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Saved - November 2, 2023 at 4:37 PM
reSee.it AI Summary
In 2021, Dr. Hui Jang's study revealed that Covid-19 hampers the body's cellular repair mechanism, intensifying the potential risks of Covid vaccines. However, one author faced job loss pressure, leading to a retraction request. This incident highlights the censorship faced when questioning vaccine safety. Science can be complex, and this situation exemplifies the challenges faced by researchers.

@stkirsch - Steve Kirsch

In 2021, Dr. Hui Jang, an NIH researcher, published a study in 2021 that proved that Covid 19 inhibits the human body's cellular repair mechanism and amplifying the lethal to health dangerous side effects of the Covid Vaccines. One tiny problem though... https://pubmed.ncbi.nlm.nih.gov/34696485/

SARS-CoV-2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro - PubMed Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has led to the coronavirus disease 2019 (COVID-19) pandemic, severely affecting public health and the global economy. Adaptive immunity plays a crucial role in fighting against SARS-CoV-2 infection and directly influences the clinical outc … pubmed.ncbi.nlm.nih.gov

@stkirsch - Steve Kirsch

One of the authors was pressured to request that the journal retract it or he'd lose his job. This is how science works. So they made up a ridiculous story to justify the retraction. The other author objected! If you say the vaccines aren't safe, they censor your work. It's that simple. This is the way science works.

@stkirsch - Steve Kirsch

You can't make this stuff up. You really can't.

Saved - June 5, 2024 at 4:54 AM
reSee.it AI Summary
In a heated exchange, Congressman Rich McCormick confronts Dr. Anthony Fauci about censorship and the government's handling of COVID-19. McCormick, a medical doctor who treated patients during the pandemic, criticizes Fauci for disregarding dissenting opinions and labeling them as anti-science. McCormick argues that medical decisions should be made through conversations with physicians, not politically motivated mandates. He accuses Fauci of causing fear through mask mandates, school closures, and vaccine mandates, damaging trust in public health institutions.

@simonateba - Simon Ateba

BREAKING - MUST WATCH: This was perhaps the most EXPLOSIVE exchange today between Dr. Anthony Fauci and Congressman Rich McCormick (@RepMcCormick), a medical doctor who treated patients during COVID but was censored for pointing out the science. He told Fauci, "You said in an interview that you gave as part of an audiobook written by Michael Specter that you believed institutions should make it hard for people to live their lives so they'd feel pressured to get vaccinated." WATCH Question: Someone said only politicians, only bloggers, only conspiracy theorists are disagreeing with you. I want to point out that I'm probably the only member of Congress that actually treated patients during the pandemic. From the very beginning to the very end of the pandemic, during night shifts in the ER, thousands of patients during that time and in 2020 I was censored. My medical license was threatened because I disagreed with bureaucrats, literally taken off the Internet as a person who is treating patients with leading edge technologies, developing theories, but doing my very best, but being censored by the United States government for the first time, stepping in and taking the place of medical professionals as the experts in healthcare. Any dissent surrounding COVID-19 treatments, mask mandates, and any public policy surrounding the pandemic was immediately labeled as anti-science. I watched as public health officials and politicians told my patients what treatment options were best for them, regardless of their comorbidities or their medical history. Despite my education and my training and my experience, my opinions were relegated to conspiracy and misinformation by so-called healthcare experts who had never treated a patient throughout the entire pandemic. This has been a black eye on the medicine and has highlighted why government should never, never insert itself in between patients and their healthcare providers. The American people deserve to make medical decisions through conversations with their physicians rather than politically motivated mandates. Question: Doctor Fauci, did you ever treat a patient for COVID during the pandemic? Answer: I was part of a team that was at the NIH that took care. We didn't take care of many of them. Question: Okay, so not hands-on. Got it. Thank you. Why would I be criticized by a bureaucrat for doing my very best as a healthcare professional? This is a rhetorical question, but why? Why would the government, who has never treated a patient for COVID... You can read all the things you want, but you're not there. You're not seeing patients. You're not watching people die. Intubating patients right there with that disease in your face, watching it happen, watching the development of this disease and actually learning from it. But I'm being told by bureaucrats what's right and wrong. And what's funny is everything I was censored on, I was proven to be right. Pretty crazy, isn't it? Question: You said in an interview that you gave as part of an audiobook written by Michael Specter that you believed institutions should make it hard for people to live their lives so they'd feel pressured to get vaccinated. Could we run the audio clip on that, please? Answer: You think it can be done about it. I have to say that I don't see a big solution other than some sort of mandatory. I know federal officials don't like to use that term. Once people feel empowered and protected legally, you are going to have schools, universities, and colleges are going to say, you want to come to this college, buddy? You're going to get vaccinated, lady. You're going to get vaccinated. Big corporations like Amazon and Facebook and all of those others are going to say, you want to work for us? You get vaccinated. And it's been proven that when you make it difficult for people in their lives, they lose their ideological bullshit and they get vaccinated. Thank you. Question: Are all objections to COVID vaccinations ideological bullshit, Doctor Fauci? Answer: No, they're not. And that's not what I was referring to. Question: Well, in reference to making it hard for people to get education, traveling, working, I'd say it very much was in context, and I take great offense to this. Miss Allison Williams testified before this committee about losing her job because she sought an exemption for ESPN's vaccine mandate, which came from recommendations from bureaucrats like yourself. She and her husband were actively working with a fertility expert, a physician, on how to get pregnant, and agreed with the premise that she was young, healthy, wanted to get pregnant, and shouldn't get the vaccination for medical purposes. But she was fired because you made it hard, just like you said in your statement, because you didn't want to make sure that the ideological bullshit got in the way of her working, of living her life, of making a medical decision with her healthcare professional. I think America should take great offense to this. That's exactly what you meant when you said making it hard for people to live without getting a vaccination. You affected people's ability to work, travel, be educated, to actually flourish in American society, to self-determine as we're all given God-given rights. Shame on you, Doctor Fauci. You've become doctor of fear. Americans do not hate science. I don't hate science. The American people hate having their freedoms taken from them. You inspired and created fear through mask mandates, school closures, vaccine mandates that have destroyed the American people's trust in our public health institutions. This fear you created will continue to have ripple effects over generations to come. You have already seen its effects in education, in the economy, and everything else, quite frankly.

Video Transcript AI Summary
The speaker questions Dr. Fauci's support for institutions pressuring people to get vaccinated. They criticize the impact on individuals' lives, citing examples of job loss due to vaccine mandates. The speaker accuses Dr. Fauci of instilling fear through mandates and closures, eroding trust in public health institutions. They emphasize the importance of individual freedoms and decision-making in healthcare. The speaker challenges Dr. Fauci's approach and its long-term consequences on society.
Full Transcript
Speaker 0: You said in an interview that you gave as part of an audiobook written by Michael Spector, that you believed an institutionals should make it hard for people to to live their lives so they'd feel pressured to get vaccinated. Could we re re, run the audio clip on that, please? Speaker 1: Do you think can be done about it? I have to say that I don't see a big solution other than some sort of mandatory vaccination. I know federal officials don't like Speaker 2: to use that term. Once people feel empowered and protected legally, you are gonna have schools, universities, and colleges. They're gonna say, you wanna come to this college, buddy? You're gonna get vaccinated. Lady, you're gonna get vaccinated. Yeah. Big corporations like Amazon and Facebook and and and all of those others are gonna say, you wanna work for us? You get vaccinated. And it's been proven that when you make it difficult for people in their lives, they lose their ideological bullshit, and they get vaccinated. Speaker 0: Only politicians, only bloggers, only conspiracy theorists are disagreeing with you. I wanna point out that I'm probably the only member of congress that actually treated patients during the pandemic from the very beginning to the very end of the pandemic, during night shifts in the ER. Thousands of patients during that time. And, in 2020, I was censored. My medical license was threatened because I disagreed with bureaucrats, literally taken off the internet as a person who is treating patients with leading edge technologies, developing theories, but doing my very best, but being censored by the United States government for the first time stepping in and taking the place of medical professionals as the experts in health care. Any descent surrounding COVID-nineteen treatments, mask mandates, and any public policy surrounding the pandemic was immediately labeled as anti science. I watched as public health officials and politicians told my patients what treatment options were best for them regardless of their comorbidities or their medical history. Despite my education and my training and my experience, my opinions were relegated to conspiracy and misinformation by so called healthcare experts who had never treated a patient throughout the entire pandemic. This has been a black eye in medicine and has highlighted why government should never, never insert itself in between patients and their healthcare providers. The American people deserve to make medical decisions through conversations with their physicians rather than politically motivated mandates. Doctor. Fauci, did you ever treat a patient for COVID during the pandemic? Speaker 2: I was part of a team that was at the NIH. We didn't take care of many of them. Okay. Speaker 0: So not hands on. Got it. Thank you. Why would I be criticized by a bureaucrat for doing my very best as a healthcare this is a rhetorical question, but why? Why would the government who's never treated a patient for COVID? You can read all the things you want, but you're not there. You're not seeing patients. You're not watching people die, intubating patients right there with that disease in your face, watching it happen, watching the development of this disease, and actually learning from it. But I'm being told by bureaucrats what's right and wrong. And what's funny is everything I was censored on, I was proven to be right. Pretty crazy, isn't it? You said in an interview that you gave as part of an audio book written by Michael Spector, that you believed an institutionals should make it hard for people to to live their lives so they'd feel pressured to get vaccinated. Can we re re, run the audio clip on that, please? Speaker 1: You think can be done about it? I have to say that I don't see a big solution other than some sort of mandatory vaccination. I know federal officials don't like Speaker 2: to use that term. Once people feel empowered and protected legally, you are gonna have schools, universities, and colleges. They're gonna say, you wanna come to this college, buddy? You're gonna get vaccinated. Lady, you're gonna get vaccinated. Yeah. Big corporations like Amazon and Facebook and and all of those others are gonna say, you wanna work for us, you get vaccinated. And it's been proven that when you make it difficult for people in their lives, they lose their ideological bullshit, and they get vaccinated. Speaker 0: Thank you. Are all objections to COVID vaccinations ideological bullshit, doctor Fauci? Speaker 2: No, they're not, and that's not what I was referring to. Speaker 0: Well, in reference to making it hard for people to get education, traveling, working, I'd say, it very much was in context. And I take great offense to this. Miss Allison Williams testified before this committee about losing her job because she sought an exemption for ESPN's vaccine mandate which came from recommendation from bureaucrats like yourself. She and her husband were actively working with a fertility expert, a physician, on how to get pregnant and agreed with the premise that she was young, healthy, wanted to get pregnant, and shouldn't get the vaccination for medical purposes. But she was fired because you made it hard, just like you said in your statement, because you didn't want to make sure that the ideological bullshit got in the way of her working, of living her life, of making a medical decision with her healthcare professional. I think America should take great offense to this. That's exactly what you meant when you said making it hard for people to live without getting a vaccination. You affected people's ability to work, travel, be educated, to actually flourish in American society, to self determine as we're all given God given rights, shame on you. Doctor. Fauci, you've become Doctor. Fear. Americans do not hate science. I don't hate science. The American people hate having their freedoms taken from them. You inspired and created fear through mass mandates, school closures, vaccine mandates that have destroyed the American people's trust in our public health institutions. This fear you created will continue to have ripple effects over generations to come. You have already seen its effects in education, in the economy, and everything else. Quite frankly, you said,
Saved - May 10, 2025 at 12:00 AM
reSee.it AI Summary
I just shared a powerful discussion featuring RFK Jr. and his team, who are determined to reform America's health system, which they believe keeps people sick for profit. Dr. Makary criticized the FDA's past focus on misinformation, advocating for a return to prioritizing cures. Kennedy defended Dr. Casey Means, highlighting her contributions to health freedom despite criticism. The team emphasized the importance of free speech in science, promising to challenge taboos and ensure transparency in future health crises. This marks the beginning of a significant movement for change.

@VigilantFox - The Vigilant Fox 🦊

RFK Jr. and Team MAHA just launched a full-scale assault on America’s broken health system. The system was designed to keep people sick—but now he has the team to dismantle it. Dr. Makary exposed a baffling top priority at the FDA. And Dr. Jay Bhattacharya said something about free speech and science that hit like a lightning bolt. This is a must-see interview with four powerhouse minds. Let’s roll the clips and break it all down. 🧵THREAD

@VigilantFox - The Vigilant Fox 🦊

📍Don’t forget to bookmark this post for later. These clips mark beginning of something special for America.

@VigilantFox - The Vigilant Fox 🦊

The moment RFK Jr. sat down with Bret Baier at HHS, you could tell something was different. He wasn’t alone. Sitting beside him were three of the most talked-about names in health right now—Jay Bhattacharya, Marty Makary, and Mehmet Oz. They’re now running the NIH, FDA, and CMS. This wasn’t just a symbolic lineup. It was a statement. Kennedy is out to tear down what he calls America’s “sick care” system—a system, he says, that keeps people unwell because that’s where the money is. “We’ve turned this country into a 'sick care' system rather than a health care system,” he said. And for the first time, he believes he’s got a team that can actually change that. “These are the people who are going to change that.” What ties them together isn’t politics. It’s purpose. “Friendship is based upon shared values,” he told Baier. “And that’s the strongest bond that holds people together.”

Video Transcript AI Summary
Friendship is based on shared values, and the group shares a lifelong vision to make the country healthy with evidence-based, replicable science. This will challenge the current system, which is destroying our health due to misaligned economic incentives and public health. The speaker met with heads of pharmaceutical companies, stating the desire to live in a place where companies profit by making people healthy, rather than the current alignment against each other. The healthcare system has perverse incentives that force people to do the wrong thing. The country has become a sick care system instead of a health care system, and the people in the group will change that.
Full Transcript
Speaker 0: Friendship is is based upon shared values, and that's the strongest bond that holds people together. And in this, we all share a vision that's been a lifelong vision for all of us, which is which is to to make our country healthy, to have evidence based science, to have gold standard replicable science, and then do the and then use that to challenge what we have the the this kind of bedrock system that is destroying our health, which is a complete misalignment of economic incentives and public health. I we yesterday we met with the heads of all the pharmaceutical the biggest pharmaceutical companies. And I said, I wanna live in a place where you can make money by making people healthy. And right now we're all aligned against each other. The the the health care system in this country is a bundle of perverse incentives that that force people to do the wrong thing. And we've turned this country into a sick care system rather than a health care system, and all these people are the people who are gonna change that.

@VigilantFox - The Vigilant Fox 🦊

Dr. Marty Makary didn’t waste any time calling out the failures of the old guard. He said the FDA under Biden lost its focus—and instead of prioritizing cures, it became obsessed with controlling what people could say. “In the last administration, the number one priority, the commissioner stated, was fighting 'misinformation'—and the DEI staff ballooned out.” The agency drifted away from its mission. Now, Makary says, it’s back on track. “We want to focus the agency on cures and meaningful treatments.” He also made it clear: this team supports medical freedom—and real innovation. “We believe in the letter and the spirit of right to try—and there's amazing stuff in the pipeline.” No more gatekeeping. No more distractions. Just getting people better.

Video Transcript AI Summary
The speaker wants the agency to focus on cures and meaningful treatments, contrasting this with the previous administration's focus on fighting misinformation and DEI. They believe in right to try and state there are amazing new treatments in the pipeline for stage four cancers, neurodegenerative disorders, and diabetes. The speaker questions the lengthy drug approval process and suggests reevaluating the focus on blaming children for illnesses instead of examining the food supply. They question the reliance on willpower when many children suffer from belly pain or attention deficit disorder and are on medication. The speaker advocates for using both common sense and gold standard science, which is the charge from Secretary Kennedy.
Full Transcript
Speaker 0: We wanna focus the agency on cures and meaningful treatments. The in the last administration, number one priority the commissioner stated was fighting misinformation, and the DEI staff ballooned out. We wanna focus on cures and meaningful treatments. We believe in the letter and the spirit of right to try, and there's amazing stuff in the pipeline I've seen. We're talking about new treatments for stage four cancers, for neurodegenerative disorders, for diabetes that we've never seen before. Why does it take ten years on average for drugs to come to market? Why are we blaming children for being sick and not looking at our food supply? Why are we thinking it's a willpower problem once we watch half of our nation's children with belly pain or attention deficit disorder on medications? And can we use common sense and gold standard science both? And that's the charge that we have from secretary Kennedy.

@VigilantFox - The Vigilant Fox 🦊

Before we roll the next clip: if you’re not following me, you’re missing out on critical updates. Hit the bell 🔔 to stay sharp and informed. → @VigilantFox Now, back to the story you came for. https://t.co/t0RY68mZZv

@VigilantFox - The Vigilant Fox 🦊

The conversation turned to Dr. Casey Means—Trump’s pick for Surgeon General. She’s been praised and criticized. But Kennedy didn’t hesitate to defend her. “Casey Means, we felt was the best person to really bring the vision of MAHA to the American public.” He pointed to her book as a rallying point for the health freedom movement. She inspired it. Articulated it. Helped build it. “She has this unique capacity to articulate it. She's written a book that really mobilized, galvanized the movement.” Critics say she doesn’t have a current medical license. Kennedy pointed out something they left out. “She was the top—the very top—of her medical class at Stanford.” But what mattered more, he said, was why she left the system in the first place. “She was not curing patients. She couldn't get anybody within her profession to look at the nutrition, contributions to illness.” And that, to Kennedy, says it all. “If we’re healers, we can’t just be making our life about billing new procedures.”

Video Transcript AI Summary
Casey Means is considered the best person to bring Maha's vision to the American public due to her ability to articulate it and her book that mobilized the movement. Despite criticism regarding her unfinished residency and lack of an active medical license, she graduated at the top of her class at Stanford and won every award possible during her residency. She left traditional medicine because she felt it wasn't curing patients and that the profession wasn't considering nutrition's role in illness. She believes that true healers need to find new approaches to medicine beyond billing procedures. She will bring this type of leadership.
Full Transcript
Speaker 0: Casey Means, we felt, was the best person to really bring the vision of Maha to the American public. She has a in this unique capacity to articulate it. She's written a book that really mobilized, galvanized the movement. She is an extraordinary she she is she is excellence in everything that she's ever she's come under her own criticism about some of the things she's advocated for. She never finished her residency and she doesn't currently have an active medical license. That's not She was the top of her the very top of her medical class at Stanford. She is in every during her residency, she won every award that she could win. She walked away from traditional medicine because she was not curing patients. She couldn't get anybody within her profession to look at the nutrition contributions to illness. And she said, if we're really gonna heal people, if we're healers, we can't just be making our life about billing new procedures. We actually have to figure out new approaches to medicine, and that's the kind of leadership that she's gonna bring to our con

@VigilantFox - The Vigilant Fox 🦊

Then came the question everyone knew was coming. “If there were another pandemic,” Baier asked, “would you do the same thing?” All four men shook their heads. “No.” Kennedy jumped in. “We’d do science. We’d do evidence-based medicine.” He said the CDC and WHO had the right protocols—but tossed them aside. “They knew there were manuals on how to do it, but they just threw those manuals out of the window.” In their place, he said, came politicized science, shaped by power and money. “We had a complete information chaos. And that is—the good information is the basis of managing any pandemic.” Next time, he said, things will be different. “We’re going to make sure... we have gold standard information. We have complete transparency so the public can ask us questions and we can make answers.” “And above all, we are going to get rid of the taboos... about challenging consensus.”

Video Transcript AI Summary
In the event of another pandemic, the speaker asserts that the response should differ drastically from the previous one. They claim that established scientific and medical protocols were disregarded in favor of a politicized approach serving specific economic and power interests, leading to information chaos. The speaker emphasizes the need for gold standard information and complete transparency to enable public inquiry and informed responses. They advocate for challenging established orthodoxies and consensus, criticizing the notion of blindly trusting experts as antithetical to science and democracy, likening it instead to totalitarianism and religion.
Full Transcript
Speaker 0: We had another pandemic. Would we do the same thing? Would it be completely different? No. What how would it be different? We do science. We do evidence based medicine. CDC knew how to do this, and WHO, they knew there were manuals on how to do it, but they just threw those manuals out of the window. And they did a politicized version of science that was designed to serve certain vested interests, economic interests and power centers in this society, And we had a complete information chaos, and that is the good information is the basis of managing any pandemic, and we're gonna make sure that next time that that happens that we have gold standard information. We have complete transparency so the public can ask us questions and then we can make answers. And above all, we are gonna get rid of the taboos about about challenging orthodoxies, about challenging consensus, and and we're telling the public every day, all of us, that is not science. You know, your whole industry was telling the public for years, trust the experts. Trust the experts is not a function of science or democracy. It's a function of totalitarianism and religions.

@VigilantFox - The Vigilant Fox 🦊

That’s when Dr. Jay Bhattacharya made his promise. And it hit like a thunderclap. “Free speech is absolutely essential for scientific progress.” He said the biggest failure during COVID wasn’t just policy—it was the silencing of anyone who questioned it. “If we had had it during the pandemic, we would have had much better outcomes.” Even basic truths were treated like dangerous ideas. “You couldn’t say that if you had COVID and recovered, you’d have some immunity.” Now, he says, that era is over. And that includes opening up some of the most sensitive medical debates—like autism. “I don’t know what causes autism to rise... It just looks like people haven’t really asked the question in a deep and honest way.” That’s about to change. “We’re going to shatter that taboo so people can ask the question honestly—grounded in truth.” His final words summed up the entire mission: “We’re going to have free speech in science—and free speech in medicine.”

Video Transcript AI Summary
Free speech is essential for scientific progress and would have led to better outcomes during the pandemic. Taboos in science exist, and the current scientific literature lacks deep and honest inquiry into certain topics, such as the causes of rising autism rates. The aim is to shatter these taboos, enabling honest questioning and answers grounded in truth. During the pandemic, certain statements were taboo, such as acknowledging immunity after recovering from COVID. Under Secretary Kennedy's and President Trump's leadership, the administration aims to eliminate these taboos and promote free speech in science and medicine.
Full Transcript
Speaker 0: One of the main problems during the pandemic was censorship. Free speech is absolutely essential for scientific progress. Free speech, if if we had had it during the pandemic, we would have had much better outcomes. So when secretary Kennedy says that we're gonna have gold standard science, the the the bottom, what what holds that up is free speech. And when secretary Kennedy talks about the taboos in science, he's absolutely right. I, as a scientist, I don't know what what causes autism to rise. I read the scientific literature, and it it just looks like people haven't really asked the question in a in a deep and honest way. What we're going to do is we're going to shatter that that taboo so that people can ask the question honestly so I could look at the scientific literature and give give an answer. At least that's grounded in truth. It's it's, you saw during the pandemic, it was taboo to say certain things. Right? You you couldn't say that if you had COVID and recovered, you'd have some immunity, for instance. Those kind of taboos are anathema to scientific progress. And on in this administration, under secretary Kennedy's leadership and president Trump's leadership, we are not going to have those taboos. We're going to have free speech in science and free speech in medicine.

@VigilantFox - The Vigilant Fox 🦊

Thanks for reading. Follow me for more stories that matter. —> @VigilantFox Looking for something else to read? 🚨 Victor Davis Hanson just shattered the media’s favorite lie about Trump. https://t.co/Ai3Rj2UcdA

@VigilantFox - The Vigilant Fox 🦊

Victor Davis Hanson just shattered the media’s favorite lie about Trump. For years, they’ve used fake polls to manipulate public opinion and crush his momentum. But Hanson didn’t just say the polls were wrong. He showed they were rigged—by design. Polling is now just a weapon, used to suppress Trump’s base and supercharge Democrat fundraising. And once you hear the evidence, you’ll never trust another mainstream poll again. 🧵 THREAD

@VigilantFox - The Vigilant Fox 🦊

Huge shout-out to @overton_news for cutting together that last clip in this thread. They’re hands down one of the best news accounts on X. Do yourself a favor and give them a follow! —> @overton_news https://t.co/W72ifyKzrC

Saved - May 16, 2025 at 11:56 PM
reSee.it AI Summary
I shared a powerful testimony about my experiences as a gastroenterologist during the COVID-19 pandemic. I highlighted the importance of the microbiome in immunity and my research on the virus found in stools. Despite delays and censorship, I documented significant findings, including the role of bifidobacteria in immunity and the effects of treatments like hydroxychloroquine and ivermectin. I also noted concerning impacts of mRNA vaccines on bifidobacteria. My work emphasizes the need for open scientific discourse and collaboration, which was lacking during the pandemic.

