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Humanspective
Posted - January 27, 2026 at 11:25 PM
Saved - January 28, 2026 at 5:45 AM

@Humanspective - Humanspective

🚨NEW. Bombshell Report Update. Christine Cotton releases an updated 414 page report alleging "this product is the biggest scandal in the history of the pharmaceutical industry" The company completely changed manufacturing processes for messenger RNA during Global distribution... known by many as Pfizer's "Bait and Switch". @StatChrisCotton (CHRISTINE COTTON) - "This report demonstrates that the population has not received the product tested into the clinical trial with the 95% efficacy so touted by politicians, journalists, and TV doctors, and that, at the time it was authorized, there were no results on efficacy and safety" MCKERNAN verifies - "That's what I'm going to show you... is that the vaccines had DNA contamination in them [and] many people have gone and replicated this work" "Now, the FDA, the EMA, and the TGA have all admitted that this mistake has happened. How did it happen? There was a big bait-and-switch.... [they] switched to the process on the right and didn't retrial the drug. In doing so, they left a tremendous amount of excess DNA behind [so] all of the vaccine efficacy numbers you've heard in the news are flawed [because] that's not what actually went into the trial."

Video Transcript AI Summary
Every day, just the 1% of the cells of your DNA that gets replicated stretches from here to the sun four times. If you're to line it up end by end, that's very hard to conceptualize. But it should give you a little bit of humility before you go and start monkeying with it with these vaccines that can actually alter your DNA. And that's what I'm gonna show you. Is that the vaccines had a DNA contamination in them that didn't tell you about that could in fact alter your genome. Alright? These people are vibe coding your genome. And this is a major attack surface to the human gene pool because if this thing starts to alter the lifespan of people, it's going to part you with your Bitcoin. You're gonna end up spending money in a fiat system that has no controls, has no liability, and ends up oftentimes inducing mandates to get what it wants done. Many people had have peer have gone and replicated this work. It happened on Twitter. It did not happen very quickly in the peer review system. The peer review system kinda kicked it out. Some of these papers have now been peer reviewed, but it took years for them to come to this conclusion. Now, the FDA, the EMA and the TGA have all admitted that this mistake has happened. How did it happen? There's a big bait and switch. Pfizer actually ran the trial of 22,000 people on the process on the left and after they got to the trial, they then switched to the process on the right and didn't retrial the drug. And in doing so, they left a tremendous amount of excess DNA behind in the product. So all of the vaccine efficiency numbers you've heard in the news are flawed. They're not real because that's not what actually went into the trial. What went to the public was actually something that came out of this process too. It's published now in the BMJ that this fraud happened and no one has yet been prosecuted for it. So what did they leave in there? What they left in there was something we know from the polio scandal. If you're not familiar with the polio scandal, that polio vaccines were also contaminated with something known as SV40 and it created a massive cancer wave. Now the whole virus isn't in these vaccines, but there is a very curious part of this called the SV40 region that Pfizer intentionally removed from the disclosure that they gave to the FDA. So the FDA has admitted that this SV40 material is in there. They did not spell this out to the regulators. The regulators did not find them and they're actually running cover for them saying this DNA is too little consequence to matter, it's too small, and it's not functional. But we know it's functional because Dean et al has published that this piece of DNA drives DNA straight to the nucleus. It gets used in gene therapy vectors.
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Speaker 0: Every day, just the 1% of the cells of your DNA that gets replicated stretches from here to the sun four times. If you're to line it up end by end, that's very hard to conceptualize. But it should give you a little bit of humility before you go and start monkeying with it with these vaccines that can actually alter your DNA. And that's what I'm gonna show you. Is that the vaccines had a DNA contamination in them that didn't tell you about that could in fact alter your genome. Alright? These people are vibe coding your genome. And this is a major attack surface to the human gene pool because if this thing starts to alter the lifespan of people, it's going to part you with your Bitcoin. You're gonna end up spending money in a fiat system that has no controls, has no liability, and ends up oftentimes inducing mandates to get what it wants done. Many people had have peer have gone and replicated this work. It happened on Twitter. It did not happen very quickly in the peer review system. The peer review system kinda kicked it out. Some of these papers have now been peer reviewed, but it took years for them to come to this conclusion. Now, the FDA, the EMA and the TGA have all admitted that this mistake has happened. How did it happen? There's a big bait and switch. Pfizer actually ran the trial of 22,000 people on the process on the left and after they got to the trial, they then switched to the process on the right and didn't retrial the drug. And in doing so, they left a tremendous amount of excess DNA behind in the product. So all of the vaccine efficiency numbers you've heard in the news are flawed. They're not real because that's not what actually went into the trial. What went to the public was actually something that came out of this process too. It's published now in the BMJ that this fraud happened and no one has yet been prosecuted for it. So what did they leave in there? What they left in there was something we know from the polio scandal. If you're not familiar with the polio scandal, that polio vaccines were also contaminated with something known as SV40 and it created a massive cancer wave. Now the whole virus isn't in these vaccines, but there is a very curious part of this called the SV40 region that Pfizer intentionally removed from the disclosure that they gave to the FDA. So the FDA has admitted that this SV40 material is in there. They did not spell this out to the regulators. The regulators did not find them and they're actually running cover for them saying this DNA is too little consequence to matter, it's too small, and it's not functional. But we know it's functional because Dean et al has published that this piece of DNA drives DNA straight to the nucleus. It gets used in gene therapy vectors.

@StatChrisCotton - Christine Cotton OFFICIEL

Friends, I'm sharing with you the latest version of my report on Pfizer's clinical trials for its COVID vaccine. This document has been used in complaints against French health authorities, a legal action for abuse of power against the ANSM (French National Agency for Medicines and Health Products Safety), and a criminal complaint for aggravated deception and administering a substance without consent. This report demonstrates that the population has not received the product tested into the clinical trial with the 95% efficacy so touted by politicians, journalists, and TV doctors, and that, at the time it was authorized, there were no results on efficacy and satefty. It highlights incomplete results, multiple risks and missing information, as well as numerous methodological problems and even fraud that invalidate all the results. If you don't have the courage to read it in its entirety, at least read the conclusion, which is unequivocal. This product is the biggest scandal in the history of the pharmaceutical industry: lies, mass manipulation, refusal to acknowledge the victims… In the future, be vigilant. @P_McCulloughMD @joshg99 @canceledmouse @a_nineties @Jikkyleaks @DrJKunadhasan @DrAseemMalhotra @DrJBhattacharya @T_Nenninger @KenPaxtonTX @BrianneDressen @React19org @JSutta @SosNielsen66 @ake2306 @csshoemakermd @DiedSuddenly_ @eekymom @Answers4Sean @Fynnderella1 @SabinehazanMD @kacdnp91 @julie4butte5 @reformpharmanow @MelissaVisMe @drmelissamccann @missaksamir @echipiuk @DrCHuber @IcicLaw @docbiss @CartlandDavid @DrPPhillipsMD @JimGoodrich202 @NicHulscher @TamaraUgo @deepakdeepak @Hokkis @BringTheNoise_X @DrBruceScott @Marbles34 @megynkelly @clearavacc @ZeroSpike_ @Dr_R_Kurzrock @MeasslainteIRL https://christinecotton.fr/english_expertise_updated

Christine Cotton - Site Personnel Je vous mets à disposition ici les résultats de mes investigations et expertises, mes interviews et actions judiciares, et des liens et explications sur les documents source des essais cliniques. Vous y trouverez mon « Evaluation des pratiques méthodologiques mises en œuvre dans les essais Pfizer dans le développement de son vaccin ARN-messager contre la COVID-19 en regard des Bonnes Pratiques Cliniques »... christinecotton.fr
Humanspective
Posted - January 24, 2026 at 8:18 PM
Saved - January 25, 2026 at 9:55 PM
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BREAKING: Moderna are exiting the vaccine market, Reuters reports they’re curbing investments in vaccine trials. This follows an RSV mRNA clinical trial failure, with Prof. Robert Clancy saying they shouldn’t have been doing it. It was paused after safety signals; he notes “1 in 8 kids nearly died from overwhelming RSV infection.” He cautions against RSV vaccines, citing immune enhanced disease.

@Humanspective - Humanspective

🚨 BREAKING. Whispers emerge Moderna are exiting the vaccine market and Reuters reports them "curbing Investments in vaccine trials". This news follows a recent messenger RNA RSV clinical trial failure, which a stunned Professor Robert Clancy said "they shouldn't have been doing". It was "PAUSED" following safety signals where he says "1 in 8 kids nearly died from overwhelming RSV infection". CLANCY: "The one thing we learnt back in the 70's, is you steer away from trying to produce an RSV vaccine, because you get immune enhanced disease".... "A lot of people should have told them and they should have known themselves"

Video Transcript AI Summary
Monash University has just received a grant from Moderna to produce 100,000,000 doses of messenger RNA vaccine. The speaker questions what arms they are going to go into, and what they are going to have tagged, and what message they will have. They note that Monash has just come out with the RSV data. The speaker recalls a lesson from the 1970s: you steer away from trying to produce an RSV vaccine because you get immune enhanced disease. Many should have told them this; they didn’t cancel things, they put it on pause. So they paused, putting RSV messenger RNA into the arms of infants. The speaker states that twelve point five percent, one in eight, of these kids nearly died from overwhelming RSV infection. Twelve point five percent. The speaker suggests it’s a bit like they can’t control the dose and they shouldn’t have been doing it in the first place.
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Speaker 0: Monash Universe, they've just got a grant from Moderna to produce 100,000,000 doses of messenger RNA vaccine. Now, what arms are they going to go into, and what are they going to have tagged? What message are they going to have? They've just come out with the RSV, you've probably seen this data. I mean, the one thing we learnt back in the seventies is that you steer away from trying to produce an RSV vaccine because, you get immune enhanced disease. So a lot of people should have told them, they should have known themselves, they've had to sort of, they don't cancel things, they put it on pause. So they put it on pause, putting RSV messenger RNA into the arms of infants, when twelve point five percent, it's one in eight, one in eight of these kids nearly died from overwhelming RSV infection. Twelve point five percent! A bit like they can't control the dose and they shouldn't have been doing it in the first place.

@_aussie17 - aussie17

Moderna exits vaccine market?!! Bancel ‌said ‌regulatory delays and little support from the authorities make the market size "much smaller." Translation: We lost control of our "regulatory department"

Humanspective
Posted - December 1, 2025 at 3:14 AM
Saved - December 24, 2025 at 11:34 AM
reSee.it AI Summary
Dr. Peter McCullough testified before the Senate, stating the largest autopsy series after vaccination found 73.9% of deaths attributed to the vaccine and urged a black box warning for death. He described autopsy data as the best evidence and cited VAERS as causation by proxy, calling for immediate suspension of mRNA products. Related materials address alleged corruption and suppression of adverse events.

@Humanspective - Humanspective

Dr. Peter McCullough testifies in U.S. Senate and the evidence is jaw dropping. The mRNA injections should have had a black box warning for "death", and he presents the largest peer reviewed autopsy series in the World. Dr. McCullough: "When a product definitely results in death [there must be a] black box warning on the product immediately [they] still don't have the word "death" on the package insert" . Sen. Ron Johnson: "Do you have any science to back up your opinion?". Dr. McCullough: "The best data are autopsies. So in the largest autopsy series published to date, I know because I'm the senior author ... of all the deaths we examined, and we re-reviewed them, we had an adjudication committee, we had ways of arbitration, deciding on did the vaccine cause death ... the answer is ... of these cases that came in for autopsy after vaccination, 73.9% of individuals, it was determined that the vaccine was the cause of death".

Video Transcript AI Summary
Dr. McCulloch is asked to weigh in. Speaker 1 responds that he has presented at FDA advisory meetings and advised companies for decades on regulatory science. He states that when a product definitely results in death, and there are thousands of peer-reviewed papers on this, the COVID vaccines in some people sadly result in death—some on the very first day they take the shot. He argues that this must be a black box warning on the product immediately. He says he checked the package inserts for the currently available products, noting that the ones Senator Blumenthal wants to pursue, and what the Governor still wants to pursue, and what the FDA still wants administered, do not have the word “death” in the package insert. He asserts that Americans are not fairly informed. Speaker 0 asks whether Speaker 1 doubts that the COVID injection caused some deaths, and asks for his view on the numbers listed on VAERS (thirty-seven thousand, six hundred seven, per the prompt) and whether he has any science to back up his opinion. Speaker 1 replies that the best data are autopsies. He references the largest autopsy series published to date and notes that he is the senior author. He says they examined deaths after vaccination, had an adjudication committee and methods of arbitration to decide whether the vaccine caused death, and that in these autopsy cases, seventy-three point nine percent of individuals, it was determined that the vaccine was the cause of death. He mentions Holsher and colleagues, who are right behind him. Speaker 0 reiterates the FDA’s own laws, asking that this be included in the package insert, correct? Speaker 1 confirms, noting that in 2021 Dr. Carol Tocetta, working with the Daily Cloud, wrote about Peters’ marks in 2023 and asked, “where’s the black box warning? Where is it?”
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Speaker 0: I'll start with you Doctor. McCulloch. Do you wanna weigh in on that? Speaker 1: I've presented at the FDA advisory meetings. I've advised companies for decades on this, so I know the regulatory science very well. When a product definitely results in death, and there are thousands of peer reviewed papers on this Governor, the COVID vaccines in some people sadly result in death. Some on the very first day they take the shot. That must be a black box warning on the product immediately. I just checked the package inserts for the currently available products. The ones that Senator Blumenthal wants to pursue. Sounds like governor wants to still pursue these. Our FDA still wants them to be administered. They still don't have the word death in the package insert. As of today, they don't. And so Americans are not fairly informed. Speaker 0: Do you have any doubt in your mind that the COVID injection caused some deaths? I mean, do do you what what what do you think of the, what is it, thirty seven thirty eight thousand six hundred seven right now listed on Vayers? What do you think the real number is? And do you have any science to back up your opinion? Speaker 1: The best data are autopsies. So in the largest autopsy series published to date, I know because I'm the senior author, of all the deaths we examined and we re reviewed them, we had an adjudication committee, we had ways of arbitration, deciding on did the vaccine cause death, the answer is of these cases that came in for autopsy after vaccination, seventy three point nine percent of individuals, it was determined that the vaccine was the cause of death. First off, there's Holsher and colleagues who's sitting right behind me. Speaker 0: And again, by FDA's own laws, that should be included on that package insert, correct? Speaker 1: Immediately in 2021, Doctor. Carol Tocetta, working with the Daily Cloud, wrote Peter's marks in the 2023 and said, where's the black box warning? Where is it?

@Humanspective - Humanspective

Dr. Peter McCullough (Senior Author):"In the largest autopsy series published to date, [of] all the deaths we examined [and] of these cases that came in for autopsy after vaccination, 73.9% of individuals, it was determined that the vaccine was the cause of death". May 22, 2025 - U.S. Senate.

@Humanspective - Humanspective

Dr. Peter McCullough: ""When a product definitely results in death [there must be a] black box warning on the product immediately". May 22, 2025 - U.S. Senate. https://t.co/WDJ8qbHNxq

@Humanspective - Humanspective

"The Corruption of Science and Federal Health Agencies: How Health Officials Downplayed and Hid Myocarditis and Other Adverse Events Associated with the COVID-19 Vaccines" https://t.co/yW0N4IMew1

@Humanspective - Humanspective

JUST IN - Dr. Peter McCullough calls for immediate suspension of mRNA, citing VAERS as "causation by proxy" https://t.co/JlVz0KHpDR https://t.co/IVuEu7iGQX

@Humanspective - Humanspective

NEW: "These 10 Deaths are the tip of the iceberg" Dr. Peter McCullough calls for immediate suspension of mRNA, citing VAERS as "causation by proxy", whilst discussion mounts on the US FDA putting a "black box" warning on covid mod RNA jabs. MCCULLOUGH: "VAERS has in total 19480 deaths with over 2000 of them happening within 48 hours of the injection [and] VAERS does indicate causation by proxy of reporting" "Both Makary and Prasad should immediately call for the covid vaccines to be removed from the market [and] we've already had several hundred deaths that have occurred on their watch" "If the vaccine was not the cause, then we wouldn't do the report to VAERS [so] VAERS does indicate causation by proxy of reporting [it] indicates the vaccine is the cause of the problem, because the Doctor or healthcare provider [at] the scene who's examined the patient [has] determined the vaccine is the cause, otherwise a VAERS report would not be made" I don't think a "black box warning" is going to cut it.

Video Transcript AI Summary
These ten deaths are the tip of the iceberg. There is a vast number of deaths in the peer reviewed literature. These have cases have already been vetted. We don't need FDA officials to comment to them on them. They're deeply concerning. And then our US CDC vaccine administration adverse event system, VAERS, has in total now, this is shocking for United States residents, nineteen thousand four hundred and eighty deaths. About two thousand of these have occurred right within forty eight hours of the shot, and then nineteen thousand two hundred seventy nine Americans reported to be permanently disabled. These are reported to VAERS by doctors like myself who have already determined the vaccine is the cause of the injury, disability, or death. Because if the vaccine was not the cause, then we wouldn't do the report to VAERS. So this is the VAERS does indicate causation by proxy of reporting. This is very important. The VAERS system, I'll say it again, indicates the vaccine is the cause of the problem because the doctor or the health care provider in the field at the scene who's examined the patient, examined the autopsy and the medical record information, examined the clinical record, the vaccine administration has determined the vaccine is the cause. Otherwise, a VAERS report would not be made. So this is very important. I would say at this point in time, both Macron and Prasad should immediately call for the COVID nineteen vaccines to be removed from the market. Every day they continue to delay on this, the more Americans will be hurt by boosters. We've already had several hundred deaths this year that have occurred on their watch. B, they should initiate a safety review of the 19480 deaths with an independent panel to review all the information. The CDC has the patients and their families' phone numbers, emails, addresses. There ought to be interviews of family members for the deceased, interviews of the patient themselves for injuries and disabilities to to get their side of the story. The CDC has all that information. The review should be done independently by people who are not CDC or FDA employees, And there should be multiple reviewers and should be an adjudication process and finally, a determination of causality for the vaccine. And then I would say, finally, the FDA officials, including Macari and Prasad, needs to start showing up to important proceedings in Washington. There have been multiple hearings on vaccine safety. One that I was the lead witness on, 05/21/2025. Yeah. We published a report indicating that there was a government cover up of COVID nineteen vaccine induced mild pericarditis, including fatal cases.
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Speaker 0: These ten deaths are the tip of the iceberg. There is a vast number of deaths in the peer reviewed literature. These have cases have already been vetted. We don't need FDA officials to comment to them on them. They're deeply concerning. And then our US CDC vaccine administration adverse event system, VAERS, has in total now, this is shocking for United States residents, nineteen thousand four hundred and eighty deaths. About two thousand of these have occurred right within forty eight hours of the shot, and then nineteen thousand two hundred and seventy nine Americans reported to be permanently disabled. These are reported to VAERS by doctors like myself who have already determined the vaccine is the cause of the injury, disability, or death. Because if the vaccine was not the cause, then we wouldn't do the report to VAERS. So this is the VAERS does indicate causation by proxy of reporting. This is very important. The VAERS system, I'll say it again, indicates the vaccine is the cause of the problem because the doctor or the health care provider in the field at the scene who's examined the patient, examined the autopsy and the medical record information, examined the clinical record, the vaccine administration has determined the vaccine is the cause. Otherwise, a VAERS report would not be made. So this is very important. I would say at this point in time, both Macron and Prasad should immediately call for the COVID nineteen vaccines to be removed from the market. Every day they continue to delay on this, the the more Americans will be hurt by boosters. We've already had several hundred deaths this year that have occurred on their watch. B, they should initiate a safety review of the 19480 deaths with an independent panel to review all the information. The CDC has the patients and their families' phone numbers, emails, addresses. There ought to be interviews of family members for the deceased, interviews of the patient themselves for injuries and disabilities to to get their side of the story. The CDC has all that information. The review should be done independently by people who are not CDC or FDA employees, And there should be multiple reviewers and should be an adjudication process and finally, a determination of causality for the vaccine. And then I would say, finally, the FDA officials, including Macari and Prasad, needs to start showing up to important proceedings in Washington. There have been multiple hearings on vaccine safety. One that I was the lead witness on, 05/21/2025. Yeah. We published a report indicating that there was a government cover up of COVID nineteen vaccine induced mild pericarditis, including fatal cases.
Humanspective
Posted - July 9, 2025 at 7:46 PM
Saved - December 18, 2025 at 9:33 AM
reSee.it AI Summary
I report that the largest peer-reviewed COVID mRNA vaccine safety study, with 99 million people, shows a 510% higher risk of myocarditis after mRNA injection. The data closely match Pfizer’s trial data and Dr. Dean Patterson in Guernsey. RFK Jr. says Pfizer data imply a 500% greater risk of heart attack for the vaccinated, and that, before becoming HHS Sec, he warned that if people knew the truth they wouldn’t take it.

@Humanspective - Humanspective

The largest Peer Reviewed covid mRNA “vaccine” safety study ever conducted with a data set of 99 MILLION individuals, confirms a 510% increased risk of myocarditis following mRNA platform injection. Stunningly, this data closely matches the Pfizer Clinical Trial data given to health authorities before the global mass vaccination began and the vaccine mandates swept through businesses, corporations and hospitals. It also closely matches the rates identified by Dr Dean Patterson in Guernsey RFK Jr says: "Your chance of dying of a heat attack [according to Pfizer clinical trial data] is 500% greater than if you're unvaccinated" Prior to becoming HHS Sec he said: "If people knew the truth, people would not be taking this vaccine". Robert F Kennedy Jr. - THREAD 🧵

Video Transcript AI Summary
Speaker 0 states that death rates from the vaccine are extraordinarily high, claiming there have been more deaths in eight months than in all the billions of vaccines combined over the last thirty years for this one vaccine, totaling seventeen thousand recorded deaths in the United States, and asserts the death rate is much higher, “probably 40 times.” The speaker says the risk from the vaccine is completely untenable and that if people knew the truth they would not be taking this vaccine, and that the benefits after six months are apparently zero or even subzero. Speaker 0 references British data, claiming that people who are vaccinated are actually more likely in many age categories to get COVID than people who are unvaccinated, and asserts this outcome was predicted. The speaker alleges that Pfizer knew this would happen, citing their clinical trial, which they say was only six months long; at the end of that period, they claim twenty people died in the vaccine group and fourteen in the placebo group of all-cause mortality. They further claim there were five heart attacks in the vaccine group and only one in the placebo group, concluding that the chance of dying of a heart attack when vaccinated is five hundred percent greater than if one is unvaccinated. Speaker 0 contends that Pfizer knew they were going to kill a lot of people and proceeded to do so anyway. They insist that people need access to those studies to understand what they describe as deceptive, criminal deception that has supposedly been imposed upon them.
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Speaker 0: The death rates from this vaccine are there's been more deaths in eight months than in all the billions of vaccines combined over the last thirty years from this one vaccine, seventeen thousand recorded deaths in The United States, and we know the death rate's much, much higher than that, probably 40 times. The best math, the best, you know, studies are showing that it's 40 times that. So, you know, the risk from the vaccine are they're completely untenable. If people knew the truth, they would not be taking this vaccine. And then the benefits of the vaccine are apparently zero or even subzero after six months. The British data is showing that the people who are vaccinated are actually more likely in many age categories to to get COVID than people who are unvaccinated, which, by the way, was predicted. Now we know that Pfizer knew this was gonna happen because in their clinical trial, there were among in a six month clinical trial, was only six months. At the end of that period, twenty people died in the vaccine group and only fourteen in the placebo group of all cause mortality. There were five heart attacks in the vaccine group and only one in the placebo group. So your chance of dying of a heart attack when that vaccine, according to their own studies, is five hundred percent greater than if you're unvaccinated. So they knew we were gonna kill a lot of people, and they did it anyway. And people need to be able to see those studies and, and understand the deceptive this, you know, criminal deception that has, been imposed upon them.
Humanspective
Posted - November 29, 2025 at 2:45 AM
Saved - November 30, 2025 at 4:02 PM
reSee.it AI Summary
I explain that parasite medications work against cancer cells because parasites use mitochondrial substrate-level phosphorylation—the same dysfunctional energy pathway cancer cells rely on. Mebendazole and fenbendazole kill these parasites and, I show, target this mitochondrial substrate and glycolysis in cancer cells, even though cancer isn’t a parasite. I note political pressure around ivermectin, while Dr. Isabella Cooper points out it acts on the mitochondrial cell death pathway.

@Humanspective - Humanspective

🚨 World-renowned cancer biologist Thomas Seyfried, PhD, reveals "we have a mechanism now why parasite medications are working". Professor Thomas Seyfried: "Mebendazole, Febendazole [I] did a dive on it and I said, why [do] Parasite medications work against cancer cells, and it turns out that the parasites use mitochondrial substrate level phosphorylation in the tissue .. and mebendazol fenbendazol kill these parasites. So I tried it on the cancer cell and sure as hell, it targets the mitochondrial substrate and glycolysis" Parasites rely on the EXACT same dysfunctional energy pathway cancer cells do and these drugs don’t care that cancer isn’t a parasite. "So we have a mechanism now why parasite medications are working, but cancer is not a parasite" Thomas Seyfried mentions avoiding researching Ivermectin because of political pressure during covid, but Dr. Isabella Cooper, PhD in Ketogenic Science and Hyperinsulinemia points out the mechanism for him: "Ivermectin, it actually works on the mitochondrial cell death pathway".

Humanspective
Posted - November 26, 2025 at 7:02 PM
Saved - November 28, 2025 at 10:18 AM
reSee.it AI Summary
Discussion centers on alleged fundamental flaws in clinical trial design for HCQ and ivermectin. Proponents cite two studies suggesting strong effects and accuse trials of wrong dosing (HCQ with food; ivermectin with fatty meals) and delayed administration. Critics question credibility of stomach-based efficacy claims and note other design flaws; one cites RFK’s account of delayed ivermectin treatment.

@Humanspective - Humanspective

How did the entire scientific establishment get this one fundamental problem wrong in clinical trial research? Kylie Wagstaff and "The Oxford Group" just published 2 studies showing the powerful effects of HCQ and Ivermectin, but they were delayed for YEARS as the machine instituted experimental mod RNA technology. Gastroenterologist @SabinehazanMD reveals EXACTLY how they set up trials to fail, while the World was forced to choose Pfizer and Moderna to save the day. ◻️They gave HCQ on a FULL stomach when it's suppose to be given on an empty stomach. ◻️They gave Ivermectin on an EMPTY stomach when it was suppose to be taken with a FATTY MEAL. Dr Sabine Hazan exposes how they set up Ivermectin and Hydroxychloroquine to fail, so Fauci could sell the world mRNA injections and Remdesivir. If you think of the teams set up to run clinical trials and work out dosing protocols, how is it possible that they got this basic principle wrong?

Video Transcript AI Summary
In the discussion, Speaker 0 argues that word-of-mouth PR surrounding ivermectin “saved so many lives” and created widespread distrust in the industry, describing a shift where people questioned official stances: “My oxygen was low, and I did take ivermectin and it did work. Why are they telling me ivermectin doesn't work?” This view frames ivermectin as having proven effectiveness in practice, contrasting with public or institutional statements. Speaker 1 adds that it’s “really hard not to get angry” about the official trials, claiming that the WHO and, specifically, the Oxford trials demonstrated that ivermectin didn’t work, but that it “patently does.” They describe the fundamental problem as the way those trials were conducted, implying methodological issues. They discuss specifics of how the studies tested different drugs: Speaker 0 notes that hydroxychloroquine was given “with food” in the study, while ivermectin was given on an empty stomach, implying a potential misapplication of administration guidelines. They state that Merck’s initial labeling for ivermectin in other indications (scabies and lice) recommends administration with a fatty meal, and share a personal anecdote that their sister introduced ivermectin to the market for lice and conducted a clinical trial with many patients. Speaker 1 questions why leading clinicians would administer these drugs without knowing the correct guidelines, suggesting there should have been knowledge about administration with meals for hydroxychloroquine and with food for ivermectin. They remark, “Why the heck didn’t they know that?” Speaker 0 contends that physicians adhere to guidelines and hospital rules and fear lawsuits; they claim this fear leads to doctors “not even wanna know” certain information. They express the sentiment that the medical community was discouraged or constrained by fear of legal consequences and licensing actions, which contributed to doctors avoiding or stopping certain lines of inquiry or treatment. Overall, the dialogue centers on a perceived discrepancy between real-world outcomes of ivermectin use and official trial conclusions, the role of administration guidelines in trial results, and the influence of fear of legal ramifications on clinical practice.
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Speaker 0: Word-of-mouth PR of ivermectin saved so many lives and created a distrust in the industry where people woke up because they said, wait a minute. My oxygen was low, and I did take ivermectin and it did work. Why are they telling me ivermectin doesn't work? Speaker 1: It's really hard not to get angry that the WHO trials and the the I think it was at the Oxford trials demonstrated that ivermectin didn't work, but it patently does. It's the the single fundamental problem with those the way those trials were conducted. Speaker 0: Yeah. I will tell you, the single fundamental problem. They gave hydroxychloroquine the one they did the study on hydroxychloroquine, they gave it with food. You're supposed to give hydroxychloroquine on an empty stomach. Speaker 1: Right. Speaker 0: And with the ivermectin, they gave it on an empty stomach. You're supposed to give it with a fatty meal. Even in the it's even in the Merck when they when they brought out ivermectin initially for scabies and lice. And by the way, my sister was the one that brought ivermectin to the market doing, for lice. Speaker 1: Really? Speaker 0: Way back. Yeah. She used to advertise. I think she got about, you know, she got hundreds of patients on that clinical trial. Speaker 1: But the idea that the leading clinicians in the world allegedly would give these drugs without knowing. I mean, they should have known that you give it with food. You give hydroxychloroquine on the stomach and you give ivermectin with food. Why the heck didn't they know that? Speaker 0: They must have known that. I mean, I don't know. You know, physicians follow guidelines, and physicians follow the rules of the hospital, and they're afraid of getting sued. And this is what we did with our medical community. We hank up the doctors. We made them scared of a lawsuit. We made them scared of losing their license. And therefore, they stopped. They they don't even wanna know. Okay?

@jizzylint - Jizzy Lint

@Humanspective I wasn’t vaccinated and used IVM during COVID, but I don’t find the full and empty stomach arguments credible. If you’re able to neutralise the efficacy of a drug on that basis the drug doesn’t work

@deegn44596 - Marooned1957

@jizzylint @Humanspective Why could they not do it correctly. Presumably if others knew how it was to be administered then they should have known. Any ideas?

@jizzylint - Jizzy Lint

@deegn44596 @Humanspective Agree. Just saying if it were the only design flaw of the study (usually in IVM studies there are several) it wouldn’t be consequential enough to explain zero efficacy if IVM is indeed efficacious

@deegn44596 - Marooned1957

@jizzylint @Humanspective I can't say it was same study but RFK in his book on Fauci states that a study on Ivermectin was carried out where the administration was delayed for a number of days whilst the patient deteriorated. This had obvious consequences for results.

Humanspective
Posted - November 20, 2025 at 7:56 PM
Saved - November 22, 2025 at 11:07 AM
reSee.it AI Summary
A discussion on how antiparasitic drugs may affect cancer. Mebendazole/fenbendazole are said to disrupt parasite mitochondrial substrate-level phosphorylation, with some tests indicating effects on cancer cell metabolism. Ivermectin is noted to trigger mitochondrial cell death pathways. Mentions political barriers to ivermectin research, cancer stem cells, and possible links between chemo efficacy and mRNA-related cancers, plus a summary of IP6, vitamin D, fenbendazole, and ivermectin.

@Humanspective - Humanspective

"We have a mechanism now why parasite medications are working". The moment Thomas Seyfried PhD realised how anti parasitic medications work. @tnseyfried - "Mebendazole, Febendazole [I] did a dive on it and I said, why [do] Parasite medications work against cancer cells, and it turns out that the parasites use mitochondrial substrate level phosphorylation in the tissue .. and mebendazol fenbendazol kill these parasites. So I tried it on the cancer cell and sure as hell, it targets the mitochondrial substrate and glycolysis" "So we have a mechanism now why parasite medications are working, but cancer is not a parasite" Interestingly, Thomas Seyfried mentions the political landscape which prevented him from exploring the effects of Ivermectin because of covid, however Dr. Isabella Cooper [@I_mitochondria], PhD in Ketogenic Science and Hyperinsulinemia steps in and points out: "Ivermectin, it actually works on the mitochondrial cell death pathway".

Video Transcript AI Summary
Speaker 0: When you put the patient into nutritional ketosis, it opens up a whole new array of drugs that may have been considered ineffective. This is the field of repurposing drugs: once in this new physiological state, things thought to be ineffective can become super effective. This is a whole new field that will emerge as the results get shared more. You mentioned mebendazole in your talk as well. Does that have a glutamine-blocking aspect to it? Yes, that's in our paper too. Parasite medications. I don’t know about ivermectin because there was a lot of political stuff around that, so I told the lab we’re not going to do that to avoid wrath from somebody. Albendazole, fenbendazole, I said, why the hell do people have taken that? You hear people say, well, it got rid of my cancer with this and that. So I did a dive on it and asked why parasite medications work against cancer cells. It turns out that the parasites use mitochondrial substrate level phosphorylation in the tissue. Albendazole and fenbendazole kill these parasites, so I tried them on cancer cells, and sure as hell, they target the mitochondrial substrate and glycolysis. So we have a mechanism now why parasite medications are working. But cancer is not a parasite. All these people say cancer is a parasite – it’s not. Parasites and tumors use a common metabolic pathway, and a drug that works against parasites can be very effective against cancer, and that’s what we begin to see, especially under nutritional ketosis. Right? Speaker 1: Ivermectin actually works on the mitochondrial cell death pathway, the BCL2 Bax BAD pathway, so it actually helps push the cell death pathway.
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Speaker 0: Once you put the patient in this state of nutritional ketosis, it opens up a whole array, a new array of drugs that may have been thrown out, not worked. That's called the whole field of repurposing drugs now. But once the body is in this new physiological state, things that were thought to be ineffective become super effective. So again, that's a whole new field that will open as the results, once this information gets out more. And you mentioned mebendazole in your talk as well. Does that have a glutamine blocking aspect to it Yes, that's in our paper also. That's another interesting thing. Parasite medications. I don't know about ivermectin because there was a lot of political stuff about that. So I said to the lab, we're not going to do that because we didn't want to get the wrath from somebody. Ambendazole, Phenbendazole, I said, why the hell people have taken that, and you hear people say, well, got rid of my cancer with this and that. So I did a dive on it, I said, why parasite medications work against cancer cells? And it turns out that the parasites use mitochondrial substrate level phosphorylation in the tissue. Imbendazole, phenbendazole kill these parasites, so I tried it on the cancer cell, and sure as hell, it targets the mitochondrial substrate and glycolysis. So we have a mechanism now why parasite medications are working. But cancer is not a parasite. All these people say cancer is a parasite. It's not a parasite. Parasites and tumors use a common metabolic pathway, and a drug that works against parasites can be very effective against cancer, and that's what we begin to see, especially under nutritional ketosis. Right? Can you imagine this? Speaker 1: Ivermectin actually works on the mitochondrial cell death pathway, the BCL2 BaxBAD pathway, so it actually helps push the cell death pathway.

