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In my hospital, my patients had a mortality rate of 4.4% while the rest of the country ranged from 25 to 40%. Unfortunately, I faced censorship whenever I mentioned the potential benefits of ivermectin on social media. This censorship, which I refer to as "Facebook jail," prevented me from sharing important information. I strongly believe that many lives were lost unnecessarily due to this censorship. Don't forget to subscribe to our alerts newsletter to stay updated.

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The speaker claims that unvaccinated individuals entering hospitals were deliberately killed. According to the speaker, every unvaccinated person they interviewed who went to the hospital reported not receiving the same treatments as vaccinated patients. Instead, they were allegedly given remdesivir, ventilation, and fentanyl, leading to their deaths. Another speaker adds that hospitals had financial incentives to produce COVID-related deaths, allegedly receiving up to $500,000 per death in California. The first speaker agrees, stating that hospital coders and whistleblowers revealed that patients were repeatedly tested for COVID until a positive result was obtained, triggering payments. They claim hospitals received additional payments for each drug and piece of equipment used, totaling over $500,000 per person. One person allegedly said their daughter was worth more dead than alive.

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It is nearly impossible to publish data that goes against the national public health narrative, preventing doctors from finding solutions. The speaker has conducted clinical trials for pharmaceutical companies, including vaccine studies, and has brought vaccines and other drugs to market. Some drugs never made it to market because they killed people. Clinical trial guidelines ensure safe drugs, but these guidelines were not followed during the pandemic, affecting everyone. COVID should have been a time for doctors to unite, but interference with research occurred. Science evolves through experiments, skepticism, and an open mind. Challenging current knowledge must be allowed to move science forward, but what the speaker witnessed during the pandemic was not science.

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A speaker claims remdesivir, an experimental drug, caused COVID-19 patient deaths in hospitals between days one and nine of a ten-day treatment. The speaker states that Dr. Anthony Fauci claimed in May 2020 that remdesivir was found safe and effective in an African drug trial in February 2019, and he hyperlinked the study in a memo to hospitals. The speaker says that the African trial actually showed a 53% death rate, leading the safety board to suspend remdesivir use and notify funders of its toxicity. The speaker alleges that Dr. Fauci and his NIH department funded the Ebola trial in Africa. The speaker accuses Fauci of lying to Congress and the American people by claiming the drug was safe and effective when the safety board deemed it too deadly and toxic.

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Speaker 0: They think I'm dangerous for speaking the truth. Speaker 1: Dr. Stella Emmanuel was part of a video claiming, without evidence, that hydroxychloroquine is a cure for COVID-19. The video was taken down by social media platforms for spreading misinformation. Despite the backlash, Dr. Emmanuel insists that hydroxychloroquine could be part of a cure. Dr. Anthony Fauci disagrees, stating that scientific data consistently shows hydroxychloroquine is not effective in treating COVID-19.

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Before the pandemic, Dr. Fauci tested Remdesivir in an Ebola trial in Africa alongside four other drugs. However, the institutional review board (IRB), responsible for ensuring safety in clinical trials, intervened and removed Remdesivir from the trial due to its high fatality rate. Ebola typically kills 53% of those infected, but Remdesivir was causing even more deaths. It seems illogical to then administer this drug to individuals with a disease that has a much lower infection fatality rate of 1%. This decision appears questionable, but unfortunately, there is a history of similar actions being taken.

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Actions were taken to promote the vaccine by inflating COVID numbers through protocols in 2020. Hospitals were incentivized to label patients as COVID, put them on ventilators, administer Remdesivir, and profit from deaths. The goal was to instill fear and push vaccinations. Hospital administrators, driven by financial incentives, unknowingly contributed to unnecessary deaths. This greed-driven system continues to harm people.

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Ralph Barrick, the inventor of coronavirus and developer of Remdesivir, a drug used to treat COVID, had a hand in both. However, Remdesivir had a high kill ratio of 53% and was pulled by the World Health Organization for Ebola treatment. Despite this, in 2020, Anthony Fauci and others decided to use Remdesivir on COVID patients, knowing it would cause deaths. This was premeditated murder, with the criminals sitting next to President Donald Trump. There are other individuals involved as well. Efforts are being made by courageous sheriffs and DAs to compile evidence of the deaths caused by Remdesivir and take legal action to end these felonies.

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Patients are dying not from COVID, but from treatments like remdesivir causing organ failure. One person's mother died after being given remdesivir against their wishes, leading to organ shutdown. There was a financial incentive for hospitals to admit patients and put them on ventilators, resulting in unnecessary treatments and deaths.