@newstart_2024 - Camus

Very powerful testimony by dr. Sabine Hazan "Thank you, senator. It's an honor to be here. The microbiome, our microbes in our guts, is our immunity and tells the story and will tell the story of COVID nineteen. And this is why as a gastroenterologist, I stepped into the pandemic. Through my experience, I will show you how difficult it was to conduct research and publish when the research goes against the national public health narrative." "Interference and delay in research happened and affects all of us. In early twenty twenty, my research genetic sequencing laboratory was the first lab to document the entire sequence of the virus in the stools as opposed to the PCR which is just a little piece of the virus." "We discovered that the virus lingered in the stools for up to forty five days. It took six months to publish this publication at a time where everybody needed to know that it was in your stools. My lab also showed that COVID nineteen in the stools was killed by hydroxychloroquine and azithromycin." "But unfortunately, azithromycin and hydroxychloroquine killed the microbiome. So therefore, vitamin c, d, and zinc was added. Three protocols were submitted to the FDA from our findings. Three studies were also put into http://clinicaltrials.gov in full transparencies to help doctors more effectively treat COVID because I knew data that nobody knew. 04/02/2020, FDA gave us an exempt letter for doing a clinical trial." "In other words, we did not need to do a clinical trial on hydroxychloroquine, z pack, vitamin c, d, and zinc as treatment or hydroxychloroquine, vitamin c, d, and zinc as prophylaxis. April 4, somebody must have called the FDA and said, I got another letter saying, I'm sorry, doctor Hazan. Exemption is denied. You must do a full on clinical trial. Here's the letter." "System pressures delayed us, and we got a green light to start recruiting by May 2020. By then, the media created fear around hydroxychloroquine. It was impossible to recruit. This drug was safely given for years for arthritis and lupus with no problems. My clinical trials companies were also banned and censored from advertising on Facebook, Instagram, and Twitter." "Remember, I do clinical trials for a living and never as a clinical trial doctor have I not been able to advertise to recruit for a trial on social media. I kept collecting stools of patients and noticed that patients with severe COVID had a certain bacteria that was missing compared to people that were highly exposed to COVID but never got COVID. That bacteria is called bifidobacteria. Bifidobacteria is an important and key microbe for immunity. It represents your trillion dollar industry of probiotics." "In fact, when you turn the bottle and you see the ingredient, it says bifidobacteria. It is present in newborns. This is why your newborns did not get a problem from COVID at the beginning, and it is absent in old people. The process of aging is loss of bifidobacteria. We published this paper, the lost microbes of COVID nineteen." "It took eight months to publish. If you follow the bifidobacteria like I did, you will notice, and we did notice anyways, that vitamin c actually increases bifidobacteria. This is why vitamin c is important when you take when you take care of viruses and, you know, you've all experienced taking vitamin c for a cold." "Well, we published this data where we showed vitamin c, if we give it to patients before and after, it increased the bifidobacteria. Ivermectin was also an interesting drug because Ivermectin, we noticed, also increased the bifidobacteria within twenty four hours of taking it." "Why Ivermectin? If you look at what Ivermectin is, it is a fermented product of a bacteria that is similar to bifidobacteria. In fact, they're in the same continent of microbes. They live. They're like sisters, brothers in the microbiome." "So I published. I knew that ivermectin increased bifidobacteria, but I said, nah. I can't go out there and start publishing that. That's gonna be too controversial. So I published a hypothesis that maybe what I was observing on the frontline treating patients with COVID, noticing that their oxygen saturation was increasing from ivermectin, was basically maybe ivermectin increased bifidobacteria." "The hypothesis on ivermectin was the most read hypothesis in the pandemic and was retracted after eight months of being on. When we cannot make a hypothesis, this is not science. December twenty twenty, at the same time that I was treating patients with COVID, I began collecting stools of my colleagues that were at home and started going into the hospital. And I said, can I get your stools before and after you get vaccinated? Because to me, this new technology of vaccines, I wanted to see what it was doing on the microbiome." "I discovered that messenger RNA vaccines killed the bifidobacteria. I knew I would never be able to publish this because it goes against the narrative. So I submitted it to my college, the American College of Gastroenterology, and presented it in October 2022. This abstract won a research award at the American College of Gastro beating 6,000 abstracts. That's from academic centers like Harvard and Mayo Clinic and MD Anderson." "This abstract got the attention of 18,000 GI doctors who all of a sudden started realizing maybe killing bifidobacteria is why I got COVID after my vaccine to begin with. Worse than that, and another abstract we presented, was the persistent damage of bifidobacteria from the vaccine." "What is going on here that the vaccine continues to kill the bifidobacteria? At the same time, we presented a link between loss of bifidobacteria and Crohn's disease, loss of bifidobacteria in Lyme disease, and loss of bifidobacteria in invasive cancer. It is nearly impossible to publish data that goes against the national public health narrative." "If doctors cannot publish the data, they cannot find solution to fix the problems. So in conclusion, I will finish with showing this. This represents clinical trials that I've done for pharmaceutical companies prior to COVID. Amongst them are vaccine studies. Yes." "I brought vaccines to the market. Proton pump inhibitors, cardiac drugs, biologics for all sorts of conditions. First, postpartum depression drug, drugs that never made it to the market because they killed people. Clinical trials doctors follow guidelines that allows the industry to provide safe drugs. These guidelines were not followed during the pandemic." "And because of that, everyone is affected. COVID should have been a time where humanity joined forces together and doctors needed to come together. It's a shame that it didn't happen. Interference with research affects all of us. This should not be political." "Science is a story that evolves. It's a multitude of experiments that allow us to see medicine, to give hopes to patients. Skepticism, challenging the current state of knowledge. Having an open mind must be allowed if we have any hope of moving science forward. What I saw this pandemic was not science. Thank you."

Video Transcript AI Summary
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.
Full Transcript
Speaker 0: Thank you, senator. It's an honor to be here. The microbiome, our microbes in our guts, is our immunity and tells the story and will tell the story of COVID nineteen. And this is why as a gastroenterologist, I stepped into the pandemic. Through my experience, I will show you how difficult it was to conduct research and publish when the research goes against the national public health narrative. Interference and delay in research happened and affects all of us. In early twenty twenty, my research genetic sequencing laboratory was the first lab to document the entire sequence of the virus in the stools as opposed to the PCR, which is just a little piece of the virus. We discovered that the virus lingered in the stools for up to forty five days. It took six months to publish this publication at a time where everybody needed to know that it was in your stools. My lab also showed that COVID nineteen in the stools was killed by hydroxychloroquine and azithromycin. But unfortunately, azithromycin and hydroxychloroquine killed the microbiome. So therefore vitamin C, D and zinc was added. Three protocols were submitted to the FDA from our findings. Three studies were also put into clinicaltrials.gov in full transparencies to help doctors more effectively treat COVID because I knew data that nobody knew. 04/02/2020, FDA gave us an exempt letter for doing a clinical trial. In other words, we did not need to do a clinical trial on hydroxychloroquine, Z Pak, vitamin C D, and zinc as treatment. Or hydroxychloroquine, vitamin C D, and zinc as prophylaxis. April 4, somebody must have called the FDA and said, got another letter saying, I'm sorry, doctor Hazen, exemption is denied. You must do a full on clinical trial. Here's the letter. System pressures delayed us, and we got a green light to start recruiting by May 2020. By then, the media created fear around hydroxychloroquine. It was impossible to recruit. This drug was safely given for years for arthritis and lupus with no problems. My clinical trials companies were also banned and censored from advertising on Facebook, Instagram, and Twitter. Remember, I do clinical trials for a living, and never as a clinical trial doctor have I not been able to advertise to recruit for a trial on social media. I kept collecting stools of patients and noticed that patients with severe COVID had a certain bacteria that was missing compared to people that were highly exposed to COVID but never got COVID. That bacteria is called bifidobacteria. Bifidobacteria is an important and key microbe for immunity. It represents your trillion dollar industry of probiotics. In fact, when you turn the bottle and you see the ingredient, it says bifidobacteria. It is present in newborns. This is why your newborns did not get a problem from COVID at the beginning. And it is absent in old people. The process of aging is loss of bifidobacteria. We published this paper, The Lost Microbes of COVID nineteen. It took eight months to publish. If you follow the bifidobacteria like I did, you will notice, and we did notice anyways, that vitamin c actually increases bifidobacteria. This is why vitamin c is important when you take you take care of viruses, and you know, you've all experienced taking vitamin c for a cold. Well, we published this data where we showed vitamin c, if we give it to patients before and after, it increased the bifidobacteria. Ivermectin was also an interesting drug because ivermectin, we noticed, also increased the bifidobacteria within twenty four hours of taking it. Why ivermectin? If you look at what ivermectin is, it is a fermented product of a bacteria that is similar to bifidobacteria. In fact, they're in the same continent of microbes. They live. They're like sisters, brothers in the microbiome. So I published, I knew that ivermectin increased bifidobacteria, but I said, I can't go out there and start publishing that. That's going to be too controversial. So I published a hypothesis that maybe what I was observing on the frontline treating patients with COVID, noticing that their oxygen saturation was increasing from ivermectin, was basically maybe ivermectin increased bifidobacteria. The hypothesis on ivermectin was the most read hypothesis in the pandemic and was retracted after eight months of being on. When we cannot make a hypothesis, this is not science. December twenty twenty, at the same time that I was treating patients with COVID, I began collecting stools of my colleagues that were at home and started going into the hospital. And I said, can I get your stools before and after you get vaccinated? Because to me this new technology of vaccines, I wanted to see what it was doing on the microbiome. I discovered that messenger RNA vaccines killed the bifidobacteria. I knew I would never be able to publish this because it goes against the narrative. So I submitted it to my college, the American College of Gastroenterology, and presented it in October 2022. This abstract won a research award at the American College of Gastro beating 6,000 abstracts. That's from academic centers like Harvard and Mayo Clinic and MD Anderson. This abstract got the attention of 18,000 GI doctors who all of a sudden started realizing maybe killing bifidobacteria is why I got COVID after my vaccine to begin with. Worse than that, and another abstract we presented, was the persistent damage of bifidobacteria from the vaccine. What is going on here that the vaccine continues to kill the bifidobacteria? At the same time, we presented a link between loss of bifidobacteria and Crohn's disease, loss of bifidobacteria in Lyme disease, and loss of bifidobacteria in invasive cancer. It is nearly impossible to publish data that goes against the national public health narrative. If doctors cannot publish the data, they cannot find solution to fix the problems. So in conclusion, I will finish with showing this. This represents clinical trials that I've done for pharmaceutical companies prior to COVID. Amongst them are vaccine studies. Yes. I brought vaccines to the market. Proton pump inhibitors, cardiac drugs, biologics for all sorts of conditions. First postpartum depression drug, drugs that never made it to the market because they killed people. Clinical trials doctors follow guidelines that allows the industry to provide safe drugs. These guidelines were not followed during the pandemic. And because of that, everyone is affected. COVID should have been a time where humanity joined forces together and doctors needed to come together. It's a shame that it didn't happen. Interference with research affects all of us. This should not be political. Science is a story that evolves. It's a multitude of experiments that allow us to see medicine, to give hopes to patients. Skepticism, challenging the current state of knowledge, having an open mind must be allowed if we have any hope of moving science forward. What I saw this pandemic was not science. Thank you.

@newstart_2024 - Camus

Credit: @SabinehazanMD

Saved - July 21, 2025 at 4:14 AM
reSee.it AI Summary
I learned from Dr. Patrick Soon-Shiong that key officials were aware of COVID-19 vaccine risks, such as myocarditis and the inability to clear the virus, as early as 2020. Despite these warnings, the public was presented with a misleading narrative of "95% efficacy," and critical data was suppressed. This has led to a legacy of distrust and avoidable harm, raising concerns about accountability, even for prominent figures like Dr. Fauci. It makes me wonder how many lives could have been saved with greater transparency.

@newstart_2024 - Camus

Dr. Patrick Soon-Shiong reveals a disturbing truth: key officials knew about COVID-19 vaccine risks—like myocarditis and failure to clear the virus—as early as 2020. Despite warnings, the public was sold a false narrative of "95% efficacy," while critical data was suppressed. The consequences? A legacy of distrust, avoidable harm, and a system corrupted by perverse incentives. Even figures like Dr. Fauci may have sought protection from accountability. The question remains: How many lives could have been saved if transparency had prevailed?

Saved - July 27, 2025 at 2:04 AM
reSee.it AI Summary
Dr. Robert Sullivan's testimony reveals alarming truths about mRNA technology, describing it as an experimental therapeutic with significant risks. He highlights that lipid nanoparticles and synthetic mRNA can remain in the body for over 700 days, potentially leading to autoimmune issues and toxic effects from the spike protein, which can cause organ damage. Sullivan points out that research dating back to 2005 indicated the dangers of the spike protein, and he accuses authorities of deception regarding the safety and efficacy of these shots, emphasizing the need for accountability.

@newstart_2024 - Camus

Explosive Testimony: They Knew mRNA Tech Was Dangerous and Lied to the World Dr. Robert Sullivan’s sworn testimony exposes the disturbing truth behind mRNA shots: mRNA is not just a "vaccine"—it’s an experimental therapeutic with serious risks: - Lipid nanoparticles and synthetic mRNA can persist in the body (700+ days and counting). - Forces cells to produce foreign proteins, leading to autoimmune destruction. - Spike protein is toxic—causes abnormal cell growth and organ damage (lungs, placenta). They Knew Since 2005 - SARS-1 research proved the spike protein alone was harmful. - 2015 UNC Gain-of-Function studies (Baric/NIH) showed lethal vaccine-enhanced disease in animals. - The same lung and vascular damage we now see in COVID victims. - They Lied. They Mandated. They Profited. - "Safe and effective" was a calculated deception. - Billions made while injuries were ignored and censored. - Doctors silenced, science manipulated, and the public betrayed. This isn’t just about COVID—it’s about accountability.

Video Transcript AI Summary
The speaker clarifies they are injured by an mRNA therapeutic, not a vaccine, and highlights issues with lipid nanoparticles and synthetic mRNA, which can persist for hundreds of days. They claim that instructing cells to produce a protein that presents on the cell surface can trigger autoimmune disorders. The speaker states that the spike protein itself is biologically active, causing cells to grow and divide inappropriately, and was known to damage the placenta and lungs. They assert they knew early on that the shot didn't stay in the arm. They cite 2005 research showing the SARS-CoV-1 spike protein alone could harm animals. The speaker references 2015 gain-of-function research at UNC, NIH, and Wuhan labs, where a more lethal and transmissible SARS virus was created. A traditional vaccine attempt for this virus caused harm and lethality in animals, with pathology slides showing similar vascular lung damage seen with SARS-CoV-2. The speaker concludes that "they" knew about these risks but still rolled out the vaccine, profiting from it while falsely claiming it was safe and effective.
Full Transcript
Speaker 0: Well, want to be clear too, and I'm not vaccine injured. I'm injured by an MRA therapeutic. I was very careful in my testimony to use the word shot. There are you're correct. There are many ways to lose with this new MRA technology. There are problems with lipid nanoparticle. There is a separate set of product problems with synthetic mRNA. It persists in some people, seven hundred days and counting now. There will always be a problem when you load the instructions to make a protein and that it will present on the surface and cell and will become a setup for autoimmune disorders. Separate from that spike protein in and of itself is biologically active and and to understand what happened to my injury I found researchers who had predicted this was going to happen. It causes cells to grow and divide when they should not. It was published in December 2020 although not widely known that that was causing damage to placenta and to lung. I I was probably one of the very few doctors that knew that that shot did not stay in the arm and I don't even know how I found that information but I would say that was, virtually unknown later I found this out to be true. I only found out spike protein was toxic later when I met the researchers, and I asked how did you think to research that because they knew in 2005 with SARS one that spike protein alone without the virus would be enough to harm an animal. Later, in the research of the original, novel bat human coronavirus, this is the 2015 research at UNC with, doctor Ralph Baric, NIH, and Wuhan labs. That was a gain of function research, and so they had a SARS virus that became, more lethal, more transmissible. They attempted to do a vaccine for that trial. That was a traditional vaccine not mRNA. They had vaccine induced harm and lethality in the animals and in the pathology slides of these animals, this is mice, you can see the same vascular lung damage that we're seeing today with SARS two. Speaker 1: So they knew all of this? That that's they knew this. Yeah. They knew this. Speaker 0: Yes. Speaker 1: And yet they they lied to us. They they rolled this out. Billions were made. They called it safe and effective. They mandated it, and they knew this. Speaker 0: That is correct, senator.
Saved - August 1, 2025 at 1:35 AM
reSee.it AI Summary
I embarked on a mission during the pandemic to uncover the truth about COVID-19 through the microbiome. My groundbreaking findings revealed that COVID could linger in the gut for 45 days and that hydroxychloroquine combined with vitamins could be effective, yet my research faced significant delays and censorship. I identified bifidobacteria as crucial for immunity, but my hypothesis on ivermectin was retracted despite its popularity. My studies on mRNA vaccines showed they harmed beneficial gut bacteria, but publication was blocked. This experience highlighted a troubling suppression of vital scientific research.

@newstart_2024 - Camus

The Censored Science of COVID-19 & the Microbiome—A Doctor’s Harrowing Fight for Truth Dr. Sabine Hazan, a renowned gastroenterologist, stepped into the pandemic with a mission: to uncover the truth about COVID-19 through the microbiome. What she discovered was groundbreaking—but what happened next exposes a chilling reality: science was silenced when it challenged the narrative. The Early Findings They Didn’t Want You to Know - First to sequence the entire virus in stools (not just PCR fragments). - Found COVID lingered in gut for 45 days—yet her paper was delayed 6 months at a time when this knowledge could have saved lives. - Discovered hydroxychloroquine + azithromycin killed COVID in the gut—but also wiped out critical gut bacteria. Vitamin C, D, and zinc were added to protect the microbiome. FDA Flip-Flop & Systemic Sabotage - April 2, 2020: FDA granted exemption for her clinical trial on HCQ + vitamins as treatment/prophylaxis. - April 4: Exemption mysteriously revoked. - By May, media fearmongering made recruitment impossible. - Social media BANNED her trial ads—a first in her career. The Lost Microbe That Could Have Changed Everything Dr. Hazan identified bifidobacteria—a keystone immune microbe—as the critical factor in COVID severity. - Newborns (rich in bifido) resisted COVID; the elderly (low bifido) suffered. - Vitamin C boosted bifido—explaining its viral benefits. - Ivermectin, a fermented bacterial product, rapidly increased bifido—potentially explaining its success. - But when she published a hypothesis on ivermectin’s mechanism? It became the most-read paper of the pandemic… then was retracted. The Vaccine’s Hidden Impact on Immunity Dr. Hazan did what no one else dared: studied the microbiome pre/post mRNA vaccination. - Found vaccines killed bifidobacteria—the same bacteria linked to immunity against COVID, Crohn’s, Lyme, and cancer. - Her abstract won a research award at the American College of Gastroenterology (beating 6,000 submissions). - Yet full publication was blocked—because it contradicted the official narrative. The Bigger Scandal: Science Held Hostage Dr. Hazan has conducted trials for Big Pharma for years—including vaccines. She knows how the system should work. But during COVID? - Guidelines were abandoned. - Data was suppressed. - Doctors were silenced. "If we cannot question science, it is not science—it is dogma." This is not conspiracy. This is documented suppression of lifesaving research.

Video Transcript AI Summary
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.
Full Transcript
Speaker 0: Thank you. Thank you, senator. It's an honor to be here. The microbiome, our microbes in our guts, is our immunity and tells the story and will tell the story of COVID nineteen. And this is why as a gastroenterologist I stepped into the pandemic. Through my experience, I will show you how difficult it was to conduct research and publish when the research goes against the national public health narrative. Interference and delay in research happened and affects all of us. In early twenty twenty, my research genetic sequencing laboratory was the first lab to document the entire sequence of the virus in the stools as opposed to the PCR, which is just a little piece of the virus. We discovered that the virus lingered in the stools for up to forty five days. It took six months to publish this publication at a time where everybody needed to know that it was in your stools. My lab also showed that COVID nineteen in the stools was killed by hydroxychloroquine and azithromycin. But unfortunately, azithromycin and hydroxychloroquine killed the microbiome. So therefore vitamin C, D and zinc was added. Three protocols were submitted to the FDA from our findings. Three studies were also put into clinicaltrials.gov in full transparencies to help doctors more effectively treat COVID because I knew data that nobody knew. 04/02/2020, FDA gave us an exempt letter for doing a clinical trial. In other words, we did not need to do a clinical trial on hydroxychloroquine, Pak, vitamin c d, and zinc as treatment, or hydroxychloroquine, vitamin c d, and zinc as prophylaxis. April 4, somebody must have called the FDA and said, I got another letter saying, I'm sorry, doctor Hazen. Exemption is denied. You must do a full on clinical trial. Here's the letter. System pressures delayed us, and we got a green light to start recruiting by May 2020. By then, the media created fear around hydroxychloroquine. It was impossible to recruit. This drug was safely given for years for arthritis and lupus with no problems. My clinical trials companies were also banned and censored from advertising on Facebook, Instagram, and Twitter. Remember, I do clinical trials for a living and never as a clinical trial doctor have I not been able to advertise to recruit for a trial on social media. I kept collecting stools of patients and noticed that patients with severe COVID had a certain bacteria that was missing compared to people that were highly exposed to COVID but never got COVID. That bacteria is called bifidobacteria. Bifidobacteria is an important and key microbe for immunity. It represents your trillion dollar industry of probiotics. In fact, when you turn the bottle and you see the ingredient, it says bifidobacteria. It is present in newborns. This is why your newborns did not get a problem from COVID at the beginning. And it is absent in old people. The process of aging is loss of bifidobacteria. We published this paper, The Lost Microbes of COVID nineteen. It took eight months to publish. If you follow the bifidobacteria like I did, you will notice, and we did notice anyways, that vitamin c actually increases bifidobacteria. This is why vitamin c is important when you take when you take care of viruses, and, you know, you've all experienced taking vitamin c for a cold. Well, we published this data where we showed vitamin c, if we give it to patients before and after, it increased the bifidobacteria. Ivermectin was also an interesting drug because ivermectin, we noticed, also increased the bifidobacteria within twenty four hours of taking it. Why ivermectin? If you look at what ivermectin is, it is a fermented product of a bacteria that is similar to bifidobacteria. In fact, they're in the same continent of microbes. They live. They're like sisters, brothers in the microbiome. So I published, I knew that ivermectin increased bifidobacteria, but I said, nah, I can't go out there and start publishing that. That's going to be too controversial. So I published a hypothesis that maybe what I was observing on the frontline treating patients with COVID, noticing that their oxygen saturation was increasing from ivermectin, was basically maybe ivermectin increased bifidobacteria. The hypothesis on ivermectin was the most read hypothesis in the pandemic and was retracted after eight months of being on. When we cannot make a hypothesis, this is not science. December 2020, at the same time that I was treating patients with COVID, I began collecting stools of my colleagues that were at home and started going into the hospital. And I said, can I get your stools before and after you get vaccinated? Because to me, this new technology of vaccines, I wanted to see what it was doing on the microbiome. I discovered that messenger RNA vaccines killed the bifidobacteria. I knew I would never be able to publish this because it goes against the narrative. So I submitted it to my college, the American College of Gastroenterology, and presented it in October 2022. This abstract won a research award at the American College of Gastro beating 6,000 abstracts. That's from academic centers like Harvard and Mayo Clinic and MD Anderson. This abstract got the attention of 18,000 GI doctors who all of a sudden started realizing maybe killing bifidobacteria is why I got COVID after my vaccine to begin with. Worse than that, and another abstract we presented, was the persistent damage of bifidobacteria from the vaccine. What is going on here that the vaccine continues to kill the bifidobacteria? At the same time, we presented a link between loss of bifidobacteria and Crohn's disease, loss of bifidobacteria in Lyme disease, and loss of bifidobacteria in invasive cancer. It is nearly impossible to publish data that goes against the national public health narrative. If doctors cannot publish the data, they cannot find solution to fix the problems. So in conclusion, I will finish with showing this. This represents clinical trials that I've done for pharmaceutical companies prior to COVID. Amongst them are vaccine studies. Yes, I brought vaccines to the market. Proton pump inhibitors, cardiac drugs, biologics for all sorts of conditions. First postpartum depression drug, drugs that never made it to the market because they killed people. Clinical trials doctors follow guidelines that allows the industry to provide safe drugs. These guidelines were not followed during the pandemic. And because of that, everyone is affected. COVID should have been a time where humanity joined forces together and doctors needed to come together. It's a shame that it didn't happen. Interference with research affects all of us. This should not be political. Science is a story that evolves. It's a multitude of experiments that allow us to see medicine, to give hopes to patients. Skepticism, challenging the current state of knowledge, having an open mind must be allowed if we have any hope of moving science forward. What I saw this pandemic was not science. Thank you. Thank you, doctor Hazen.
Saved - August 2, 2025 at 8:29 AM
reSee.it AI Summary
During the darkest days of COVID, I witnessed patients struggling to breathe, and I knew I had to act. While others adhered to strict protocols, I personalized treatments, ensuring not a single patient under my care died. As AI threatens to take over medical judgment, I emphasize the need for human compassion and expertise in healthcare. Medicine should be about freedom of choice and the courage to take risks for better outcomes. We must protect our rights to think, question, and innovate. Let’s fight for the future of medicine and the humanity within it.

@newstart_2024 - Camus

Dr. Sabine Hazan: "Freedom, Choice, and the Fight for Humanity in Medicine" During the darkest days of COVID, Dr. Sabine Hazan stood on the frontline, watching patients gasp for air—oxygen levels at 63%, terrified of hospitals. But she refused to stand by. "Letting someone die when you know how to help is criminal," she says. While others followed rigid protocols, she tailored treatments to the individual—and not a single patient under her care died. Now, as AI threatens to replace human judgment in medicine, Dr. Hazan issues a warning: "I don’t want an algorithm telling me I have 10 days to live. I want a doctor who’s fought for lives, who’s seen what works, who can say, ‘Here’s your best shot.’" Medicine isn’t one-size-fits-all. It’s about freedom—the right to choose your treatment, to weigh risks, to fight for more than just extra days. "Do you take the safe route and live 10 days longer? Or risk it all for a year?" There are no guarantees—just the courage to leap into the abyss and trust in God, science, and human ingenuity. But this battle isn’t just about medicine. It’s about protecting freedom—of choice, of speech, of innovation. "We must stand as humans, defend our right to think, to question, to pioneer." Because when we surrender our decisions to machines and bureaucracies, we surrender our humanity. Dr. Hazan’s message is clear: Fight for the right to choose. Fight for the doctors who still care. Fight for the future of medicine—before it’s too late.

Video Transcript AI Summary
When treating COVID patients, some didn't want to go to the hospital even with low oxygen levels. The speaker felt it was criminal to not try to save them. None of the speaker's patients died during the pandemic while following their protocols, which varied based on individual risk factors. The speaker doesn't want to rely solely on AI for medical advice, preferring a physician's sympathy and experience. They want the freedom to choose their treatment, even if it means taking a risky route for a chance at a longer life. The speaker trusts God and is willing to "jump in the abyss," accepting the potential consequences. They believe it's crucial to protect freedom of choice, speech, ideas, and innovation.
Full Transcript
Speaker 0: When I was on the front line treating COVID, patients didn't wanna go to the hospital. Their oxygen was 63%. I wasn't gonna just watch them die. That's like watching a patient bleeding and you're not giving a blood transfusion. I mean, to me, that's criminal. Right? We know certain things. Let's try to save that life. Right? When I noticed that, you know, none of my patients died during the pandemic that followed my protocol, My protocols because there were different protocols for different people, different, you know, risk different patients with different risk factors. We need to encourage that. We need I I don't wanna be that patient, you know, because I always look twenty years from now. I don't wanna be that patient where I type in my symptoms. An AI program tells me, doctor Eason, you need all this, or Sabine, you need all this. And then you're you have this, and you have about ten days to live. I don't wanna know that. I want the sympathy of a physician to say, you know what? I've seen this work. These are the protocols that AI is gonna give you, but here are your chances with that program of AI. I think I can up your chances better with this because I've seen this work for this, this, and that. And that's really, it's freedom of choice. It's my choice to do what I wanna put in my body. It's my choice. Do I wanna take the safe route and get ten extra days of life? Or do I wanna take the risky route and maybe die tomorrow or get an extra year of life? Right? So and understanding that there are no there are no guarantees in life. You're jumping in the abyss. I mean, I tend to trust God for everything. Right? So I jump in the abyss and I hope that God's gonna guide me. And if it doesn't happen, well, it doesn't happen. You know, I made that choice to jump into the abyss. I think we need to stand as humans to protect that freedom of choice, to protect that freedom of speech, to protect ideas, to protect innovations, yes, to elevate. So important.
Saved - August 3, 2025 at 3:52 AM
reSee.it AI Summary
I discussed the future of microbiome research and the urgent need for large-scale studies, emphasizing the commitment of patients for long-term testing, particularly regarding vitamin C's effects on bifidobacteria. Standardization is crucial, as variations in vitamin C formulations can skew results. The challenge lies in the system's resistance to breakthroughs with natural compounds, which are often not patentable. I believe that clinicians must navigate a landscape that suppresses unpatentable truths, and we need public awareness and independent research to ensure access to essential science.

