Video yükleniyor...

Video Yüklenemedi

Ana Sayfaya Dön

Spike Is Generated Forever Once Integrated Into Stem Cells‼️ Professor Emeritus Yasufumi Murakami of Tokyo University of Science was interviewed about what researchers have proven incontrovertibly about DNA and SV40 contamination and the implications now for human life‼️ Once DNA integration occurs within stem cells, it is permanent and...

sophiadahl1's profile picture

Sophia Dahl

84,324 subscribers

13,513 görüntüleme • 7 ay önce •via X (Twitter)

LIVE

Anya Rossi• Live Now

Private livecam show

0 Yorum

Yorum bulunmuyor

Orijinal gönderinin yorumları burada görünecek

Benzer Videolar

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.
6:34

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.

You

574,563 görüntüleme • 2 yıl önce

🚨🚨🚨🚨 Oh-oh! First experiments of genetic vaccines getting absorbed by human cells completed - Prof Sucharit Bhakdi reveals. ----------------------------- Our two lady scientists who are just brilliant, they took cells, human cells, and immersed these cells in the vaccine and they found, and these are the first experiments that have ever been done, okay, that the human cells immediately took up the vaccines and the DNA and the chromosomes, and the chromosomes, bacterial chromosomes, entered the cells and these cells immediately started making the spike protein in horrendous quantity and they have quantified this, they have shown what happens to the spike protein, that it is stable, that it is shed into the blood, into the circulation, they have shown that they can measure this in the blood, they can measure this anywhere actually, and they have shown that the plasmid and the spike production goes on for many, many days. So, what did our girls do? They sent their human cells that had been transfected to Kevin McKernan, begging the question, Kevin, can you find any chromosomal integration of bacterial DNA in the human cell chromosomes? Do you know the answer? He put it up in his substack one week ago, and the answer is yes. He's found it. ------------------------------------- Kevin McKernan
5:27

🚨🚨🚨🚨 Oh-oh! First experiments of genetic vaccines getting absorbed by human cells completed - Prof Sucharit Bhakdi reveals. ----------------------------- Our two lady scientists who are just brilliant, they took cells, human cells, and immersed these cells in the vaccine and they found, and these are the first experiments that have ever been done, okay, that the human cells immediately took up the vaccines and the DNA and the chromosomes, and the chromosomes, bacterial chromosomes, entered the cells and these cells immediately started making the spike protein in horrendous quantity and they have quantified this, they have shown what happens to the spike protein, that it is stable, that it is shed into the blood, into the circulation, they have shown that they can measure this in the blood, they can measure this anywhere actually, and they have shown that the plasmid and the spike production goes on for many, many days. So, what did our girls do? They sent their human cells that had been transfected to Kevin McKernan, begging the question, Kevin, can you find any chromosomal integration of bacterial DNA in the human cell chromosomes? Do you know the answer? He put it up in his substack one week ago, and the answer is yes. He's found it. ------------------------------------- Kevin McKernan

aussie17

333,911 görüntüleme • 2 yıl önce

A bombshell scientific publication confirms a critical danger in the Pfizer/BioNTech COVID-19 vaccine, and the implications are as severe as they are alarming. The core issue is plasmid DNA contamination. New research confirms this contaminating DNA is not just present in the vial; it is capable of entering human cells. This fact alone is concerning, but the true danger lies in what this DNA contains. Scientists have identified the presence of an SV40 viral promoter/enhancer sequence within Pfizer's plasmid DNA. For decades, SV40 has been known to be a potent tool for driving gene expression and is associated with potential genomic integration risks. Here is why this is a catastrophic failure in regulatory disclosure and vaccine design: 1. Nuclear Entry & Genomic Integration: The SV40 promoter is functionally active in human cells. Its presence means the contaminating plasmid DNA has a non-zero chance of entering the nucleus of a human cell. Once inside the nucleus, it runs a tangible risk of integrating into the human genome. 2. Uncontrolled, Long-Term Gene Expression: If integration occurs, it could effectively turn the vaccine into an unintended and uncontrolled gene therapy. This could force the body to produce the SARS-CoV-2 spike protein indefinitely—for months, years, or permanently, with unknown health consequences. 3. A Deliberate Omission? Most damningly, Pfizer never disclosed the presence of this known biohazard, the SV40 sequence, to regulatory bodies during the approval process. There was no functional reason for its inclusion, as Moderna's production process utilized a standard bacterial plasmid without such dangerous components. The authors of this pivotal study are now calling for the immediate suspension of these mRNA vaccines until a full understanding of their long-term genomic risks is achieved. They further state that Pfizer and BioNTech must be held accountable for exposing the global population to a risk this significant without informed consent. This is no longer speculation. This is published, peer-reviewed science confirming a pathway for potential permanent alteration of the human genome. The demand for transparency and accountability has never been more urgent.
3:00

