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Could a "universal vaccine" protect us from future virus outbreaks? 🦠 A Cambridge team has developed an entirely new way of making vaccines. Using data from virus surveillance programmes around the world, they used AI to design a ‘super antigen’. This can create a single vaccine that provides lasting... show more

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🚨 BILL GATES' DREAM JUST CAME TRUE: AI IS NOW CREATING "UNIVERSAL VACCINES" TESTED ON HUMANS Bill Gates has been pushing this hard for years, and now it’s here. Scientists just announced a world first: an AI designed vaccine component created entirely by computer simulations has entered human trials. They’re calling it a potential universal vaccine that could protect against entire families of viruses and stop future pandemics before they start. They’ve already run a human trial on a Covid version and are now moving toward flu. Gates tied his massive wealth from Microsoft straight into his “second career” of pouring money into vaccines, gene editing, and now AI innovation in health. He even referenced Warp Speed style breakthroughs to “cure and eradicate” diseases like HIV and sickle cell. This is all being sold as saving millions of lives. But when the same man who has openly talked about using vaccines to reduce population growth is now teaming up with AI to create universal shots for whole virus families… a lot of people are asking the obvious question. Is this really about saving humanity… or is Bill Gates using AI to build the ultimate population control weapon disguised as a “universal vaccine”?

🚨 BILL GATES' DREAM JUST CAME TRUE: AI IS NOW CREATING "UNIVERSAL VACCINES" TESTED ON HUMANS Bill Gates has been pushing this hard for years, and now it’s here. Scientists just announced a world first: an AI designed vaccine component created entirely by computer simulations has entered human trials. They’re calling it a potential universal vaccine that could protect against entire families of viruses and stop future pandemics before they start. They’ve already run a human trial on a Covid version and are now moving toward flu. Gates tied his massive wealth from Microsoft straight into his “second career” of pouring money into vaccines, gene editing, and now AI innovation in health. He even referenced Warp Speed style breakthroughs to “cure and eradicate” diseases like HIV and sickle cell. This is all being sold as saving millions of lives. But when the same man who has openly talked about using vaccines to reduce population growth is now teaming up with AI to create universal shots for whole virus families… a lot of people are asking the obvious question. Is this really about saving humanity… or is Bill Gates using AI to build the ultimate population control weapon disguised as a “universal vaccine”?

HustleBitch

17,495 Aufrufe • vor 1 Monat

RFK Jr. says they are in the process of developing a new universal vaccine that could change the way we fight viruses. He explains this vaccine is designed to mimic natural immunity, making it effective against any type of mutation that may emerge. According to him, it will offer protection against both COVID-19 and the flu, and he describes it as “safe and effective.”

RFK Jr. says they are in the process of developing a new universal vaccine that could change the way we fight viruses. He explains this vaccine is designed to mimic natural immunity, making it effective against any type of mutation that may emerge. According to him, it will offer protection against both COVID-19 and the flu, and he describes it as “safe and effective.”

Shadow of Ezra

221,195 Aufrufe • vor 1 Jahr

Kennedy also gave legitimacy to what was deemed a “conspiracy theory” for the longest time. He suggested the COVID-19 shots, marketed as “safe and effective,” could have CAUSED the virus to mutate more quickly and EXTENDED the pandemic altogether. He explained: “The [mRNA] vaccine [platform] paradoxically encourages new mutations and can actually prolong pandemics. As the virus constantly mutates to escape the protective effects of the vaccine, millions of people, maybe even you or someone you know, caught the Omicron variant despite being vaccinated. That’s because a single mutation can make mRNA vaccines ineffective.”

Kennedy also gave legitimacy to what was deemed a “conspiracy theory” for the longest time. He suggested the COVID-19 shots, marketed as “safe and effective,” could have CAUSED the virus to mutate more quickly and EXTENDED the pandemic altogether. He explained: “The [mRNA] vaccine [platform] paradoxically encourages new mutations and can actually prolong pandemics. As the virus constantly mutates to escape the protective effects of the vaccine, millions of people, maybe even you or someone you know, caught the Omicron variant despite being vaccinated. That’s because a single mutation can make mRNA vaccines ineffective.”

