FDA Petitioned to Launch Nationwide Testing for 'Post-Vaccine Syndrome' Among Covid-Vaxxed

The U.S. Food and Drug Administration (FDA) is under mounting pressure to launch nationwide testing for silent but deadly adverse events among people who received Covid mRNA “vaccines.”

A viral Change.org petition is sounding the alarm, calling on federal health agencies and Congress to finally confront the devastating long-term public health implications of the mass vaccination campaign.

It calls for diagnostic testing among the Covid-vaccinated to identify individuals suffering from post-vaccine syndromes.

It comes as thousands of Americans say they’ve suffered through in silence with post-vaccine injury and so-called “long Covid.”

The petition demands that the FDA, the National Institutes of Health (NIH), the Biomedical Advanced Research and Development Authority (BARDA), and even Congress take immediate action to approve and fund lab-based diagnostic testing for persistent spike protein, vaccine-derived mRNA, and DNA fragments in affected individuals.

In short, Americans want proof, not vague guesses or gaslighting from the medical establishment.

“We need real diagnostics—not dismissal,” the petition reads.

The calls are clear:

• Fast-track FDA approval of assays.

• NIH and BARDA funding for validation studies.

• CMS insurance coverage for those suffering.

Supporters say this could be a lifeline for thousands who’ve been medically ignored for too long.

But this grassroots push is more than just a demand for testing.

It’s a reckoning, and the government knows it.

However, if the FDA greenlights these diagnostics, it’s more than just approval; it’s an admission.

It would serve as a silent concession that those who questioned the narrative, who sounded the alarm on vaccine harm, may have been right all along.

The petition isn’t just emotional, it raises sharp, technical questions that federal agencies haven’t answered:

• Do valid, scalable tests for spike protein and vaccine mRNA even exist? Research labs have them, but FDA-cleared, reproducible clinical diagnostics? Not yet.

• Can these tests even distinguish spike protein from natural infection vs. the jab? That’s a scientific minefield.

• Could testing lead to false hope or overtreatment if fragments of spike protein are found but misunderstood?

• And most crucially: Would approving these tests be the first real institutional acknowledgment of vaccine-related harm?

These questions are exactly why the system is stalling.

Because if these tests are validated and deployed nationwide, it rips the lid off a scandal that legacy media and government officials have tried to bury for years.

The mRNA injection narrative was sold as “safe and effective.”

Any questioning of that mantra was dismissed as fringe conspiracy.

Yet, with millions reporting long-term complications, there is now a growing movement demanding objective biological evidence.

And the silence from federal agencies? Deafening.

The truth is, people are suffering today.

They don’t need a commission next year or a white paper in 2027.

They need answers now.

The Biden-era policies, kept alive by bureaucrats and Big Pharma loyalists, don’t want to admit the fallout from the rushed “vaccine” rollout.

However, this petition may force their hand.

If they don’t act, the message is clear: they care more about political damage control than about human lives.