reSee.it - Related Video Feed

For years, I claimed that none of the 72 vaccines mandated for children underwent proper safety testing in placebo-controlled trials. When I confronted Fauci about this, he couldn't provide the study he claimed existed. After suing him, we received confirmation that no such study was ever conducted. The lack of liability and safety testing saves pharmaceutical companies significant costs, leading to a rush to add unnecessary vaccines to the schedule. This has resulted in a dramatic increase in chronic diseases among American children since 1989, including a rise in neurological disorders and autism, which has skyrocketed from 1 in 10,000 to 1 in 34 today.

Speaker 1 claims that no vaccines, including the COVID vaccine, have been properly tested. They assert that no childhood vaccine has undergone a placebo-controlled clinical trial of sufficient duration and power to assess its safety before being injected into millions of children in America. Speaker 1 states this is not just their opinion, but can be verified by anyone who examines the FDA website, specifically the package inserts and underlying clinical trial documents.

It is claimed that ethical concerns prevent double-blind placebo trials for childhood vaccines already on the schedule that never underwent safety testing. The first step should be honesty about the clinical trial data underlying childhood vaccines. One proposed method involves comparing health outcomes of vaccinated versus unvaccinated individuals using existing datasets. If unvaccinated children are equally or less healthy than vaccinated children, this should be published to reassure parents. However, if vaccinated children are less healthy, the claim that these products cannot harm anyone should be reconsidered. It is asserted that comparative studies between vaccinated and unvaccinated individuals have been conducted, but not published because they allegedly show that the unvaccinated are healthier. Publishing a study showing vaccinated individuals are healthier would have discredited Robert Kennedy Jr., but the fact that it wasn't published suggests a problem.

The speaker questions the safety of 5,000 micrograms for children under six. They claim many vaccine trials use an aluminum adjuvant containing placebo or other aluminum-containing vaccines as the control group. The speaker argues that because the control group receives aluminum, the study is invalidated. They further claim that countries with less aggressive vaccine schedules do not have significant trends in autistic diagnoses. They state that the Amish community, which is largely unvaccinated, has extremely low rates of autism diagnoses.

Speaker 0 argues that the myth that vaccines are safe and necessary and that they eradicated childhood disease is false. He claims vaccines have never been tested for safety and that there are no placebo-controlled trials; in trials, the control group is given the immunogens that are in the vaccine, making the comparison deceptive. He emphasizes that vaccines typically contain a protein plus an accompanying substance—the adjuvant or immunogen—that stimulates an immune response, and that these adjuvants (such as aluminum or other substances) by themselves are dangerous. When the control group receives these adjuvants along with the experimental group, he says the side effects are similar, describing this as a “slight hand trick” and “extremely deceptive.” He notes that for the last forty years people have been shouting that there has not been a true placebo-controlled trial with saline. He then argues that if one looks at the history of all the childhood illnesses that vaccines target, they were almost all nearly eradicated before the introduction of the vaccine. He claims that the impression vaccines stop childhood illnesses is not true; almost all illnesses had reduced to extremely low levels due to sanitation and hygiene, development, and some antibiotics. Regarding the vaccines themselves, he states that the true data and history of these vaccines are “really horrible.” He mentions a history of lack of safety and relates it to sudden infant death syndrome, asserting that it “suddenly came out of nowhere as we suspended the schedule” and asks when death occurs. He asserts that sudden infant death syndrome is reproducible in that it occurs at two months, four months, and six months, and that most of those deaths occur within days to a couple of weeks of the vaccine. He concludes with a strong personal stance: if he had his young children today, he would not give them a single vaccine.

Speaker 0 asserts that there is no safe vaccine on the childhood schedule and labels themselves an anti-vaxxer because no vaccine has been properly tested for safety. They state that, in the book Vax Facts, you are more likely to die from the vaccine than from the disease for which there is a vaccine, and that this is true for every single vaccine on the childhood schedule. They acknowledge that death from the vaccine is still a death and “super rare,” but claim you are much more likely to die from the vaccine. They ask which do you want: a greater chance of dying from the vaccine or a lesser chance of dying from the disease, noting that for many of these diseases, the risk is zero.