The Vigilant Fox 🦊

280,316 Aufrufe • vor 1 Jahr

REPORT: Researchers are now pushing an AI-powered “super-vaccine” designed to “prevent pandemics.” This makes the COVID jab look like child’s play. And chances are, they’ll try to mandate it. The first “super-vaccine” has already been created and was tested in humans by researchers at the University of Cambridge. The team fed AI systems genetic sequences from multiple coronaviruses gathered through ongoing surveillance programs. The algorithm then assembled a “super-antigen” intended to train the immune system to recognize entire virus families rather than individual strains that constantly mutate. The problem is that this approach is flawed from the outset because these surveillance systems already depend on fraudulent testing methods such as PCR. And once a digital ID system is in place, refusing a pandemic-prevention vaccine could come with real-world consequences. No shot, no access. No compliance, no participation. Watch ZeeeMediaOfficial’s report for the full details. I just hope we’re ready for what’s coming.

REPORT: Researchers are now pushing an AI-powered “super-vaccine” designed to “prevent pandemics.” This makes the COVID jab look like child’s play. And chances are, they’ll try to mandate it. The first “super-vaccine” has already been created and was tested in humans by researchers at the University of Cambridge. The team fed AI systems genetic sequences from multiple coronaviruses gathered through ongoing surveillance programs. The algorithm then assembled a “super-antigen” intended to train the immune system to recognize entire virus families rather than individual strains that constantly mutate. The problem is that this approach is flawed from the outset because these surveillance systems already depend on fraudulent testing methods such as PCR. And once a digital ID system is in place, refusing a pandemic-prevention vaccine could come with real-world consequences. No shot, no access. No compliance, no participation. Watch ZeeeMediaOfficial’s report for the full details. I just hope we’re ready for what’s coming.

The Vigilant Fox 🦊

56,791 Aufrufe • vor 2 Monaten

🚨 BILL GATES SAID VACCINES COULD LOWER THE POPULATION BY 10-15% — NOW AI JUST CREATED A “UNIVERSAL VACCINE” Years ago, Bill Gates stood in front of a crowd and said: “If we do a really great job on new vaccines, health care, reproductive health services, we could lower that [population] by perhaps 10 or 15%.” He later described vaccines and gene editing as the focus of his “second career.” Now, researchers have just announced a new AI-designed “universal vaccine” that has passed its first human clinical trial. It’s being called a breakthrough that could "protect" against entire families of viruses. Now people are connecting the dots again. When Bill Gates said vaccines could reduce the population by 10-15%, do you still think he was talking about saving lives?

🚨 BILL GATES SAID VACCINES COULD LOWER THE POPULATION BY 10-15% — NOW AI JUST CREATED A “UNIVERSAL VACCINE” Years ago, Bill Gates stood in front of a crowd and said: “If we do a really great job on new vaccines, health care, reproductive health services, we could lower that [population] by perhaps 10 or 15%.” He later described vaccines and gene editing as the focus of his “second career.” Now, researchers have just announced a new AI-designed “universal vaccine” that has passed its first human clinical trial. It’s being called a breakthrough that could "protect" against entire families of viruses. Now people are connecting the dots again. When Bill Gates said vaccines could reduce the population by 10-15%, do you still think he was talking about saving lives?

HustleBitch

15,378 Aufrufe • vor 14 Tagen

#WATCH | Delhi: On India's first indigenous dengue vaccine, Dr. Rajeev Bahl, DG, ICMR, says, "Indian company Panacea Biotec initially worked with technologies provided by the National Institutes of Health, but they have since developed an indigenous vaccine. They have used that initial technology, but they have transformed it into a vaccine that covers all four Dengue strains. This vaccine has completed phase one and phase two studies, and has been found to be safe and capable of generating immunity. Currently, a phase three dengue vaccine trial is underway..."

#WATCH | Delhi: On India's first indigenous dengue vaccine, Dr. Rajeev Bahl, DG, ICMR, says, "Indian company Panacea Biotec initially worked with technologies provided by the National Institutes of Health, but they have since developed an indigenous vaccine. They have used that initial technology, but they have transformed it into a vaccine that covers all four Dengue strains. This vaccine has completed phase one and phase two studies, and has been found to be safe and capable of generating immunity. Currently, a phase three dengue vaccine trial is underway..."