A bombshell scientific publication confirms a critical danger in the Pfizer/BioNTech COVID-19 vaccine, and the implications are as severe as they are alarming. The core issue is plasmid DNA contamination. New research confirms this contaminating DNA is not just present in the vial; it is capable of entering human cells. This fact alone is concerning, but the true danger lies in what this DNA contains. Scientists have identified the presence of an SV40 viral promoter/enhancer sequence within Pfizer's plasmid DNA. For decades, SV40 has been known to be a potent tool for driving gene expression and is associated with potential genomic integration risks. Here is why this is a catastrophic failure in regulatory disclosure and vaccine design: 1. Nuclear Entry & Genomic Integration: The SV40 promoter is functionally active in human cells. Its presence means the contaminating plasmid DNA has a non-zero chance of entering the nucleus of a human cell. Once inside the nucleus, it runs a tangible risk of integrating into the human genome. 2. Uncontrolled, Long-Term Gene Expression: If integration occurs, it could effectively turn the vaccine into an unintended and uncontrolled gene therapy. This could force the body to produce the SARS-CoV-2 spike protein indefinitely—for months, years, or permanently, with unknown health consequences. 3. A Deliberate Omission? Most damningly, Pfizer never disclosed the presence of this known biohazard, the SV40 sequence, to regulatory bodies during the approval process. There was no functional reason for its inclusion, as Moderna's production process utilized a standard bacterial plasmid without such dangerous components. The authors of this pivotal study are now calling for the immediate suspension of these mRNA vaccines until a full understanding of their long-term genomic risks is achieved. They further state that Pfizer and BioNTech must be held accountable for exposing the global population to a risk this significant without informed consent. This is no longer speculation. This is published, peer-reviewed science confirming a pathway for potential permanent alteration of the human genome. The demand for transparency and accountability has never been more urgent.

Camus

205,889 görüntüleme • 10 ay önce

New Research Deep Dive: The "Shedding" Conversation Just Got More Serious A new in-vitro study (using human cells in a lab) on the Pfizer mRNA vaccine has revealed critical findings that can no longer be ignored. Let's break it down. The researchers confirmed two major things: 1️⃣ Spike Protein Production: The cells successfully took up the mRNA and began producing the SARS-CoV-2 spike protein, displaying it on their surface. This was expected. 2️⃣ Spike Protein "Shedding" via Exosomes: Here's the crucial part. The cells didn't just keep the spike protein to themselves. They packaged it into exosomes—tiny extracellular vesicles cells use to communicate—and excreted them into the environment. Why does this matter? This provides a potential mechanistic blueprint for how spike protein could travel systemically throughout the body after vaccination. These spike-laden exosomes can enter the bloodstream and, theoretically, deliver their cargo to distant organs and other cells. But the most alarming part? The authors note a profound lack of safety data. They explicitly state: We have no scientific studies to determine if this exosome-mediated spread of spike protein is toxic to other human cells. Even more concerning, they observed "pathological changes" and toxicity within the cells producing the spike. And these weren't weak cells—they were robust, immortalized embryonic kidney cells, chosen for their resilience. If these cells showed adverse effects, what is the impact on our more delicate primary cells? The authors themselves caution that proper toxicology studies on normal human cell lines are urgently needed... and are currently unavailable. This isn't conspiracy theory. This is cell biology. The conversation must evolve from if spike protein can travel, to what are the systemic consequences when it does. The call for rigorous, independent safety science has never been louder.
2:20

New Research Deep Dive: The "Shedding" Conversation Just Got More Serious A new in-vitro study (using human cells in a lab) on the Pfizer mRNA vaccine has revealed critical findings that can no longer be ignored. Let's break it down. The researchers confirmed two major things: 1️⃣ Spike Protein Production: The cells successfully took up the mRNA and began producing the SARS-CoV-2 spike protein, displaying it on their surface. This was expected. 2️⃣ Spike Protein "Shedding" via Exosomes: Here's the crucial part. The cells didn't just keep the spike protein to themselves. They packaged it into exosomes—tiny extracellular vesicles cells use to communicate—and excreted them into the environment. Why does this matter? This provides a potential mechanistic blueprint for how spike protein could travel systemically throughout the body after vaccination. These spike-laden exosomes can enter the bloodstream and, theoretically, deliver their cargo to distant organs and other cells. But the most alarming part? The authors note a profound lack of safety data. They explicitly state: We have no scientific studies to determine if this exosome-mediated spread of spike protein is toxic to other human cells. Even more concerning, they observed "pathological changes" and toxicity within the cells producing the spike. And these weren't weak cells—they were robust, immortalized embryonic kidney cells, chosen for their resilience. If these cells showed adverse effects, what is the impact on our more delicate primary cells? The authors themselves caution that proper toxicology studies on normal human cell lines are urgently needed... and are currently unavailable. This isn't conspiracy theory. This is cell biology. The conversation must evolve from if spike protein can travel, to what are the systemic consequences when it does. The call for rigorous, independent safety science has never been louder.

