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Pharmaceutical companies paid $1.06 billion to reviewers at leading medical journals, including the New England Journal of Medicine, JAMA, Lancet, and BMJ, allegedly corrupting the peer review process. Studies from the CDC, FDA, and Pfizer purportedly revealed major breaches in safety signals for COVID-19 vaccines in pregnancy, but these findings were ignored. Independent researchers who published findings contradicting pharmaceutical industry narratives faced persecution, censorship, and threats to their medical licenses and board certifications. The speaker claims this happened to them personally.

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The speaker, a gastroenterologist, discusses research on the microbiome's role in COVID-19 and challenges faced publishing findings that went against the public health narrative. Early research documented the virus in stools for up to 45 days and showed hydroxychloroquine and azithromycin killed COVID-19 in stools, but also harmed the microbiome, necessitating vitamin C, D, and zinc. The FDA initially granted an exemption for clinical trials using this combination, then revoked it. Media-fueled fear around hydroxychloroquine hindered recruitment. Research revealed that severe COVID-19 patients lacked bifidobacteria, a key microbe for immunity, which is abundant in newborns but declines with age. Vitamin C and ivermectin were found to increase bifidobacteria. A hypothesis that ivermectin increased bifidobacteria was retracted after being widely read. Research on mRNA vaccines showed they killed bifidobacteria, presented at a gastroenterology conference, linking bifidobacteria loss to Crohn's disease, Lyme disease, and invasive cancer. The speaker concludes that research interference during the pandemic hindered scientific progress and that clinical trial guidelines were not followed.

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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 study claimed chloroquine does not inhibit SARS CoV 2 in tissue culture. The speaker examined the study, noting it used CaLU3 lung cells. The speaker contacted the author, stating the study showed chloroquine allows the virus to attack a cancer cell, while protecting a normal cell. The speaker believes the study authors misinterpreted the data and hid the fact that they used KLU3 lung cells, which was found in the appendix. The speaker accuses them of a disinformation campaign, claiming they misrepresented the study's findings to suggest chloroquine is unlikely to work against SARS CoV 2. The speaker believes the study actually proved chloroquine is effective because it allows viruses to attack cancer cells, but not normal cells.

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Speaker 0 argues medicine is becoming like magazines, with journals turning into gossip columns. He calls a group of journals "predatory journals" that are smart because they do have an impact factor, they're brand new journals, they send you emails constantly. He says, "they can manipulate or retract the data to make you look bad." He describes his Frontiers experience: he submitted "a hypothesis on ivermectin increasing the bifidobacteria," and it was accepted by the peer review. "Nine months later, the paper was the number one read at Frontiers with 59,000 views." He says this is an interesting hypothesis "right? Because we're seeing ivermectin has a role potentially in cancer. So maybe increasing the benefit of bacteria is how we're doing it, right?" He notes that because it got so much attention, "it lit up ivermectin, which they don't want to do, you understand?"

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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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The speaker, a gastroenterologist, discusses their research on the microbiome and COVID-19. They found that the virus lingers in stools, hydroxychloroquine kills the virus but harms the microbiome, and bifidobacteria is crucial for immunity. Their studies on vitamin C, ivermectin, and mRNA vaccines' effects on bifidobacteria faced challenges in publication due to going against the mainstream narrative. They highlight the importance of unbiased research and collaboration in finding solutions. The speaker also raises concerns about pharmaceutical companies prioritizing profits over patient safety during the pandemic.

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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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A recent study claimed that the malaria drug chloroquine doesn't inhibit SARS-CoV-2, but the study used KLU-3 lung cells. After looking at the study, I realized KLU-3 cells are lung cancer cells. I contacted the author, pointing out that the study inadvertently demonstrated that chloroquine allows viruses to attack cancer cells while protecting normal cells because cancer cells are de-differentiated with different receptors. The author misinterpreted the data. The fact that they used KLU-3 lung cells was hidden in the appendix. This is disinformation. They're saying chloroquine is unlikely to work against SARS-CoV-2. On the contrary, this proves that chloroquine is incredibly smart because it lets viruses attack cancer cells, not normal cells.

