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Speaker 0 asked about a report and how concerning it is, questioning whether “10” is the real number. Speaker 1 said the main concern is that the report “dramatically understates the problem.” They argued that analyses rely on doctors and that it was difficult to obtain autopsies during the pandemic. Speaker 1 stated that medical professors did not want to know, resulting in very few autopsies. They said NIH, CDC, and FDA reviewed 96 autopsies of children and identified about 10 cases they considered possible or probable. Speaker 1 then pointed to VAERS, stating there are almost 1.7 million total adverse events and 39,000 deaths worldwide. They said that of the 39,000 deaths, 24% occurred on the day of vaccination or within one or two days. They acknowledged FDA officials say VAERS does not prove causation, but said that if someone was perfectly healthy and died on that day or within one or two days, they would assign blame. Speaker 1 also said there may be cases where people were already in bad health and vaccination “tipped them over,” with death ultimately caused by something else. Speaker 1’s “bigger revelation” was described as information they said was not covered by mainstream media. They stated that on 03/01/2021, Peter Marks, head of CBR within FDA, was briefed that their algorithm analyzing VAERS safety would hide and mask safety signals. Speaker 1 said that 26 days later, Marks ran a new algorithm that unmasked 49 cases of extreme masking and 25 safety signals, including sudden cardiac death, pulmonary infarction, Bell’s palsy, and different types of strokes. Speaker 1 said that in the next three months, similar data runs with the new algorithm showed more safety signals and more types of sudden death. They said the report described not “pin[ning] a badge” on doctor Anna Scharzman (identified as the dad of Speaker 1’s expert), ordering her to cease and desist, and continuing to use the algorithm the briefing warned would hide safety signals “to this day.” Speaker 1 said Peter Marks later went to work for Eli Lilly and claimed that the world is in denial. They stated they could not get the story broadcast or interviews on CBS, ABC, NBC, PBS, MS Now, or CNN, and said they challenged Jake Tapper, sending the report and requesting an additional appearance.

The speaker states the hearing is titled "What Are They Hiding?" and cites over 60 oversight letters to federal health agencies as evidence. These letters cover issues like hot lots and VAERS analysis procedures. The speaker says their oversight letters were prompted by Anthony Fauci's emails released under FOIA in February, requiring someone to go to court to obtain them. After requesting unredacted versions of the initial 4,000 pages in June 2021, they received the same redacted pages by July. In September 2021, a request was narrowed to 400 pages. From October 2021 to January 2022, they were allowed to review 50 pages at a time in a reading room, without the ability to make copies. The last 50 pages have not been released after nearly two years. The speaker suggests the unreleased documents may contain incriminating information and should be accessible to Congress and the public.

The record that they're gonna rely on to make these decisions? Will you make it transparent for the American people? All the evidence is transparent. All evidence is transparent for the first time in history. You can characterize it any way you want. I quoted them today. What I said was accurate. What you said were lies. Are you saying that the mRNA vaccine has never been associated with myocarditis or pericarditis into I am simply trying to say that the people that you have put on that panel after firing the entire You're evading the question. The senator, they deserve the truth and that's what we're gonna give them for the first time in the history of that agency.

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.'

The transcript alleges that multiple senior FDA officials, not just Peter Marks, are “complicit.” It claims American people believed these officials, and that each day the officials lie “compounding the lie day after day, week after week, month after month, year after year.” It says this makes honesty “less likely” over time. The speaker then references a member of Congress who “cut videos” tied to “the jab,” arguing the videos would “end the pandemic.” The transcript asserts that the advocacy for the injections “killed people” and “permanently disabled them,” adding that doctors, federal health officials, and Stephen Colbert “wouldn’t want to do that.” The speaker describes what they call a “global state of denial,” saying other governments relied on federal health officials and “forced it down there,” with administration mandates requiring the injections “in complete violation” of the Nuremberg Code, which the speaker frames as prohibiting forcing medical treatment. The transcript claims that people died as a result. It contrasts political claims about the pandemic, saying Biden blamed “the pandemic of the unvaccinated” while “losing patients,” and then asserting, “Now we’re losing patients too.” The speaker says the central issue is that “your injection didn’t stop transmission” and that “your injection killed people” and “permanently disabled people.”