Camus

48,219 görüntüleme • 8 ay önce

How many billions of doses would have gone into peoples arms, if the "safe and effective" message was replaced with: "The DNA contamination will be protected within a lipid nano particle so that the SV40 sequences can be escorted into the cells cytoplasm and that "animal work" has shown that the mRNA injection will go to the Nucleus of your cells". New discussion with Dr Clare Craig, who reveals to John Campbell that an Australian FOI request revealed an immunofluorescence study that showed : "you can also see some in the Nucleus...so the lipid nano particles were entering the Nucleus". New peer reviewed research showed that for DNA impurities: ◻️"Pfizer exceeds limits by 36-153 fold" ◻️"Moderna exceeds limits by 112-627 fold" Published by Speicher et al (McKernan, Rose). Any contaminants are protected and bypass the immune systems detection, so that all of its contents is ushered into the cells cytoplasm, for the event of hijacking the cells machinery to make spike protein.
1:24

How many billions of doses would have gone into peoples arms, if the "safe and effective" message was replaced with: "The DNA contamination will be protected within a lipid nano particle so that the SV40 sequences can be escorted into the cells cytoplasm and that "animal work" has shown that the mRNA injection will go to the Nucleus of your cells". New discussion with Dr Clare Craig, who reveals to John Campbell that an Australian FOI request revealed an immunofluorescence study that showed : "you can also see some in the Nucleus...so the lipid nano particles were entering the Nucleus". New peer reviewed research showed that for DNA impurities: ◻️"Pfizer exceeds limits by 36-153 fold" ◻️"Moderna exceeds limits by 112-627 fold" Published by Speicher et al (McKernan, Rose). Any contaminants are protected and bypass the immune systems detection, so that all of its contents is ushered into the cells cytoplasm, for the event of hijacking the cells machinery to make spike protein.

Humanspective

108,069 görüntüleme • 9 ay önce

Allahu Akbar‼️‼️ Professor Henry Klassen, MD, Ph.D., at the University of Pittsburgh, accepted Islam on the first day of Ramadan Professor Klassen is a pioneer in the field of Stem Cell research and Retinal Regeneration He accepted Islam, because it is the truth ☝️❤️
2:52

Allahu Akbar‼️‼️ Professor Henry Klassen, MD, Ph.D., at the University of Pittsburgh, accepted Islam on the first day of Ramadan Professor Klassen is a pioneer in the field of Stem Cell research and Retinal Regeneration He accepted Islam, because it is the truth ☝️❤️

ONE

626,154 görüntüleme • 2 yıl önce

A whole new wave of disease therapies have started to arrive. They're based on lab made stem cells that can reprogram the body. Folks like Jeff Bezos, Sam Altman and Brian Armstrong have invested billions of dollars into this technology. @nabsicle is trying to mass produce these new stem cells to make the therapies cheaper and more widespread. This is our full episode with her where we get deep into iPSCs and how this technology works. The Core Memory podcast is on all major platforms and on YouTube down below. Brex and @e1ventures are very smart and help us bring the world's smartest podcast to you. Enjoy! Timestamps 00:00 Intro 01:22 Cell Rejuvenation 02:30 AI and Biotech 06:18 Lab-Made vs Natural Stem Cells 08:25 Programming Cell States 10:07 Reversing Parkinson's 12:15 Japan’s Stem Cell Trials 16:46 Personalized Cells 21:19 Cellino’s Laser Bubble Technology 31:34 Stem Cell Fabs 38:33 Personalized Medicine 43:02 Lowering Stem Cell Therapy Costs 46:31 Can Humans Live Forever?
1:17:51

