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Aaron Siri's Senate Hearing Bombshell: "Not a Single Routine Childhood Vaccine Was Licensed on a Trial That Affirmed Its Safety" In a powerful address to the U.S. Senate, attorney Aaron Siri delivered a damning indictment of the foundation of childhood vaccine policy. He testified that when he deposes typical...

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The Unsettling Truth: Not One Childhood Vaccine Was Tested Against a True Placebo In a Senate hearing, attorney Aaron Siri was asked by Sen. Ron Johnson to clarify the research behind childhood vaccines. His answer was staggering. Siri submitted a 66-page document to the Senate citing FDA clinical trial data. His finding? NOT A SINGLE routine childhood vaccine on the current CDC schedule was licensed based on a placebo-controlled trial where the control group received an inert saline placebo. The "control" groups were given another vaccine—which itself was not tested against a true placebo. This circular referencing means the entire schedule lacks a foundational gold-standard safety benchmark. Why does this matter? Because we are in the midst of a silent pandemic. A pandemic of chronic disease. Since the early 1980s, chronic illness in American children has skyrocketed from under 13% to over 50%. Most of these diseases—asthma, allergies, autoimmune disorders—are forms of immune system dysregulation. What has changed in that same timeframe? The childhood vaccine schedule. In 1986, when vaccine manufacturers were granted legal immunity, the schedule was 3 injections. Today, a child following the full CDC schedule receives 29 injections by their first birthday, including in utero. Every one of those vaccines was licensed by a company that knew it would not be liable for any injuries. In the face of a catastrophic rise in childhood chronic illness, is it not the most basic duty of public health to honestly and transparently investigate all environmental insults, including the exponential increase in vaccines? This isn't anti-vax. It's pro-science. It's a demand for the rigorous safety science our children deserve.

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96,137 Aufrufe • vor 11 Monaten

Attorney Aaron Siri exposes that not one childhood vaccine on the CDC schedule was licensed with a true placebo-controlled trial, as chronic diseases skyrocket in kids. Is this why over 50% of children now face a health crisis? Attorney Aaron Siri’s explosive testimony exposes a critical gap in vaccine safety research that demands attention. As Siri detailed in his 66-page submission to Congress, not a single routine childhood vaccine on the CDC’s current schedule (except COVAXIN for ages 12+) was licensed based on a clinical trial using a true placebo control group. If a control group received another vaccine, that vaccine also lacked a placebo-controlled trial. These claims are backed by FDA clinical trial documents—undeniable evidence that challenges the narrative of “settled science.” Siri’s testimony raises a pressing question: Why haven’t we studied the safety of childhood vaccines with the rigor they deserve? He points to a pandemic of chronic disease plaguing America’s children. In the early 1980s, less than 13% of kids had a chronic illness. Today, over 50% suffer from conditions like asthma, allergies, and autoimmune disorders—many rooted in immune dysregulation. What’s changed? Siri notes the CDC’s vaccine schedule has ballooned from 3 injections in 1986 to 29 by age one today, including in utero shots. This staggering increase, coupled with the 1986 National Childhood Vaccine Injury Act shielding manufacturers from design defect liability, raises red flags. Siri argues we must investigate all environmental factors—including vaccines—driving this crisis. The absence of long-term, placebo-controlled trials leaves a gaping hole in our understanding of vaccine safety. When Robert F. Kennedy Jr. pressed Dr. Anthony Fauci for such studies, none were produced. CDC and FDA officials, when questioned, have similarly failed to provide evidence. Siri’s call to action is clear: we need transparent, unbiased research to rule out vaccines as a contributor to the chronic disease epidemic. “We’re in a pandemic right now,” he warns, urging HHS Secretary nominee Kennedy to prioritize this issue. The health of our children hangs in the balance. Will we have the courage to demand answers, or will we ignore the data staring us in the face?

Camus

347,306 Aufrufe • vor 1 Jahr

"Never a Placebo-Controlled Group": How Our Children's Vaccines Were Licensed on a Foundation of Flimsy Science. We are told the vaccine schedule is the most tested and safest in medical history. But what if that claim collapses under the weight of the actual data? Attorney Aaron Siri delivers a stunning fact that should halt every parent and citizen in their tracks: "Almost all childhood vaccines were licensed based on trials in which safety was reviewed for days or weeks after injection, underpowered, not enough kids, and there was never a placebo-controlled group for a single of the routine childhood vaccines injected into children, not one of them." Let that sink in. Not one. The gold standard of scientific research—the placebo-controlled trial—was abandoned for the entire routine childhood vaccine schedule. Why the Double Standard? For prescription drugs, companies run years-long, placebo-controlled trials. Why? Not ethics—economics. They are liable for damages. A harmful drug means financial ruin. For vaccines, the incentive is perversely flipped. With liability removed, the corporate boardroom's bottom-line calculus is simple: do the absolute minimum required for licensure. The Hep B Example is Jaw-Dropping Proof. The Combovax HB vaccine, given to babies on their first day of life, was licensed based on a "trial" that: - Monitored safety for just FIVE DAYS. - Included only 147 children. - Had NO control group whatsoever. This isn't just inadequate; it's scientifically indefensible. The recent COVID vaccine trials, often criticized as rushed, were vastly more comprehensive than this. The Root Cause? The Liability Shield. There is no doubt: if vaccine manufacturers were financially liable for injuries, the safety science would be exhaustive. They would never risk their profits on such flimsy data. The absence of liability created an absence of scientific rigor. This isn't conspiracy. It's cold, hard corporate calculus, and our children are the ones living in the experiment. It's long past time to demand the same gold-standard safety proof for vaccines that we demand for every pill we swallow.

