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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.

The speaker claims adverse events from the vaccine rollout were covered up and dismissed as rare and coincidental. They state that regulators approved the vaccines based on relative risk data (95%), which they describe as misleading, while the absolute risk reduction was only 0.84%, meaning 120 people had to be vaccinated to prevent one infection. The speaker alleges that Pfizer has 31 convictions, including withholding data, presenting false data, and bribing clinicians and regulators. They claim over 100 doctors have written to various health organizations, including the NHS and MHRA, about the vaccine program, but received only one response. The speaker concludes that science is dead because discussion, analysis, and debate are no longer allowed, and decisions are being made without scientific basis.

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus a month after rollout in November 2020. They allege Pfizer knew the third most common side effect was COVID. Within months, Pfizer supposedly needed to hire 2,400 staffers to process adverse event reports. The speaker asserts Pfizer and the FDA knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The speaker states the CDC initially claimed the injection materials stayed at the injection site, but Pfizer knew they biodistributed throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

Congress investigated ACIP over two decades ago, finding conflicts of interest. In 2002/2003, four of five people who added the rotavirus vaccine had direct financial interest; one voted the rotavirus vaccine onto the schedule and sold his rotavirus vaccine for $186 million. Congress found that 97% of ACIP members had undisclosed conflicts. According to the speaker, a critical issue is adding new vaccines without pre-licensing safety studies. In 1986, there were 11 vaccines on the schedule; now, children must take 69 to 92 vaccines to stay in school in some states, none of which have been safety tested in pre-licensing placebo-controlled trials. The speaker states that the people in charge are now gone, and new, credentialed scientists and physicians will be brought onto the ACIP panel to do evidence-based medicine and make objective public health determinations based on science.

Changes to ACIP are occurring after over two decades of congressional investigation. In 2002/2003, a government oversight committee found conflicts of interest, citing that four out of five people who added the rotavirus vaccine to the schedule had direct financial interest in it. One individual voted the rotavirus vaccine onto the schedule and then sold his rotavirus vaccine in development for $186 million. That year, Congress stated that 97% of ACIP members had undisclosed conflicts. The speaker claims that adding new products to the schedule without pre-licensing safety studies is malpractice. In 1986, there were 11 vaccines on the schedule, but now children must take between 69 and 92 vaccines to stay in school in some states, and none have been safety tested in prelicensing placebo-controlled trials. The speaker states that the people in charge are now gone, and new credentialed scientists and physicians will be brought onto the ACIP panel to do evidence-based medicine and follow the science.

Speaker 0 frames the issue as 'the corruption of science' and the 'capture of the agencies' by pharmaceutical industries, stating the goal is to restore integrity and credibility to science. Speaker 1 cites a CDC internal study: 'black boys who got the vaccine on time had a two hundred and sixty percent greater chance of getting an autism diagnosis than children who waited.' He adds that 'The chief chief scientist on that, Doctor. William Thompson, the senior said vaccine safety science at CDC, was ordered to destroy that data. And then they published it without that fact.' Finally, he asserts, 'So, you know that story. And you know of hundreds of stories like that. It happens all the time. We are being lied to by these agencies, and we're gonna change that right now.'

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.

The discussion centers on the credibility of vaccine safety claims made by various health organizations and the FDA. One speaker argues that vaccines undergo rigorous testing, while the other contends that no vaccine has ever completed a long-term placebo-controlled trial before being licensed. They express distrust in the FDA, citing past issues with drugs like Vioxx and opioids, suggesting that the FDA misled doctors and the public about their safety. The speaker believes that pharmaceutical companies influence these agencies, leading to misinformation about vaccine safety. The goal is to address and rectify this perceived corruption.

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.

Speaker 0 presented a chart and asserted that due to “radical transparency” they have access to close to 11,000,000 pages showing signals that were hidden in VAERS analyses. The speaker stated they uncovered that a signal on myocarditis was hidden, and they also recently uncovered a signal on ischemic stroke for people aged 65 and older in 2022–2023. They claimed both signals were downplayed, but that a hearing would be held next week and a draft report would be issued in conjunction with that hearing. The speaker alleged that Peter Marks was made aware on 03/26/2021 that the inventors of the algorithm analyzing VAERS data were going to mask adverse events, and that by using a different system they uncovered 49 examples of extreme masking, including 25 significant adverse events such as sudden cardiac death, Bell’s palsy, and pulmonary infarction. The speaker emphasized that this is not a matter requiring a sophisticated mathematical model to identify safety signals, stating that the chart shows deaths associated with vaccines dating back to 1990, with several hundred per year initially, and that in 2021 there were over twenty thousand deaths in a five-year span, contrasting with the FDA’s assertions that no signal exists. They characterized these as signals screaming that there has been a covering up to the present day. The speaker claimed that a number of individuals involved in the cover-up continue to work within HHS, the CDC, and the FDA. They requested a commitment that those people will be made available for interviews, and stated that they would subpoena others as needed to dig into the matter, announcing an intention to scrutinize the massive government apparatus and its handling of vaccine safety signals. The speaker concluded by reiterating their commitment to pursue interviews and investigations.