A whole new wave of disease therapies have started to arrive. They're based on lab made stem cells that can reprogram the body. Folks like Jeff Bezos, Sam Altman and Brian Armstrong have invested billions of dollars into this technology. @nabsicle is trying to mass produce these new stem cells to make the therapies cheaper and more widespread. This is our full episode with her where we get deep into iPSCs and how this technology works. The Core Memory podcast is on all major platforms and on YouTube down below. Brex and @e1ventures are very smart and help us bring the world's smartest podcast to you. Enjoy! Timestamps 00:00 Intro 01:22 Cell Rejuvenation 02:30 AI and Biotech 06:18 Lab-Made vs Natural Stem Cells 08:25 Programming Cell States 10:07 Reversing Parkinson's 12:15 Japan’s Stem Cell Trials 16:46 Personalized Cells 21:19 Cellino’s Laser Bubble Technology 31:34 Stem Cell Fabs 38:33 Personalized Medicine 43:02 Lowering Stem Cell Therapy Costs 46:31 Can Humans Live Forever?

Ashlee Vance

21,622 görüntüleme • 4 ay önce

Scientists just figured out how to reverse aging using AI. And this is a massive breakthrough. We can now reprogram any human cell back to age 20. Heart cells, brain cells, skin cells, all reset to their biological prime. And here’s the wildest part…the technology to do this, has already existed since 2012 (it won the Nobel Prize). But the real breakthrough wasn’t possible until this year, when they supercharged it with AI. It’s a wild story. So in 2006, scientists discovered Yamanaka factors. They’re proteins that can basically convert any normal cell into a universal stem cell. Now this was a huge deal, because these stem cells are basically like magic healers. If you have torn muscle tissue, you could inject these stem cells into the area and they will turn into the youthful muscle cells you need. So Yamanaka factors were this insane breakthrough, because they allowed any human to turn any cell you already have into these magic healers. But, there was one big problem… It turns out, the original Yamanaka factors weren’t very good at this stem cell conversion. They could do it, but they just weren’t very reliable. Enter OpenAI...and this is where things get crazy. OpenAI designed a special AI model built specifically to create new proteins. Think of it like ChatGPT but for protein engineering. So they took all the Yamanaka research and asked this new AI to go ham on improving it. And get this… Their version was 50x more effective than the original. They tested it on 50 year old cells and it successfully started repairing 30% of their cells in just 7 days. This is just science fiction…it actually happened. And it sounds crazy, but in a few years, humans will be able to take a shot that will literally reverse the age of their cells.
1:32

Scientists just figured out how to reverse aging using AI. And this is a massive breakthrough. We can now reprogram any human cell back to age 20. Heart cells, brain cells, skin cells, all reset to their biological prime. And here’s the wildest part…the technology to do this, has already existed since 2012 (it won the Nobel Prize). But the real breakthrough wasn’t possible until this year, when they supercharged it with AI. It’s a wild story. So in 2006, scientists discovered Yamanaka factors. They’re proteins that can basically convert any normal cell into a universal stem cell. Now this was a huge deal, because these stem cells are basically like magic healers. If you have torn muscle tissue, you could inject these stem cells into the area and they will turn into the youthful muscle cells you need. So Yamanaka factors were this insane breakthrough, because they allowed any human to turn any cell you already have into these magic healers. But, there was one big problem… It turns out, the original Yamanaka factors weren’t very good at this stem cell conversion. They could do it, but they just weren’t very reliable. Enter OpenAI...and this is where things get crazy. OpenAI designed a special AI model built specifically to create new proteins. Think of it like ChatGPT but for protein engineering. So they took all the Yamanaka research and asked this new AI to go ham on improving it. And get this… Their version was 50x more effective than the original. They tested it on 50 year old cells and it successfully started repairing 30% of their cells in just 7 days. This is just science fiction…it actually happened. And it sounds crazy, but in a few years, humans will be able to take a shot that will literally reverse the age of their cells.

Whiplash347

68,643 görüntüleme • 8 ay önce

🚨THREE INDEPENDENT SOURCES CONFIRM: Pfizer/Moderna mRNA Shots Alter the Human Genome 📌 Aldén et al: Pfizer mRNA reverse-transcribed into DNA in liver cells—within 6 hours 📌 InModia Lab (Germany): Spike + SV40 found in human tissue years later 📌 Neo7Bioscience + Univ. of North Texas: Persistent synthetic RNA, SV40, and cancer-linked gene dysregulation in vaccinated blood Some may become permanent spike factories—driving chronic inflammation, immune collapse, and cancer. As regulators remain silent, we will continue to study these deeply worrisome findings.
0:57

🚨THREE INDEPENDENT SOURCES CONFIRM: Pfizer/Moderna mRNA Shots Alter the Human Genome 📌 Aldén et al: Pfizer mRNA reverse-transcribed into DNA in liver cells—within 6 hours 📌 InModia Lab (Germany): Spike + SV40 found in human tissue years later 📌 Neo7Bioscience + Univ. of North Texas: Persistent synthetic RNA, SV40, and cancer-linked gene dysregulation in vaccinated blood Some may become permanent spike factories—driving chronic inflammation, immune collapse, and cancer. As regulators remain silent, we will continue to study these deeply worrisome findings.

