HHS and FDA keep COVID jabs on the market, invest in new mRNA jabs, DIVIDING MAHA

The U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) have long positioned themselves as guardians of public health, yet mounting evidence suggests these agencies have concealed catastrophic risks tied to mRNA COVID-19 vaccines—risks that include unprecedented death rates, reproductive harm, and systemic fraud. Despite Pfizer’s own internal documents revealing 1,223 deaths within 90 days of rollout—alongside thousands of adverse events—federal regulators under the direction of Robert F. Kennedy Jr. and Dr. Marty Makary continue endorsing these shots, even for vulnerable subsets of the population.
This betrayal of trust raises urgent questions: Why has the FDA refused to pull these dangerous injections from the market? Why does the CDC still recommend them for sick people, but not healthy people, despite peer-reviewed studies and whistleblower data proving their lethality? And why was the mRNA platform suspiciously omitted from the recent “MAHA Report,” a document meant to address medical harms? The answers point to a disturbing pattern of cowardice and institutional corruption, where profit and control eclipse human life, and where towing the line and appeasement takes precedence over enforcing accountability for mass medical error and wrongful death.
Key points:
- Pfizer’s confidential post-marketing data exposed 1,223 deaths and thousands of severe injuries within three months of rollout, yet HHS and FDA ignored the warnings.
- VAERS and v-safe data reveal COVID-19 vaccines as weapons of mass injury, with disproportionate harm to pregnant women—including skyrocketing miscarriage rates.
- Despite overwhelming evidence, the FDA and CDC still recommend mRNA shots for certain demographics, a policy that health freedom advocates see as a distraction from doing the right thing – taking decisive action and pulling the jabs from the market.
- The MAHA movement, a bipartisan coalition, demands accountability, but federal agencies respond with “linguistic misdirection” and hollow promises.
Pfizer’s concealed catastrophe: A deadly cover-up
When Pfizer’s 90-day post-marketing report was forced into public view through legal battles led by attorney Aaron Siri, the findings were staggering: 1,223 fatalities, 158,000 adverse events, and nine pages of “Adverse Events of Special Interest,” including heart failure, neurological damage, and pregnancy complications. Dr. James Thorpe, a maternal-fetal medicine specialist, analyzed the data and found miscarriage rates exceeding 80% in some cohorts—a figure that should have triggered immediate suspension. Instead, the FDA doubled down, green-lighting boosters while dismissing injuries as “rare” or “unverified.” Internal emails later revealed that Pfizer executives privately acknowledged “signal[s] of serious concern” as early as February 2021, yet publicly declared the shots “safe and effective.”
VAERS and v-safe: The smoking guns being ignored
The Vaccine Adverse Event Reporting System (VAERS), though notoriously under-reported, logged over 37,000 deaths post-COVID vaccination by 2023—a number that dwarfs all other vaccines combined over 30 years. Similarly, v-safe, the CDC’s own surveillance tool, recorded thousands of pregnant women reporting miscarriages and fetal abnormalities within days of injection. Yet, when confronted with this data, CDC Director Rochelle Walensky dismissed it as “anecdotal,” while HHS quietly altered v-safe’s interface to obscure pregnancy-related outcomes.
Today, Secretary Kennedy and FDA Commissioner Makary have removed recommendations for COVID jabs for pregnant women and are requiring the vaccine manufacturers to warn recipients about myocarditis risks from the vaccine, but the elephant in the room remains: the leaders that MAHA put in place are failing to take decisive action to remove the shots from the market in the first place. A new precedent must be set in medicine, but this has not taken place under the new MAHA leadership.
RFK Jr.’s hollow reforms and the MAHA revolt
Recent policy shifts under HHS Secretary Kennedy and FDA Commissioner Dr. Makary—such as limiting mRNA shots to “sick individuals” while keeping them on the market—have been framed as progress. But the real health freedom movement call this so-called progress a cynical sleight-of-hand. “Recommending these shots for anyone is indefensible,” said Dr. Peter McCullough, a cardiologist and outspoken vaccine safety advocate. “The data demands a full recall, not a PR stunt.”
Instead of taking action against COVID jabs, Secretary Kennedy is quelling MAHA “anxiety” and has green lit new mRNA experiments, providing Moderna with more taxpayer funds to bring forth “gold standard science.” However, the latest research on new replicon samRNA technology finds that they induce severe blood abnormalities in upwards of 93% of trial participants.
The MAHA (Make Americans Healthy Again) movement, a grassroots alliance of parents, doctors, and liberty activists, has united across political lines to demand accountability. Their open letter to HHS and FDA condemns the agencies’ “distractions and watered-down policies” as a betrayal of public trust. “We don’t need more studies,” the letter states. “We need action.”
Yet, with the FDA still touting its “gold standard of science” while ignoring corpses in the data, the question remains: How many more must die before the truth prevails?
Sources include:
HSGAC.Senate.gov [PDF]
Source: https://naturalblaze.com/2025/06/hhs-and-fda-keep-covid-jabs-on-the-market-invest-in-new-mrna-jabs-dividing-maha.html
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