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" Cancer? Cancer, you know, we're we're seeing certain cases here and there." "for those three cases, you know, there was success. You know, I know two of the patients." "it's not for everybody." "why is it again that some patients are improving with high dosages of mebendazole, ivermectin, etcetera, and some patients are not?" "we did fecal transplant using her grandson, and we extended her life. She improved her appetite." "She improved her hemoglobin, but it wasn't continuous." "we've shown that loss of bifidobacteria is a problem in invasive cancer." "I think there's gonna be in a future where we're gonna have, every cancer is gonna have a microbe attached to it." "Think about HPV cervical cancer, H. Pylori, gastric cancer, Burkitt's lymphoma, Epstein Barr virus." "there's gonna be a link to a cancer and a microbe that's lacking that needs to be repopulated." "in other words, is it over is the tumor growing because of a microbe that's in there that’s allowing it to grow?" "suppression of that microbe would be first to to kill off the tumor." "the methods that we have right now at killing the tumor is we kill off everything. Kind of like what we do with hydroxychloroquine." "We kill off the virus, but then we kill the whole microbiome." "that's not necessarily a solution because the problem is, well, you've killed the virus this time, but then what happens now you've killed your microbiome and your bifidobacteria, and now you're gonna get another virus and another virus." "Knowing what I know today, which is once you kill your microbiome, it takes years to recover."

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Speaker 0 asks: first, what impacts the loss of bifidobacterium? and second, what can we do to replenish it and keep it strong and populated? Speaker 1 responds that the microbiome is still in its infancy, and urges not to assume you can test your stools in the market because the FDA doesn’t have a test approved for testing stool. Regarding buying Bifidobacterium, he says that the problem with replenishing is you may suppress your own ability to make Bifidobacteria, and what Bifidobacteria needs is good nutrition, good vitamins, and good yogurt. He cites the case of a woman who lived to 117 years old in India, noting that remnants of bifidobacteria were found in her stools, and that she ate yogurt three times a day. When asked how much she ate, he replies that there aren’t studies on that, but yogurt is happening. Speaker 1 continues: in a world where we constantly dodge viruses, parasites, and bacteria that secrete toxins, survival involves doing one’s best. There are things that kill the microbiome, notably antibiotics. Therefore, when you take antibiotics, that’s the time to supplement with a good probiotic and good vitamins. He notes a problem: 16 out of 17 probiotics on the market do not have Bifidobacteria. He explains why he began focusing on Bifidobacteria: in the trillion-dollar probiotic industry, if you turn a bottle around and read the ingredients, the bacteria listed are Bifidobacteria. That observation during the pandemic sparked his interest in Bifidobacteria. He says the whole path is to save the Biff, referencing the idea that during stressful moments—political division, hate, anger—seeing the power of a microbe becomes important.

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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.

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While treating COVID patients with hydroxychloroquine, the speaker discovered ivermectin's effect on oxygen saturation. This led to the realization that ivermectin is in the same phylum as bifidobacteria, which were found to be lacking in severe COVID cases. Antibiotics are essentially microbes, illustrated by the discovery of penicillin from apple mold killing bacilli. Similarly, vaccines are microbes or pieces of microbes. The speaker notes that drugs are made somehow. Ivermectin is the fermented product of a soil bacteria. The speaker poses the question of whether ivermectin's secretion feeds bifidobacteria, potentially boosting immunity, while emphasizing that this is still under research.

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Speaker argues that the majority of doctors lack the private-sector tools to "go outside the box"—no FDA portal to write INDs, no funds, no genetic sequencing labs, and no in-house scientists. They say doctors are "limited to what the guidelines are telling them to do" because stepping outside risks lawsuits; achieving this requires "'a regulatory board... FDA oversight... lawyers' costs." This isn't a field for all doctors. Cites examples like Peter McCullough and others (Pierre Corre, Paul Merrick, Jackie Stone, Mary Bowden). Peter McCullough is praised as "'published thousands of papers'"; most doctors merely receive data from sources and may miss data. During the pandemic, they faced rushed conditions and propaganda—"hydroxychloroquine was a bad drug, Ivermectin was a horse paste"—"they didn't get to see the data." The speaker notes three FDA-tracked trials and asserts FDA jurisdiction in off-label work, and that "'I had an FDA approval to run these trials.'"