Nicolas Hulscher, MPH

138,008 görüntüleme • 1 yıl önce

Genomics Expert Kevin McKernan on How He Discovered DNA Contamination in the COVID Vaccines, Which Has Been Replicated in Labs Across the Country "Ask yourselves, do we want to be injecting billions of people with billions of molecules of DNA that could potentially into stem cell genomes or into gametes...When you start getting into stem cells and germ cells, you're in the territory where they put people in jail for doing this. And we've done this not on two CRISPR babies – we've now done this on billions of people who did not consent to this." Kevin McKernan MeehanMD The HighWire Peter A. McCullough, MD, MPH® @P_J_Buckhaults
30:43

Genomics Expert Kevin McKernan on How He Discovered DNA Contamination in the COVID Vaccines, Which Has Been Replicated in Labs Across the Country "Ask yourselves, do we want to be injecting billions of people with billions of molecules of DNA that could potentially into stem cell genomes or into gametes...When you start getting into stem cells and germ cells, you're in the territory where they put people in jail for doing this. And we've done this not on two CRISPR babies – we've now done this on billions of people who did not consent to this." Kevin McKernan MeehanMD The HighWire Peter A. McCullough, MD, MPH® @P_J_Buckhaults

Chief Nerd

477,662 görüntüleme • 2 yıl önce

🚨Here's what a lot of people misunderstand about cancer treatment, says drpaulmarik: "Cancer is not homogeneous. The somatic mutation theory—which is the current theory in which treatment is based—posits that you have a mutation in a single cell, and that gives rise to a whole population of cells that look the same and have the same mutation. But the Cancer Genome Atlas has shown that that theory is completely wrong. The cancer cells are very heterogeneous, so they're made up of very different populations of cells with different mutations, and one of the populations is the cancer stem cell. It's a sub-population of the cancer. These are generally slow-growing, but they're distinct in that they have the ability to divide indefinitely and grow indefinitely, and can change their characteristics. Basically, if you get rid of the fast-dividing cells, which is the cancer, you're left with the stem cells, which then become the roots, which grow back to form the tumor" sometimes years later. Conventional chemotherapy gets rid of the fast-dividing regular cancer cells but *NOT* the stem cells. So the key question is: how do you get rid of the stem cells? “There are a number of repurposed drugs that do it, and this has been well-established in scientific medical literature. One of the most effective treatments to knock out the stem cell is the famous horse deworming medicine," says drpaulmarik. Yes, ivermectin. Independent Medical Alliance
6:30

🚨Here's what a lot of people misunderstand about cancer treatment, says drpaulmarik: "Cancer is not homogeneous. The somatic mutation theory—which is the current theory in which treatment is based—posits that you have a mutation in a single cell, and that gives rise to a whole population of cells that look the same and have the same mutation. But the Cancer Genome Atlas has shown that that theory is completely wrong. The cancer cells are very heterogeneous, so they're made up of very different populations of cells with different mutations, and one of the populations is the cancer stem cell. It's a sub-population of the cancer. These are generally slow-growing, but they're distinct in that they have the ability to divide indefinitely and grow indefinitely, and can change their characteristics. Basically, if you get rid of the fast-dividing cells, which is the cancer, you're left with the stem cells, which then become the roots, which grow back to form the tumor" sometimes years later. Conventional chemotherapy gets rid of the fast-dividing regular cancer cells but *NOT* the stem cells. So the key question is: how do you get rid of the stem cells? “There are a number of repurposed drugs that do it, and this has been well-established in scientific medical literature. One of the most effective treatments to knock out the stem cell is the famous horse deworming medicine," says drpaulmarik. Yes, ivermectin. Independent Medical Alliance