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"Your government doesn't censor those people as a way to do the best that it can." The speaker recalls being interviewed by a major newspaper and "I bring up doctor Peter McCullough every time" when asked "what evidence? What proof?" They argue that "the world's leading heart doctor" and "the most published heart doctor in the world was censored during COVID." They question whether "the government was just doing the best that it could under the circumstances," answering "Like, no." The speaker asserts that "The best a government that considers itself to be in a free nation does not go out of its way to censor world renowned scientists, doctors, the number one heart doctor in the world in doctor Peter McCullough, the most published ICU doctor the world in doctor Paul Merrick, the inventor of the technology itself, doctor Robert Malone." "Your government doesn't censor those people as a way to do the best that it can."

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Speaker 0 argues that ivermectin and hydroxychloroquine were suppressed because they are well-established drugs with safety records and billions of doses used; ivermectin is a human drug that also works on horses and won the Nobel Prize for its effectiveness in humans. He states there is a federal law that says an emergency use authorization (EUA) for a vaccine cannot be granted if there is any approved medication shown effective against the target disease, so admitting effectiveness of hydroxychloroquine or ivermectin would have made EUA for vaccines illegal and would have collapsed a “200,000,000,000 enterprise.” Speaker 1 notes this is the first time hearing that assertion, acknowledging it’s in the book. He suggests that if the medical community had been saying ivermectin is an effective COVID treatment, EUA for vaccines could not have been granted. Speaker 0 explains that many in the medical community supported effectiveness, citing a petition signed by 17,000 doctors and numerous peer-reviewed publications, but Fauci aggressively crusaded against it, labeling it a horse medication and alleging danger and overdosing to drown out those reports. Speaker 1 asks why Fauci continued to push the claim after EUA was granted. Speaker 0 answers that, even with EUA, the law may require withdrawal if a functioning medication exists, implying a motive to undermine ivermectin and hydroxychloroquine. He mentions a strong incentive for Fauci to kill these medications and cites several doctors who treated tens of thousands of COVID patients and supported the claim that the science shows many lives could have been saved. He names Harvey Reich at Yale, Peter McCulloch as the most published doctor in history and prominent in biostatistics/epidemiology, and Peter Quarry in connection with the doctors who treated many patients. They allegedly state that half a million Americans did not need to die.

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Fauci filled the world with mRNA, claiming control over science to prevent deaths. Pfizer's jab didn't work, media manipulation ensued. People blindly followed big pharma, ignoring rising deaths. The truth will surface eventually.

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Monoclonal antibodies worked very well and quickly, and were initially readily available. The speaker believes the government intentionally made them harder to get to encourage people to take the COVID shot. The speaker didn't use ivermectin until the government took over distribution of monoclonal antibodies. In March, the government put out information on why people should not take ivermectin for COVID on the FDA's website. At the same time, they launched COVID-nineteen Community Core on 04/01/2021, an $11,500,000,000 slush fund to feed out propaganda.

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At home, it is recommended to treat viral replication by giving zinc and other zinc-enhancing remedies like hydroxychloroquine and Ivermectin. However, the protocol followed by hospitals was to provide no treatment until admission, and then use ventilators and Remdesivir, which were known to be harmful. Tony Fauci was aware of the dangers of Remdesivir, as it caused lethal side effects in Ebola patients. Despite this, he manipulated a study to make Remdesivir the standard of care, resulting in kidney failure, heart failure, and organ collapse in COVID-19 patients. The deaths attributed to the virus were actually caused by Remdesivir.

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In 2018, remdesivir was considered unethical for Ebola clinical trials in Africa due to a 53% kill rate, higher than Ebola's typical mortality. Despite this, it was chosen to treat COVID in April and May 2020, with Anthony Fauci and Deborah Burke advocating for its use despite the World Health Organization's ethical concerns. The speaker claims that a conflict of interest exists because the same entities that financially benefit from promoting certain products are declaring the pandemic. These entities are allegedly linked to the Eugenics office at Carnegie Mellon in 1913 and the establishment of the World Health Organization in 1953. The speaker expresses concern about the influence of eugenics on these decisions.