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.

Doctor Moran, a senior advisor to Fauci, discussed deleting emails to avoid FOIA requests, which goes against NIH policies. He also mentioned avoiding "smoking guns" in emails. Moran shared internal discussions with Daszak and helped craft responses to FOIAs, actions not in line with NIH policies. Tabak expressed concern over these actions. Moran is still employed by NIH. The questions raised highlight potential transparency issues within the NIH. Translation: Doctor Moran, a senior advisor to Fauci, discussed deleting emails to avoid FOIA requests, which goes against NIH policies. He also mentioned avoiding "smoking guns" in emails. Moran shared internal discussions with Daszak and helped craft responses to FOIAs, actions not in line with NIH policies. Tabak expressed concern over these actions. Moran is still employed by NIH. The questions raised highlight potential transparency issues within the NIH.

There was a recent FDA rejection of an MDMA-based therapy for PTSD, a program that had achieved, on its own terms, two successful phase three studies. The speaker notes that the trials were designed exactly as the FDA told them to design, but the episode is tied to the rise of advisory committees—FDA panels of so-called experts who opine on data and recommendations. The FDA is not bound by their recommendations, but they often follow them, sometimes not. In the speaker’s view, the FDA uses these advisory committees as a cover for what they actually want to do, a dynamic the speaker has observed across years in biotech as an investor and company builder. He has sat in eight-hour advisory committee sessions in Maryland, taking detailed notes, and while he didn’t attend the most recent one, he believes it smelled like the briefing documents provided to the committee were used to guide the outcome. He suspects the advisory committee recommended against approval, and the FDA then moved to that outcome. The speaker argues this is a travesty for PTSD patients who have very few options. He focuses on the reasoning the FDA gave for denying approval: the trial was functionally unblinded. Typically, trials use placebo and active drug arms with participants unaware of which treatment they receive, to ensure that observed effects are not merely placebo. The FDA claimed that patients knew whether they were on the MDMA-based therapy because some experienced euphoria, a side effect of the treatment. Therefore, the therapy could appear to work due to unblinding and a placebo effect, rather than a true therapeutic benefit. The speaker emphasizes that the possibility of euphoria being part of the drug’s mechanism—and thus related to its therapeutic effect—was ignored in their assessment, and that this unblinding was, in his view, anticipated by the FDA before agreeing to the phase three protocol, which also added tens or hundreds of millions of dollars in development costs. The speaker criticizes the public record, including biotech press coverage, for focusing on “trial irregularities” or an unblinding issue rather than on the broader cost-benefit and mechanistic considerations. He asserts that the public is left with the notion that there were unblinding issues, not recognizing that the unblinding related to the drug’s therapeutic properties was anticipated and approved by the FDA. He concludes that the episode reveals how the bureaucratic machinery operates, with advisory committees and briefing documents shaping outcomes in a way that aligns with the FDA’s underlying aims.

In the message described, Speaker 0 highlights a key claim: the CDC and FDA were fully aware of the masking phenomenon within their empirical Bayesian analysis. The speaker emphasizes that this awareness was part of the information being conveyed in a letter to Bobby Kennedy. The central issue raised is not about general safety signals, but about the timing of deaths relative to vaccination. The speaker notes a concern that began earlier, stating that back in October there were discussions with Mike Eden about these injections. The concern is tied to what was observed in the data, specifically that “early on in March and April” the data appeared to be "screaming at us" when looking at thousands of deaths. The speaker provides a concrete statistic: “forty six percent of those deaths were occurring on the day of vaccination than one or two days.” The speaker then updates the figure, saying that they are “up to almost thirty nine thousand deaths” in total, and adds that “Twenty four percent of those deaths occurred on the day of vaccination or within one or two days.” The speaker asserts that this information “has been available month by month by month since about March, April 2021,” yet alleges that “the federal officials are still not acknowledging it.” Instead of acknowledging these signals, the speaker claims officials point to other metrics, stating they “go to these, you know, PRR, the proportional reporting ratios, or a more sophisticated” approach. The claim continues that when PRRs were showing safety signals, officials reacted as if, “oh, we're not using those. We're using empirical Bayesian analysis. They set the trigger.” In summary, the transcript presents a narrative in which the CDC and FDA are described as being aware of a masking phenomenon identified through empirical Bayesian analysis, with specific, alarming timing data linking a significant proportion of deaths to the day of vaccination or the following couple of days. The speaker contends this information has been publicly accessible on a monthly basis since early 2021, but accuses federal officials of not acknowledging it and of favoring a different analytic framework (PRR) or of claiming to use empirical Bayesian analysis after the fact, implying that the trigger for safety signals was set within that framework. The overall emphasis is on the alleged discrepancy between available data and official acknowledgment, as well as the choice of analytic methods used to interpret safety signals.