Jan Jekielek

96,002 görüntüleme • 1 yıl önce

A toxicologist's devastating testimony on how COVID-19 mRNA vaccines could cause cancer and alter the human gene pool. This is a must-read. Dr. Lindsay Janci just laid out a harrowing case. The concern isn't just short-term side effects; it's the potential for genetic vaccines to drive cancer and be passed to future generations. Her summary is a masterclass in scientific alarm. Here are the 9+ potential pathways to cancer she detailed: 1. LNP Delivery to Stem Cells: Lipid Nanoparticles (LNPs) don't just go to muscle cells. They readily transfect hemopoietic stem cells—the origin of all our blood cells. 2. Cancer Metastasis: LNPs may cause pre-existing cancer cells to spread more easily by inducing "endothelial leakiness." 3. Inherent LNP Oncogenicity: The LNPs themselves might have cancer-causing effects, which have never been studied. 4. The SV40 Promoter: Hidden plasmid DNA in the vaccines contains the powerful SV40 promoter. If this genetic switch integrates near an oncogene, it could explosively drive cancer growth. 5. SV40 Enhancer (Nuclear Targeting): This sequence is designed to rush DNA into the cell nucleus—a key step for "insertional mutagenesis," where foreign DNA disrupts our own genes. 6. Spike Protein & p53: The spike protein itself has been shown to inhibit p53, a critical tumor suppressor protein that stops cancer from developing. 7. Insertional Mutagenesis & Frameshifts: Plasmid DNA doesn't need SV40 to get into the nucleus. Once integrated, it can cause frameshift mutations, leading to aberrant, cancer-causing proteins. 8. mRNA Reverse Transcription: The mRNA can be reverse-transcribed back into DNA and integrated into our genome, a known cancer mechanism, especially in ovaries & testes where reverse transcriptase is high. 9. Immunosuppression: The vaccines may suppress specialized T-cells that act as "guards" keeping dormant cancer clones in check. Weakening this guard can lead to a surge in cancers, similar to what we see in aging pets. But it gets worse. Dr. Janci issued a grave warning about heritable genetic damage: The DNA plasmids and reverse-transcribed DNA can potentially integrate into sperm and ova (gametes). This means the genetic payload could be passed to our children and "contaminate the gene pool." She reveals two mechanisms: - Genomic Integration: Direct insertion into the gamete's DNA, likely causing cancer in offspring rather than functional spike production. . Sperm-Mediated Gene Transfer (SMGT): A process where sperm can carry extra-chromosomal DNA and pass it on to the next generation without full genomic integration, leading to constitutive spike protein expression in children. The most chilling part? Dr. Janci states that this is "not being investigated at all." Despite reaching out to multiple labs, no one is testing sperm or ova from vaccinated individuals for these integrations. This isn't conspiracy theory. This is a credentialed toxicologist presenting a plausible, mechanistic roadmap for a public health catastrophe. The absolute lack of curiosity from health agencies is deafening. The question is no longer if there are risks, but why those in charge are refusing to look.
8:42

A toxicologist's devastating testimony on how COVID-19 mRNA vaccines could cause cancer and alter the human gene pool. This is a must-read. Dr. Lindsay Janci just laid out a harrowing case. The concern isn't just short-term side effects; it's the potential for genetic vaccines to drive cancer and be passed to future generations. Her summary is a masterclass in scientific alarm. Here are the 9+ potential pathways to cancer she detailed: 1. LNP Delivery to Stem Cells: Lipid Nanoparticles (LNPs) don't just go to muscle cells. They readily transfect hemopoietic stem cells—the origin of all our blood cells. 2. Cancer Metastasis: LNPs may cause pre-existing cancer cells to spread more easily by inducing "endothelial leakiness." 3. Inherent LNP Oncogenicity: The LNPs themselves might have cancer-causing effects, which have never been studied. 4. The SV40 Promoter: Hidden plasmid DNA in the vaccines contains the powerful SV40 promoter. If this genetic switch integrates near an oncogene, it could explosively drive cancer growth. 5. SV40 Enhancer (Nuclear Targeting): This sequence is designed to rush DNA into the cell nucleus—a key step for "insertional mutagenesis," where foreign DNA disrupts our own genes. 6. Spike Protein & p53: The spike protein itself has been shown to inhibit p53, a critical tumor suppressor protein that stops cancer from developing. 7. Insertional Mutagenesis & Frameshifts: Plasmid DNA doesn't need SV40 to get into the nucleus. Once integrated, it can cause frameshift mutations, leading to aberrant, cancer-causing proteins. 8. mRNA Reverse Transcription: The mRNA can be reverse-transcribed back into DNA and integrated into our genome, a known cancer mechanism, especially in ovaries & testes where reverse transcriptase is high. 9. Immunosuppression: The vaccines may suppress specialized T-cells that act as "guards" keeping dormant cancer clones in check. Weakening this guard can lead to a surge in cancers, similar to what we see in aging pets. But it gets worse. Dr. Janci issued a grave warning about heritable genetic damage: The DNA plasmids and reverse-transcribed DNA can potentially integrate into sperm and ova (gametes). This means the genetic payload could be passed to our children and "contaminate the gene pool." She reveals two mechanisms: - Genomic Integration: Direct insertion into the gamete's DNA, likely causing cancer in offspring rather than functional spike production. . Sperm-Mediated Gene Transfer (SMGT): A process where sperm can carry extra-chromosomal DNA and pass it on to the next generation without full genomic integration, leading to constitutive spike protein expression in children. The most chilling part? Dr. Janci states that this is "not being investigated at all." Despite reaching out to multiple labs, no one is testing sperm or ova from vaccinated individuals for these integrations. This isn't conspiracy theory. This is a credentialed toxicologist presenting a plausible, mechanistic roadmap for a public health catastrophe. The absolute lack of curiosity from health agencies is deafening. The question is no longer if there are risks, but why those in charge are refusing to look.