According to the speaker, most vaccines have never been tested in a randomized, placebo-controlled trial to evaluate their safety. The speaker claims that vaccines contain aluminum compounds because many dead vaccines don't mount an immune response without them. The speaker alleges that in a Gardasil vaccine study, the placebo group received an aluminum adjuvant instead of a true placebo, resulting in similar side effect profiles between the active vaccine and placebo groups. The speaker asserts that Merck used a novel aluminum compound and that data suggests aluminum in vaccines is profoundly toxic. The speaker states that the only true randomized controlled trial involving a vaccine was conducted on sheep with blue tongue disease. The results allegedly showed that the aluminum in the vaccine was toxic, causing the sheep to become sick, unsociable, and, in some cases, die. The speaker concludes that the assumption that aluminum adjuvants in vaccines are safe is unfounded and has never been tested.

Speaker 1 claims that no vaccines, including the COVID vaccine, have been properly tested. They assert that no childhood vaccine has undergone a placebo-controlled clinical trial of sufficient duration and power to assess its safety before being injected into millions of children in America. Speaker 1 states this is not just their opinion, but can be verified by anyone who examines the FDA website, specifically the package inserts and underlying clinical trial documents.

Vaccine recommendations typically come from the Advisory Committee of Immunization Practices (an outside consulting committee at CDC) and VRBPAC (within FDA), which recommends vaccine licensure. These committees only adopted evidence-based medicine about twelve years ago. The speaker states that during their administration, they want safety studies prior to vaccine licensure and recommendation. They claim vaccines are exempt from pre-licensing safety testing, and the COVID vaccine was the only one tested in a full placebo trial. They assert that the other 76 shots children receive between birth and 18 have not been safety tested against a placebo, meaning the risk profile is not understood. The speaker intends to remedy this.

None of the 72 vaccines for children have been tested against a placebo. The speaker sued HHS in 2016 to find placebo studies for vaccines, but none were found. The safety testing for the polio vaccine was only 48 hours, while the hepatitis b vaccines were tested for 4-5 days. This means that any adverse events occurring after that time period were not considered. Without placebo testing, the risk profile of current vaccines is unknown, and it cannot be determined if vaccines cause more harm than good. The speaker questions the ethics of mandating medical products with unknown risks for children.