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

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

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The speaker discusses an ivermectin study showing ivermectin increased bifidobacteria before and after, noting it rose with ivermectin but didn't last: "Goes up, goes back down." He questions whether this yo-yo effect explains cancer patients' lack of improvement and whether timing matters. When someone reports a patient improved kidney cancer with ivermectin, mebendazole, he asks to see the microbiome before and after, blood work, and markers to understand why some survive while others don't. He praises courageous physicians who push the art of medicine to save lives, citing a seven-year-old with a brain tumor who was headed to hospice; he urges trying everything with informed consent. He concludes: "I don't know. This is research. I don't know, but I'm willing to try. These are the risks. Your kid may die on my protocol." He emphasizes weighing the risk-benefit ratio.

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Speaker discusses anecdotal findings on bifidobacteria from vitamin C and ivermectin, and the publish‑or‑perish obstacle in research. "I took a lot of vitamin c at the beginning of the pandemic. Grams a day." "I do not recommend it to anybody." He did it as a guinea pig, and notes that vitamin C "increases bifidobacteria." He then tested about 20 patients to see what happened. "Ivermectin increases bifidobacteria," but publication was blocked by research interference, making long-term effects unclear—"could there be kidney problems? Could there be liver problems?" He laments that you cannot advance research if you don't publish, because publication validates work. When he published "the lost microbes of COVID," labs, Japan, China, and Italy, reproduced the data, confirming replication. "If that paper is real, it gets reproduced into three, four, five papers." He emphasizes colonization as the essence of the work and notes cross‑population questions about who it helps.

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" I'm a big believer of vitamin c. " "This doesn't mean it's going to work for everyone and we're not making any claims. " "There is definitely something about vitamin C through the years that have said to people, wait, vitamin C is pretty safe. " "But then we looked at the in vitro studies and that's how they grow the bitter bacteria. " "In vitro studies of vitamin C effect on the microbiome, you actually see increased Bifidobacteria with in vitro. " "So we just proved on a human clinical model what the in vitro model did. " "I'm on this big push of increasing the betrobacteria. " "That's my science... my vision. " "Are antibiotics good? Are they good long term? " "Now we're in the world of biologics. What are biologics doing to the microbiome? " "Maybe all disease starts with lots of bifidobacteria. " "As I'm improving the benefit of bacteria, I see improvement in the disease clinically as a physician."

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The speaker observed that patients with severe COVID were missing bifidobacteria compared to those highly exposed but uninfected. Bifidobacteria is a key microbe for immunity and is present in newborns but absent in older people. The speaker's research indicated vitamin C increases bifidobacteria, which may explain its use for treating colds. Ivermectin also increased bifidobacteria within 24 hours, possibly because it's a fermented product of a similar bacteria. The speaker hypothesized that ivermectin's observed benefits in COVID patients might be due to increased bifidobacteria. This hypothesis was the most read during the pandemic but was later retracted. The speaker believes the retraction of a hypothesis is not in the spirit of science.

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

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I'm Karen DeVore, a dermatologist in South Carolina. I've been prescribing hydroxychloroquine and Ivermectin for over 30 years, off-label. In 2020, the FDA called Ivermectin horse medicine and doctors couldn't prescribe it. I knew these drugs were safe and effective, and I saw great results in my patients. None of the patients I treated with these drugs were hospitalized or died from COVID. They had no side effects and felt better within hours. It's frustrating that insurance companies and pharmacies denied access to these drugs. Even terminally ill patients on ventilators couldn't try them. How many lives could have been saved?