Camus

18,244 görüntüleme • 9 ay önce

🚨 JOE ROGAN & BRET WEINSTEIN: “It’s clear fraud.” This wasn’t a debate — it was an autopsy of the entire COVID narrative. Weinstein revealed that independent tests on leftover vaccine vials showed DNA contamination — including the SV40 promoter, a carcinogenic genetic element once found in early polio vaccines. “What was tested was not what was injected into billions of people. That’s fraud.” Let that sink in: The public was told there was no DNA. But there was — and not just any DNA, but DNA capable of altering human cells. Rogan’s reaction said it all: “They tested one product for safety… and injected another.” Billions trusted the process. Now evidence suggests the process itself was corrupted — swapped, concealed, and justified with garbage computer models claiming “millions of lives saved.” If even half of this is true, it’s not a scandal. It’s the biggest medical fraud in human history. The question now isn’t if it happened — but who knew, who signed off, and who profits from silence.
5:03

🚨 JOE ROGAN & BRET WEINSTEIN: “It’s clear fraud.” This wasn’t a debate — it was an autopsy of the entire COVID narrative. Weinstein revealed that independent tests on leftover vaccine vials showed DNA contamination — including the SV40 promoter, a carcinogenic genetic element once found in early polio vaccines. “What was tested was not what was injected into billions of people. That’s fraud.” Let that sink in: The public was told there was no DNA. But there was — and not just any DNA, but DNA capable of altering human cells. Rogan’s reaction said it all: “They tested one product for safety… and injected another.” Billions trusted the process. Now evidence suggests the process itself was corrupted — swapped, concealed, and justified with garbage computer models claiming “millions of lives saved.” If even half of this is true, it’s not a scandal. It’s the biggest medical fraud in human history. The question now isn’t if it happened — but who knew, who signed off, and who profits from silence.

Jim Ferguson

18,257 görüntüleme • 8 ay önce

Kevin McKernan issues a warning about the "genomic integration" story. Big Pharma wants you to get lost in proving integration, when the DNA contamination is "inhibiting p53", which is an oncogenic driver. Kevin McKernan: "I think the integration story is a little bit of a misdirection." "Pharmaceutical companies are asking everyone to look for that, and unless you find that, it doesn't matter." "That's not true. In fact, the moment the DNA gets into the cell, it triggers a particular pathway that can be oncogenic, known as the cGAS-STING pathway." "It's an inflammatory response because it sees bacterial DNA in a cell, and it thinks you're septic. So, you get this massive cytokine and interferon response. The transfection of the DNA into the cells is the problem because it comes from bacteria. Since it's bacterial DNA, it has some methylation signals that trigger a certain response." "I think that's the main issue that we're probably seeing in more of the acute side of the reactions. If it's proven that they've integrated that, of course, it might be playing a role in cancer. But once that DNA has gotten into the cell, it's inhibiting p53. That's where it should end. If any shot has a p53 inhibitor that was never disclosed, it should be banned from the marketplace, and the people who did it and hid it from the regulator should be in jail." Kevin McKernan also mentioned in another podcast the amount of regulatory red tape that scientists have to go through to prove integration is immense. This is why Big Pharma want you to focus on that.
1:42