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In March, I started researching my protocol and started writing the protocols; there were like contraindications to hydroxychloroquine. There were three pages of medications. The protocol was approved by the FDA within twenty four hours and “move to market... start giving it to patients, proceed.” Twenty four hours later, “the politics” and lobbyists allegedly said, “we can't have a cheap drug… kill the market.” A Bill Gates letter asked, “when do you think you're going to, you're anticipating finishing your protocol?” Twitter destroyed it for being open label, and the effort was described as “a political move to destroy a drug.” The Lancet paper is claimed fake: “There is no way that four or five authors took 17,000 records” and “sixty… 96,000 patients”; “Australia doesn't even have COVID yet” and “Ninety six thousand… fraudulent.” NIH notes “chloroquine and hydroxychloroquine toxicity” with “excellent oral absorption and bioavailability” and retinal toxicity is the concern, but in ICU patients the death overshadows it: “He's dead. It doesn't matter that he's got retinal toxicity.”

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Doctors were aware that hydroxychloroquine was safe until the media suggested otherwise. They claimed it was both safe and effective, but when the narrative shifted to it being unsafe, despite its 70-year history and a government database showing it to be safer than Tylenol, it raised concerns. The assertion of its lack of safety felt like a significant deception.

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The forest plot shows COVID medicines, with only expensive ones approved in the US. Cheaper options were ignored. Study endpoints were changed when results weren't as expected. Despite positive outcomes in trials, hydroxychloroquine and Ivermectin face negative perceptions in the US. Over 420 trials on hydroxychloroquine and 100 on Ivermectin show significant benefits, but they are still viewed negatively.

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Speaker 0: There were four drugs that were being tested for Ebola. Remdesivir killed more people than placebo, and the data safety monitoring board had actually stopped the study where literally fifty three percent of Speaker 1: the patients died in the failed Ebola trial and was repurposed. It was a failed Ebola drug because it caused more harm than good in Ebola trials. It was still unpatent. It was Tony Fauci's drug of choice. The majority of hospital deaths were actually caused by Anthony Fauci because his NIH put out protocols that if the hospital systems adhered to, they got bonuses, big bonuses, lots of money, $3,000 per for putting an IV in of remdesivir. Boom. $3,000. But guess what? On top of the entire hospital stay, a 20% bonus, that could be hundreds of thousands of dollars. Speaker 0: The data was so overwhelming that remdesivir killed patients more so than placebo. The drug had to be stopped, and this was published in the New England Journal in the 2019. Speaker 2: What happened during COVID could not have happened without propaganda and censorship. And how do we overcome that propaganda and censorship? It's primarily through people not being willing to shut up.

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Pharmaceutical companies paid $1.06 billion to reviewers at major medical journals, allegedly corrupting the peer review process. Studies from the CDC, FDA, and Pfizer purportedly revealed major breaches in COVID-19 vaccine safety signals during pregnancy, but these findings were allegedly ignored. Independent researchers who published findings contradicting pharmaceutical industry narratives faced persecution, censorship, and threats to their medical licenses and board certifications. The speaker claims this happened to them personally.

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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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A recent study claimed that 17,000 people died from Hydroxychloroquine, but Robert Kennedy Jr. pointed out flaws in the study. The drug was given to COVID patients already in the hospital instead of within the first 10 to 14 days when it is effective. The dosage administered was also much higher than recommended. While these mistakes may have contributed to deaths, it is important to consider how many lives could have been saved if the drug was used correctly. Hydroxychloroquine has been widely used for malaria and sometimes drugs are discovered to have additional benefits. The politicization of these drugs is unfortunate, especially considering their affordability.