ANI

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Dr. Andy Wakefield says he’s deeply concerned about what we’ve done by inoculating the entire population with imperfect vaccines. He warns it could drive new viral mutations — and that we’ve lost faith in nature’s ability to protect us. “We saw this with COVID, when you introduce a vaccine that’s imperfect, you put a genetic selection pressure on the virus to mutate and adapt — and you’ll get the emergence of new strains.” “Pfizer saw that as a tremendous market potential, generating new vaccine after new vaccine, chasing the virus to cover the strains they helped create.” “So are we now going to see the emergence of more dangerous strains of measles precisely as a consequence of vaccination policy?” “My personal opinion is that we need to invest our trust in nature and allow that decline in mortality and seriousness of disease to play out naturally.” Dr. Andy Wakefield

Dr. Andy Wakefield says he’s deeply concerned about what we’ve done by inoculating the entire population with imperfect vaccines. He warns it could drive new viral mutations — and that we’ve lost faith in nature’s ability to protect us. “We saw this with COVID, when you introduce a vaccine that’s imperfect, you put a genetic selection pressure on the virus to mutate and adapt — and you’ll get the emergence of new strains.” “Pfizer saw that as a tremendous market potential, generating new vaccine after new vaccine, chasing the virus to cover the strains they helped create.” “So are we now going to see the emergence of more dangerous strains of measles precisely as a consequence of vaccination policy?” “My personal opinion is that we need to invest our trust in nature and allow that decline in mortality and seriousness of disease to play out naturally.” Dr. Andy Wakefield

Children’s Health Defense

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Dr. Patrick Soon-Shiong Reveals the T-Cell Vaccine That Could Have Changed Everything The current COVID vaccines target the ever-mutating spike protein, forcing endless boosters. But what if there was a universal T-cell vaccine—one that attacked the virus at its core and worked against all variants? The Breakthrough That Was Ignored Dr. Patrick Soon-Shiong and his team developed a T-cell vaccine targeting COVID’s nuclear capsid protein—a part of the virus that doesn’t mutate. - Phase 1 trials proved it worked—he even tested it on himself. - Unlike antibody-based vaccines, this approach could have provided long-lasting immunity and stopped transmission. - Yet when he asked to deploy it as a booster, the FDA placed it on hold—with no clear explanation. The Consequences of Delaying Science - Without strong T-cell immunity, COVID keeps replicating inside the body, potentially leading to long COVID, autoimmune issues, and turbo cancers. - Billions were spent on temporary spike-protein vaccines, while this durable solution was overlooked. - Dr. Soon-Shiong even offered the technology for free—but no one took it. There’s Still Time to Fix This With new leadership at the FDA, this lifesaving vaccine could still be revived. The question is: Will they finally act—or will politics keep blocking the cure we needed all along?

Dr. Patrick Soon-Shiong Reveals the T-Cell Vaccine That Could Have Changed Everything The current COVID vaccines target the ever-mutating spike protein, forcing endless boosters. But what if there was a universal T-cell vaccine—one that attacked the virus at its core and worked against all variants? The Breakthrough That Was Ignored Dr. Patrick Soon-Shiong and his team developed a T-cell vaccine targeting COVID’s nuclear capsid protein—a part of the virus that doesn’t mutate. - Phase 1 trials proved it worked—he even tested it on himself. - Unlike antibody-based vaccines, this approach could have provided long-lasting immunity and stopped transmission. - Yet when he asked to deploy it as a booster, the FDA placed it on hold—with no clear explanation. The Consequences of Delaying Science - Without strong T-cell immunity, COVID keeps replicating inside the body, potentially leading to long COVID, autoimmune issues, and turbo cancers. - Billions were spent on temporary spike-protein vaccines, while this durable solution was overlooked. - Dr. Soon-Shiong even offered the technology for free—but no one took it. There’s Still Time to Fix This With new leadership at the FDA, this lifesaving vaccine could still be revived. The question is: Will they finally act—or will politics keep blocking the cure we needed all along?

Camus

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Bill Gates is optimistic about the future of mRNA vaccine technology, referring to it as "a treasure to the world". He admits that the mRNA Covid vaccine "doesn't block you from getting infected", but remains excited about the development of mRNA vaccines for cancer, measles, tuberculosis, HIV, and even animal vaccines.

Bill Gates is optimistic about the future of mRNA vaccine technology, referring to it as "a treasure to the world". He admits that the mRNA Covid vaccine "doesn't block you from getting infected", but remains excited about the development of mRNA vaccines for cancer, measles, tuberculosis, HIV, and even animal vaccines.