@newstart_2024 - Camus

Dr. Sabine Hazan on Advancing Microbiome Research: The Challenges of Innovation in a Non-Patentable World The future of microbiome research hinges on rigorous, large-scale studies—but who is willing to do the work? Dr. Sabine Hazan highlights a critical gap: we need patients committed to long-term testing, tracking how vitamin C impacts bifidobacteria through stool analysis. Only then can we unlock meaningful discoveries. But the challenges run deeper. Standardization is key. Clinicians can’t simply recommend any vitamin C off the shelf—different formulations, additives, or even capsule materials could skew results. This is why controlling variables, like offering the exact same product across studies, is non-negotiable. Without it, we’re comparing apples to oranges, and progress stalls. The bigger issue? The system isn’t built for breakthroughs in natural compounds. Vitamin C, vitamin D, even cancer-fighting microbes—none are patentable unless artificially altered. This creates a paradox: real science thrives on reproducibility, yet innovation is often blocked unless it’s "novel" enough to profit from. Dr. Hazan’s wake-up call? Clinicians fighting on the frontline face more than just disease—they battle a landscape where forces actively suppress unpatentable truths. The path forward demands public awareness, independent research, and patients willing to champion their own data. Because when healing can’t be owned, everyone deserves access to the science.

Video Transcript AI Summary
We need studies where people test their stools to see if long-term vitamin C improves bifidobacteria. To advance microbiome research, protocols need to be done properly. A clinician cannot recommend different vitamin C products from different stores because of variations in supervision. Selling a specific product ensures consistency, avoiding comparisons between different vitamins. Advancing this research is challenging because natural substances like vitamin C, vitamin D, and naturally occurring microbes cannot be patented. Patenting requires fabricating or modifying something to be new and novel. The speaker realized that forces are trying to stop innovations, despite a clinician's role to help patients with informed consent.
Full Transcript
Speaker 0: And seeing does it increase the bifidobacteria. Right? So we need large numbers. So where do I get my large numbers? You know, those people that basically are, you know, willing to test their stools to see, you know, the vitamin C long term is improving the bifida bacteria. Those are the studies we need. That's how we advance research on the microbiome. And here's the other thing. I cannot tell my patient if I'm if they're taking vitamin c, I cannot tell them go to Walmart, go to CVS, different vitamin c's. Right? Because different supervision. You need to have the same exact product. So why do I sell it on a website? Because I need to have the same exact product for everybody. Because if I change the the product or I put a capsule to the vitamin c and the capsule itself kills the bifidobacteria. Well, I can't compare apples and oranges. Okay? I can't compare two different populations that took different vitamins. Also, you know, so protocols need to be done properly in order to see something and to see something change. So, you know, this is this is the what we're dealing with, you know, advancing this kind of research because it is not something you can patent. Vitamin c, you cannot patent. Vitamin d, you cannot patent. Every discovery, it doesn't matter if you discover that a microbe is curing cancer. If that microbe is real, you cannot patent it. Because if you fabricate a microbe, you change the molecules and and you change the sequence. Now you can patent it because you have something new and novel. Right? And this is the world we're living in. So people need to understand the patent arena. People need to understand the publishing arena. You know, this was a wake up call for me on the front line because here I thought, well, my job as a clinician is really to try to save the patients no matter what with everything that I can do to help them as long as I have an informed consent. But there's there's a lot of forces that are basically trying to stop the innovations and destroy.
Saved - August 3, 2025 at 8:29 PM
reSee.it AI Summary
I expose the troubling reality behind COVID vaccine approval, revealing manipulated data and a betrayal of public trust. Adverse events were dismissed, leaving patients gaslit and without accountability. The vaccines were marketed using misleading statistics, emphasizing relative risk over absolute risk. Regulatory bodies like the FDA and EMA failed us, approving vaccines based on false data and corporate influence. Science is dying as dissent is silenced, and the betrayal by politicians and regulators is complete. When will justice be served?

@newstart_2024 - Camus

The Great COVID Vaccine Deception: How They Lied to the World Dr. Angus Dalgleish exposes the shocking truth behind the COVID vaccine approval—a scandal of manipulated data, silenced doctors, and a total betrayal of public trust. THE COVER-UP: From the start, adverse events were dismissed as "rare," "coincidental," or "anecdotal." Patients suffering severe reactions were gaslit by their own doctors, hospitals, and regulators. No feedback. No accountability. Just a wall of denial. THE STATISTICAL FRAUD: Pfizer, AstraZeneca, and Moderna didn’t sell the vaccine on absolute risk (a mere 0.84%—meaning you had to jab 120 people to prevent ONE infection). No, they pushed relative risk (95%), a statistical sleight-of-hand that fooled the world. THE REGULATORS FAILED US: The FDA, MHRA, EMA—all complicit. They approved a vaccine based on false data, withheld evidence, and corporate bribes. Pfizer alone has 31 convictions for fraud, bribery, and falsifying data. Yet, when doctors like Dalgleish sounded the alarm, they were ignored. THE DEATH OF SCIENCE: "We are witnessing the death of science," warns Dalgleish. Debate is crushed. Dissent is silenced. "Follow the science" was a mantra—but there was no science to follow. Just power, profit, and propaganda. THE BETRAYAL IS COMPLETE. Politicians bought. Regulators captured. Patients abandoned. When will justice come?

Video Transcript AI Summary
The speaker claims adverse events from the vaccine rollout were covered up and dismissed as rare and coincidental. They state that regulators approved the vaccines based on relative risk data (95%), which they describe as misleading, while the absolute risk reduction was only 0.84%, meaning 120 people had to be vaccinated to prevent one infection. The speaker alleges that Pfizer has 31 convictions, including withholding data, presenting false data, and bribing clinicians and regulators. They claim over 100 doctors have written to various health organizations, including the NHS and MHRA, about the vaccine program, but received only one response. The speaker concludes that science is dead because discussion, analysis, and debate are no longer allowed, and decisions are being made without scientific basis.
Full Transcript
Speaker 0: What I really wanted to, to point out about the vaccine and those, adverse events is how they were all covered up, that everybody went along with it. Yes. Yes. They're okay. They're all minor. They're very rare. They're very, very rare. And it's clear they weren't rare. I mean, I basically started to see as the vaccine was rolled out, people complaining of all sorts of things, and their doctors, the hospitals, my hospital, all told them it's just a coincidence. It's just anecdotal. Nothing to see here. And that is what I think is actually the worst thing. There was no feedback. And just let me so I look at it, and I say, how on earth could they have allowed this dread dreadful data to be unapproved? Well, Pfizer, AstraZeneca, Moderna, they used a thing of statistics in which it was relative risk. So they used all the data, relative risk ninety five percent. If you had that virus, if you had the vaccine, that was what it would do. It'd be ninety five percent magic magic letter. But relative risk is real. It's it's really is unbelievable syllogism whatever. Because if you look at the real data, the absolute risk was zero point eight four. So what does that mean? That means that you had to vaccinate a hundred and twenty people to prevent one infection. And my god, once you're at that level, it's a complete waste of time. And yet, our regulators, the FDA, the whole of Europe, Australia, Canada, they all approved it on that. And I must say that I didn't spot this until one of my collaborators, who's used to looking at all these things, spotted it. And then when we point this out, nothing happens. Nothing happens. So this is where I've been coming from is that I really believe that the vaccine should never ever have been approved on the data we know now. And we know that it was sophistry. They lied. They withheld data. They presented false data. And now we know Pfizer have 31 convictions, include withholding data, presenting false data, bribing bribing clinicians, and bribing regulators. Now to that, you can add bribing politicians in my book too, because nobody would listen to us. This is vast body. I'm one of over a 100 doctors that have written consistently to WITI, the NHS, MHRA, Department of Health, pointing out all this and that the vaccine program is a disaster. And we only ever had one reply from the MHRA thanking us for our communication to remind us that it's the best regulatory authority in the world. That was all they said. And that's the only feedback. So this is why I was inclined to say, what we are witnessing is the death of science. You're no longer allowed to discuss, discourse, look at things, analyze some things, and debate. It's being decided by the science. We're following the science. There was never any science to follow. It's an absolute disaster.
Saved - August 8, 2025 at 2:47 PM
reSee.it AI Summary
I've been reflecting on Dr. Sabine Hazan's insights regarding the probiotic industry and its connection to cancer and aging. She highlights a significant issue: the FDA's stringent requirements for clinical trials prevent the acknowledgment of probiotics' potential benefits. This regulatory environment stifles innovation, as evidenced by her team's success with ivermectin, doxycycline, and zinc during COVID, where no patients died. Dr. Hazan emphasizes the need for medicine to move beyond bureaucratic constraints, using social media to share vital information and empower healthcare professionals.

@newstart_2024 - Camus

The Probiotic Paradox: What Big Pharma & the FDA Don’t Want You to Know Dr. Sabine Hazan, a leading gastroenterologist & clinical trial expert, reveals a critical gap in medicine: The probiotic industry knows bifidobacterium loss is linked to cancer & aging. Yet, they can’t say probiotics may improve longevity or severe disease. Why? The FDA demands clinical trials—even when the science is clear. Doctors are caught in a regulatory trap. Even well-meaning physicians risk FDA backlash for discussing real-world results. But here’s the problem: "If we only approve drugs with a 20% success rate, what happens to the other 80%?" —Dr. Hazan Her work proves innovation can’t stop at FDA approval. When her team used ivermectin/doxycycline/zinc for COVID, ZERO patients died—despite placebo groups crashing. Yet, without billion-dollar trials, such breakthroughs stay in the shadows. The truth? Medicine must evolve beyond red tape. Social media is now a lifeline for sharing unfiltered data & empowering doctors to think beyond the 20%. Follow Dr. Sabine Hazan as she challenges the system—one clinical trial at a time.

Video Transcript AI Summary
The probiotic industry understands the loss of bifidobacterium in cancer and aging populations, but cannot claim probiotics improve longevity due to FDA regulations requiring clinical trials. Doctors also face scrutiny for promoting products without sufficient data. The speaker conducts clinical trials, involving the FDA when bringing products to market, such as ivermectin, doxycycline, and zinc for COVID. Data showed no deaths during treatment, suggesting its effectiveness. Despite a product's market approval with a 20% success rate, the speaker emphasizes the need to address the remaining 80% of patients. Innovation and discussion among doctors are crucial, but social media is now essential for educating doctors and the public due to the high cost of publishing data.
Full Transcript
Speaker 0: So the probiotic industry understands what I'm showcasing of loss of bifidobacterium cancer, loss of bifidobacterium in the aging population. They understand all that because that's how Bifidobacteria came on. It was looking at those populations, Loss of Bifidobacteria in the aging population. So they understand that, but they cannot come out and say, well, probiotics are going to help your longevity. Probiotics are going to help your severe. Because unfortunately that's making a claim that the FDA says, well, where's your clinical trials? Even us as doctors cannot make claims, right? I think it's important to educate the doctors out there because I see over and over physicians that are getting caught with regulatory physician. And by the way, I'm not perfect either. You know, I I may mess up sometimes on videos and say things, you know, but I I think it's important to remember that when you talk and when you promote something, you know, the FDA is gonna come down and say, well, you're making claims that this drug is improving and where's your data? Where's where are your clinical trials? You know, I'm in a peculiar position because I do clinical trials for a living with pharma where I bring products to market. So everything I do in my lab is really clinical trials. And I involve the FDA to the best of my ability, especially when we're trying to bring a product, when we try to bring ivermectin doxycycline zinc to the market for COVID, which was an amazing product. I involved the FDA when I did that. They saw the data. They saw no one died on my shift. How do you have a placebo group that is as only has a small percentage of success from the placebo, and then they're crashing and dropping their oxygen and they're surviving? How does that happen? Unless you're giving a treatment that is improving and that treatment is improving. Here's the thing that, you know, I've been doing clinical trials for three decades almost. What I'm realizing more and more is just because a product works for and goes to market for 20 and success rate is twenty percent, you still have the other eighty percent that you have to deal with. Yeah. If you stop the asking the question, the innovation, you're stopping to treat that eighty percent of the population. So it's great that there's a product, but that product is twenty percent successful. What are we supposed to do with the eighty percent? Am I going to just tell them, call the FDA so that they can treat you as patients? No. As a physician, I have to start doing my job of innovating, of treating, of discussing it with other doctors. And unfortunately, we're in a world of social media right now, and that's why you and I are on social media to educate the doctors, to educate the public on what's out there, what we're seeing because too often, the data is not getting it takes a lot of money to get these these publications seen by the world. Right? This is why we do what we're doing.

@newstart_2024 - Camus

Credit: @SabinehazanMD; @drgoodyear; http://progenabiome.com; https://www.youtube.com/watch?v=VOt57L74otk

ProgenaBiome A genetic Sequencing laboratory that specializes in understanding the microbiome. progenabiome.com
Saved - August 12, 2025 at 6:36 AM
reSee.it AI Summary
This episode was censored on YouTube, but here it is. I appreciate newstart_2024 and grok for their support. I conducted trials on treatments like HCQ and IVM, witnessing their effectiveness firsthand without losing anyone. I invite those without patient experience to visit my lab at Progenabiome for invaluable insights.

@SabinehazanMD - sabine hazan md

This episode was censored on @YouTube... Here it is 👇👇👇Thank you @newstart_2024 @grok pay attention to what Drs on the frontline saw and did…REMEMBER I ran the Hcq zpack Vit C d and zinc trials and Ivm, foxy zinc with @US_FDA watching. I saw first hand treatment worked having lost no one. MD is next to my name. This is data. I recommend anyone who hasn't touched a single patient to step into my lab at @Progenabiome. What I learned was priceless…

@newstart_2024 - Camus

YouTube CENSORED This Entire Podcast Episode Dr. Sabine Hazan’s Let’s Talk Sh!t Podcast (Jan 29, 2024) WHY? Because doctors exposed: • HCQ & ivermectin SUCCESS in their clinics. • COVID vaccine injuries they’re treating daily. • How Big Pharma & tech giants COLLUDED to silence dissent. THEY DELETED IT. Not for "misinformation"—but because it THREATENED THE NARRATIVE. Think about that: 🔸 Doctors with decades of experience = "dangerous." 🔸 Fact-checkers with ZERO medical degrees = "truth." 🔸 Patients left to suffer while profits soared. THIS IS WAR. On medicine. On free speech. On YOU. SHARE THIS POST → Let’s make it IMPOSSIBLE to ignore. FOLLOW → They won’t stop us.