Speaker 0 asks if the speaker knew about stopping humanization before it entered the market and if they are willing to share the data with the committee. Speaker 1 responds that they did not know about it before it entered the market and had to move at the speed of science to understand what was happening.

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 thanks the committee for a complimentary introduction and for dedication to transparency and accountability. Speaker 0 says they are a career CIA operations officer. They report that they were on joint duty at the Office of the Director of National Intelligence, working with the National Intelligence Directors Initiatives Group (DIG), from March 2025 to April 2026. Speaker 0 states their responsibilities included leading the DIG’s investigation into COVID origins, anomalous health incidents, and unidentified anomalous phenomena. Speaker 0 says they are appearing to discuss “the COVID cover up,” the national security implications tied to the DIG’s investigative findings, CIA refusal to comply with lawful oversight, and how to remedy these problems. Speaker 0 describes how intelligence community leaders and senior analysts downplayed the possibility that the COVID pandemic originated as the result of a lab incident. Speaker 0 says that motives were difficult to define given the scope of the DIG’s review. Speaker 0 then states that, “intentional or not,” the IC’s actions resulted in a cover up, wasted resources, and a failure to properly inform policymakers. Speaker 0 says that public health policy would have been very different if the American public had been made aware that a virus from a lab in China was going to serve as the foundation for emergency use authorization mRNA products that were mandated by the former administration. Speaker 0 then addresses Doctor Fauci’s role. Speaker 0 states that Doctor Fauci’s role in the cover up was intentional. Speaker 0 says Fauci influenced the analytical process and findings by using his position to ensure that the intelligence community consulted with a conflicted list of curated subject matter experts, public health officials, and scientists. Speaker 0 states that this included some of the authors of the paper “The Proximal Origin of SARS CoV-two.” Speaker 0 further says the process included other public health experts who have been in Fauci’s orbit for the last twenty plus years. Speaker 0 frames these points in relation to the DIG investigative findings and ties them to national security implications, CIA refusal to comply with lawful oversight, and proposed remedies for the problems Speaker 0 describes.

Speaker 0 asks about a report and how concerning it is, suggesting that if the reported figure is 10, there is a “real number” that could be higher. Speaker 1 says the main concern is that the analysis “dramatically understates the problem.” They describe the difficulty of getting autopsies during the pandemic and say medical professors didn’t want to perform them, resulting in very few autopsies. They state that NIH/CDC/FDA reviewed 96 pediatric autopsies and concluded about 10 were possible or probable. Speaker 1 then argues that safety signals were “screaming,” and points to VAERS. They claim there are almost 1.7 million total adverse events and 39,000 deaths worldwide. They say 24% of the 39,000 deaths occurred on the day of vaccination or within one or two days. Speaker 1 also references the point that VAERS doesn’t prove causation, while stating that if a person who was “perfectly healthy” died that day or within one or two days, they would “be blaming” the jab. They add that in some cases people may have been in bad health already, with death tipped over by another cause. Speaker 1 says the “bigger revelation,” which they claim was unveiled three weeks ago and is “still not being covered by the mainstream media,” involves FDA’s VAERS algorithm. They state that on 03/01/2021, Peter Marks (head of CBER/FDA’s division approving vaccines and surveilling post-approval safety) was briefed that their algorithm analyzing VAERS would “hide and mask safety signals.” They say that 26 days later, a new algorithm unmasked safety signals, producing 49 cases of extreme masking revealed and 25 safety signals, including sudden cardiac death, pulmonary infarction, Bell’s palsy, and different types of strokes. They claim that similar data runs over the next three months showed more safety signals and more sudden death. Speaker 1 further claims that FDA did not “pin a badge” on Anna Scharzman, referred to as the father of their expert, and instead “shunned her off to the side,” ordered her to cease and desist, and decided to use the algorithm they had been warned would hide safety signals, which they say is still being used. Speaker 1 states that Peter Marks left for Eli Lilly and claims “the entire world” is in denial. They say they have been unable to broadcast the story or get interviews on CBS, ABC, NBC, PBS, MSNBC, or CNN, and that they challenged Jake Tapper, who they say agreed to read the report but has not invited them back yet.