Wide Awake Media

78,706 Aufrufe • vor 8 Monaten

“In America there are 19-30% who refuse to vaccine” “Would it be nice if the Government could some how disseminate the vaccine quietly - in a way people wouldn’t even realise it” One way or another they want this new mRNA technology inside of you - question it why?

“In America there are 19-30% who refuse to vaccine” “Would it be nice if the Government could some how disseminate the vaccine quietly - in a way people wouldn’t even realise it” One way or another they want this new mRNA technology inside of you - question it why?

Concerned Citizen

77,479 Aufrufe • vor 1 Jahr

🚨 Dr. Scott Gottlieb Worries That Moving the U.S. to the Denmark Vaccine Schedule Could Make Vaccine Makers Liable Again “If they move away from recommending these vaccines and move them to a different configuration on the CDC schedule called shared clinical decision making, there's a question of whether or not they will still have liability protection under the vaccine injury compensation program.”

🚨 Dr. Scott Gottlieb Worries That Moving the U.S. to the Denmark Vaccine Schedule Could Make Vaccine Makers Liable Again “If they move away from recommending these vaccines and move them to a different configuration on the CDC schedule called shared clinical decision making, there's a question of whether or not they will still have liability protection under the vaccine injury compensation program.”

Chief Nerd

524,256 Aufrufe • vor 7 Monaten

The COVID Vaccine That Could Have Ended the Pandemic—And Stopped a Looming "Pandemic of Cancer." The FDA Blocked It. In a stunning account, Dr. Patrick Soon-Shiong reveals the story of the vaccine that was—a true sterilizing shot designed not just to reduce symptoms, but to eliminate the COVID-19 virus from the body entirely. While "Operation Warp Speed" championed antibody-based vaccines, Dr. Soon-Shiong's "BioStrike/BioShield" took a different path. It was engineered to activate T-cells and Natural Killer cells—the body's elite forces for hunting and destroying viruses. His vaccine was the only candidate in a key primate trial that successfully cleared the virus. It promised not just temporary protection, but long-term immunity that could prevent transmission and stop the virus in its tracks. Yet, when he applied to the FDA for a Phase II trial to deploy it as a crucial booster, he was met with a wall of silence and refusal. At the same time, the manufacturing ecosystem was entirely consumed by the major players, leaving no resources for this superior alternative. Dr. Soon-Shiong issues a dire warning rooted in science: COVID-19 is a systemic vascular virus. When it lingers, it causes chronic inflammation. This inflammation, he states, has a "sad, sad chance" of triggering a looming global pandemic of cancer with a 5-10 year latency. The world was given a tool to reduce immediate mortality. But it was denied the tool that could have cleared the virus, potentially prevented long COVID, and averted a future cancer crisis. This is not just a story of a missed opportunity; it's a warning we must now heed.

The COVID Vaccine That Could Have Ended the Pandemic—And Stopped a Looming "Pandemic of Cancer." The FDA Blocked It. In a stunning account, Dr. Patrick Soon-Shiong reveals the story of the vaccine that was—a true sterilizing shot designed not just to reduce symptoms, but to eliminate the COVID-19 virus from the body entirely. While "Operation Warp Speed" championed antibody-based vaccines, Dr. Soon-Shiong's "BioStrike/BioShield" took a different path. It was engineered to activate T-cells and Natural Killer cells—the body's elite forces for hunting and destroying viruses. His vaccine was the only candidate in a key primate trial that successfully cleared the virus. It promised not just temporary protection, but long-term immunity that could prevent transmission and stop the virus in its tracks. Yet, when he applied to the FDA for a Phase II trial to deploy it as a crucial booster, he was met with a wall of silence and refusal. At the same time, the manufacturing ecosystem was entirely consumed by the major players, leaving no resources for this superior alternative. Dr. Soon-Shiong issues a dire warning rooted in science: COVID-19 is a systemic vascular virus. When it lingers, it causes chronic inflammation. This inflammation, he states, has a "sad, sad chance" of triggering a looming global pandemic of cancer with a 5-10 year latency. The world was given a tool to reduce immediate mortality. But it was denied the tool that could have cleared the virus, potentially prevented long COVID, and averted a future cancer crisis. This is not just a story of a missed opportunity; it's a warning we must now heed.