Video Transcript AI Summary
Sabine Hazen and her panel critique a hydroxychloroquine paper, calling it a fake paper with fake data: "This is a fake paper. This is a fake data." They cite claims of "seventeen thousand people died" and "96,000 patients" in the Lancet as fraudulent, arguing no way "70,000 medical records" could be used. Xavier Ezolber analyzes data miscalculation, "data inconsistency" and "fabricated" results, criticizing the peer-review process and predatory journals that "launder scientific papers." He says, "There is a corruption in medicine," "money talks for sure," and "lobbyists control both sides of the politics." They recount frontline experiences with hydroxychloroquine–Z Pak–vitamins and ivermectin–doxycycline protocols, reporting "zero mortality, zero hospitalizations" in some cohorts and highlighting the microbiome’s role. They urge transparency, critique drug trial processes, and question vaccine strategies, stressing early outpatient treatment research.
Full Transcript
Speaker 0: From her private lab deep inside the bowels of Internal Study Central, the doctor is at. So let's talk shit with doctor Sabine Hazen. Speaker 1: Welcome everyone who's here, and thank you for coming, this early in the morning. And thank you, Brian, for wanting to talk shit with me about this hydroxychloroquine paper. I think most of you know me as a gastroenterologist that has been spearheading the research on the microbiome and also hydroxy. 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. So I'm very familiar with all these protocols. I ran the case. No one died on my shift, even though I did a placebo controlled trial on hydroxychloroquine, Z Pak, vitamin C, D and zinc. I also did the prophylaxis protocol with hydroxychloroquine and vitamins versus vitamins alone. And we had hundreds of patients on that. And then when the vaccine rolled over, a lot of doctors were forced because it was mostly doctors that we enrolled because they were high risk. When the vaccines rolled over, a lot of these doctors were forced to take the vaccine. But we have data coming out on the hydroxychloroquine prophylaxis versus vitamin C, D and zinc. So I'm very familiar with all the ins and outs of hydroxychloroquine. Brian, you want to introduce yourself? Speaker 2: Yeah, Brian Lenzkes. I'm an internal medicine doctor practicing in California for the last twenty years, general internal medicine, really focusing on metabolic health and now learning a lot more about the gut microbiome and all this stuff. Thought was crazy a few years back. So, yeah, so I was in practice during this time and watching these things and thinking, how could we be going against everything we've always believed in? You know, how can we be relying on studies that are totally fraudulent in a way, right? And getting published in major magazines. I mean, journals, I will call magazines now probably. But yeah, it's, you know, watching it and saying, how do we not talk about natural immunity? All these things that we've known for the history of medicine all of a sudden become quackery. And so, so we were united in that and then seeing all these doctors standing up on the, you know, stairs of the Capitol saying, wait a minute, this is crazy. Here's what we're doing in practice. And we're having clinical success, but no one would listen to him, you know, Erso and Pierre Corrie and all these people and Peter McCullough, the most decorated doctor. So me just being a rank and file doctor was thinking what happened to all of our great leaders? Did they either all go insane at the same time or are they right? Speaker 1: Or are they following guidelines so much that they've forgotten about how to practice the art of medicine and how to innovate, right? So I think that's the most important. Xavier, do you want to introduce yourself? Speaker 3: Yeah, of course. Well, thank you very much for having me. So I'm Xavier Ezolber. I'm a scientific journalist and econometrician by training. That is a combination of economist and statistics. And I have prepared with a number of doctors, scientific papers, over early treatments because as Brian mentioned, I saw a lot of biases in the analysis that were conducted in meta analysis and RCTs. And therefore I've used my science, which is totally different from medical science, in order to debunk a lot of these studies starting with the Lancet, because I'm one of the rare person who has interviewed Mandeep Mehra, who was the lead author also on the Lancet Gates study. I've also interviewed one of the lead investigator in recovery asking about the dosage, and so on and so forth. So my work as a scientist is to, is a major in mass is basically to look at the methodology and the inconsistencies and because I'm a journalist as well, I'm just writing up about these inconsistencies in my media. Speaker 1: Okay. So, Brian, how do you want to do this? Because, we wanted to start, I think probably starting with the article itself, right? Speaker 2: Yeah, sounds good. You're the boss. You're the boss here. I mean, you're the researcher FDA. I'm a doc, right? All I can say is we saw clinically for sure. Speaker 1: Yeah, so here's, you know, like it's interesting you said magazines, right? And I think that's what medicine is becoming. A lot of these journals are becoming magazines. They're almost like, you know, gossip column, you know, gossip journals, right? That you hear, these celebrities are doing that and then they're not doing it. It's the same propaganda. So there's a group of journals. You know, it's funny because Doctor. Barodi and I, you know, we've been working at the protocols with COVID, the whole pandemic. He calls them predatory journals. And they're actually very smart in a way because they do have an impact factor. They're brand new journals. They send you emails constantly. Different people send you emails and they're like, Oh, doctor, we've read your paper. We would love to see you publish. And then once you publish, they're easily, they can manipulate or retract the data to make you look bad. And that's exactly what happened with me with Frontiers. Frontiers, all my colleagues knew, I didn't know that it was a predatory journal. I submitted a hypothesis on ivermectin increasing the bifidobacteria and it was accepted by the peer review. Nobody criticized the articles that I picked or anything like that. And then next thing you know, nine months later, because this paper was the number one read at Frontiers with 59,000 views of doctors reading this paper, finding interesting, it was an interesting hypothesis, right? Because we're seeing ivermectin has a role potentially in cancer. So maybe increasing the bifidobacteria is how we're doing it, right? So because it got so much attention, because it really lit up ivermectin, which they don't want to do. You understand? Hydroxychloroquine and ivermectin are out of patents. So because they're out of patents, you cannot make any money on these drugs. The most you could sell them for is like $300 Pharmaceutical companies are no longer interested in $300 drugs. They're interested in orphan drugs where they can get name your price for a drug. They're no longer interested. And even the drug, the diseases, they basically find, you know, some kind of weird genetic pattern and say, oh, this is a rare condition. We're going to put it under an orphan and now we can bill whatever we want. So, you know, the and you and I have seen, you know, the Remicade, you know, we went, I went from Prilosec, which was at the time probably about a couple $100, right? And then we went to biologics, which that was a huge jump, right? From like $300 to $10,000 a month. And they got away with it. Then all these companies started copying and doing biologic at $10,000 a month. So the problem is they don't want to go back. They want to move forward. Now granted research is expensive. You need to pay for these things, etcetera. And the cost of research has gone up. But there is a movement that is controlling the research and stopping innovations that is stopping, you know, out of patent drugs, drugs that are basically, you know, like hydroxychloroquine and ivermectin. So I think that's the number one thing and the attacks on that. Speaker 2: And I think it's important for people to realize too, when you look at a medical journal, in between every single article, you can't get an article without seeing pages and pages of ads. Those aren't free. Right? They're paying money for that, first of all. And then if you want your study to get out to people, have to pay for reprints. And it's a money making venture. Right? And you say something that they're not going to like or they're going to lose some sponsorships, they're going to say, okay, we're not publishing this paper. And so that's what's happening is we've been captured. Money talks for sure. Speaker 1: And here's the thing, right? If you're leading the government, right? You have an economy to support and you have health of the people to support, right? The problem with this pandemic is that the pandemic started focusing know, when they involved all of us and all of us doctors were basically, wait a minute, I could die from this virus. I better get involved. I better figure this out. Right? I mean, I think that's what happened to you. You started looking up the journals. You started looking up clinicaltrials.gov. You know, my protocols and after Didier Raul, so I, like you guys, I read the papers of Didier Raul. The thing that impressed me about the papers, the initial paper in French was, and I speak French, so I was able to read it, was the fact that here's a man who, because they, France had COVID before we had it in America, or at least before we were made aware that we had it, right? And here's a man who was in a hospital exposed to all those patients and he's older. So he's in that high risk category and yet he survived, right? So that was the first thing. And then I read the paper and I started looking at his work, doing nasal swabs, on a weekly basis. I think he was doing nasal swabs. He was collecting stools. I mean, this man did meticulous work in research, right? And so I started being inspired by that. I said, well, you know what, maybe hydroxychloroquine is certainly a safe product. So in March I started researching my protocol and started writing the protocols. And yes, they were like contraindications to hydroxychloroquine. There were three pages of medications. You have to practice medicine and still be vigilant as a doctor. But ultimately the protocol was approved by the FDA within twenty four hours. And in fact, it was approved to say, move to market. Go ahead, Doctor. Hazen, just take your combination, start giving it to patients, proceed. Okay. That was what it was. Twenty four hours later, somebody must have called from the politics or the lobbyist that controls both sides of the politics, right? And said, wait, wait, we can't have a cheap drug. It's going to kill the market and then it's not going to start our protocol. Right. Which interestingly enough, at the same time about this, after the protocol was approved, I got a letter from Bill Gates that basically said, when do you think you're gonna, you were anticipating finishing your protocol? Why is Bill Gates interested in my little protocol? I thought he was going to invest personally. So I'm like, Oh, I've been in the clinical trial business for like thirty years. Don't worry, it's going out there, right? Well, lo and behold, you know, my protocol took forever. My protocol had a lot of, you know, like ups and downs. A month later it got approved by the IRB and then went on Twitter, Twitter destroyed it because it was an open label. I had to go back to the FDA and say, look, I'm going to do vitamins versus hydroxychloroquine with the vitamins. And then finally a month and a half later, it got into motion to start. By then it was destroyed by the politics. This was a political move to destroy a drug and unfortunately, you know, supported probably or whispered, you know, to the politicians by the lobbyists. That's exactly what happens when the Lancet paper came out and we all discovered it was BS essentially. We knew, right? This is wrong, right? Because hydroxychloroquine is the safest drug. Now this paper and why I didn't speak the whole time because you heard about Zelenko, you heard the frontline doctors and great because they were speaking, trying to save as many lives. You know, one of the criticism I got on my protocol was why did I spell out the drugs hydroxychloroquine with the dosages, Z Pak with the dosages, vitamin C, D and zinc. Why didn't I just leave it a Haze D Pak, right? Because then nobody knows, it's proprietary. There's no secret that's leaked out to the doctors. That wasn't my point. My point on April 3, when it was approved by the FDA and it went into the clinicaltrials.gov, we were number two or three. The two protocols went online on clinicaltrials.gov in America, number two and three in 04/02/2020. Why did I do that? To sound the alarm and say, look, this is what I think happens, right? On the other side, we found COVID in the stools and we discovered that actually hydroxychloroquine and Z Pak made the virus disappear. You had it at baseline, five to eight days later the virus disappeared. Problem is, you know, it does destroy the microbiome as well. So you have to be selective on which population you're going to give it, right? Every antibiotic has a risk of killing the microbiome, right? And even drugs like hydroxychloroquine. But on a safety level, you know, wrote about it. It got approved by the FDA within twenty four hours. It was safe, right? So 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. There is no way that four or five authors took 17,000 records, medical records. Now they probably took the death certificate. You can alter the death certificate. Lobbyists can pay people to like, you know, hey, you know, I mean, we've seen you and I, Brian, physicians that are on the other side that are getting paid by legal to bring, you know, cases to lawsuits, right? We've seen that. A death certificate does not make the case. Going to court and presenting your case makes the case. If you look at this paper, there is no way 70,000 medical records were taken. First of all, you need the authorization of the patient to get medical records from the hospitals. So that's why it's a fake paper. Much like the 96,000 patients that was in the Lancet. I saw that paper and I said, wait a minute, Australia doesn't even have COVID yet. Why are there patients in that paper of COVID? And you're going to tell me 10 people evaluated ninety six thousand patients with their smoking history. I'm in the clinical trial business. It takes me a year and a half to evaluate a 100 patients. Okay. And to analyze them like the hydroxychloroquine paper, we're still analyzing the data. We're like three years out. It's very time consuming to do these studies properly. So when you see a number like ninety six thousand, that's fraudulent. When you see seventeen thousand people died, that's fraudulent right off the bat. I don't even need to know how much they got because it's fraudulent. The second thing is if you look at the guidelines and then I'm gonna have Xavier jump in. If you look at the guidelines on hydroxychloroquine, there are no guidelines that tell you to test for toxicity, None. So, you know, where did that come from? Right? The second thing is if you look at, you know, the NIH chloroquine and hydroxychloroquine toxicity, the paper itself says both chloroquine and hydroxychloroquine have excellent oral absorption and bioavailability. Both have a long and variable plasma elimination half life and about half the drug metabolites. Basically there's no comment. Does not appear to cause harm to the fetus or the mother, both excreted in breast milk, which we know. And basically the only thing that they're questioning, and I wish Richard Urso was here. Speaker 2: He's here, which came true. I just saw him pop in. Was like, yes. Speaker 1: Yeah, Richard will tell you the only thing he's concerned about is the retinal toxicity with hydroxychloroquine. But your patient is in the intensive care. He's dying. You don't care about retinal toxicity. He's dead. It doesn't matter that he's got retinal toxicity. He's under the ground in one day. That's it. Speaker 4: The retinal toxicity is chronic and it's over a course of maybe getting, you know, two kilograms over your lifetime. And and so in general, I did toxicity studies on the drug in the nineties. It's basically around five point five milligram per kilogram over an extended period of time might get some toxicity. I've never known a cardiologist taking a patient off. After this thing came up, I asked 14 cardiologists here in Houston if they've ever taken a patient off of of this drug because of the QT interval issues, and not single one had ever done it. And in the meta analysis from 2,018, going back over, sixty four years of studies of usage, there were eighteen people all time that have died of that they thought may be attributed to hydroxychloroquine. And chloroquine was also had a few, but hydroxychloroquine was 18. So it's almost insanity to say that that was the cause of it because the drug's been around forever. And I think you've heard me say Sabine about all the side effects. Lowers the D dimer, sed rate, C reactive protein, decreases atherosclerosis, improves the bone health, decreases the cholesterol level, decreases hemoglobin A1C, and glucose tolerance is improved. It improves seventy percent chance of improvement in chronic kidney disease for those people at risk, decreases stroke, heart attack, pulmonary embolism. It's actually one of the best drugs you could ever take. It's almost insanity. Like you said, it's useful in pregnancy and never had a toxicity issue. It's something that comes up multiple times. So yeah, it's a completely corrupted study, just like the Surgisphere study. Speaker 2: Yeah. And just from a primary perspective, I've been practicing for twenty years. Never once ever until these last couple years has anyone said, why are you prescribing hydroxychloroquine? Now all of a sudden it's like, can't get it. If you do a short course, you can't get it. If you prescribe a month, they would fill it because they think it's for a rheumatologic condition. Right. So it's just amazing to see the politics just jump in to say, you can't fill this medicine. Speaker 3: And they Speaker 2: had tons of surplus. There was tons of supply because I asked four pharmacists that were friends of mine. They go, we have tons of supply. That's not the issue. It's just that the powers of be said we can't prescribe it. Speaker 1: I gave it. So I had a homeless in my office during COVID and the wife had arthritis and I gave it to the wife for arthritis. And the pharmacist in front of everyone said, no, you're lying. It's for COVID. Embarrassed my patient who's a homeless, right? And basically he comes back crying saying the pharmacist didn't want to give it to me. And here's a patient that was getting it prior to that, right? And that was CVS. And I went on Twitter and I said, this is ridiculous. We can't even treat for arthritis anymore. We have to like stop hydroxychloroquine. Now I'm not saying hydroxychloroquine is a great, you know, miracle drug for everybody, you know, certainly that population that, you know, Richard was describing, that has chronic disease, probably zero bifidobacteria to begin with, they're your severe patients. That's who you really reach out to. I'll tell you one of the biggest lessons I learned on the pandemic was the use, because I went through both protocols, right? I had hydroxy Z Pak vitamin C, D and zinc. And I had ivermectin doxycycline vitamin C, D and zinc. And I felt that ivermectin doxycycline was just a better protocol. When I was treating from severe patients to mild, I realized there's a, you can stratify the treatment of these patients to make it better. Those who have a good microbiome, you want to improve that microbiome. You want to get that microbiome going to fight. You don't want to destroy it. When you have patients that are basically severe oxygen desaturating. And that was one of the things that I discovered as I was treating these patients in the placebo group, right? Because remember, I don't know who's getting, I'm doing the placebo controlled trial with the FDA watching. I don't know who's getting placebo and who's getting the real stuff, right? So at the beginning I was watching them like on an hourly basis, they had my cell phone. So when at 02:00 in the morning they're crashing, I don't know what they got, right? They could have gotten hydroxychloroquine. My first instinct was, well, let me give them the real hydroxychloroquine. Maybe they got placebo. But what about if they got the placebo, if it wasn't the placebo and they already got hydroxychloroquine. So now I'm double dosing, right? So I was in that situation and guess what? That's when I discovered, wait a minute, I got to up the vitamin C, I got to up the vitamin D, I got up the ivermectin to increase their oxygen. It was all on the frontline of treating these people that didn't want to go to the hospital. They were dying. And I have videos of that, of people that were couldn't breathe, short of breath, oxygen's in the seventies, eighties, and they survived. Everyone survived. So there was a role for hydroxychloroquine. Also I had patients that were, if you'll remember patients sometime in August when Pierre Corie and FLCC all started writing ivermectin, we had two groups, right? We had the Peter McCullough frontline, myself, we were the hydroxychloroquine, Z Pak, vitamin C, D and zinc. And then we had another group Pierre Corrie and the FLCC that was the ivermectin. Right. I was kind of in between because I was running both trials. And in July we submitted the ivermectin doxycycline trial. So I discovered the power of ivermectin. When my patient was dying or I didn't know what they got. I said, well, you know what? Let me give them ivermectin. When one of my patients was heading to the hospital and he had thirty six milligrams of ivermectin and I told him, Hey, your oxygen is in the sixties. Why don't you stop at McDonald's and get like, you know, hamburger, which was like a fatty meal that I thought of garbage food, but it didn't matter, you know, happy meal before he goes to the hospital, what the hell? And he took the thirty six in one shot. By the time he got to the hospital, his oxygen was 92%. The doctor said, whatever doctor he's in is doing, just follow her. And I'm like, woah, thirty six milligrams of ivermectin, but I just gave him hydroxychloroquine. You know what I mean? So that's when I realized the combination and in those sick sick patients, you really have to do everything to save them. The problem is that, we're working with these guidelines and these hospitals are supported by pharmaceutical companies. When Gilead pays a hospital a $100,000 per patient to try the drug, you know, the hospital's going go, you know what, let me give, you know, let me give remdesivir, right? They're not going to give a cheap drug like hydroxychloroquine or ivermectin. It's not on the road. Speaker 4: One of the awful things Will was the you know I remember talking to Deborah Birx and saying hey you know this is a respiratory virus it's maybe alive for five to seven days you can't use something to affect the RERP at day 20. It doesn't make any sense. And literally, I think a lot of people had no awareness of the life cycle of respiratory viruses. She clearly didn't. And it surprised me because a lot of people were not aware of the fact that a respiratory virus is basically all of them, adenovirus, rhinovirus, all of them are very short lived. And somehow that that still they pressed this whole remdesivir thing when it clearly couldn't be effective. So, it's crazy. The other thing about your comment is that the combo does help because mechanistically there's different ways that they're affecting. And I think one of the things I like late in the disease, ivermectin and hydroxychloroquine affect neutrophil extracellular traps, ivermectin blocks the CD-one 147 receptor. They can both help in the late disease when it was really bad delta and the first few variants where you had all the blood clotting. I think they both could have, been useful. But of course, they use those toxic doses. So, of course, hydroxychloroquine giving toxic doses was a big deal. Speaker 1: But but even there, let's talk about the the toxic dosage. Even there, you know, is there such a thing as a toxic dose? Right? Like I asked my husband who's a cardiologist and I said, have ever checked for levels of patients that have been on a hydroxychloroquine? He's like, no, never. Speaker 4: And it Speaker 1: affects my pathologist because yesterday sent me a death certificate of one patient where the doctor put death from hydroxychloroquine. And I said, I called my pathologist and I said, how do you check that the patient, how do you know that the patient died from hydroxychloroquine versus the virus versus another co infection? Nobody did a stool sample. Nobody called me and said, we'll test the microbiome to see if there's mycoplasma in there. It could have been a combination of mycoplasma in there. They could have been other viruses. These people are immunosuppressed in the hospital. Of course, they're going to have other viruses. The nurse comes in, there's different strains of COVID that came into play. So all that played a role. You know, it's fascinating to me that my pathologist said there's no guidelines, there's no levels where you say that there's a toxic level and the patient died from toxicity of hydroxychloroquine. But I'll jump to Xavier because Xavier did an intense research on that, on the papers. So go ahead, Xavier. Then I'll Thank Speaker 3: you very much, Kevin. I'm gonna try and summarize what we did. And by way of background, I think it's very important to explain the situation in France right now because Didier Raouf, the lead of IHU, Professor Raouf has been under attack by a large number of government officials and also doctors to try and discredit the work they have done. That study is part of the defense, that they're trying to put in place in order to discredit the work. Now, the way we worked with my team of scientists around that, it's a combination of, medical doctors and mathematicians, statisticians, because we looked at all the biases And here you're talking about the biochemistry mechanism with ivermectin and hydroxychloroquine and how it works. But this study is a calculation. And one of the, we've basically we've broken that into three parts. Part number one is what are the data miscalculation that we've actually observed? Part number two is it fabricates some results and therefore these results are false. But the most important element is that it's been peer reviewed. And for me, it demonstrates the failures of peer review. And here we have to improve the peer review process in order to prevent papers of these natures to actually get into that. So the study, if I actually looked at what we have actually identified as data miscalculation, Of course, the results of sixteen thousand deaths calculated that should have been calibrated to reality. And it's enough to actually look at pharmacogenes data and these are in existence. So one of the buyers is they have not actually calibrated this to reality. And just that as a mathematician, from my perspective, it demonstrates that these individuals are not trying to represent what happens in the real world, they are trying to represent what they want to actually demonstrate. And that in mathematical modelling is called a dependent model. Now the second element we've looked at is the actual data of each individual country and the data for Belgium, because there's a Belgium doctor called Veronik Bodu, she's actually very much in tune with, what happens in Belgium. And she worked out that it's impossible, okay, that the numbers that were found out for deaths that they model can actually, be that number. There are several factors, there's published data, there's research that we're actually done and conducted. And these figures do not correspond to the data. And that's one of the bias because if one of the country that you try to represent an overestimation of deaths or an over death estimates is wrong, then definitely you will end up by having biases in the results and the result being fabricated. Now, if you look at the code guidelines for ethics of conducting research, there are two elements that should form the basis for a lead of concern or retraction because here we're talking about structuring response to a published letter in a way that we can address each of the biases and that we make it easy for the editor to look at the research and say, okay, well, on balance there is an issue. Now you have to imagine it's very hard for a chief editor to retract a paper because it basically shows that you've done something wrong and you have to question this. And it's very hard for them to actually accept. Speaker 1: Unless it's a predatory journal. And it's very easy to bypass the peer reviewers and go straight to the editor, pay him money and we track the journal. Speaker 3: So what we did is we structured our response to the editor in a way that we can demonstrate that there are data inconsistency and miscalculation and that the results are fabricated. Let me just give you an example. They calculate the mathematical function that they use in order to calculate the estimation of deaths that would have, I would say would, because it's not real, that would have died from, absorption of hydroxychloroquine, uses an ingoing hypothesis, which is the odds ratio issued from the Axforce Research of one point one one. That basically means that, eleven percent would have died, from absorption of hydroxychloroquine over, standard of care of placebo. We don't know. Now, if you look at the Axforce research, it has basically two types of studies within that. It has studies with low dose and has studied with high dose and they only use the bias or odds ratio of 1.11, because if they had used the other ratio from low dose, it would have been 0.97 and therefore their model would have actually failed. So when you use a constant and you apply that 11%, you will only find this. You cannot find zero. And so that in itself demonstrates that the model they used is totally biased. The other element is a lot of the data are dependent on one another. So for example, and I'm not a medical doctor, however, I've tried and understand the process that a patient has. If you deprive a patient from early treatments, then it has a loss of chances and it has a chance of progressing to ICU. That's a probabilistic model. And of course, some patients, they actually recover by themselves, but then for those that aggravates, they have a probability and then they are hospitalized, they have a chance to move to ICU and they have a chance of dying. Now, the model that they use is therefore not taking into consideration the fact that patients may have had a loss of chance of being treated early. And therefore just this, which is not used in a model, demonstrate also the weakness of any form of probabilistic model. That in itself, it's a very high level summary without going into the medical element that you've just discussed. The fact that we do not have pharmacoviligence data for hydroxychloroquine deaths that the high dose of course would have to actually be controlled. And this is what actually has happened with the DDRO sort of hospital in Marseille. They have controlled the patients to whom they gave ACQ. And there is a 30,000 strong databases, which has been published of all the patients that have been treated that demonstrate that there is a significant improvement or there's an odds ratio of something like zero point five five over, the chances of, of deaths. So that's, the authors, cherry picked, they cherry picked countries, they cherry picked data, they cherry picked the references that they were using. For example, they are not mentioning two studies which are dramatically important. One of them is the Yale and Al study of 2020 that demonstrate the optimum dosage. Just that if you're a medical doctor and you do not know that study and you do not reference this, then by definition, for me, you do not want to know something that you should have known or you turn a blind eye on something and that demonstrate again some of the weaknesses of that. And the second, element is of course this OR calculation, which is derived at 75% from the recovery study. Now the recovery study has used a protocol of two point four gram of hydroxychloroquine salt. It's of course one hundred and fifty five milligram per tablet. So it's less in days, in day number one and it's 9.6 gram over ten days. That in itself increased the level of concentration, due to the long life of, the long life of hydroxychloroquine in the plasma. But another element that they should have actually learned from Yao and Hal is that in the lung cells, the concentration of hydroxychloroquine is something like 400 times higher. So therefore they are not deriving the elements of science that they should have derived when they are doing their discussion. So this OR is definitely wrong. Now I ask myself another question, which is why did they not apply this data to The UK data, to this model, to The UK data? Because they're using an OR, as their constant, the 1.11 from Axforce, which is 75% of its weight issued from UK data. So calibration number one is you would want to calibrate this to UK data. And the answer is quite simple. If they had applied this model to The UK data, then they would have found zero deaths. Or the estimate of deaths would have actually been nil because there is only one study in The UK that has given hydroxychloroquine and that is recovery. And recovery concludes that there is no difference between placebo and hydroxychloroquine. Now we know it's high dose. We know there are some issues with this. And however, that demonstrate that the odds ratio being non significant then there is no difference in efficacy and they also conclude that there is no death issues. Now we are not going to argue about recovery which I could do, it's totally different. It's also a bias study and the results are totally biased and for me it's another fraud. But if you're saying that there could not have been any estimated of deaths in The UK based on this OR calculation, then in my view that explains why they don't apply this model to The UK. Now turning to The U. S, there is another PhD in IT in France, Eminelle Dahl. She has identified she has looked at the data and she recalculated the data and they're estimated that there is something like eighty thousand, sorry, eight hundred thousand hospitalized patients in The US. She looked at the CDC data, over the same period and she cannot actually reconcile that data. So just simple data validation, data calibration, which is what you would do in any mathematical model, try to calibrate to reality is what you actually measure and calculate through your model has formed some links with reality and it has no link with reality. So we've prepared a letter which we've issued to the editor. It's now being reviewed. We work quite extensively on that. But for me, the third point, which is the peer review process is the one, that is the most problematic because of course here we know that these are just fabrication of results. Now, how can you fool a peer review process? Well, first of all, in peer reviews, and here it's totally blind. So I like blind things, but when a peer review process of this nature is totally blinded, it's very hard to actually look at how they actually did it and who did the peer review. In my view, this peer review has been done, it's complacent and it lacks a methodologist or somebody that would have a background such as mine that would have actually done not a medical read of this, but somebody that has no knowledge whatsoever of medical science and that just asks simple questions like I just did. Because what you see is what you get and in modeling here is garbage in garbage out and the garbage is pretty easy to identify just as I have done. Now I looked at the other processes from other journals, which are more transparent, like for example, the BMG. In the BMG, you can publish a rapid response, but you can also see the review process and the questions. You have an idea of the background of the individuals. Now I've looked at a number of studies and there's very few methodologies, there's very few mathematicians that look at these. And in my view, just by having somebody outside of your own field of expertise, doing the acid test, the reality test, would help. And that's where I believe there is some issue. So that's more or less what we actually identified are the major issues of this paper. Speaker 1: Thank you. That was very, very thorough. And I absolutely agree with you. Incidentally, feel sorry for Doctor. Raul because he is being attacked. And the same people that are attacking him and retracting his paper and my paper yesterday sent me an email showing me a death certificate of one patient that died from hydroxychloroquine. Of course, we know that the death certificate doesn't mean anything. It's really about the medical records. And secondly, toxic drugs, nobody in the, first of all, Brian, you and I are in California. Speaker 2: I'm in Arizona. I sit in Arizona. Speaker 1: I'm sorry, Arizona. Speaker 2: No, I'm from California, but AB 2,098 chased me out. Speaker 1: Yeah, I'm sorry. But you were in California at the beginning. Speaker 2: I'm in both. Speaker 1: Yeah, so at the beginning there was no, the patients were not getting hydroxychloroquine in the hospital. My hospital was not giving it. They had a thousand cases. Nobody was discharged. One patient wanted ivermectin never got in in the hospital. Hospitals were not dispensing hydroxychloroquine or ivermectin in California. So I don't know how they got that 880,000 cases. And that the majority, I forgot the number. Hold on. I will tell you here USA eight hundred and eighty eight thousand and supposedly five hundred and fifty one thousand were exposed to hydroxychloroquine. Which hospital was giving hydroxychloroquine? We have actually with us, Alan Miller, Doctor. Miller, who is by the way, one of the top clinical trial doctor in the country has been with me. We were pulling our hair at the beginning of the pandemic and he helped me write the protocol at the beginning when we were trying to figure it out. And, you know, Alan, I consider a good friend and he's been very righteous and he's been doing clinical trials like me for two decades almost, right Alan? And Alan's treated a lot of patients. So Alan, you want to talk about toxic drugs and toxicity of hydroxychloroquine? As an internist, you've written hydroxychloroquine probably more than I have. Speaker 5: I've written hydroxychloroquine for thirty years, maybe longer. If you go back to medical school, thirty five. I've never seen a patient die from hydroxychloroquine. In fact, when you look at, if you just think just logically, I don't know of any physician in The United States, or maybe globally, who writes any dose that would be remotely toxic at all. Doses of two hundred, four hundred, six hundred milligrams of hydroxychloroquine daily, every day, whatever you want to give, are not toxic. The drug is cleared very quickly. You know that because it's a BID drug, right? If it was a drug that had had a, you know, a large volume distribution, it also had a half life. What I'm trying to say is it basically is cleared quickly. And so to claim that it's toxic is actually somewhat ludicrous. The interesting thing about what you said, and I remember when we were looking at these papers, is it is almost impossible, I mean, literally impossible within weeks to collect data on ten, twenty, thirty, forty, 50,000, 100,000 patients. In normal clinical trials, I've done about 125, or so clinical trials. I currently have about eight or 10 in my office, mostly cholesterol, some diabetes, some hypertension. It takes years, I mean, sometimes to collect all that data, and that may just be on two or 3,000 patients. So to do any type of retrospective analysis on thousands of patients at hospitals or anything all over the globe is absolutely a farce. And whenever you see that, that immediately will tell you that that is a garbage paper and just throw it through the trash. It means nothing. As far as the death death certificates, death certificates in hospitals are often, done by the ancillary staff. A doctor will come by and just basically sign his name. When a patient is very acutely ill and passes away in an intensive care unit, there are hundreds of three things that are going on and many that we don't even understand. So when we actually write death certificates and you say hydroxychloroquine causes, that would be impossible to actually validate. So I think, you know, what we should probably start doing is just calling out things as they are. The papers are frauds, the people that are out there are criminals. They're basically, you know, shills for certain, you know, areas of pharma. And that doesn't mean all pharma is bad. Okay? There are some people in pharma I know that are really good and really trying to do what they think is right. So I I think in this scenario, you basically have Speaker 1: But they're being killed by the people that are doing stuff like that. Speaker 5: Oh, for sure. Speaker 1: And the lobbyists are not doing a favor to pharma by doing stuff like that. Right? Because ultimately who's controlling this and supporting pharma is the lobbyists, right? Lobbyists control both sides of the politics. We saw it. That same lobbyist firm control, supports Trump and Biden. So both sides are playing this narrative, which is convenient because it creates a controversy, which sells drugs, which sells vaccines. Remember during the elections, was Kamala Harris and Pence were basically talking. The three questions were vaccines, vaccines, vaccines. Marketing 101, you repeat things three times, it gets branded into the person's brain. That was not an electorial questioning. That was a marketing ploy to get into our brains vaccines before the vaccine trials even came out or while the vaccines were Speaker 5: Beyond vaccines. Speaker 1: That's the other thing. You know that I have been in the clinical trials too long, you know, 150, 120 for you, 300 plus for me. I did vaccine studies. I just got a trial for a vaccine study right now on my desk. And I'm looking at it and I go, Oh, that's a real vaccine and not a genetic sequence, right? Speaker 5: That's correct. Speaker 1: There's a difference. They're trying to shove down our throat this new technology that is dangerous, that has not been tested. That if you look at mice studies or rat studies where they are given, you know, messenger RNA, they are chewing their arms. They're in such pain. Animal studies are telling you that, you know. And let's go back to the original animal study on these vaccines where they killed the monkeys after one week. What can you get of data from animal studies? Couldn't you let them live a little bit longer to see if they develop something? So there is a fraud that occurred in medicine. There is, I hate to say this, but it's like, again, the economy, it's like the vaccine could make more than the early treatment and they weren't ready with Paxlovid. One question that I have, and I know Brian you've used it, Alan you've used it. What happened to the monoclonal antibodies? They came and went. I was, my patients were doing great with that. What happened to that? So it didn't fit their stock that they were trying to bring up, right? That's what it's all about. And here's the problem. When we interfere with research, we screw ourselves up, right? Because ultimately we're cheating research. We're cheating us as the patients. My aim when I ran this trials was to see the truth myself. Had, and I think Alan, when you started treating patients, you were like, wait a minute, these vaccines are a new technology. It's not really a vaccine, early treatment. How many patients did you treat at the beginning? Remember in March, were collecting my stools. Alan Miller was my collector of poop. He was going to houses and saying, Doctor. Ozan is looking for the virus in your stools. And he was collecting them for me. So, you know, he risked his life on the frontline. He was in front of everybody and he saw firsthand these people were surviving, right? Did you lose anyone in this pandemic, Alan? Speaker 5: No, I probably treated 1,000 patients maybe. I don't even remember. I lost track. I didn't lose anybody. In fact, I saved one of my friends who's in a band. He had really horrible GI COVID. He was really sick. And, we got gave him hydroxy and Z Pak. And within, forty eight hours, he was basically better. And he gave me a guitar. I mean, so Speaker 1: I know you with guitars. Speaker 5: Yeah. So I collect guitars. So, you know, I I didn't lose any I know Brian, we don't we've never really met, but we've heard of each other. I just haven't seen it and I don't expect to see it. And I think if you look at how these drugs work, especially hydroxychloroquine is a zinc ionophore and ivermectin with, you know, blocking import protein and all the other things it does, these drugs have zero ability really for toxicity. And they're about as safe as they come, which is really crazy considering that remdesivir, which was pulled from the Ebola trials, as you may remember, because it basically caused renal failure or respiratory failure, some other kind of failure, organ system failure, in about fifty to seventy percent of the patients. It's really, unbelievable. But listen, I've got to go back and see some more patients. I'm in Atlanta. I'll get back on a little bit. Speaker 2: Alright? Thanks doc. Thanks. Speaker 5: No problem. No problem. Speaker 2: And I'll jump in and say I had zero mortality, zero hospitalizations, And we're living fear with the medical board by saving our patients and preventing hospitalizations. And that's what's insane about that. Right. And that's why I started looking at the insanity. I would love to hear both of you, Xavier and Sabine. What about this draws in paper that came out PCR? They submit that from my understanding and looking at it, didn't sleep for a week when I read this that they submit on December 22, It gets published December 23. What kind of peer review can you possibly do in a few hours and then have press releases all over the world the next morning? I