The speaker states that a board was fired for being a "sock puppet" for the industry it regulated. In 2002, a government oversight committee held hearings about the Advisory Committee on Immunization Practices (ACIP), finding that 97% of its members had undisclosed conflicts of interest. As an example, the speaker claims that when the ACIP approved the rotavirus vaccine, four of the five members had direct financial interests in it. One member, Paul Offit, allegedly voted to add the rotavirus vaccine to the schedule while he had a rotavirus vaccine in development. The approved vaccine was withdrawn due to causing intussusception. Offit's vaccine then replaced it. The speaker claims that Offit and his business partners sold that vaccine to Merck for $186 million.

The speaker claims that when the rotavirus vaccine was approved, four out of five board members had direct financial interests in it, working for the companies that made the vaccine or receiving grants to do clinical trials on it. One board member, Paul Offit, allegedly voted to add the rotavirus vaccine to the schedule while he had a rotavirus vaccine in development. The speaker says that because it's now on the schedule, his developing vaccine is virtually guaranteed to get on the schedule. The rotavirus vaccine that Offit voted on was withdrawn within a year because it was causing intussusception in kids. Offit's vaccine then replaced it. The speaker states that Offit and his business partners sold that vaccine to Merck for $186,000,000. The speaker says that Offit told Newsweek that he won the lottery and that it's been said of him that he voted himself rich.

The speaker describes a committee conflict investigated by the office of inspector general and Congress, who urged change, but nothing happened. They claim medical malpractice by this group is evident in the approval of vaccines. The speaker states that in 1986 there were 11 vaccines, which increased to 69, then 92. They assert that, except for the COVID vaccine, none had a pre-licensing safety trial involving a true placebo. According to the speaker, these vaccines were introduced without safety studies, resulting in a lack of understanding regarding the risk profiles of these products. The speaker attributes this to corruption and agency capture.

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.

The speaker states the vaccine recommendation panel has been under attack for 20 years. A 2002 congressional investigation allegedly found 97% of panel members had conflicts of interest with the pharmaceutical industry. One instance cited four out of five members working for a company when they approved its vaccine, and one voting member held a patent on that vaccine, later sold for $186 million. The speaker says the goal is to ensure the panel consists of individuals without conflicts of interest who are not profiting from their votes. The speaker claims that since the panel's inception in 1986, the vaccine schedule has expanded from 11 doses of five vaccines to 69 to 92 doses of 19 vaccines, none of which have been tested for safety. The speaker asserts this is malpractice and aims to ensure all vaccines are tested for safety so physicians and patients understand the risk profile and benefits of each vaccine.

The speaker claims COVID vaccines are not actually vaccines and have caused unbelievable problems and damage. They allege the virus escaped from a lab with six manipulated inserts and the vaccine was 80% homologous to humans, causing major side effects. The speaker states that governments were informed but ignored warnings. They further claim the vaccines' quality control was appalling, the manufacturing process changed, and they were full of contaminants that can integrate into the genome, leading to massive excess deaths and a rise in cancer. The speaker questions why the vaccines haven't been banned, given COVID's diminished threat. They criticize the vaccination of children and call the vaccines "horrible gene therapies" causing "turbo cancers." They advocate for trials for those involved and accuse medical officers and regulatory bodies like MHRA, TGA, and FDA of incompetence and negligence, likening the situation to the Nuremberg trials. They assert the vaccines were never effective or safe, citing Pfizer's initial submissions to the FDA.