Speaker 0: I find information like this, you know, inserts for the vaccine. Paper's there, and there's nothing printed on it. I find that very interesting, disheartening, disgusting, and lots of other words, but then it gets better. It just keep wait. There's more. It just keeps happening. The CDC redacts every single word of a 148 page study on a myocarditis after COVID vaccination. So I asked research to print the study for me. 148 pages. The entire thing is redacted. What good does a study do if there's nothing there? Then I wanna know, wait, what might have been there that they needed to redact it? That's even scarier. Speaker 1: We're witnessing an active cover up of a colossal consumer product safety debacle that is is basically affecting the entire world. Mhmm. So in The United States, our CDC, National Institutes of Health, and the FDA are actively involved in a cover up. And the same is occurring in The UK with the MHRA, Europe with European medicine agencies, and Australia with the Therapeutic Goods Administration. Something is going on that's very big. Each one of these companies that puts out a product has an obligation to produce ninety days of safety monitoring after their product comes out. It's a regulatory dossier. If somebody has a problem with the new product and they call the company like Pfizer, Pfizer has to report, write down what happened, and they have to collate that in a report and produce it and make it publicly available. When it came to ninety days with Pfizer, the first vaccine that came out, remember Pfizer was approved 12/10/2020. Pfizer didn't produce the report. And then people started asking, well, what's happening with your vaccine? And Pfizer would not disclose what happened. And then it went to court. And the lawyer for the FDA stepped in and said they don't wanna release Pfizer's dossier for fifty five years. Mhmm. Oh. Fifty five years. And the the the plaintiff pushed. And finally, slowly, the Pfizer dossier came out. Pfizer recorded one thousand two hundred and twenty three deaths with their product within ninety days of release. People were calling Pfizer in desperation watching their family members die after taking the vaccine. Pfizer recorded over twelve hundred new adverse events, new problems that doctor Boden has talked to you about that we are grappling with the entire time. But the point is our FDA worked to cover this up. The FDA should be regulating this company. FDA should have been having at least monthly meetings and fully disclosing what was going on with these novel vaccines, which are a genetic transfer technology platform.