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An experimental drug called remdesivir will be responsible for people's deaths. People diagnosed with COVID-19 in the hospital died between day one and day nine, specifically on day nine of a ten-day remdesivir treatment. Dr. Anthony Fauci claimed in May 2020 that remdesivir was found safe and effective in a drug trial in Africa a year earlier (02/2019), and hyperlinked the study in a memo to hospitals. However, in that trial, remdesivir killed 53% of people, and the safety board suspended its use at month six, deeming it too deadly and toxic for Ebola patients. Dr. Anthony Fauci and his department at the NIH funded the Ebola trial in Africa in 02/2019. Therefore, Fauci lied to Congress and the American people by claiming the drug was safe and effective against Ebola, when the safety board had deemed it too deadly and pulled it from the trial.

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In 2018, remdesivir was described as one of the speaker’s “favorite targets,” but it was said to have been considered too unethical for Ebola clinical trials in Africa because a “53% kill rate” was published in medical journals. The speaker contrasts this with the choice made in April and May 2020 to use remdesivir as the drug of choice to treat COVID, stating that the drug was still treated as unacceptable for African trials due to the alleged 53% kill rate. The speaker claims that Anthony Fauci and Deborah Birx were present next to the president advocating for remdesivir, while stating that the World Health Organization said it was unethical to use. The speaker frames the issue as a lack of accountability and justice as long as financial interests determine what product is promoted, arguing that if the entity declaring a pandemic is also driven by financial interests, there is no possibility for accountability. The speaker also alleges that the decision-makers were formed out of the Eugenics Office at Carnegie Mellon in 1913, and that the same group established the World Health Organization in 1953. The speaker asserts that this group was making the decision in 2020 regarding remdesivir and says they have a problem with eugenics.

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Speaker 0 explains that people wonder why ivermectin and hydroxychloroquine were suppressed, noting these are well established drugs with safety profiles and billions of doses given. He says ivermectin is a human drug and also works on horses, but it would win the Nobel Prize because it works so well on human beings. Speaker 1 responds “Mhmm.” Speaker 0 states there is a little known federal law that says you cannot give an emergency use authorization (EUA) to a vaccine if there is any medication approved for any purpose that is shown effective against the target disease. So if Tony Fauci or anybody had admitted that hydroxychloroquine or ivermectin are effective against COVID, it would have been illegal to give the EUAs to the vaccines, and they could never have gotten them approved. He suggests this would have collapsed a “200,000,000,000 enterprise.” Speaker 1 says, “That is fascinating,” noting they had been covering this for two years and that this is the first time hearing that; if the medical community had been saying ivermectin works, it would have affected EUA. Speaker 0 responds that the medical community did say that—17,000 doctors signed a petition, and there are many peer reviewed publications consistently saying so. Yet Fauci aggressively crusaded against it, insisting it’s a horse medication, that people are overdosing, and so on. He asks why Fauci kept saying it. Speaker 1 asks why Fauci continued to say it after he got the authorization. Speaker 0 offers possible explanations: one, even if you have an EUA, the law appears to say you can't have it anymore if there is a functioning medication. He acknowledges, though, that he cannot read Fauci’s mind but speculates there is a strong incentive for Fauci to kill ivermectin and hydroxychloroquine. He cites several doctors who treated tens of thousands of COVID patients successfully and who argue that half a million Americans did not need to die, naming Harvey Reich at Yale, Peter McCulloch, and Peter Quarry.