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"I did a case where I did fecal transplant on a patient with Alzheimer's, and he could remember his daughter's date of birth six months after the procedure. So when I changed his microbiome, his poop in his colon, and gave him his wife's microbiome, who was super with it, started remembering things. So, when we start looking, and we're actually publishing stuff at ACG, because the deadline's today actually to publish for ACG American So, College of we have six abstracts coming up, and so we're showing the data on Alzheimer's, autism, long haulers. So, can't say vaccine injured because then it's not gonna be, you know, it's too controversial. So we have to stay within the but here's the problem. It should not be controversial. In order to advance science, in order to advance medicine, we need to be, better. We need to be better at listening"

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"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?"

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I discovered that patients with severe COVID lacked a key bacteria, bifidobacteria, which is crucial for immunity. Newborns have this bacteria, while the elderly do not due to aging. Vitamin C and Ivermectin were found to increase bifidobacteria levels. I published a hypothesis linking Ivermectin to bifidobacteria increase, which gained attention but was retracted. Hypotheses are essential in science.

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In December 2020, the speaker began collecting stool samples from colleagues before and after their COVID vaccination to study the vaccine's impact on the microbiome. The speaker discovered that mRNA vaccines killed bifidobacteria but believed these findings were unpublishable due to the prevailing narrative. The speaker presented this research as an abstract at the American College of Gastroenterology in October 2022, where it won a research award, beating 6,000 other abstracts. This abstract drew the attention of 18,000 GI doctors, who began to consider that the loss of bifidobacteria may explain why they contracted COVID after vaccination. Further research indicated persistent damage to bifidobacteria from the vaccine. The speaker's presentation also linked the loss of bifidobacteria to Crohn's disease, Lyme disease, and invasive cancer.

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Speaker 0 explains that in the probiotic market, one out of 17 probiotics on the market has real bacteria in there, meaning 16 out of 17 say Bifidobacteria on the label but don’t actually have it. He adds that three out of 26 yogurts or drinks that say bifidobacteria on the market have bifidobacteria; the rest do not. He then asks about verification and testing. Speaker 1 asks if there is any way to know by looking at the label, and whether testing exists. Speaker 0 says you can call the lab Progena Biome to test, and there are other labs that do spot checks. He notes another problem: whether the microbe is alive or dead. Bifidobacteria in the gut are anaerobic, so exposing capsules to air may kill them, and stomach acid could also kill them before they reach the gut. He reframes the question: what does dead bacteria do to a live microbiome? He compares it to sleeping with corpses and suggests eventual effects on the microbiome and potential diseases, reflecting his viewpoint. Speaker 0 then raises another issue: by taking probiotics, are you suppressing your own gut production, similar to taking pancreatic enzymes which helps digestion but may shut down the pancreas’s own secretion? He questions whether taking oral enzymes could cause damage by reducing the body's own production. He explains that their approach is research-focused: they test patients with a stool test in the research world, then determine what the probiotic is doing, and implement a protocol with the right probiotic, the right prebiotic, the right bovine, and the right vitamins to see if the patient improves. If it works, great; if not, they reassess why the probiotic didn’t work—whether the probiotic was killed in the gut or interacted with certain bowel areas and became inactivated or transformed. Speaker 0 notes that he doesn’t talk about which probiotics upfront because they are still testing. He mentions several probiotics he is testing and acknowledges that not everybody responds similarly. They must understand why a probiotic works in some patients but not in others. Overall, the discussion centers on probiotic quality, viability, and personalized testing to determine effectiveness, along with concerns about dead bacteria, potential suppression of natural gut processes, and the need for ongoing research to explain variable patient responses.