Speaker 0: They argue that because the vaccine is classified as such, they don’t have to worry about being sued. They claim immunity from liability is dependent on there being no fraud, and there clearly was fraud. Speaker 1: They say there is fraud. They note that immunity from liability depends on fraud, and in light of that, it matters. They explain that there was fraud. Speaker 0: Expresses surprise and asks for caveats about fraud. Acknowledges there were caveats. Speaker 1: Confirms there is fraud and says it makes the situation more interesting. Speaker 0: Asks how fraud is defined, noting that drugs were sold with multiple studies and only one was good. Speaker 1: Responds with a point about safety testing for the mRNA vaccines. States that the insufficient safety testing was done before release, and that the product injected into billions of people involved DNA plasmids. There is massive contamination in the shots actually delivered, including the SV40 promoter from simian virus 40. The point is that safety testing for one drug was completed, but people were injected with something different that had other components that were not tested, which is described as fraudulent. Speaker 0: Requests an explanation of the SV40 issue for the audience. Speaker 1: Describes production techniques used to generate the product. Explains that a plasmid, a circular piece of DNA, was used to produce the product in vats, with bacteria performing the production, later coated in lipid nanoparticle. There is a requirement to purify DNA and set standards for DNA contamination, with limits that cannot be exceeded. In this case, the problem isn’t only poor quality control but that there was a more painstaking way to produce the same product that did not involve DNA plasmids at all. Consequently, leftover material in vials injected into people contained DNA contamination across the board. Kevin McKernan tested vials, finding DNA contamination in the samples. Speaker 1: Explains that the DNA left over includes the SV40 promoter, a genetic trigger from simian virus 40, which is known to be carcinogenic. Since this promoter is left in the vials from injections given to people, it challenges the claim that the mRNA shots could not integrate into the genome. While acknowledging that there are cellular processes such as reverse transcription, the speaker asserts that even the claim of “no DNA” is false because there is DNA in the vials, specifically DNA with the SV40 promoter, a genetic engineering tool with carcinogenic potential. The speaker concludes that this appears to be fraud: injecting a different product into the public on the basis of safety testing that was conducted with a product produced by a different process. Speaker 0: Reiterates the conclusion: you can’t inject a different product into the public on the basis of safety testing that was done with something produced by a different process.

Senator Johnson is asked about a “COVID cover-up” and why legacy media such as CNN is not covering it. The interviewee claims that Peter Marks knew on March 1, 2021 that “their algorithms were hiding safety signals,” and that 26 days later it was discovered they had 25 serious adverse events, including sudden cardiac death, pulmonary infarction, bells and pauses, and different types of strokes. The interviewee says the information was “buried” and “hid,” calling it a major scandal that major media is ignoring for almost six weeks. When asked whether people could sue the U.S. government over the COVID cover-up, the interviewee says legal ramifications are hard to say, noting the government’s ability to protect itself and people carrying out its mission. They frame their role as exposing the issue and mention “radical transparency” from Secretary Kennedy as enabling access to more documents and more people to interview. The interviewee calls it the biggest scandal of their lifetime, saying people were not warned and were mandated to take the shot or were coerced or convinced without the kind of information needed for informed consent. They claim that millions suffered adverse events and that at least tens of thousands died after the March 1 date. In response, a commentator asserts that “conspiracy theorists were right again,” reiterating that 25 serious adverse events with the COVID vaccine were hidden from the public. They describe “masking” as obscuring and then list categories of side effects, focusing on neurological and cardiac effects (including sudden death and cardiac failure) and pulmonary effects associated with stroke, along with other “obscure” items. They conclude that people should have been warned about these side effects before getting the vaccine, rather than being told it was 100% safe and effective.

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 claims a committee experienced typical conflict, but a specific conflict was particularly obvious. The Office of Inspector General and Congress investigated and urged change, but nothing happened. The speaker asserts this group committed medical malpractice by approving vaccines, increasing the number from 11 in 1986 to 69 and then 92. They state that, except for the COVID vaccine, none had pre-licensing safety trials with a true placebo. According to the speaker, these vaccines were introduced without safety studies, meaning the risk profiles are unknown. The speaker attributes this to corruption and agency capture.

Speaker 0 states that the committee now has over 8,000,000 pages of information. In the first tranche, they discovered that someone in the federal health agencies, through interagency communication, hid the signal and admitted there was a signal on myocarditis, but they hid it and didn’t warn the public or doctors. This is described as one instance of corruption and lies told by the CDC, with many more to be rolled out. He notes that they held their first hearing in permanent subcommittee investigation on that hiding of the signal myocarditis and that they have heard a lot of studies. He mentions that, as he has looked into science, it has been thoroughly corrupted, and he requests to enter a data sheet into the record, saying he has been publishing this chart since early 2021. He references being on talk radio shows where they get deplatformed due to censorship in the Biden administration. He then presents what he calls “the facts” about the VAERS system, which was touted in October 2020 as a great safety surveillance system on COVID. A few months later, they denigrated their own system. Despite this, VAERS shows that there have been 38,742 deaths reported on VAERS worldwide associated with the COVID vaccine. He specifies that 9,252 of those deaths occurred on the day of vaccination within one or two days.