Kevin McKernan issues a warning about the "genomic integration" story. Big Pharma wants you to get lost in proving integration, when the DNA contamination is "inhibiting p53", which is an oncogenic driver. Kevin McKernan: "I think the integration story is a little bit of a misdirection." "Pharmaceutical companies are asking everyone to look for that, and unless you find that, it doesn't matter." "That's not true. In fact, the moment the DNA gets into the cell, it triggers a particular pathway that can be oncogenic, known as the cGAS-STING pathway." "It's an inflammatory response because it sees bacterial DNA in a cell, and it thinks you're septic. So, you get this massive cytokine and interferon response. The transfection of the DNA into the cells is the problem because it comes from bacteria. Since it's bacterial DNA, it has some methylation signals that trigger a certain response." "I think that's the main issue that we're probably seeing in more of the acute side of the reactions. If it's proven that they've integrated that, of course, it might be playing a role in cancer. But once that DNA has gotten into the cell, it's inhibiting p53. That's where it should end. If any shot has a p53 inhibitor that was never disclosed, it should be banned from the marketplace, and the people who did it and hid it from the regulator should be in jail." Kevin McKernan also mentioned in another podcast the amount of regulatory red tape that scientists have to go through to prove integration is immense. This is why Big Pharma want you to focus on that.

Humanspective

45,236 görüntüleme • 9 ay önce

Some vials of the Covid 19 mRNA ‘vax’ has over 600 x more DNA contamination than is permitted including the SV40 printer gene, which is linked to cancer and was undisclosed to regulators by Pfizer. No wonder cancer rates have risen enormously‼️🙏👇
2:16

Some vials of the Covid 19 mRNA ‘vax’ has over 600 x more DNA contamination than is permitted including the SV40 printer gene, which is linked to cancer and was undisclosed to regulators by Pfizer. No wonder cancer rates have risen enormously‼️🙏👇

Sophia Dahl

27,443 görüntüleme • 8 ay önce

🚨 THIS SHOULD HAVE STOPPED. IT DIDN’T. 🚨 Why would DNA still circulate in someone’s bloodstream months — even years — after vaccination? In this clip, researchers and clinicians discuss disturbing findings: 🧬 DNA detected in vaccine vials 🩸 DNA reportedly circulating in blood long after injection ⏳ Spike protein production that never “shuts off” 🏥 Serious unanswered questions for blood banks and transfusions The body is supposed to clear foreign DNA quickly. So why is it still there? Some scientists say the only plausible explanation proposed is integration — and if true, the implications for health, informed consent, and blood safety are massive. This isn’t “anti-science.” This is science asking questions that authorities refuse to answer. Watch. Decide for yourself. 👀👇
1:58

🚨 THIS SHOULD HAVE STOPPED. IT DIDN’T. 🚨 Why would DNA still circulate in someone’s bloodstream months — even years — after vaccination? In this clip, researchers and clinicians discuss disturbing findings: 🧬 DNA detected in vaccine vials 🩸 DNA reportedly circulating in blood long after injection ⏳ Spike protein production that never “shuts off” 🏥 Serious unanswered questions for blood banks and transfusions The body is supposed to clear foreign DNA quickly. So why is it still there? Some scientists say the only plausible explanation proposed is integration — and if true, the implications for health, informed consent, and blood safety are massive. This isn’t “anti-science.” This is science asking questions that authorities refuse to answer. Watch. Decide for yourself. 👀👇

Tom Renz

26,235 görüntüleme • 6 ay önce

Genomics Expert Kevin McKernan Shares Summary of DNA Contamination Found in the COVID mRNA Vaccines & Preliminary Evidence of DNA Integration "The fact checkers who told you this DNA won't get into the cell are proven wrong by this data. We can see DNA in there. It's a very high copy number...We've also found two genome integrations. This has not been replicated like all of our qPCR data, so this is very early, but we have fusions of DNA between the spike sequence and Chromosome 12 and between the spike sequence and Chromosome 9. This needs to be confirmed with long read sequencers where we can span the entire integration event...But we shouldn't be seeing any of this...So a little bit more validation to do in this but still a little bit concerning." *From the 2/23/2024 International Crisis Summit-5 in Washington DC. Quote is taken from the 9:50 mark. ➡️chiefnerd
12:54

Genomics Expert Kevin McKernan Shares Summary of DNA Contamination Found in the COVID mRNA Vaccines & Preliminary Evidence of DNA Integration "The fact checkers who told you this DNA won't get into the cell are proven wrong by this data. We can see DNA in there. It's a very high copy number...We've also found two genome integrations. This has not been replicated like all of our qPCR data, so this is very early, but we have fusions of DNA between the spike sequence and Chromosome 12 and between the spike sequence and Chromosome 9. This needs to be confirmed with long read sequencers where we can span the entire integration event...But we shouldn't be seeing any of this...So a little bit more validation to do in this but still a little bit concerning." *From the 2/23/2024 International Crisis Summit-5 in Washington DC. Quote is taken from the 9:50 mark. ➡️chiefnerd

Dr Dave Cartland BMedSc MBChB Ex-MRCGP

20,109 görüntüleme • 6 ay önce