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The forest plot shows COVID medicines, with only expensive ones approved in the US. Cheaper drugs were ignored. Studies manipulated endpoints and faced negative PR. Over 420 trials on hydroxychloroquine and 100 on Ivermectin show significant benefits, but they are dismissed in the US.

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Big Pharma, they own everything. There's a number of past chief editors of journals, and we're not talking just, you know, like some throwaway journals. We're talking New England Journal of Medicine, Lancet, British Medical Journal. Okay. Some of the biggest journals in the world. Those are top three out of the top four that I just named. Journal of American Medical Association is the other one. But chief editors in the last twenty years, at least six of them have come out and said that at least 50% of the science that's published is fake. Come on. Read their quotes. Marcia Angel is one of them that I can remember her name. There's a guy by the name of Richard something or other from the British Medical Journal who said the same thing. I just read an article about it the other day. I'll I'll send it to you because it's I'm not surprised. I mean, depth of corruption is is stunning and and the fact that pretty much nothing's been done about it makes you wonder how long this can all last.

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panel discusses hydroxychloroquine and early treatments. Hazen states: "I did the clinical trial. I wrote those protocols on hydroxychloroquine, Z Pak, vitamin C, D and zinc, passed them through the FDA within twenty four hours." She adds, "No one died on my shift, even though I did a placebo controlled trial on hydroxychloroquine, Z Pak, vitamin C, D and zinc," and "And we had hundreds of patients on that." They argue the Lancet paper is invalid: "This paper is to me is not just, you know, I'm not going to criticize it and say, oh, well they overdosed. I'm going to say, no, this is a fake paper. This is a fake data." They insist: "There is no way that four or five authors took 17,000 records." They discuss predatory journals: "predatory journals" and "they can manipulate or retract the data to make you look bad." They claim: "Hydroxychloroquine and ivermectin are out of patents." They report outcomes: "zero mortality" and "zero hospitalizations," and critique media: "they control the media and they push all this narrative out there." They urge: "stop publishing papers that are so fraudulently, so obviously fraudulent." They reference the microbiome: "the microbiome is all shit," and advocate: "everybody needs a fecal transplant right now."

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In the discussion, Speaker 0 argues that word-of-mouth PR surrounding ivermectin “saved so many lives” and created widespread distrust in the industry, describing a shift where people questioned official stances: “My oxygen was low, and I did take ivermectin and it did work. Why are they telling me ivermectin doesn't work?” This view frames ivermectin as having proven effectiveness in practice, contrasting with public or institutional statements. Speaker 1 adds that it’s “really hard not to get angry” about the official trials, claiming that the WHO and, specifically, the Oxford trials demonstrated that ivermectin didn’t work, but that it “patently does.” They describe the fundamental problem as the way those trials were conducted, implying methodological issues. They discuss specifics of how the studies tested different drugs: Speaker 0 notes that hydroxychloroquine was given “with food” in the study, while ivermectin was given on an empty stomach, implying a potential misapplication of administration guidelines. They state that Merck’s initial labeling for ivermectin in other indications (scabies and lice) recommends administration with a fatty meal, and share a personal anecdote that their sister introduced ivermectin to the market for lice and conducted a clinical trial with many patients. Speaker 1 questions why leading clinicians would administer these drugs without knowing the correct guidelines, suggesting there should have been knowledge about administration with meals for hydroxychloroquine and with food for ivermectin. They remark, “Why the heck didn’t they know that?” Speaker 0 contends that physicians adhere to guidelines and hospital rules and fear lawsuits; they claim this fear leads to doctors “not even wanna know” certain information. They express the sentiment that the medical community was discouraged or constrained by fear of legal consequences and licensing actions, which contributed to doctors avoiding or stopping certain lines of inquiry or treatment. Overall, the dialogue centers on a perceived discrepancy between real-world outcomes of ivermectin use and official trial conclusions, the role of administration guidelines in trial results, and the influence of fear of legal ramifications on clinical practice.