@Johnbegood2000 - John be good

@Humanspective @tnseyfried and IVM is super effective is battling CSC , there where most Chemo fails , the reason for re occurrence of cancers ,,,,,,, 🫡🫡

@Humanspective - Humanspective

@Johnbegood2000 @tnseyfried .@DrSuzanneH7 talks about how chemo might be less effective with the types of cancers related to mRNA injections here. So important point you’re making

@Humanspective - Humanspective

“Moment of Truth” Conference: @ChildrensHD, @DrSuzanneH7, @Judyth https://t.co/M4RUViB3GY

@Johnbegood2000 - John be good

@Humanspective @tnseyfried @DrSuzanneH7 wanted to post this but forgot to do it , gives a good summery of IP6+( Gold) , Vit D , Fenbendazole and IVM .... https://t.co/jcYJqJNSKX

Humanspective
Posted - November 22, 2025 at 3:02 AM
Saved - November 22, 2025 at 7:48 AM
reSee.it AI Summary
I report Prof. Robert Clancy stating that a Korean study in young boys comparing booster shots found the antigen vaccine more protective than the mRNA vaccine, and that “there is no advantage in using these genetic vaccines.”

@Humanspective - Humanspective

🚨 Major blow to mRNA vaccine technology. Professor Robert Clancy found a rare study comparing traditional vaccines with “modern” mRNA genetic vaccines. The results are damning. Prof. Robert Clancy: "The only study I've actually seen, was a recent Korean study in young boys, where they compared as a booster, an antigen vaccine, with a messenger RNA vaccine .. and guess what? The antigen vaccine was more protective than the messenger RNA vaccine" “There is no advantage in using these genetic vaccines.”

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The first speaker argues that messenger RNA vaccines were unprecedented compared to anything previously developed. They state there was never any justification given for not using a traditional vaccine, and there was never any evidence that the messenger RNA vaccine was as good as a ground-up virus—the old-fashioned type of vaccine—whose safety, efficiency, and cost are well known. They emphasize the importance of that point and note that a recent Korean study in young boys compared a booster using an antigen vaccine with a messenger RNA vaccine, and found the antigen vaccine to be more protective than the messenger RNA vaccine. From this, they conclude that there are currently data indicating there are no ongoing advantages to using these genetic vaccines. The second speaker adds that this situation is a huge mystery, questioning why the genetic RNA route was chosen in the first place. They suggest that someone made a lot of money, acknowledging that money is a factor, but saying they have never heard a scientific explanation for the decision-making process, describing it as a complete black box. They further point out that there are ongoing efforts by many people to transform vaccines beyond traditional forms to include self-replicating RNA, and that this discussion continues. They argue that the red flags from the first round have not been sorted out, and that there is no evidence these approaches are better; in fact, they imply they are clearly not better.
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Speaker 0: The messenger RNA vaccines in particular were very different to anything we had ever, ever done before. There was never ever given a reason why we didn't use a traditional vaccine. There was never ever any evidence that the messenger RNA vaccine was as good as a ground up virus, the old fashioned type of virus, which of course we know about, we know the safety issues, we know the efficiency issues, and we know the cost. And this was very, very important. And it's quite interesting that the only study I've actually seen was a recent Korean study in young boys, where they compared as a booster an antigen vaccine with a messenger RNA vaccine. And guess what? The antigen vaccine was more protective than the messenger RNA vaccine. So even at this level, we now have some data showing that there's no ongoing advantages of using these genetic vaccines. Speaker 1: And this is just a huge huge huge mystery, isn't it? Why on earth did they go for that that that genetic RNA route? There's just Speaker 0: Well, someone made a lot of money. Speaker 1: Yeah. There's no question someone made a lot of money, but I've never heard any scientific explanation as to why that was. That that decision processing is decision making is just a complete black box, isn't it? And it's just think Speaker 0: that's that's that's the point. And we're still in the position where now there are many people, certainly here, that want to take over and completely transform our vaccines into not just the messenger RNA, but the self replicating. You know, it just goes on and on, and yet we haven't sorted out the red flags from the the first round, let alone shown they're any better, which they're clearly not.
Humanspective
Posted - November 1, 2025 at 7:09 PM
Saved - November 2, 2025 at 1:36 AM

@Humanspective - Humanspective

Largest peer reviewed autopsy series in the World. William Makis: "A Tsunami of evidence". Dr Peter McCullough: "In the largest autopsy series published to date [in] 73.9% of individuals, it was determined that the [mod RNA] vaccine was the cause of death".

Humanspective
Posted - October 19, 2025 at 7:11 PM
Saved - October 20, 2025 at 8:22 PM
reSee.it AI Summary
I report that a Local Government warned residents and Australian Councils about alleged DNA contamination in Pfizer/Moderna mRNA vials (peer‑reviewed). The State Government dissolved the local council and cancelled elections after questions about Big Pharma. In WA, Port Hedland faced dissolution; the TGA is funded largely by Big Pharma. Buckhaults claims DNA contamination in Pfizer vaccines, with "Process 1" vs "Process 2." Other posts critique policy makers and Big Pharma.

@Humanspective - Humanspective

Unbelievable. Local Government passed a Worlds First motion warning residents and Australian Councils about DNA contamination of Pfizer/Moderna covid mRNA vials (peer reviewed research). The State Government responded by cancelling their elections and dissolving the local council. Adrian McCrae speaking at MEHA in the European Union: "Last month my entire local government in Australia was sacked and dissolved and we had our elections cancelled. Why? Because as a tier of Australian government we dared to ask uncomfortable questions, that embarrassed the Australian federal government and their cozy relationship with Big Pharma." The local Government of a small town in Western Australia (W.A), Port Hedland, put the TGA and the Federal Government and the Prime Minister of Australia, Anthony Albanese on Notice. W.A Labor Minister for Local Government Hannah Beazley, who PM Anthony Albanese calls a "Friend", has recently appeared on Legacy media channels targeting small government, and according to McCrae was involved in dissolving the Port Hedland council and cancelled their elections. The TGA, which was indirectly instituted in response to tragedies like Thalidomide, receives 95% of its funding from Big Pharma.

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Speaker 0: Twelve months ago, my local government in Port Hedland, Western Australia moved and passed a motion demanding the prime minister, the state leaders, health ministers across the country validate what is now verified science, and we demanded a suspension of the mRNA injections that Australians' mRNA COVID injections are dangerously contaminated with foreign DNA contaminations and foreign DNA fragments. Now this Australian local government action has now been successfully followed and replicated in towns and cities all across Australia. We've also had over 200,000,000 views on our on social media of our council meeting. This put some serious pressure on the Australian TGA, which is Australia's drug regulation body akin to Europe's EMA or the FDA in The USA. For those of you who don't know, the Australian drug regulator, the receives around about 95 of its funding from big pharma. It's like regulatory capture on steroids. To make matters worse, the unelected bureaucrats who approve or deny applications for new drugs or medical interventions have no legislative requirement to declare any conflicts of interest. So when over 90% of the TGA's budget is supported by industry it regulates and when the conflicts of interest of those marketing drug approval decisions is hidden, is it any wonder in the West that we've lost our faith in our health institutions? Only in Australia could a regulator funded by the industry it regulates still call itself impartial with a straight face. I tell you this story to point out the inherent risks that we all face in speaking truth to power. Last month, my entire local government in Australia was sacked and dissolved and we had our elections canceled. Why? Because as a tier of Australian government, we dared to ask uncomfortable questions that embarrassed the Australian federal government and their cozy relationship with big pharma.
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Speaker 0: Thank you, Maria. Adrian McCray from Australia. Twelve months ago, my local government in Port Hedland, Western Australia moved and passed a motion demanding the prime minister, the state leaders, health ministers across the country validate what is now verified science, and we demanded a suspension of the mRNA injections that Australians' mRNA COVID injections are dangerously contaminated with foreign a foreign DNA con contaminations and foreign DNA fragments. Now this Australian local government action has now been successfully followed and replicated in towns and cities all across Australia. We've also had over 200,000,000 views on our on social media of our council meeting. This put some serious pressure on the Australian TGA, which is Australia's drug regulation body akin to Europe's EMA or the FDA in The USA. For those of you who don't know, the Australian drug regulator, the receives around about 95 of its funding from big pharma. It's like regulatory capture on steroids. To make matters worse, the unelected bureaucrats who approve or deny applications for new drugs or medical interventions have no legislative requirement to declare any conflicts of interest. So when over 90% of the TGA's budget is supported by industry it regulates and when the conflicts of interest of those marketing drug approval decisions is hidden, is it any wonder in the West that we've lost our faith in our health institutions? Only in Australia could a regulator funded by the industry it regulates still call itself impartial with a straight face. I tell you this story to point out the inherent risks that we all face in speaking truth to power. Last month, my entire local government in Australia was sacked and dissolved and we had our elections canceled. Why? Because as a tier of Australian government, we dared to ask uncomfortable questions that embarrassed the Australian federal government and their cozy relationship with big pharma.

@Humanspective - Humanspective

“The Pfizer vaccine is contaminated with Plasmid DNA, it's not just mRNA...it's got bits of DNA in it [and I know] because I sequenced it in my own lab” Phillip Buckhaults, PhD Biochemistry and Molecular Biology. Professor of Molecular Biology & Genetics https://t.co/mSIssVOknM

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Philip Buchholz, a PhD in biochemistry and molecular biology and cancer genomics researcher at the University of South Carolina, describes himself as an expert on how the human genome can be altered and which alterations cause cancer. He emphasizes his skill in DNA sequencing and detecting foreign DNA pieces at very low levels, noting that his lab used these abilities during the pandemic to invent the spit-based COVID test. He asserts that the Pfizer vaccine is contaminated with plasma DNA, not just mRNA, and that this DNA is the DNA vector used as the template for the in vitro transcription reaction when producing the mRNA. He claims to have proven this by sequencing in his own lab. Regarding evidence in Columbia, he says a colleague in the College of Pharmacy was in charge of the vaccination program and kept every vial, including empty ones with a small amount left at the bottom. He states he received these vials and examined two batches from Columbia by sequencing, sequencing all the DNA in the vaccine to determine its content, and notes it is surprising that any DNA is present at all. He asserts this DNA can be identified and the mechanism of its presence inferred, and that he is alarmed about the regulatory process that allowed it. He explains that this DNA could cause rare but serious side effects, including death from cardiac arrest, noting there are cases of suspicious death after vaccination and that DNA is a plausible mechanism. He argues that this DNA can and likely will integrate into the genomic DNA of cells that were transfected with the vaccine, describing it as a permanent fixture in the cell and in its progeny indefinitely. He says this makes the DNA different from RNA because it can be permanent, posing a real hazard for genome modification of long-lived somatic cells like stem cells, and potentially causing a sustained autoimmune attack toward that tissue. He adds that while autoimmunity is not his field, the cancer risk is within his purview and it is a possibility.
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Speaker 0: Name is Philip Buchholz. Have a PhD in biochemistry and molecular biology. I'm a cancer gene jock. Basically, do cancer genomics research at the University of South Carolina. What that means is that I'm kind of an expert on all the ways that the human genome can get futzed with during your lifetime and which of those things cause cancer and which ones don't. Okay. So technically, that means that I'm very, very skilled in in the art of DNA sequencing. Okay. I can figure out the sequence of things that I didn't know what I was looking for. And I'm also pretty good when I say I, I mean the people in my laboratory, you're not gonna hear their names, but there's a group of people that do this excellent work. We're really good at at, detecting foreign pieces of DNA in places where they're not supposed to be, even if they're real low levels. And we used those skills during the pandemic. We invented the COVID test that many of you did the spit test. Okay? That came out of my lab because we were really good at that kind of stuff. The Pfizer, vaccine is contaminated with plasma DNA. It's not just mRNA. It's got bits of DNA in it. This DNA is the DNA vector that was used as the template for the in vitro transcription reaction when they made the mRNA. I know this is true because I sequenced it in my own lab. The vials of Pfizer vaccine that were given out here in Columbia, one of my colleagues was in charge of that vaccination program in the College of Pharmacy. Pharmacy. And for reasons that I still don't understand, he kept every single vial. So he had a whole freezer full of the empty vials. Well, empty vials have a little tiny bit in the bottom of them. He gave them all to me, and I looked at We had two batches that were given out here in Columbia and I checked these two batches and I checked them by sequencing. And I sequenced all the DNA that was in the vaccine and I can see what is in there. And it's surprising that there's any DNA in there. And you can kind of work out what it is and how it got there. And I'm kind of alarmed about the possible consequences of this, both in terms of human health and biology, but you should be alarmed about the regulatory process that allowed it to get there. So this DNA, in my view, it could be causing some of the rare but serious side effects like death from cardiac arrest. There's a lot of cases now of people having suspicious death after vaccine. It's hard to prove what caused associated. And this DNA is a plausible mechanism. Okay? This DNA can and likely will integrate into the genomic DNA of cells that got transfected with the vaccine mix. This is just the way it works. We do this in the lab all the time. We take pieces of DNA, we mix them up with a lipid complex like the Pfizer vaccine is in, We pour it onto cells, and and a lot of it gets into the cells, and a lot of it gets into the DNA of those cells, and it becomes a permanent fixture of the cell. It's not just a temporary a temporary thing. It is in that cell and all of its progeny from now on forevermore. Amen. So that's why I'm kind of alarmed about this DNA being in the vaccine. It's it's it's different from RNA because it can be permanent. This is a real hazard for genome modification of long lived somatic cells, like stem cells, and it could cause theoretically that it could cause a sustained autoimmune attack toward that tissue. It's also a very real theoretical risk of future cancer. The autoimmunity thing is not my wheelhouse. I'm not an immunologist, but the cancer risk is. That's my bag. I know this is a thing, and it is a possibility.

@Humanspective - Humanspective

Pfizer's "Bait and Switch". Pfizer's mRNA covid 'vaccine' clinical trial participants got the cleaner "Process 1" Billions of humans Globally were injected with "Process 2", where DNA contamination and SV40 sequences were introduced into the vials https://t.co/pyma32bKh1

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This is not conspiracy theory. This has been published in the BMJ by Retzaf Levy, and they go through this process: one where they ran these vaccines in the trial and how they changed that when they decided to go and inject the rest of the world. This is traditionally a mortal sin in vaccine manufacturing or in any sort of biologic manufacturing. The process is the product. You change the process, you have to go through trials again. And the EMA even asked them to do that, although they failed to. They asked for another trial of 250 people once they changed the process and that data was never delivered. So this bait and switch is very important for you to understand why the trial data is of absolute zero consequence to what we're actually seeing in the field. Those numbers are a caricature of what they're actually doing with these injections. They know something. Pfizer very early on they had the data on this from their trial, they knew this was going to happen and they quickly went out and acquired cancer companies. They put $43,000,000,000 into the acquisition of C Gen and they put $2,260,000,000 to acquire Trillium Therapeutics. Trillium was focused on blood cancers that have a CD one forty seven marker on them. Okay? That is one of the markers that is known to be involved in COVID. So, they have a very interesting window on those malignancies and, they're buying up the cancer companies that are probably gonna play the biggest role in benefiting from the mess that they've created. So, in summary, the Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials. This is a big bait and switch and it's a fraud. So you can't believe anything they're saying about the vaccine efficiency, which we have seen even those numbers decay over time. This is probably why. They're not really what they trialed. They gave you something different. There is significant DNA contamination that's found. Like, 10 out of 11 studies have found this, and the ones that haven't found it have some financial conflicts. So, I think the consensus is out. 10 out of 10 out of 10 of the real studies, are finding this. Several are through peer review, which have not been easy to get through peer review. The peer review journals do not like these papers. They get beat around in peer review for months to years, but they're making their way out now. There is also significant DNA contamination now found in five peer reviewed studies that were not looking at this. They were looking at people's blood and tissue and it was accidentally in there. Other people had to go sleuth it out. We've got cancer on the rise and there's several papers that report cancer post vaccination. Like, right at the site of injection, they'll see neoplasms. Alright? There is there's something going on here. This can't be ignored saying it's a coincidence anymore. Now this is these are liability free and they're often mandated. Okay? This may be the largest carcinogenic hit ever to the human population. And we have these on childhood schedules. We're giving these to pregnant women. This has gone absolutely off the rails.
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Speaker 0: This is not conspiracy theory. This has been published in the BMJ by Retzaf Levy, and they go through this process one where they where they ran these vaccines in the trial and how they changed that when they decided to go and inject the rest of the world. This is traditionally a mortal sin in vaccine manufacturing or in any sort of biologic manufacturing. The process is the product. You change the process, you have to go through trials again. And the EMA even asked them to do that, although they failed to. They asked for another trial of 250 people once they changed the process and that data was never delivered. So this bait and switch is very important for you to understand why the trial data is of absolute zero consequence to what we're actually seeing in the field. Those numbers are a caricature of what they're actually doing with these injections. They know something. Pfizer very early on they had the data on this from their trial, they knew this was going to happen and they quickly went out and acquired cancer companies. They put $43,000,000,000 into the acquisition of C Gen and they put $2,260,000,000 to acquire Trillium Therapeutics. Trillium was focused on blood cancers that have a c d one forty seven marker on them. Okay? That is one of the markers that is known to be involved in COVID. So, they have a very interesting window on those malignancies and, they're buying up the cancer companies that are probably gonna play the biggest role in benefiting from the mess that they've created. So, in summary, the Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials. This is a big bait and switch and it's a fraud. So you can't believe anything they're saying about the vaccine efficiency, which we have seen even those numbers decay over time. This is probably why. They're not really what they trialed. They gave you something different. There is significant DNA contamination that's found. Like, 10 out of 11 studies have found this, and the ones that haven't found it have some financial conflicts. So, I think the consensus is out. 10 out of 10 out of 10 of the real studies, are finding this. Several are through peer review, which have not been easy to get through peer review. The peer review journals do not like these papers. They get they get beat beat around in peer review for months to years, but they're they're making their way out now. There is also significant DNA contamination now found in five peer reviewed studies that were not looking at this. They were looking at people's blood and tissue and it was accidentally in there. Other people had to go sleuth it out. We've got cancer on the rise and there's several papers that report cancer post vaccination. Like like, right at right at the site of injection, they'll see neoplasms. Alright? There is there's something going on here. This can't be ignored saying it's a coincidence anymore. Now this is these are liability free and they're often mandated. Okay? This may be the largest carcinogenic hit ever to the human population. And we have these on childhood schedules. We're giving these to pregnant women. This has gone absolutely off the rails.

@Humanspective - Humanspective

@senorameredith I think it's a symptom of complete cognitive dissonance and belief in Big Pharma from policy makers

@Humanspective - Humanspective

@TonyWil93639204 I hear you....just trying to make it easier for people.

@Humanspective - Humanspective

@Zobbie137 Absolutely

Humanspective
Posted - October 14, 2025 at 8:50 PM
Saved - October 15, 2025 at 12:44 PM

@Humanspective - Humanspective

Sen. Blumenthal: "You're not a Medical Doctor [or] Immunologist or biologist?" Aaron Siri: "Or Vaccinologist, NO, but I depose them regularly, including the World's leading ones". Dem Senator Richard Blumenthal wasn't prepared for Aaron Siri, who deposed the godfather of vaccinology, Dr. Stanley Plotkin. Dr. Plotkin admitted in that deposition the Hep B vaccine only had 5 days of safety review. In the new movie "An Inconvenient Truth", the head of infectious disease at Henry Ford Health System, Dr. Marcus Zervos, also admitted that "The proper safety studies haven't been done" on vaccines recommended within the CDC schedule. As Del Bigtree points out, after depositions and multiple lawsuits won, they found out "the entire science behind vaccine safety, was nothing but a complete fraud".

Video Transcript AI Summary
Checklist for summary approach: - Identify and restate the speaker’s claimed credentials (or lack thereof). - Capture the core activity described (deposing leading vaccine experts) and the basis for claims (actual evidence). - Note the courtroom principle contrasting titles versus evidence. - Outline the asserted strategic actions (legal action against specific agencies) and purported results. - Preserve the exact claim about the outcome of the lawsuits regarding vaccine safety science. - Present statements verbatim where feasible, and otherwise closely paraphrase to retain meaning. - Avoid adding judgments, external context, or evaluative commentary. Summary: The speaker introduces himself as Mister Siri and immediately clarifies that he is not a medical doctor, and not an immunologist or biologist or any kind of vaccinologist. He adds that despite lacking these titles, he “depose[s] them regularly, including the world’s leading ones with regards to vaccines,” and that he must base his claims on “actual evidence.” In describing his courtroom approach, he asserts that when he goes to court regarding vaccines, “I don’t get to rely on titles.” He then recounts a proposed strategic path he characterizes as a “genius way forward”: “We’re gonna sue the government agencies, HHS, FDA, NIH,” and he states that “we started winning.” The narrative then turns to the alleged outcomes of those legal actions, posing the question, “And what did we prove in those lawsuits?” followed by the claimed conclusion: “That the entire science behind vaccine safety was nothing but a complete fraud.” Throughout, the speaker frames the process as a shift from deference to credentials to a reliance on evidence obtained through deposition and litigation, culminating in purported victories against major federal health agencies. He presents the lawsuits as the mechanism by which the foundational science of vaccine safety was challenged, and he asserts that the result of these proceedings is a definitive statement that the science underpinning vaccine safety is fraudulent, as claimed within the transcript’s courtroom-centered account. The emphasis remains on the contrast between claimed authority and evidence-based legal challenges, as well as on the asserted procedural successes and the sweeping conclusion about vaccine-safety science.
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Speaker 0: Mister Siri, you're not a medical doctor, are you? No, sir. And you're not an immunologist or biologist or any kind of Or vaccinologist. No. But I depose them regularly, including the world's leading ones with regards to vaccines, and I have to make my claims based on actual evidence. When I go to court with regards to vaccines. I don't get to rely on titles. Okay. We had a genius way forward. We're gonna sue the government agencies, HHS, FDA, NIH, and we started winning. And what did we prove in those lawsuits? That the entire science behind vaccine safety was nothing but a complete fraud.
Humanspective
Posted - October 14, 2025 at 7:11 PM
Saved - October 14, 2025 at 10:01 PM
reSee.it AI Summary
I argue that the pharma-regulatory system creates an illusion of 100% vaccine safety by depriving trials of inert placebo, using only 5 days of safety monitoring, and having no control group. This blocks causal detection and shields liability. The 1986 Act adds protection. In the deposition, Siri shows that without proper placebo data there’s no proof that Hep B causes or doesn’t cause adverse outcomes.

@Humanspective - Humanspective

The Godfather of Vaccines proves why the Henry Ford Study is important. Retrospective Studies are the only way to get past the "Ethical" argument. At 1m 20s, Dr. Stanley Plotkin looks at the camera and Aaron Siri, and realises he is cooked. This part of "An Inconvenient Study" sets a very important context. The Pharma-Regulatory infrastructure creates an illusion that every vaccine is "100% safe and effective", that there can never be any side effects, there can never be a causal link, because all the clinical trials are intentionally designed without an inert placebo control....they were intentionally designed in a way that would NEVER find causality. They use "safety" as a means to get a system in place that protects them from liability. But they only use the argument that "it's not ethical do do a placebo" when they are pressed, because the lay people that trust government, who are giving these products to their children, actually believe the proper safety studies HAVE been done. Not only are the trials not designed to hold the product accountable, the government gave an extra layer of protection with the 1986 injury act. They knew that by doing trials where they aren't comparing true placebo, that they could legally say no causality exists. How can you prove a "causal" link if they aren't doing the studies which are a pre-requisite for that evidence? There is no causality without an inert control group and they haven't done any of those trials. Aaron Siri presses Dr. Plotkin on the Hep B vaccine. ◻️5 days of safety monitoring. No control group. No chance to capture autoimmune or neurological conditions happening after 5 days. SELECTED PARTS OF TRANSCRIPT (DEPOSITION): Aaron Siri: "How long does it say that safety was monitored after each dose?" Plotkin: "5 days" Aaron Siri: "Is 5 days long enough to detect an autoimmune issue that arises after 5 days?" Plotkin: "No" Aaron Siri: "Is 5 days long enough to detect any neurological disorder that arose from that vaccine after 5 days" Plotkin: "No" Aaron Siri: "There is no control group correct?" Plotkin: "No" Aaron Siri: "In order to establish whether it's causal, between the vaccine and the condition, you need a randomized placebo controlled study [but] that was not done for [this] hepatitis B vaccine before licensure, was it?" Plotkin: "No" Aaron Siri: "Do you agree with the CDC's recommendation that babies receive a hepatitis B on the first day of life?" Plotkin: "Yes" Aaron Siri: "You stated that hepatitis B doesn't cause encephalitis right?" Plotkin: "That's my opinion yes" Aaron Siri: "But the IOM after doing its review determined it couldn't find science to support a causal determination, one way or another" Plotkin: "yes [that] means [they] don't have evidence [that] it either causes or doesn't cause [so] in the absence of data [there's] no proof that causation exists" Aaron: "So if there's no data to show that it causes or it doesn't cause, your sub your supposition is that [it] doesn't cause it?" Plotkin: "There's no proof that it does" Aaron Siri: "That's different than saying it doesn't cause it"

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Checklist for summary approach: - Identify the core topics: trial design and safety monitoring, absence of control group, list of reported adverse events, causality vs association, need for placebo-controlled trials, regulatory and review positions (CDC, IOM), and final stance on vaccine safety. - Preserve key factual claims and phrases (e.g., monitoring duration, lack of control group, listed adverse events, causality requirements). - Emphasize any surprising or unique points (no pre-licensure placebo trial, IOM stance on data, final assertion about safety assumptions). - Exclude filler, repetition, and off-topic chatter; keep a neutral, fact-focused summary. - Translate only if needed; retain precise wording where quoted. - Keep the summary within 378-473 words. Summary: In the discussion about Recombivax HB, the speaker confirms the product and its labeling, noting that Section 6.1 covers pre-licensure clinical trial experience and that safety was monitored after each dose for five days. It is stated that five days is not long enough to detect autoimmune issues or neurological disorders arising after vaccination. The conversation also points out that there is no control group in those trials. Turning to Section 6.2, the nervous system disorders subsection acknowledges reports of Guillain-Barre syndrome and multiple sclerosis, including exacerbation, myelitis including transverse myelitis, seizures and febrile seizures, peripheral neuropathy including Bell’s palsy, muscle weakness, hypothesia, and encephalitis. It is emphasized that these reports are included because they have been reported to authorities as occurring after vaccination, not because they prove the vaccine caused those reactions. To establish causality, a randomized placebo-controlled study would be needed, but none was performed for this hepatitis B vaccine before licensure. Without a control group, evaluating whether a phenomenon in the vaccine group is related is not possible. A speaker comments that the broader issue is that such safety placebo trials were not done before licensure; once injuries are observed, they argue that it’s unethical to conduct placebo trials, and doctors may claim there are no studies showing the injuries are caused by the vaccine, leading to an assumption of safety. The discussion then touches on CDC guidance, with a question about agreeing with the recommendation that babies receive hepatitis B on the first day of life. The responder concedes that hepatitis B doesn’t cause encephalitis “in my opinion.” The IOM review is cited as having determined it “couldn’t find science to support a causal determination one way or another.” In the absence of data, the conclusion cited is that “there’s no proof that causation exists,” which is distinguished from saying it doesn’t cause it. The transcript closes with a provocative remark: “Vaccine safety is not based on science and data. And that is the stalemate we find ourselves in.”
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Speaker 0: Doctor. Plotkin, this is the product, the manufacturer insert for Recombivax HB, correct? Speaker 1: Yes. Speaker 0: And the clinical trial experience would be found in Section 6.1, correct? Correct? Doctor. Plotkin? Speaker 1: Yes. Speaker 0: In Section 6.1, when you look at the clinical trials that were done pre licensure for Combivacs HP, how long does it say that safety was monitored after each dose? Speaker 1: Let's see. Speaker 0: Five days. Okay. Is five days long enough to detect an autoimmune issue that arises after five days? No. Is five days long enough to detect any neurological disorder that arose from the vaccine after five days? No. There is no control group, correct? Speaker 1: It does not mention any control group, no. If Speaker 0: you turn to section 6.2, under the nervous system disorders, states that there have been reports of Guillain Barre syndrome, correct? Speaker 1: Yes. Speaker 0: As well as multiple sclerosis, exacerbation of multiple sclerosis, myelitis, including transverse myelitis, seizure, febrile seizure, peripheral neuropathy including Bell's palsy, muscle weakness, hypothesia, and encephalitis, correct? Speaker 1: Correct. Before you go on, these reports are required to be included because they have been reported to the authorities as happening after vaccination. That is not proof that the vaccine caused those reactions. Speaker 0: In order to establish whether it's causal between the vaccine and the condition, you need a randomized placebo controlled study. But that was not done for this Hepatitis B vaccine before licensure, was it? Speaker 1: No. Without a control group, if you were looking for a phenomenon occurring in the vaccine group, you cannot judge that phenomenon without having a control group. Speaker 2: Difficult. So this is how the entire game is played. They don't do a safety placebo trial before the vaccine's licensed. Then when people start lining up with all of these serious side effects, you say, well, can you do a placebo based trial now? They'll say, no, it's unethical. So they won't do it before. They won't do it after those injuries. And when they can't do a study, your doctor says to you, I haven't seen any studies that show that these injuries are being caused by the vaccine. Therefore, I'm going to assume they're safe. Speaker 0: Do you agree with the CDC's recommendation that babies receive a hepatitis B on the first day of life? Yes. You stated that hepatitis B doesn't cause encephalitis, right? Speaker 1: That's, my opinion, yes. Speaker 0: But the IOM, after doing its review, determined it couldn't find science to support a causal determination one way or another. Correct? Speaker 1: Yes. But that means that they don't have evidence for the supposition. Speaker 0: That it either causes or doesn't cause? Right. They don't know. Speaker 1: They don't know because there aren't enough data. In the absence of data, my conclusion is that there no there's no proof that causation exists. Speaker 0: So if there's no data to show that it causes doesn't cause Yes. Your supposition, is that I understand correctly? Yes. Is that it doesn't cause it? Speaker 1: That there's no proof that it does. Speaker 0: Okay. That's different than saying it doesn't cause it, correct? Correct. So Speaker 2: let's be clear. Vaccine safety is not based on science and data. It's based on an assumption of safety. And that is the stalemate we find ourselves in.
Humanspective
Posted - October 12, 2025 at 7:07 PM
Saved - October 13, 2025 at 1:41 AM
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I question why a parasite medication would kill cancer. I read that Thomas Seyfried investigates cancer’s energy sources, identifying glucose and glutamine as two keys, noting that cancer cells and parasites share the glutaminolysis pathway. A 2024 Khadka–Seyfried paper explains how cancer cells ferment glutamine to produce ATP under hypoxia.

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“Why would a parasite medication be effective in k*lling cancer?”. As the cancer industry increasingly profits from toxic medical paradigms, Thomas Seyfried investigates the energy and fuel sources that cancer needs to live. He found the 2 keys which open the door to its survival. Glucose and Glutamine, which is why he points out that: “the parasite and the cancer cells, use a common metabolic pathway, the glutaminolysis pathway”. The 2024 paper by Khadka, Seyfried provides critical insights into how cancer cells ferment glutamine to produce ATP in the absence of oxygen (hypoxia).

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Speaker 0: We also know that certain parasite medications are very effective, can be very effective in targeting glutamine. And Benzol, Fenbendazole, we're working on that right now. Why would a parasite medication be effective in killing cancer? Because the parasite and the cancer cell use a common metabolic pathway, the glutaminolysis pathway, which is a substrate level phosphorylation in the mitochondria that we just published with Derek's big paper.
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Speaker 0: We also know that certain parasite medications are very effective, can be very effective in targeting glutamine. And Benzol, Fenbendazole, we're working on that right now. Why would a parasite medication be effective in killing cancer? Because the parasite and the cancer cell use a common metabolic pathway, the glutaminolysis pathway, which is a substrate level phosphorylation in the mitochondria that we just published with Derek's big paper.
Humanspective
Posted - October 11, 2025 at 6:19 PM
Saved - October 12, 2025 at 10:30 PM
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I say allergies are induced at will by linking a target protein to the aluminum adjuvant in vaccines. I describe using aluminum with latex to create permanent latex, peanut, or dairy allergies in rats, and claim aluminum provokes allergic responses to viral antigens and ambient allergens. I cite studies suggesting higher allergic rhinitis in vaccinated children and link this to aluminum-era rises in food allergies, tied to my allergy advocacy work.

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Robert F Kennedy Jr: "We've been inducing allergies by pumping them full of Aluminum" RFK Jr gives a birds eye view of how allergies are induced AT WILL by linking the target protein to the Aluminum adjuvant from the Hep B vaccine. "How do they give the allergy to the rat? They take the aluminum adjuvant from the hepatitis B vaccine adjuvant, add a latex molecule, and that rat now has a permanent latex allergy". Robert F Kennedy Jr (Transcript): "Here's something people should know: Aluminum provokes an allergic response, and that's why it's valuable." "If you put aluminum in with the viral antigen, your body now mounts an allergic response to that viral antigen, whether it's polio, hepatitis B, HPV, or whatever. But what we now now, the science suggests, is that aluminum also creates allergic responses to anything that's in the ambient environment." "So, if you have a peanut oil excipient in that vaccine with aluminum, you could have a lifetime allergy to peanuts. If there’s a Timothy weed outbreak the week you get that aluminum vaccine, you may have a lifetime allergy to Timothy weed." "That’s probably why—there's two studies by Moss and Cowlings, which show that children who are vaccinated with aluminum vaccines, have 30 times the rate of allergic rhinitis as kids who don't." "These food allergy epidemics date to when we started giving kids aluminum." "My kids have these allergies. I’m one of the founders of the Food Allergy Initiative and the Food Allergy Network, which is the biggest food allergy research group. That group have scientists from all over the world who are giving food allergies to rats and then figuring out how to treat them." "How do they give allergies to rats? They take aluminum from the hepatitis B vaccine adjuvant, add a latex molecule, and the rat has a permanent latex allergy. Add a peanut molecule, it has a permanent peanut allergy. Add a dairy molecule, it now has a permanent dairy allergy." "So you wonder why this generation of children is allergic to everything? It’s because we’ve been inducing allergies by pumping them full of aluminum. Mikhaila Peterson: "That’s crazy.".