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Speaker 1 discusses probiotics and the current state of microbiome science: taking random probiotics may be questionable because the technology of the microbiome is not FDA-approved yet. The reason is that there are many bacteria in the microbiome and we don’t know what they are, what they do, whether they’re good or bad. For example, blotia and Rosaburia are poorly understood; 90% of GI colleagues don’t know blotia is a microbe, and 90% don’t know there’s such a thing as Rosaburia. Historically trained on Klebsiella pneumoniae, E. coli, Salmonella, C. difficile, Clostridium perfringens, but not on nonpathogenic microbes. The question remains: is blotia a good bug or a bad bug, and who has too high or too low levels? This represents the abyss of the microbiome and is still research, not consumer product or standard medical practice. Speaker 1 explains that doctors cannot be told to use a new stool test or to start using microbiome data broadly until researchers reproduce findings and doctors see the data for themselves. The idea is that oncologists may notice correlations, such as loss of bifidobacteria in invasive cancer, and observe improvements in cancer alongside bifidobacteria, which could influence acceptance of the gut-brain or microbiome link. However, such observations need replication to move from incidental findings to established conclusions. An example given is Colleen Kelly at Brown University, who published two cases of alopecia areata with C. difficile where hair grew back after fecal transplant. The question is whether fecal transplant for alopecia areata is valid; however, an academic center trying to reproduce the data could not. The speaker suggests uncertainty about whether a specific microbe caused hair regrowth or if exposure during treatment led to it. Until data are reproduced, no one can claim alopecia areata is improved by fecal transplant or microbiota transplant. Concluding guidance: if you’re healthy, keep doing what you’re doing and do nothing else; if you’re not healthy and have multiple diseases and you’ve tried a probiotic, if it works, continue, but if it doesn’t work, then it’s probably not a great probiotic. The overarching theme is careful interpretation, replication, and recognition that microbiome science is still evolving and not yet ready for universal clinical application.

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Speaker 1 notes that ivermectin has broken through to the public sphere beyond COVID and is now discussed for many diseases. Speaker 0 asks where ivermectin stands in the scientific and medical community today and what other use cases exist for the medicine. Speaker 1 responds that thousands of doctors follow their data; 18,000 GI doctors see their data when they publish or present at the American College of Gastroenterology. Word-of-mouth in the medical community is a major form of marketing, with one doctor speaking to another. Referencing the COVID era, Speaker 1 mentions corruption and retractions, then describes ivermectin as having created a healthcare revolution where doctors have lined up to work to see other benefits of ivermectin without needing to ask permission to treat patients. A whole branch of healthcare is moving away from the same institute that Speaker 1 helped create drugs to market with his sisters. He says a group of doctors who had sponsored or helped pharma are turning away from pharma and exploring other methods to treat patients. He states his job is to unite doctors to see the truth, while bringing pharma back to being righteous and stopping data manipulation and scientist censorship. Speaker 1 references his book, Let’s Talk SH.T, acknowledging he could be wrong and challenging others to prove him wrong and reproduce the data to retract the hypothesis or paper. He emphasizes that the scientific process should be followed, especially when everything was done by the book and as well as he could. He adds that the research was not funded by others; it was funded by his savings. He created the microbiome research foundation with the goal of raising money to study kids with autism and to push an IND to the FDA, which cost about $600,000 to obtain FDA approval. He clarifies that no external party paid for this work, and he continues to struggle to raise funds to treat poor autistic kids who cannot afford expensive stool testing, drugs, and vitamins; they need help and everyone should step in to assist these kids. Speaker 1 concludes that their focus is fixing autism, with the aim of later addressing Parkinson’s, Alzheimer’s, and cancer.

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Speaker 0: Bifidobacteria was absent in kids with autism, that Bifidobacteria was absent in Alzheimer's. Bifidobacteria was absent in long haulers, vaccine injured, Lyme patients, Crohn's patients, invasive cancer. When you look at who has Bifidobacteria, the newborns have a lot of Bifidobacteria, old people have zero Bifidobacteria. Nursing home dying, zero Bifidobacteria. The process of aging is really this loss of Bifidobacteria. Expanded: if you look at and you believe the Bible, you know, people lived a lot longer. In biblical times than we are right now. We're barely making it to seventy, eighty and not really healthy seventy, eighty. You know, the mind starts going. So, is the mind starting to go because of the loss of Bifidobacteria? And, when you start looking at, well, what improves Bifidobacteria, right? So, our lab discovered vitamin C improves Bifidobacteria. Okay. Our lab discovered bovine immunoglobulins, the blood of the cow spun around that clear stuff, provided that the cow is not on a lot of antibiotics, is not given a lot of hormones, is not given like thousands of vaccines. So when you start looking at all that, you start seeing the importance of Bifidobacteria and you start seeing, like even me, you know, with Progena Biome, looking at the stool samples before the pandemic, during the pandemic and after the pandemic, there is a lot of disappearance of Bifidobacteria. Is that why we're having an increase in Alzheimer's, increase in cancer? Have we demolished this bifidobacteria? So, to me, that's a very important microbe that I believe is our longevity, if we can retain it. And it's not easy to retain in a world that's toxic in a way and in a world where we are, you know, put you know, given media full of stress, where we are divided, where we are, you know, constantly nervous of the next pandemic or the next virus, you know, it's it's almost like this bottle that you're shaking and it's full of gas and you just need to put it on the counter and let it just calm down, right? So, I think that's, it's a very important microbe.