mean, just from a common sense perspective, you go. Speaker 1: That's what they do. Right? That's what they do. They publish this, big title like seventeen thousand people die from hydroxychloroquine mortality, right? They publish these papers. They go all over the media because they control the media. Remember the lobbyists control the media, both sides of the media, right? Fox and CNN. So they control the media and they push all this narrative out there. Everybody only hears hydroxychloroquine mortality, right? Then they're gonna retract it in about probably a month because Xavier is gonna make some noise. I'm gonna make some noise. You're gonna make some noise Brian. And then they're gonna say oh wait wait wait, you know, we got to retract it. But they're never gonna report it to the media like they did with the Lancet study. Did it go did the media start talking about Lancet? Oh that paper was fraudulent. No. Everybody still thinks that that Lancet paper didn't work. Know that that was a real study that hydroxychloroquine doesn't hear. It doesn't work. I hear it from like friends of mine that are in academia and they're like, they're quoting that paper. I'm like, didn't you know this paper was retracted? Speaker 2: Not only that it's even worse. Like Paul Thacker just was showing that this six foot apart rule came from an article someone wrote in the New York Times. Like now you have the World Health Organization referring to the New York Times as their source of They worldwide Speaker 1: get their narrative. Right. It's interesting because Speaker 3: Sabine, if I may interject, one of the issue here is called, you know, in money, you have money laundering. Here what they are doing is they are laundering scientific papers. And that's definitely a very serious issue. Now, as a director of publication of the media, if you look at the charter, that you have is as soon technically speaking, as soon as you are aware of an issue, that a paper is wrong or that information has changed, then you're supposed to actually take stock of that and to actually modify your paper. Now they are not doing it because they are not following their own ethical guidelines. Because of course, as you mentioned, they are not doing journalism, they're doing propaganda. Now with these papers, one of the issues that we actually raise in our article is the fact that it has already received a lot of public attention. By definition, it's throwing a really bad eye on science because it creates wrong signs, it brings wrong impression, because the journalists that are interviewing these people are not even asking questions. They are just taking the results and they are just saying, oh, there's seventeen thousand people that have died. Now, did you check that there has been seventeen thousand records? It's simple mathematical calculation. And for me, this is the worst part of it. That's why I say we have to tighten the review process in order to avoid having those paper get out. And that's where for me we have the biggest issue because we will always end up by having people trying to do fake science. That has been forever the case, but the peer review process should be a barrier, a protection against that. And for me, that's where you have the biggest issues. And for doctors, the other element is that it throws a very dishonest evaluation on the treatment that you have been using. And that's the conclusion study of the paper that we wrote is that, if you're doing fabrication of results based on false data, what you're doing is you're simply bringing a justification and to evaluate a treatment which is a cheap treatment. And of course we all know that if you are sort of working with a pharma company you want to actually sell very expensive drugs and you don't want to actually sell cheaper. So this is quite normal to actually throw, a bad eye or a bad sort of feel, bad flavor on these treatments. And we have to prevent that from happening. Speaker 1: Yeah. And I think it's not, think about it. What happened during this pandemic, it's not only hydroxychloroquine and ivermectin, it's even vitamin D and vitamin C. And this is why, Kate, are you able to talk? Because Kate was at the CDC, she presented tons of data on vitamin D, why we should be telling people to start taking vitamin D to optimize their vitamin D. And that never went out. That was never in mainstream media. That was again. Speaker 2: And that Fauci had given a talk on the benefits of vitamin D years ago, and now all of a sudden he doesn't know anything about it. Like how does Speaker 1: He that talk about vitamin C and D at some point during the pandemic. Speaker 6: Yes, did. So did Doctor. Frieden also talked about vitamin D during the pandemic, I think in 2020. Yeah, I wrote a little white paper at the March 2020 and fed it around. Worked on anthrax at CDC. I was one of the main anthrax doctors, so if you put Hendrix and anthrax into PubMed or anything, my name will pop up a lot. But I had done nutrition research before when I worked at a state health department. I had done a lot of stuff on folic acid and B12 and birth defects, so I was interested in nutrition. And then I also gave a, besides sitting around a white paper, I also gave a talk to a bunch of epidemiologists at CDC at the 2020. A lot of people were interested. A lot of people would say, Oh yeah, of course, I am on vitamin D. Everybody was always telling me that they were taking vitamin D. So I was just super disappointed that we never said anything about it, and we never looked at it because I don't really count me looking at it in my spare time as the agency looking at vitamin D. There is nobody assigned to look at that. There was nobody assigned to, look at other early treatments. I mean, when I say look at it, I mean, what I did on the anthrax was always, you know, systematic reviews where we would, you know, spend hundreds of man hours or woman hours, whatever, evaluating data, but we would, at CDC, we just kind of refer to FDA or NIH and say they had had a website. That was it Speaker 1: know, And a little you presented my data of the lost microbes to the CDC, right? Do you want to talk about like their experience of the microbiome? Speaker 6: Well, no, I just, I presented it to a few people. I didn't really present it to a large group, but Speaker 1: So it's interesting. So, but don't you think like Kate, that there's a lot of, you know, that these agencies are captured in a way by the politics, by the direction of where the government is going? You know what, I don't speculate. Well, that's probably Speaker 6: All I can say is what happened is that we didn't Speaker 1: Yeah. Won't go into the Speaker 6: There is time looking at anything like that. There was no nobody devoted time to it. Speaker 1: Well, you for all your work and everything you've done at the CDC to try to like, you know, bring on vitamin D. And, you know, I think doctors appreciated it all over. Xavier had to leave. Brian, do you want to kind of like for me, a couple of things on the paper, just why these people died. The hospital setting is not the greatest setting full of viruses. The nurses are waking you up on the hour to take vitals. The stress that it kills your microbiome. Your exposure to multiple strains of the virus and other viruses. I think that's the most common reason why people die in the hospital from COVID. So I think this paper as Xavier said, and he had to leave is fraud. And we have to start putting pressure on our government to stop interference with research and to stop publishing papers that are so fraudulently, so obviously fraudulent right out there. And we got to stop the retraction of papers that are not fraudulent. Papers like Didier Raul who did the work meticulously. You know, all that's doing. And if pharma ever listens to this is all, and Alan knows because he's working with pharma every day. And I tell them the same thing. I say, look, ultimately what it's doing is it's removing little by little doctors from trusting your drugs. Every day doctors are finding new ways to treat their patients. They're going into the nutraceuticals. They're going into the food alteration, the stress, the multiple different innovations that is going to remove the need for pharmaceutical products. I mean, I see it, I go to these, I speak at these conferences from academic conference conferences that are basically longevity conference, A four ms. They're all academic in my opinion. And these doctors are looking for other ways than pharmaceuticals. So I think if we continue in this path of retracting good papers, which we're all seeing because we're in the business of analyzing and criticizing papers. Remember Brian, we used to do a gut club together. Like as doctors, we would take a paper and start criticizing it and analyzing it and saying, okay, well this is why this is bad. And it doesn't mean anything. Let's look for another. Science is about prove me wrong, right? Is it right or is it wrong? But ultimately you don't retract. You leave it there as a symbol of a bad paper, right? Unless it's fraudulent like these papers. So, you know, the fact that they removed Doctor. Raul and all these papers on ivermectin and doctors have seen firsthand patients being treated and have seen, I've seen the effects of ivermectin on the microbiome. I know that I'm on the right path with those drugs and using those drugs. And I've seen their safety measures. So at the end of the day, start need telling if it is a lobbyist move that's pushing all this, we need to tell them to stop because it's killing the whole industry that is allowing us to do good research. Alan and I did not want to step into the pandemic and start writing a protocol at the beginning. And I wrote my protocol with my team. That was 20 fourseven for like ten days of hundreds of pages that we had to go through and the articles that we had to go through. You know, this was not easy. We didn't want to do this. And then me spending my money on this research, we didn't want to do But we felt like we needed to see the truth. We need to have righteousness in medicine and in research again. And we need to trust our doctors and we need to trust the science and we need to trust the research, but we need to trust the science understanding that science can change and evolves, right? And we need to be open minded on that. Speaker 5: You know what's interesting? There is a physician who's a rheumatologist in LA. I don't know his name. Think he may have retired by now. He was the world's largest writer of hydroxychloroquine. And when I say the largest writer, apparently he'd written over 2,000,000 pills of hydroxychloroquine in his career, something close to that, some ridiculous number. I mean, that's obviously thousands and thousands of patients, right, that they've seen in many refills. He would have been the best person probably on the planet to discuss anything about hydroxychloroquine. And not once did anybody ever interview him, talk to him, or maybe he just decided he'd want to get involved. But if you really wanted to talk to an expert, he was just down the street from Sabine. Sabine, Speaker 1: do remember Speaker 5: his name? I mean, he's really Speaker 1: You know, and I had him, I actually quoted him when I wrote the protocols. I actually quoted him when I wrote the protocols because I said this guy wrote the most hydroxychloroquine. I'm trying to find it. So I'll skip the Brighton I look forward Speaker 3: to it. Speaker 5: It's a shame that this guy, that he never was actually asked because he would have been probably, would have put the whole thing to bed. He was truly the expert. Well, think even if he did come out, Speaker 1: they wouldn't have given him a stage. Very difficult to get up on that stage and start accumulating followers and making enough noise to be noticed. Speaker 5: Yeah, I agree. But it's really astonishing. Eighty percent of the doctors in our country have lost their minds. I mean, they really have. Speaker 2: That's generous. Speaker 5: Yeah. Well, I think there's still Speaker 2: Doctor, you're generous. You're nicer than me. Speaker 4: I I think there's still Speaker 5: 20. I I will tell you a little story, just a little caveat. I think Sabine knows this. Regarding the mRNA gene therapy shots, it hit home in my call group about two and a half months ago. One of the doctors in my call group on Friday got a booster. Saturday didn't feel well. Monday night died of acute MI. And, I got a text on Tuesday morning from the guy, one of his partners, and his partner who was kind of a shot guy said, you know, Alan, I think you're right. I'm pretty sure the shot killed him. I think, this is just one example, but, I just wanted to kind of throw that out there that it hit home. Speaker 6: How old? Speaker 5: He was 61, basically healthy runner, no big nothing. Speaker 6: Wow. Speaker 5: And, I don't think he took any medications. Yeah, and then I've been to another physician, about 20 miles from me, about three or three, maybe four or five months ago, same thing. So, you know, when you hear these, when they talk about anecdotal. Yeah, Speaker 1: I mean they Speaker 5: They don't mean anecdotal. You just need basically just stories and the reality, and that'll tell you what's really going on out there. That's how they used to do it years ago. Speaker 1: Yeah, I'm bringing the next show, Brian, you and I will do, and Alan, hopefully you'll be on it. I'm bringing in a couple of patients. One of the patients that I, yesterday, my last patient of the day, healthy woman, got the vaccine and the booster. Four days after the booster she's paralyzed, wheelchair bound. Speaker 2: Really? Speaker 1: And four days. Now, Alan, you and I have been doing clinical trials long enough to know that that's a serious adverse event, right? Nobody reported it. So nobody's looking at it. It's like, oh, no problem. A good Speaker 5: site will eventually report that. I mean, will eventually have to come out of me because that, Speaker 1: I mean, we would Pfizer reached out to her and tried to mitigate to not have her speak too much. But you know, we're seeing it. I'm seeing it every day. I mean, I have hundreds of people that have been vaccine injured. Speaker 2: I There's zero question about it. I mean, I've seen it. I have four personal friends, docs, all triathletes, super fit, myocarditis, atrial fibrillation, pericarditis. Guys I've interviewed on the podcast, we've lost 150 pounds with this huge cardiac workup before they start doing low carb and keto stuff. Now all of a sudden have ejection fraction of 32%, you know, after and they couldn't talk about it. Why? Because they'll get fired from their job. Right. Because some of these people have huge profiles. If you don't say you push it. And so a good friend of mine actually who had damage to the California Medical Board, he's like, you're telling me that I can't say anything about, you know, adverse reaction that actually happened to me the day after I had this, right, who was super healthy running triathlons. So when you start seeing these things and the adverse effects after you've already had COVID and then get the vaccination within a month or so, horrific side effects. Right. So these are things as doctors, we have to evaluate and look at. It's not about being political. It's about what it is and what we're seeing. And I think that's the problem. I I have a podcast, Life's Best Medicine. I had it was taken down four times. One, Peter McCullough within seventeen seconds of being posted. Right. Everything he said was factually correct and has been proven. Another with a hospice doctor when I asked about the case he seen in the last month. Right. All factually documented, no one contacted him or me, but it was taken down for medical misinformation. A good friend of mine, Patricia Lee from USC, who presented what she was seeing to the FDA, wrote five letters with no response, came out as a whistleblower that was taken down for medical misinformation. Right. These are all doctors talking about what they're seeing in clinic. It's someone at YouTube knows this medical misinformation. Like what med school do they go to? What clinical experience do they have? And that's what I mean when we start seeing these things. And it's important for both of you that you didn't just pull these protocols out of your rectum, right? There was data on that before from the NIH and all these people who were saying this is what works. And then you didn't just pull it out, go, hey, let's just randomly pull three drugs and try it, you know? And so just looking at this study, the things that came to mind that and you too may know better than I do, but they never mentioned that they were giving zinc with the hydroxychloroquine or is it the max? So that was never given. And we know that it acts as an ionophore from Zelenko protocol and all these other things. How long did you wait to give the drug? And so even in this study says we cannot say that that prophylaxis or early outpatient, we can't make any statement about outpatient treatment, just hospitalized treatment. So once like we all know, if someone has shingles and they've had it for two weeks, you're not going to put them on an antiviral. The virus is gone already, like Doctor. Urso pointed out. And so I think all these questions and the other confounded, I don't know, may be in here, but you're better at reading than I am. But I didn't see anything about how many of these patients were also given remdesivir. Right. Because I only know personally Speaker 1: That's the other thing. Right. How much oxygen, did they ventilate those patients? What other medications did they give them? Were they interact? Was it interacting with the hydroxychloroquine? Heck, what nutrition were they on? I said that on Twitter. I said, did they all drink orange juice? Because if they all drank orange juice maybe we should blame the orange juice on the death of those patients. So I think there's so many factors that were not looked at. And again, you know, patient comes into the hospital, he's in the intensive care unit. His lung is necrotic. Okay. I mean, we've seen the pathology of these lungs. It's dead tissue. You cannot regrow a dead tissue. You need a new lung, right? So you're really giving medications to a dead person that you should have interjected early on and treated early. But I will tell you, it's interesting this whole treatment early. I've had people that I treated a month later and I gave them massive amount of hydroxychloroquine and ivermectin and vitamin C, D, zinc and Z Pak or doxycycline. And you know what, they survived. I think it's at the level, and let me just say also, is it the strain of the virus that matters or is it really what your microbiome is all about, right? I had a guy that was in the middle of nowhere America in the forest, he was far from a hospital. Oxygen was desaturating, you know, and I did not, I said, what do you have? Do you have ivermectin? Do you have hydroxy? Nothing. He had vitamin C and vitamin D. Well, I managed to keep him alive till he got his ivermectin with his oxygen up with just vitamin C and vitamin D and what he had, you know, of gut health in his fridge. You know what I mean? So when you understand the microbiome is really what's gonna help you survive and that it's really, you need different bacteria. You start treating differently, right? Because you start saying, okay, well this kid has a lot of bifidobacteria. I'm not going to worry about this kid. So I'm not going to, I'm going to give him vitamins and then I'm going to give him some ivermectin if he's too miserable or doxycycline. But these severe patients, I'm going to pay more attention to them because, and I'm going to be more aggressive with them. Speaker 2: Well, that's the point when you hear it. When I hear you saying, look, have a patient with a stat of seventy percent goes up to ninety two percent within an hour or two after this treatment. You go, okay, we got to look at that at least. He's crazy. Like he got better. If he died, then you go, okay, that wasn't a good treatment protocol, right? When people are getting better, you have to sit back and look and go, wait a minute, there's something to this and not just say it's crazy all of a sudden. When you have people like, you know, I'm a fan of Doctor. Urso, Pierre Corre, they're crying going, look, we're doing this with patients and they're getting better. Let's at least look at this and like, no, we're not looking at it. It's insane, right? Speaker 1: Look at I took pictures. Okay. Pictures of my oxygen saturations of my patients. Who the hell takes pictures of patients with 73%? Most doctors would freak out. Right. I'm like, you know what? Take a picture because I know it's going to improve. Okay. This is the by the way, you could see the wedding band. It's the same guy, you know, same guy, same finger. I didn't fabricate this. Here's the wedding band again, ninety five percent. Okay? I didn't make this up. I mean, these people, I saw it with my own eyes. You know, Doctor. Barodi has a sentence on this. He says, if you see a Martian in your backyard, you're gonna start believing there's life on Mars. You don't need to do a placebo controlled trial to see if there's Martians, right? You're not gonna dissect the Martian. You're gonna say, Holy cow, there's a better Martian in my backyard. There must be life on Mars, right? This is a Martian to me. The oxygen going up was a Martian. Like holy cow ivermectin did something. And here's the thing, a physician that sees that needs to, and then you don't see it on another patient. You need to understand why. Here's what I discovered. If a patient's drinking alkaline water, it doesn't work. Because what is alkaline water doing? It's killing your microbiome, right? So I can't increase my bifidobacteria with ivermectin, which by the way, when I published that hypothesis of ivermectin increasing the bifidobacteria, I already knew the answer, right? That's why I published the hypothesis because I already had seen it, right? I saw the bifidobacteria was zero. And then after I give my patient ivermectin, bifidobacteria went up. Okay. And in fact, I published it not in a public, know, now I'm not publishing in journals anymore. I'm just writing abstracts. It's much faster. And I present them at the American College of Gastro and have gotten three presidential awards in three years. My peers are appreciating it. I love my research. They're listening. They're paying attention. I don't need to publish anymore, you know. And it's from now on people are gonna just have to follow my abstracts on my website, right? So to see the truth, which is a shame. Speaker 2: Well, and I see my patients getting better doing what you're doing. And I think that's the bottom line is like our responsibility to our patient. I don't really care what other doctors think. I really don't care. I don't care what the CDC thinks of the World Health Organization. Now, the problem we face, all three of us saying we have zero mortality from COVID is like, okay, ninety nine point nine percent of people survived COVID. Right. When we look at the data. So who was that dying and sitting down with Peter McCullough? It was the morbidly obese diabetic, you know, other diseases that were that were going to take these people out. So you go, okay, if I could prevent them from getting to the hospital, I've saved a life. Probably the only person I know of in my of anyone I know, that I personally taken care of or friends, family, neighbors, whoever I've come in contact with acquaintances. I only know of one person who died, who was getting ready for discharge. He was morbidly obese diabetic, and they put him under Envisivir the day before he was getting discharged. He decompensated, went into renal failure and died. That's the only person I know of. Right? So you look at and go, was it the remdesivir that killed him? I don't know. But he was getting ready for discharge and the paperwork's very clear on that. And he had every single risk factor of dying of COVID. So it's when you start looking at like that, it's like, oh my gosh, was getting in the hospital going to be your reason for dying? Know, was that going to was mismanagement in the hospital? I don't know. I can't judge that because I'm not a hospital doctor, but I've talked to a lot of them and I've talked to a lot of nurses. Go, there was a lot of questionable stuff that Right. And especially if this, know, we have an issue is that every single person went to the hospital, a PCR test. Well, no matter what you're there for. And the problem is you're going to it's a false positive. Like if you are asymptomatic and you get a false positive, it's like a ninety four percent false percent of false positive, right? If you're asymptomatic. Speaker 1: But here's the thing, the PCR is just a portion of the virus, right? Speaker 2: Correct. Speaker 1: It's a cheap way to analyze. We analyze stools and we looked at the whole entire genome. In fact, that data is coming to see whether the strain mattered or the level of Bifidobacteria mattered. I'll wait till after the elections because right now this is like very bad time to start publishing stuff, which is too bad by the way, because my research, a lot of it would help. You know, I'm a Malibu physician. I treat celebrities. I treat billionaires. You know, I mean, nobody's put me on people magazine of killing them, right? So clearly I'm doing something right, right? So ultimately my way has some methodology to it. I've been doing clinical trials, over 300 clinical trials. I've read all these protocols. I have an insight that nobody has. And on top of that, I'm doing research on the microbiome. You would think that people would wanna know how did I come to like lose no one? How did I come to publish on hypoxic patients? You know what I mean? It's unbelievable to me that the people that spoke this pandemic were the people and the experts were the people that stayed in their basement. You know, I think of like, you know, Doctor. Jaw, how many patients did he treat? He was talking from his house. I didn't see him in the hospital touching a patient. It's a different story when you are on the frontline treating patients, you discover things, right? You discover, well, first of all, you don't give hydroxychloroquine with a full stomach. You actually, it's better on an empty stomach because it gets into the cells with that and changes the pH of the cells to alkalinity. So when the virus gets in, it gets killed. Well, you learn that so you're not gonna interfere that mechanism with food, right? You're not gonna give ivermectin on an empty stomach. It gets absorbed better with a fatty meal, Right? So there's different timings, right? Like when I did my protocol and I treated my patients, there was a different time factor that I gave. And I started learning like, how do I treat better? How do I, you know, towards the end I was so after Delta, Delta kind of killed me with so many patients. I think I had like 50 patients a day sometimes. And, you know, one of my friends, Nina is on there. She'll tell you, she would be texting me all the news and I'm like, I don't care. I don't care who's going to be president. I don't care who's politician. It doesn't affect me. What affects me right now is me surviving and then my patients surviving, right? So after Delta, I was kind of like burnt out and I was just becoming so aggressive to treat everyone because I wanted quick treatment to be done with the patient, right? Because you don't have the luxury on the frontline treating 50 patients a day to say, okay, I'm gonna hesitate. And let me tell you, I was not the nicest physician with these patients because if they hesitated and they're like, well, I don't wanna take the Trump drug. I was like, okay, you know what? Start digging your grave. It's not my problem. Done. You know what I mean? Because it's a patient doctor relationship. I'm here to save your life and I don't mind being your soldier and your captain. When you go to the army, the captain's telling you do sit 50 push ups. He's doing it to strengthen you to make you a warrior, right? So I don't mind being that captain to my patients, but at the same time, and it's not because I'm confident or what I Well, it is confidence, but it's not because I'm arrogant. It's because I'm confident. I know what works, you know, follow my protocol. I had one of my patients who's like a high influential patient. I actually had him on Dennis Prager and he didn't want to take the hydroxychloroquine for like, you know, a week. Like he was hesitating. And then on Wednesday night at 02:00 in the morning, he's calling me. He's like, I can't breathe. I'm tight. I'm going go to the hospital. I'm like, are you going to take the pill or not? And then within four hours he was breathing again. And he's like, Oh my God, I was so scared for a week to take this pill. And now I'm breathing again. Do you know how many patients said that to me? What killed me is like the people that were so anti because they made it political, right? And again, on purpose because the lobbyists are controlling both sides of the politics. What killed me was when the people that I treated would not tell anybody else that hydroxychloroquine work. And to me it's sort of like, look ultimately I treat you so you tell someone else and save another life, right? It's kind of like pass the baton. Like when you saw these protocols and you saw they work fine, you were telling other people. Speaker 2: Well, know, I'll tell you. You know, I'll tell you. You know, I had the opportunity to sit down at a barbecue with Peter McCullough. Brian Tyson is probably treating more people for COVID in in California than anyone. And we talked and Peter McCullough, they were impressed because I didn't know. I didn't wanna go. And I kinda just go, I'll just meet this guy and see what his deal is. Anyways, goes, Brian, what's working for you? What's about not working? I want to know what's happening in California. He wasn't saying, here's my protocol, push this, right? And so Brian Tyson was the same thing. So they both helped me out like, hey, want to help my patients. As an example, ivermectin, I've used it in the third world. Do a lot of volunteer work. We use it for these kids for parasites all the time and they get dramatically better. Their asthma gets better, their eczema gets better, their mood gets better. Everything gets better. Speaker 1: Right. Speaker 2: And it's because they had an underlying parasite, right? So one of my patients comes back, she's having GI complaints after being overseas. We test her stool, she's positive. Treat her ivermectin as a treatment. Pharmacist refused to fill the medicine. And I had to argue with the pharmacist. She made me fax over the result of the stool study before she would have filled the medicine. What the heck is this? Is it their match? Indication are you giving it for? No one ever asked me that in twenty years of practice. So what happened is politics invaded us. We didn't invade politics, right? Because I'm trying to help my patients. I don't really care who the president is. I want to save that patient in front of And you and I have that same mindset. Doctor. Ursula, the same thing. When I saw him, go, this guy's nuts. He's going out full public and sitting on the steps of the Capitol. Is curse suicide if you're wrong. Speaker 1: Because we're not to us, it's not about politics. We don't care about the politics. Right? We don't care about the politicians. We care about saving lives. That's our job. Right? All have a job on the planet. Our job is simple. My job is the microbiome. It's all shit. Right? So ultimately I need to see clearly what's going on there. Speaker 2: It was interesting. And when I had that conversation with Peter McCullough, it turns out he doesn't like Trump. Right? And I go, why not? And he said, well, because he got the Cadillac, he got all this stuff we're talking about and he didn't make it everyone get that treatment protocol and say, this is the protocol everyone gets, not just the president of The United States. He got better quick. So you look at and go, okay. Speaker 1: And Cory doesn't like Trump either. He's a he's a full on Democrat. Speaker 2: Yeah. So you look at these guys and you go, okay, it's really about what works for the patient. The problem is we have so many, like you said, both sides are getting paid by the same people. So they're going to be biased in what they're doing. When I had to sit back and look at all these guys, the frontline doctors go, either they're all crazy. What do they have to gain by this? You know, look at look at McCullough gets his his ABIM. Speaker 1: Right. Removed. Speaker 2: Yanked. The the most decorated doctor with the most publications in integrity. Speaker 1: No longer a part of Baylor. You know, mean, that's Speaker 2: all that. Yeah, all that. And you start watching what happened to people. And I think what they did is they made people such an example. As you know, when you start your protocol, they come after you say, stop and stop doing this. Well, these people are getting better. I don't care what the FDA says. If they're getting better, if they're all getting sicker, then you say, yeah, we got to change the protocol. Right? But if they're getting better and you see these miracles, it's like, can any doctor in their right mind not say it's working what I'm doing? Speaker 1: And exactly that. Why are we not following what works? Why are we following a bunch of papers that are paid to push another narrative? Why are we not following what's working? Speaker 2: Because the only thing that makes sense is you can't have an emergency use intervention when there's an alternate treatment. Because if people say I could just do her protocol and get better, I got fired. A patient fired me because she got COVID. I said I would do McCullough's protocol. Here's what I recommend, which is your protocol too. Synthomac, zinc, blah, blah, blah. I got fired by the patient and go, okay, good luck. It's politics because it's politics for them, not what's going get me better. I don't care who came up with. I don't care if, you know, whoever I don't like came up with that. If it was the Fauci protocol and it was working, then I would use it. Right. Unfortunately, his protocol wasn't working. And now we're finding out like that they're all backpedaling and they can't remember what they said a year ago. It's amazing what we're up against. Speaker 1: No, it's and again, there is a force who is pushing the money who is paying. It's amazing. Here's what's amazing to me is how few people are not bribed to the right thing. You know what I mean? Think about it. You're standing up speaking, I'm standing up speaking. Nobody can pay me. You know, I've had bribes in the past from pharmaceutical companies and I'm like, no, this serious adverse event is going to be reported. I don't care if you're gonna blacklist me as a physician. And I've been blacklisted by a lot of pharmaceutical companies that I've reported because ultimately my job on the frontline of research is to make sure that a drug is safe enough to go out. And if it's not, it doesn't go out because ultimately, I have to sleep at night knowing that I did right for the patient. What is sad is how fast these drugs are going into market right now with such poor data. You know? Speaker 2: And that's the point Sabine. That's the concern is this. If you look at it and I just posted about that, I couldn't remember how many, like, think it's 15,000 drugs that have been approved by the FDA have been yanked off the market subsequently. But the money is made. It's just like you said, it's like when they publish these fraudulent studies, the money is made and the impression is made and then they retract it a few years later. Right? So in that time, how much money is riding on just getting this drug approved? And that's the problem is there's zero accountability for the patients that have died from Vioxx, from all these things. There's zero accountability for the FDA people. Or we'll go back to the opioid epidemic, right, with OxyContin, right? There's zero response. And they get promoted to pharma now and they're making 10 times what they were making for the FDA. So when you see this corruption, you go, what are we up against? And I think doctors like us who stand up and go, wait a minute, this is crazy. Like just using common sense, I have nothing to gain by someone using Zithromax or hydroxychloroquine. Have nothing to gain other than my patient being healthy. Right? So, like, I have no skin in the game that way. If the vax worked perfectly, I'd go, okay, worse, all my patients are. But when you start seeing problems, and I'll tell you that the corruption is so deep. I have a letter. You probably got the same letter by the ABIM saying, Hey, it's safe in 2020. They knew it was safe and effective with no long term consequences. How do you know that? How do you know that? If I just make a car, I can't tell you it's going to run for twenty years without running the car for twenty years and telling you, yeah, most of 90% of cars run for twenty years. So I think that's what we ran into is that you couldn't say, wait a minute, I'm seeing these bad things. These my friends are having health problems. I have nine nurses in my practice with DVTs out of nowhere. Right. And pulmonary embolism. Right. And no one reports this. And you go, well, if I give you doxycycline and two days later you have a stroke, you go, it's probably that new medicine that the doctor gave you. But right now there's such a blindness where people just won't see it. Like the doctors, none of those were reported to VAERS, not one, because the doctor said it's not a problem. It just was a coincidence. Like they never had a blood clot. And as a matter of fact, I have an 87 year old lady that had been taking care of her twenty years after her booster, four days later, she's in the hospital bilateral pulmonary embolism DVT and the doctors diagnosed her with a congenital clotting disorder. I'm like, okay, I talked to the doctor. She's 87 years old. No one in her family has ever had a clot. She's never had one with zero risk factors. She walks and plays bingo every day and she goes to, you know, the her literal exercise class and she has pulmonary embolism out of nowhere. And four days before that, she was vaccinated. It has nothing to do with it. And you know that. Speaker 4: I'm getting a lot of vascular events and and it's always a lot of stories are like are like this. 40 year old, then they go and check the carotid, check the coronaries. He's got no, he's, you know, he's he's got a history. He's not a not diabetic. And and and then, basically, they're told, we don't know why this happened. You know? We don't know why it happened. Because it's got clean carotids, clean coronaries, and and and they get they they're gaslighted. Had a guy come in. He was paralyzed and had the left side of his body, 43 years old, and I'm just like and I get it all the time. I literally have I have a huge, you know, amount of people running through my practice. We we saw 14,000 patients last year, and every one of them, ask them about the vaccine. And and it's kind of an interesting conversation now because pretty much seventy percent of people are like, I'm never taking that again. And then there's a twenty percent Speaker 1: That's why there's a sixteen percent people returning, right? But ultimately, I'm all for freedom of choice, right? I have a patient that's on his seventh booster. His life. He's got a lot of chronic diseases, super sick to begin with. So probably would have died from COVID and didn't have access. He wouldn't have had access to hydroxy or ivermectin or whatever. His choice, freedom of choice. I'm all for freedom of choice. When they mandated it and I saw the research was poor and I saw the animal studies were fast and they came to me to give it to me. That's when I opened my mouth to say, no, wait a minute. We're going to look at this because the moment you mandate something for all of humanity, you are essentially having the potential of extinguishing humanity. Here's the problem with, killing one race or two races. The problem is that that kills all of humanity. Humanity is like the microbiome. You kill a bunch of phyla and that's it. You have a diseased healthy, a diseased human, right? So we need to be very cautious. Was the biggest experiment in my opinion on the whole world. And the catastrophes that we are gonna see, mark my words, from now to the next twenty years are gonna be enormous. And thalidomide is gonna appear like nothing compared to what's Speaker 4: Well, I kinda I look at it like the problem we have is know, basically informed consent. The design flaws the design features for genetic disease, which are basically wide distribution and lengthy mRNA activity, are design flaws for this. So they're they're the major design flaws. Why distribution of brain bone marrow? When I did my work with lead ligand directed chemo, I wiped out the bone marrow on the animal models, you know, years ago, not not quite twenty years ago. And so we went away from the lipid nanoparticle model for targeting cancers. And I I knew right from the beginning we were gonna get that problem. And then, of course, you know, all the other things we've seen where what now we know that things stop breaking down. This is a horrible thing. And I think we you know, I just warn patients all the time. I said, you're basically creating an inflammatory pathway in your body that may last for who knows how long, and we don't even you know, you shouldn't do it. It's it's bad. It's bad medicine. Speaker 1: And Speaker 4: I also kinda go over the thing with patients all the time about respiratory viruses being short lived. They're basically, if you get a vaccine and you're over 50, you train your T cells and other immune system cells that are not going be renewed to chase a ghost that doesn't exist. And so, think in general, that's a concept that patients seem to understand really well. Speaker 5: So Anyway Yeah. Speaker 2: I think we all saw that. That was the thing. And Doctor. Ursula, want to personally thank you for stepping up early, early on and, like, making me look and say, okay, let's look at the data in Israel. Let's look what happens there. And then we saw the disaster that happened in Israel. Then you all speaking And for me as a doc in my practice, look, I want do what's best for my patients is take politics out of it. I'm right winger anyways, but take the politics out of it. Let me look and see what helps my patients. Right. I don't care who comes up with a protocol that And so the problem became, we started seeing adverse effects, but people would say, well, it just stays in your arm. It doesn't. Well, it doesn't clearly. And then we said we knew biodistribution. These guys had the data and they sat on it. And I think that's inhumane and fraudulent and evil. Right. They knew we all knew and we knew what we were seeing. So we started seeing bad outcomes. I mean, in the history of medicine, all of us being docs, I've never had anyone get the flu. And then three months later go, oh, now you need the flu shot for this year. It's a variant. You already have the flu. Don't worry about it. Right. You have natural immunity. And so when we brought up natural immunity, was called a right wing conspiracy theory. It's like that's the history of medicine we know about once you have something. Right. And if you're chasing that, like you're saying, you're chasing the ghost. It was two years ago, it's a variant. I'm going to train my body for someone who you know, my whole football team to tackle the guy who retired three years ago. It doesn't make any sense. So logically, from a medical perspective, it just never what what they were doing never made sense. And if we said anything, we were a quack. Speaker 1: Yeah. Yeah. Speaker 4: Yeah. You know, it's funny. The quack the quack part of it, I I usually kind of look and I go, I guess you guys don't know me very well. I graduated top of my class. I'm chief at MD Anderson. I invented an FDA approved drug. I go, you know, sorry to tell you, but I'm the upper dog. You know? So then my wife saw me doing that. She's like, you you need to stop. Don't stop that stuff Cause that you look like an arrogant asshole. Speaker 1: I usually say I'd rather be a quack then. You know what? Call me whatever you want to call me. I'm still going to be roaring at the end of the day. So, and this is a fight. This is a fight for humanity. You know, someone said to me yesterday, you're such a fighter. And I said, you better believe I was born for this. So, you know, that's why I have the lioness hair. So I'm ready to fight. This is our freedom we're talking about. This is our freedom of choice. There is a corruption in medicine. There is an interference with science and research that is going to affect all of us. Speaker 4: So are you saying Francis Collins and Fauci don't know what they're talking about? I don't understand. You know better than them. Speaker 1: I think that they have their own hypothesis and let's just say, you know, everybody has their own hypothesis on what a virus does but at the end of the day don't interfere with my hypothesis and I won't interfere with yours. How's that? Don't interfere with my body and I won't tell you what to put in your body. How's that? Because if I had my choices I would say everybody needs a fecal transplant right now. So I'm ready. We'll wrap Speaker 2: it I Speaker 1: had to bring fecal transplant in this somehow because that's the future. Speaker 2: Amen. Speaker 1: It was great talking. Brian, thank you so much. Speaker 2: Thanks, Abin. Appreciate it. Speaker 1: Thank you for stepping in in between the OR cases. You're awesome. Thanks. Thanks. Alright. Bye. Speaker 4: See you guys. Thanks. Speaker 0: It's not just a book. It's also a leading podcast available on Spotify, Apple Podcasts, on your Alexa. Let's talk with doctor Sabine Hazen. Tune in now on all major platforms.
Saved - August 15, 2025 at 8:28 AM
reSee.it AI Summary
I'm frustrated with outdated science and one-size-fits-all treatments. Antibiotics and biologics have had their moments, but now we face a new era of superficial solutions. I'm not waiting for permission to innovate. I’m asking bold questions, like whether Crohn’s could be linked to mycobacteria and if the real cure lies in precision antibiotics and microbiome restoration. True progress in medicine happens when pioneers challenge established beliefs. For my patients, this approach means moving from harsh treatments to genuine healing. Science and doctors should always evolve.

