
For years, independent doctors, scientists, and journalists have been censored, de-platformed, and smeared for asking basic questions:
- Why were early treatments like ivermectin and hydroxychloroquine demonized while untested mRNA jabs were pushed as the only solution?
- Why did natural immunity—which studies showed was 13x more protective than vaccination—get erased from the conversation?
- Why were vaccine-injured Americans abandoned, with no compensation, no answers, and no justice?
Now, as the Trump administration considers pulling the plug, the pharmaceutical-industrial complex is scrambling. The same media outlets that shamed the unvaccinated are suddenly quiet. The same "fact-checkers" who labeled concerns about blood clots as "misinformation" have gone dark.
But the damage is done. Millions of lives altered. Families destroyed. Trust in medicine shattered.
If the COVID vaccine is finally removed from the market, it won’t be because the system worked. It will be because the truth overcame the censorship, propaganda, coercion, and exposed a system that was weaponized to deceive and kill.
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