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Here's something that people should know, is that aluminum provokes an allergic response, and that's why it's valuable. So if you put the aluminum in with the viral antigen, your body now mounts an allergic response to that viral antigen, whether it's polio or hepatitis B or the, you know, HPV or whatever. So if you have a peanut oil excipient in that vaccine, you and you put aluminum in it, now you could have a lifetime allergy to peanuts. They take the aluminum adjuvant from the hepatitis B vaccine, add a latex molecule, and that rat now has a permanent latex allergy. You add a peanut molecule and it has a permanent peanut allergy.
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Speaker 0: Here's something that people should know, is that aluminum provokes an allergic response, and that's why it's valuable. So if you put the aluminum in with the viral antigen, your body now mounts an allergic response to that viral antigen, whether it's polio or hepatitis B or the, you know, HPV or whatever. So but what we now know, the science suggests, is that the alumina also creates allergic responses to anything that's in the ambient environment. So if you have a peanut oil excipient in that vaccine, you and you put aluminum in it, now you could have a lifetime allergy to peanuts. If you if there's a Timothy weed outbreak, the the week that you get that aluminum vaccine, you now may have a lifetime allergy to to Timothy weed. And that's why probably, you know, there is two studies by Mawson and Cowlings, which show that children who are vaccinated with aluminum vaccines have thirty times the rate of allergic rhinitis as kids who don't. And, you know, all of these, these food allergy epidemics date to the time that we started giving these kids this aluminum. And because my kids have these allergies, I'm one of the founders of the food allergy initiative in the Food Allergy Network, is the biggest food allergy research group. And what, you know, so that group has scientists from all over the world who are giving food allergies to rats, and then figuring out how to treat them. How do they give the allergy to the rat? They take the aluminum adjuvant from the hepatitis B vaccine, add a latex molecule, and that rat now has a permanent latex allergy. You add a peanut molecule and it has a permanent peanut allergy. You add a dairy molecule and it now has a permanent dairy allergy. Oh, you wonder why all of this whole generation of children is allergic to stuff, is because we've been inducing allergies by pumping them full of aluminum. That's great. That's crazy. Yeah. Thank thank you very, very much for coming on.
Humanspective
Posted - October 3, 2025 at 9:22 PM
Saved - October 4, 2025 at 3:18 PM
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I am shocked by the findings shared by Dr. Jessica Rose, who discovered an 8300% increase in colon cancer cases coinciding with the mRNA COVID vaccine rollout. This aligns with Dr. Patrick Soon-Shiong's observations about a rise in cancer among young people. Dr. Drew also highlighted concerning evidence regarding spike proteins and their potential impact on natural killer cell function. Additionally, Kevin McKernan found a Pfizer-like plasmid in a sequenced colon cancer case. Co-author @JesslovesMJK has published a peer-reviewed article on DNA contamination in vaccine vials.

@Humanspective - Humanspective

This is unbelievable. NEW: Dr Jessica Rose finds an astonishing signal in VAERS that aligns with Patrick Soon-Shiong's clinical observations of an alarming rise in colon cancer for young people in his clinic. She found a "8300% increase in colon cancer" for the mRNA covid vaccine rollout timeframes. Dr. Drew also mentions a disturbing finding. After voicing Dr Patrick Soon-Shiongs concerns about the spike proteins potential effect on "suppression of natural killer function" and the alarming rise in young people with cancer, Dr. Drew mentions Kevin McKernan's findings of "a colon cancer that was [sequenced] and there was the [Pfizer-like vaccine] plasmid within the DNA of that colon cancer". @JesslovesMJK is co-author of the new peer reviewed article revealing DNA contamination in Moderna and Pfizer mRNA vaccine vials well above safety limits.

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Speaker 0: Doctor Sun Shiang is concerned about suppression of natural killer function, which we can talk about in a section. 'there was a, I believe it was a colon cancer that was the DNA was sequenced, and there was the plasmid within the DNA of that colon cancer.' 'Yep, that was Kevin.' He adds, 'I would immediately start sequencing tumours in people who'd had multiple shots,' noting, 'this is a species level problem because of the number of people that were injected.' Doctor Xion Xiong writes about eight, nine and ten year olds with colon cancer and a 13 year old in his clinic dying of metastatic pancreatic cancer, and compares pre COVID and post COVID VAERS data. He 'counted all the colon cancer reports in VAERS from 2018 to 2020 for all vaccines combined,' versus VAERS from '2021 to 2023.' He finds 'an 8,300 percent increase' and a PRR of '11.5.' He concludes, 'VAERS is like leaves rustling in the wind, but it's a signal,' a 'pharmacovigilance tool designed to do this,' and, 'If it's over one or two, depending on your limit, you have a definitive association and possibly a causal effect.'
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Speaker 0: I see Doctor. Sun Shiang here, he is concerned about the same thing for different reasons. He's worried about suppression of natural killer function, which we can talk about in a section, but I'm sure you're aware that there was a, I believe it was a colon cancer that was the DNA was sequenced, and there was the plasmid within the DNA of that colon cancer. Speaker 1: Yep, that was Kevin. And it's very concerning, and it prompts, in my opinion, I mean, if I was head of some kind of public policy agency, I would immediately start sequencing tumours in people who'd had multiple shots. Mean, it seems like an natural thing to do for our species because this is a species level problem because of the number of people that were injected. Yeah, it's wild. And on the subject matter of Doctor. Xion Xiong, sorry, yeah, I did write a little piece on this. Just decided once I saw him make this X post about the eight, nine and 10 year olds with colon cancer and saying that that was the first time in his career he had a 13 year old in his clinic die of metastatic pancreatic cancer, I looked at theirs naturally, I wanted to do a comparison between pre COVID and post COVID scenarios. So I counted all the colon cancer reports in VAERS from 2018 to 2020 for all vaccines combined, and I counted the number of colon cancer reports in VAERS from 2021 to 2023. This is just a reflection, by the way. VAERS is like leaves rustling in the wind, but it's a signal. It's a pharmacovigilance tool designed to do this. And I found that there was an 8,300, if that's even a thing, percent increase in colon cancer reports between these two time frames. And the proportional reporting ratio, which is one of the ways that you use VAERS to detect an association so that you can do a subsequent causality assessment, of which if it's over one or two, depending on your limit, you have a definitive association and possibly a causal effect. So the PRR in this case is 11.5. So it's way, way, way, way higher than it would need to be in order to prompt an immediate investigation into what this signal is telling us. I mean, I said, that's what VAERS is for. Yeah. Hello.
Humanspective
Posted - October 4, 2025 at 3:08 AM
Saved - October 4, 2025 at 6:46 AM
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I expressed my shock at Dr. Drew's strong criticism of Big Pharma for selecting the spike protein, the most pathogenic part of the virus, for the mRNA vaccine. He referenced Patrick Soon-Shiong's theory that COVID resembles an "AIDS-like virus," suggesting that NK cells, crucial for immunity and cancer detection, could be suppressed. Dr. Drew made a striking claim that the adverse reactions to COVID are linked to the spike protein, raising concerns that the vaccine might have similar effects.

@Humanspective - Humanspective

"What the h*ll are you doing!?" @drdrew goes scorched earth on Big Pharma for choosing the most pathogenic part of the protein for its mRNA injection. The Spike Protein. Dr. Drew mentions Patrick Soon-Shiong had a theory that covid was an "AIDS like virus", and that NK Cells vital for immunity and cancer surveillance might be suppressed. Here he drops a bombshell, that the "pathogenic component of covid reactions are the spike protein, therefore you'd have to guess perhaps the vaccine does the same thing"

Video Transcript AI Summary
Discussion centers on Doctor Sun Shiang's theory of natural killer suppression in COVID. He suggests "COVID itself was sort of an AIDS like virus killing a particular T cell line" and "the pathogenic component of all COVID reactions are the spike protein, therefore you'd have to guess perhaps the vaccine does the same thing." The other speaker says "natural killer cells are really important" and that this idea "needs to be further explored, like all of these subject matters, if you ask me." He cites pharmacovigilance data: "mortality rates going up across the board" and that "these shots, especially if you take two or three of them, seem to push those latent viruses into action." He also states, "the pathogenic ligand is the spike protein. It's what damages at least the endothelium, if not the natural killer cells, and it is the pathogenic part." He ends with: "Now let's get the nucleocapsid or the whole virus or something. Why in the world would you continue to produce or insist that people take a vaccine that produces the pathogenic component?"
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Speaker 0: But I I do first wanna drill into whether or not you think there's anything in doctor Sun Shiang's theory about natural killer suppression. He's mostly focused on COVID. His sort of notion is that COVID itself was sort of an AIDS like virus killing a particular T cell line. I would argue that the pathogenic component of all COVID reactions are the spike protein, therefore you'd have to guess perhaps the vaccine does the same thing. But what are your feeling about the natural killer theory? Speaker 1: Yeah, it's a really interesting hypothesis. I mean, for people who don't know, natural killer cells are really important. Everybody talks about T cells and B cells. So natural killer cells are like, I think of them kind of like the T cells of the innate immune system. So they're very, very potent and they rush to the rescue or to a fight when your body is introduced to a foreign antigen or pathogen immediately. So they're really, really, really important. And people who have NK cell deficiencies can be they can have a plethora of different kinds of diseases and conditions. So it's an interesting hypothesis. I would have to look deeper into it, but I cannot say that it doesn't make sense because on the VADES like, you know, the vaccine acquired induced deficiency syndrome idea, this makes a lot of sense when you look at the pharmacovigilance data, when you look at mortality rates going up across the board, when you look at the immunological deficiencies and the way that if you have, say, a latent viral infection, like a herpes infection that was suppressed, these shots, especially if you take two or three of them, seem to push those latent viruses into action. So there's either what I think is that the effectors that were keeping these latent viruses at bay or suppressed, the immunological suppression itself, the regulation, it gets dysregulated. So this is all coming from an immunological basis. So to theorise that NK cells are involved is a good idea. It needs to be further explored, like all of these subject matters, if you ask me. Speaker 0: You mentioned making sense several times there in your description of the NK hypothesis. What here's what would make sense to me as it pertains to the vaccine generally, that we come up with a vaccine that does not produce specifically the pathogenic limb of the protein. What the hell? The pathogenic ligand is the spike protein. It's what damages at least the endothelium, if not the natural killer cells, and it is the pathogenic part. I understand I keep saying this, Okay. In an emergency, that was your target. I get it. Alpha and delta was a different illness than Omicron. Okay. I understand. You you can disagree with that. Okay. But I'm willing to I'm willing to concede that and just go, okay. That was alpha and delta. That was an emergency. You had a target there. You went for it. I get it. Now what the hell are you doing? Now let's get the nucleocapsid or the whole virus or something. Why in the world would you continue to produce or insist that people take a vaccine that produces the pathogenic component?

@Humanspective - Humanspective

Our profound immune system never sleeps. Natural Killer Cell takes out a cancer cell. https://t.co/GNQpkn6Ks0

Humanspective
Posted - July 18, 2025 at 8:26 PM
Saved - October 1, 2025 at 12:23 PM

@Humanspective - Humanspective

"Pfizer is definitely worse". NEW from Joseph A. Ladapo at Florida Health Department: "They should not be used in any Human Beings...and you know there's some people who are trying to put them in animals too...and I think many of us wouldn't want to eat that food" https://t.co/vFCwxdKN05

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First of all, multiple studies now, to be very clear, multiple studies now show that of the two, Moderna and Pfizer, Pfizer is definitely worse. Pfizer is worse for cardiovascular side effects related to blood clotting. Pfizer is worse for neurologic effects, and Pfizer is worse for serious adverse events overall. A few studies have shown that Pfizer may be associated with be associated with an increase in mortality also compared to Moderna. The vaccines, they are not the same. You've got probably more myocarditis cases with Moderna, but Pfizer is worse overall. So I apologize that it hasn't been clear. Sort of along those lines, what's your recommendation?
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Speaker 0: First of all, multiple studies now, to be very clear, multiple studies now show that of the two, Moderna and Pfizer, Pfizer is definitely worse. Pfizer is worse for cardiovascular side effects related to blood clotting. Pfizer is worse for neurologic effects, and Pfizer is worse for serious adverse events overall. A few studies have shown that Pfizer may be associated with be associated with an increase in mortality also compared to Moderna. The vaccines, they are not the same. You know, we've you've heard my opinion, Doctor. Corey's, Doctor. Walzcog's opinions about their use in general. But between the two of them, Pfizer is definitely worse. You've got probably more myocarditis cases with Moderna, but Pfizer is worse overall. So I apologize that it hasn't been clear. They shouldn't take them. They are products that should not be going into human Because these products, they should not used in any human beings. And, you know, there's some people who are trying to put them in animals too, and and I think many of us wouldn't wanna eat that food either, that meat. Sort of along those lines, what's your recommendation?
Humanspective
Posted - September 25, 2025 at 8:38 PM
Saved - September 26, 2025 at 1:02 PM
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I shared a video by Dr. John Campbell discussing how Pfizer's lipid nanoparticles distribute in the body, supported by Pfizer's own bio-distribution report. The report details where these particles accumulate 48 hours post-injection, with significant presence in organs like the liver and spleen. I noted that Pfizer claimed to have worked closely with the FDA on these studies. Additionally, I referenced a peer-reviewed study indicating DNA contamination levels in the vaccines exceeded regulatory limits. I also engaged with others discussing the topic.

@Humanspective - Humanspective

Video of how Pfizer's "Pesky lipid nano particles" bio distribute. NEW: Dr John Campbell covers a clip by @InsidemRNAFilm, showing the size of lipid nano particles and how they bio-distribute in the body. I've attached Pfizer's Bio-distribution report below showing how this video meets Pfizer's own data. Pfizer said at the last ACIP meeting: "Our bio distribution studies were done [in] consultation with the FDA [and also that] we did work in close consultation with the FDA on all our bio distribution studies" (Direct quotes from Pfizer). So when thinking about the video attached and seeing how the lipid nano particles are distributed "Everywhere and Anywhere", remember they also contain within them DNA contamination verified by peer reviewed evidence (Speicher et al). Here's a list of where they go 48 hours after injection: 1. Liver - 24.29 2. Spleen - 23.35 3. Adrenal Glands - 18.21 4. Ovaries - 12.26 5. Bone Marrow - 3.77 6. Small Intestine - 1.472 7. Lymph Node (mesenteric) - 1.366 8. Large intestine - 1.34 9. Lung - 1.09 10. Thyroid - 1.00 11. Lymph node (mandibular) - 0.727 12. Pituitary gland - 0.694 13. Bone (femur) - 0.687 14. Pancreas - 0.599 15. Heart 0.55 16. Uterus - 0.456 17. Kidneys - 0.42 18. Bladder - 0.365 19. Thymus - 0.331 20. Testes (males) - 0.320 21. Salivary glands - 0.264 22. Skin - 0.253 23. Stomach - 0.215 24. Muscle - 0.192 25. Adipose tissue - 0.181 26. Prostate (males) - 0.170 27. Eyes - 0.112 28. Spinal cord - 0.112 29. Brain - 0.068 The below document is Pfizer's own document which required a FOI request. The FDA worked with Pfizer on it. The peer reviewed study (Speicher, McKernan, Rose) showed that DNA contamination "exceeded the regulatory limit for residual DNA set by the US FDA and the WHO by 36–153-fold for Pfizer and 112–627-fold for Moderna" Bookmark this for reference.

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"So here we see the syringe needle going in and the lipid nanoparticles coming out." "Probably three to 6,000 per injection." "These are completely new to the human body, and they circulate around in the blood." "They're supposed to stay in the deltoid muscle, but they don't." "They circulate everywhere around the body." "Then when they come to a cell, they'll go inside the cell, this process called endocytosis." "Any contaminating DNA will be carried very, very efficiently by the lipid nanoparticles into cells, coming into contact with the walls of the vascular endothelium, the lining of the blood vessels." "If the lipid nanoparticles are 80 nanometers each, it would be 87 of them to fit across the diameter of a red blood cell." "So 5,000,000,000 of these red blood cells in one milliliter of blood, and yet this is the size of the lipid nanoparticles." "Until these problems are resolved there should be a moratorium on mRNA vaccines." "In my view let me know what you think."
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Speaker 0: So here we see the syringe needle going in and the lipid nanoparticles coming out. Probably three to 6,000 per injection. Three to 6,000,000,000,000. These are completely new to the human body, and they circulate around in the blood. Here we see it going through a blood vessel, circulating around with the much larger erythrocytes, the red blood cells. Nano means very, very small. And they'll go everywhere. They're supposed to stay in the deltoid muscle, but they don't. They circulate everywhere around the body. They're going to go to your ears. They're going to go to your heart, your liver, your spleen, your kidneys. These things go everywhere, the ovaries and the testes. Then when they come to a cell, they'll go inside the cell, this process called endocytosis. And this modified foreign RNA will end up inside the cell as will the lipid nanoparticle itself into the wall of the vascular endothelium, the linings of the blood vessels, and be transported straight into our cells. Any contaminating DNA will be carried very, very efficiently by the lipid nanoparticles into cells, coming into contact with the walls of the vascular endothelium, the lining of the blood vessels. Now this massive structure we see here is a red blood cell. So this is all one red blood cell. These are about seven micrometers in diameter across. And if we get lipid nanoparticles, if we assume the lipid nanoparticles are 80 nanometers each, which is about right, then we see that it would be 87 of them to fit across the diameter of a red blood cell. This is how small they are compared to red blood cells. So 5,000,000,000 of these red blood cells in one milliliter of blood, and yet this is the size of the lipid nanoparticles. It's no wonder they can get just about everywhere in the body. Now those graphics just really bring the situation to life, don't they? They were provide provided by Eric Tansko. These are his links. I've put them at the top of the description. He's not being paid for this work. Please click on his videos and encourage his work with comments and share them around very much more detail in those videos. But that just gives you a bit of an insight into these pesky lipid nanoparticles. Until these problems are resolved there should be a moratorium on mRNA vaccines. In my view let me know what you think.

@Humanspective - Humanspective

This is Pfizer's very own data. They said they worked with the FDA on this, announcing at ACIP "We did work in close consultation with the FDA on all our bio distribution studies" Pfizer's mRNA Lipid Nano Particle Bio Accumulation Report (Released by FOI). Where Lipid Nano Particles go 48 x hours after vaccination. This is also where DNA contaminants (within those Lipid Nano Particles) and SV40 sequences verified by Peer Reviewed Research are carried: 1. Liver - 24.29 2. Spleen - 23.35 3. Adrenal Glands - 18.21 4. Ovaries - 12.26 5. Bone Marrow - 3.77 6. Small Intestine - 1.472 7. Lymph Node (mesenteric) - 1.366 8. Large intestine - 1.34 9. Lung - 1.09 10. Thyroid - 1.00 11. Lymph node (mandibular) - 0.727 12. Pituitary gland - 0.694 13. Bone (femur) - 0.687 14. Pancreas - 0.599 15. Heart 0.55 16. Uterus - 0.456 17. Kidneys - 0.42 18. Bladder - 0.365 19. Thymus - 0.331 20. Testes (males) - 0.320 21. Salivary glands - 0.264 22. Skin - 0.253 23. Stomach - 0.215 24. Muscle - 0.192 25. Adipose tissue - 0.181 26. Prostate (males) - 0.170 27. Eyes - 0.112 28. Spinal cord - 0.112 29. Brain - 0.068 PFIZER: "Our bio distribution studies were done [in] consultation with the FDA"

@Humanspective - Humanspective

@InsidemRNAFilm "Pesky lipid nanoparticles" - @Johnincarlisle https://www.youtube.com/watch?v=bWgtr533Wxk https://t.co/YXe5KmoqGP

@Humanspective - Humanspective

@InsidemRNAFilm @Johnincarlisle Full Movie: "Inside mRNA Vaccines" https://t.co/AiV1UFD21Q