Senator Ron Johnson introduces Aaron Siri at the Kennedy Center, praising Siri as a highly consequential attorney and highlighting Siri’s work since the COVID era. Johnson recounts how his own oversight role in Congress evolved to rely on the adversarial legal process to extract information from a large government, noting that enforcement power rests in the courts. He frames Siri as someone who, through litigation and testimony, has exposed what he views as flaws in vaccine science, regulation, and safety oversight. Johnson describes Siri’s rise to prominence during the COVID period, beginning with public hearings on vaccine injuries in Milwaukee (June 2021) and Washington, DC (November 2021). He notes that Siri represented Dr. Patricia Lee, a physician who publicly discussed vaccine injection injuries and medical treatment obstacles, illustrating how federal health agencies and the CDC/FDA were perceived to respond to reports of injury. Siri’s testimony is credited with exposing calls to his practice from vaccine-injured doctors seeking treatment and the CDC/FDA officials’ defense of VAERS. Johnson highlights Siri’s 2022 and 2025 hearings, including the release of the VAERS data via the v-safe system, which Siri reportedly showed indicated higher rates of medical care sought and activity impairment among the vaccinated. Siri’s deposition of Stanley Plotkin and other experts is cited as foundational to his arguments about safety science, conflicts of interest, and the integrity of the vaccine schedule. Johnson points to the Institute of Medicine’s (IOM) conclusions as being insufficient to prove vaccine safety for the entire childhood schedule, and to Siri’s presentation of the Henry Ford study (vaccinated vs. unvaccinated children) showing higher rates of chronic illness among the vaccinated. A central claim Johnson attributes to Siri is that vaccines have immunity from liability, due to the National Childhood Vaccine Injury Act of 1986 (NCVIA). Siri’s summary is that vaccines are the only product in America with blanket liability protection for manufacturers and administrators, preempting design-defect claims via the Supreme Court interpretation that “the National Childhood Vaccine Injury Act preempts all design defect claims.” Siri argues this immunity removes the market incentive to develop safer vaccines and leaves safety oversight to federal health authorities (HHS agencies: NIH, CDC, FDA) rather than to private manufacturers. Siri’s account of the 1986 act is that it created a mandate for safer childhood vaccines, with three provisions: (1) the general rule placing the secretary of HHS in charge of vaccine safety; (2) a task force of NIH, CDC, and FDA to make safety recommendations to the secretary; and (3) a biannual report to Congress on actions to improve vaccine safety. Siri contends that the biannual reports have never been submitted, and the task force produced only one report (in 1998) before disbanding, with Secretary Kennedy recently reinstating the task force. Siri’s firm ICANN has filed FOIA requests and submitted recommendations to HHS about how to improve vaccine safety, asserting that the current safety framework is not adequate. Siri then surveys the landscape across federal agencies. He asserts that the absence of liability incentives undermines safety, citing industry-pricing and trial designs, and he presents specific examples of licensure trials for routine vaccines that he claims were inadequate by design. Examples include: - Hepatitis B vaccines (Recombivax HB and Engerix B): five days of safety monitoring in trials with 147 participants, according to package inserts and FDA reports he obtained; he notes a lack of long-term safety data and questions the adequacy of control groups. - Prevnar 7 and Prevnar 13 (pneumococcal vaccines): uses Prevnar 7 as a control for Prevnar 13; safety data show notable serious adverse events but are deemed acceptable for licensure; subsequent trials used Prevnar 13 as control for Prevnar 15 with continued concerns about safety signals. - DTaP vs DTP: claims DTP served as control and that DTP itself was not licensed on placebo-controlled trials; cites a Guinea-Bissau study showing higher mortality with DTP vaccination and other studies suggesting increased overall mortality with DTP. - Dengue vaccine: notes long-term, placebo-controlled data showing increased severe harm and death in certain age groups; argues that non-placebo, ethically problematic trial designs can mask safety issues. Siri asserts a categorical claim based on FDA licensure documents: not a single routine neonatal vaccine on the CDC schedule has been licensed based on a placebo-controlled trial; when another vaccine served as control, that control was never a placebo. He presents this as evidence that safety assessments were compromised, especially for early-life vaccines administered in the first six months. Regarding autism, Siri frames it as a litmus test for vaccine safety studies. He recounts IOM findings that were inconclusive about DTaP (and related vaccines) causing autism, citing the lack of sufficient studies and the absence of unvaccinated comparison groups in many analyses. He describes ICANN’s FOIA drive to obtain CDC studies showing vaccines do not cause autism, asserting that most of the CDC’s own 20-study list did not address the vaccines in question. In deposition clips, Siri indicates that the IOM and CDC have not produced adequate evidence to rule out a causal link for several injuries, and that the only mainstream “no autism” position has come under legal scrutiny when the agencies faced court-ordered settlements and deposition testimony. Siri concludes with reform recommendations across agencies: - FDA: remove conflicted personnel from vaccine safety reviews, require clear licensure standards, mandate proper controls and longer safety monitoring, require practitioner notification of trial details, and post pre-registered study protocols; regain transparency of de-identified health data. - CDC/HRSA: align vaccine injury compensation with statutory requirements; expand the VICP to cover more injuries; ensure the CICP is reformed and funded to reflect safety concerns; reduce conflicts of interest; promote alternative, non-pharmaceutical approaches for root causes of chronic illness. - NIH: limit pharma involvement in vaccine development, focus taxpayer-funded research on root causes and replication, and avoid patent-related partnerships that create conflicts. - CMS/HHS-wide: require automated VAERS reporting and public access to de-identified health data; ensure religious exemptions are preserved; depoliticize vaccines and end mandates as political tools; end chronic disease by addressing vaccines as a contributing factor to immune dysregulation. Siri closes by insisting that mandating vaccines is a political act that undermines informed consent, arguing that safety should be decoupled from politics and that safety and efficacy claims should be grounded in rigorous, transparent science. He emphasizes that informed consent, not mandates, should govern medical decisions.