Camus

300,407 Aufrufe • vor 10 Monaten

You might have heard this week’s announcement from RFK Jr. and the MAHA Action account on X about a new universal vaccine being developed—with his blessing. If you didn’t, it may be because, after racking up nearly half a million views and an enormous backlash, MAHA Action deleted the post. That’s strange. Here’s the announcement they didn’t feel confident leaving up: “Right now we're developing a universal vaccine at NIH, which is a vaccine that addresses the entire phylum of viruses. And so it's a vaccine that mimics natural immunity, and it is effective against any kind of mutation, so it doesn't drive the virus to mutate and it could be effective. We believe it's going to be effective, against not only coronaviruses, but also flu. And it's going to be a much more, much safer and much more effective vaccine.” — RFK Jr. The backlash was intense. More vaccines are clearly not what the public wants. The comments rebuked the announcement, and the post was deleted. Beyond the odd commitment from RFK Jr. to introduce more vaccines after years of warning about their dangers, this announcement comes with even more surprises. Dig deeper, and you might be horrified by what you find. The trail leads to a product already listed as “reasonably anticipated to be a human carcinogen”—meaning more cancer. A product that is funded by none other than Bill Gates and linked to Anthony Fauci.

You might have heard this week’s announcement from RFK Jr. and the MAHA Action account on X about a new universal vaccine being developed—with his blessing. If you didn’t, it may be because, after racking up nearly half a million views and an enormous backlash, MAHA Action deleted the post. That’s strange. Here’s the announcement they didn’t feel confident leaving up: “Right now we're developing a universal vaccine at NIH, which is a vaccine that addresses the entire phylum of viruses. And so it's a vaccine that mimics natural immunity, and it is effective against any kind of mutation, so it doesn't drive the virus to mutate and it could be effective. We believe it's going to be effective, against not only coronaviruses, but also flu. And it's going to be a much more, much safer and much more effective vaccine.” — RFK Jr. The backlash was intense. More vaccines are clearly not what the public wants. The comments rebuked the announcement, and the post was deleted. Beyond the odd commitment from RFK Jr. to introduce more vaccines after years of warning about their dangers, this announcement comes with even more surprises. Dig deeper, and you might be horrified by what you find. The trail leads to a product already listed as “reasonably anticipated to be a human carcinogen”—meaning more cancer. A product that is funded by none other than Bill Gates and linked to Anthony Fauci.

The Vigilant Fox 🦊

50,846 Aufrufe • vor 1 Jahr

Hepatitis B is a tiny virus with just 4 genes. But it kills hundreds of thousands globally per year, mostly by infecting babies and causing liver disease or cancer over the following decades. In a new episode of HARD DRUGS, we tell the story of the hepatitis B vaccine, which became the first of many milestones: It was the first viral protein subunit vaccine, the first recombinant vaccine, and the first vaccine to prevent a type of cancer. Key stats: • Hepatitis B virus has just 4 genes, some of which overlap, making it one of the most genetically compact human pathogens • It has a very unusual life cycle for a DNA virus: it forms a stable mini-chromosome (cccDNA) inside liver cell nuclei, and uses reverse transcription, similar to HIV. • It integrates itself into your liver cells' DNA, causes repeated cycles of cell damage and repair, and inflammation that eventually leads to cancer. • During infection, the virus produces ~500 quadrillion (5 x 10¹⁷) copies of its surface antigen in the bloodstream. They act as decoys, soaking up our antibodies and helping the virus evade immunity, and it sticks around in our cells for decades. Over time, it causes one of the most common and deadliest liver diseases and cancers: ~300 million people worldwide are living with chronic hepatitis B ~600,000 people die from hepatitis B each year, mostly from cirrhosis and liver cancer While only ~5–10% of adults infected develop chronic infection, ~90% of infants infected at birth do. Around a third of those infants will eventually die from liver failure, cirrhosis, or liver cancer. But there's a vaccine against it: the hepatitis B vaccine. It is so efficient that it helps us block the virus by training us to recognize just one protein (the surface antigen) quickly, before it can overwhelm us. The first hepatitis B vaccine (1981) was made from human plasma, through multiple brutal inactivation steps that kill other microbes and contaminants. The second hepatitis B vaccine (1986) was the first recombinant DNA vaccine ever, made by factories of yeast cells churning out the antigen in bulk. The payoff has been enormous. Large cluster randomized trials have shown that hepatitis B vaccination reduces liver cancer rates by 85% and deaths by 70%. Universal vaccination of newborns has led to massive drops in hepatitis cases, liver failure, and liver cancer in younger generations. As the first viral protein subunit vaccine, it was built upon a series of breakthroughs in immunology, advances in virology and vaccinology. In this episode, we trace the discovery of hepatitis, hepatitis B virus, the development of vaccines, and their impact. And we explore how we even got to subunit vaccines at all: the great battle of immunology, the discovery of antibodies and their incredible diversity, and how that understanding could be used to test, study, and build better vaccines. If you want to understand how modern vaccines actually came to be, or why hepatitis B vaccination still matters today, this one’s for you. Timestamps: 0:00:00 Introducing the hepatitis B vaccine 0:15:46 The mysterious trail of jaundice outbreaks and the search for an invisible liver pathogen 0:28:03 How a tiny virus causes cirrhosis and liver cancer, and the struggle to identify it 0:53:19 How Maurice Hilleman developed the safest, purest vaccine in history 1:17:36 Turning the hep B vaccine recombinant 1:29:14 The impact of hep B vaccination 1:39:27 How we got here: the 19th century battle for the soul of immunology 2:01:34 How the body builds an infinite library of defenses 2:19:25 Why scientists thought immunology was solved in the 1960s 2:30:57 How better immunology led to precise subunit vaccines 2:45:33 Conclusion