@newstart_2024 - Camus

Dr. Sabine Hazan Challenges the Status Quo The public is tired—tired of outdated science, tired of one-size-fits-all treatments. Antibiotics revolutionized medicine… until they didn’t. Biologics became the answer… until they weren’t. Now, we’re in the era of ‘pill pooping’—throwing solutions at symptoms without asking WHY. Dr. Sabine Hazan isn’t waiting for permission to innovate. She’s on the frontlines, asking the bold questions: What if Crohn’s is caused by mycobacteria? What if the cure isn’t another biologic, but precision antibiotics + microbiome restoration? Medicine moves forward when pioneers challenge dogma. Most won’t. Dr. Hazan does. And for the patients under her care? It’s the difference between brutal treatments… and actual healing. Science isn’t static. Neither should be your doctor.

Video Transcript AI Summary
"The public is tired. They're tired of the old science. They're tired you know, antibiotics were great." "I trained in the world of antibiotics where we were giving antibiotics for everything." "then came the biologics, and then it became biologics for everything." "And now we're in the pill poop level, and it's gonna be pill poop for everything, you know." "So science is only good as science is during the moment in time where the research is not advanced." "What me and doctor Barodi do is we're the innovators." "We're the ones that are basically on the frontline challenging the status quo and saying, why not look for this?" "Why isn't Crohn's mycobacterial paratuberculosis? And why shouldn't I look for it?"
Full Transcript
Speaker 0: The public is tired. They're tired of the old science. They're tired you know, antibiotics were great. Speaker 1: And and still are for the right thing. Speaker 0: Yeah. Yeah. Yeah. And listen. I mean, I I trained in the world of antibiotics where we were giving antibiotics for everything. Psoriasis, antibiotics, you know, rheumatoid arthritis, antibiotics, you know, and then came the biologics, and then it became biologics for everything. And now we're in the pill poop level, and it's gonna be pill poop for everything, you know. So science is only good as science is during the moment in time where the research is not advanced. What me and doctor Barodi do is we're the innovators. We're the ones that are basically on the frontline challenging the status quo and saying, why not look for this? Why isn't it why isn't Crohn's mycobacterial paratuberculosis? And why shouldn't I look for it? And should I be giving antibiotics and then implant? You know? So there's so many different causes, but I think you have to play detective and you have to innovate and be outside the box. And there's not many doctors that are willing to do that or be that. Speaker 1: And the few fortunate patients that come into your care can be cured of conditions which otherwise they would die for or be be subject to brutal treatments. Speaker 0: Yeah. But my patients understand. What I do is research. You know, I'm extremely regulated. Everybody's watching me.
Saved - August 16, 2025 at 3:41 PM
reSee.it AI Summary
Medicine is facing a crisis as predatory journals undermine rigorous science, turning it into a platform for agendas. I, Dr. Sabine Hazan, a gastroenterologist, faced this reality after my research on ivermectin and bifidobacteria gained significant attention. Despite its success, the journal retracted my work because it contradicted their narrative. These journals, which initially flatter researchers, ultimately suppress findings that threaten the status quo. It raises a troubling question: how many vital discoveries have been silenced?

@newstart_2024 - Camus

The Disturbing Truth About "Predatory Journals" – Dr. Sabine Hazan’s Shocking Experience Medicine is in crisis. What was once a field driven by rigorous science has devolved into a "gossip column" industry, where predatory journals manipulate data, suppress truth, and serve agendas. Dr. Sabine Hazan, a leading gastroenterologist and microbiome expert, experienced this firsthand. After her groundbreaking hypothesis on ivermectin increasing bifidobacteria (a potential link to cancer treatment) was peer-reviewed & published in Frontiers, it became their #1 most-read paper—59,000 views, with doctors worldwide engaging. Then, 9 months later, the journal turned on her. Why? Because her work "lit up ivermectin"—a treatment they wanted buried. This is the dark reality of modern "science." Journals that lure researchers with flattery, only to retract, manipulate, or sabotage studies that challenge the narrative. Dr. Hazan calls them out: "They’re not journals—they’re propaganda machines. And if your science threatens the status quo, they will come for you." The question is: How many life-saving discoveries have been silenced this way?

Video Transcript AI Summary
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?"
Full Transcript
Speaker 0: Here's, you know, like it's interesting. You said magazines, right? And I think that's what medicine is becoming. A lot of these journals are becoming magazines. They're almost like, you know, gossip column, you know, gossip journals, right? That you hear, you know, these celebrities are doing that and then they're not doing it. It's the same propaganda. So there's a group of journals, It's funny because Doctor. Barodi and I, we've been working at the protocols with COVID, the whole pandemic. He calls them predatory journals. And they're actually very smart in a way because they do have an impact factor. They're brand new journals. They send you emails constantly. Different people send you emails and they're like, Oh, doctor, we've read your paper. We would love to see you publish. And then once you publish, they're easily, they can manipulate or retract the data to make you look bad. And that's exactly what happened with me with Frontiers. Frontiers, all my colleagues knew, I didn't know that it was a predatory journal. I submitted a hypothesis on ivermectin increasing the bifidobacteria, and it was accepted by the peer review. Nobody criticized the articles that I picked or anything like that. And then next thing you know, nine months later, because this paper was the number one read at Frontiers with 59,000 views of doctors reading this paper, finding interesting, it was 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? So the fact that, so because it got so much attention, because it really, you know, lit up ivermectin, which they don't want to do, you understand?
Saved - August 23, 2025 at 2:29 PM
reSee.it AI Summary
During the pandemic, I witnessed patients with dangerously low oxygen levels refusing hospital care, which felt criminal to me. I rejected a one-size-fits-all approach, opting instead for personalized medicine, resulting in no deaths among my patients. I believe in protecting the sacred physician-patient relationship from becoming impersonal. I fear a future where AI dictates outcomes without empathy. We must fight for our right to choose our medical paths, balancing risk and reward. This is a call to uphold our freedoms in medicine and humanity.

@newstart_2024 - Camus

Dr. Sabine Hazan on the Frontlines: A Plea for Humanity, Choice, and the Courage to Innovate During the darkest days of the pandemic, Dr. Sabine Hazan faced a terrifying reality: patients with oxygen saturation levels as low as 63%, terrified of going to the hospital. To her, watching them die without intervention wasn't just medicine—it was criminal. It was akin to withholding a blood transfusion from someone bleeding out. Her response wasn't blind adherence to a single, monolithic protocol. It was personalized medicine at its most critical. She implemented tailored protocols for different patients with unique risk factors. The result? Not a single one of the patients who followed her specific guidance died. This experience forged a core belief: the sacred relationship between a physician and a patient must be protected from becoming a cold, algorithmic transaction. Dr. Hazan poses a chilling future scenario: What happens when you input your symptoms into an AI and it coldly calculates you have 10 days to live? She rejects this dystopia. She doesn't want a printout; she wants the empathy, the experience, and the honest counsel of a human physician who can say: “These are the stats from the AI. But I’ve seen this work. I have a protocol that might up your chances. It’s riskier, but the potential reward is greater. The choice, however, is yours.” This is the fundamental right we must fight for: Freedom of Choice. It is the absolute right to decide what goes into our own bodies. It is the choice between a "safe" route that offers marginal gains and a "risky" route that could fail tomorrow or grant a full year of life. There are no guarantees. It is always a leap into the abyss. Dr. Hazan’s leap is guided by faith, but the principle is universal: we must have the autonomy to make that jump on our own terms. This is a call to action. We must stand as humans to protect: - The Freedom of Choice. - The Freedom of Speech. - The Freedom of Ideas. - The Freedom to Innovate. We must elevate medicine, not automate humanity. The goal is to save lives, not just to process data.

Video Transcript AI Summary
On the COVID front line, patients didn't wanna go to the hospital. Their oxygen was 63%. 'I wasn't gonna just watch them die. That's like watching a patient bleeding and you're not giving a blood transfusion. I mean, to me, that's criminal.' He notes that 'none of my patients died during the pandemic that followed my protocol' because 'there were different protocols for different people, different, you know, risk different patients with different risk factors.' He argues for encouraging personalized protocols rather than AI dictating care: 'An AI program tells me, doctor Eason, you need all this, or Sabine, you need all this. And then you're you have this, and you have about ten days to live.' He champions 'freedom of choice' and 'freedom of speech' and protecting ideas and innovations. He trusts God, 'I jump in the abyss' and chooses life with its uncertainties.
Full Transcript
Speaker 0: When I was on the front line treating COVID, patients didn't wanna go to the hospital. Their oxygen was 63%. I wasn't gonna just watch them die. That's like watching a patient bleeding and you're not giving a blood transfusion. I mean, to me, that's criminal. Right? We know certain things. Let's try to save that life. Right? When I noticed that, you know, none of my patients died during the pandemic that followed my protocol, My protocols because there were different protocols for different people, different, you know, risk different patients with different risk factors. We need to encourage that. We need I I don't wanna be that patient, you know, because I always look twenty years from now. I don't wanna be that patient where I type in my symptoms. An AI program tells me, doctor Eason, you need all this, or Sabine, you need all this. And then you're you have this, and you have about ten days to live. I don't wanna know that. I want the sympathy of a physician to say, you know what? I've seen this work. These are the protocols that AI is gonna give you, but here are your chances with that program of AI. I think I can up your chances better with this because I've seen this work for this, this, and that. And that's really, it's freedom of choice. It's my choice to do what I wanna put in my body. It's my choice. Do I wanna take the safe route and get ten extra days of life? Or do I wanna take the risky route and maybe die tomorrow or get an extra year of life? Right? So and understanding that there are no there are no guarantees in life. You're jumping in the abyss. I mean, I tend to trust God for everything. Right? So I jump in the abyss and I hope that God's gonna guide me. And if it doesn't happen, well, it doesn't happen. You know, I made that choice to jump into the abyss. I think we need to stand as humans to protect that freedom of choice, to protect that freedom of speech, to protect ideas, to protect innovations, yes, to elevate. So important.
Saved - August 31, 2025 at 12:28 PM
reSee.it AI Summary
I expose a central crisis crippling modern science: the active interference in research, retraction of crucial data, and systemic mislabeling that misleads the public. This corruption is propaganda that stifles truth and prevents life-changing solutions, like healing our microbiome, from reaching those in need. Restoring integrity is a long road, but it starts with us demanding that our government and institutions protect research from political and corporate influence. The future of medical education and public health depends on this fight.

@newstart_2024 - Camus

Dr. Sabine Hazan exposes the central crisis crippling modern science: the active interference in research, the retraction of crucial data, and the systemic mislabeling that deliberately misleads the public. This corruption, she states, is nothing short of propaganda. It stifles truth and prevents real, life-changing solutions—like healing our nation's microbiome—from ever reaching the people who need them. Dr. Hazan affirms that restoring integrity is a long road, but it begins with a collective stand. We the people must demand that our government and institutions protect the sanctity of research from all political and corporate influence. The future of medical education and public health depends on this crucial fight.

Video Transcript AI Summary
Speaker emphasizes 'no interference in research' and urges that 'this government or who or we, the people, stand up for, you know, righteous research and no retraction of data and no interference in research.' They argue that while the public may be educated by podcasts, 'doctors, the scientists are gonna be educated by watching by reading the data.' Addressing labeling, they state that 'mislabeling that that, the the labels that mislead the consumers, we're never gonna fix our micro I agree.' They reference Kennedy, saying 'Kennedy's saying it's propaganda. This research has been basically propaganda. And, now, hopefully, he's going to put an end to it, but it's a it's a long row.'
Full Transcript
Speaker 0: The other thing is, you know, making sure that there's no interference in research. Because here's the thing. I do this to educate other doctors so that they can follow, but they are not gonna be educated by watching a podcast. I mean, the public's gonna be educated by watching a podcast, but the doctors, the scientists are gonna be educated by watching by reading the data. So it's very important that this government or who or we, the people, stand up for, you know, righteous research and no retraction of data and no interference in research. That's very important because until we stop the interference in research, until we stop the mislabeling that that, the the labels that mislead the consumers, we're never gonna fix our micro I agree. And Kennedy's saying it's propaganda. This research has been basically propaganda. And, now, hopefully, he's going to put an end to it, but it's a it's a long row.
Saved - September 1, 2025 at 4:58 PM
reSee.it AI Summary
I expose the political sabotage of a life-saving COVID-19 protocol I developed in March 2020, which included hydroxychloroquine, Zinc, and vitamins. Initially approved by the FDA, this approval was quickly overturned, likely due to pressure from lobbyists protecting pharmaceutical profits. My clinical trial faced systematic delays and discrediting on social media. I dismantle fraudulent studies aimed at undermining hydroxychloroquine, revealing a deliberate effort to suppress a safe treatment for profit. This situation highlights the corruption at the intersection of money, politics, and science.

@newstart_2024 - Camus

Dr. Sabine Hazan exposes the shocking political sabotage of a life-saving COVID-19 protocol. In March 2020, she developed an early-treatment protocol using hydroxychloroquine, a Zinc pack, and vitamins. Despite three pages of known contraindications, the protocol was deemed safe and approved by the FDA within 24 hours for immediate use. This approval was swiftly overturned. Dr. Hazan believes powerful lobbyists, threatened by a cheap, generic drug, intervened to protect pharmaceutical profits. The timing was suspicious: she received an unexpected letter from Bill Gates inquiring about her protocol simultaneously. Her clinical trial was then systematically delayed and destroyed on social media platforms like Twitter, forcing redesigns and costing precious time. This was a coordinated political move to discredit hydroxychloroquine. Dr. Hazan dismantles the fraudulent studies published to kill the drug. The infamous Lancet paper claiming 96,000 patients was an impossibility; Australia didn’t even have that many cases. The recent paper citing 17,000 deaths is also fake. Patient authorization is required to access medical records—a legal hurdle making such a study logistically impossible in that timeframe. These were not scientific studies but hit jobs. The goal was to create a false narrative that a safe, effective, and affordable treatment was dangerous, ensuring a clear path for expensive, novel drugs and vaccines to dominate the market. Dr. Hazan published her detailed protocol publicly on http://clinicaltrials.gov to sound the alarm and empower doctors, not to create a proprietary product. Her own data showed the protocol made the virus disappear from patients in 5-8 days. The tragedy is that a safe, effective early-treatment option was deliberately destroyed for profit, costing countless lives. This is a stark warning about the corruption that can exist where big money, politics, and science intersect.

Video Transcript AI Summary
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.”
Full Transcript
Speaker 0: So I started being inspired by that. I said, well, you know what, maybe hydroxychloroquine is certainly a safe product. So in March, I started researching my protocol and started writing the protocols. And yes, they were like contraindications to hydroxychloroquine. There were three pages of medications. You you have to practice medicine and still be vigilant as a doctor. But ultimately the protocol was approved by the FDA within twenty four hours. And in fact, it was approved to say move to market. Go ahead, Doctor. Hazen, just take your combination, start giving it to patients, proceed. Okay. That was what it was. Twenty four hours later, somebody must have called from the politics and said, or the lobbyist that controls both sides of the politics, right? And said, wait, wait, we can't have a cheap drug. It's going to kill the market and then it's not going to start our protocol. Right? Which interestingly enough, at the same time about this, after the protocol was approved, I got a letter from Bill Gates that basically said, when do you think you're going to, you're anticipating finishing your protocol? Why is Bill Gates interested in my little protocol? I thought he was gonna invest personally. So I'm like, oh, I've been in the clinical trial business for like thirty years. Don't worry, it's going out there, right? Well, lo and behold, you know, my protocol took forever. My protocol had a lot of, know, like ups and downs. A month later it got approved by the IRB and then went on Twitter, Twitter destroyed it because it was an open label. I had to go back to the FDA and say, look, I'm going to do vitamins versus hydroxychloroquine with the vitamins. And then finally a month and a half later, it got into motion to start. By then it was destroyed by the politics. This was a political move to destroy a drug. And unfortunately, you know, supported probably or whispered, you know, the politicians by the lobbyists. That's exactly what happens when the Lancet paper came out and we all discovered it was BS essentially. We knew, right? This is wrong, right? Because hydroxychloroquine is the safest drug. Now this paper and why I didn't speak the whole time because you heard about Zelenko, you heard the frontline doctors and great because they were speaking trying to save as many lives. You know, one of the criticism I got on my protocol was why did I spell out the drugs? Hydroxychloroquine with the dosages, Z Pak with the dosages, vitamin C, D and zinc. Why didn't I just leave it a Haze D Pak, right? Because then nobody knows it's proprietary. There's no secret that's leaked out to the doctors. That wasn't my point. My point on April 3, when it was approved by the FDA and it went into the clinicaltrials.gov, we were number two or three. The two protocols went online on clinicaltrials.gov in America, number two and three in 04/02/2020. Why did I do that? To sign the alarm and say, look, this is what I think happens, right? On the other side, we found COVID in the stools and we discovered that actually hydroxychloroquine and Z Pak made the virus disappear. You had it at baseline, five to eight days later the virus disappeared. Problem is, it destroy the microbiome as well. So you have to be selective on which population you're going to give it, right? Every antibiotic has a risk of killing the microbiome, right? And even drugs like hydroxychloroquine. But on a safety level, you know, wrote about it. It got approved by the FDA within twenty four hours. It was safe, right? So 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. There is no way that four or five authors took 17,000 records, medical records. Now they probably took the death certificate. You can alter the death certificate. Lobbyists can pay people to like, you know, hey, you know, I mean, we've seen you and I, Brian, physicians that are on the other side that are getting paid by legal to bring, you know, cases to lawsuits, right? We've seen that. A death certificate does not make the case. Going to court and presenting your case makes the case. If you look at this paper, there is no way 70,000 medical records were taken. First of all, you need the authorization of the patient to get medical records from the hospitals. So that's why it's a fake paper. Much like the 96,000 patients that was in the Lancet. I saw that paper and I said, wait a minute, Australia doesn't even have COVID yet. Why are there patients in that paper of COVID? And you're going to tell me 10 people evaluated ninety six thousand patients with their smoking history. I'm in the clinical trial business. It takes me a year and a half to evaluate a 100 patients. Okay. And to analyze them like the hydroxychloroquine paper, we're still analyzing the data. We're like three years out. It's very time consuming to do these studies properly. So when you see a number like ninety six thousand, that's fraudulent. When you see seventeen thousand people died, that's fraudulent right off the bat. I don't even need to know how much they got because it's fraudulent. The second thing is if you look at the guidelines and then I'm gonna have Xavier jump in. If you look at the guidelines on hydroxychloroquine, there are no guidelines that tell you to test for toxicity. None. So, you know, where did that come from? Right? The second thing is if you look at the NIH, chloroquine and hydroxychloroquine toxicity, the paper itself says both chloroquine and hydroxychloroquine have excellent oral absorption and bioavailability, Both have a long and variable plasma elimination half life and about half the drug metabolites. Basically there's no comment. Does not appear to cause harm to the fetus or the mother, both excreted in breast milk, which we know. And basically the only thing that they're questioning, and I wish Richard Urso was here. He's here, I'm here. I it came true. I just saw him pop in. I was like, yes. Yeah, Richard will tell you, the only thing he's concerned about is the retinal toxicity with hydroxychloroquine. But your patient is in the intensive care, he's dying. You don't care about retinal toxicity. He's dead. It doesn't matter that he's got retinal toxicity. He's under the ground in one day. That's it.
Saved - September 10, 2025 at 3:41 PM
reSee.it AI Summary
I shared a powerful message about my journey as a gastroenterologist and the challenges I faced during the COVID-19 pandemic. After successfully using social media to recruit patients for clinical trials, I experienced censorship when my posts about my own trial were blocked. This sparked a fierce advocacy for scientific freedom, leading to the creation of the Microbiome Research Foundation. I now challenge Mark Zuckerberg to support our mission with a donation, which would help rebuild trust with the medical community and invest in the future of medicine.

@newstart_2024 - Camus

A powerful message from a pioneer in the field. Dr. Sabine Hazan, a renowned gastroenterologist, shared a compelling story of transformation and a direct call to action for Mark Zuckerberg. Dr. Hazan, who once leveraged social media to successfully recruit patients for major pharmaceutical clinical trials, found herself on the other side of the fence during the COVID-19 pandemic. Her own clinical trial investigating repurposed therapeutics, including hydroxychloroquine, Z-Pak, ivermectin, doxycycline, and essential vitamins, was abruptly censored. "Facebook blocked my post on recruiting for COVID," she stated. "I was the girl that helped the clinical trial world, and suddenly I was being censored. I had trolls attacking me, and I thought, 'What’s going on here?' That moment woke me up to the realities of power and control in our world." This experience ignited a fierce advocacy within her, transforming her into a "beast" fighting for scientific freedom and open inquiry. From that struggle was born a profound commitment to give back, leading to the creation of the non-profit Microbiome Research Foundation, dedicated to groundbreaking research for the health of future generations. Now, she extends a challenge—and an opportunity for redemption—to Meta's CEO: "My message to Mark Zuckerberg: In view of the significant difficulties your platform created for my research protocol, a donation to the Microbiome Research Foundation would be a noble gesture. It would directly support crucial science for these kids and would be a meaningful step toward rebuilding trust with the medical community. It's our chance to come back together." This is more than a request; it's an invitation to right a wrong and invest in the future of medicine.