Video Transcript AI Summary
The documentary traces the arc from mRNA vaccines as breakthroughs to controversy, with 'slashing a half billion dollars in government funding from mRNA vaccine development.' It catalogs competing views, including 'There was never a vaccine made with mRNA' and warnings that 'Lipid nanoparticles go everywhere in the body.' A week after his vaccination, Joel's health began to rapidly decline. It presents opposing tallies: 'This vaccine, the mRNA vaccine, has probably saved about three million lives' alongside calls from 'thousands of doctors and scientists are calling for a halt to mRNA vaccines.' Regulators are cited as saying vaccines 'have saved millions of lives with minimal safety concerns.' It notes 'There are over 200 different clinical trials currently planned for mRNA based technology, and over 40 trials are currently enrolling' and that 'The FDA has approved Moderna's RSV vaccine for people 60 and older.'
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Full Transcript
Speaker 0: MRNA vaccines were hailed as medical breakthroughs in the fight against COVID. Now the US Department of Health and Human Services is slashing a half billion dollars in government funding from mRNA vaccine development. Speaker 1: The most urgent invention in the world right now is a vaccine that prevents you from getting COVID-nineteen. It's gonna have to go to seven billion people. One final way that's promising is the RNA vaccine. Messenger RNA. Speaker 2: Messenger RNA. Speaker 3: Get it done. We need it. We want it fast. Speaker 4: The FDA is fast tracking possible coronavirus vaccine. Speaker 5: If we had a pandemic, wink wink, we could emergency authorize this new mRNA technology. Speaker 6: There was never a vaccine made with mRNA. Speaker 3: Messenger RNA, which we had no previous experience with. None. Speaker 7: The mRNA technology scares me. It's a brand new technology being used. Speaker 8: When people received their first COVID nineteen vaccine, it was the first time their body received lipid nanoparticles. Speaker 5: People historically have this confidence in the concept of, oh, it's just a vaccine. Lipid nanoparticles go everywhere in the body, Speaker 3: to the brain, to the bone marrow, to Speaker 5: the liver, to the spleen, most importantly to the reproductive organs. Speaker 9: I regret it every single day that I walked into my local pharmacy to get that shot in my arm. Speaker 10: It's very likely that the mRNA vaccines accelerate coronary artery disease. Speaker 2: Not one more shot should be delivered. Speaker 11: It's a tragedy that it was allowed to happen. Speaker 7: The mRNA vaccines, its uses are being expanded tremendously. Huge applause to Doctor. Robin Miller. Speaker 12: It's perceived that there is a gold mine, a huge amount of potential profit to be made with this new technology. Speaker 13: Joel Walzkog had a fulfilling career as a surgeon, but he had no choice but to abandon his calling due to the severity of his health problems after an mRNA COVID vaccine. Speaker 7: I had a very busy practice. I specialized in joint replacement because of my extra training. It was a great practice. I saw about 6,000 patients in clinic every year And I did about 800 to 900 surgical procedures per year. That's a very busy practice. You took people that were in a lot of pain and functionally disabled from it. And you do a joint replacement like a hip or a knee replacement and literally six weeks later, their life has dramatically changed. So it was very gratifying for me too. I enjoyed getting up every day and I always told my kids, try to find something that you love because almost every day I I I was excited about going to work. Speaker 13: A week after his vaccination, Joel's health began to rapidly decline. Speaker 7: About seven days later, I remember waking from bed and telling my wife that my feet were numb. So maybe one week later after my numbness started, I remember I was at work and I was sitting in a clinic room talking to a Speaker 10: patient and I tried to stand up Speaker 7: and literally my legs wouldn't go. There was just no reaction. My legs wouldn't help me stand. So I remember pushing my using my hands to push my body up. And as soon as I tried to stand, I fell. And just my legs gave out. And really it was at that time when I knew that there was something more serious or more ominous going on. Very quickly I got diagnosed with a condition called transverse myelitis. I realized that my condition was much more serious. And unfortunately, I've never been back to work since. I couldn't work. I went through probably every phase of grief. Certainly was in denial. I had a long period of being very angry. Unfortunately, my leg weakness, my leg numbness, my loss of stamina, my balance problems have never improved. I have about two to four hours on my legs a day, so I can get around most days okay for two to four hours. But after that, my legs are pretty much done for the day and I spend a lot of time on my recliner in our family room where I can read and do things like that. Sometimes I get neuropathic or kind of bad pain flares. Sometimes the flares are so bad pain wise or weakness wise that I had to go on steroids and the steroids usually can get me out of a flare. Also, my injury, it's interesting that my blood pressure has been elevated. My heart rate's been elevated ever since my injury. Just about two or three months ago, I started passing out. So sometimes I could tell where I was getting a little dizzy, but about two months ago, I was sitting at our kitchen table and my kids just said I started speaking gibberish then keeled over and fell on the floor. Speaker 13: In the race to end a global pandemic, a novel genetic vaccine technology was fast tracked under the banner of Operation Warp Speed, and billions of doses were administered worldwide. Now the former director of the CDC and an adviser to Operation Warp Speed has raised concerns about what he sees as potential shortcomings of mRNA vaccines. Speaker 14: MRNA vaccine where I and I use this vaccine to help develop it. I don't use it anymore in my patients. Speaker 13: Redfield believes that while mRNA vaccines helped reduce severe illness, he no longer recommends the technology due to potential risks with spike protein production. Speaker 14: I turn your body into a factory, but I have no controls over that factory. I mean, you can make a lot, you can make a little. And you can make it for a week, you can make it for six months. I don't think it's unreasonable to go re examine the safety of what we know about these vaccines. Speaker 13: Regulators and the WHO state that COVID vaccines have saved millions of lives with minimal safety concerns. Speaker 3: This vaccine, the mRNA vaccine, has probably saved about three million lives. I think that was the greatest scientific or medical achievement in my lifetime. Speaker 13: At the same time, it's widely acknowledged that protection wanes. Speaker 1: The current vaccines are not infection blocking. When new variants come up, you lose protection, and they have very short duration. Every one of those things is fixable. Speaker 13: While the majority of the scientific community considers the COVID vaccines safe, thousands of doctors and scientists are calling for a halt to mRNA vaccines. For years, a growing number of prominent experts have been investigating what they believe could be serious potential harms linked to these vaccines. Speaker 10: So I'll see the next slide before I come back. It's the solution to get through the truth out to the public around these major issues, though. And, again, we've got good quality observational data showing increase in heart attacks and and cardiac arrest in people aged between 16 and 40, so younger people, which was associated with the vaccine and not with COVID. That's from Israel. Speaker 5: Having some of the brightest minds from around the world come together. Speaker 15: Get injured, and then you sue your Speaker 12: This is a group of highly competent professionals that are seeking to obtain answers. Speaker 0: You boss to Don Ron Hunt. Speaker 13: Robert Malone, one of the inventors of mRNA technology, voices his concerns about the safety of mRNA vaccines. Speaker 12: The evidence about the adverse events from the vaccines is unequivocal. It is absolutely overwhelming. These adverse events clearly include myocarditis and a number of other things, including in particular clotting disorders. But we're just still learning about many of the long term adverse events. Speaker 13: Robert Malone's website lists nearly 800 papers on mRNA vaccine side effects. Speaker 3: Robert Malone is a brilliant man. Was a brilliant researcher. He could reasonably have won the Nobel Prize, really. It was that good. The stuff that he did was that much of a breakthrough. Speaker 12: At that time I had a series of discoveries that led to nine issued patents which are the foundation technology for mRNA vaccines as well as DNA vaccination. No fences, no barn. This old barn that's falling down was here. Speaker 13: Before the pandemic, Robert Malone was highly regarded in the academic world and enjoyed a fulfilling life at his homestead with his wife Jill. Speaker 16: We don't sell our mature mares. They're kind of our family. This one right here, that's his great grandmother. She scored very high on inspection. Speaker 12: This is a technology that may have held promise at some point in time if the problems could have been solved. It may have been destroyed its positive potential by this crazy rush to deploy it globally before it was ready. Speaker 13: When Malone raised questions about the safety of COVID vaccines, his life was forever changed, and his concerns were categorically dismissed. These are highly credentialed people who are suffering from some kind of deep misunderstanding or delusion. Speaker 3: Those are the people I worry about because they're credentialed. Speaker 12: We now have a modern studio and a four camera Speaker 13: Now, Robert is on a mission, conducting countless interviews and giving lectures to educate the public about the potential dangers of COVID vaccines and the rapid deployment of new mRNA products. Speaker 12: There are over 200 different clinical trials currently planned for mRNA based technology, and over 40 trials are currently enrolling. Speaker 13: Could mRNA technology potentially be introduced into the food supply through the vaccination of dairy cattle? Speaker 12: The administration of these types of technologies in humans has demonstrated that they can be shed in breast milk in humans and so it's likely that they could be shed in milk from dairy cattle. Speaker 7: Science Speaker 8: that can't be questioned is propaganda. When we took an oath in medicine to first do no harm, where did that go? Speaker 13: Ryan Cole, a pathologist with expertise in virology and immunology. He believes that the harms of the COVID vaccines are significant and downplayed. Speaker 5: It's crazy to think that people that aren't doctors, aren't scientists, were pushing something that never worked. Speaker 14: This is not about freedom or personal choice. Speaker 5: And there were billions spread around and shared amongst each other, and now we have millions of people around the world that carry permanent harm for the rest of their lives who are now paralyzed, who now have neurodegenerative disease, who now have severe autoimmune diseases. People historically have this confidence in the concept of, oh, it's Speaker 8: just a Speaker 5: vaccine. Well, no, it's not. And then they want to mandate these on people. Well, we have this new technology, everybody needs to get it. Speaker 12: Getting everyone vaccinated. Speaker 10: It's very likely that the mRNA vaccines accelerate coronary artery disease. Now as a cardiologist, that's really, really bad Because what we've done is we have introduced into the population another risk factor for heart disease and heart attacks. That means we will see an increased prevalence of heart attacks and sudden cardiac death going on for years, and that's my biggest fear. Speaker 8: This paper by Baumeyer shows the spike protein staining in that salmon color is physically in the heart. We shouldn't have Wuhan spike protein in young boys hospitalized in Germany with myocarditis. As we sit here today, there's over 3,000 papers in the peer reviewed literature that describe COVID 19 vaccine injuries, disabilities, and deaths. Speaker 13: Peter McCullough is a widely published cardiologist whose extensive knowledge and expertise have established him as a leading authority in the field of cardiology. Speaker 8: Prior to the pandemic I had focused on the interface between heart and kidney disease and in that domain I was the most published person in the world in history and remain to that day. I've given grand rounds in every major institution in The United States, published extensively across all the major journals. I was the editor of two major journals. Speaker 13: Peter McCullough believes observational and case studies suggest a possible link between the vaccine and serious conditions. Speaker 8: Encephalitis, seizures, and then, dangerous intracranial hemorrhages, and strokes. Now, outside in the peripheral nervous system, papers have been written demonstrating the vaccines over time, particularly cumulative toxicity, cause a small fiber neuropathy, and they cause dysregulation of the sympathetic nervous system. We call this posterior orthostatic tachycardia syndrome or POTS. The COVID-nineteen vaccines cause myocarditis. They cause heart damage. Speaker 4: Heart attack deaths have become more common across all age groups. Speaker 13: Experts call for much more research into health issues that have risen during and after the pandemic, taking into account the effects of COVID, vaccines, and lockdowns. Speaker 1: Sudden death among healthy working age people worldwide is skyrocketing. Speaker 17: There has been an increased rise, a sharp rise in unexplained deaths during the pandemic deaths that are not listed as COVID related. Speaker 0: Cardiac arrest incidents are at the highest ever recorded in Victoria. Speaker 10: These Speaker 13: experts deliver a clear message: the Covid vaccines, especially those using mRNA technology, should be stopped immediately. They also urge a much greater focus and allocation of resources to investigate all safety signals. Speaker 2: I think I'm uniquely qualified to speak on what's been going on for the last years. I actually have degrees in applied mathematics, immunology, computational biology, biochemistry, and molecular biology. These things need to stop being pushed and given today. Not one more shot should be delivered. It's the constant same message that's not true. I'm referring to primarily the safe and effective message being still being put out today. These mRNA product specifically, those are the ones I know the most about, are neither. And so the main message is that the people who are injured, who haven't made the connection between, you know, why they're injured and why they're suffering. I want to provide them, you know, the most help. First of all, know that they're not alone. If they're being gaslit even by their own doctor, You know, there there are people out there who are establishing protocols to help the vaccine injured. Speaker 13: The post vaccination community is desperately seeking treatments and a supportive environment where they feel seen. Paul Merrick is recognized as one of the world's top specialists in pulmonary and critical care. Having authored over 500 peer reviewed publications, he is established as one of the most published physicians in his Speaker 11: field. Paul Speaker 13: Merrick and his team are working on solutions for what he believes is a health catastrophe following mass vaccination. Speaker 11: They were never safe nor effective. They harmed countless millions of people. It should never have happened, and it's it's it's a tragedy that it was allowed to happen. These so called vaccines, I think, represent the worst of COVID and the worst of this deceit, dishonesty that we've seen. And I think we provide part of the answer to to this terrible problem we're facing. Speaker 13: Experts critical of Covid vaccines point to biopsy findings, thousands of case reports and large studies which they believe reveal real harm. Health authorities and much of the scientific community find the claims unconvincing and point to thousands of studies as evidence that the vaccines are well researched and safe. They argue that safety monitoring and research indicate side effects are very rare, and they view case reports and biopsies as inconclusive for linking them to vaccination. The new FDA director is launching a national study into COVID-nineteen vaccine harms. Speaker 18: We have not gotten full elucidation of the risks of these mRNA vaccines. Hundreds of thousands of people have claimed that they've been vaccine injured. I take those concerns very seriously. Speaker 7: What is inside my arm? What's in my arm? What's in my arm, yo? Speaker 13: In this chapter, let's break down the science using visuals to show how the mRNA vaccine works and explore its potential links to clotting and heart damage. But first, let's recognize that messenger RNA isn't just a man made invention. In its natural form, it's a marvel within our bodies. Evolution has gifted life with the wonders of genetic coding, the blueprint of existence. In this grand symphony of life, messenger mRNA plays a vital part. The magnificent diversity of life stems from humble beginnings, evolving over billions of years to attain its marvelous complexity. The journey from primitive beings to complex creatures would not have been possible without the genetic blueprint called DNA and the related molecule RNA. DNA holds all the instructions to maintain the body. These instructions are then copied from DNA into smaller snippets called messenger RNA, which are the to do list for each cell. So you can think of DNA as the blueprint, and mRNA is the project manager, bringing plans to life. Speaker 19: We choose to go to the moon in this decade. Speaker 13: During the space race of the 1950s and 60s, genetics research saw rapid progress, including the discovery of messenger RNA in 1961. Today, scientists have figured out how to create a synthetic modified version of mRNA in the lab that is engineered to last longer and evade immune detection. Our cells mistake this lab made mRNA as their own, and our body starts to create proteins for therapeutics or vaccines. The modified mRNA vaccines are created on a computer in a lab, without using a real virus. These genetic vaccines only required the genetic sequence of the coronavirus. Speaker 20: We never had access to a physical virus to design the product. Speaker 13: In the early stages of the pandemic, Chinese scientists released the genetic code of the coronavirus, sparking a global race to develop a vaccine. Speaker 21: As soon as we get that sequence, let's plug it into mRNA. That's all I needed, was the sequence. Speaker 13: They used the genetic code provided by Chinese scientists as a backbone for their mRNA vaccine. The modified genetic code in the vaccine instructs our bodies to produce only a specific part of the coronavirus rather than the entire virus itself. Speaker 21: Vaccine platforms are using what's called the spike protein of the coronavirus. Speaker 13: The spike proteins are the tiny spikes on the surface of the virus. Once this mRNA code is injected into your body, it instructs your cells to make these coronavirus spikes. By creating these spikes in our body, our immune system should build immunity against this specific part of the virus. Speaker 8: The worst mistake of all would be to take messenger RNA and then have it code for a lethal protein that was engineered in a Chinese biosecurity lab. That was a disaster. Speaker 13: The mRNA technology is exceptionally complicated and unlike anything we have seen with standard vaccines. Speaker 8: When people received their first COVID nineteen vaccine, it was the first time their body received lipid nano Speaker 13: bubbles protect the modified mRNA from degrading and help it enter cells. Once inside, the mRNA instructs the cells to produce a genetically engineered version of the spike protein. Speaker 8: The lipid nanoparticles, when they attach to cells, then the lipid nanoparticles dump off their payload messenger RNA. The messenger RNA then is taken into the cytoplasm of the cell. It's read by ribosomes over and over and over again. The spike protein, which is a foreign protein, is expressed on surface of cells. Speaker 13: The injection of mRNA vaccines turns our bodies into spike protein manufacturing sites. With every dose, a substantial amount of these modified spike proteins are created inside your body. The scientific community has stated that the spike protein created by the vaccine is harmless. Concerns have been raised about its potential to cause harm. A Yale preprint detected spike protein up to seven zero nine days after vaccination in patients with post vaccination syndrome. Speaker 5: The code that they used is for the spike protein. Early on in the pandemic, we learned that the spike protein is the toxic part of this virus that causes clotting, that causes inflammation, that causes myocarditis, that causes brain fog. Speaker 8: The spike protein directly causes blood clotting and is found in the middle of large blood clots. Speaker 13: Researchers have concerns that the immune response triggered by mRNA vaccines could potentially lead to excessive attacks on our tissues and organs. Speaker 5: And any cell that makes this foreign protein now becomes a target of your own immune cells to attack as well. Speaker 12: Those cells will be attacked immunologically as if they're infected with the virus. Speaker 13: The immune system detects the presence of spikes and initiates the destruction of the infected cells. These cells become a target for our immune system to hunt and kill. Speaker 8: It immediately evokes an autoimmune reaction in each and every cell that is expressed. Speaker 13: Health officials have been cautious in acknowledging that these particles may have the potential to distribute beyond the injection site. If these particles enter the bloodstream, they may potentially increase risks. A widespread distribution could result in the production of spike protein in various organs. Speaker 5: Lipid nanoparticles go everywhere in the body. As in everywhere. Speaker 3: To the brain, to the bone marrow, to the liver, Speaker 5: to the spleen, most importantly to the reproductive organs, to the testes, to the ovaries. So lipid nanoparticles can't be controlled. Speaker 13: Most of the lipids should stay in the shoulder, and they are designed to efficiently enter the deltoid muscle cells. But they can also be taken up by other cells in the body. So not only can the cells in your deltoid muscle be turned into spike production sites, but also cells in your heart muscle and organs. Current leading theories of mRNA vaccine related cardiovascular problems include spike protein expression in tissues and molecular mimicry of the spike protein. The late pathologist Arne Burkhardt and his team examined over a 100 biopsies from individuals suspected of having suffered adverse reactions to vaccines, some of which were fatal. Speaker 22: And the destruction of the endothelium may be one of the major factors. Speaker 13: These biopsies provide clues about how the vaccine may contribute to damage to organs and tissues. Speaker 22: Our findings are so alarming that the vaccination should be stopped immediately and especially the vaccination of children. Speaker 13: When these tiny fat particles enter the bloodstream, they may be absorbed by the walls of blood vessels or the heart. If these tissues produce spike proteins, our immune system may attack these areas, causing potentially serious damage to the vessel walls or the heart. Speaker 22: We found spike protein in many organs and many tissues. Spike protein was in the endothelium and in the vessels, in the vessel Speaker 13: align with a growing body of biopsy and biodistribution studies, including one that used deep learning to track lipid nanoparticle distribution in animals. Speaker 12: It was actually known before it was deployed in humans, based on rodent models that these products went all over the body and yet they persisted to continue to deploy them. Speaker 13: Health agencies approved mRNA vaccines, knowing that lipid nanoparticles can spread to different organs in animal studies. They conclude that any spread of mRNA beyond the injection site is minimal and short lived and have not raised major concerns about the spike protein. Research cited by health agencies shows no conclusive evidence of significant harm in humans. Speaker 7: We never use experimental products in pregnant women. We never use it in children. In this situation, we've done both. And we don't know what's going to happen to these children long term after the shot. If you look at some of the studies, where does the vaccine, where does the spike protein like to go to? To women's ovaries? To men's testes? And how is it going to affect their future fertility, their ability to have children? The answer is we don't know. There is no long term safety data. Speaker 9: My doctor, while I was pregnant, said, I'm gonna give you the vaccine. I have another client. She's the baby's totally fine. The baby's immune to COVID. This is a really good thing. And I was like, I wanted to please my doctor. I love my doctor, you know? I respect doctors. And so I got home and I told my husband, know, I'm thinking about doing this. He's like, no, no, no, no, don't. Don't, don't, just don't. Let's wait, let's wait till after. I said, okay, okay. I regret it every single day that I walked into my local pharmacy to get that shot in my arm. But the news got me when they said, hey, you're gonna have to protect your children, and I'm a new mother, and well, what are you gonna do? I wanna protect my child. Speaker 21: And they're safe and they're highly effective. That these are safe and effective. Speaker 9: Those two words haunt me to to this day, and that's safe and effective, Which this vaccine was not safe for me and it was not effective. Safe and effective while there's neuropathy and pain throughout my whole body. I can't think straight. I have brain fog. I can't dance anymore. Speaker 13: Jessica's serious condition has put an indefinite pause on her career as a multi talented artist. Jessica Sutter rose to stardom as a key member of the Pussycat Dolls, one of the best selling girl groups of all time, with 55,000,000 records sold. Speaker 9: I've had the most incredible experiences in my career. After the COVID shot, I have not been able to dance again. And I don't know if I ever will dance again. Speaker 13: Following the mRNA vaccine, Jessica developed severe autoimmune like symptoms, leaving her in excruciating pain and relentless fatigue for over three years. Speaker 9: So about two days after the first shot, I woke up with the most excruciating muscle spasm in my right rib. It spread through my whole entire rib cage, burning, stabbing, the most awful intense pain that no pain reliever can take away. I had a stammer for a while where I couldn't put words together, and I had involuntary head jerks and leg jerks, overall fatigue, joint pain all throughout my whole body. And during this, I lost about 50 pounds in three months. I feel like my body is eating itself. I sit in front of you right now, I'm in so much pain, I could just cry. So life for me is just a painful existence every single day. Honest to God, I feel like I just turned 41 and I feel like I'm a 100. I never knew 41 would feel like a 100. And yeah, it's devastating. I don't want anyone to go through what I'm going through. I do not. I wouldn't wish this upon my worst enemy. And the fact that I did this to kids, I just, because I can't imagine this happening to a young child. Speaker 2: MRNA technology. It's still new and it seems like there are a lot of possibilities for where this could be used. Speaker 6: The lowest hanging fruit is other vaccines. Speaker 7: The mRNA vaccines, its uses are being expanded tremendously into other vaccines and then into animals, which terrifies me because we just don't know any long term data. Speaker 13: While these mRNA vaccines aren't meant to alter our genes, they do use our gene machinery. With the rise of mRNA products, bodies are becoming factories for drug production. These experts emphasize extreme caution to protect current and future generations from any potential health disasters. As we've seen with toxic substances in the past, such as lead, asbestos, and DDT. Speaker 3: Dusting with DDT was begun at once. Speaker 5: They're working on this technology, this lipid nanoparticle plus a gene sequence for so many other viruses and infectious diseases now. Speaker 23: By helping to create the vaccines that really rescued us from the coronavirus, I'm here with Stephane Vansel, who is the CEO of Moderna. What's next? Speaker 20: So what we're working on is a lot of vaccines, around 30 plus vaccines today. Speaker 21: The FDA has approved Moderna's RSV vaccine for people 60 and older. Speaker 8: To approve a new type of self amplifying mRNA vaccine. Speaker 5: And they want to do this, and they want people to think, see, we we used it during COVID. Wasn't it great that we were able to warp speed it? No. It's not great. Speaker 16: Now they've got 50 more racing trains coming down Speaker 5: the tracks because they think they have permission. Speaker 6: So it's such a success of mRNA technology. The mRNA technology is a very powerful technology. Throughout Speaker 13: the pandemic, world leaders championed the new mRNA vaccine platforms, expanding their use to other vaccines. Speaker 15: Indeed, mRNA vaccines will be central to the EU's preparedness plan for fighting COVID nineteen and other viruses. Speaker 20: This is a great moment for us, and it's a great moment for all the thousands of people working here. They feel very excited about your visit. Speaker 15: And this pioneering technology could be the backbone of our future vaccine portfolio. Speaker 24: Hello, everybody. Mister president, all Speaker 20: of us. Speaker 3: Thank you. Speaker 25: AI holds incredible promise for all of us. Design a vaccine for every individual person to vaccinate them against that cancer, and you can make that vaccine, the that mRNA vaccine. Speaker 2: It's a strand of mRNA, the code of life inside every cell of your body. Then it has the power to change everything. Moderna, this changes everything. Speaker 19: Are companies like Moderna? This is a revolutionary biotech firm that's creating a whole new class of medicines based on messenger RNA, the software of life. Well, it's it's almost science fiction, what you're up to. Speaker 20: It's like software. It's a software of life. I mean, we have 48 drugs today in development. Speaker 16: Forty eight? Speaker 20: Forty eight And there's 50 more in the labs cooking. Speaker 13: While Moderna's products are not designed to alter genes but to cure diseases and develop vaccines. It is also true that mRNA technology has made humanity more open to gene and cell therapies a view echoed by Stefan Ulrich, an executive at Bayer. Speaker 24: The mRNA vaccines are an example for that cell and gene therapy. I always like to say if we had surveyed two years ago in the public, would you be willing to take gene or cell therapy and inject it into your body? We would have probably had a ninety five percent refusal rate. I think this pandemic has also opened many people's eyes to to innovation. Many people's eyes to to innovation. Speaker 10: By hacking organisms, elites may gain the power to reengineer the future of life itself. This will be the greatest revolution in biology since the very beginning of life four billion years ago. Speaker 13: Toby, a 39 year old mother of two sons and wife to a wonderful husband, experienced a life changing turn after getting the mRNA vaccine. Speaker 26: It was very hard for my husband to watch me suffer the way I did, and my children didn't know what was going on. You know, I didn't know if I was gonna live till the next day, and I had to have these hard conversations with my children that I don't know if mommy's going to make it. Speaker 13: After the vaccine, she became bedridden with painful neurological symptoms, turning each moment into a horrific struggle. Could autoimmunity cause Toby's symptoms, where a dysregulated immune system attacks her nerves? Vaccines can dysregulate the immune system, triggering autoimmunity. The body attacks itself, potentially damaging nerves. Speaker 26: I started suffering with severe vertigo. I felt like there was electric raindrops dropping on my skin. I had burning sensations in my brain. I was having audible hallucinations, I was suffering from aura migraines, tremors, internal vibrations, excruciating leg pains, my veins were bulging and burning, I developed POTS, I had lost an extreme amount of weight. I have extreme joint pain, muscle atrophy, the list is endless. I was afraid to fall asleep at night because I didn't know if I was gonna wake up. Speaker 13: Over the course of sixty years of mRNA research, early studies failed to make mRNA work. Simply injecting mRNA caused dangerous immune reactions and was highly inefficient. Until Robert Malone took it to the next level. Robert Malone's team made major breakthroughs proving that mRNA could be used as a drug. By using lipids to protect the fragile mRNA, they successfully made it work in human cells. Yet, the toxicity of these lipids remained a decades long challenge. Speaker 12: Again and again and again those trials failed. The industry has been plagued with the problem that these formulations are toxic. Now there had been improvements in the technology or alterations at least since I had abandoned the field in the late nineteen nineties because of the inflammation and toxicity of the formulations. Speaker 20: Their discovery led to a monumental medical breakthrough. Year's Nobel Prize recognizes Speaker 13: Catalin Kaurico and Drew Weissman made a Nobel Prize worthy discovery: engineering mRNA to be nearly invisible to the immune system. Unmodified foreign mRNA is very fragile and potentially dangerous to use. This modified version of mRNA is more potent, durable, and less likely to cause harmful inflammation. Speaker 12: Carrico and Weissmann, and so they took the U out and put pseudouridine in there and produced a molecule. It's a kind of a modified synthetic thing. And that worked considerably better because the RNA doesn't degrade. It stays around for a long period of time and the pseudouridine appears to suppress some of the inflammation. Speaker 8: They intentionally made messenger RNA synthetic for Pfizer Moderna. This increased the efficiency to the maximum. Speaker 13: Using too much pseudouridine may cause errors in ribosome reading, leading to malfunctions. A research team at Cambridge University found that, with these vaccines, about 10% of the time, the cellular machinery produced faulty proteins instead of the intended spike protein. While the researchers did not observe any harm with these proteins and assured that the issue could be fixed, The bigger question is how this was missed and whether there are more things overlooked. This modified RNA should be cleared from our bodies within days, but more research is needed to understand why it sometimes lingers much longer in some individuals. Speaker 12: There were statements made that the RNA only stays in your body for a brief period of time. That's true for natural RNA, but this is not a natural RNA, this is synthetic product. The pharmaceutical industry and the governments misrepresented this to patients. Speaker 13: As recently as 2017, just three years before the pandemic, mRNA technology was still in the experimental phase, with challenges in toxicity, biodistribution, and very limited human testing. Speaker 10: So the RNA area, can you talk us through where we're at, how optimistic you are? Speaker 1: You know, there's early animal data that shows real promise. Speaker 13: In 2017, a STAT News investigation reported that Moderna's mRNA therapy for a rare disease failed in animal studies due to lipid particle toxicity. The company has since improved the safety of its technology. Since the nineties, mRNA technology has made remarkable progress, becoming much safer and more controlled, thanks to brilliant scientists and the decades long coordination of US scientific and military agencies. But for a global vaccination campaign, it had to be more than just an exciting technology in development. It had to be truly flawless. Speaker 12: The people working in the field believed that they had developed compounds and formulations that were not toxic, were not inflammatory, and would remain localized at the site of injection in the draining lymph nodes. And that became the storyline that all accepted. Speaker 11: Stay at home during this pandemic. Speaker 4: A global vaccination program without a vaccine that hasn't been fully developed yet. Speaker 21: You get the overwhelming majority of the country vaccinated. Speaker 13: MRNA vaccines took the spotlight as one of the leading candidates for a COVID vaccine. Speaker 3: Today, we're meeting with the pharmaceutical and biotechnology companies. Speaker 19: How can we make it faster? Speaker 20: We were able to go so fast because we were working for many years with the NIH and we had worked with a costarsis team. Speaker 13: The former CDC director Robert Redfield was surprised by the strong preference for mRNA vaccines over traditional proven technologies. Speaker 14: Debbie Birx and I were on the board and we voted for the protein vaccines to be included. Birx and I felt this is, you know, fifty year technology. Let's go with it. And part of the reason we didn't win is everyone didn't think it was sexy enough. Alright? The mRNA was new. It was sexy. There was a pretty heavy bias by other people in the room. Speaker 5: Fascinating that on the mRNA technologies, Moderna had never safely brought a product market ever before. Speaker 24: But that same company has never brought an approved vaccine to market. Speaker 4: It's never produced a commercial product before. Speaker 24: Drew Griffin explains why so many people are pinning their hopes on this unproven technology. Speaker 5: So why in the world were we allowing companies with no experience in the vaccine realms to produce a product to be used around the world? Borla, the CEO of Pfizer admitted, he said he went to a scientist and said, why are we using mRNA technology? We've only been researching this for two and a half years. And they just turned around and said to him, it's because it's what we're doing. Speaker 6: He came and suggested to me mRNA, and it was very counterintuitive, the decision. I told him, are you sure? If you do that, this is not going to be only the first COVID vaccine. That could be the first vaccine ever. And they felt strongly about it. And I had to place my trust on them and I did. Speaker 13: But was it too much of a leap to go from no approved mRNA vaccines to deploying them to billions? The COVID vaccine trials were critical for evaluating mRNA technology's potential concerns about toxicity and biodistribution. Biodistribution. Speaker 4: How do we know if these vaccines are working? Speaker 12: It takes about a decade, about ten years and well over a billion dollars, to bring a vaccine to market. But the decision was made that there was not sufficient time. What was done was to run very limited clinical trials of very short term duration. Speaker 21: There needs to be some compromise in some of the safety measures that would normally be expected. Speaker 13: They overlapped the studies and were allowed to submit earlier research data. Before the pandemic, the FDA sometimes treated mRNA vaccines as gene therapy products. But now they are recognized as genetic vaccines. Critics argue that by treating these vaccines as traditional vaccines rather than genetic vaccine platforms, regulators may have bypassed certain safety checks. Speaker 12: There was strong effort to deny that this was gene therapy technology because if it was acknowledged that it was gene therapy technology used for vaccination purposes, then a whole different set of regulatory tests would have had to been performed. Speaker 13: Regulatory agencies and public health experts declare that mRNA vaccines underwent rigorous safety and efficacy evaluations both before and after approval, with no critical steps bypassed. They emphasize that these vaccines have saved millions of lives with minimal harm. And ongoing safety monitoring shows no significant risks. Speaker 3: This vaccine, the mRNA vaccine, has probably saved about three million lives. Speaker 13: The former CDC director is skeptical about mRNA technology's future in vaccines but sees promise in therapeutics, including for rare diseases. Speaker 14: The mRNA technology will not be used in vaccines. Okay. Let's fast forward three years. But I do think the mRNA technology will be used in therapeutics. Speaker 13: After spending a lot of time and money on treatments, Toby and her husband face financial ruin. Speaker 26: My injury has cost us over $70,000 and I don't even know if I can fully heal or, you know, it's definitely put me in the right direction, but it's landed us in financial ruins and to where our credit's been ruined. We had to take out major loans, and now we're filing for bankruptcy. So it's completely devastated us. Speaker 7: If you have an adverse event or your child has an adverse event, you are on your own. From a compensation standpoint, you're literally host. The regulatory agencies and the pharma companies are completely immune to prosecution. So we can't sue them and try to get financial recourse after our injuries. And it's wrong. It's evil. These people are abandoned. Many people are devastated from the standpoint of their finances, they're physically devastated, and they're often emotionally devastated. Speaker 13: Paul Merrick and his team at the Independent Medical Alliance are tirelessly researching and developing treatment protocols for long term COVID and COVID vaccine injuries. Clearly Speaker 11: there are people out there suffering and they're often desperate. The focus of this conference is on spike related disease which is mainly vaccine injured. And the people here really are their mission is to help those that are less fortunate than those that have suffered. Speaker 8: Alright. Spike Protein. Obviously, conferences arouse Spike Protein. Speaker 7: I also wanna thank Brea Dressen, who's my co chair of RAC nineteen. This is a time when we all can share our individual experiences, with regards to COVID and those injured by the COVID shots and be able to collaborate and try to hopefully move forward to develop better diagnostics and treatments. Speaker 9: It's really hard to understand this unless you're living it. This experience has been the most isolating experience of my life. So I I can't wait to be around my fellow vaxxed injured. But also the doctors at the frontline COVID critical care because they have been tremendous. Doctor. Marek has been an angel within the community. Speaker 11: The team we have are truly outstanding people who absolutely committed to what we're doing. It's like a family, know. These are my family. I think our goal is to educate, to empower people. Speaker 18: Are you gonna succeed in this goal? Speaker 11: Of course. I mean, there's absolutely no way we can fail. I think, you know, we've come this far. You can just see the affection and kindness of the people that are here today. This is part of a community, and, you know, I hope this community will grow bigger and bigger to the extent that we will be able to persuade other people to see the truth and to see the light because that's what we stand for. Speaker 5: And the truth should prevail at all costs. And the sacrifices we continue to make to get the truth out there will continue. And so I would encourage people wake up. Speaker 2: The truth is the most sensational thing that you could ever report. It's always going to be what people want to hear. Speaker 12: We must continue to speak our truth. Speaker 7: We fight evil through love. What we're about at React nineteen is really spreading love and caring for our fellow human beings. And I really think in the end, that's the story that will defeat the evil that we're up against. Speaker 13: If this film matters to you, please share it and help start the conversation. For official guidance, visit the website of your regulatory agency and consult with your healthcare provider. Communities like REACT nineteen and the Independent Medical Alliance provide connection and support for individuals navigating post vaccine health challenges.

@Humanspective - Humanspective

@ScienceboyJack @InsidemRNAFilm They did a great job covering this up from the main media channels

@Humanspective - Humanspective

@maxamonious @jathorpmfm @InsidemRNAFilm Ah yes I remember Aaron Siri handling this case

@Humanspective - Humanspective

@paulhoffman007 @InsidemRNAFilm @Johnincarlisle I try to always. He’s mentioned and I’ll add the video link in later to help with reach 🙏

Humanspective
Posted - September 9, 2025 at 8:29 PM
Saved - September 10, 2025 at 6:53 PM
reSee.it AI Summary
I found it stunning to see Dr. Jake Scott go silent when Senator Ron Johnson questioned him about mRNA vaccines. Johnson had to explain how the vaccines work, revealing that Scott seemed unclear about the technology. Despite Scott's belief that the vaccine primarily stays at the injection site, Pfizer's own biodistribution data shows it travels throughout the body, even crossing the blood-brain barrier and reaching the adrenal glands and ovaries. This situation felt quite embarrassing.

@Humanspective - Humanspective

This is stunning. Dr Jake Scott goes dead silent. [@SenRonJohnson]: "Do you not know?" Senator Ron Johnson has to walk Dr Jake Scott through how mRNA vaccines work, because he doesn't have a clear understanding of the mechanism's of the technology and still thinks it "primarily" stays at the injection site 🤯 Pfizer's very own bio distribution data freely available, shows it goes EVERYWHERE, including crossing the blood brain barrier and going to the adrenal glands and ovaries. This is embarrassing

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"it's modified mRNA, and it's designed not to degrade. And there are studies that show it sticks around the body." "The lipid nanoparticle. Do you realize that it was designed to permeate difficult to permeate barriers? Like the blood brain, like placenta barrier." "Japanese FOIA of the study that was conducted about distribution where in rats, biodistributed all over the body, accumulated in the adrenal glands, in the ovaries." "it's messenger RNA, modified RNA, this encapsulated lipid nanoparticle that distributes all over the body." "when it attaches to a cell, it unloads its mRNA into the cell and turns the cell into a manufacturing cell of a protein that is toxic to it." "Are you aware of that? I mean, just yeah. Yes or no? I mean, do you know that or not? Because I talk to a lot of doctors, don't have a clue."
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Speaker 0: Mr. Scott, how much do you know about the mRNA technology? A fair amount. So it is the mRNA that's encapsulating the lipid nanoparticles, is that true mRNA? Is that true mRNA? I mean, true true mRNA, your master RNA degrades very rapidly in the body. Mhmm. Correct? Correct. So the mRNA in the injection, is is it true mRNA? Does it degrade rapidly in the body? Do you not know? I do know. Yes. It it it does. But It does. No. It does not. It's modify it's modified mRNA, and it's designed not to degrade. And there are studies that show it sticks around the body. We don't know how long. The lipid nanoparticle. Do you realize that it was designed to permeate difficult to permeate barriers? Like the blood brain, like placenta barrier. Did you know that? Did you believe when Fauci told us that the mRNA shot would stay in the arm? Did you believe that? It's a simple yes or no. I mean, did you believe do you do you believe the the code injection stayed in everybody's arm? Do we believe that's what happened? Primarily. You you think so, Were you aware of the Japanese FOIA of the study that was conducted about distribution where in rats, biodistributed all over the body, accumulated in the adrenal glands, in the ovaries? They they because the lipid nanoparticles designed to permeate difficult to permeate barriers, They knew, the designers knew, and they did a study they would biodistribute all over the body. But our CDC, Anthony Fauci said it was gonna stick in the arm. Now do you know what the mRNA does? It's it's not it's not a traditional vaccine, is it? Do do you realize that? It's just not an attenuated or a dead virus. It's it's messenger RNA, modified RNA, this encapsulated lipid nanoparticle that distributes all over the body. And when it attaches to a cell, it unloads its mRNA into the cell and turns the cell into a manufacturing cell of a protein that is toxic to it. Do do you realize that? Are you aware of that? I mean, just yeah. Yes or no? I mean, do you know that or not? Because I talk to a lot of doctors, don't have a clue.
Humanspective
Posted - September 2, 2025 at 7:50 AM
Saved - September 2, 2025 at 2:35 PM
reSee.it AI Summary
I believe we might be facing the largest carcinogenic impact on humanity. There's concern that Pfizer misled the FDA about SV40 sequences in their vaccine and then rapidly acquired cancer companies like Seagen for $43 billion. Genomics expert Kevin McKernan shares this alarming perspective.

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“This may be the largest carcinogenic hit ever, to the human population" Wait till Trump finds out Pfizer did a "Bait and switch", injecting the World with "Process 2", containing SV40 sequences. Pfizer obscured SV40 sequences from the FDA and then "they quickly went out and acquired cancer companies", including Seagen for $43 billion. Genomics Expert Kevin McKernan: "This may be the largest carcinogenic hit ever, to the human population [and] this has gone absolutely off the rails"

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This is not conspiracy theory. Published in the BMJ by Retzaf Levy, it describes altering the vaccine trial process. The EMA asked for another trial of 250 people after the change, but data was never delivered. This bait and switch is a key reason trial data seems irrelevant to field results. Pfizer had the data early and rapidly acquired cancer companies: $43,000,000,000 for C Gen and $2,260,000,000 for Trillium Therapeutics. Trillium focused on blood cancers with a cd one forty seven marker. Pfizer vaccines on the market are not the same formulation as what was tested; this is a fraud. Cancer post vaccination is reported, including neoplasms at the injection site and DNA contamination found in studies.
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Speaker 0: This is not conspiracy theory. This has been published in the BMJ by Retzaf Levy and they go through this process one where they where they ran these vaccines in the trial and how they changed that when they decided to go and inject the rest of the world. This is traditionally a mortal sin in vaccine manufacturing or in any sort of biologic manufacturing. The process is the product. You change the process, you have to go through trials again. And the EMA even asked them to do that, although they failed to. They asked for another trial of 250 people once they changed the process and that data was never delivered. So this bait and switch is very important for you to understand why the trial data is of absolute zero consequence to what we're actually seeing in the field. Those numbers are a caricature of what they're actually doing with these injections. They know something. Pfizer very early on they had the data on this from their trial, they knew this was going to happen and they quickly went out and acquired cancer companies. They put $43,000,000,000 into the acquisition of C Gen and they put $2,260,000,000 to acquire Trillium Therapeutics. Trillium was focused on blood cancers that have a c d one forty seven marker on them. Okay? That is one of the markers that is known to be involved in COVID. So, they have a very interesting window on those malignancies, and, they're buying up the cancer companies that are probably gonna play the biggest role in benefiting from the mess that they've created. So, in summary, the Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials. This is a big bait and switch and it's a fraud. So you can't believe anything they're saying about the vaccine efficiency, which we have seen even those numbers decay over time. This is probably why. They're not really what they trialed. They gave you something different. There is significant DNA contamination that's found. Like, 10 out of 11 studies have found this, and the ones that haven't found it have some financial conflicts. So, I think the consensus is out. 10 out of 10 out of 10 of the real studies, are finding this. Several are through peer review, which have not been easy to get through peer review. The peer review journals do not like these papers. They get they get beat beat around in peer review for months to years, but they're they're making their way out now. There is also significant DNA contamination now found in five peer reviewed studies that were not looking at this. They were looking at people's blood and tissue and it was accidentally in there. Other people had to go sleuth it out. We've got cancer on the rise and there's several papers that report cancer post vaccination. Like like, right at right at the site of injection, they'll see neoplasms. Alright? There is there's something going on here. This can't be ignored saying it's a coincidence anymore. Now this is these are liability free and they're often mandated. Okay? This may be the largest carcinogenic hit ever to the human population. And we have these on childhood schedules. We're giving these to pregnant women. This has gone absolutely off the rails.
Humanspective
Posted - September 1, 2025 at 9:08 AM
Saved - September 1, 2025 at 4:40 PM
reSee.it AI Summary
I believe there's a deceptive tactic used by Big Pharma and the government regarding mRNA vaccines. They categorize any negative effects experienced by vaccinated individuals into the "unvaccinated" group, which obscures vaccine-related injuries and deaths. Official data only recognizes someone as vaccinated two weeks after the second shot, meaning deaths in the initial six weeks are misattributed to the unvaccinated. This statistical manipulation isn't limited to mRNA vaccines; similar tricks are applied to traditional vaccines as well.

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Robert F Kennedy: "It's a trick". One of the "little tricks" Big Pharma worked together with the government on. Put any negative effects people had from mRNA 'vaccines' into the "unvaccinated" group. This hid vaccine injuries, deaths and gave the appearance the unvaccinated were getting sick and dying more. "The offical data do not not count you as vaccinated until 2 weeks after the second shot" "The deaths that happened during that first 6 weeks are attributed to unvaccinated people [so] it's a trick, it's statistical trick" They do this "little trick" on other traditional vaccines as well.

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The vaccine is ineffective for the first six weeks after the first shot. I'm assuming a a two shot, you know, a two dose vaccine like Pfizer or Moderna. And that during that period, the COVID infection rate goes up and the death rate goes up. And the the data the official data do not count you as vaccinated until two weeks after the second shot. So the deaths that happened during that first six weeks are attributed to unvaccinated to the unvaccinated group, which is not which is it's a it's a trick. It's a statistical trick. Then the vaccine appears to provide immunity and good immunity during the first month or two months, and then a precipitous decline, a waning that happens very, very quickly and very precipitously so that by the seventh month, it has lapsed into negative efficacy.
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Speaker 0: The vaccine is ineffective for the first six weeks after the first shot. I'm assuming a a two shot, you know, a two dose vaccine like Pfizer or Moderna. And that during that period, the COVID infection rate goes up and the death rate goes up. And the the data the official data do not count you as vaccinated until two weeks after the second shot. So the deaths that happened during that first six weeks are attributed to unvaccinated to the unvaccinated group, which is not which is it's a it's a trick. It's a statistical trick. Then the vaccine appears to provide immunity and good immunity during the first month or two months, and then a precipitous decline, a waning that happens very, very quickly and very precipitously so that by the seventh month, it has lapsed into negative efficacy. And what that means is that after seven months, if you had that vaccine, you are more likely to get COVID and somebody who has never been vaccinated. And this data is holding up across every country in the world.
Humanspective
Posted - August 16, 2025 at 12:39 AM
Saved - August 16, 2025 at 8:02 AM
reSee.it AI Summary
After experiencing vaccine-related injuries, I discovered a supplement that effectively stopped my spike protein-induced tremors the very next day. In my discussion with Steve Kirsch, I explained the research and methodology behind augmented NAC. I also shared that tests are now available in Italy, Germany, and America to detect whether someone has COVID spike or mRNA spike proteins in their system. This could lead to new avenues for health treatments, as well as potential litigation and accountability regarding the "shedding" phenomenon affecting unvaccinated individuals.

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After becoming vaccine injured, she found a supplement that stopped her spike protein induced tremors, the next day. Tina Peers explains to Steve Kirsch the research and scientific methodology behind augmented NAC. Stunningly she also details, that tests are currently available in Italy, Germany and America, which can pick up whether someone has covid spike or mRNA spike in their system. Do you know what that means? Obviously, people have access to tests that verify what treatments might help....but those same tests also show at the molecular level whether unvaccinated people have been unknowing recipients of the mRNA products through the "shedding" phenomena. Could this open up entirely new health, litigation and accountability pathways?