Speaker 1 says that throughout the Biden administration he sought records about decision-making and why the U.S. funded Wuhan, China research, including why evidence about the virus origin being from a lab accident was being suppressed, but “we got nothing.” He says the Biden administration “stiff-armed” him by preventing access to virtually any documents. He says many of the findings during the Biden administration came from Freedom of Information Act requests by people outside government and from court actions forcing disclosure. He says that after the new election, he received promises from Secretary Kennedy and others that documents would be revealed. He says it took about six months, with resistance he attributes not to Secretary Kennedy but to “minders” around him. He says that after finally receiving documents, they have been reviewed for about a month. Speaker 1 states that in communications between Anthony Fauci and others, including Francis Collins, Fauci is depicted telling others to read materials, then delete them, and that he allegedly instructed them to delete “this material” after reading. Speaker 1 says deleting emails and discussions about government business is illegal for someone in the executive branch. He adds that Fauci testified he did not do that, and says this creates “two crimes”: destroying federal records and a prior sworn statement that he wouldn’t do it. Speaker 1 identifies a “big question” involving what he calls an “auto pen pardon” and says it will have to be challenged. He says there are thousands of auto pen pardons and raises whether President Biden was aware. He says they interviewed the person running the auto pen, who said they never met the president, and that the person said they did not discuss it directly but heard about it from higher-ups who allegedly talked to the president. Speaker 1 says this provides “a lot to go on” and describes it as a chance for the issue to get into court and for the Department of Justice to fight it out. Speaker 1 says he has invited Anthony Fauci involuntarily; if accepted, they will bring him in, and if not accepted, they will subpoena him. Speaker 0 asks whether the alleged wrongdoing falls under the auto pen time frame, noting that in some earlier auto pen matters there were specific time frames. Speaker 1 responds that the “umbrella” was “a decade,” described as leading up to the end of Biden’s term, and says this raises questions about whether a pardon can cover crimes not alleged at the time, whether it can be “all inclusive,” and whether a pardon can be upheld if it doesn’t specify the crime. Speaker 1 contrasts this with how pardons are typically specific to an accused or trial-ready crime. Speaker 0 asks about specific consequences, including prison time, regarding destroying federal records. Speaker 1 says lying to Congress is the biggest issue, that it can be five years in prison as a felony, and that destroying records adds to the crime and is against the law. He then ties this to contemporaneous emails, asserting that while Fauci said publicly he had no idea the virus came from a lab and that it couldn’t have been gain-of-function, privately he was “very worried” about the lab because he knew it did gain-of-function research. Speaker 1 also says gain-of-function research was funded by the United States government with Anthony Fauci’s approval, and claims Fauci’s pandemic guidance about origins and about cloth masks was contradictory to privately discussed concerns, including that Speaker 1 says cloth masks do not prevent transmission.

The speaker discusses redacted information on vaccine inserts and a cover-up involving the CDC, FDA, and other agencies regarding vaccine safety monitoring. Pfizer failed to produce safety monitoring reports, leading to court battles and eventual disclosure of 1,223 deaths and 1200 adverse events within 90 days of vaccine release. The FDA is accused of covering up this information, despite the unprecedented use of genetic transfer technology in vaccines.

A Pfizer whistleblower within the company released documents showing that there were over 158,000 reports of adverse reactions from 12/01/2020 through 02/28/2021. The reports include serious adverse reactions and spontaneous abortions. The whistleblower states that the FDA was well aware and wanted these documents hidden for seventy five years. According to the speaker, the documents prove that the adverse events were intentionally released and that officials knew all along that the vaccine was going to cause massive heart attacks and strokes and deaths and infertility and miscarriages. The speaker claims the list of adverse effects goes on, including neurological issues, and questions how this vaccine remains on the market, noting that vaccines have been removed where ten cases of a child getting sick occurred. The speaker describes the situation as evil, intentional, and asserts that those involved must be held accountable.

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”

Speaker 0 asks if the speaker knew about stopping humanization before it entered the market and if they are willing to share the data with the committee. Speaker 1 responds that they did not know about it before it entered the market and had to move at the speed of science to understand what was happening.