In January 2022, a colleague alerted Speaker 0 that there had been a doubling or tripling of baby deaths in the last year, which sparked curiosity. Speaker 1 states that “Their own government told us a medical treatment was safe, and it killed babies.” Speaker 2 says she has “lost all faith that Health Canada is looking out genuinely for the best interests of Canadians.” Speaker 3 alleges that doctors “made extra money to push vaccines” and were given a billing code to do it, and that she has “pulled all the billing codes.” Speaker 4 asserts that “They've purchased the vaccine that hasn't been approved,” distributed it to the provinces so that once it’s approved, they can “start jabbing ourselves with it” and “start jabbing pregnant mothers with it.” Speaker 3 questions the necessity of vaccinations: “Why did we have to get these vaccinations? Like, why was this something that we had to do? You go to the hospital, you expect to have a baby, and you expect to go home, and then you don't.” Speaker 0 speculates on criminal negligence, saying, “I would suspect that there was criminal negligence on part of the government and the public health officials.” Speaker 3 notes that it is “highly recommended that pregnant women get their vaccine as soon as possible.” Speaker 0 contends that a narrative was pushed to everybody, including pregnant and breastfeeding women, that the mRNA shots were safe and effective. Speaker 2 claims wiretapping, harassment, charging, and barring expert witnesses: “They had wiretapped her phone. They had harassed her. They had charged her. They didn't allow any expert witnesses to testify.” Speaker 1 accuses police of trying to cover up Canadian babies’ deaths “to the point of stopping detective Helen Greaves from testifying about it.” Speaker 4 observes that “The dominant individuals keep the subordinates in their place by constant aggression.” Speaker 5 discusses vaccination choice versus public risk, remarking, “If you don't wanna get vaccinated, that's your choice. But don't think you can get on a plane or a train besides vaccinated people and put them at risk,” and claims CBC initially “started off with CBC running a story to implicate her and to paint her with a brush that looks uncomplimentary to the public.” Speaker 6 claims Canada must shift its understanding of what the is, describing it as “a state broadcaster pushing the agenda of the Liberal government of Canada.” Speaker 4 calls this “the most significant matter affecting our children today from a health perspective,” noting that authorities are “not investigating.” Speaker 2 concludes that everything emanates outward from this case involving law enforcement, the judicial system, the pharmaceutical industry, and health agencies, “how they work together, how they censored information. It all ties together to this one case, and that's what makes it so dangerous.”

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.

Speaker says his committee now has over 8,000,000 pages of information and that federal health agencies hid the signal about myocarditis, claiming "CD somebody in the federal health agencies, interagency communication, hid the signal. Admitted there was a signal on my architis and they hid it. They didn't warn the public. They didn't warn doctors." He calls this "one instance of corruption and lies told by the CDC" and says more will be rolled out. He notes "our first hearing in permanent subcommittee investigation on that hiding of the signal myocarditis." He asserts science has been "thoroughly corrupted" and presents "data" to enter into the record. Citing censorship during the Biden administration, he cites VAERS: "thirty eight thousand seven hundred and forty two deaths reported on VAERS worldwide associated with COVID vaccine. Thirty eight thousand seven hundred forty two. Nine thousand two hundred fifty two of those deaths occurred on the day of vaccination within one or two days." He adds, "There's not any good study on that. This is hard evidence."

Speaker 0 describes finding vaccine insert materials with no printed content and says this is disheartening and “disgusting,” then adds that it “gets better” and that “more” continues to happen. Speaker 0 claims the CDC redacted every word of a 148-page study on myocarditis after COVID vaccination, and that when they asked to have the study printed, the entire document was redacted. They question what the study could have contained that required redaction and say this is “even scarier.” Speaker 1 says they are witnessing “an active cover up” of a “colossal consumer product safety debacle” affecting the entire world. They claim that in the United States the CDC, National Institutes of Health, and FDA are actively involved, and that similar actions occur in the UK with the MHRA, in Europe with European medicine agencies, and in Australia with the Therapeutic Goods Administration. Speaker 1 states that each of these regulators requires product companies to produce ninety days of safety monitoring after a product comes out, describing this as a regulatory dossier. They say that if problems arise and are reported to a company (such as Pfizer), the company must report, compile, and produce a report that is made publicly available. Speaker 1 claims that for Pfizer, whose first vaccine was approved 12/10/2020, Pfizer did not produce a report after the ninety days. They add that when people asked what was happening, Pfizer allegedly did not disclose what occurred, leading to court proceedings. Speaker 1 states that the FDA’s lawyer allegedly said the dossier should not be released for fifty-five years, and that after pressure, the Pfizer dossier was eventually released. They then claim Pfizer recorded 1,223 deaths with their product within ninety days of release and recorded over 1,200 new adverse events. Speaker 1 also says the FDA worked to cover this up, and that FDA should have regulated Pfizer with at least monthly meetings and full disclosure about “novel vaccines,” which they describe as a “genetic transfer technology platform,” the first time human beings had been injected with foreign genetic material in world history. Speaker 1 ends by stating that two thirds of the world’s population took these.