The speaker claims that no childhood vaccine has ever undergone a safety trial using a double-blind, placebo-based study. They assert that this type of study, involving a saline injection as a placebo, is the only way to determine the safety of a pharmaceutical product. Furthermore, the speaker states that there has never been a study comparing the health outcomes of children who receive the full schedule of 72 (or potentially up to 90) vaccines to those who receive none. Because of the lack of safety studies and comparative data, the speaker chooses not to inject themselves or their children with vaccines. They want evidence that vaccines are safe and make people healthier.

We couldn't find any prelicensing safety trials for the 72 vaccines doses that are recommended for American children. Unlike other medications, vaccines were exempt from conducting safety trials that compare health outcomes between a placebo group and a vaccine group. This lack of safety trials is concerning considering the widespread use of these vaccines.

Speaker 0 claimed that none of the 72 vaccines mandated for children has ever been safety tested in relicensing placebo-controlled trials. He said Fauci has been denying this for eight years and recounted a 2016 appointment by President Trump to run a vaccine safety commission, where he asked Fauci and Collins to meet with him with White House counsel. He stated that at that meeting Fauci said, “you say I’m lying,” and promised to send the study, but he never received it. He asserted that he sued Fauci and Aaron Siri, and after a year of stonewalling, government lawyers admitted on the courthouse steps that they never had any study, and provided a written acknowledgment. He pointed to a CHC website and his own website where the letter from HHS is posted. He claimed there is “no downstream liability” and “no front end safety testing,” which he said saves vaccine makers a quarter of a billion dollars. He further argued there is no marketing and advertising cost because the federal government orders 78,000,000 school kids to take that vaccine every year. He described a “gold rush” to add vaccines to the schedule, which he argued is unnecessary for most of them, and claimed many vaccines target diseases that are not even casually contagious. He contended that once a vaccine is on the recommended schedule, it becomes a billion-dollar-a-year business for the company. He asserted that NIH bears royalties in many cases. According to him, a set of vaccines expanded to 72 shots and 16 vaccines contributed to a dramatic increase in vaccine offerings. He linked this expansion to a broader push around vaccines, including the HPV vaccine. He also claimed that in 1989 there was an explosion of chronic disease in American children, including neurological diseases, ADD, ADHD, sleep disorders, language delays, ASD (autism), Tourette syndrome, tics, and narcolepsy. He stated that autism prevalence rose from one in ten thousand generations ago to one in thirty-four children today, citing CDC data. Overall, the summary repeats assertions about the lack of placebo-controlled safety testing, the admission of no study, financial and regulatory incentives to expand vaccine schedules, and a sharp rise in diagnosed neurological and developmental conditions beginning around 1989.

In early 2017, the speaker and Robert Kennedy Jr. met with Tony Fauci and Francis Collins at the NIH to discuss vaccine safety concerns. They questioned the absence of double-blind placebo safety trials for childhood vaccines. According to the speaker, Fauci and Collins admitted that such trials are not conducted because they would be unethical. The speaker proposed a comparative study using the Vaccine Safety Data Link (VSD) to compare the health outcomes of vaccinated and unvaccinated individuals, assessing rates of cancer, diabetes, ADD/ADHD, autism, Tourette's, lupus, and leukemia. The speaker claims this study could be completed quickly, but alleges that NIH officials stated they would never conduct it. The speaker suggests that if vaccines were proven safe through such a study, concerns about vaccine safety would disappear. The speaker believes the study has been done, but the data was manipulated to make vaccinated people appear healthier.

We couldn't find a prelicensing safety trial for any of the 72 vaccines doses recommended for American children. Unlike other medications, vaccines were exempt from conducting safety trials that compare health outcomes between a placebo group and a vaccine group.

Big problem with trusting the science is not the science part, it's who's behind the science part, primarily in the area of vaccines for children. Normally, when you study a drug, you compare it with a placebo, so that way you can truly test the side effects on something, but that is not how they test children's vaccines. This so called placebo control is not really a true placebo control because it's not inert. It's an active vaccine with something called an adjuvant. The big one that they've been using for a long time is aluminum. My question is, how can you really truly test the safety and effectiveness of something if you're looking at the relative safety of an active vaccine to another active vaccine with adjuvants. That just muddies the water to this whole safe and effective claim that you keep hearing over and over and over.