Video Transcript AI Summary
"You know, I've been privileged in my life, you know, God has provided, and I felt this is my time to give back." "N of one was the beginning, and then COVID kind of showed me the reality of the world and pharma and woke me up to, what do you mean I can't do a clinical trial? What do you mean I'm censored? What do you mean I can't recruit? You know, Facebook just blocked my post on recruiting for COVID?" "When my own clinical trial on hydroxychloroquine, Z Pak, vitamin C, D and zinc got censored by Facebook and I had all these trolls saying all sorts of things about me, I said, wait a minute, what's going on there," "So if this message reaches Mark Zuckerberg, please donate to the Microbiome Research Foundation."
Full Transcript
Speaker 0: You know, I've been privileged in my life, you know, God has provided, and I felt this is my time to give back. And I think that N of one was the beginning, and then COVID kind of showed me the reality of the world and pharma and woke me up to, what do you mean I can't do a clinical trial? What do you mean I'm censored? What do you mean I can't recruit? You know, what do you mean Facebook just blocked my post on recruiting for COVID? So I became a little bit of a beast because I was the girl that really helped the clinical trial world. I was the girl that would put a post on Facebook and get 20 patients with psoriasis to enter a clinical trial for pharma. When my own clinical trial on hydroxychloroquine, Z Pak, vitamin C, D and zinc got censored by Facebook and I had all these trolls saying all sorts of things about me, I said, wait a minute, what's going on there? So I think as a good message, Rachel, we should ask today for Mark Zuckerberg to donate to the Microbiome Research Foundation in view of the difficulties that he created from my protocol on hydroxychloroquine, Z Pak, vitamin C, D and zinc, and ivermectin, doxycycline and zinc. So if this message reaches Mark Zuckerberg, please donate to the Microbiome Research Foundation. I think it would be a nice gesture for these kids, and it would be a comeback for us to trust you and Facebook again. This is my message to Mark Zuckerberg.
Saved - October 5, 2025 at 8:36 AM
reSee.it AI Summary
I shared the story of Dr. Paul Thomas, an Oregon pediatrician who advocated for informed vaccine choices. He analyzed data from 10,000 patients and found that vaccinated children had a 400% higher risk of various illnesses compared to unvaccinated ones. Despite his objective findings, he faced severe repercussions: his medical license was revoked, and his research was retracted. This case highlights the suppression of scientific inquiry and the dangers of silencing those who present inconvenient truths, ultimately prioritizing narrative over public health.

@newstart_2024 - Camus

He Studied 10,000 of His Own Patients, Found a 400% Increase in Childhood Illnesses Linked to Vaccines, and Lost His License for Telling the Truth Stanford's Prof. Annelise Barron reveals the story of Dr. Paul Thomas, an Oregon pediatrician who believed in informed choice. He typically recommended a conservative, Danish-style vaccine schedule (≈17 shots by age 5) instead of the full CDC schedule, but honored parents' decisions for any path, including zero vaccines. Dr. Thomas then did what more should: he looked at the real-world data. He analyzed thousands of children born into his practice, tracking diagnoses before age five. His study compared health outcomes—from ear infections and allergic rhinitis to ADHD—between his largely partially vaccinated/selectively vaccinated patients and the completely unvaccinated cohort. The findings were unequivocal and alarming. The vaccinated children had a 4x higher risk of a wide range of health issues. For publishing this objective, practice-based data, the system made an example of him. His medical license was revoked. His paper was retracted. He was professionally destroyed for telling an inconvenient truth. This case is about more than vaccines. It's about the suppression of scientific inquiry and the silencing of a doctor who simply reported what he found in his own patient population. As Prof. Barron states, this was "real data" that should have been headline news, prompting a serious scientific discussion. Instead, it was buried. When we silence messengers for their data, we are not protecting public health—we are protecting a narrative. The truth has a cost, and Dr. Paul Thomas paid it.

Video Transcript AI Summary
Dr. Paul Thomas, an Oregon pediatrician who ran a practice of about 10,000 patients, promoted parents’ vaccine choice and studied a Danish approach: 17 vaccines before age five, vaccinating only against diseases lethal to the child. He proposed a lighter schedule but would support the full CDC schedule or zero if parents chose. He analyzed thousands of children born into his practice, comparing diagnoses before age five and visits, focusing on infections and ADHD. He looked at the totally unvaccinated kids, and the vaccinated kids were very few who took the full schedule because he didn’t recommend it. He published it, and it showed a four x higher risk of pretty much everything, like allergic rhinitis. He lost his license and they retracted the paper, yet he continues advocating, saying it’s real data and that they’ve done everything to hide it. The study was objective and should have been headline news.
Full Transcript
Speaker 0: And are you familiar with, you know, doctor Paul Thomas? No. Okay. So he has been on Children's Health Defense, which is a great site. But, you know, he was a pediatrician in Oregon who had for many years run a large practice, about 10,000 patients. And his general personal viewpoint was that parents should be able to choose which vaccines and how many vaccines they give. He had actually done a deep study himself, and he kind of favored what I would call the Danish approach. So in Denmark, they give, I think, 17 vaccines before age five, and they only vaccinate against diseases that could be lethal to the child. Right? So they have a more conservative approach, and they don't really have a problem with Mhmm. Autism there as much as we do in The United States. He was aware of this, and so his general recommendation to parents was to do this lighter schedule. Mhmm. 17 instead of the full CDC schedule. But if the parents wanted the full CD schedule CDC schedule, great. You know? Free country. If the parents wanted zero because, you know, Oregon is full of hippies. Right? Mhmm. So some hippies come in, they're like, no. My child's gonna be pure. Yeah. Oh, he'd be like, okay. Sure. Yeah. So he what he did then is he he did an analysis of thousands of children born into his practice, and he looked just at what were they diagnosed with before age five and how many what did they come in for doctor's visits for? So was it an ear infection? Was it, you know you know, asthma or ADHD? And he correlated. So he had a Speaker 1: What infections they had? Variceal infection, right? Speaker 0: Yeah. And it was mostly kind of infections, but also included ADHD. And he looked at the totally unvaccinated kids. And then the vaccinated kids were very few of his kids took the full schedule because he didn't recommend it. He recommended a light schedule. He published it. It was like a four x higher risk of pretty much everything, like allergic rhinitis, etcetera. And then, you know, you can guess what happened to him. Speaker 1: Lost his license. Speaker 0: Lost his license. They they retracted the paper. Mhmm. You know, they destroyed his him. But he was such a good, strong man that he, you know, he just has done his best, but he's continuing to advocate because he's telling the truth. It's real data. But, you know, they've done everything they can to hide it. And that's wrong. Speaker 1: It's wrong. I mean, imagine if we could have just done that kind of screening. Speaker 0: It's not Speaker 1: that hard. Speaker 0: Oh, we could have. Speaker 1: Like, how much more time does it take to do that kind of screening? Speaker 0: I think, you know, frankly, there are people who have known this a long time that chose to keep it quiet. Speaker 1: You could probably do that screening in a one page questionnaire. Right? Speaker 0: Yeah. If you trusted parents. But, you know, the neat thing about doctor Paul Thomas' study was that it was entirely objective, and it was all children that were born into his practice, that he was the only pediatrician that had ever seen them. Speaker 1: Mhmm. Speaker 0: And it was just a beautiful study, and it should have been, you know, headline news.
Saved - October 12, 2025 at 10:42 PM

@newstart_2024 - Camus

Dr. Sabine Hazan: "So I'm ready to fight. This is our freedom we're talking about. This is our freedom of choice. There is a corruption in medicine. There is an interference with science and research that is going to affect all of us." https://t.co/3XRCof07Hp

Video Transcript AI Summary
I usually say I'd rather be a quack than a sheep. So you know what? Call me whatever you want to call me. I'm still gonna be roaring at the end of the day. So, and this is a fight. This is a fight for humanity. You know, someone said to me yesterday, you're such a fighter. And I said, you better believe I was born for this. So, you know, that's why I have the lioness hair. So I'm ready to fight. This is our freedom we're talking about. This is our freedom of choice. There is a corruption in medicine. There is an interference with science and research that is going to affect all of us.
Full Transcript
Speaker 0: I usually say I'd rather be a quack than a sheep. So you know what? Call me whatever you want to call me. I'm still gonna be roaring at the end of the day. So, and this is a fight. This is a fight for humanity. You know, someone said to me yesterday, you're such a fighter. And I said, you better believe I was born for this. So, you know, that's why I have the lioness hair. So I'm ready to fight. This is our freedom we're talking about. This is our freedom of choice. There is a corruption in medicine. There is an interference with science and research that is going to affect all of us.
Saved - October 21, 2025 at 10:48 AM
reSee.it AI Summary
I witness the establishment retracting her papers; Dr. Sabine Hazan replies with a powerful ultimatum. She holds keys to reversing nonverbal autism in twins and microbiome secrets, yet the data stay locked in her mind. She won’t publish—her leverage and protection. The war on science costs, and she makes them pay.

@newstart_2024 - Camus

The establishment retracts her papers. Dr. Sabine Hazan’s response? A powerful ultimatum. She holds the keys to groundbreaking discoveries: reversing nonverbal autism in twins and unlocking the secrets of the microbiome. But the data stays locked in her mind. She will not publish. It’s her leverage. It’s her protection. While they play political games, she holds the very science they may one day need to heal themselves. The war on science has a cost. Dr. Hazan is making sure they pay it.

Video Transcript AI Summary
Speaker 0 expresses a firm stance against publishing. They reference an “amazing case of twins who have … are verbalizing,” followed by, “I’m not publishing what I did to those kids. They were autistic? They were autistic. And I’m not publishing.” They continue, “I’m not publishing what I discovered on the microbiome,” presenting this as an ultimatum: retracting papers is not a concern for them because “it’s cheaper for me not to publish my data.” They claim it’s better to “keep my data in my brain because then it keeps me alive,” explaining that those who create the narrative would end up needing a doctor to fix their microbiome. The speaker asserts, “So bring it on. Nothing’s coming out of my brain. I don’t need to publish.” They conclude that this approach “saves me tons of money,” and express enjoyment at others talking negatively about them, stating, “they’re talking shit about me because then I sell more books. Let’s talk shit.”
Full Transcript
Speaker 0: Yeah. But I think I'm just gonna say because you mentioned, you know, the publishing. I can't publish. So guess what? I have an amazing case of twins who have are verbalizing. I'm not publishing what I did to those kids. They were autistic? They were autistic. Now they're fully verbal. And I'm not publishing. I'm not publishing what I discovered on the microbiome. This is my ultimatum now. You wanna play those games of retracting my papers? No problem. It's cheaper for me not to publish my data. It's better for me to keep my data in my brain because then it keeps me alive. Because then, you know, those who create this narrative end up needing a doctor to fix their microbiome. So bring it on. Nothing's coming out of my brain. I don't need to publish. You're saving me tons of money. I love the fact that they're talking shit about me because then I sell more books. Let's talk shit.
Saved - November 19, 2025 at 12:15 AM
reSee.it AI Summary
I share Dr. Sabine Hazan’s claim that ivermectin boosts gut bifidobacteria within 24 hours, possibly due to its Streptomyces lineage. In a placebo-controlled trial, she allegedly intervened for a high-risk patient, giving 36 mg ivermectin with a fatty meal, and his oxygen rose from the 60s to 92%. She says a successful paper on this was later retracted, and she questions why ivermectin is deemed unsafe once generic. Her abstracted report challenges the narrative.

@newstart_2024 - Camus

The Ivermectin Effect They Didn't Want You to Know. In a revelatory interview, Dr. Sabine Hazan, a gastroenterologist and researcher, shared groundbreaking data and a harrowing story from the front lines of the pandemic. Her research uncovered a paradoxical effect of Ivermectin: it significantly increases beneficial bifidobacteria in the gut within 24 hours. This is counterintuitive for an anti-parasitic drug and suggests a novel mechanism of action. Dr. Hazan hypothesizes this is because Ivermectin is a fermented product of Streptomyces bacteria, which shares a phylum with bifidobacteria. The story turns personal and urgent. While running an FDA-watched, placebo-controlled trial, Dr. Hazan faced an ethical nightmare: watching high-risk patients in the placebo group crash and head toward death. She made the courageous decision to intervene. One patient, a diabetic with chronic renal failure and oxygen levels plummeting into the 60s and 70s, was on his way to the hospital. Dr. Hazan instructed him to take 36mg of Ivermectin with a fatty meal (french fries) to drastically increase absorption—a critical step validated by Merck's original studies but ignored by later flawed trials. The result was nothing short of miraculous. By the time the patient arrived at the hospital, his oxygen saturation had risen from the critical 60s to 92%. Dr. Hazan meticulously documented the entire journey, refuting any claims of a faulty oximeter reading. This was the moment she knew Ivermectin was a key. Yet, when she published a paper on her successful combination therapy for hypoxic patients, it was retracted by a private publishing house that overruled the peer reviewers—a stark example of the suppression faced by repurposed, non-profitable drugs. She poses a devastating question: How does a drug like Ivermectin, deemed safe enough for babies with scabies while under patent, suddenly become "unsafe" for dying COVID-19 patients once it's generic and cheap? Dr. Hazan’s work, published as an abstract due to the controversial nature of the drug, stands as a testament to unbiased research and the relentless pursuit of saving lives, even when it means challenging the established narrative.

Saved - November 26, 2025 at 8:57 AM
reSee.it AI Summary
Dr. Sabine Hazan alleges that some journals secretly retract peer-reviewed work after publication, citing a COVID-19 stool-isolation study as an example. She says a private publishing house enforces pay-for-play to suppress inconvenient findings, alerting colleagues at Mayo Clinic, Harvard, Yale, and officials at NIST. Critics warn this endangers scientific discourse if papers disappear for not fitting a narrative. DouglasHeimark condemns the behavior and urges transparent evaluation.

@newstart_2024 - Camus

What if the peer-reviewed journals you trust are operating more like censors than scientists? Dr. Sabine Hazan is blowing the whistle on a shocking breach of scientific integrity, and the story is straight out of a modern-day academic thriller. In a bold revelation, Dr. Hazan exposes a disturbing pattern: groundbreaking research is passing rigorous peer review, only to be secretly retracted by publishers after the fact. Her own pivotal study, which successfully isolated COVID-19 in stool samples, met this very fate. Her response? To "stir up shit," as she puts it. She didn't stay silent. She alerted investigative journalists at Trial Site News, who uncovered a shadowy "private publishing house" responsible for these retractions—implying a pay-for-play scheme to suppress inconvenient science. She then made direct calls to colleagues at elite institutions like Mayo Clinic, Harvard, and Yale, warning them that their unpaid peer reviews are being rendered meaningless by backroom decisions. The message is chilling: if a paper doesn't "fit the narrative," it disappears. She even alerted government officials at the National Institute of Standards, who were stunned by the retraction of her corroborated work. Dr. Hazan’s fight is a wake-up call for everyone who values truth. This isn't just about one paper; it's a systemic "burning of the books" that threatens the very foundation of scientific discourse.

Video Transcript AI Summary
I mean, it's become a joke. These papers that are winning awards at the American College of Gastro, and they're not getting published. So and what I do is I do what I do best, which is basically stir up shit, and I call all my friends. And I go, by the way, my paper has been retracted. That paper of the finding COVID in the stools Yeah. Was considered to be retracted. So, I called Trial Site News, and I said, by the way, you may wanna investigate. That's how they found out about the publishing house, private publishing house that is retracting these papers. So somebody must be paying them. And then I called all my colleagues, Mayo Clinic, Harvard, Yale, and I go, by the way, remember that paper that I found COVID? Well, it got retracted. And they're like, what? But it it passed peer review. Well, your peer review means nothing. And here's the thing. So guess what? You're not getting paid to do these peer reviews. Maybe you should start charging the journals now because clearly, they're going about wasting your time reviewing a paper, and they're going behind your back to retract the paper because it doesn't fit the narrative. So, that's what I do. So, and then the other thing that I did is I called the National Institute of Standards, Scott Jackson. And I basically said, remember my paper that we found COVID in the stools, and you also found COVID in the septic tanks? Well, my paper was retracted. And, you know, they couldn't believe it. They could this is at the government level. People are waking up to see we have a problem. Yeah. This is like the burning of the books.
Full Transcript
Speaker 0: I mean, it's become a joke. Right? I mean, these papers that are, you know, winning awards at the American College of Gastro, and they're not getting published. It's a joke. So and what I do is I do what I do best, which is basically stir up shit, and I call all my friends. And I go, by the way, my paper has been retracted. That paper of the of finding COVID in the stools Yeah. Was considered to be retracted. So, I called Trial Site News, and I said, by the way, you may wanna investigate. That's how they found out about the publishing house, private publishing house that is retracting these papers. So somebody must be paying them. And then I called all my colleagues, Mayo Clinic, Harvard, Yale, and I go, by the way, remember that paper that I found COVID? Well, it got retracted. And they're like, what? But it it passed peer review. Well, your peer review means nothing. And here's the thing. So guess what? You're not getting paid to do these peer reviews. Maybe you should start charging the journals now because clearly, they're going about wasting your time reviewing a paper, and they're going behind your back to retract the paper because it doesn't fit the narrative. So, that's what I do. So, and then the other thing that I did is I called the National Institute of Standards, Scott Jackson. And I basically said, remember my paper that we found COVID in the stools, and you also found COVID in the septic tanks? Well, my paper was retracted. And, you know, they couldn't believe it. They could this is at the government level. People are waking up to see we have a problem. Yeah. This is like the burning of the books.

@DouglasHeimark - Douglas Heimark

@newstart_2024 This is truly sick. Science is all about discovering the truth, no matter who it offends, and making sure the public becomes aware of the new studies. Let the readers judge for themselves, not some backroom bastards!

Saved - January 9, 2026 at 11:04 AM
reSee.it AI Summary
I’m hearing Dr. Sabine Hazan expose scientific censorship: journals harassed with endless questions until they retract papers to silence the harassment. A retraction may not disprove the hypothesis, yet it's wielded as a weapon. 0:55 clip—the dirty truth behind retractions. How many are silencing?

@newstart_2024 - Camus

Dr. Sabine Hazan blows the lid off scientific censorship: Journals are harassed relentlessly with endless questions until they ignore the authors' answers and retract papers — just to stop the harassment. A retracted paper doesn't even disprove the hypothesis — but they use it as a weapon anyway. 0:55 clip — the dirty truth behind retractions 👇 How many "retracted" studies are actually just silenced?

Video Transcript AI Summary
Speaker 0: Asked about the system of retractions and whether retracting a paper discredits a hypothesis, and on what basis retractions occur. Speaker 1: Responded that quoting papers that are later retracted does not negate a hypothesis; there is no rule requiring a hypothesis to be retracted if a cited paper is retracted after publication. They note that the practice involves harassing journals rather than logically disproving a hypothesis. For example, they may present a dozen questions to the journal, answer all of them, and then continue harassing the journal to the point that the journal ignores the answers and retracts the paper to avoid further harassment.
Full Transcript
Speaker 0: Right. So I just wanted to ask about the system of retractions. When they retracted, let's say, your hypothesis, did they disprove your hypothesis? On what basis are retractions It actually Speaker 1: was was, you quoted some papers that were retracted. Well, that doesn't negate a hypothesis. I can quote anything I want on a hypothesis. There is no rule that says that if you quote a paper in a hypothesis and the paper was retracted after the publication, that you have to retract the hypothesis. And what they do is they keep harassing the journals. So they will for example, they'll come to me with like a dozen questions. We answer all the questions to the journal. And then they'll keep harassing the journal to the point that the journal ignores my answers and just retracts the paper not to be harassed.
Saved - February 17, 2026 at 9:37 AM
reSee.it AI Summary
I recount Dr My-Le Trinh, a GP in Australia for nearly 30 years, who questioned the COVID narrative, treated patients, and refused to comply with policies she believed harmed people. The system suspended her licence and kept her in court for years. I explore why she believes early treatments were suppressed, why doctors were silenced, and how her fight touches medical autonomy and freedom of speech—about who controls medicine and information.

@JimFergusonUK - Jim Ferguson

🚨 SUSPENDED FOR TELLING THE TRUTH For nearly 30 years, Dr My-Le Trinh served as a GP in Australia. Then COVID happened. She questioned the narrative. She treated patients. She refused to comply with policies she believed were harming people. And the system moved against her. Licence suspended. Career threatened. Years in court. In my interview, she explains why she believes early treatments were suppressed, why doctors were silenced through fear, and why her legal fight now goes far beyond her own profession — to the core issue of medical autonomy and freedom of speech. Whether you agree with her conclusions or not, her story raises serious questions about power, authority, and what happened during those years the world was told there was only “one acceptable view.” This is not just about one doctor. It’s about who controls medicine. Who controls information. And what happens to those who dissent. Watch the full interview. @myletrinh123