Hepatitis B is a tiny virus with just 4 genes. But it kills hundreds of thousands globally per year, mostly by infecting babies and causing liver disease or cancer over the following decades. In a new episode of HARD DRUGS, we tell the story of the hepatitis B vaccine, which became the first of many milestones: It was the first viral protein subunit vaccine, the first recombinant vaccine, and the first vaccine to prevent a type of cancer. Key stats: • Hepatitis B virus has just 4 genes, some of which overlap, making it one of the most genetically compact human pathogens • It has a very unusual life cycle for a DNA virus: it forms a stable mini-chromosome (cccDNA) inside liver cell nuclei, and uses reverse transcription, similar to HIV. • It integrates itself into your liver cells' DNA, causes repeated cycles of cell damage and repair, and inflammation that eventually leads to cancer. • During infection, the virus produces ~500 quadrillion (5 x 10¹⁷) copies of its surface antigen in the bloodstream. They act as decoys, soaking up our antibodies and helping the virus evade immunity, and it sticks around in our cells for decades. Over time, it causes one of the most common and deadliest liver diseases and cancers: ~300 million people worldwide are living with chronic hepatitis B ~600,000 people die from hepatitis B each year, mostly from cirrhosis and liver cancer While only ~5–10% of adults infected develop chronic infection, ~90% of infants infected at birth do. Around a third of those infants will eventually die from liver failure, cirrhosis, or liver cancer. But there's a vaccine against it: the hepatitis B vaccine. It is so efficient that it helps us block the virus by training us to recognize just one protein (the surface antigen) quickly, before it can overwhelm us. The first hepatitis B vaccine (1981) was made from human plasma, through multiple brutal inactivation steps that kill other microbes and contaminants. The second hepatitis B vaccine (1986) was the first recombinant DNA vaccine ever, made by factories of yeast cells churning out the antigen in bulk. The payoff has been enormous. Large cluster randomized trials have shown that hepatitis B vaccination reduces liver cancer rates by 85% and deaths by 70%. Universal vaccination of newborns has led to massive drops in hepatitis cases, liver failure, and liver cancer in younger generations. As the first viral protein subunit vaccine, it was built upon a series of breakthroughs in immunology, advances in virology and vaccinology. In this episode, we trace the discovery of hepatitis, hepatitis B virus, the development of vaccines, and their impact. And we explore how we even got to subunit vaccines at all: the great battle of immunology, the discovery of antibodies and their incredible diversity, and how that understanding could be used to test, study, and build better vaccines. If you want to understand how modern vaccines actually came to be, or why hepatitis B vaccination still matters today, this one’s for you. Timestamps: 0:00:00 Introducing the hepatitis B vaccine 0:15:46 The mysterious trail of jaundice outbreaks and the search for an invisible liver pathogen 0:28:03 How a tiny virus causes cirrhosis and liver cancer, and the struggle to identify it 0:53:19 How Maurice Hilleman developed the safest, purest vaccine in history 1:17:36 Turning the hep B vaccine recombinant 1:29:14 The impact of hep B vaccination 1:39:27 How we got here: the 19th century battle for the soul of immunology 2:01:34 How the body builds an infinite library of defenses 2:19:25 Why scientists thought immunology was solved in the 1960s 2:30:57 How better immunology led to precise subunit vaccines 2:45:33 Conclusion