"The myth of vaccines that, a, they are safe and, b, they are necessary and that they eradicated childhood disease, that is a myth." "They've never been tested for safety." "There are no placebo controlled trials." "They always put in the control group the immunogens that's in the vaccines." "That those adjuvants, whether it be aluminum or other substances, those by themselves are dangerous." "they refused to do a true placebo controlled trial like with saline." "they almost all were nearly eradicated before the introduction of the vaccine." "That is not true." "It's reproducible, occurs at two months, four months, and six months." "And most of those deaths are within either days to a couple of weeks of the vaccine."

The speaker states they searched for years for a pre-licensing safety trial of the 72 vaccine doses effectively mandated for American children. They claim that every other medication requires a safety trial comparing health outcomes in a placebo group versus a vaccine group before FDA licensing. The speaker assumed this was also done for vaccines. They state they found out that vaccines were exempt from this requirement.

If regulatory agencies continue to rush products to market without long-term safety trials, the planet is in danger. The speaker questions what would happen if a vaccine wipes out fertility. They state that no childhood vaccines on the schedule have gone through randomized, double-blind, placebo-controlled trials. The speaker finds it alarming that Dr. Martin Macri's statement that no future vaccine will be licensed without a proper randomized controlled placebo trial is shocking to some. They accuse mainstream media of spreading misinformation by denying the absence of placebo trials, then admitting it to avoid delaying vaccine advancement. The speaker asserts the pharmaceutical industry has lied about drugs like Fenben and Vioxx and is now making vaccines. They call for accountability from the industry and the media, warning of grave danger if this does not happen. They disapprove of five-day safety trials with no placebo, especially for products given to healthy children.

According to the speaker, vaccines have never been tested in a randomized, placebo-controlled trial to evaluate their safety. The speaker claims that vaccines contain aluminum compounds because many dead vaccines don't mount an immune response without them. The speaker alleges that in a Gardasil vaccine study, the placebo group received an aluminum adjuvant instead of a true placebo, so the side effect profiles of the active vaccine and placebo groups were the same. The speaker asserts that Merck used a novel aluminum compound and that data shows aluminum in vaccines is toxic. The speaker states that the only completely randomized controlled trial was on sheep using a vaccine for blue tongue disease. The speaker claims the aluminum was toxic, the sheep became sick, their behavior changed, and many died compared to the placebo group. The speaker concludes that the presumption that aluminum as an adjuvant is safe is unfounded and has never been tested.

Speaker 1 states that no vaccines, including the COVID vaccine, have been properly tested. They claim that no childhood vaccine has undergone a placebo-controlled clinical trial of sufficient duration and power to assess its safety before being injected into millions of children in America. Speaker 1 asserts this is not an opinion, but can be verified by anyone reviewing package inserts and clinical trial documents on the FDA website.

Speaker 0 questions Speaker 1 about the lack of clinical trial data for the MMR vaccine. Speaker 1 insists that the vaccine was extensively tested before being licensed and that millions of doses have been used. Speaker 0 asks for proof of pre-licensure clinical trials, but Speaker 1 only refers to a book and mentions studies done in the 1960s. Speaker 0 argues that the data provided is not sufficient and questions the absence of a placebo group. Speaker 1 admits uncertainty about the inclusion of control groups but maintains that safety assessments were conducted. Speaker 0 concludes that no randomized placebo-controlled study exists for the MMR vaccine. Speaker 1 agrees to provide additional information after the deposition.

None of the vaccines, including the COVID vaccine, have undergone proper testing. No childhood vaccine has completed a placebo-controlled clinical trial with sufficient duration and power to confirm its safety before being administered to millions of children in America. This is not an opinion; it can be verified by anyone visiting the FDA website, where the package inserts and clinical trial documents are available for review.

For years, I claimed that none of the 72 vaccines mandated for children underwent safety testing in placebo-controlled trials. Despite Tony Fauci's denials, I challenged him to provide evidence. He admitted he didn't have it on hand and promised to send it, but I never received it. After suing him, his lawyers confirmed there was no such study. The lack of liability and safety testing allows pharmaceutical companies to profit significantly, as the government mandates vaccines for millions of children. This has led to a surge in unnecessary vaccines, contributing to a dramatic rise in chronic diseases among American children since 1989, including conditions like autism, which has increased from 1 in 10,000 to 1 in 34.