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38,809 Aufrufe • vor 9 Monaten

Vaccine Safety "Pyramid Scheme" Exposed: The Shocking Truth They Never Wanted You to See In an amazing presentation, attorney Aaron Siri drops a truth bomb that should be heard by every parent, doctor, and policymaker. He systematically dismantles the most common defense of the childhood vaccine schedule: the claim that they were tested against saline placebos. Siri reveals a chart, built from years of work and sourced directly from FDA documents, that tracks the clinical trials for every single routine injected childhood vaccine. The categorical finding? Not one. Not a single one. Here is the stunning reality: - No Saline Placebos: There has NEVER been a routine injected childhood vaccine licensed based on a placebo-controlled trial using an inert saline solution. - The "Pyramid Scheme" of Safety: Instead, new vaccines are tested against older vaccines, which were themselves tested against even older ones. This creates a "daisy chain" where safety is only ever compared to another product that also lacked a true safety baseline. - The Proof is in the FDA's Own Documents: The source for this chart is the FDA's website. As Siri states, "If you don't agree with this information... you're arguing with the FDA." Some of the most shocking examples: - Hepatitis B: The first vaccines for newborns were licensed with no control group at all. - PCV (Pneumococcal): The original Prevnar 7 was tested against another experimental vaccine—a practice Siri compares to testing a new cancer drug against another unproven cancer drug. - Polio (IPOL): The modern IPV vaccine, a completely different technology from the Salk vaccine, was licensed with a safety review of just three days and no control group. - MMR: The clinical trials for the current MMR II, which uses human fetal cell lines, used no control group. - HPV (Gardasil): The "placebo" used in trials for thousands of young girls was not saline. It often contained the aluminum adjuvant—a known neurotoxin with no therapeutic benefit—effectively rigging the trial to mask true adverse event rates. This rigged system allows serious adverse event rates in healthy children to creep into the 7%, 8%, and even 9% range in clinical trials. Because the control group gets a similarly reactive shot, the numbers appear "similar" and are deemed "safe," hiding the true risk. The bottom line: The entire childhood vaccine schedule rests on a foundation that has never been properly tested for safety against an inert placebo. The baseline safety profile for these products is, and has always been, unknown. This isn't an opinion. It's a fact documented by the FDA itself. If this doesn't make you question everything, what will?

Camus

473,721 Aufrufe • vor 8 Monaten

🚨 **BOMBSHELL FDA REFORM EXPOSED** — Aaron Siri just delivered a jaw-dropping takedown at the Kennedy Center, proving **every single clinical trial** for routine childhood vaccines is unethical by the British Medical Journal’s own standards… … and then he dropped a no-holds-barred blueprint to fix the broken FDA. Here is **EVERY SINGLE WORD** he said (full verbatim quote from his speech; emojis are mine): “Speaking of ethics, here's what the British Medical Journal says about these trials when they're not properly done. It says quote, ‘in some trials placebos were omitted on ethical grounds. That is illogical because studies destined to produce unreliable results should themselves be considered unethical.’ And that is true of every single clinical trial relied upon to license a routine injected childhood vaccine. They're all by this definition unethical. So here are the reforms I recommend for the FDA. ✅ One: Absent public contrition, remove anyone in FDA's Office of Vaccine Research and Review (OVRR) involved in licensing any routine injected childhood vaccine. After you have unleashed these products on millions of children and you've been part of that, unless you can publicly admit that you made a mistake, you're going to be too conflicted to properly do your job going forward. ✅ Two: Notify practitioners. The FDA should be sending notice to every single practitioner — pediatrician, family doctor, OBGYN — of the details of each trial relied upon to license each routine injected childhood vaccine. They should know, they should understand. ✅ And issue minimum standards for licensure of vaccines. And I mean real licensure standards like what the controls should be, how long safety should be reviewed, proper blinding, so on and so forth. That doesn't exist for vaccines, certainly not for childhood vaccines. There was some guidance put out actually for the EUA of COVID vaccines but that's about it. ✅ And then there's a whole bunch of other recommendations in the Task Force letter below. So these would be my recommendations for the FDA.” 🙌 This isn’t theory — this is the accountability moment America has been waiting for. The captured era ends here. 👏 Who’s ready for REAL reform? 🔥 When will we see it? Credit: Aaron Siri #FDAReform 💪 #MedicalFreedom #TransparencyNow

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