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A recent study found that the malaria drug Chloroquine does not inhibit SARS CoV 2 in lung cells, although it may work in kidney cells. The speaker, who has experience in ocular oncology, contacted the author of the study and pointed out that the lung cells used in the study were actually cancer cells. This means that Chloroquine allows the virus to attack cancer cells but not normal cells. The speaker believes that this is a misinterpretation of the data and accuses the study of being part of a disinformation campaign. They argue that Chloroquine is actually a very effective drug.

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The speaker, a gastroenterologist, discusses research on the microbiome's role in COVID-19 and challenges encountered publishing findings that contradicted the public health narrative. Early research identified the full viral sequence in stool samples, where it lingered for up to 45 days, and noted hydroxychloroquine and azithromycin killed the virus in stools but harmed the microbiome, leading to the addition of vitamins C, D, and zinc to treatment protocols. An initial FDA exemption for clinical trials using this combination was revoked, and media-fueled fear around hydroxychloroquine hindered recruitment. Research revealed that patients with severe COVID-19 lacked bifidobacteria, a key microbe for immunity, which is abundant in newborns but decreases with age. Vitamin C and ivermectin were found to increase bifidobacteria levels. A hypothesis that ivermectin increased bifidobacteria was retracted after being widely read. Research on mRNA vaccines showed they killed bifidobacteria, a finding presented at a gastroenterology conference and linked to conditions like Crohn's disease, Lyme disease, and invasive cancer. The speaker concludes that interference with research during the pandemic hindered scientific progress and that established clinical trial guidelines were not followed.

Keeping It Real

Dr. Hazan on Ivermectin, COVID, and MRNA Vaccines.
Guests: Sabine Hazan
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In Keeping It Real, Jillian Michaels hosts Dr. Sabine Hazan, a gastroenterologist who has spent three decades in clinical trials and microbiome research. Hazan describes how her lab shifted focus during the pandemic to study the gut microbiome’s role in COVID-19, including attempts to detect the virus in stool and to understand how microbial balance might influence disease severity. She explains writing 57 research protocols and building standardized methods for sample collection and analysis, likening protocols to screenplays that guide experiments from stool collection to data interpretation. Hazan argues that the microbiome not only reflects health but can shape immune responses, potentially affecting asymptomatic cases and vulnerability to infection. Hazan recounts the suppression she perceives around certain treatments and findings, such as vitamin C and vitamin D protocols, hydroxychloroquine early in the crisis, and especially ivermectin. She describes censorship on social media and hesitation from institutions, arguing that political polarization interfered with scientific discourse and patient care. The discussion moves to her ivermectin work, including a personal clinical pivot from hydroxychloroquine to ivermectin and doxycycline, observations about how gut bacteria like Bifidobacteria relate to COVID outcomes, and hypotheses about how the gut-lung axis might mediate inflammation and recovery. She details a controversial arc of hypothesis, retraction, and subsequent data, contending that journals and researchers are influenced by broader forces, while insisting that listening to patients and pursuing open inquiry are essential to medical progress. The conversation then broadens to vaccines, adverse events, and the idea that mRNA technologies require careful, independent scrutiny. Hazan discusses observing changes in patients’ microbiomes after vaccination, concerns about persistent effects on beneficial microbes, and the need for transparent reporting of adverse events. She advocates for independent, nonprofit scientific work and emphasizes collaborative, global learning about the microbiome’s diversity. The episode closes with Hazan’s call for humility in medicine, a push for open dialogue, and a vision of a microbiome-informed future where different cultures’ microbial ecosystems enrich our understanding of health rather than divide it.