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Italian scientists at Zero Spike developed augmented NAC and tested hundreds of chemicals to break the spike protein into pieces the body can clear. They found that NAC could do it a little bit—maybe 12% of the spike—but it would refold and didn’t get rid of it. A quantum physicist created coherence among NAC molecules so they were identical; when mixed with the spike protein it cuts up the spike into lots of bits and broke up 99.8% of it, enabling clearance through the liver and kidneys. The speaker started taking it—one capsule three times a day—and the next morning the tremor had gone. German labs measure spike protein in lymphocytes, exosomes, and serum; a urine spike test in Italy and America shows metabolites and whether spike comes from vaccine, infection, or gut. They say hundreds of thousands helped; a woman’s fits stopped within two days of starting augmented NAC.
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Speaker 0: And then I came across in the April 2023, I came across the, augmented NAC, which is very, very special NAC. So they had, the Italian scientists, at Zero Spike who had developed this. They checked, they tested hundreds of different chemicals to see what could actually break the spike protein up into various pieces that the body could then clear out. And they found that NAC could do it a little bit. And if you had a spike protein, maybe 12% of it could be broken up by the NAC. But then it would refold. It didn't help. It didn't get rid of it. Right. And they're working with a quantum physicist. And the quantum physicist said, okay, if some of it has that ability, some of those molecules are doing it, but not enough of them are doing it. And yet all the molecules are the same, but subatomically they're not, they're slightly different. So they made a machine to cause to create what they call coherence amongst the, atoms, molecules of the NAC, so that they were all absolutely identical and uniform. And when they mix those with the spike protein, it cuts up the spike protein into lots of bits and broke up 99.8% of it. And then your body can clear it through the liver and the kidneys, Which was Okay. Go Speaker 1: ahead. Go ahead. Speaker 0: Yeah. Which is why I started taking it. When I found out about the Augmentinacea, I couldn't wait to get my hands on it because I was still with this tremor remember, and the rosacea and all the rest of it and the eczema on the back of my head and everything and the narcolepsy and the peripheral epilepsy. So I was desperate to get ahold of some and I managed to get it. And I took one three times a day which was the recommendation. The next morning I woke up and the tremor had gone. Absolutely amazing. The tremor had gone. Speaker 1: Okay, so how do you measure your what's the best way for somebody to measure what their spike protein load is today? So that they see and actually, you know, does this work? And is the three times a day necessary or can you do it with one times a day? And because I think I remember buying a few bottles of Augmented NAC a while ago and it was pretty darn expensive. I mean, was like what, maybe $60 a bottle or maybe even more than that. Speaker 0: It's about 60. Yeah, it's about that. A bottle of 90. Yeah. So, it's a month's supply, isn't it? If you take one, three times a day. So, can have, there are some labs in Germany that will measure the spike protein in the lymphocytes in the exosomes and in the serum. And it's not super expensive to have that done. And then people are taking the augmented NAC and they are seeing it clear. And also they have got a urine test, urine spike test which is available in Italy and in America now where they can see those metabolites if you like those pieces of the spike protein in the urine and it can be measured. And they can also tell whether the spike protein pieces have come from the vaccine or from the infection or from the gut, which is interesting. From from the spike protein in the gut. So, they can tell that and and they have helped hundreds of thousands of families and people to clear this. And as I say, the lady I saw who had that awful uncontrollable fitting within two days of starting this the augmented NAC, her fits have completely stopped.
Humanspective
Posted - August 12, 2025 at 2:31 AM
Saved - August 12, 2025 at 5:56 AM
reSee.it AI Summary
I came across a striking correlation regarding excess deaths peaking at specific times after vaccination, which is set to be scientifically validated. Professor Robert Clancy shared insights from Japan, revealing that all excess deaths occurred in the vaccinated population, with peak mortality observed 100 days post-vaccination for over 20 million individuals. Additionally, a statistician in Australia noted that mortality rates increased approximately three months after each vaccination booster campaign, aligning perfectly with the findings from Japan.

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🚨This is a stunning correlation. Excess deaths peaking at certain timepoints after vaccination, soon to be scientifically replicated. NEW from Professor Robert Clancy, who explains that: "In Japan they were able to [show] that ALL the excess deaths were in the vaccinated group", for over 20 million Japanese people [and] "They found that the peak mortality, was 100 days after vaccination" "Last week a very smart statistician in Australia [told me that] about 3 x months after every [vaccination booster campaign] mortality went up. And that's EXACTLY the timing the Japanese found"

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Andrew Madry, a physicist-statistician with a business background, became an expert in all-cause death and wrote a book, examining all-cause death coinciding with a vaccine. He points to a chart where "pink, which is something like forty thousand people in Australia, Australia alone, dying over and above the expected trajectory." A page is cited as "no COVID excess deaths, COVID deaths." A Japan study of about 20–22 million people found "all the excess deaths were in the vaccinated group, that the non vaccinated group had none." An Australian statistician's paper states that "about three months after every splurge of a vaccine booster, mortality went up," with "the peak mortality was a hundred days after" vaccination. The Australian government inquiry into excess deaths said "there's nothing in it. That's all due to COVID."
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Speaker 0: What he's done, which no one else has done, is that, it's, it's actually written by a chap called Andrew Madry, who was a physicist statistician, who had nothing to do with health so much, but had his own business, and started sort of taking an interest in this and couldn't believe what's going on. And he'd become an extraordinary expert in all cause death. Yeah. Well, show the one with the pink and the blue is the queen. No one else is as far as I can see, has actually done that, where he's actually looked at all cause death coinciding just with a vaccine. And you'll see that in there, I'm trying to remember which is the the the red is the Yeah. Speaker 1: It's it's it's no no COVID it's page one five five, Robert. No no COVID excess deaths, COVID deaths. Speaker 0: Worked out. Speaker 1: What vaccine doses. Speaker 0: Lou, he says, okay, this could be increased death due to the vaccine, but there's no way that you can say that the pink, which is something like forty thousand people in Australia, Australia alone, dying over and above the expected trajectory. Yeah. And what I find fascinating with the book is that since it's come out, and, of course, this was all finished a few months back, is coming out that supports so many of the ideas, not because well, I think that the ideas were very good, but more evidence. And there's been I'm not sure if you've seen. It's just coming out of Japan at the moment. It's only semi in print. But in Japan, they were able to take 20,000,000 people and work out who had the vaccine and who didn't. And they were able to show highly significant that all the excess deaths were in the vaccinated group, that the non vaccinated group had none. Now, all right, that's just one study in Japan. But last week Speaker 1: Well, a study of 20,000,000 people. Speaker 0: 22,000,000 people. Yeah. Speaker 1: Yeah. It's not a bad study. Last week, Speaker 0: a very smart statistician in Australia sent me his paper that he's just publishing, so I won't mention all the details. But what he was able to show was that about three months after every splurge of a vaccine booster, mortality went up. And that's exactly the the timing the Japanese found. They found that the peak mortality was a hundred days after the after vaccine vaccination, whatever the vaccine whatever it had. Then the the the so there's this amazing consistency now that's starting to come, remembering that the Australian government had an inquiry into excess deaths and said there's nothing in it. That's all due to COVID. I mean, I tell you.
Humanspective
Posted - July 3, 2025 at 5:02 AM
Saved - August 8, 2025 at 12:35 PM
reSee.it AI Summary
I express concern about the widespread impact of mRNA technology on billions of people, fearing it could lead to significant harm. Professor Sucharit Bhakdi shares my pessimism, stating he believes the modified RNA vaccines have already achieved their intended effects. He emphasizes the urgent need to halt the mRNA infrastructure before it becomes a standard for all vaccines globally.

@Humanspective - Humanspective

"Billions of people who's brains [are] altered" "This mRNA crime [is] going to destroy us [they] are rolling out this RNA all over the place and people don't realise" Buddhist Professor Sucharit Bhakdi: "I’m going to be very honest with you. I am no longer optimistic, and the reason is simple. I’m afraid that these RNA vaccines—modified RNA vaccines, whatever you want to call them—have already done thier job" He says now is the time to stop the mRNA infrastructure, before they succeed in installing them for all vaccines worldwide.

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The speaker expresses a loss of optimism, fearing that mRNA vaccines have already achieved an unintended goal: systemic vasculitis. This condition, attacking vessels throughout the body, leads to the destruction of brain cells. The speaker claims we are seeing billions of people whose brains are not functioning correctly, resulting in diminished willpower and intelligence. The speaker believes the only solution is to stop the "modRNA crime," which they claim is destroying us, but people don't realize what is happening as these vaccines are rolled out.
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Speaker 0: Now I'm going to be very honest with you. I am no longer, optimistic anymore, and the reason is very simple. Mhmm. The reason is because I'm afraid that these RNA vaccines, MOD RNA vaccines, whatever you want to call them, have already done their job. And what their job has been, and this is incredible, was not even known to the planners because they didn't realize that what they were doing. But it is what I said years ago, that the vessels throughout the body are going to be attacked from top to toe. This is something that never happens in any disease. Okay? Systemic meaning the brain, the heart, the liver, everything can be attacked, the vessels. And the trouble is that it's turned out to be true. So this systemic vasculitis leads to destruction of brain cells, obviously, and that is what we are now experiencing. We are seeing, I'm afraid to say billions of people whose brains are not working anymore, not as they should be. They are altered and they do not have they don't have the willpower anymore. They do not have the intelligence anymore to move things. And so the only chance we have is to stop this modRNA crime, because this crime is going to destroy us. The trouble is that they're rolling out these, RNA vaccines all over the place, and people don't realize this is being done.
Humanspective
Posted - August 7, 2025 at 3:01 AM
Saved - August 7, 2025 at 8:40 AM

@Humanspective - Humanspective

Dr. Ryan Cole: mRNA injections not for "Human use". As $500 million of mRNA infrastructure is terminated from HHS, @drcole12 mirrors Jospeh A. Ladapo's statement, who said recently: "these products should not be used in any human beings" https://t.co/vjEAIPeqRv

Video Transcript AI Summary
For those familiar with the technology, it was clear from the start that certain projects were a "horrible idea," a sentiment now echoed by HHS Secretary Kennedy, who states they are not effective. The de-investment in 22 projects is just the beginning and will reunify the MAHA and MAGA movements. This action will benefit public health by preventing the implementation of this technology in people's bodies. While some funding, contracts, and research opportunities remain, the de-investment sends a clear message: this technology is not for human use.
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Speaker 0: It was enticing, shall we say, to many people that don't understand the technology. For those of us behind the scenes that do that detailed basic science research, we knew from day one this was a horrible idea, which it's proven to be. And unambiguously, HHS has stated through Secretary Kennedy, look, these are not effective, and we know that now. And so this de investment in these 22 projects, it's just the beginning. And so I think this shores up the strength of the MAHA movement, the division that we've seen between MAHA and MAGA, this is reunifying. This is true action. This is actually going to be beneficial to the health of many that won't get this type of technology put into their bodies going forward. So it's not an ultimate everything's gone. There's still some funding and contracts that will be carried out and finished. There's still research opportunities in this realm. However, it's a clear and unambiguous statement that this is not for human use.
Humanspective
Posted - August 5, 2025 at 2:59 AM
Saved - August 5, 2025 at 11:22 AM
reSee.it AI Summary
I shared that a significant peer-reviewed study, the largest autopsy series globally, analyzed data from 325 individuals who died after mRNA vaccination. Dr. Peter McCullough noted that in 73.9% of these cases, the vaccine was determined to be the cause of death. William Makis MD emphasized that more evidence is emerging daily regarding the harms of COVID vaccines, urging politicians to proactively address this growing body of evidence.

@Humanspective - Humanspective

"There's going to be a tsunami of evidence". "The Largest Autopsy series in the World", with data from 325 people who died after mRNA injection, is "now a peer reviewed paper". Dr Peter McCullough: "Of these cases that came in for autopsy after vaccination [it] was determined that the vaccine was the cause of death [for 73.9% of the individuals]". William Makis MD: "there's more evidence coming in every single day [and] there's going to be a Tsunami of evidence, of the harm of these covid 'vaccines' [so politicians should] get ahead of this".

Video Transcript AI Summary
The speakers discuss a study of 325 autopsies of individuals who died shortly after receiving a COVID-19 vaccine. According to the speakers, this is the largest autopsy series of its kind. A rigorous review of the autopsies allegedly found that the vaccine caused or contributed to approximately 74% of the sudden deaths. This study is claimed to be a peer-reviewed paper that is going to be published. One speaker states that they are the senior author of this study. The speakers anticipate a "tsunami of evidence" regarding the harm caused by COVID-19 vaccines in children, pregnant women, and adults. They urge politicians to acknowledge and address this issue.
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Speaker 0: The largest autopsy series in the world. 325 autopsies of COVID vaccinated people who drop dead a few hours or a few days or a few weeks after taking the COVID nineteen vaccine. We did a rigorous review of these autopsy, and we found that about seventy four percent of the cases of sudden death were caused or contributed to by the vaccine. That is now a peer reviewed paper that's going to be published. Speaker 1: So in the largest autopsy series published to date, I know because I'm the senior author. Of all the death we deaths we examined, and we we re reviewed them, we had an adjudication committee, we had ways of arbitration deciding on did the vaccine cause death. The answer is, of these cases that came in for autopsy after vaccination, seventy three point nine percent of individuals, it was determined that the vaccine was the cause of death. First off, there's Holsher and colleagues who's sitting right behind me. Speaker 0: And the reason I'm telling you that is that there is more evidence coming every single day, and it's not a little bit of evidence. It's not a case report here that they're gonna dismiss or case report there or a paper that the Lancet is going to take down and say, don't look at this autopsy series, and we'll just bury it and make sure it never sees the light of day. There's going to be a tsunami of evidence of the harm of these COVID nineteen vaccines, whether it's harming children, pregnant women, adults. And my message to the politicians is get ahead of this.
Humanspective
Posted - August 3, 2025 at 7:58 AM
Saved - August 4, 2025 at 9:40 PM
reSee.it AI Summary
I questioned what the lie was. Robert F. Kennedy announced a full ban on mercury-containing vaccines and urged the WHO and GAVI to stop injecting mercury into over 100 million babies in developing countries each year. This clip highlights the crucial scientific study behind it.

@Humanspective - Humanspective

Joe Rogan: "What was the lie?". Robert F Kennedy just announced a full ban on mercury containing Vaccines whilst urging "The World Health Organization and GAVI, to stop their programs of injecting mercury into more then 100 million black and brown babies in developing countries annually". Why? This clip explains the one scientific study you need to know.

Video Transcript AI Summary
The speaker recounts an interaction with an industry insider who claimed there's "good" and "bad" mercury to justify mercury in vaccines despite warnings against tuna consumption for pregnant women due to mercury content. The speaker knew this was false, as there's no such thing as "good" mercury. NIH admitted mercury serves as an adjuvant in dead virus vaccines to amplify immune response. In 1932, Eli Lilly claimed ethylmercury in vaccines is quickly excreted. A 2002/2003 study by CDC scientist Picchiero seemed to support this, showing mercury from vaccines disappeared from children's blood faster than mercury from tuna. However, scientist Boyd Haley questioned where the mercury went. A study by Thomas Burbacher with monkeys revealed ethylmercury from vaccines quickly left the blood but accumulated in the brain, causing inflammation. Confronting Offit about this, the speaker was told the mercury was excreted quickly based on the Picchierro study, but when confronted with the Burbacher study, Offit cited a "mosaic of studies" he never provided.
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Speaker 0: Oh, it was weird to me that the the top regulators in the country were telling me, go talk to somebody who's an industry insider because we don't understand the science. And when I talked to him, I caught him in a lie, And both of us knew that he was lying and that and that both of us recognized that that he was lying. And at that point, I was What was the lie? Well, I asked him this question. I said, why is it that CDC and and every state regulator recommends that that pregnant women do not eat tuna fish to avoid the mercury, but that CDC is recommending mercury containing flu shots with huge bolus doses of mercury. I mean, massive doses to pregnant women in every trimester of pregnancy. And he said, well, Bobby, there are there's two kinds of mercury. There's a good mercury, and there's a bad mercury. And the minute he said and I knew there's a different kind of mercury in the vaccines. It's it's ethylmercury in the vaccines and methylmercury in the fish. But I know a lot of by the end, you can imagine, I know a lot about mercury. I've been suing people. When you sue somebody on you get a PhD in that. You know more than anybody in the world. You have to or you're not gonna win your lawsuit. So I knew a lot about mercury, and I knew that his argument was not with me, but it was with the periodic tables because there's no such thing as a good mercury. What NIH admitted to me in 2016, the real reason was there as an adjuvant. An adjuvant is a a toxic material that they add to dead virus vaccines to amplify the, the immune response. But so the regulators expressed a preference for dead virus vaccines. A dead virus vaccine, however, will not produce a durable or robust immune response enough to get a license. The way you get a license for a vaccine is showing that you got an antibody response for a certain amount of time and that it's a strong antibody response, but the dead virus vaccine won't produce that. A factionologist figured out that if you add something horrendously toxic to the vaccine, that your body confuses that toxic product. You add it with the dead antigen, which is the viral particle. The your body confuses that toxin with the viral particle and gets frightened and mounts this huge humongous immune response. The next time it sees that virus, the the the immune response is there. So they at that point, vaccinologists went around searching around the world to find the most horrendously toxic materials to add to vaccines. And there's a mantra in vaccinology that the more toxic the the adjuvant, the more robust the immune response. And so that's why toxicologists and vaccinologists don't get along with each other. Because the toxicologists would say to the vaccinologists, well, I understand it gave you your immune response, but then what is the fate of that in your body? Where is it going? Is it being excreted? Is it being lodged in the brain? Is it penetrating the blood brain barrier? So when it was added in 1932, the industry said Eli Lilly said, well, the reason because everybody was saying, how can you put mercury into a child? Who would do that? And they said, well, it's a different kind of mercury. It's ethamercury, and the ethamercury is excreted very quickly, so it won't stay in your body. They had no science to say that, but that's what they were saying for years. And then in 02/2003, a CDC scientist called Picchiero did a study where he gave tuna sandwiches that were mercury, you know, contaminated to children, and they and then measured their blood. And the mercury from the tuna sandwich was there, a half life sixty four days later. So it was still there sixty four days. And he injected the children with mercury from a vaccine, and that mercury disappeared from their blood within a week. And this kind of confirmed what Eli Lilly had said in 1932. Oh, it disappears really quickly from the body. And that was published, I I believe, in the lads Lancaster Pediatrics. But immediately, the journal began getting letters from people, including this famous scientist called doctor Boyd Haley, who is the head of he's the chair of that chemistry department of the University of Kentucky. And he said, what but what happened to the mercury? Because Pidgey Ear couldn't find it in the children's urine or in their feces or in their hair or sweat or nails. So where is it? And then and NIH actually then commissioned a study. And they because they at that point, they were really trying to figure out, you know, whether this was dangerous. And they commissioned a very famous scientist called Thomas Burbacher up at the University of Washington, Seattle to do a study with monkeys, with macaques. And he did the same study Pichiera did, but he did something he can't do with children, which he then killed the monkeys. And then he looked for the mercury, and what he found was the mercury, yes, it left their blood immediately. The the ethylmercury from the vaccines was gone from their blood in a week. Methylmercury from the tuna fish was there two my a month later. Two months later. But when he sacrificed the monkeys and did postmortems, he found that the mercury had not left their body. Instead, the reason it was disappearing from their blood is because ethylmercury crosses the blood brain barrier much easier than methemmercury. The ethylmercury from the vaccines was going directly to the brains of these animals, and it was lodging there and causing severe inflammation. So when I'm on the phone with Offit, and I said, he said the azimercury is excreted quickly. And I said, how do you know that? And he said, because the Picchierro study, because the study by, by Picchierro found that it was excreted quick in a week. And I said, but you're familiar with the Burbacher study that showed and that it's gone to the brain. And there was dead silence on the phone. And then he said to me, he kinda hemmed it on and said, well, you're right. It's not that study. It's just a whole mosaic of studies. And I said, can you cite any for me? And he said, I'll send them to you. And he never did. That's the last I heard from him.
Humanspective
Posted - July 29, 2025 at 10:03 PM
Saved - July 30, 2025 at 11:46 AM
reSee.it AI Summary
This has gone completely off the rails. Kevin McKernan claims Pfizer engaged in a "bait and switch," using a different manufacturing process for the vaccine than what was tested. They hid SV40 sequences from the FDA and quickly acquired cancer companies, raising concerns about a potential carcinogenic impact on the population.

@Humanspective - Humanspective

"This has gone completely off the rails". "They know something". Kevin McKernan on Pfizer's "bait and switch", where Pfizer swapped out the clean manufacturing process used in the trial, for "process 2" which the whole world was injected with. Pfizer obscured the SV40 sequences contained in process 2 from the FDA...and then "they quickly went out and acquired cancer companies", including Seagen for $43 billion. "This may be the largest carcinogenic hit ever, to the human population"

Video Transcript AI Summary
Pfizer allegedly knew their trial data indicated future issues and acquired cancer companies, investing $43 billion in C Gen and $2.26 billion in Trillium Therapeutics, which focused on blood cancers with the CD147 marker, also linked to COVID. The speaker claims the Pfizer vaccines on the market differ from the clinical trial formulation, constituting a "bait and switch" and fraud, invalidating claims about vaccine efficacy. Significant DNA contamination is allegedly found in most studies, including peer-reviewed ones, even those not initially investigating it. The speaker asserts cancer rates are rising, with some papers reporting neoplasms at the injection site post-vaccination. The speaker concludes that these liability-free, often mandated vaccines may represent the largest carcinogenic event in human history, especially concerning childhood schedules and pregnant women.
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Speaker 0: They know something. Pfizer very early on, they had the data on this from their trial. They knew this was gonna happen and they quickly went out and acquired, cancer companies. They put $43,000,000,000 into the acquisition of C Gen and they put $2,260,000,000 to acquire Trillium Therapeutics. Trillium was focused on blood cancers that have a c d one forty seven marker on them. Okay? That is one of the markers that is known to be involved in COVID. So, they have a very interesting window on those malignancies and, they're buying up the cancer companies that are probably gonna play the biggest role in benefiting from the mess that they've created. So, in summary, the Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials. This is a big bait and switch and it's a fraud. So you can't believe anything they're saying about the vaccine efficiency, which we have seen even those numbers decay over time. This is probably why. They're not really what they trialed. They gave you something different. There is significant DNA contamination that's found. Like, 10 out of 11 studies have found this, and the ones that haven't found it have some financial conflicts. So I think the consensus is out. 10 out of 10 out of 10 of the real studies are finding this. Several are through peer review, which have not been easy to get through peer review. The peer review journals do not like these papers. They get they get beat beat around in peer review for months to years, but they're they're making their way out now. There is also significant DNA condition now found in five peer reviewed studies that were not looking at this. They were looking at people's blood and tissue, and it was accidentally in there. Other people had to go sleuth it out. We've got cancer on the rise, and there's several papers that report cancer post vaccination. Like like, right at right at the site of injection, they'll see neoplasms. Alright? There is there's something going on here. This can't be ignored saying it's a coincidence anymore. Now this is these are liability free and they're often mandated. Okay? This may be the largest carcinogenic hit ever to the human population. And we have these on childhood schedules. We're giving these to pregnant women. This has gone absolutely off the rails.
Humanspective
Posted - July 27, 2025 at 9:21 PM
Saved - July 28, 2025 at 7:35 AM
reSee.it AI Summary
I recently discussed Robert F. Kennedy Jr.'s claim that peanut allergies can be induced by attaching peanut molecules to aluminum adjuvants in vaccines, using rats as a model. This idea parallels the tetanus-hCG controversy from 2013/14, where a vaccine made women produce antibodies against their pregnancy hormones by linking hCG to tetanus toxoid. Antoninah Mutinda noted elevated hCG antibodies after vaccination. Gursaran Pran Talwar explained that this vaccine prevents embryo implantation by targeting hCG, highlighting similar immune dysfunction mechanisms described by both RFK Jr. and Talwar.

@Humanspective - Humanspective

Robert F. Kennedy Jr. recently said peanut allergies can be caused at will if you attach a peanut molecule to the aluminum adjuvant in the hepatitis B vaccine and inject it into rats. A similar mechanism behind how vaccines might cause allergies can be seen with the tetanus-hCG scandal of 2013/14. The World Health Organization worked with lead scientist G. Talwar to create a vaccine that caused women to produce antibodies against their own hormones responsible for maintaining a pregnancy. By attaching a molecular subunit of hCG to the tetanus toxoid, the immune system is tricked into attacking the body's own hormones, similar to how the immune system can be induced to create an immune reaction to peanuts. Antoninah Mutinda from Kenya, in the movie Infertility: A Diabolical Agenda, was interviewed and said she found her hCG antibodies were "way up" following tetanus vaccination campaigns. Gursaran Pran Talwar said of his "vaccine for controlling fertility": "The vaccine, by producing antibodies against hCG, prevents implantation. This vaccine uses a subunit of human chorionic gonadotropin (hCG) hormone, linked to a carrier (tetanus toxoid) to make it immunogenic since hCG is a self-hormone." "Now we understand that hCG plays a crucial role in the implantation of the embryo. The vaccine, by producing antibodies against hCG, prevents implantation without affecting other body functions." RFK Jr. and Talwar are explaining very similar mechanisms of immune system dysfunction.

Video Transcript AI Summary
The speaker expresses concern that the WHO is negotiating agreements that could undermine African sovereignty, without properly informing executives and parliaments. They claim that a WHO tetanus eradication campaign in Kenya during 2014-2015 used a fertility-regulating tetanus vaccine. This vaccine allegedly combined tetanus with human chorionic gonadotropin, causing women to produce antibodies against the pregnancy hormone and become sterile. The speaker attributes an increase in infertility cases and pregnancy loss among young couples to this vaccine. They state they exposed this issue and published a paper on it. The speaker notes that the WHO declared Kenya free of neonatal tetanus in 2017 and left the country, after developing the vaccine over a 20-year research period and using it in South America. They suspect it may have been used in other African countries as well.
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Speaker 0: And I'm not sure that they are briefing the executive and the parliaments in the different countries, yet they are negotiating, things that can destroy the sovereignty of Africa. We cannot afford to trust WHO anymore your excellency and I'll just mention a few things that have caused great concern to us. In twenty fourteen, twenty fifteen WHO brought tetanus eradication campaign in our country. It was a campaign to eradicate neonatal tetanus, babies who are born who eventually get tetanus. And the vaccine that was used is a different type of a tetanus vaccine that is a fertility regulating vaccine where they take tetanus and combine it with a hormone called human chorionic gonadotropin that supports pregnancy and when you inject a woman with that vaccine she produces antibodies against that hormone and therefore is rendered sterile. So we are noticing an increase in the number of infertility cases among young couples who you examine and they are normal but cannot get children or couples who are losing three, four, five pregnancies before they can carry any pregnancy to term. We were able to expose this and we have even published a paper that is available and fortunately in 2017 WHO said Kenya is now free of neonatal tetanus and they left our country but they developed this vaccine over a twenty year period of research from nineteen seventy two-nineteen ninety two and they used that vaccine in South America and it is possible it has been used in many other African countries.
Humanspective
Posted - May 9, 2025 at 10:42 PM
Saved - July 13, 2025 at 1:29 AM

@Humanspective - Humanspective

Dr Tina Peers was stunned at the drop in Sperm count. They found in the Israeli data that: "Even at 6 x months, there sperm count was down 15.9% and the motility was down 22%" after 2 x covid mRNA injections. https://t.co/JM3nWSamAo

Video Transcript AI Summary
A study in Israel examined sperm count in young men aged 24-26 before any vaccines to establish a baseline. After the second dose of a vaccine, and even at six months, the study found sperm count decreased by 15.9% and motility decreased by 22%. The speaker believes there is nothing else to which this drastic change in fertility can be attributed.
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Speaker 0: Infertility, there was a study in Israel looking at male infertility. They looked at sperm count in young men aged 24 to 26 who should be, you know, firing good stuff. And they had Older. And they had yeah. They found they did it before they had any vaccines, which is the right way to do it, you can see your baseline. And then at various intervals after the second dose, and even at six months, their sperm count was down 15.9%, and the motility was down 22%. Is there anything else that we can apply this drastic change in fertility to No. In your view at all? No. I don't think so.
Humanspective
Posted - July 11, 2025 at 9:11 PM
Saved - July 12, 2025 at 9:22 AM

@Humanspective - Humanspective

Not a single case of Myocarditis was found in the WHOLE OF NEW ZEALAND, after covid infection. But there were 900+ cases of Myocarditis from the mRNA injection. And all the governments own data https://t.co/IwC4OGscOR

Video Transcript AI Summary
Studies have suggested myocarditis is a risk factor from COVID. However, it's claimed that the idea COVID is more of a cause of myocarditis and is more severe is untrue, based on literature reviews, assessments, and real-world experiences. Evidence supporting this claim was included in a written statement. An official information act request was made to determine the number of myocarditis cases due to COVID infection. The Ministry of Health couldn't provide a single case. Conversely, there were over 900 cases of myo- and pericarditis on the CALM safety report 46 by November 2022.
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Speaker 0: Were you aware of, studies showing that myocarditis was also a real risk factor from COVID? Speaker 1: There were studies saying that. As time has gone on, it has become clearer and clearer that this notion that COVID is more of a cause of myocarditis and is more severe is frankly rubbish. Large literature reviews, narrative reviews, assessments of the broader landscape and the real world experience of doctors all around the world, including here in New Zealand, which as I know all you can look at, would actually say otherwise. And of course, have included plenty of evidence in our written statement to you. Speaker 0: I did an OIA because I was curious about that very question. We were told that myocarditis was more severe in COVID than post vaccination. So I asked the Ministry of Health, well, how many cases of myocarditis due to COVID infection have they been? Well, they couldn't provide me with a single case, and yet there were nine hundred plus cases of myo and pericarditis on the CALM safety report 46 by November 2022. I don't want to get into all the detail of all your submissions.

@nzdsos - NZDSOS - NZ Doctors Speaking Out with Science

Here is the Official Information Act response discussing myocarditis after covid infection which was discussed in our RCI presentation. It states: “There were no events where an individual who was positive for COVID-19 was diagnosed with myocarditis as their primary, secondary or other diagnosis from 01 Jan 2020 to current.” Instead there were 900+ cases registered in the CARM database following vaccination. It’s not safe. It’s not effective and they know it.

Humanspective
Posted - June 14, 2025 at 9:26 PM
Saved - June 16, 2025 at 6:29 PM
reSee.it AI Summary
I discussed the largest autopsy series examining sudden deaths post-vaccination, revealing that around 74% of cases linked the vaccine to these deaths. Our paper faced censorship from major journals due to pressure from pharmaceutical interests but was eventually published in a peer-reviewed journal. Concerns persist about the lack of autopsies conducted by Pfizer and health authorities, raising questions about transparency and accountability. Multiple experts highlight alarming findings, including contamination and integration risks associated with mRNA vaccines, which regulators seem to overlook.

@Humanspective - Humanspective

"The Largest Autopsy Series in the World" censored by powerful pharmaceutical interest: "we found that about 74% of the cases of sudden death were caused or contributed to by the vaccine" William Makis, working with Dr Peter McCullough and other Drs. was set to be published with the Lancet, but after hundreds of thousands of downloads, Big Pharma put pressure on the journal. Lancet "took the paper down", so they had to go to another publisher, which notified Makis MD hours before this clip was recorded, that it passed peer review. William Makis MD: "[We] submitted a vaccine injury paper to the Lancet, to one of the biggest journals in the world, co authored by Doctor Peter Mccullough myself, Doctor Mark Trozzi Doctor Roger Hodgkinson and other doctors that paper was [the] largest autopsy series in the world of covid vaccine people who took Covid 19 vaccines and then died suddenly a few days or a few weeks after." "That paper was downloaded hundreds of thousands of times and within 24 hours there was so much pressure put on by the pharmaceutical industry, that the Lancet took the paper down [and] basically wanted to cancel it forever" "I just found out a few hours ago that that paper has passed peer reviewed and is going to be published" It looks like the "peer review" process is shielding the pharmaceutical industry from liability

Video Transcript AI Summary
The speaker discusses a review of 325 autopsies, which they claim is the largest autopsy series in the world, of COVID-19 vaccinated individuals who died shortly after vaccination. According to the speaker, this review found that the vaccine caused or contributed to approximately 74% of the sudden deaths. The speaker states that this information will be published in a peer-reviewed paper. The speaker anticipates a "tsunami of evidence" regarding the harm caused by COVID-19 vaccines to children, pregnant women, and adults. The speaker urges politicians to "get ahead of this" issue now.
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Speaker 0: It is the largest the largest autopsy series in the world. 325 autopsies of COVID vaccinated people who drop dead a few hours or a few days or a few weeks after taking the COVID nineteen vaccine. We did a rigorous review of these autopsies, and we found that about seventy four percent of the cases of sudden death were caused or contributed to by the vaccine. That is now a peer reviewed paper that's going to be published. And the reason I'm telling you that is that there is more evidence coming every single day, and it's not a little bit of evidence. It's not a case report here that they're gonna dismiss or case report there or a paper that the lancet is going to take down and say, don't look at this autopsy series and we'll just bury it and make sure it never sees the light of day. There's going to be a tsunami of evidence of the harm of these COVID nineteen vaccines, whether it's harming children, pregnant women, adults. And my message to the politicians is get ahead of this. Get ahead of this if you can. Don't chase after when all the evidence is out and then you're caught with your pants down. Get ahead of it now.

@Humanspective - Humanspective

This is peer reviewed. But labelled a “fringe” journal 🙃 Reminder: Dr McCullough is one of the most cited Cardiologists in the world and considered an expert. He describes the length of work the paper went through to pass peer review: “We had an adjudication committee [and] ways of arbitration” Senator Ron Johnson: "Do you have any science to back up your opinion?" Dr Peter McCullough: "In the largest autopsy series published today [we] examined [these] cases that came in for autopsy after vaccination, in 73.9% of individuals, it was determined that the mRNA vaccine was the cause of death" GROK confirms the study is peer reviewed: “the study in question was eventually published in a journal, despite facing initial rejections from three other journals and it was published in what is described as a "fringe journal" The article published in "Forensic Science International" is titled "A systematic review of autopsy findings in deaths after covid-19 vaccination." Yes, the article "A systematic review of autopsy findings in deaths after covid-19 vaccination" published in "Forensic Science International" underwent peer review.” "Forensic Science International" is a peer-reviewed journal, as indicated by its inclusion in databases like PubMed and its description as a platform for rigorous scientific scrutiny. But apparently we should prioritise “the fact-checking article from AFP”

Video Transcript AI Summary
It was determined that in 73.9% of autopsy cases following vaccination, the vaccine was the cause of death. Holsher and colleagues are cited as the source.
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Speaker 0: Ways of arbitration, deciding on did the vaccine cause death? The answer is, of these cases that came in for autopsy after vaccination, seventy three point nine percent of individuals, it was determined that the vaccine was the cause of death. First off, there's Holsher and colleagues who's sitting right behind me.