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

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But I think there's you know, what's beautiful now because so many doctors are stepping up and seeing something and talking about something, I'm not saying that's the right thing. 'Is ivermectin improving cancer? Certainly some doctors have seen it.' 'So is that the way we is it improving for everybody? What is it in ivermectin that improves the microbiome of certain people and not in others? What is it in ivermectin that helps certain cancers and not others? Right? So we really need to be better to say, okay, look, I'm courageous enough to add ivermectin to my protocol of the chemo or the bio or the immunotherapy that I'm giving or maybe I don't.' 'And maybe at least I look at the microbiome. I look at the microbiome on what is believed right now, you know, a a good look at it.'

Keeping It Real

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

The Peter Attia Drive Podcast

283 ‒ Gut health & the microbiome: improving and maintaining the microbiome, probiotics, & more
Guests: Colleen Cutcliffe
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The microbiome is a mutable ecosystem of microbes, including bacteria, viruses, fungi, and yeasts, residing in and on the human body. Colleen Cutcliffe, with a background in biochemistry and molecular biology, discusses her journey from academia to founding Pendulum, a company focused on microbiome-based products. She emphasizes the potential of microbiome interventions, particularly through fecal microbiome transplants, to improve health outcomes. Cutcliffe explains that the gut microbiome is established at birth, primarily influenced by the mode of delivery and early exposure to maternal microbes. The diversity of the microbiome peaks in early adulthood and declines with age. While the idea that microbes outnumber human cells is debated, the functional importance of these microbes is clear, as they contribute significantly to bodily processes. The conversation shifts to the differences between prokaryotic bacterial cells and eukaryotic human cells, highlighting that bacteria can replicate independently and evolve rapidly, which is a factor in antibiotic resistance. The relationship between humans and their microbiota is generally symbiotic, although some bacteria can become pathogenic under certain conditions, such as *Clostridium difficile*, which can proliferate when antibiotics disrupt the balance of the microbiome. Cutcliffe discusses the Human Microbiome Project, which revealed significant variability in microbiomes across individuals, influenced by factors like genetics, diet, and environment. The complexity of the microbiome makes it challenging to draw definitive conclusions about specific strains and their functions. The conversation also touches on the role of different microbes, including the potential benefits of *Akkermansia muciniphila*, which is associated with metabolic health and glucose regulation. Cutcliffe describes how *Akkermansia* can stimulate GLP-1 secretion, a hormone that helps regulate blood sugar levels and appetite. Pendulum's product, Glucose Control, was developed based on clinical trials showing its efficacy in lowering A1C and blood glucose spikes in individuals with type 2 diabetes. The formulation includes multiple strains to enhance metabolic function. Cutcliffe notes the importance of rigorous scientific validation in the supplement industry, which is often plagued by unsubstantiated claims. The discussion highlights the challenges of studying the microbiome, including the need for longitudinal data and the difficulty of controlling for dietary factors. Cutcliffe emphasizes the importance of understanding individual microbiome responses to interventions, as well as the potential for future research to uncover more about the gut-brain connection and the impact of diet on microbiome health. Overall, the conversation underscores the evolving understanding of the microbiome's role in health and disease, the potential for targeted microbiome therapies, and the importance of scientific rigor in developing effective products.
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