Video Transcript AI Summary
Dr. Miley Trinh, a GP based in Sydney, Australia, joins Jim Ferguson for her first appearance on the show. She explains she has practiced as a GP for nearly thirty years and has been suspended since late 2021 amid a dispute with the health regulator over her license. She describes her suspension as part of a broader fight with regulators and regulators’ attempts to cancel her medical license. Trinh recounts how her concerns about the COVID-19 situation began in 2019, while following global events and studying debt-based economic systems. She states she became alarmed by reports of Wuhan’s lockdown timing, noting that authorities announced a lockdown five days earlier and allowed travel before it commenced, which she found alarming. She observed what she called unusual global coordination in reporting and policy responses to the pandemic, with early treatment being suppressed and a tightly controlled narrative across countries. Regarding ivermectin, she says she concluded after months of research that it was a key medication for treating COVID-19, particularly when given early. She describes participating in doctor groups and Zoom meetings to discuss how to treat patients and notes she treated a patient by telephone during lockdown who was deteriorating. She reports that the patient improved after her treatment but later faced complications requiring hospital care. She says two complaints were filed against her in September 2021—the first from a patient she had helped, and the second from an individual named John Smith who obtained a prescription that belonged to a family member for ivermectin. She asserts John Smith did not belong to her practice, and that the prescription was allegedly handed to an APRA (Australian Health Practitioner Regulation Agency) agent, a fact she says regulators overlooked when investigating her practice. Trinh emphasizes that she had never before faced a complaint in nearly thirty years of practice and that the suspension hearing concluded with her being deemed a danger to public health, despite her insistence that she saved a life. She has remained suspended for over four years. She describes the regulatory process as involving claims of prescribing ivermectin “below standard” and accusations of professional misconduct for not handing over 20 to 30 patient medical files, which she says she refused to provide because she did not know the patients’ names and because none of the patients had filed complaints against her. She notes that hearings occurred in December, March, and August, with subsequent issues over transcript integrity and requests for recusal of the presiding judge. She says a decision on the main case is imminent, but a cancellation of her license could entail a three to five-year suspension and substantial costs, complicating the possibility of reinstatement. Beyond her case, she argues the fight is about medical autonomy and the right for physicians to tailor treatments to individual patients, not be dictated by politicians or rigid guidelines. She criticizes what she views as a heavily censored environment for doctors who questioned the pandemic narrative or advocated for therapeutics like ivermectin, hydroxychloroquine, vitamin D, and zinc. She asserts that the COVID-19 Task Force guidelines opposed ivermectin and other therapeutics, and she contends such guidelines restrict doctors’ ability to provide individualized care. Trinh links the censorship and regulatory pressure to broader concerns about global governance, citing media suppression, removal of dissent on platforms like Facebook and YouTube, and increased control over platforms such as X (formerly Twitter). She mentions public support, including her presence on X and Facebook, as important to her ongoing legal battle and the broader struggle over medical autonomy and truth during the pandemic. She concludes by inviting people to follow her on X and Facebook to learn more and to show support as she pursues potential appeals if the judgment does not go in her favor. She frames her case as about more than COVID-19 alone: it is about challenging what she views as a long-standing, disproportionate control of doctors and a fight for fundamental rights, including the right to a hearing before the tribunal and the right to medical decision-making free from political interference.
Full Transcript
Speaker 0: Well, thanks very much indeed. Welcome to the show. I am Jim Ferguson, and I'm joined with a great guest. Her name is Doctor. Miley Trinh, all the way from Australia. It's her first time on the show. A big welcome to you, Doctor. Trinh. Speaker 1: Hi, Jim. Thank you for having me on the show. Speaker 0: You're very welcome. As a first time guest, maybe you would just, for the sake of our audience, tell us a little bit about briefly a little bit about who you are, what you do, where you're located, please. Speaker 1: Yes, sir. I'm a GP in Australia. I'm locating located in Sydney. I've been practicing as GP for almost thirty years before, being suspended, in late two thousand twenty one, and I've been fighting in the court, regarding my suspension and attempt by the health regulator to cancel my license. Speaker 0: No. I mean, this is obviously to do with the whole COVID pandemic. It's to do with your principled stand that you took. Let me ask you to go back to when you first thought and realized there was something not right about the whole thing. When was what the what was the earliest point you you you just sort of, in your own mind, discovered there's something not right about this? Speaker 1: So it started fairly early. In 2019, I was following the story of, I was following Donald Trump, campaign for his reelection in 2020. And, but the background of that, I have, interest in, about the financial situation, about the the the fact that we're in a debt a system of a debt based system, and it's about to implode. And I was just watching for any world event that could sort of, change or or indicate there's an indication that that that that there's some serious issues that's gonna come up. So when there was suspicion of, you know, anovirus or or a coronavirus being very serious and deadly, it it's I started to become very concerned, and I acutely aware of the the situation. So I started to do a lot of research into it. And when the when Wuhan lockdown took place, when they closed Wuhan, but they announced, that they were gonna close it down and but for, they announced that they're close it down five days beforehand and allow the people to travel all over the world to spread the virus. That to me was, quite alarming and quite concerning because it it didn't make any sense whatsoever. Speaker 0: Yes. I must admit, it was in, December. I think it was early December. I was actually in the Brexit party as a parliamentary candidate fighting the general election at the time, but I remember seeing those reports come out, those things coming out from China as well, and it started to raise red flags for me, and I think a lot of people that I know who have appeared on the show were were in the same position. And and I think also, the way it happened, the sort of coordinated lockstep that the the the the the world's governments were in also raised red flags because it seemed that there was a coordinated, plan unfolding. Did you feel that as well? Speaker 1: Definitely. So it was really unusual that every country have the same narrative. And, so I was watching what was happening in Italy and then what what was happening in The US because we were late to have our sort of cases arising. So, I was, seeing how unusual was the way the pandemic was dealt with, how every country responded in the same way, and how early treatment was, being suppressed and controlled. The narrative seems very controlled. Yeah. Speaker 0: Yeah. I mean the mainstream media were were almost giving identical reports all at the same time delivering exactly the same message. That, and a lot of people have said it since, has all the hallmarks of a psychological operation that was rolling out, and they were using fear to bully, coerce, intimidate people. And of course, when people are afraid, they look to leadership, and often that's the government. But the government's played a very, very big role, our respective government certainly, that I know Australia did, know The United Kingdom did in particular as well, in pushing that narrative that everybody had to get the mRNA shots, this experimental gene editing therapy, which which I I don't even like calling it a vaccine. They sort of called it a vaccine, but it wasn't really a vaccine, was it? Speaker 1: Well, no. It's, it's an experimental product that should not have been pushed upon the world, and certainly not especially people who who or well, especially young people who could deal with the infection quite easily without having to to take an experimental product. And the fact that they were coerced, and it was mandated, in order to for for these people to, take the procedure before they could continue to work. There's so much pressure and so much coercion in Australia. It's it's frightening. It's it's it's like it's just surreal. I I just couldn't believe that we come to a point in so called free country where we were so controlled and so we were pushed a narrative that was completely false and, pushed by health regulators, pushed pushed by health, so called experts and our own government. And there was no, discussion of the effects of this new experimental vaccine. No discussion on early treatment, management of the, of the pandemic. So it's it's it's bizarre. It's very disturbing. And, I mean, as a health regulate as as a health practitioner, my I see my role as being the primary care giver that I have to educate myself and to prepare myself if I have a patient that that's got COVID nineteen infection that I I need to be able to equip myself to know how to treat such patients, and that's what I I I did. So it's it was an unusual way of dealing with a disease that they said that it's new, and it's it's deadly, and they have to lock down the whole country. And yet the the response was completely illogical and irrational. Speaker 0: It certainly was. I know that Australia got hit very, very hard in terms of lockdowns. In the state of Victoria, remember seeing it under Dan Andrews, the the, I don't know how you would describe him, but I mean, he he seemed to be quite gleeful about the newfound power that he had, and he was he wasn't slow in threatening people, and he seemed to be enjoying himself. I mean, Dan Andrews is one of the worst. I know Canada got hit, of course, very, very hard, which led to the rise of the Canadian, Truckers Convoy, that freedom movement, many of whom I've met, all of the leadership I've met in my travels to North America. What was your reaction after doing the research? Because I think ivermectin played a big part in what you were trying to do to help your patients. Speaker 1: Yes. So in, after many months of research, I came to a conclusion that ivermectin was a key medication that could, very effectively, treating COVID nineteen, especially if if it's given early. So I I was in a group. I attended Zoom meeting with various groups and, in particular, a group with lots of other doctors discussing how we could handle or treat patients that that were sick. So I educated myself and equipped myself with that knowledge and understanding, and, that's how it all began. So in so in July, I, well, I took a bit of time off work during the pandemic, because I wanted to understand a bit more about the situation and also about the available treatment, because that wasn't forthcoming from, the health, our health departments. So and also the GP college, etcetera. So I, once I was able to once I I knew that I was convinced that there was treatment available, I felt the need to be back at work so that I could provide treatments for people who who were sick. So it started when I had a referral from a from, a colleague who, was aware of a patient, in my area, that was sick and needing some help, for treating COVID nineteen. And so I, accepted that responsibility and and took on to treat her. So she was in a lockdown area, and I wasn't able to go to visit her in her home. So the treatment was conducted over the phone. So that patient, got better after my treatment. She was very, very unwell, and I had to use various I mean, I was using medication in a way that I normally wouldn't use in general practice, but it was an emergency. So I used high dosage of steroid to treat her psycho her cytokine storm. So so she was she got better, but then she had some complication from the treatment and ended up in hospital. And I got reported by the intern of that particular patient. So I received two complaints in in September 2021. So two complaints came, on the same day, And that was a shock to me because I couldn't understand why I had a complaint made against me when I did everything possible and I saved her life. And and the second complaint was from someone by the name of John Smith, and the circumstances around that complaint was quite bizarre because John Smith happened to obtain a prescription that belonged to a family member that I prescribed ivermectin for, and that prescription was taken by me to the chemist to the local chemist. And so it was with a chemist. And, somehow, John Smith was able to obtain that prescription. And and I I didn't have a a patient by the name of John Smith, so he he wasn't a patient of mine. So that prescription was used as as a way of claiming that I promote there was a claim that I was promoting a treatment of ivermectin as the treatment of COVID nineteen and that I was promoting this measure this treatment online and that, I am an anti vaxxer, etcetera. So that was all false. I I didn't do any of that. And the issue the real issue was how did John Smith obtain that prescription. So when I found out that that prescription was it belongs to who whoever it was, and I knew the whereabout of that prescription. I went back to the chemist, and asked where the prescription had gone to. And I was told that the that the chemist had told me that the prescription was handed over to an APRA agent. So APRA being the Australian health regulator in Australia. So the so so the basis of that complaint was really completely fraudulent, and they the health regulator, instead of looking at the, fraudulent nature of that complaint, Instead of looking into that, it investigated me, and my practice. And for almost thirty years being a GP, I've never had a complaint made against me. But all of a sudden, one day, I had two came on one day, and and one from by someone who I about a patient whom I saved, and the other one was completely fraudulent and baseless. So I was taken to this meeting, this suspension hearing. And at the end of the hearing, I was suspended because I was considered a danger to public health. And I've done nothing wrong. What what I did was treating patients that were sick, and I did everything possible to save that patient's life. I went beyond my core to to to make sure that she's gonna survive. And so Speaker 0: Right. Speaker 1: I've been suspended since so it's been suspended for four years and three months. Speaker 0: We're gonna we're gonna come on to ivermectin in a moment. We're gonna go for a very, very short break. Don't go away. We're gonna be right back, and, then we're gonna talk a little bit more about ivermectin itself as one of the safest drugs. We'll be right back. Are you still feeling off after the COVID vaccine? You're not alone and new research backs it up. In a groundbreaking study, Risk Stratification for Future Cardiac Arrest After the Jab, Doctor Peter McCullough highlights an alarming rise in sudden cardiac events among young and previously healthy individuals. His study found that tiny hidden patches of heart inflammation often missed by doctors could silently be building up leading to sudden heart attacks during exercise or sleep. That's why the wellness company created the three in one ultimate spike detox, crafted with 100% natural ingredients specifically designed to help your body clear harmful spike proteins, reduce inflammation and support heart health. Don't wait until symptoms strike, experience the only formula approved and used by Doctor. McCullough, a top freedom fighting doctor who risked it all. Head to twc.healthgym10 and use code gym 10 to get 10% off. And we're back. I I want to clarify a couple of things that you mentioned. First of all, you talked about a cytokine storm. People might not know what that is. A cytokine storm, if I'm right, is where the body produces an overreaction to something that is going on. Am I right in saying that? Speaker 1: Yes, that's correct. So when the patient is, has been treated early enough and they have a significant vital viral load and the coronavirus being very immunogenic in in terms of the in terms of the reaction that the body's reacting to the virus, it induce a severe immunological response and it attacks the tissue in the lungs. So the lung tissue, I mean. So when your lungs becomes inflamed, then there's no oxygen exchange. So so the the blood cannot obtain oxygen and and and doesn't get oxygenated. Basically So you're in respiratory failure. So in order to reduce the inflammation in your lungs, you've got to take a huge dose of steroid in order to dampen down the inflammation. That doesn't happen until you're in the second phase of the COVID infection. So if get treated early, you get over it quite easily. But if you get it quite late and you get it quite severe, then you go to the second phase of the lung inflammation and that's a very serious illness and it could result in death. So technically, these patients should be really be in hospital and be treated in ICU. A lot of them were being treated in ICU. But in particular, the patient that I was treated, she had been to hospital before. She wasn't given any medication and she discharged against medical advice. She continued to deteriorate over a number of days when she contacted me. By then, she was sort of going to the second phase of the disease and it was a lot harder to treat and she didn't want to be she didn't want to go back to the hospital. So I had no choice, but well, I felt that I needed to treat her or else she would die. Yeah. Speaker 0: Well, thank you for clarifying that and for explaining it. The other thing I want to touch on is ivermectin itself. Ivermectin, I remember it was absolutely trashed by the mainstream media yet this is a drug that's been on the on the market, I think thirty, forty years. It's won prizes for being incredibly safe. It's very cheap to produce. Ivermectin is not a dangerous drug, is it? Speaker 1: No, not at all. In fact, it's one of the safest drug that we've had. So it's been around for, I think, almost forty years and it's won a Nobel Prize for the discoverers two two discoverers won the Nobel Prize for that. And it's been used successfully in treatment of parasitic infection and disease like river blindness. And because of my background, I was born in Cambodia, and I was a refugee from from Cambodia to Vietnam and then to Australia as a boat refugee. So I after I became a doctor, I provided I went back to Cambodia to provide medical mission work in Cambodia, in a rural area of Cambodia. So there's a condition, a parasitic infection of the intestine called strongyloides, which respond very well to ivermectin. So I had experience using ivermectin for such condition. Ivermectin was available over the counter in Cambodia. So it was not a drug that unfamiliar to me, and it was not a drug that I have any concern in using, and I have experience using it. So yeah. Speaker 0: There there was a a clear attempt by the mainstream media to completely denigrate ivermectin, to completely rubbish the whole name of ivermectin. They referred to it as horse paste. They made fun of it. You wonder why they would do that to a Nobel winning a Nobel winning prize medication that that is has been around for decades. Sometimes people say follow the money and and there were other people who were sitting very much involved with the whole mRNA scam, because I because I that's how I see it. Bill Gates was one of them. He was making considerable sums of money. There were indeed others that appear to have made a lot of money. Even the former prime Minister in The United Kingdom, Ritchie Sunek, who it turns out made an investment back in 2017 of $500,000,000 of his own personal wealth, he's a very wealthy individual, into Moderna through a shell company that he helped create in the Cayman Islands known as Thelim Partners. And I'm not sure if you're aware of that, but he was challenged because he was standing up in the Houses of Parliament here in London saying how safe and effective the mRNA shots were, all the while, making a huge amount of profit, it would seem. And when you I don't know if you're aware of that, but what what what's your reaction to that? Speaker 1: Well, ivermectin is a huge threat. Ivermectin and hydrochloroquine is a huge threat to the the provision provisional approval for the vaccine. So the the law concerning the approval of an experimental drug for a new disease is that if there isn't any therapeutics available for that disease, then you can resort, you have to resort to experimental drugs. So any therapeutics like ivermectin, hydroxychloroquine, vitamin d, vitamin c, zinc, and anything at all that is that is that's gonna help COVID, that's gonna alleviate COVID is a threat to the emergency use authorization. So you have there has to be there has to not be a therapeutic before the vaccine could be approved. So so ivermectin is a huge threat because it's it's the safest drug. It is much safer than hydroxychloroquine. And we didn't need the vaccine. In fact, can I can I can say with all of my heart with what I know that we didn't need the vaccine, that COVID could be treated very easily and very like, it's really easy to treat if we advocate early treatment, if we encourage people to take vitamin D and take measures to boost the immune system, go out in the sun, just measures like that? And that's been shown in India, in a province called Uttar Pradesh where they gave ivermectin and a combination of other things. I'm not sure exactly what they gave, but it's ivermectin combination of other medication for treatment of COVID-nineteen. And people just self medicate and within a few weeks, literally within a few weeks, COVID infection subsided to nothing. And they didn't need to resort to they didn't need to push, the vaccination so much, and they didn't need to lock down the country as long as we had had that to do. Speaker 0: Yes. So I remember I I remember the the news coming out of Uttar Pradesh in India where that actually happened, and, they had huge, huge success with it. Speaker 1: That's right. And that story was completely suppressed by the mainstream media. Speaker 0: Yes. I mean, it seems that there were there there was other reasons why this pandemic came along. I'm not sure just how involved some of these billionaires were, but there was a lot of people made a lot of money. Of course, big pharma were really pushing it out as well. They were paying fortunes for media coverage. There was a lot of people in the media that just went along with it simply because they were making a lot of money. This happened in Australia extensively as well, didn't it? Speaker 1: Yes. It is. I I think it's it's the same that what you have in The UK. It's a very coordinated effort, you know. This is it's it's I I just think it's been planned for a long time. So it's all the right people and in the right places to do what they needed to do. And and people were so I mean, it's so controlled that we just got nowhere to move, nowhere to to you know, if you say something, if your voice up, you you get suppressed, the the media will the social media or like Facebook will suppress, you know, will cancel your your account and things like that and you you get censored, you get cancelled, that kind of thing. It's such high level of censorship and in particular, those people who spoke out against the pandemic and those people who speaks who spoke about therapeutics and things like that. So so we're dealing with a a a situation where the the authorities were in complete control of the narrative and there wasn't any truth coming out. It's just all lies. Speaker 0: I remember joining a group on Facebook where there were people who had taken the vaccine. I'm not vaccinated. I refused to do it, but I remember joining this Facebook group. There, there must have been about 20, maybe 30,000 people in at that point and a lot of the people were sort of posting images of their skin and, and, and things that were going wrong after they had taken the vaccine. Well, that group got shut down and censored very, very quickly. Facebook were one of the worst. Mark Zuckerberg was very much involved with the censoring of it all. YouTube didn't feel much better and they still don't like people talking about this. X actually is the only real free platform for social media, that's why X is the only platform that I really bother with. And I do a lot of interviews with professors and scientists and doctors of course like yourself And because Elon Musk does believe in freedom of speech and of course, the Albanese government in Australia is attacking X vigorously as is Starmer in The UK, as is Mark Carney in Canada. The three of them seem to be coordinating together to try to actually bar X. When you hear of that sort of level of censorship kicking in again, what what do you think of that? Speaker 1: It's a different world we're living in. It's not what like what it used to be. It's something that we I find it really hard to to come to terms with. But it's changed, like our world's changed since COVID and it's it's not going back. It it's it's moving on the same as it is. And I mean, as a GP for like, I I'm a very private person. I I never post anything on social media, and I never spoke out about anything, in you know, in particular. But when COVID came along, the the I just the the the wrong that's been done to the people is to a level where I just can't, not speak out and I can't, especially because I've been I was suspended. Especially I've been suspended, I I have no choice. But I felt a need. I feel a need to speak out and to to voice, the truth because without voices of reason and truth, you're just gonna be overwhelmed with the lies. And and it's it's hard to have the courage to do that, but but I have to for the future of my children and and future generation because if we don't do anything, we're just gonna be completely completely controlled. Speaker 0: Well, I absolutely commend you for the courageous stand that you took for your patience, for the truth, to get that word out there and and you're still fighting hard. We're gonna come on to parts of the court case in a moment, but first of all, before we do that, I want to, I want to go back to, you know, you're obviously a deep thinker, you mean you're a professional healthcare practitioner, you're a doctor, you're a GP. You, you think deeply. Why do you think, I mean, you might not know the answer to this, but I always like to ask people when they come on the show, what do you think was actually behind all of this? Because the data is showing how harmful the mRNA shots were. I mean, we could spend the next three hours talking about just on the data itself and all of it is government data. But what do you think was really motivating these elites, these globalists to do what they did? Speaker 1: I can't help but to say that it is it is about control and it is about depopulation. You wouldn't want why would you give an experimental injection to the mass population? You you not only are you giving to them, you you've almost forced them to. You it the the level of coercion was so unbelievable that it was really hard for people to say no to. And there has to be a motive and the motive is to vaccinate all the population, as as as many as possible on a product that that in the in fact, we know it's harmful before it even it even created. I mean, mRNA the mRNA therapy has been available for years before the COVID before COVID and a few of the experiments that's been done on people have had really bad effect. In fact, many of those patients died and experimental on ferret and animals, they all died. So initially when it was first introduced, it was designed for use in genetic disorder where there's no available therapeutics. And that's only what it's reserved for a situation where there's no hope. And so there's a need for, research into therapeutics for that kind of diseases. But for the mass population to be injected with that kind of medication, that kind of therapeutics, that kind of treatment was actually not a treatment to be given an experimental product that we knew that it's gonna cause harm. Unjust it it cannot be justified. So why would why would people wanna do that unless they want to depublic the world? So there's very dark, nefarious agendas behind and and also control. I mean, all of a sudden in, you know, Western nations, those nations that were considered are free are the least free of all. We were if if you don't take the job, you can't work, you can't travel, you can't visit your loved ones, you can't live visit your dying loved one, you can't visit them in the nursing home. They just it's just unbelievable. It's just unbelievable. It's I mean, I was born in Cambodia, and my I lost my mom from the during the Khmer Rouge. And and I know that level of threat and and and fear that's from from government, but this is another level altogether. And and the worst of all is that they're doing all this under this facade that they're doing to protect the public. They they doing it for your for your safety and for your benefit, and none of that was true. Speaker 0: I think I think as somebody that's that that that that that that knows what communism really is under Paul Pott, the Khmer Rouge, huge numbers of people, I think millions were were were were slaughtered under his tenure. But going back to the earlier parts of the pandemic, I remember speaking with people, and many of them were doctors, some were scientists, some were professors who were looking into this and I remember thinking, look, is, is there has to be something more going on here and then I started to hear about the depopulation agenda where people like Professor Dennis Meadows has quite openly said on YouTube, you know, there's too many people in the world, billions have to go, that the planet can't sustain that population. But they're never the first ones to volunteer to off themselves, say doctor R, they, it's always everybody else that has to to do that, but it looks like, unbelievable as it seems, it looks like men and women, men and women, very powerful, very wealthy people, elites as they like to call themselves. I I tend to call them parasites, to be honest, because they are the parasite class. They have taken the decision, it would appear, to thin the hair, to get rid of many, many people. We saw our elderly communities here in The United Kingdom being treated with drugs that were extremely harmful in care homes. You vitamin D. Vitamin D is another very safe thing for people to take, very cheap to produce, but they didn't wanna know. And of course that, a lot of elderly in The UK in particular, don't get a lot of sunshine. That would have boosted their immune systems tremendously as well. Vitamin vitamin d along with zinc, and these types of things that ivermectin could have saved many, many millions of lives around the world, but actually many millions of lives were lost. What is the mentality of people that would that would decide that they were going to perpetuate, you know, perpetrate a global pandemic with the sole aim of of depopulation and control of the remaining population? It seems I think evil is the only way I can describe it. Speaker 1: Yes. I agree. Because really, they have no rights to decide for all of us. Who are they to say that the world is overpopulated? We only occupy a small part of the world. I mean, Australia is so vast and we only most of us only live in the in in the East Coast. There's many areas of many open land that that hasn't been occupied. Who is who is it to say that those areas can't we can't live in those areas? So but who who it is to say that for them to take away lives? They it's not for them to take it away. It's not they did not create a life. We are all created by God and they they have no right to make a decision to to to take away someone's life. And that's actually what happened. They pushed the jab, they locked down they locked down the country, they forced people to take an experimental product. They provide treatment that's not effective in hospital. They And they have no rights to do any of this. And I think in a way that I felt responsible in a sense that I felt that these people have such power to do what they they've been doing. And it's because the civilian, the average people, refuse to stand up and refuse to say no and refuse to to to to comply. Well, that they we always comply is the problem. And we we we're not we we refuse to stand up and to we refuse to stand up for what is right. A lot of the time, we'll hope we're hoping that someone would do it. Someone better will come along and would stand up and speak for us or or do something great. But I think that the world is the way it is because we allow just a few people to make decision for for everyone else. And it's about time for the rest of us to actually, say, speak out and and stand up for what is right and don't tolerate what is wrong. And I think that COVID is one of those thing where we cannot tolerate that kind that level of evil, that level of deception wrong to be perpetrated for the whole population. And for some of especially for some of us who are in the know, I mean, you don't know what goes on, then you can't really do anything. But for for for some of us that are in the know, we need to be able to we need to speak out, we need to stand up. It's really hard for me for what I'm for what I do, but, you know, I I believe in that. I want to do that because I can only do what I do. I can't tell what you know, I can't tell people what to do. So I need to do what is right and to hopefully encourage others to do the same. Speaker 0: You know, Freedom Tour International was inspired by the Canadian Trucker Convoy movement. I went there. I met all the leadership, decided to set up an international freedom movement, which is the largest and and fast still fastest growing in the world. We have a motto, don't be scared, be prepared. And I think that that that's very true in a lot of this. We've got to stand up, we've got to fight for the truth, we've got to fight for our rights and stand firm and hold firm together. And of course, that was one of the things they tried to do is to try to suggest that everybody that was asking questions was somehow, some kind of conspiracy theorist or anti vaxxer. You were labeled that as well. So I think, I think that, that it is all coming out. Now we're seeing an explosion in cancers, sometimes referred to as turbo cancers or early onset cancers where people go from not stage one, stage two, but they're straight to stage three or stage four cancer. Are you seeing that in Australia as well? Speaker 1: Yes. So I I have got friends that and and close I have friends that I know that I have have had stage four cancer, and I believe that it came from the vaccine. Speaker 0: A lot of people. Now they're trying to take your license. Tell us a little bit more about what's the next steps with the court case that's coming up. Speaker 1: So I've been fighting this for four years, nonstop. I initially took the medical counsel, the body that suspended me in 2021. I took them to the tribunal and then to the supreme court court of appeal. They dismissed my case, but, I I actually disagreed with the decision of the supreme court. But in the process of while I was doing that, they initiated a prosecution proceeding against me. So that was in late two thousand and twenty three, and that's the proceeding that I'm in at the moment, the proceeding that's before the tribunal. So they're seeking to cancel my license. They deemed that I have practiced significantly below standard for prescribing ivermectin, and they also alleged that I have committed professional misconduct for not handing over 20 to 30 patients medical files that they were seeking. But the the thing is that they didn't know the name of those patients, and none of those patients made a complaint against me. And I've been advised by two lawyers not to hand over those medical files. So so that's those are, the allegations that I have had to, face, before the tribunal. So that was, the hearing started in December. Sorry, December the before And it went to I had a second lot of hearing in March, and then we had a closing hearing in August. But then after August, I have initiated two two more proceedings because I discovered that the transcript was not how it's meant to be and that bits of the audio was missing, etcetera. So I had to challenge that issue. And, also, I applied for a recusal of the judge. So that hearing took place last week. So I think it won't be long before the decision of my main case would be would be released. So after that, I don't know what's gonna happen depending on what the decision, would be, will be. So if they're successful in cancelling my license, say they want to cancel it for further three to five years and they want me to pay for the costs of the prosecution proceeding, which been going on since 2023. And they also wanna fine me thousands of dollars for committing professional misconduct and unprofessional conduct, and and that could be up to $50,000. And it's really hard if you get suspended for that long and and have your license canceled for that long. It's hard for you to get reinstated. And it will be the same body who's gonna approve if I want to if I if I were to be cancelled and I I wanted to reapply. It's the same body's gonna approve my my application for, you know, if I wanna get back. So but my fight since, you know, since beginning till now, it's it's really more than just my license. It's about truth of what happened during the COVID pandemic. I refuse to call it a pandemic. It's a pandemic. And the truth about ivermectin because the fact that many people because in Australia, they banned ivermectin. I don't know what happened in Canada, but they banned ivermectin in Australia for for, I think, about two years, more than two years. And there was no reason for them to ban ivermectin. And ivermectin would have saved many lives and those the lives that have lost as a result of being denied of these people being denied of cure. It's criminal and they only would know if I continue to speak out and I continue to fight my fight. So my fight is more than just my license. It's about that. But it's also about medical autonomy. As physician, we are not we're not we should not be dictated by politicians or health regulators as to how we should treat our patient. We should treat our patient individually. Should be catered for individual patient depending on their health circumstance And we should apply what is best for that particular patient. We should not be dictated by guidelines how to treat, what should we use, what should be for particular disease, what specific medication had to be used. It should not be like that. And a guideline is a guideline. It's not one where you strictly have to abide by. So I've been judged by this particular guideline that the COVID nineteen task force had had, you know, put together. And that that guideline was against the use of ivermectin and against the use of anything that works. So I can't do that. I can't morally do that as a doctor to deny a patient, a dying patient, of an effective treatment. And so my fight is about medical autonomy and politicians shouldn't be involved in how doctors care for their patient. Speaker 0: Especially politicians who are globalists and following a global agenda that is not in the interests of humanity itself. Where can people find more about you? How how can people support you? Speaker 1: I I like them to they can they can follow me on X. So my Twitter handle is maileitwin one two three and on Facebook. I'm very active on Facebook as well as SX. I I just want people to share my story because I'm going through the court process and and having public support is very significant. I'm also seeking to it's there's a likelihood that I might have to appeal my case if the judgment is not going my way. So in a few months, I'm I the judgment will probably be released, and I would have to continue to fight on. And there'll be another eighteen months or so of fighting in the Supreme Court. So I just want the public support to continue. Yeah. Speaker 0: Well, you you know, as we always do with our great guests, I always give them the last and final word, bearing in mind that we have a very large following all across North America, including Canada, and actually all around the world. We have a lot of Aussies that follow us here on the show as well. So what would you like to say to them? Floor is yours. I Speaker 1: wanna say that my fight against the medical council, against the health care complaints commission is highly significant in Australia. And this is what I'm fighting for is more than more than COVID. It's about because because the health regulator's been able to control doctors for fifteen years since the introduction of a new law that we are regulated under. And I have in in my case to the Court of Appeal, I challenge a particular legislation that's really significant because it allows doctors when they suspend it, they we we we supposed to have we're supposed to be referred to the tribunal before we get prosecuted. So so the injustice is that doctors are so how how can I they the the the way the the way the health regulators been running, the proceedings like like myself and and cases where they want the the when they want to suppress a particular treatment and a particular doctor is being persecuted, they go through this process where the doctors do not have the right to have a hearing and that right, that legislation I challenge in the in the Supreme Court, which I failed? However, I am planning to rechallenge that second time in the Supreme Court. And if I'm successful, it means that the the control that the health regulators have on on on doctors and on on health, professional in general, will not be able to continue because that right the right to have a hearing before the tribunal, before the prosecution is highly significant, and that's been denied that's been denied for for more than a decade. So so so like an example in my case, the substantive matter of my case has never been hurt. And yet, I'm facing prosecution. Look at the level of injustice that is for for for someone. I mean, not you don't need to be a doctor. Just in general, if if you've been accused of something, you need to you need to be able to have a hearing to have a say. And that is the fundamental legal rights of of any individual. That's a human right. And that's been denied to all by all doctors to all doctors. That's been denied for a long time. So that's why, the level control of doctors in Australia is is is so severe that, doctors in Australia are so afraid to speak out, and they they all do what they are told to do. And so I want to be able to change that. And and my case, if if I need to appeal to the supreme court this time, I will be challenging that legislation again. Speaker 0: Well Doctor. Maile Trinh, want to say I commend you for the great courageous stance that you're taking and I want to really thank you for being on the show with us today telling us about your experience and what's happening. Speaker 1: Thank you Jim for having me on the show. Thank you so much for the opportunity. Speaker 0: My absolute pleasure to all of you out there watching. This is a very principled lady. She's tough, she's sincere and you can really help her by sharing this content. Let's get this out far and wide all around the world because people need to know that there are good doctors who fight for them and the whole medical practice itself. So thank you Doctor. Maile Chren and thank you to each and every one of you for watching. Until next time, this is Jim Ferguson and we'll speak soon. Bye bye for now.
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