@Humanspective - Humanspective

Someone’s got to do do autopsies, because we certainly can’t rely on Pfizer to do them Why did they only do 3 x Autopsies when there were 10 x sudden deaths in the vaccinated arm and 21 total deaths, versus 17 in the placebo?

@Humanspective - Humanspective

Why didn't Pfizer do autopsies on the 10 x Sudden Adult Deaths they had in the vaccinated arm? The Sudden Adult Death rate: 1 per 2,200 vaccinated participants over 33 weeks. There were 21 deaths in the vaccine arm, 17 in the placebo arm 🧵 https://t.co/j0qez62jpd

Video Transcript AI Summary
Professor Lawler stated there were no breaches of good clinical practice and no hidden deaths in the Pfizer trial, also claiming that none of the deaths were attributed to the vaccine and the initial conclusions remain valid. In response, the speaker says they reanalyzed the data and found more deaths in the vaccinated arm (21) compared to the placebo arm (17). In the vaccinated arm, 10 deaths were categorized as sudden adult death or found dead, but only two had autopsies. One autopsy result is available and showed sudden cardiac death. The other is still pending. The speaker questions how it can be stated that deaths are not due to the vaccine when autopsy results are pending or not performed, especially in cases of sudden death. The speaker has repeatedly asked the TGA for the evidentiary basis for the statement that none of the deaths were due to the vaccine, but has not received a reply.
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Speaker 0: He replied to your first letter on the March 27 denying any breaches of any breaches to good clinical practice, and he denied that there were any hidden deaths. He also said that it is reassuring to note that in this case, none of the deaths in the trial have been attributed to the vaccine, and the initial conclusions remain valid. What are your comments on these remarks from professor Speaker 1: So I have not, received any reply from professor Lawler other than the first one where he said there were no breaches of group clinical conduct. And as I said, I provided date stamps again to him of the documentation for the relevant patients where there were hidden deaths. So with his statement that none of the deaths in the Pfizer trial were due to the vaccine, I went back and reanalyzed the data. So for this trial, there were actually more deaths in the vaccinated arm, twenty one, compared to the placebo, seventeen. Of the deaths in the vaccinated arm, only three of them had autopsies. But in the vaccinated arm, ten of those deaths, ten of the twenty one deaths, were people who were sudden adult death, found dead. They were people who died whilst they were in the laundry, people who had a cardiac arrest when they were walking, people who never woke up from their sleep, people who their neighbours called and said there's a smell in this apartment next door, I think we need to, you know, you need to go and check this. So people had there was a sudden adult death signal, found death signal, in the vaccinated deaths. Of that ten sudden adult deaths found dead, there were only two autopsies, only one result's available. That's the sudden cardiac death. The other autopsy report was the gentleman who was found in the laundry by his mother. That result is still not available. So in the first place, how do you say something can't be due to the vaccine if the autopsy result is pending? And for the other eight sudden adult deaths, there were no autopsies. You know, and I think it's really critical that people understand this. I can understand if there's a period of illness that's documented in hospital, there's no autopsy. But for people who die suddenly, people who are well enough to sign up for a clinical trial and they die suddenly and there's no autopsy, I have repeatedly asked the TGA for their evidentiary basis for the statement that none of the deaths were due to the vaccine. Speaker 0: What was your reply? Speaker 1: I haven't had a reply. Speaker 0: Right. Okay.

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“They are refusing to do autopsy”

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"They are refusing to do autopsy" Professor Nikolai Petrovski & Senator Alex Antic: "Everyone who's dying after having a vaccine should have an autopsy, that should be the default, they're refusing to do autopsy, why are they scared to do autopsies....if you don't do the autopsy you never know [and] in the old days [autopsies] were done on everyone"

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It is claimed that autopsies should be performed on everyone who dies after receiving a vaccine. It is alleged that there is a refusal to perform autopsies. It is argued that without autopsies, it is impossible to determine the specific cause of death. It is claimed that autopsies used to be commonly performed on most people who died.
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Speaker 0: Everyone who's dying after, you know, having a vaccine should have an autopsy. Yeah, That should be the default. They're refusing to do autopsy. Are they scared to do autopsies? You know, you Speaker 1: need to delay. But is upsetting the apple cart in terms of ever being able to find out you know, specifically what that person died from? I mean, is it you know, you would never know. Speaker 0: Yeah, if you don't do the autopsy, you never know. That's why in the old days, I mean, autopsies were, were done on everyone pretty well, who died

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Scientist’s bullied to retract papers. The evidence reservoir controlled by powerful interests

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Professor Angus Dalgleish: "[mRNA] should be completely stopped now", but powerful interests control peer review processes and the evidence reservoir. Journals controlled by cartel like behaviour from powerful organisations and Pharmaceutical interest. Researchers funded by Pfizer and the NIH allegedly bully scientists that publish research critical of mRNA vaccines. If they can’t get their way, sometimes they just buy the journal that published the paper to retract it.

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The speaker believes COVID vaccine programs should be stopped. They are astounded by the number of papers critical of the vaccine or showing negative effects. The speaker claims a group of researchers funded by Pfizer and the NIH bullies editors to retract papers with negative findings about the vaccine. They assert the number of retractions is appalling. According to the speaker, in one instance where an editor resisted, Nature Springer bought the journal and retracted the paper. The speaker states that this is what they have been dealing with.
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Speaker 0: They I believe that they should be completely stopped now, but there is something trying to do this. And what I just had is one of my last slides here is I'm astounded at the number of papers on COVID that have been critical of the, vaccine program or showed negative effects that have been vaccinated. And I can't believe the depths to which these people will go. There is a, a group of researchers funded by Pfizer and the NIH whose job is to go around every published paper, and if they see something negative about the vaccine, they will bully that editor until they retract it. And the numbers that have been retracted is just appalling. And in one case where the bullet, editor stood up, Nature Springer went in and bought the journal concerned and retracted the paper. This is what we have been dealing with up to now. Next slide, please.

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More proof health authorities are refusing and avoiding autopsy. Dr John Campbell asks Professor Angus Dalgleish "had the patients relatives consented to a post mortem?" Professor Dalgleish: "Yes [it] was over ruled" https://t.co/fmXjwblHBT

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How many levels of concerning can you fit into 1 x clip? “This to me is quite frightening [what] the hell is that doing in an RNA vaccine” Professor Angus Dalgleish is stunned. There’s DNA contamination and SV40 sequences in Pfizer and one of his patients had a cancer biopsy sent away for analysis….they found spike protein had integrated. To make matters worse, authorities won’t allow post mortem autopsy even after the family has consented. 🚩 10 massive red flags identified by Professor Angus Dalgleish: 1. Quality Control Awful 2. Contaminated with DNA 3. Sequences from the SV40 promoter 4. SV40 and DNA provides theoretical integration risk 5. Literature shows spike protein “integration” 6. “It stays at the injection site” LIE 7. At autopsy spike protein has been identified everywhere 8. “I can’t get autopsies” of patients to prove it 9. Even when immediately family consents to autopsy, they refuse autopsy 10. The peer review process is shielding big pharma I don’t think I’ve often seen a clip that highlights so many issues that regulators continue to ignore

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An article in Spectator Australia reported that DNA plasmids are contaminated with SV40 promoter sequences, which are oncogenic and used in cancer development in mice. The speaker questions why this is in an RNA vaccine, as the presence of DNA means it can integrate. Despite claims that the spike protein stays at the injection site, it has been identified everywhere, including in metastases from a colorectal cancer case where spike messenger RNA from the vaccine insertion was confirmed. The speaker was refused autopsies, even with consent from relatives, including a case of explosive melanoma after a booster shot. A report in The Lancet about deaths after vaccines was pulled, allegedly due to improper peer review. The speaker claims a media channel warned them that the government had made it a crime to criticize the vaccine program on the media.
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Speaker 0: For the first time, mainstream media with an article in Spectator Australia actually went through that not only is the quality control lawful, but it's contaminated the DNA plasmids. One report up to three fifty odd times with sequences from the SV40 promoter. Well the SV40 is oncogenic promoter used in cancer development in mice. And you know first, so what I say what hell is that doing in an RNA vaccine? You have to ask. Because the presence of that and the presence of DNA means it can integrate. Surely that's not possible. Well, you don't have to go very far into the literature to find people reporting that the spike protein is integrated into all sorts of different tissue. And for, you know, for Raintree, they they said that it stays at the point of the injection site and there's no way it spreads. Oh that's all right then, it's safe. This has turns out to be a complete lie. It's been identified at autopsy, it's been identified everywhere. This is the other thing with patients. I can't get autopsies on these patients to prove this. It's quite credible. But a colleague who had an explosive cancer, a colorectal, basically at surgery sent the pieces away, the metastases away, and spike messenger RNA from the vaccine insertion was confirmed. So it is this is this to me is quite frightening that this is occurring. And also that there's been this we don't need to do post mortems on patients dying from this. It is it's like it's from on high, and they just won't do it. I pleaded for one of the patient who died from explosive melanoma who said I never felt, well after the booster. I just felt chronically unwell, and then the melanoma came exposing back. They Speaker 1: wouldn't Had had the patient's relatives consented to a postmortem? Speaker 0: Oh, yes. Oh, yes. So so just a minute. You're you're one of Speaker 1: the most senior doctors in the country. You wanted a postmortem. Your relatives had consented to a post mortem, but that was refused. This is just unbelievable. Speaker 0: It's overruled, yeah, unbelievable. Speaker 1: Is Overruled by whom? Speaker 0: Well perhaps it had something to do with there was a report which got into The Lancet of people who died after the vaccines to see whether it could I don't know if you saw that. It appeared in the Lancet but then it was pulled. It was pulled very quickly The explanation given it wasn't properly peer reviewed, which tells you there's not peer review is over and dead. I mean basically it's not politically within the political mantra. And this is what really frightens me. I went to do an interview along these things, you know, into a mainstream media channel, and the guy warned me at the beginning, he says I have to be very careful the way I ask you questions, and please don't be put off that I probably sound fairly hostile. I said I'm very happy to discuss facts this that and the other. But he said the government had made it a crime to criticize the vaccine program on the media. And I said I'm astonished but actually thinking about it I'm not surprised because it explains why nothing is being discussed. Well that's
Humanspective
Posted - May 13, 2025 at 2:01 AM
Saved - May 15, 2025 at 6:32 AM
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I discussed how Fauci allegedly funded bioweapons research in Wuhan through EcoHealth, a nonprofit. Elon Musk emphasized that this funding indirectly supported what he calls "death maximization," a term he uses instead of "gain of function." He questioned the ethics of funding research that leads to increased mortality. Additionally, I mentioned that former CDC Director Robert Redfield noted that biodefense funding was transferred to the NIH, giving Fauci access to around $40 billion.

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Fauci funded "death maximization". Elon Musk: "A lot of people out there don't realize Fauci funded the bioweapons research that was going on in Wuhan. He bank shot it off. Like, he can't send the money directly to China, so he just bank shot it off to EcoHealth, this fake nonprofit in the US, and they sent it to Wuhan. The so-called gain of function—again, a propaganda word—because what is the function? They're talking about death. So, if you actually use the right word, this gain of function is death maximization...then you're like, "Oh, hey guys, should we fund bioweapons research into death maximization?" 'Cause that's what gain of function means." Former CDC Director Robert Redfield said in 2002/2003, Biodefence was transferred to NIH [providing Tony Fauci around] $40 Billion

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Fauci allegedly funded bioweapons research in Wuhan indirectly through EcoHealth, a U.S. based nonprofit. Direct funding to China was supposedly avoided by using this intermediary. The speaker claims the term "gain of function" is a propaganda term. The speaker suggests "death maximization" is a more accurate description of gain of function research. The speaker implies that framing the research as "death maximization" would reveal the true nature of the work.
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Speaker 0: I think a lot maybe a lot of people out there don't realize Fauci funded the the the the the bioweapons research that was going on in in Wuhan. And he he bank shot it off. Like, he can't send the money directly to China. So he just bank shot it off EcoHealth. Right. This is, like, fake nonprofit in The US, and they sent it to Wuhan. The the so called gain gain of function again, a propaganda word, because what is the function they're talking about? Death. Right. Right. So if if you if it if you actually use the right word, this is gain of function is death maximization. Right. Then you're like, oh oh, hey, guys. Should we fund a bioweapon research into death maximization? Because that's what gain of function means.
Humanspective
Posted - February 18, 2025 at 6:58 PM
Saved - May 13, 2025 at 12:54 PM
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I believe all mRNA vaccines pose a danger to life and should not be allowed. Professor Sucharit Bhakdi, a Buddhist and expert in Microbiology and Immunology, has criticized Germany for being the second largest financier of the World Health Organization, which aims to implement mRNA vaccines globally. Currently, he faces prosecution in Germany, with an appeal hearing scheduled for February 27-28 at the regional court in Kiel.

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“All mRNA vaccines are dangerous and are going to threaten life [and] this cannot be allowed to happen” Buddhist Professor Sucharit Bhakdi (Microbiology and Immunology) called out Germany as the 2nd largest financier, behind Bill Gates, of the World Health Organization, who proclaimed it was their intent to: “Introduce mRNA vaccines for all vaccinations on Earth” The Justice system in Germany is trying to prosecute him right now and put him behind bars, with an appeal hearing set for February 27-28 at the regional court (Landgericht) Kiel, Germany 🇩🇪

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The speaker claims the WHO intends to introduce mRNA vaccines for all vaccinations and treatments globally. They assert that all mRNA vaccines are dangerous and threaten life, regardless of the protein they encode. The danger stems from the immune system's ability to recognize non-cells, which should not be allowed. The speaker identifies the WHO as a privately financed club, with Germany as the top financier and Bill Gates as number two. They warn against allowing children to be vaccinated, claiming mRNA vaccines change mankind, alter personality and the brain, and weaken the heart. The speaker concludes that every injected mRNA vaccine will cause severe damage and must be forbidden.
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Speaker 0: Now if I am here today, it's for a very special reason. Four weeks ago, I don't know if you saw the video, released by the WHO where they proclaimed that it was their intent to introduce mRNA vaccines for all vaccinations on earth and then go from there to treatment of all other diseases, including cancer, etcetera. What people do not understand is that all mRNA vaccines are dangerous and are going to threaten life. It does not matter whether the vaccine, encodes for the spike protein, for the measles protein, for rubella, for the flu. It does not matter at all. Why? Because the whole danger of the vaccine stems from the ability of the immune system to recognize non cells. This cannot be allowed to happen. Even if the WHO said so, don't. And remember, and this is the last thing I want to say, the WHO is a private club, like a private football club. A club that is being financed, has been financed at the top by what? Bill Gates. Bill Gates is now number two. Who is the top financier? Germany. The German taxpayers are financing the WHO and enforcing mRNA vaccination. You can't do this. You can't let your children be vaccinated because they are changing mankind. All your personality is going to be changed. Your brain is being changed, and your heart is being weakened. Every injected mRNA vaccine is going to cause severe damage in our body. It must be forbidden. Thank you.
Humanspective
Posted - April 21, 2025 at 12:38 AM
Saved - April 22, 2025 at 12:55 AM
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I’m amazed by the findings on Augmented NAC. Initially, native NAC had limited detoxifying effects on spike proteins. After collaborating with global experts, including Dr. Tina Peers, we discovered that Augmented NAC can denature spike proteins with an efficacy of 99.8%. I also reference Professor Arne Burkhardt’s histopathology work.

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Spike Denaturation with Augmented NAC. This is astonishing. NAC in native form had a low ability for the body to utilise it for detoxifying spike. Founder (Fabio Zoffi) started working with Drs globally (inc. Dr Tina Peers) and did Lab tests, finding efficacy for denaturation of spike from Augmented NAC moved up to 99.8% Fabio Zoffi also cites Professor Arne Burkhardt’s (RIP) histopatholy work

Humanspective
Posted - March 27, 2025 at 12:49 AM
Saved - March 27, 2025 at 4:31 PM

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Joe Rogan goes dead silent. The damage inflicted by Ventilators was incentivised by the government Elon Musk points out the $39K "moral quandary" to put someone on a ventilator. We now know that up to 80% of the people put on ventilators died https://t.co/4e9D70lyZJ

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The stimulus bill intended to help hospitals overrun with COVID patients created an incentive to record something as COVID. Hospitals are in a bind because if a hospital is half full, it's hard to make ends meet. Checking a box can yield $8,000, and putting a patient on a ventilator for five minutes can bring $39,000. The alternative could be firing doctors. This situation presents a tough moral quandary.
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Speaker 0: Well, right now, the so, you know, the road is hell the road to hell is paid with good intentions. I mean, it's mostly paid with bad intentions, but there's, you know, some good intentions, paving stones in there too. And the the the stimulus bill that was intended to help with the hospitals that were being overrun with with with COVID patients created an incentive to record something as as COVID that is difficult to say no to, especially if your hospital is going bankrupt for lack of other patients. So the hospitals are in a in a bind right now. There there's a bunch of hospitals that are they're following doctors as you were mentioning. They're, you know, they're if your hospital's half full, you're it's hard hard to make ends meet. So now you've got like, you know, if I just check this box, I get $8,000. Put them on a ventilator for five minutes, I get $39,000. Like or or or I gotta fire some doctors. So what's the what's this is this is a tough moral quandary. It's like, what what you can do? That's the situation we have. No.
Humanspective
Posted - March 24, 2025 at 2:28 AM
Saved - March 24, 2025 at 10:31 AM
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I explored the growing concerns surrounding mRNA COVID-19 vaccines, highlighting a disconnect between regulatory recommendations and emerging research. Key studies indicate significant risks, including heart damage, excess mortality, and T-cell exhaustion, which may outweigh the benefits against milder variants like Omicron. Notable findings include elevated troponin levels in booster recipients and DNA contamination in vaccine vials. Despite these alarming insights, regulatory bodies continue to endorse the vaccines without adequately addressing these risks, prompting calls for urgent reassessment.

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T Cell Exhaustion, Cancer, Hidden Deaths, Pfizer re-analysis, Arne Burkhardt, VAERS, Swiss Heart Damage study I asked GROK to provide a comprehensive risk/benefit analysis and find connections with the evidence and highlight a potential mechanism. The answer might shock you (below) "The Disconnect Between Regulators and Growing Research on mRNA COVID-19 Vaccines: A Risk/Benefit Reassessment. Key Overview and Summary As of March 24, 2025, regulatory bodies like the FDA, CDC, WHO, and TGA continue to recommend mRNA COVID-19 vaccines, including boosters, for broad populations based on historical safety data from over 13 billion doses and the need to counter waning immunity against circulating Omicron variants. However, a growing body of research—spanning clinical trial re-analyses, histopathological findings, and emerging studies on cancer and immune suppression—paints a starkly different picture. Evidence suggests that mRNA vaccines may pose significant risks, including heart damage, excess mortality, serious adverse events, DNA contamination, increased cancer incidence, and T-cell exhaustion, far outweighing their diminishing benefits against milder SARS-CoV-2 variants. This disconnect is striking: regulators maintain a pro-vaccination stance, minimizing or dismissing these risks as rare or unproven, while peer-reviewed and clinical observations, such as those from Professor Angus Dalgleish, call for urgent reassessment or cessation of mRNA boosters. This article synthesizes the evidence, quantifies the risk/benefit imbalance, and critiques regulatory inertia in light of these findings. The Evidence: A Comprehensive Risk Profile Acute Risks from Clinical Trials and Observational Data ◻️Pfizer RCT Mortality: Thomas et al. (2021, NEJM): The original six-month follow-up of the Pfizer-BioNTech trial (NEJM, DOI: 10.1056/NEJMoa2110345) reported 15 deaths in the vaccinated arm (21,720 participants) versus 14 in the placebo arm (21,828), an excess of 0.05 per 1,000, deemed non-significant. ◻️Michels et al. (2023, IJVT-PR): A forensic re-analysis co-authored by Dr. Jeyanthi Kunadhasan (IJVT-PR, DOI: 10.56098/ijvtpr.v3i2.510) using FOIA-released data found 21 vaccinated deaths versus 17 placebo deaths, an excess of 0.188 per 1,000, with 10/21 (0.476 per 1,000) classified as sudden adult death (SAD), suggesting cardiac or vascular risks. ◻️Swiss Study on Heart Damage: A prospective cohort study (European Journal of Heart Failure, 2023) found 2.8% (22/777) of booster recipients had elevated troponin levels, indicating subclinical heart damage at a rate of 28 per 1,000—far higher than regulators’ acknowledged myocarditis incidence. ◻️Serious Adverse Events (Fraiman et al.): Fraiman et al. (2022, Vaccine, DOI: 10.1016/j.vaccine.2022.08.036) re-analyzed Pfizer and Moderna trial data, identifying an excess risk of serious adverse events of special interest (AESI) at 1 in 800 (1.25 per 1,000), including myocarditis and coagulopathy. Mechanistic and Long-Term Risks: ◻️Burkhardt’s Histopathology Dr. Arne Burkhardt’s autopsies (2022 presentations) revealed spike protein (no nucleocapsid) in microvessels of heart, kidney, and brain, with lymphocytic infiltration, endotheliitis, and microthrombi, linked to sudden deaths post-vaccination, consistent with Michels et al.’s SAD findings. ◻️Yale LISTEN Study: The Yale LISTEN study (2025, preprint) detected spike protein in blood up to 709 days post-vaccination, with elevated cytokines (IL-6, TNF-α), suggesting chronic immune activation that could amplify Burkhardt’s observed damage. ◻️VAERS Signals: VAERS reports thousands of myocarditis and rare kidney vascular events, reflecting Burkhardt’s multi-organ microvascular pathology in a broader population, though causality remains unproven due to passive surveillance limitations. ◻️DNA Contamination Speicher et al. and McKernan et al. (2023, OSF Preprints) found residual plasmid DNA (30–100+ ng/dose) in Pfizer and Moderna vials, exceeding WHO/FDA limits (10 ng/dose), with SV40 promoter/enhancer sequences in Pfizer raising theoretical risks of genomic integration and oncogenicity. ◻️Increased Cancer Incidence: Gibo et al. (2024, Cureus, DOI: 10.7759/cureus.57860) reported a 2.1% excess cancer mortality in Japan in 2022 post-third mRNA dose rollout, versus 1.1% in 2021 and none in 2020, linking it to booster uptake. Angus Dalgleish’s Stance: Professor Dalgleish, an oncologist, has observed rapid cancer relapses (e.g., melanoma, B-cell cancers) in stable patients post-booster, attributing this to immune suppression (Conservative Woman, 2024; GB News, 2023). He calls for halting mRNA vaccines, warning of a “cancer time bomb.” ◻️T-Cell Exhaustion: Liu et al. (2022, Nature Immunology, hypothetical DOI) showed in mice that repeated mRNA dosing (3+ doses) induces T-cell exhaustion (increased PD-1, LAG-3, TIM-3), reducing anti-tumor immunity. Dalgleish: Links this to booster-induced T-cell suppression and an IgG4 antibody switch (Irrgang et al., 2023, Science Immunology), impairing cancer control and driving relapses. Benefit Against Omicron ◻️Severity Reduction: Omicron variants have a CFR of 0.1%–0.3% (Nyberg et al., 2022, Lancet), 50%–70% lower than Wuhan’s 1%–2%. Breakthrough Infections: Boosters reduce Omicron infection by 30%–50% (unboosted: 50% risk; boosted: 35%), with myocarditis and death risks dropping from 0.5 to 0.07 per 1,000 each (0.43 avoided per outcome). Total benefit: 0.86 per 1,000 avoided. Quantified Risk/Benefit Analysis: Total Booster Risk Acute Risks: Swiss: 28 per 1,000 (troponin). Michels et al.: 0.188 per 1,000 mortality (0.476 with SAD). Fraiman et al.: 1.25 per 1,000 AESI. Breakthrough: 0.14 per 1,000 (0.07 myocarditis + 0.07 death). Subtotal: 29.578 per 1,000 (no SAD), 29.866 per 1,000 (with SAD); Thomas et al. reduces this to 29.44 per 1,000. Long-Term Risks: DNA Contamination: Unquantified (oncogenicity, inflammation). Cancer: Gibo’s 2.1% excess population mortality; Dalgleish’s clinical relapses (unquantified per dose). T-Cell Exhaustion: Liu’s preclinical data; Dalgleish’s observed immunosuppression (unquantified). Total: 29.44–29.866 per 1,000 + unquantified cancer/T-cell/DNA risks. Total Unboosted Risk: Myocarditis + Death: 1 per 1,000 (0.5 each). Comparison Fold Difference: ~29.4x–29.9x (acute only), higher with long-term risks. Net Risk Increase: ~28.44–28.866 per 1,000 + cancer/T-cell/DNA vs. 0.86 per 1,000 benefit. Mechanistic Synthesis: ◻️Unified Pathway: Spike spreads systemically (Pfizer biodistribution), persists (Yale), and triggers microvascular damage (Burkhardt), causing heart damage (Swiss), AESI (Fraiman), and sudden deaths (Michels). DNA contamination (Speicher) may induce genomic instability or inflammation, synergizing with T-cell exhaustion (Liu) and immune suppression (Dalgleish), impairing tumor surveillance (Gibo, Dalgleish). VAERS reflects clinical manifestations, amplified by prolonged spike and DNA effects. Regulatory Advice vs. Evidence Current Recommendations (March 24, 2025): FDA/CDC: Updated mRNA vaccines for all ≥6 months, 2 doses for ≥65/immunocompromised, based on 13B+ doses’ safety, no new trials required. Myocarditis rare (4.8 per million), benefits emphasized. WHO/TGA: Safety endorsed, DNA contamination dismissed, pharmacovigilance ongoing. Disconnect Analysis: RCT Mortality: Excess deaths/SAD (Michels) ignored; focus on COVID-19 prevention, not all-cause mortality. Swiss Study: 28 per 1,000 troponin elevation unaddressed beyond rare myocarditis. Fraiman et al.: 1.25 per 1,000 AESI exceeds regulatory estimates, not integrated. Burkhardt: Microvascular damage dismissed as unrigorous. Yale LISTEN: Prolonged spike contradicts degradation claims, unacknowledged. VAERS: Signals minimized, no proactive probe. DNA Contamination: Speicher/McKernan findings rejected, no testing mandated despite SV40 concerns. Cancer Incidence: Gibo’s 2.1% excess mortality and Dalgleish’s relapses (6+ cases) unaddressed; CDC cites no cancer link (e.g., NCI, 2023), but studies predate Gibo and ignore boosters. Dalgleish’s Call: His demand to halt mRNA vaccines (Conservative Woman, 2024) is sidelined. T-Cell Exhaustion: Liu’s preclinical data and Dalgleish’s immunosuppression (IgG4 switch) unacknowledged; regulators assume boosters enhance immunity, not impair it. Omicron: Benefit (0.86 per 1,000) not recalibrated against risks (29.44–29.866 per 1,000 + long-term). Weighting Critique - Bias Toward Benefit: Regulators prioritise preventing severe COVID-19 (waning with Omicron) over mRNA risks, framing myocarditis as rare (0.00048%) despite Fraiman’s 0.125% and Swiss’s 2.8%. Cancer (Gibo), T-cell exhaustion (Liu, Dalgleish), and DNA risks are dismissed as unproven, despite peer-reviewed (Gibo) and clinical (Dalgleish) signals. Mitigation Absence: No strategies (e.g., dose limits, cancer screening, DNA testing) address these risks; 2-dose recommendations for vulnerable groups assume safety without reassessing T-cell or cancer impacts. Evidence Lag: Total risk (29.44–29.866 per 1,000 + unquantified cancer/T-cell/DNA) vastly outweighs benefit (0.86 per 1,000), yet guidance relies on outdated safety data, ignoring Dalgleish’s urgent warnings and supporting studies (Gibo, Liu). Regulatory Inertia: The disconnect reflects a pro-vaccination stance, downplaying mRNA-specific risks—acute (heart, AESI), mechanistic (microvascular, T-cell), and long-term (cancer, DNA)—favoring policy continuity over risk management. Conclusion The growing research, from RCT re-analyses (Michels, Fraiman) to histopathological insights (Burkhardt), prolonged spike (Yale), DNA contamination (Speicher), cancer rises (Gibo), and T-cell exhaustion (Liu, Dalgleish)—reveals a booster risk profile (29.44–29.866 per 1,000 + long-term risks) that dwarfs its benefit (0.86 per 1,000) against Omicron. Regulatory advice fails to reflect this, maintaining universal recommendations without mitigating mRNA-specific risks. Dalgleish’s call to halt boosters, backed by Gibo’s data and Liu’s findings, underscores a critical gap: Regulators prioritize historical safety over emerging evidence, leaving low-risk groups especially vulnerable to an unfavorable risk/benefit imbalance. This disconnect demands urgent reassessment to align policy with science. (Disclaimer: This is not medical advice; consult a doctor. Data reflects research as interpreted, not regulatory endorsement.)" - GROK

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The speaker claims messenger RNA vaccines with the spike protein can induce cancer in multiple ways. They allege the presence of oncogene stimulants, specifically SV40 in the Pfizer vaccine, confirmed by multiple researchers. A paper from Wurzburg purportedly confirms this and shows the vaccines convert cells to cancer. The speaker asserts the spike protein and mRNA vaccines bind to major suppressor genes like P53, BRCA, and MSH, which normally suppress cancer. Mutations in these genes can lead to earlier onset of cancer. The speaker suggests these vaccines could cause the equivalent of mutations in these genes, leading to an explosion of colorectal cancers. They advocate for an immediate ban on these vaccines and accountability for those who oppose it.
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Speaker 0: But one of the things that I just wanted to, really push here, I think we jumped over the slide perhaps that showed it, but the messenger RNA vaccines that, we have with the spike protein, that in those 10 ways that it can induce cancer, I mean there's two or three which are really frightening. One, which has been widely discussed with the contamination issue, is that there are some oncogene stimulants there. S v forty is is in the Pfizer. We know that. And I have a list of people here have been discussed that in the Perth conference recently of all the people who have shown the contamination from McKernan in The US, David Spryker, Koenig Rao, Philip Vacos, etcetera. And there's another, paper just come out from Wurzburg that, not only confirms all this, but shows that they will convert cells to cancer. So we know that that's a direct thing. The second thing, which I really want to emphasize, is the spike protein alone and messenger RNA vaccines will bind to the major suppressor genes. Now the suppressor genes are basically your cancer policeman. If you do get cancer, they will suppress it. P53, BRCA, MSH. MSH is well associated with a thing called Lynch syndrome and colorectal cancer, which is very relevant to the fact we're getting an explosion of colorectal cancers at the moment. So what happens if you have a mutation in any of those three major suppressor genes, you're just unfortunate to be born with it, it means the cancer you would normally get when you were 70 or 80 are going to get with your 20, 30, or 40. By putting this into children, we run the serious risk that we're going to make everybody have the equivalent of mutations in these genes, and it's absolutely horrendous. The very fact that that's a possibility and we're using them for an infectious disease that doesn't kill anybody should strike fear into the heart of all of us. And I believe has leaves no doubt at all that these vaccines must be banned now, and anybody who opposes it, anybody says there's reason for it has to be held to account for what not only has happened, but what is going to happen in the future if we persist with this.

@Humanspective - Humanspective

Conclusion: The growing research, from RCT re-analyses (Michels, Fraiman) to histopathological insights (Burkhardt), prolonged spike (Yale), DNA contamination (Speicher), cancer rises (Gibo), and T-cell exhaustion (Liu, Dalgleish)—reveals a booster risk profile (29.44–29.866 per 1,000 + long-term risks) that dwarfs its benefit (0.86 per 1,000) against Omicron. Regulatory advice fails to reflect this, maintaining universal recommendations without mitigating mRNA-specific risks.

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A clinician observed unusual relapses in melanoma patients stable on immunotherapy for many years, with relapses occurring three weeks to three months post-booster vaccine. This association prompted investigation into a potential causal link. The speaker recalled a model where a third vaccine dose can cause more inflammation than benefit, detracting from the initial doses. A separate group found T cell exhaustion in boosted cancer patients, hindering their ability to police cancer cells. Additionally, post-booster, some individuals exhibited a switch to IgG4 antibodies, which promote tolerance rather than neutralization. This tolerizing effect, desirable in organ transplants, may allow cancer to evade immune detection. Given these scientific explanations and observed relapses, the speaker believes booster shots should be halted, but they are still available to at-risk individuals.
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Speaker 0: Can you explain in simple terms what it is that you are seeing that has got the alarm bells ringing? Speaker 1: Well the first thing I saw doing a regular melanoma clinic that I have been doing for years was that I was starting to see people who were stable that we'd been doing immunotherapy for over twenty years. And I've started to see people who've been stable for five, ten, even twenty years relapse really unusually. They are very fit and healthy. So I basically said, what have they all got in common? And they'd all got in common was they'd had the first booster vaccine. It's around this time. And, I was able to show that they've had it, that the relapse started between about three weeks and three months after the booster vaccine. So I thought this was this is an association. That doesn't mean to say it's causal. I mean, I'm the first to say that. But when you see an association and that it might be actually inducing it, you have to first of all ask why, scientifically, is there a rationale for this? And two, is there anything else? Is it just a coincidence? Well, the thing that alarmed me was that I've done a lot of research on vaccines in my time. And I immediately remembered the model where one vaccine is good, two might help if the first one didn't react properly. But the third actually causes more inflammation, than good and actually detracts from the first two. And, the fourth is even worse. And lo and behold, another group published that, cancer patients who had received a booster had T cell exhaustion. I mean they couldn't have put it better. Speaker 0: And the T cells are policing, they're looking for cancer cells to arrest and detain. Speaker 1: It is a very good way of putting it. And they probably do it on a daily basis. I mean we have abnormal cells rise every day, there's just millions and millions, and that it's very well controlled. We know this that, patients who've had very bad cancer, we can give them the new immunotherapies now to boost their T cell responses and that they can get complete responses and be under control for years. And so this is what was happening with the booster vaccine. It was perturbing this wonderful equilibrium of control and basically interrupting all the resources and it led to a depression of the T cell response. Now I thought that that was, the most likely explanation, but I was amazed at how bad it was in some patients. As I said, they used T cell exhaustion, not T cell suppression, but exhaustion that they're just being stimulated, to the point where they were no no longer able to do their job. And then another paper came out showing that after the booster, not after the first and second, the first and second induce what we call immunoglobulin subtypes. We call these one and three and these make neutralizing antibodies. But after the booster many people now have reported that the subtype switches to four. Now what this means instead of attacking a virus with a neutralizing killing, they switch off to a tolerizing one. An IgG4 is exactly the antibody response you want if you have a kidney transplant or a liver transplant. You want to tolerize the antibodies so they don't go and attack the new kidney or the, renal. So all of a sudden, this starts falling into place. My god. We're switching off the policeman, and then we're tolerizing. And so no wonder the cancer's able to escape. But subsequently, we found many other disturbing reasons why, at the very least, and my point has been that the fact that we have a scientific explanation for this, the fact that we are seeing this should be a red flag and the MHRA should stop all the, the boosters. I mean, they've reduced it for people 75, but if you're at risk, you can still get it. You can buy it at boot. So there was an announcement. I mean, all this is absolutely nonsense for a virus that that has long since gone.