This Past Weekend

Robert F. Kennedy Jr. | This Past Weekend w/ Theo Von #370
Guests: Robert F. Kennedy Jr.
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On this episode, Theo Von welcomes Robert F. Kennedy Jr., whose book The Real Anthony Fauci is a central topic of discussion. Kennedy describes his research process, including a 300‑plus‑member email list of actors, MDs, and scientists that lets him see new studies in real time and hear critical analyses of them. He argues that agency capture taints public health and environmental regulators, with the FDA funded largely by pharmaceutical companies and fast‑track approvals turning regulators into partners of industry. He contends the COVID response prioritized profits over lives, noting that early treatment was minimized and hospitalizations and ventilator use followed Fauci’s regimens. He cites hydroxychloroquine and ivermectin as effective in early treatment, says NIH studies in 2005 and later showed HCQ's potential, and accuses Gates and others of funding studies designed to discredit these drugs by using hospitalized patients and overdosing. He claims there were coercive incentives for hospitals to code deaths as COVID and to use Remdesivir, driving up counts and profits. Kennedy criticizes social and traditional media for pharma‑driven censorship, recounting his experience with Fox News where advertising revenue from pharma influenced editorial choices. He links Big Tech to the pharmaceutical industry, claiming Google and Facebook manage vaccine content and data to protect profits. He asserts direct‑to‑consumer advertising fueled this power and notes the lack of liability for vaccine manufacturers under the EUA framework, arguing that the Pfizer trial’s six‑month data showed vaccines did not clearly prevent death or transmission and appeared to increase all‑cause mortality. The discussion covers Event 201, gain‑of‑function research funded through USAID and DARPA, and the Wuhan lab network. Kennedy connects these to broader concerns about surveillance, vaccine passports, programmable money, and the erosion of civil liberties, urging three daily acts of civil disobedience to reclaim rights. He highlights autism links with vaccines in some studies and defends publishing with extensive references. The interview closes with praise for the book, a call to resist, and thanks to Kennedy for joining.

The Joe Rogan Experience

Joe Rogan Experience #2427 - Bret Weinstein
Guests: Bret Weinstein
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In this episode, Bret Weinstein challenges the conventional Darwinian narrative by proposing a powerful, overlooked layer in evolution that accelerates the emergence of diverse forms. He argues that random mutations in protein-coding genes can explain nanoscale changes well, but fail to account for major leaps such as the transition from limb to wing. The conversation delves into EvoDevo, developmentally oriented biology, and the idea that organisms store and manipulate a broad library of variables in the genome—numbers and timing signals that govern development, growth, and adaptive leaps. Weinstein uses telomeres, microsatellites, and dosage effects as entry points to illustrate how non–protein-based information could modulate phenotypes, potentially expanding the adjacent possible and enabling rapid shifts in form once new ecological opportunities arise, such as flight in bats. The discussion weaves through how such a framework would be Darwinian in spirit, subsuming, rather than overturning, classical mechanisms, while highlighting gaps in mainstream evolutionary theory and the need for a more integrated view of mechanisms and selective processes. He then connects these ideas to broader questions about technology and culture, arguing that humans employ an intercoupled system of biological and cultural evolution—where the “campfire” of shared ideas and tools accelerates adaptation. The guests explore how human cognition functions as an explorer mode, testing designs mentally and prototyping them in the world, a process that may explain cultural explosions and rapid shifts in behavior. They examine the capacity of the genome to store variables, the role of variable number tandem repeats, and the possibility that development is steered by “integers” in DNA that influence timing, expression, and morphogenesis. A recurring theme is the tension between gradualism and leap-taking in evolution, and the potential for a more powerful, quantitative toolkit to illuminate how ordinary mechanisms can generate extraordinary diversity without abandoning Darwinian logic. The conversation also covers current debates around vaccines, repurposed drugs such as Ivermectin, and medical science’s reliance on randomized trials. The speakers critique institutional incentives and media narratives surrounding COVID-19, vaccines, and public health policy, while contrasting the elegance of simple, transparent analyses (for example, chi-squared tests) with complex trials that can be biased or manipulated. They reflect on the role of free speech, censorship, and digital platforms in shaping scientific discourse, and contemplate how to sustain robust, open inquiry in an era of rapid tech-driven change and political polarization.
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