Saloni

32,424 Aufrufe • vor 7 Monaten

RFK Jr. on Pfizer Trial: 23% Higher Death Rate in Vax Group Debunks "100% Effective" Myth In a stunning exposé, RFK Jr. dismantles the narrative by highlighting the shocking results of the original Pfizer trial: a 23% higher all-cause mortality rate in the vaccinated group versus the placebo group after six months. This alarming fact from the Pfizer's own clinical trial underpins what he calls the "data chaos" of the initial rollout. He eviscerates the famed "100% effective" claim that emerged from that same trial, revealing it was built on a dataset of just three COVID deaths total—two in the placebo group and one in the vaccinated group. This statistically fragile result was disingenuously spun into a universal promise of complete protection. Kennedy breaks down the brutal math from the trial data: to prevent a single COVID death, nearly 20,000 people had to be vaccinated. He argues that with the vaccine itself showing a higher mortality risk, this minuscule benefit would be instantly canceled out, potentially making the intervention net harmful. This history makes the current shift so critical. Kennedy outlines the new FDA-approved vaccine’s stark reality: it is primarily for those 65+ or with profound comorbidities under a unique and telling agreement—every recipient becomes part of an actual clinical trial. After years of mandates and declarations of "safe and effective" without robust long-term data, this new policy is a quiet admission. They are finally conducting the trial that should have been done first, using the public as participants.

RFK Jr. on Pfizer Trial: 23% Higher Death Rate in Vax Group Debunks "100% Effective" Myth In a stunning exposé, RFK Jr. dismantles the narrative by highlighting the shocking results of the original Pfizer trial: a 23% higher all-cause mortality rate in the vaccinated group versus the placebo group after six months. This alarming fact from the Pfizer's own clinical trial underpins what he calls the "data chaos" of the initial rollout. He eviscerates the famed "100% effective" claim that emerged from that same trial, revealing it was built on a dataset of just three COVID deaths total—two in the placebo group and one in the vaccinated group. This statistically fragile result was disingenuously spun into a universal promise of complete protection. Kennedy breaks down the brutal math from the trial data: to prevent a single COVID death, nearly 20,000 people had to be vaccinated. He argues that with the vaccine itself showing a higher mortality risk, this minuscule benefit would be instantly canceled out, potentially making the intervention net harmful. This history makes the current shift so critical. Kennedy outlines the new FDA-approved vaccine’s stark reality: it is primarily for those 65+ or with profound comorbidities under a unique and telling agreement—every recipient becomes part of an actual clinical trial. After years of mandates and declarations of "safe and effective" without robust long-term data, this new policy is a quiet admission. They are finally conducting the trial that should have been done first, using the public as participants.

Camus

127,530 Aufrufe • vor 10 Monaten

This video shatters the entire basis. “There are many books on polio vaccines and how they came to market.” “One of my favorite books is called The Virus and the Vaccine by Debbie Bookchin and [Jim Schumacher].” “Dr. Michael Carbone, who is a PhD and a researcher, had been looking at the fact that the polio vaccines were contaminated with Simian Virus 40 that came from the monkey kidney cells that they used to make the polio vaccine.” “They were just normal contaminants inside of monkeys, but inside of humans, they contributed to … slow-growing cancers.” “It’s a cancer-causing virus.” “The second half of the book is all about him and how he tried to get the FDA to look at this and stop using monkey kidney cells to develop the polio vaccine because of the contaminants … and how his lab was shut down and all of his money was taken away.” “His credentials were ruined—just like every other researcher that has stood up against the government and against the pharmaceutical industry.” Dr Sherri Tenpenny Alex Clark