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- The discussion opens with a critique of how public health authorities in the United States and much of the media discouraged experimentation with COVID-19 treatments, instead pushing vaccination and portraying other approaches as dangerous. The hosts ask why treatments were sidelined and treated as heretical to question. - Speaker 1 explains that the core idea was to stamp out “vaccine hesitation,” which he frames not as a purely scientific issue but as a form of heresy. He notes a broad literature on vaccine hesitancy and contrasts it with the perception of the vaccine as a liberating savior. He points to a Vatican €20 silver coin (2022) commemorating the COVID-19 vaccine, described by Vatican catalogs as “a boy prepares to receive the Eucharist,” which the speakers interpret as an overlay of religious iconography with vaccination imagery. They also reference Diego Rivera’s mural in Detroit, interpreted as depicting the vaccine as a Eucharist, and a South African church banner reading “even the blood of Christ cannot protect you, get vaccinated,” highlighting what they see as provocative uses of religious symbolism to promote vaccination. - They claim that the Biden administration’s COVID Vaccine Corps distributed billions of dollars to major sports leagues (NFL, MLB) and that many mainline churches reportedly received money to push vaccination, with many clergy not opposing the push. The implication is that monetary incentives influenced public figures and organizations to advocate for vaccines, contributing to a climate in which questioning orthodoxy was difficult. - The speakers discuss the social dynamics around vaccine “heresy,” using Aaron Rodgers’ experience with isolation and shaming in the NFL and Novak Djokovic’s experiences in Australia to illustrate how prominent individuals who questioned or fell outside the orthodoxy faced punitive pressure. They compare this to a Reformation-era conflict over doctrinal correctness and describe a psychology of stigmatizing dissent as a tool to enforce conformity. - They argue the imperative driving institutions was the belief that the vaccine was the central, non-negotiable public-health objective, seemingly above other medical considerations. The central question they raise is why vaccines became the sole priority, seemingly overriding a broader, more nuanced evaluation of medical options and individual risk. - The conversation shifts to epistemology and the nature of science. Speaker 1 suggests medicine often relies on orthodoxies and presuppositions, rather than purely empirical processes. He recounts a Kantian view that interpretation depends on preexisting categories, and he uses this to argue that medical decision-making can be constrained by established doctrines, which may obscure questions about optimization and safety. - They recount the 1986 National Childhood Vaccine Injury Act and discuss Sara Sotomayor’s dissent, which argued that liability exposure is a key incentive for safety and improvement in vaccine development. They argue that the current system creates minimal liability for manufacturers, reducing the incentive to optimize safety, and they use this to question how the system encourages continuous safety improvements. - The hosts recount the early-treatment movement led by Peter McCullough and others, including a Senate hearing organized by Ron Johnson in November 2020 to discuss early-treatment options with FDA-approved drugs like hydroxychloroquine. They criticize what they describe as aggressive pushback against such approaches, noting that McCullough faced professional sanctions and lawsuits despite presenting peer-reviewed literature. - They return to the concept of orthodoxy and dogma, arguing that the medical establishment often suppresses dissent, citing YouTube removing a McCullough interview and the broader pattern of silencing challenge to the vaccine narrative. They stress that the social and institutional systems prize conformity and punish those who deviate, creating a climate of distrust toward official health bodies. - The discussion broadens into metaphysical and philosophical territory, with references to the Grand Inquisitor from Dostoevsky’s The Brothers Karamazov. They propose that elites—whether religious, political, or scientific—tend to prefer “taking care” of people through control rather than preserving individual responsibility and free will. The Grand Inquisitor tale is used to illustrate a recurring human temptation: to replace personal liberty with a protected, paternalistic order. - They discuss messenger RNA (mRNA) technology as a central manifestation of Promethean or Luciferian intellect—humans attempting to “read and write in the language of God.” They describe the scientific arc from transcription and translation to mRNA vaccines, noting Francis Collins’s The Language of God and the idea of humans “coding life.” They caution that mRNA vaccines involve injecting genetic material and point to the symbolic and ritual power of vaccination as a form of modern sacrament. - The speakers emphasize that the mRNA approach represents both a profound scientific achievement and a source of deep concern. They discuss fertility signals and potential adverse effects, including myocarditis in young people, and cite the July 2021 NEJM case study as highlighting safety concerns for myocarditis in adolescent males. They reference the FDA deliberative-committee discussions, noting that some influential voices publicly questioned the risk-benefit calculus for young people, yet faced pressure or dismissal within the orthodox framework. - They describe post-hoc investigations and testimonies suggesting that adverse events (like myocarditis) might have been downplayed or obscured, and they assert that public trust in health institutions has eroded as a result. They mention ongoing debates about whether vaccine-induced changes might affect future generations, referencing studies about transcripts of mRNA in cancer cells and liver cells, and they stress the need for independent scrutiny by scientists not “entranced” by the vaccine program. - The dialogue returns to the broader human condition: a tension between curiosity and restraint, knowledge and humility. They return to Dostoevsky’s moral questions about free will, responsibility, and the limits of human knowledge, concluding that scientific hubris can lead to dangerous consequences when it overrides open inquiry and accountability. - In closing, while the guests reflect on past missteps and the need for integrity in medicine, they underscore the ongoing questions about how evidence is interpreted, how dissent is treated, and how society balances scientific progress with humility, transparency, and respect for individual judgment.