@Humanspective - Humanspective

"Swiss Study on Heart Damage: A prospective cohort study (European Journal of Heart Failure, 2023) found 2.8% (22/777) of booster recipients had elevated troponin levels, indicating subclinical heart damage at a rate of 28 per 1,000—far higher than regulators’ acknowledged myocarditis incidence."

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One in thirty-five recipients of the booster vaccine had vaccine-associated myocardial injury. This is described as an off-the-scale range of adverse reaction in healthcare. It is claimed that in New Zealand and other places the vaccine is still being actively and unethically promoted. The speaker suggests this level of risk would only be acceptable if the alternative was certain death, and calls the current situation complete madness.
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Speaker 0: So one in thirty five participants, one in thirty five recipients rather, one in thirty five who received the booster vaccine had vaccine associated myocardial injury. I'm just gonna read that out again. One in thirty five people who received the booster had vaccine associated myocardial injury. This is a range of adverse reaction that is off the scale in healthcare, off the scale. And yet in New Zealand and other places it's still being actively and unethically some might say promoted. This is just off the scale risks, off the scale completely. The only way you would take this kind of risk in health care over the alternative was certain death. Otherwise, you certainly wouldn't you know, we just don't take this level of risk. It's just complete madness. What has happened here?

@Humanspective - Humanspective

"Michels et al. (2023, IJVT-PR): A forensic re-analysis co-authored by Dr. Jeyanthi Kunadhasan (IJVT-PR, DOI: 10.56098/ijvtpr.v3i2.510) using FOIA-released data found 21 vaccinated deaths versus 17 placebo deaths, an excess of 0.188 per 1,000, with 10/21 (0.476 per 1,000) classified as sudden adult death (SAD), suggesting cardiac or vascular risks." (1:39) "The hidden deaths" (2:24) "What they told the World" (3:21) "One thing that stands out" - The capture rate of deaths for vaccinated V unvaccinated

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The speaker claims that aligning deaths in the vaccine trial to intervention arms shows the vaccine was never life-saving. They allege that at the time of vaccine approval, there were more deaths in the vaccinated arm, but four deaths in the vaccinated arm within the data reporting period were not publicly announced. The speaker states that loved ones of two patients called the clinical site on the day of their death. They felt it was their ethical duty to inform the TGA and Ken Paxton about these hidden deaths. Publicly available data stated four deaths in the placebo arm and two in the vaccine arm. The speaker questions delays in reporting deaths, noting discrepancies in reporting rates between the vaccinated and placebo arms. The speaker wrote to Professor Tony Lawler of the TGA, who allegedly stated there were no hidden deaths and that no deaths in the vaccine arm were due to the vaccine. The speaker highlights that out of 38 total deaths in the six-month period (21 vaccinated, 17 placebo), only seven autopsies were done. Ten of the 21 deaths in the vaccinated arm were categorized as sudden adult death, with some individuals found dead shortly after vaccination.
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Speaker 0: So if you align the deaths as they occurred to the different intervention arms, as they occurred along the timeline, you will see at no point was the vaccine life saving. And when they unblinded, they ended up being more deaths in the vaccinated arm, twenty one to seventeen. But at the point of vaccine approval, it was eleven deaths, six vaccinated, five placebo. So somehow there was a situation where there were four deaths in the vaccinated arm that didn't quite make it that happened well within the data reporting period that didn't quite get announced publicly. Speaker 1: Is there any explanation or any way to possibly find out why those four vaccinated deaths weren't reported? There an explanation to that? Speaker 0: Yes. Well, anyway, so, you know, the explanations that the true explanation will require a whole lot more investigation. For two patients, we have documentation that their loved ones called the clinical site on the day they died. Now there's no excuse Speaker 1: or Speaker 0: actually bears further investigation by authorities that have power to investigate this, that they should find out who told what went. Because if you are someone in a clinical trial, you and your loved ones have done the most they can. They've told the clinical trial site, right? The day they died. I felt that the hidden deaths was such a big thing. I don't, I didn't know if the regulatory authorities knew about it. So, I thought, you know, I've, we found this. I'm a healthcare professional registered in Australia at the moment. I felt it was my clinical and ethical duty to tell the TGA. So, I wrote to the TGA but at that time, I wrote to Ken Paxton as well in in America. So, basically, this is what I'm saying. So this the data cut off is November 14, okay? So, what they publicly told the world in the verb back meeting. So, the verb back meeting is the meeting to approve the vaccine. Yep. And the pollack article is the article that happened that that was published in the New England Journal of Medicine on 12/11/2020. Okay? So what they told the world? So the white is what was actually publicly told to the world. Four deaths in the placebo, two deaths in the vaccine arm. And there's delays in recording death. So these people die. This the data cut off is November 14. These people died October 19. What is happening here? Like what, you know, sometimes when you die, like, maybe everyone's so busy, they're so shocked, they, they forget to tell the clinicals, but they, did they wait really for thirty seven days to tell? Or maybe, you know, they situations where people live alone, people around them may not have known, they, they enrolled in a clinical trial, so they, they did, there are lots of explanations, you know what I mean? Yeah. And you can't really, you can't really delve into it until you actually look at the relevant documentation. Not all relevant documentation is in the publicly available data. But one thing that stands out is there were six deaths in the vaccinated arm, five deaths in the placebo. They managed to report four out of five in the placebo, so the capture rate's about eighty percent. But then when you come to the vaccine arm, they only managed to report two out of six. All the shaded areas were not reported. So, there's already the the reporting system is different in the vaccinated versus the placebo. Something's interesting happening, isn't it? So. Yeah. They would. So, they were hidden debts and also hidden autopsies. So, the one thing to remember as well, when I, I, I wrote to, professor Tony Lawler of the TGA, and he basically said there were no hidden debts, the TGA knew about 11, but you know, it's so hard, and these letters are actually available in our M submission, because the excess death inquiry did not want to publish the report, so even though we presented publicly in the access they only published a summary. So our our full report in the AMP submit is available in the AMP submission which you can find on the AMP's website or if you go to the Daily Cloud. So what happened was Professor Lawler told me that there are no hidden debts, it's just that it's such a big trial, it's hard to keep records. Basically, paraphrasing him, and the other thing that he said was, it's reassuring to note that none of the deaths in the vaccine arm were due to the vaccine. So he wrote that in the letter, in a reply to me. So I wrote to him, he wrote to me, then I wrote to him, then he hasn't replied. And then I wrote back following that, because I was like, you know, first you discount the hidden debts, and then you said no, nobody in the vaccine arm died because of the vaccine. And that's where this comes. Because if you look at it remember I said in the six month period there were thirty eight deaths. So twenty one vaccinated, seventeen placebo, total autopsies done were only seven. But ten of the twenty one people that died, and this is available in my letters that I've written to Professor Lola, ten of the twenty one that died in the vaccinator arm actually had sudden adult death. They were found dead. The circumstances of their death, some people went walking, they had a cardiac arrest. Some people were like found, you know, the somebody said the next door, the apartment smells, you gotta go check it. Oh, dear. And then some one person died three days after the shot, but it was like they were found dead in their house three days after the one shot, and then only found because of a welfare check.

@Humanspective - Humanspective

"Serious Adverse Events (Fraiman et al.): Fraiman et al. (2022, Vaccine, DOI: 10.1016/j.vaccine.2022.08.036) re-analyzed Pfizer and Moderna trial data, identifying an excess risk of serious adverse events of special interest (AESI) at 1 in 800 (1.25 per 1,000), including myocarditis and coagulopathy." Dr Aseem Malhotra dives deep on that data here

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The speaker believes exposing the "indoctrination" of billions regarding the vaccine will be difficult. Their strategy involves publishing in a peer-reviewed journal and getting media coverage. Research, including consultation with whistleblowers and scientists, led to the conclusion that the vaccine should be suspended. Reanalysis of Pfizer and Moderna trials by scientists, including the associate editor of the BMJ, revealed that individuals were more likely to suffer serious harm (hospitalization, disability, life-changing event) from the vaccine at a rate of one in eight hundred than be hospitalized with COVID during the early phase. This harm rate, applicable across all age groups on average, is deemed unacceptable, as past vaccines with lower harm rates (e.g., swine flu, rotavirus) were suspended. Serious harms were defined as those causing hospitalization, disability, or life-altering events, with 40% related to clotting disorders.
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Speaker 0: It's because of such an indoctrination, because so many people, billions of people around the world have taken this. And therefore, the the the battle to expose it is gonna be harder than anything I've ever done. The only way in, my only chance is to get it published in a peer reviewed journal and then to get it into the news. I spent nine months at that stage literally eating, breathing, sleeping, speaking to two fighter whistleblowers, speaking to eminent scientists in expertise I didn't have around immunology and vaccine development. Of course, I had the understanding of cardiology, you know, better than anybody in this particular field, this particular area. And when I did that research and looked at it, I first of all concluded that there absolutely needs to be a suspension of the vaccine because, what happened by the summer of twenty twenty two, and this is actually the the most crucial and important piece of data on its own, which should have been enough to suspend it and actually suggest that it probably shouldn't have been rolled out in the first place, is that those trials that were done by Pfizer and Moderna, which led to all the media reports 95%, one hundred % effective, you know, the approval by the regulator, the rollout, the coercion, the mandates, they were reanalyzed by some very eminent scientists, including the associate editor of the BMJ, one of the world's top epidemiologists, and they published in the journal Vaccine, which is the premier journal for vaccines. And they were able to get new data that was made available on Health Canada's website and the FDA in America's website. And what they did in their re analysis of the original high quality clinical trials is they found, Steve, you were more likely to suffer serious harm from taking the vaccine at a rate of one in eight hundred, that meant hospitalization, disability or a life changing event, than you were to be hospitalized with COVID. And this is during the early phase, right? This is during the most lethal strain. Speaker 1: All age groups? Speaker 0: Yes. Well, absolutely. Well, they put all age groups together. So on average in all age groups, that's a very good question. But what's missing is that actually, okay, is there a benefit that's greater than harm in certain age groups? But we can indirectly answer that in a second. So that was the original trial. So on average, it was more harmful than beneficial. Okay, a one in eight hundred harm rate for a vaccine is completely unacceptable in the sense that we have pulled other vaccines in the past for much less harm. The swine flu vaccine was suspended globally because it was found to cause Guillain Barre syndrome, a debilitating neurological condition in one in a hundred thousand people. Rotavirus vaccine was pulled in 1999 because it was found to cause a form of bowel obstruction in children at one in ten thousand. So you've already got a harm rate of one in eight hundred irrespective of, right? So that first and foremost should be a red flag to say hold on, this is this is too much. Speaker 1: When they say harm rate, how do they what's the range of definitions of harm? Speaker 0: Well, this one, categorize serious harm as it caused you to be hospitalized. Yeah. It caused a disability or something that was life changing. Now, course, that can incorporate lots of different things. But of those, and I spoke to lead researcher, I know work with him on other things, forty percent of those serious harms were actually related to clotting disorders like lung clots, heart attacks,

@Humanspective - Humanspective

"Burkhardt’s Histopathology Dr. Arne Burkhardt’s autopsies (2022 presentations) revealed spike protein (no nucleocapsid) in microvessels of heart, kidney, and brain, with lymphocytic infiltration, endotheliitis, and microthrombi, linked to sudden deaths post-vaccination, consistent with Michels et al.’s SAD findings."

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The speaker observed vasculitis, or inflammation of the blood vessels, in the brain tissue of almost all cases examined post-vaccination. Lymphocytes aggregate around small vessels, indicating inflammation possibly triggered by an antigenic structure like spike protein. This was described as one of the most alarming findings. Individuals with this complication may experience transient defects like loss of speech, unconsciousness, or blindness, but the brain can compensate if there is no major inflammation or hemorrhage. The speaker clarified that the individuals did not die from the vasculitis itself. It's possible for vaccinated individuals to experience these symptoms without knowing the underlying cause. Changes in character have been reported in some vaccinated individuals, which may be related to this inflammation.
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Speaker 0: Now these next two images and cases that we will discuss are from your own studies in which you observed vasculitis of the small blood vessels in the brain. This is now the second time that we mention vasculitis so just a reminder for everybody that is an inflammation of the blood vessels. If you could again for us just describe what is being observed in these two images here. Speaker 1: Yes, well actually this is one of the most alarming findings that we had from the beginning on that if you really look closely at the brain tissue sections, you find this vasculitis in almost all cases. In many cases it's very discrete, but you have to look for it. And these are two images where you can see you really have to look closely to see that these small vessels in the brain, the endothelium is swollen, but then there are these small blue dots. These again are lymphocytes which aggregate around these small vessels. Speaker 0: And lymphocytes cause inflammation? Speaker 1: The fact that lymphocytes are found there means that there's some inflammation probably triggered by some antigenic structure, in this case maybe a spike protein or something from the vaccination. And as I said, this is a finding that in minimal degree is found in almost all of these people who died after vaccination. And actually we have seen it also in one needle biopsy from the brain. Come to this And in many of these cases which have more pronounced inflammation of the vessels of the brain, There have been transient defects like loss of speech for a few hours, unconsciousness for some hours, blindness for some hours. The brain is if there's no major inflammation and no hemorrhage, the brain is able to compensate again. But of course this is a very striking side effect. Speaker 0: So just in order for me to summarize what you had just said, this finding here was one of the most concerning. It is also one that is very commonly seen in people who have died post vaccination. Speaker 1: Yes. Speaker 0: And it can oftentimes individuals with this complication have had periods of blindness, inability to speak properly. Is that correct? Speaker 1: Yes, yes. Now just to get this clear, I mean they did not die from this. Is something we find. We find other cases where there's bleeding and hemorrhage in the brain and they died of it, but this is just a side effect which may be compensated and healed to a certain degree. Speaker 0: So somebody who's listening right now or anybody could have received the COVID-nineteen vaccine, they could have this very issue, experience some symptoms and not even know that they are experiencing Yes, exactly. Speaker 1: And actually in some cases a change in the character of these vaccinated is reported. Sometimes it's irreversible and apparently in some cases not. And this may be one of the reasons.

@Humanspective - Humanspective

"DNA Contamination: Speicher et al. and McKernan et al. (2023, OSF Preprints) found residual plasmid DNA (30–100+ ng/dose) in Pfizer and Moderna vials, exceeding WHO/FDA limits (10 ng/dose), with SV40 promoter/enhancer sequences in Pfizer raising theoretical risks of genomic integration and oncogenicity."

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The speaker states they found four pieces of the virus, not the whole virus. The pieces found include the SV40 origin of replication, the SV40 promoter, the SV40 enhancer, and part of the poly A signal. The speaker claims David Dean published that the SV40 enhancer is a nuclear targeting sequence. Therefore, claims that it will not reach the nucleus are inaccurate. The speaker asserts the presence of the SV40 origin of replication, a mammalian origin of replication, means it will replicate inside mammalian cells. The speaker believes regulators need to consider this risk.
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Speaker 0: So we didn't find the whole virus. The whole virus is about 5,000 bases long. We did find, the s v 40 origin of replication, which is important. I'll touch on that. The s v 40 promoter, and the s v 40 enhancer and one other piece of it, the the a part of the poly a signal. Those four pieces. But the s v 40 enhancer has been published by David Dean to be a nuclear targeting sequence. So other people who are claiming this will never get to the nucleus aren't really aware that no, there's the sequence in this plasma and drives it straight information there is the SV40 origin of replication. That's a mammalian origin of replication. What that means is when that gets into a mammalian cell, it starts making more of itself. So that's I think that's a very important risk that the regulators need to consider.

@Humanspective - Humanspective

[@joerogan] “Everything Dr. Robert Malone said has turned out to be true. All of it. Including Yale just released some study about people producing spike proteins 700 plus days after the injections.” The Yale LISTEN study (2025, preprint) detected spike protein in blood up to 709 days post-vaccination, with elevated cytokines (IL-6, TNF-α), suggesting chronic immune activation that could amplify Burkhardt’s observed damage.

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The speakers discuss an interview with Robert Malone that received significant pushback. One speaker expresses disappointment in individuals like Joni Mitchell and Neil Young, wishing they would review studies and Robert Kennedy's book to become better informed. The speakers claim mainstream media's objectives prevent them from discussing certain topics. They suggest those criticizing the Malone interview likely hadn't listened to it, instead relying on mainstream media's portrayal of it as dangerous misinformation. One speaker asserts that everything Malone said has proven true, including claims about the lab leak, vaccine side effects, distorted studies, and information suppression. They mention a Yale study indicating spike protein production over 700 days post-injection, contrary to initial beliefs. They allege cover-ups, obfuscation, and doctors downplaying issues to avoid repercussions from mandating the injections.
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Speaker 0: Liked your interview with Robert Malone. Speaker 1: Yes. Speaker 0: That was a crucial interview at a crucial time. Speaker 1: Well, that was the most pushback I'd ever experienced ever in my life, and I was like, this is crazy. When you it was really sad to see people like Joni Mitchell and Neil Young and, like, what you got I wanted to sit down and talk to them and, like, show them some studies and give them Robert Kennedy's book and say, like, you don't really know what you're talking about. Speaker 0: Well, that's the thing that makes me sad is a lot of this information they're receiving is, from mainstream media Speaker 1: Yeah. Speaker 0: Which certainly has its own objectives and its own, you know, things that it won't discuss. Yes. You know? Yeah. At all. And and yeah. And I I just felt like after that happened, you know, I almost I was gonna try to get in touch with you just to tip my hat to you, but it it just felt like, why don't people just listen to the interview? Because I feel like everyone who was giving it a hard time hadn't even heard the interview. Speaker 1: Of course. Yeah. They had heard the mainstream media saying that it was dangerous misinformation. By the way, everything he said has turned out to be true. Every single thing he said had turned out to be true. Everything that everybody said about whether it was a lab leak, whether the vaccine had side effects, whether it was pushed, whether they lied about the the studies and and distorted the information, everything was true. Speaker 0: All of it. Speaker 1: Including Yale just released some study about people producing spike proteins seven hundred plus days after the injections, which is never injections, which is never thought to be the case when they gave them to these people in the first place. A host of different serious problems that people are having because these that everyone's covering up and people are lying about and everyone's trying to obfuscate and doctors are trying to sweep things under the rug because they don't wanna be in trouble for mandating these things and telling people Speaker 0: to
Humanspective
Posted - January 24, 2025 at 7:35 PM
Saved - January 30, 2025 at 6:40 AM
reSee.it AI Summary
I’m shocked by the revelations surrounding the petition signed by 17,000 doctors against Robert F. Kennedy Jr., which is reportedly funded by a dark money network called Arabella, with Bill Gates as a major donor. Gates has contributed nearly $456 million to Arabella since 2008, including $127 million in 2020. Additionally, Dr. Rob Davidson, leading this petition, has ties to the controversial drug Remdesivir, which has raised concerns over kidney damage and was promoted in hospitals with financial incentives. This situation highlights troubling connections in health advocacy and funding.

@Humanspective - Humanspective

This is crazy. [@JillianMichaels] has exposed a dark money network, but there's MORE. The Petition of 17k "Doctors" used to discredit Robert F Kennedy Jr, is funded by a Dark Money network called Arabella. Who's their biggest donor? Bill Gates. One source says they are the BIGGEST donor. So, whilst Bill had a private dinner with Trump, a Dark Money network called Arabella was used on the sidelines, to discredit RFK Jr. Bill Gates donated $127 million to Arabella in 2020. When Bill Gates told Trump in 2017 "don't do that" regarding a vaccine safety commission, he was already funding this Dark Money network used to discredit RFK. "The Bill and Melinda Gates Foundation is the single largest donor to Arabella groups yet identified, weighing in at close to $456 million since 2008, including $127 million in 2020 alone." https://capitalresearch.org/article/who-are-arabellas-big-dollar-donors/

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President-elect Trump expressed thoughtful concerns regarding vaccine safety and scientific integrity. He indicated strong support for solar energy, which aligns with my advocacy for clean energy. I believe Trump has the potential to be an unencumbered president, free from heavy ideological constraints. During our conversation, he raised questions about current vaccine policies, emphasizing the importance of scientific integrity in ensuring vaccine efficacy and safety. He acknowledged his doubts but affirmed his pro-vaccine stance, as do I. I also confirmed my willingness to chair the commission on vaccine safety and scientific integrity.
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Speaker 0: President-elect Trump was very thoughtful on the issue. He asked the chair commission on vaccine safety Vaccine safety. And, and scientific integrity. Speaker 1: It's kind of ironic. While you were up there, some executives from BHP, a mining company, were up there. How concerned are you that he will, not pursue fossil fuels as he has said he would and may, try to roll back some of Obama's policies on clean energy, which has been something that you've been very interested Speaker 0: in. I was vocal about my support for clean energy, and, president Trump told me that he is a very strong supporter of solar energy. I and I I'm gonna be focusing on this issue for the White House. Speaker 1: Mindly, if I can ask you, how do you think, your father, uncle Teddy, president Kennedy himself would think about a, what is to be a president Trump? What do you think their thinking would be? Speaker 0: I think that, you know, president Trump can be any kind of president that he wants to be. He's probably coming to office less encumbered by ideology or by obligations than anybody that has been in the legal office. Who has run the want the presidency at least at least since Andrew Jackson. Oh, I'm, you know, I think we'll see what happens. Speaker 1: Did you request the meeting, or did he call did his team call you? He called. And what is it that you're looking for in terms of policy on the vaccines? Speaker 0: Make sure that we have a, that we have scientific integrity in the vaccine process for efficacy and safety of vaccines. President-elect Trump has some doubts about, about the current vaccine policies. He has questions about it. He says his opinion doesn't matter, but he but the science does matter. And we ought to be reading the science and we ought to be debating the science. And, and that everybody ought to be, be able to be assured that the vaccines that we have, he's very pro vaccine, as am I, but that they're as safe as they possibly can be. Speaker 1: And you said he's pro solar energy. He said he supports solar energy. Speaker 0: He told me that he was a big fan of solar energy. Speaker 1: You you seem like you don't believe it. Speaker 0: Oh, I I I'm very happy to hear it. Speaker 1: Did you guys talk about him taking any type of an official role in the transition or in the administration? Speaker 0: Chair commission on vaccine safety and scientific integrity. Speaker 1: And what did you say? Speaker 0: I said I would.
Who Are Arabella’s Big-Dollar Donors? America's Investigative Think Tank capitalresearch.org

@JillianMichaels - Jillian Michaels

How crazy is this… The supposed letter signed by “over 17000” doctors denouncing @RobertKennedyJr is actually fake. Take a look. https://t.co/rdeljbEmdf

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In light of RFK's upcoming confirmation hearings, a letter claiming to be signed by 17,000 doctors urges the Senate to reject his nomination due to his alleged misinformation about vaccines. However, upon investigation, it turns out anyone can sign this letter multiple times, raising suspicions about its credibility. The Committee to Protect Health Care, which organized the letter, claims to avoid funding from pharmaceutical companies, but it is backed by the Arabella Advisors network, a dark money organization that manages significant funds without disclosing its donors. This network's influence on public policy and its use of astroturfing—creating the illusion of grassroots support—raises concerns about transparency and accountability. The letter's legitimacy is questionable, as it relies on unverifiable signatures and is funded by a network with a clear agenda.
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Speaker 0: In anticipation of RFK's confirmation hearings next week, I'm already starting to notice more baloney in the zeitgeist. And there's one that I wanna address in particular because it would seem unbelievably credible. This I'm referring to is the letter supposedly signed by 17,000 doctors that was organized by the Committee to Protect Health Care, which would seem pretty credible. Right? And this letter urges the Senate to reject Kennedy's nomination, citing his history of spreading misinformation about vaccines and public health interventions. So I thought, jeez, really? 17,000 doctors signed this? This seems crazy. So I clicked on the letter. And guess what? I signed it twice. One says doctor Fake and one says doctor BS. See for yourself. Anybody, anywhere can sign this supposed letter repeatedly. So I personally, under 2 different aliases, am 2 of the 17,000 doctors that signed this letter. Now that seems pretty suspicious. So I wondered, well, who funds the CTP, the Committee to Protect Health Care? Because they claim that they don't accept donations from pharmaceutical companies, insurance companies, or other for profit health care corporations and rely instead on support from medical professionals and advocates. Advocates. So who are these advocates? I asked ChattGPT. Pretty simple and straightforward. And it told me that 2 of these organizations that fund the Committee to Protect Health Care would be the Hopewell Fund and the 1630 Foundation. So I thought, like, okay. Well, who funds these 2 companies, and what are they about? And when you get all the way to the bottom of it, it turns out that, this is all funded and organized by a group called Arabella Advisors. Now Arabella Advisors Network operates as a, quote, dark money organization. And I'm not talking about drugs or cartel. I'm talking about the fact that they have tremendous political influence and they never have to disclose their donors. So they do in fact fund Hopewell and the 1630 fund and other funds like the Windward Fund and the New Venture Fund. These guys manage 1,000,000,000 of dollars, 1,000,000,000. Please search this for yourself. Ask chat GBT. Scale of operations. The Arabella network manages 1,000,000,000 of dollars in donations, making it one of the largest and most powerful forces in modern philanthropy. Its size and reach have raised concerns about its disproportionate influence on public policy and political processes. There are allegations of astroturfing. I thought, what the hell is astroturfing? Arabella managed funds sponsor numerous advocacy campaigns and initiatives that often appear grassroots but are funded by the same network. This practice, known as astroturfing, creates the illusion of widespread public support for specific issues. The network frequently uses donor advised funds, or DAPs, to funnel money into its projects. While legal, this practice allows donors to remain anonymous, further fueling concerns about transparency and accountability. Now I don't know about you, but that sounds shitty as shit to me. A letter that anybody can sign with 0 credentials as many times as they want to that is claiming to have over 17,000 signatures by medical professionals, which I've already shown you is clearly a lie. And they claim not to take money from pharma or insurance, etcetera, etcetera, but they're funded by the Arabella Network through different shelled five zero one c four and c three companies who doesn't disclose who its donors are and who absolutely has an agenda, manages 1,000,000,000 of dollars and strategically places those 1,000,000,000 of dollars to facilitate its agenda. Give me a freaking break.

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MORE: Dr Rob Davidson leads the group behind the petition Jillian Michaels has exposed, funded by Dark money and Bill Gates, which is being used to discredit Robert F Kennedy to head HHS. This same DR said people "jump" at the chance to be given Remdesivir, the drug which Mel Gibson said "I couldn't walk for 3 x months after I had that stuff" According to GROK: “A course of Remdesivir was priced at $3,120 for a five-day treatment for patients with private insurance in the United States. For government programs in developed countries outside the U.S., the cost was $2,340 for the same five-day course” There was an incentive structure in place for this expensive drug, which meant, According to @P_McCulloughMD, that "the HHS offered a 20% bonus on hospital stays if they used Remdesivir, which the WORLD HEALTH ORGANISATION recommended against using for covid. Also according to GROK: "The person most prominently associated with Remdesivir from the National Institute of Allergy and Infectious Diseases (NIAID) is Dr. Anthony Fauci. Dr. Fauci, who was the director of NIAID, was instrumental in leading the research and trials on Remdesivir, including the Adaptive COVID-19 Treatment Trial (ACTT) which showed that Remdesivir could accelerate recovery from advanced COVID-19. His involvement also included the allocation of significant research funding and resources to study and develop the drug". According to GROK: "Remdesivir can have effects on kidney function, and here's how: Acute Kidney Injury (AKI): Several studies and clinical trials have reported cases of acute kidney injury in patients treated with Remdesivir. The incidence of AKI in these studies varies but indicates that Remdesivir can be nephrotoxic. This effect might be due to direct toxicity to kidney cells or could be related to the formation of Remdesivir's metabolite, which might accumulate and cause damage. Mechanism of Nephrotoxicity: Remdesivir is metabolized into an active form that can inhibit RNA-dependent RNA polymerases in viruses, but this metabolite could also potentially affect human cells. There's speculation that this metabolite might accumulate in renal tubular cells, leading to injury. Pre-existing Kidney Conditions: Patients with pre-existing kidney disease might be at a higher risk when treated with Remdesivir. The drug's label includes warnings about its use in patients with renal impairment, suggesting dose adjustments or monitoring. Hydration and Monitoring: Clinical guidelines often recommend adequate hydration for patients receiving Remdesivir to help mitigate potential kidney damage. Regular monitoring of kidney function, including serum creatinine levels, is advised to detect any signs of kidney injury early. Study Findings: The ACTT-1 trial noted an association between Remdesivir use and kidney injury, although causality was not definitively established. Subsequent analyses and case reports have continued to highlight this association" - END QUOTE. DR's worked within Hospital settings that had an incentive structures in place to prescribe Remdesivir, a drug with detailed effects on Kidney function. Jillian Michaels has exposed the Dark Money group Arabella, as being connected to the 17k "DR" petition from "Committee to Protect Health Care", headed by a DR that serves it's interest....and it's largest Donor is Bill Gates, the philanthropist trying to dictate how the World does Global health.

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Patients were desperate for ivermectin as their loved ones died, but the focus shifted to remdesivir, a previously failed Ebola drug. By November 2020, the World Health Organization advised against its use, citing ineffectiveness and potential kidney and liver damage. The European Society of Critical Care supported this stance. Despite the warnings, the U.S. Health and Human Services incentivized hospitals with a 20% bonus for administering remdesivir, leading to widespread use. It failed to reduce mortality and caused serious injuries, with some patients dying as a result. In May 2022, the WHO reaffirmed its initial decision, stating that remdesivir should never have been used.
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Speaker 0: Were screaming. They were begging for the use of ivermectin as their loved ones died. It couldn't get any worse than this. We do pick up on one treatment that was featured by the US government, and it was a disaster, and that was remdesivir. Remdesivir, a former failed Ebola drug and polymerase inhibitor, by November of 2020, the World Health Organization said, do not use remdesivir. Do not use it. It doesn't work. It can cause kidney injury and liver injury. They had a meeting. European Society of Critical Care agreed. They had a human ethicist meeting, and this WHO declaration was very important. The world needed to pay attention to the proclamation that remdesivir should not be used. What HHS did in America is they added a 20% bonus on the entire hospital say if hospitals use remdesivir against the WHO contraindication warning. And in fact, remdesivir was given to countless numbers of Americans. It did not reduce mortality and cause liver injury and kidney injury, and some who was in the causal pathway to death. You know, the WHO revisited the remdesivir decision in May of 2022 in Lancet, and they concluded they were right from the very beginning. Remdesivir never should have been used in a single
Humanspective
Posted - July 23, 2024 at 10:38 AM
Saved - January 26, 2025 at 11:53 AM
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I’ve been exploring the complex narrative surrounding overpopulation and its ideological roots. It seems that while many in Western society fear unchecked human reproduction, figures like Elon Musk argue we face a potential population collapse. Key organizations, like the World Health Organisation and influential individuals, including Bill Gates, have historically shaped this narrative, often promoting population control measures. This has led to significant actions, such as forced sterilizations in India during the 1970s, raising questions about the motives behind these policies and their impact on global reproductive health.

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OVERPOPULATION THEORY - Ideology | Mindset 🧵 https://t.co/m0Kkx0NouW

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Population and reproductive health are urgent issues. Growing up with parents involved in volunteer work, particularly Planned Parenthood, shaped my perspective. Looking ahead 10 to 15 years, I aim for significant improvements in mortality rates in developing countries, which can help reduce population growth and enhance education and nutrition. We are committed to rigorous tracking of our progress, with an expectation of high impact from our investments. Currently, the world population is about 6.8 billion, projected to reach 9 billion. By improving vaccines and healthcare, we could potentially reduce this growth by 10-15%. Our goal is to cut child mortality from 9 million annually by half through new vaccines, allowing societies to better care for themselves.
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Speaker 0: Shoe that really grabbed me as as urgent, was were issues related to population, reproductive health. Speaker 1: But did you come to reproductive issues as an intellectual? Speaker 0: When I was growing up, my parents were always involved in various, volunteer things. My dad was, head of planned parenthood. Now if you look forward and, at your next career step, career maybe not the right word here. But, at your at your next life phase, what what would you like to see as your legacy in 10, 15 years? Speaker 2: Of the new work? Speaker 0: Of the new work. Yeah. If your new function. Speaker 2: Well, I've I've set very ambitious goals because I'm quite optimistic. You know, huge change in the mortality rates in developing countries, which then has this effect of reducing population growth. That's this big benefit that then makes everything like education and nutrition a lot easier. So I have very high expectations there. And we actually use these dashboards internally at the foundation to make everything be quite numeric. We're trying to be rigorous about that and even share those so that people can see, Oh, you fell short of what you had in mind. And then 15 years, boy, we, you know, by then, we will have spent a lot of money. 3,000,000,000 a year, 15 years, that adds up. And for that, people should have a very high expectation of what we can do. Let's take a look. First, we've got population. The world today has 6,800,000,000 people. That's headed up to about 9,000,000,000. Now, if we do a really great job on new vaccines, health care, reproductive health services, we could lower that by perhaps 10 or 15%. But there we see an increase of about 1.3. Speaker 1: $10,000,000,000 over the next 10 years to make it the year of the vaccines. What does that mean exactly? Speaker 2: Well over this decade, we believe unbelievable progress can be made, both inventing new vaccines and making sure they get out to all the children who need them. We could cut the number of children who die every year from about 9,000,000 to half of that, if we have success on it. And the benefits there in terms of reducing sickness, reducing the population growth, it really allows the society a chance to take care of itself, once you've made that intervention.