This video shatters the entire basis. “There are many books on polio vaccines and how they came to market.” “One of my favorite books is called The Virus and the Vaccine by Debbie Bookchin and [Jim Schumacher].” “Dr. Michael Carbone, who is a PhD and a researcher, had been looking at the fact that the polio vaccines were contaminated with Simian Virus 40 that came from the monkey kidney cells that they used to make the polio vaccine.” “They were just normal contaminants inside of monkeys, but inside of humans, they contributed to … slow-growing cancers.” “It’s a cancer-causing virus.” “The second half of the book is all about him and how he tried to get the FDA to look at this and stop using monkey kidney cells to develop the polio vaccine because of the contaminants … and how his lab was shut down and all of his money was taken away.” “His credentials were ruined—just like every other researcher that has stood up against the government and against the pharmaceutical industry.” Dr Sherri Tenpenny Alex Clark

Children’s Health Defense

37,502 Aufrufe • vor 7 Monaten

A stunning and damning indictment from renowned oncology Professor Angus Dalgleish. He dismantles the entire premise of the COVID-19 vaccine program, revealing a catastrophic failure in scientific understanding and public health policy. His argument, in summary: 1. The Fundamental Flaw: From the start, it was impossible to create an effective vaccine for a coronavirus. Their rapid 3-month mutation wave far outpaces the 6-7 month development of mRNA vaccines. By the time a vaccine is deployed, it targets a virus that is already gone. 2. The "Worse Than Useless" Effect: This is not merely a case of outdated vaccines. It's about "Antigenic Sin" or "Immunological Imprint." The vaccine locks the immune system onto a non-existent version of the virus, using its energy to fight a ghost. This actively impairs the body's ability to recognize and respond to new, real-world variants. 3. The Inconvenient Data: This theory was borne out by real-world evidence. Data began to show that the vaccinated were more likely to get infected by subsequent variants than the unvaccinated. The official response? A circular logic that dismissed the clear signal of harm. 4. The Omicron Blindspot: When Omicron emerged, our health officials saw a disaster. Dalgleish saw "the very best vaccine ever"—a highly infectious, airborne variant that conferred broad immunity with minimal illness. Instead of embracing this natural path to endemicity, they doubled down on boosters, despite evidence linking more jabs to higher infection risk. 5. The Final Betrayal: We now know the foundational claim—that vaccines prevent transmission—was never backed by data. The program continued unabated, creating a cycle of dependency on ineffective shots that potentially worsened population-wide immunity. Professor Dalgleish concludes that the actions of key medical officers amount to "supreme incompetence, if not manipulation against the better interests of the country." A powerful call for accountability and a stark lesson in the dangers of ignoring fundamental immunology.

A stunning and damning indictment from renowned oncology Professor Angus Dalgleish. He dismantles the entire premise of the COVID-19 vaccine program, revealing a catastrophic failure in scientific understanding and public health policy. His argument, in summary: 1. The Fundamental Flaw: From the start, it was impossible to create an effective vaccine for a coronavirus. Their rapid 3-month mutation wave far outpaces the 6-7 month development of mRNA vaccines. By the time a vaccine is deployed, it targets a virus that is already gone. 2. The "Worse Than Useless" Effect: This is not merely a case of outdated vaccines. It's about "Antigenic Sin" or "Immunological Imprint." The vaccine locks the immune system onto a non-existent version of the virus, using its energy to fight a ghost. This actively impairs the body's ability to recognize and respond to new, real-world variants. 3. The Inconvenient Data: This theory was borne out by real-world evidence. Data began to show that the vaccinated were more likely to get infected by subsequent variants than the unvaccinated. The official response? A circular logic that dismissed the clear signal of harm. 4. The Omicron Blindspot: When Omicron emerged, our health officials saw a disaster. Dalgleish saw "the very best vaccine ever"—a highly infectious, airborne variant that conferred broad immunity with minimal illness. Instead of embracing this natural path to endemicity, they doubled down on boosters, despite evidence linking more jabs to higher infection risk. 5. The Final Betrayal: We now know the foundational claim—that vaccines prevent transmission—was never backed by data. The program continued unabated, creating a cycle of dependency on ineffective shots that potentially worsened population-wide immunity. Professor Dalgleish concludes that the actions of key medical officers amount to "supreme incompetence, if not manipulation against the better interests of the country." A powerful call for accountability and a stark lesson in the dangers of ignoring fundamental immunology.

Camus

59,264 Aufrufe • vor 10 Monaten