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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\u2014risks that include unprecedented death rates, reproductive harm, and systemic fraud. Despite Pfizer\u2019s own internal documents revealing 1,223 deaths within 90 days of rollout\u2014alongside thousands of adverse events\u2014federal regulators under the direction of Robert F. Kennedy Jr. and Dr. Marty Makary continue endorsing these shots, even for vulnerable subsets of the population.<\/p>\n
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,\u00a0despite peer-reviewed studies and whistleblower data proving their lethality<\/a>? And why was the mRNA platform suspiciously omitted from the recent \u201cMAHA Report,\u201d 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.<\/p>\n Key points:<\/strong><\/p>\n When Pfizer\u2019s 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 \u201cAdverse Events of Special Interest,\u201d\u00a0including heart failure, neurological damage, and pregnancy complications<\/a>. Dr. James Thorpe, a maternal-fetal medicine specialist,\u00a0analyzed the data<\/a>\u00a0and found miscarriage rates exceeding 80% in some cohorts\u2014a figure that should have triggered immediate suspension. Instead, the FDA doubled down, green-lighting boosters while dismissing injuries as \u201crare\u201d or \u201cunverified.\u201d Internal emails later revealed that Pfizer executives privately acknowledged \u201csignal[s] of serious concern\u201d as early as February 2021, yet publicly declared the shots \u201csafe and effective.\u201d<\/p>\n The Vaccine Adverse Event Reporting System (VAERS), though notoriously under-reported, logged over 37,000 deaths post-COVID vaccination by 2023\u2014a number that dwarfs all other vaccines combined over 30 years. Similarly, v-safe, the CDC\u2019s 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 \u201canecdotal,\u201d while HHS quietly altered v-safe\u2019s interface to obscure pregnancy-related outcomes.<\/p>\n 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\u00a0myocarditis risks from the vaccine<\/a>, 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.<\/p>\n Recent policy shifts under HHS Secretary Kennedy and FDA Commissioner Dr. Makary\u2014such as limiting mRNA shots to \u201csick individuals\u201d while keeping them on the market\u2014have been framed as progress. But the real health freedom movement call this so-called progress a cynical sleight-of-hand. \u201cRecommending these shots for\u00a0anyone<\/em>\u00a0is indefensible,\u201d said Dr. Peter McCullough, a cardiologist and outspoken vaccine safety advocate. \u201cThe data demands a full recall, not a PR stunt.\u201d<\/p>\n Instead of taking action against COVID jabs, Secretary Kennedy is quelling MAHA \u201canxiety\u201d and has green lit new mRNA experiments, providing Moderna with more taxpayer funds\u00a0to bring forth \u201cgold standard science.\u201d<\/a>\u00a0However, the latest research on new replicon samRNA technology finds that they induce\u00a0severe blood abnormalities in upwards of 93% of trial participants<\/a>.<\/p>\n The MAHA (Make Americans Healthy Again) movement, a grassroots alliance of parents, doctors, and liberty activists, has united across political lines to demand accountability.\u00a0Their open letter<\/a>\u00a0to HHS and FDA condemns the agencies\u2019 \u201cdistractions and watered-down policies\u201d as a betrayal of public trust. \u201cWe don\u2019t need more studies,\u201d the letter states. \u201cWe need action.\u201d<\/p>\n Yet, with the FDA still touting its \u201cgold standard of science\u201d while ignoring corpses in the data, the question remains: How many more must die before the truth prevails?<\/p>\n Sources include:<\/strong><\/p>\n<\/div>\n X.com<\/a><\/p>\n FreedomLibrary.Hillsdale.edu<\/a><\/p>\n HSGAC.Senate.gov<\/a>\u00a0[PDF]<\/p>\n CNN.com<\/a><\/p>\n X.com<\/a><\/p>\n TheFocalPoints.com<\/a><\/p>\n<\/div>\n<\/div>\n \n\t<\/div>\n\n
Pfizer\u2019s concealed catastrophe: A deadly cover-up<\/strong><\/h4>\n<\/p>\n
VAERS and v-safe: The smoking guns being ignored<\/strong><\/h4>\n<\/p>\n
RFK Jr.\u2019s hollow reforms and the MAHA revolt<\/strong><\/h4>\n<\/p>\n