The speaker questions how many people injected with mRNA products knew they weren't receiving a traditional vaccine, suggesting many, including medical professionals, are unaware due to the perception of conspiracy. The speaker claims there was a sufficient safety signal in VAERS to halt the rollout in January, citing almost 90,000 VAERS entries and nearly 700 deaths within the first month. They state that historically, products causing over 50 deaths have been pulled from the market. The speaker questions why the CDC, HHS, and FDA aren't investigating this data.

A physician who experienced an adverse reaction to the Moderna COVID shot states that the COVID shots should never have been authorized for children and pregnant women. After receiving the Moderna shot, the speaker developed transverse myelitis, autonomic dysfunction, and an unspecified immune disorder, leading to medical retirement. The speaker is now co-chair of React19, representing Americans injured by the COVID shots. The speaker claims that the clinical trials were rushed, safety data was withheld or altered, and reporting systems like VAERS and V-Safe have failed. The speaker questions whether regulatory agencies have a conflict of interest. The speaker alleges that instead of proving safety and efficacy, the COVID-19 shots were assumed to be safe and effective, with short follow-up data, and were given to pregnant/lactating women and children without long-term safety data. The speaker is appreciative that the COVID-19 shots have been removed from the childhood vaccination schedule for healthy children, but much damage has already been done. The speaker advocates for recognition, research, medical care, and compensation for those injured by the COVID-19 shots.

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.

A law called Vika was passed in 1986, making it illegal to sue vaccine companies, regardless of recklessness or negligence. As a result, the number of mandated vaccines has increased from 3 to 79, none of which have been safety tested. The speaker claims that vaccines are exempt from pre-licensing safety testing, a claim that Anthony Fauci publicly denied. When President Trump appointed the speaker to run a vaccine safety commission, the speaker asked Fauci to provide safety studies on vaccines. Fauci claimed he left them in his office and never sent them. Subsequently, the speaker and Aaron Siri sued Fauci. After a year of stonewalling, HHS provided a letter stating that there has never been a pre-licensing safety study of any vaccine on the childhood schedule.

Speaker 0 says they found “information like this,” such as vaccine insert paper, with “nothing printed on it,” which they call disheartening and disgusting. They add that it “just keeps happening” and claim the CDC redacts “every single word” of a 148-page study on a myocarditis after COVID vaccination. Speaker 0 says they asked someone to print the study, and that the entire 148 pages are redacted. They ask what a study does if “there’s nothing there,” and they ask what might have been there that required redaction. Speaker 1 says they are “witnessing an active cover up” involving “a colossal consumer product safety debacle” affecting the entire world. They claim that in the United States, the CDC, National Institutes of Health, and FDA are actively involved in a cover up, and that similar cover ups are occurring in the UK with the MHRA, in Europe with European medicine agencies, and in Australia with the Therapeutic Goods Administration. Speaker 1 states that each company that puts out a product has an obligation to produce “ninety days of safety monitoring” after the product comes out, describing it as a regulatory dossier. They claim that if someone has a problem and reports it to a company like Pfizer, Pfizer must report, write down what happened, collate it into a report, and make it publicly available. Speaker 1 says that when the ninety days elapsed for Pfizer’s first vaccine approved on 12/10/2020, Pfizer “didn’t produce a report.” They add that people asked what was happening with the vaccine, and Pfizer allegedly would not disclose what happened, leading to a court case. Speaker 1 says the lawyer for the FDA stepped in to say they did not want to release Pfizer’s dossier for fifty-five years. Speaker 1 then says that after the plaintiff pushed, the Pfizer dossier “slowly” came out. They claim Pfizer recorded one thousand two hundred and twenty-three deaths with their product within ninety days of release, and they say people called Pfizer in desperation watching family members die after taking the vaccine. Speaker 1 also claims Pfizer recorded “over twelve hundred” new adverse events and refers to “doctor Boden” discussing problems they say they have been grappling with. They conclude by claiming the FDA worked to cover this up and should have been regulating the company with at least monthly meetings and full disclosure about novel vaccines, described by Speaker 1 as a genetic transfer technology platform and as the first time human beings were injected with foreign genetic material in world history, after which “they were getting it full on.” Speaker 1 ends by saying “Two thirds of the world’s population took”