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Remdesivir, one of four drugs tested for Ebola, allegedly killed more people than the placebo, leading the Data Safety Monitoring Board to halt the study. According to the transcript, 53% of patients died in the failed Ebola trial, but the drug was repurposed. It is claimed that Remdesivir was Anthony Fauci's drug of choice, and that the NIH protocols, which provided hospitals with bonuses for using remdesivir, caused the majority of hospital deaths. Reportedly, hospitals received $3,000 for each remdesivir IV and a potential 20% bonus. The data allegedly showed that remdesivir killed more patients than the placebo, resulting in the drug trial being stopped. One speaker stated that it is inexplicable that remdesivir became the standard of care, and that doctors seemingly shut off their brains and followed directions from above without questioning the use of remdesivir in every hospitalized patient.

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Monoclonal antibodies worked very well and quickly, and were initially readily available. The speaker believes the government intentionally made them harder to get to encourage people to take the COVID shot. The speaker started using ivermectin when monoclonal antibodies became difficult to obtain. In March, the government put out information on the FDA's website about why people should not take ivermectin for COVID. Simultaneously, the government launched COVID-nineteen Community Core on 04/01/2021, an $11,500,000,000 slush fund for propaganda.

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In 2018, remdesivir, described as one of my favorite targets, was deemed too unethical to put into Ebola clinical trials in Africa because it had a fifty-three percent kill rate published in medical journals. The speaker notes that Ebola doesn’t have a fifty-three percent kill rate, yet in April and May 2020 it was chosen to be the drug of choice to treat COVID. The drug was considered too unethical to use in an African clinical trial because it was killing fifty-three percent of the people to whom it was given. The speaker asserts that Anthony Fauci and Deborah Birx were sitting next to the president advocating the use of remdesivir despite the World Health Organization stating it was unethical to use it. The central problem identified is that, as long as the financial interest that dictates which product is promoted is the one making the declaration of the pandemic, there is no possibility for accountability and no possibility for justice. The speaker argues that the decision-making is influenced by a lineage described as having emerged from the Eugenics office, specifically naming Carnegie Mellon in 1913, the same group of people that established the World Health Organization in 1953. The speaker claims that this same group is the one making the current decisions. The speaker asks the audience to consider their feelings about Eugenics and concludes by expressing a problem with it, tying these connections to the governance and promotion of pandemic responses.

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Speaker 0: Remember that in 02/2018, remdesivir, one of my favorite targets, remdesivir was too unethical to put into Ebola clinical trials in Africa because it had a fifty three percent kill rate published in medical journals. Ebola doesn't have a fifty three percent kill rate, but it was chosen in April and May 2020 to be the drug of choice to treat COVID. This drug was too unethical to use in an African clinical trial because it was killing fifty three percent of the people that it was given to. And we had Anthony Fauci, Deborah Burke sitting next to the president going, we need to use remdesivir despite the fact that the World Health Organization said it was unethical to use it. Here's the problem. The problem is as long as the financial interest that dictates what product is going to be promoted is the one making the declaration of the pandemic, We have no possibility for accountability. We have no possibility for justice. And what we do is we allow people who were formed out of the Eugenics office, Carnegie Mellon in 1913, that same group of people that were the same group of people that established the World Health Organization in 1953, that same group of people are the ones who are making this decision. And I don't know how you feel about Eugenics, but I have a problem with it.

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I've stated since May 2020 that remdesivir will result in at least 30% death in those who receive it in the hospital. I had data pulled for Medicare patients in New York, and found that 26.9% of those who received remdesivir died. As of October 2020, the cardiovascular toxicology journal found that remdesivir causes death of heart cells and can lead to cardiac arrest. Yet, in December, the NIH decided to update all guidelines for treatment drugs allowed for COVID-19, and remdesivir was the only FDA-approved drug for hospitalized Americans, despite the WHO publishing that it causes increased acute kidney failure. As of January of this year, the FDA extended an emergency use authorization, making remdesivir the only authorized medication that can be administered to newborns to 18-year-olds.

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According to the speaker, hospital protocols differed for vaccinated and unvaccinated COVID-19 patients, with more aggressive protocols used on the unvaccinated. The unvaccinated patients interviewed were often given remdesivir, a repurposed drug from a failed Ebola trial where about half the patients died. The speaker claims the efficacy data for remdesivir was "sketchy at best," but hospitals received large reimbursements for its use. The speaker alleges that patients would then be put on oxygen, then mechanical ventilation, then ICU, and finally, if they resisted, a cocktail of sedatives and sometimes four-point restraints to prevent them from leaving. The speaker states that "a lot of the patients died." The speaker claims that at each step, the hospital received more reimbursement, and there was "lockstep adherence" to the protocol.
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