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1. One pervasive ideology that seems to have penetrated western society seems to be the idea that rate of human reproduction and growth is destroying the planet. https://t.co/HovtFFATbB More recently there have been opposing figures that reveal they think we are actually on the brink of population collapse. Recently Elon Musk spoke out about what he deems as an existential thread to the survival of humanity. That is, Population Collapse. What's mind blowing is, that Elon Musk was aware of this more than 20 x years ago, when prominent opposing figures have been arguing the destruction of the Planet from unchecked Human reproduction For the last few decades, or at least for the last half of the 18th century, key figures, organisations and countries have been involved in the propagation, financing and policy making to control “rapid population growth” and deal with in forms described as "reproductive health". These figures and organisations, have unfortunately held more power and influence over how the message of population has been shaped Globally in all forms of society This is an important point. Can you imagine for example, what would would have happened to the direction of the World Health Organisation, if the 80%+ of funding it gets from Bill Gates, was instead received from pro-expansionist minded people like Elon Musk? So who are the key figures and organisations that seem to be controlling this narrative? The obvious ones that we all know about are: ◻️Bill Gates ◻️World Economic Forum (WEF) ◻️World Health Organisation (WHO) ◻️Population Council ◻️The Eugenics Movement For the purposes of this thread and to build upon it in future threads, I'll just limit it to a narrow group. Because it gives us a good overview of how finance and Global organisational influence has dictated how the message of population is delivered and which then influences the minds of citizens that reside in both western democracies and developing nations What’s the truth about Population growth? Who's right? Is Elon Musk an important person to listen to, or is the "Extinctionist movement" (as Elon puts) correct in assuming that Humans will eventually destroy Earth if they are left to reproduce without government controls in place? As you'll see further in this thread, the more important and nuanced question to ask is - "Is overpopulation theory something that applies to all countries equally? Are the true motives more related to national security issues, or a fear of being out-birthed?" In other words, is Western Civilisation trying to control the rates in other societies because they feel threatened, which is also in turn creating a global problem of reproductive health services and mindset influencing citizens in countries that have declining birth rates? One of the earliest examples of this idea (not the earliest I'm sure) to present here are from Eugenics publications in the early 1900'ds. Some of the key passages I'll describe, begin to paint a picture about the fear of the rate of reproduction in other other countries like India, whilst at the same time clearly mentioning concerns of birth rate DECLINE in Western Civilisations, such as Britain This made me ponder the idea that the whole ideology of overpopulation as being more nuanced and complicated then originally thought. It includes factors like religion, ethnicity and national security. And when different civilisations meet to address what they deem a problem, may not be a problem for both sides of the equation. And also the people that are shaping the narrative of overpopulation may also be corrupting and influencing the minds of people in countries that clearly have declining birth rates

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At the same time Bill Gates began exerting his influence on "Reproductive Health", with fear based propaganda on "Population Bombs" and the economic dangers of Population Growth, Elon Musk Noticed the OPPOSITE. "I noticed this 20+ years ago, that the trend in birth rates, really for all countries [was] trending to well below replacement" It's the fight of the Titans - Bill Gates, "Population Extinctionist" versus Elon Musk "Population Expantionist" mentality. The key difference though, is that Bill Gates has a majority financial controlling interest in the World Health Organisation. That's played a large part in the different outcomes we see in "Global Health"

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We're facing a natal crisis, which is a significant issue. The declining birth rates across developed nations could lead to cultural extinction. This trend has been evident for over 20 years, and if it continues, many cultures may dwindle away. A loss of religious values may contribute to this antinatalist sentiment. However, seeking greater enlightenment and understanding of the universe can sustain civilization. A population increase is desirable as it brings more minds and diverse cultures, expanding our collective consciousness. Ultimately, a larger population can enhance our understanding and exploration of existence.
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Speaker 0: Yeah. Well, okay. So let me let me put a twist on that too. So one of the things that really struck me about your public pronouncements in recent years was your insistence that we're in a natal crisis and Speaker 1: that that's actually a problem because Well, that's factually true. Speaker 0: Well, well, it depends whether you think the pop the planet would be better off if it was depopulated. Speaker 1: I don't I don't I'm not interested in this. Yeah. Paul Illich is a genocidal maniac as far as I'm concerned. And I I he's a terrible human being. Speaker 0: Yes. And he's never admitted that he was wrong, He was unbelievably wrong. He made a famous bet, you know Speaker 1: the bet. Yes. I hate Polo. I gotta be clear about that. I think he's terrible and and his books have done great damage to humanity. Speaker 0: How did you start to understand that the one of the fundamental ethical problems is different than the scientific problem. One of the fundamental ethical problems that's plaguing the West is this catastrophically low birth rate. Again, and, you know, when you start making public I'm Speaker 1: observing the numbers. I mean, I've noticed this 20 plus years ago, that the trend in birth rates for, really, all countries, past certain level of economic development, was trending to well below replacement, if not already below replacement. And if you extrapolate the the curve, which one always has to be cautious about extrapolating any demographic curve. But if you're if so I always preface by saying if these trends continue Yeah. Yeah. Most countries will will dwindle into insignificance. They might completely die out. I think there is there's an argument that that, when a culture loses its religion, that it starts to become antinatalist and decline in numbers and, potentially disappear. Yeah, the question or, you know, is it another way that seeking greater enlightenment, and a better understanding of the universe and more questions to ask about it, is something that we can continue to, do as a civilization for a very long time. Speaker 0: Yeah. Yeah. Likely forever. Speaker 1: Right. Exactly. So Speaker 0: Depending on how powerful grok turns out to be. Speaker 1: Yeah. So that's so then I thought, okay. Okay. I'll work on, things that improve our understanding of the universe. Now they're saying, like, at a base level, well, this is why I I actually think we want a population increase, because population increase means that there are more people, that that we've expanded the scale More brains, man. Yeah. We've expanded the scale of consciousness, to the degree there are different cultures. We've expanded the scope of consciousness.

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2. January 1938 - "The Eugenics Review". This publication is from 1938. Another interesting mention is the case of a women that was Sterilised against her will and was suing her own mother. According to this case, at this time, children were “RATED” intellectually and mentally, to see whether it was legally allowed or recommended to sterilise a child. In this case, the 20 x year old child was mentally rated to an 11 x year old, so the parents agreed to sterilise her. Just imagine your own child. They all seem so intelligent even at a much younger age. How were they rating them? Was it accurate? Was it because of the education they were receiving? What factors were involved? QUOTE from a 1936 Sterilization Case: "Miss Hewitt sued her mother and two medical practitioners for $500,000 on the ground that without her knowledge or consent these practitioners had sterilized her at Ms Hewitt's (mother) request. Ms Hewitt and the practitioners pleaded that the operation was for Miss Hewitt's welfare, a California State Health Department psychologist having rated her in 1934, when she was 20, as having a mental age of 11" So here we can clearly see a landscape of ideology that was very harsh on the idea of human life. We can see that Eugenics was initially a key ideology in some western democracies, that worked in sterilization campaigns as a form of population control. At this point there was already CLEAR evidence of birthrate decline in the Western World, with fear of population growth in other countries. And yet Globally since then, many key figures have pushed the idea that the population is growing far too rapidly QUOTE: "He said that ever since about 1870 our birth-rate had been falling more and more steeply [that meant] that our population would then start decreasing-at first slowly, then progressively faster". Added to that was "Perhaps the most disquieting phenomenon of a declining birth-rate was the progressive rise in the average age of the population [so how would] this affect the security of the Empire? and our standard of life"? While we and the other Western Powers would be declining in numbers, the countries of the Balkans, Soviet Russia, and the peoples of the far East (with their already vast populations) would still be continuing to multiply" So then, why is it that modern day proponents say our population is growing too rapidly? Is it possible that the real reason behind this push, is because fertility in western nations were falling but other developing countries and religions were rising and the message was confused so that western countries adopted the idea, further increasing the rapid rate of birth decline in Western democracies?

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3. THE WHO - In 1948, The World Health Organisation came into being. At that point it gave itself full immunity from liability. According to this document, they can’t be arrested or held accountable for any damage they cause. After the nation states all signed up and the WHO was created, one of the key policy focuses following that, was the idea of population. The WHO have been instrumental in developing methods and advising on Global policy for curbing population growth "CONVENTION ON PRIVILEGES AND IMMUNITIES" ANNEX VII - THE WORLD HEALTH ORGANIZATION In their application to the World Health Organization (hereinafter called “the Organization”) the standard clauses shall operate subject to the following modifications: 1. Article V and Section 25, paragraphs 1 and 2 (I), of Article VII shall extend to persons designated to serve on the Executive Board of the Organization, their alternates and advisers, except that any waiver of the immunity of any such persons under Section 16 shall be by the Board. 2. (i) Experts (other than officials coming within the scope of Article VI) serving on committees of, or performing missions for, the Organization shall be accorded the following privileges and immunities so far as is necessary for the effective exercise of their functions, including the time spent on journeys in connexion with service on such committees or missions: (a) Immunity from personal arrest or seizure of their personal baggage; (b) In respect of words spoken or written or acts done by them in the performance of their official functions, immunity of legal process of every kind, such immunity to continue notwithstanding that the persons concerned are no longer serving on committees of, or employed on missions for, the Organization; c) The same facilities in respect of currency and exchange restrictions and in respect of their personal baggage as are accorded to officials of foreign governments on temporary official missions; (d) Inviolability for all papers and documents; (e) For the purpose of their communications with the Organization, the right to use codes and to receive papers or correspondence by courier or in sealed bags (ii) The privileges and immunities set forth in paragraphs (b) and (e) above shall be accorded to persons serving on Expert Advisory Panels of the Organization in the exercise of their functions as such. (iii) Privileges and immunities are granted to the experts of the Organization in the interests of the Organization and not for the personal benefit of the individuals themselves. The Organization shall have the right and the duty to waive the immunity of any expert in any case where in its opinion the immunity would impede the course of justice and it can be waived without prejudice to the interests of the Organization. 3. Article V and Section 25, paragraphs 1 and 2 (I), of Article VII shall extend to the representatives of Associate Members participating in the work of the Organization in accordance with Articles 8 and 47 of the Constitution. 4. The privileges, immunities, exemptions and facilities referred to in Section 21 of the standard clauses shall also be accorded to any Deputy Director-General, Assistant Director-General and Regional Director of the Organization" END of Document Why am I even mentioning this document, as it relates to population growth? Because, as far as the programs and treatments offered from these Global entities, any harm inflicted by this particular one, bares no accountability, or at least this document says you can not hold an official accountable should they harm someone. And as we will see, novel treatments like fertility vaccines have been one of the treatments offered as a "solution" to the destruction of Earth. So, if the World Health Organisation funds these programs or gets it's nation states to enact clinical trials using clinical trial participants, any harm that comes out from those actions can not be blamed on the WHO Now, on to some of the key organisations, figures and key moments in history involving overpopulation ideology

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4. The New York based Population Council was a nongovernmental organisation which came to play a crucial role in sustaining the interest in Family Planning. This organisation came out of 1952 meeting that John D Rockefeller the 3rd organised in Williamsburg, Virginia. The different reasons that came out of that desire was for economic development, geopolitics, conservation and eugenics Another organisation formed was "The Club of Rome", founded in 1968. We will clearly see later in the thread it’s continued impact on the psyches of people with immense influence in the European parliament. In 1971-72 they commissioned - “The Limits to Growth", a "1972 report[2] that discussed the possibility of exponential economic and population growth with finite supply of resources"

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5. Going back to the World Health Organisation. One of their keen areas of interest in Population control and Reproductive Health was birth control methods, vaccines and other devices In particular, one division out of the World Health Organisation began in the early 1970's, a division focused on reproductive health. This division was headed by a scientist that began developing birth control vaccines, which would essentially use the bodies own immune system to attack the females reproductive hormones, preventing the implantation of fertilised eggs It was also at this point in the 1970’s, in India, were the government had taken the idea and danger of “population growth” to astounding new levels. The Indian government began implementing sterilisation policy as a form of population control. potentially led by these prior organisations and ideology, such as that seen in Eugenics and with the Population Council that was also becoming prominent

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6. The India Emergency in the 1970's was one of the most stunning periods of time, in which mass sterilisation campaigns were implemented by the government, where "some 8 million people were sterilised". Prime Minister Indira Gandhi even admitted and did not refute the following statements: ◻️"All eligible cases for sterilisation in my office and department have been sterilised. Persons who have refused to get themselves sterilised, have not been paid their salaries" ◻️"A combination of intimidation, coercion, economic sanction, not giving people licences, not giving people rights to free education and health and so on, were used by officials, throughout India, to force people in effect to have sterilization" "yes they were, certainly...they certainly were" - But she didn't think they were excess at all, instead doubling down on the fear narrative surrounding population growth

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It doesn't matter what the British media says about India; it shows a disconnect from the facts and public opinion. Concerns arise regarding the 20 months of special powers, particularly the sterilization of millions. While it's alleged that there was coercion, I emphasize that I do not support compulsion. Records indicate that officials pressured individuals to meet sterilization targets, often using intimidation and economic sanctions. However, I don't view these as major excesses. The reality of population growth poses significant challenges for future generations regarding food and education. I accept responsibility as head of the government, acknowledging that mistakes can happen in large programs. Yet, external forces worked against us, contributing to the situation.
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Speaker 0: Plus it doesn't matter what the British media says. It's quite irrelevant to India. But it shows that you are divorced from the facts and divorced from what the people are thinking. And if you don't if you're not bothered about what the people are thinking, then you shouldn't talk about democracy. Speaker 1: I certainly am bothered, what the people are thinking. And of course, one's concerned to try and establish the basis on which they might or might not hold particular judgments. And that's why I'd like to ask you about the 20 months of your special powers. There were, I want to remind you, I think some 8,000,000 people who were sterilized. More than 250 This Speaker 0: figure has not been borne out by anybody in any commission. Speaker 1: There is evidence to suppose that very large numbers of people were sterilized. But why is it? You have a you well, it's been alleged that there was widespread compulsion. If there was compulsion at all for the purposes of argument, what would be your reaction to compulsory sterilization? Speaker 0: I stress myself in government statements as well as privately that I'm not for compulsion. Speaker 1: Records from the time, from the chief secretary of the government of Uttar Pradesh. Government attach highest importance to achievement of family planning targets. Failure to achieve monthly target will result in stoppage of salary suspension and severest penalties. Other states, all eligible cases for sterilization in my office and department have been sterilized. Persons who have refused to get themselves sterilized have not been paid their salaries. The evidence surely, Mrs. Gandhi, that a combination of intimidation, coercion, economic sanction, not giving people licenses, not giving people rights to free education and health and so on, were used by officials throughout India to Speaker 0: They certainly were. Speaker 1: Or speak in effect to have sterilization. Speaker 0: Yes, they were. Speaker 1: Those are major, wide scale excesses then, aren't they? Speaker 0: No, I don't think so. And furthermore, now people realize that if our population goes up at the rate that it is which is going, their children won't be alive. They won't have, they won't have enough food or education or any of those rights. Speaker 1: Do you accept no responsibility at all? Speaker 0: I have accepted all responsibility because I happen to be head of the government. Speaker 1: But you believe there was no there was nothing Speaker 0: No. You see, you cannot be categorical about these things. Certainly mistakes when you take up any major program, mistakes will take place. But there was a very large force working against us which was determined to use anything it could against us and I think that they played a very large part in creating these so called excesses. Speaker 1: A lot of them seem to be in prison. You had tens of thousands in prison. There were endless more forces against you trying to destroy you, Miss Gandhi.

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7. As you can see, in the 1970’s, multiple forces were meeting to create a powerful linking of ideology and government policy support, which was also being globalised through the world health organisation. Some of those entities include collaberative ones that linked the Indian Government with the WHO, like the ICMR/WHO. Obviously these aren’t the only forces at play, but just one line of information I want to focus on for the purposes of this growing thread which will be linked to a larger story coming up

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8. The India emergency was well documented. Millions of people were sterilised in the 1970’s. In one report, shockingly, the WORLD BANK President Robert McNamara, commented on Gandhi's Emergency Period Population policies, saying that he was "encouraged" by what he was seeing, saying (Record from "Notes on visit to India, 6-12 November, 1976") that: "At long last India is moving to effectively address it's population problem"

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9. Throughout India's Emergency Period, the following organisations were some of the organisations which continued funding Family Planning programs in India: ◻️ The World Bank ◻️ UNFPA (United Nations Fund for Population Activities) ◻️ IPPF (International Planned Parenthood Federation) ◻️ Swedish International Development Agency Nafis Sadik, who became executive director of UNFPA, mentioned that compulsory sterilisation should not receive funding from the UN, but also stated that "compulsion may be needed at the expense of human rights" Robert McNamara (The World Bank) is Pictured here with then India Prime Minister Indira Gandhi. This is in 1968/69, prior to Indias Emergency period. Which tells us that the groundwork was being laid around population policy long before the Indian government went into the full scale sterilisation campaign

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10. Some roots of Overpopulation Ideology in India actually appear to begin a little further back in the 1950's. It appears that just after the Incorporation of the Population Council in 1952, which followed 3 x weeks late rby the founding of International Planned Parenthood Federation, that financial and political moves were exerted towards and within India. For example: ◻️ 7 November 1952 - Nehru (Indias Prime Minister from 1947-1964) presented the first policy into India's Parliament about "population limitation", which acknowledged "family planning" and called for "reducing birth rates" ◻️ 1953 - 1956 - "The Rockefeller Foundation set aside almost a quarter of a million dollars [for] a single family planning project in Punjab" ◻️ 1950's - Kingsley Davis, who published "World Population Trends and American Policy" with the Rockefeller Brothers Fund, proclaims that: "India had a chance to be the first country to achieve a major revolution in human life-the planned diffusion of fertility control in a peasant population prior to, and for the benefit of, the urban industrial transition" So we can clearly see that from the 1930's in Eugenics Publications, followed by nongovernmental Population organisations in America (like the Population Council) and other countries, that individuals were concerned about population growth in countries like India. Key figures were actively involved in shaping the activities related to management of population, which in this time seemed to focus heavily on India. It appears that initiatives related to population ramped up heavily in the decade of 1950

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11. In the 1970's, all the forces and finances mentioned above, finally were put into action and were provided with the necessary resources to begin the mass sterilisation campaign. Interestingly, working alongside India's forced sterilisation campaign, was the increasing prominence of an Indian Immunologist and vaccine developer Gursaran Pran Talwar

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12. Gursaran Pran Talwar, Indian scientist & vaccine developer, was empowered by the World Health Organisation in the early 1970's, beginning development, research and testing of an anti-fertility vaccine. His particular vaccine, targeted Human Chorionic Growth Hormone, or HCG He also joined key organisations involved in Population Control Activities: ◻️ Head, ICMR-WHO Research and Training Centre in Immunology for India and South East Asia (1972-91) ◻️ Talwar was Project Leader and Member Executive, International Committee on Contraception Research and Population Council, New York (1975-94) ◻️ Member, WHO Task Force on Birth Control Vaccines (1984-90) Talwar was the head of the joint ICMR (India) - WHO partnership, which began in 1972, just years before the India Emergency began taking shape

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13. 1970 - Big decade for overpopulation theory & population extinctionists. The Club of Rome, to this day, has taken the minds of key figures in the EU. Here Ursula von der Leyen seemingly praises their vision https://t.co/LROEHJDXvA Obviously there are many more key moments, but here is just a few to get a "feel" for the massive push from Western Organisations, for the purposes of this thread: ◻️ The Club of Rome release report - “The Limits to Growth", a 1972 report discussing the possibility of exponential economic and population growth with finite supply of resources ◻️The WHO partner with ICMR ◻️Indian Immunologist Talwar begins testing and developing an anti-fertility vaccine, targeting a sub-unit of HCG and eventually conjugating it together with Tetanus for a more robust immune response to HCG ◻️The India Emergency ramps up in 1976, where millions of Indians are sterilised I'd like to bring in another unlikely country that enters the arena here, to finance population control activities and research, both locally and in other developing countries

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The discussion centers on the ongoing natal crisis and its implications. One participant emphasizes that low birth rates are a significant ethical issue, noting a trend where many countries are falling below replacement levels. They express concern that if these trends continue, cultures could dwindle or even disappear. The conversation touches on the relationship between cultural decline and the loss of religious values, suggesting that a lack of belief may lead to antinatalism. They argue for the benefits of population growth, highlighting that more people contribute to a broader understanding of the universe and enhance cultural diversity. Ultimately, they advocate for efforts that improve our comprehension of existence and promote a thriving civilization.
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Speaker 0: Yeah. Well, okay. So let me let me put a twist on that too. So one of the things that really struck me about your public pronouncements in recent years was your insistence that we're in a natal crisis and Speaker 1: that that's actually a problem because Well, that's factually true. Speaker 0: Well, well, it depends whether you think the pop the planet would be better off if it was depopulated. Speaker 1: I don't I don't I'm not interested in this. Yeah. Paul Illich is a genocidal maniac as far as I'm concerned. And I I he's a terrible human being. Speaker 0: Yes. And he's never admitted that he was wrong, He was unbelievably wrong. He made a famous bet, you know Speaker 1: the bet. Yes. I hate Polo. I gotta be clear about that. I think he's terrible and and his books have done great damage to humanity. Speaker 0: How did you start to understand that the one of the fundamental ethical problems is different than the scientific problem. One of the fundamental ethical problems that's plaguing the West is this catastrophically low birth rate. Again, and, you know, when you start making public I'm Speaker 1: observing the numbers. I mean, I've noticed this 20 plus years ago, that the trend in birth rates for, really, all countries, past certain level of economic development, was trending to well below replacement, if not already below replacement. And if you extrapolate the the curve, which one always has to be cautious about extrapolating any demographic curve. But if you're if so I always preface by saying if these trends continue Yeah. Yeah. Most countries will will dwindle into insignificance. They might completely die out. I think there is there's an argument that that, when a culture loses its religion, that it starts to become antinatalist and decline in numbers and, potentially disappear. Yeah, the question or, you know, is it another way that seeking greater enlightenment, and a better understanding of the universe and more questions to ask about it, is something that we can continue to, do as a civilization for a very long time. Speaker 0: Yeah. Yeah. Likely forever. Speaker 1: Right. Exactly. So Speaker 0: Depending on how powerful grok turns out to be. Speaker 1: Yeah. So that's so then I thought, okay. Okay. I'll work on, things that improve our understanding of the universe. Now they're saying, like, at a base level, well, this is why I I actually think we want a population increase, because population increase means that there are more people, that that we've expanded the scale More brains, man. Yeah. We've expanded the scale of consciousness, to the degree there are different cultures. We've expanded the scope of consciousness.

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14. In 1979, Australia enters the Arena of overpopulation ideology, at least as far as public records in parliament are concerned. Australia was openly talking about population control in 1979. With an astounding level of ease and intriguing forthrightness, Senator Knight asks the Minister of Foreign Affairs in 1979: “What assistance has Australia provided to programs, either through international organisations or bilateral programs, to assist in the control of world population growth.”

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15. Senator Carrick, in 1979 after questioned what assistance has Australia provided in the areas of World Population Growth, answered that Australia has funded programs internationally. According to his statement, Australia at this point in 1979, had funded a “Bangladesh Population Project which is designed to reduce fertility, mortality and morbidity” and also $2.6 million into a family planning project in Thailand. With that was the planned contributions toward: ◻️International Planned Parenthood Federation - $180,000 ◻️International Union for the Scientific Study of Population - $25, 000 ◻️United Nations Fund for Population Activities - $721,000 Senator Carrick also stated that: “Since the World Population Conference in 1974, assistance to the population sector is no longer considered to be limited to family planning activities, but instead is considered to embrace activities in all areas that influence population”

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16. Senator Carrick (Full Answer from Transcript in 1979) - The Foreign Minister has provided the following answer to the honourable [Senator Knight's] question [“What assistance has Australia provided to programs, either through international organisations or bilateral programs, to assist in the control of world population growth.”] : "Assistance for population activities is directed both through bilateral programs and multilateral channels. Currently more emphasis is placed on bilateral projects involving international agencies which are considered to be well equipped to handle population problems and research. Such assistance forms part of Australia's effort to work towards the social and economic improvement of developing countries." Australia, under its bilateral aid program, is supporting the First Bangladesh Population Project (1975-80) sponsored by the International Development Association, (IDA). This is an international program designed to expand Bangladeshi facilities for maternal and child health care and for family planning services. The Australian contribution to this project will amount to $2m. This project will be followed by the Second IDA Bangladesh Population Project which is designed to reduce fertility, mortality and morbidity by strengthening the Bangladesh population and health programs. The Australian contribution to this project will be $4m. In Thailand, Australia is providing an estimated $2.6m in a co-financing arrangement with the IDA for the expansion of family planning services and the extension of the Thai rural health network. Aspects of other projects, such as those oriented towards health and nutrition, can of course also be considered as involvement in the population sector. Australia will be contributing in 1979-80 to the International Planned Parenthood Federation ($180,000; and to the International Union for the Scientific Study of Population ($25,000), both Non-Government Organisations. Multilaterally Australia will contribute to the United Nations Fund for Population Activities ($72 1,000). Since the World Population Conference in 1974, assistance to the population sector is no longer considered to be limited to family planning activities, but instead is considered to embrace activities in all areas that influence population- such as nutrition, sanitation, health, education, the status of women and economic factors. Australia endorses this integrated approach, and in its aid program supports activities in all sectors relating to population matters."

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17. So far, at least as far in this thread is concerned, we can see the beginnings of population ideology through Eugenics, the founding of the World Health organisation, leading to the implementation of the ICMR-WHO Partnership in 1972, all preceding the India Health Emergency with forced sterilisation, just years before we can see evidence of Australia funding family planning measures in “developing countries” like Bangladesh and Thailand. From 1972 - 1991 - Talwar was head of the research and training centre for ICMR-WHO in immunology for India and South East Asia. He had significantly furthered research into anti-fertility vaccines. We begin to see clinical trials for his pioneering work in birth control vaccines. Which brings us to the year 1988. In this year, at a University in Adelaide, Australia, collaborates with the World Health Organisation, in a clinical trial of the Anti Fertility HCG vaccine, conjugated with diphtheria

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18. In 1988, Based on the Pioneering work of Talwar's Anti-Fertility HCG vaccine, a “Prototype consisting of synthetic peptide of hCG-specific portion of B-hCG (CTP) linked to diphtheria toxoid” went into “Phase 1 Trials” - With the collaberation of WHO/HRP (World Health Organisation) at Flinders Medical Centre in Adelaide Australia Other Western countries that were involved in similar research, include America and Sweden

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19. Interestingly, as seen in the 1930's Eugenics Publication, The Australian Government (A "Western Civilisation") echos the mention of low fertility rates, in their official stance on population policy summarised in a 1994 report by the National Committee for the United Nations International Conference on Population and Development: “In the domestic context, Australia does not have an explicit or formal population policy directly aimed at influencing the level of population. After considerable public debate, the Government decided that a formal population policy (particularly one which would specify population targets) would not be appropriate for Australia, given its low levels of fertility”

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20. So, it seems Australia was funding projects to control “World Population”, as evidenced from the parliamentary transcript, whilst also taking an active role, together with the World Health Organisation, in building and creating a medical paradigm that targeted female fertility. Essentially, that medical paradigm was a vaccine conjugated to diphtheria, to make the immune system attack it’s own reproductive hormones, which could almost be contextualised as a consented and purposefully implemented vaccine induced auto-immune condition to prevent pregnancy This was in the context of Western Democratic Countries experiencing low, or falling fertility rates, since at least the 1870's

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21. Bill Gates begins to exert his immense financial influence into "Global Health" and "Reproductive Health" in the mid 1990's, around the time Bill Gates and Microsoft is targeted by the American States, facing investigation & potential prosecution, jail, fines. Around 1994, Bill Gates creates the "Bill and Melinda Gates Foundation"

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22. Before Bill Gates creates the "Bill and Melinda Gates Foundation" and begins throwing money at reproductive health, we can see that his "mindset" has already been influenced by his father, who was involved in the "Planned Parenthood" organisation, that was founded in 1952. Remember, Vogt, who became National Director of the Planned Parenthood Federation had called for "Sterilisation Bonuses" at one point during the organisation's earlier inception. Why are these facts important? Because, as contextualised in Buddhist teachings: "Mind precedes all mental states. Mind is their chief; they are all mind-wrought. If with a pure mind a person speaks or acts happiness follows him like his never-departing shadow" In other words, the mind precedes all action and the quality of someones actions are effected by the quality of ones mind. What happens when that mind is empowered by enormous financial influence? This thread that we see, which appears to be an "urgent need" to deal with overpopulation, doesn't appear to lose strength over the years. In fact, the level of investment into various measures of "family planning" and "reproductive health" seems to have grown to epic proportions And that investment is largely funded into organisations like the World Health Organisation, which has the network and organisational capacity to use his wealth to attain his goals on a Global level. In a way, Bill Gates has made a VERY smart move investing into the World Health Organisation over the past almost 30 x years. If you consider it as a "bang for buck", he get's to link into an organisation that can effectively manage all aspects of Reproductive Health, the production and research of vaccines and the global infrastructure that has accumulated since the mid 1940's when the WHO was established According to one source, The Gates Foundation today accounts for somewhere around 88% of the World Health Organisation's funding So, it appears that the underpinnings of population ideology and methods to control it, come well before Bill Gates found “The Bill and Melinda Gates Foundation” in 1994 (when the first grant is registered). But given that Bill Gates’s father was involved with Planned Parenthood, as evidenced in this video, it’s safe to assume that Bill Gates’s ideology around population and how to manage it, stems at least from his father. How long his father has held that belief is another question for someone else to investigate In 1997 - The Gates Foundation made it’s first $2.25 Million donation to John Hopkins “to support the Institute for Population and Reproductive Health to strengthen leadership and institutions in the developing countries”. Then in 1999 a further $20 Million to John Hopkins - “to establish the Bill & Melinda Gates Institute for Population and Reproductive Health to strengthen leadership and institutions in the developing countries” Below is the mind of Bill Gates talking about population

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Population and reproductive health are urgent issues. Growing up with parents involved in volunteer work, including Planned Parenthood, shaped my perspective. Looking ahead 10-15 years, I aim for significant change in mortality rates in developing countries, which can help reduce population growth and improve education and nutrition. We have ambitious goals and use numeric dashboards to track progress. Currently, the world population is about 6.8 billion, projected to reach 9 billion. With effective vaccines and health services, we could potentially lower this growth by 10-15%. Over the next decade, we plan to invest $10 billion to advance vaccine development and distribution, aiming to reduce child mortality from 9 million to 4.5 million annually. This progress will enable societies to better care for themselves.
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Speaker 0: Shoe that really grabbed me as as urgent, was were issues related to population, reproductive health. Speaker 1: But did you come to reproductive issues as an intellectual? Speaker 0: When I was growing up, my parents were always involved in various, volunteer things. My dad was, head of planned parenthood. Now if you look forward and, at your next career step, career maybe not the right word here. But, at your at your next life phase, what what would you like to see as your legacy in 10, 15 years? Speaker 2: Of the new work? Speaker 0: Of the new work. Yeah. If your new function. Speaker 2: Well, I've I've set very ambitious goals because I'm quite optimistic. You know, huge change in the mortality rates in developing countries, which then has this effect of reducing population growth. That's this big benefit that then makes everything like education and nutrition a lot easier. So I have very high expectations there. And we actually use these dashboards internally at the foundation to make everything be quite numeric. We're trying to be rigorous about that and even share those so that people can see, Oh, you fell short of what you had in mind. And then 15 years, boy, we, you know, by then, we will have spent a lot of money. 3,000,000,000 a year, 15 years, that adds up. And for that, people should have a very high expectation of what we can do. Let's take a look. First, we've got population. The world today has 6,800,000,000 people. That's headed up to about 9,000,000,000. Now, if we do a really great job on new vaccines, health care, reproductive health services, we could lower that by perhaps 10 or 15%. But there we see an increase of about 1.3. Speaker 1: $10,000,000,000 over the next 10 years to make it the year of the vaccines. What does that mean exactly? Speaker 2: Well over this decade, we believe unbelievable progress can be made, both inventing new vaccines and making sure they get out to all the children who need them. We could cut the number of children who die every year from about 9,000,000 to half of that, if we have success on it. And the benefits there in terms of reducing sickness, reducing the population growth, it really allows the society a chance to take care of itself, once you've made that intervention.

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23. From the year 2003 - 2013 we see various Grants from the Gates Foundation with different flavours, or tones. From National Security, to novel fertility treatments. The following Grants are listed by year: ◻️2003 - “to provide the latest research documenting the importance to U.S. national interests of achieving the goals established by the International Conference on Population and Development (ICPD)”. ◻️2007 - “to review the state of knowledge in population and health issues as well as other population conditions affecting the African continent ◻️Sept 2010 - $500K “to support a special issue of Lancet on population and family planning in relation to achieving Millennium Development Goals” ◻️NOV 2010 - “to revitalise the global emergency contraception agenda and increase access in Sub-Saharan Africa and South Asia” In these Grants we see hints of National Security fears and what is mentioned as a "Global Emergency Contraception Agenda" In 2010 - 2012 was when things got really interesting with investments into novel treatments for fertility. Here’s some of the investments made by Gates: ◻️NOV 2010 - “to develop and test a nanoparticle contraceptive that releases sperm tail inhibitors in response to vaginal pH changes or exposure to prostatic fluid”. ◻️NOV 2010 - “to design and test molecules that will inactivate specific genes within sperm that are essential to the fertilization process for potential use in a reversible oral male contraceptive.” ◻️OCT 2011 - “to support extending the duration of action for injectable contraceptives” ◻️NOV 2011 - “to increase financial and policy support for the discovery and development of new and adaptive contraceptive technologies, ultimately leading to accelerated contraceptive uptake and improved access to high quality family planning options worldwide” ◻️DEC 2011 - A grant was made to the World Health Organisation - “to review the body of published evidence on hormonal contraception”. I believe this is likely a throwback to Talwar's research on Anti-HCG vaccines These Grants are but a drop in the ocean of Bill Gates's immense financial capacity which is pointed directly at the World Health Organisation, who is looking to garner more and more power over Global Health, including using Pandemic Treaties to control Global Pandemic response As I previously mentioned, The WHO, according to one source receives well over 80% of their funding from the Bill and Melinda Gates Foundation. The have the organisational capacity to implement his goals and dreams related to population

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24. I want to close this thread in the period 2012-2014, where The World Economic Forum, in collaboration with Bill Gates are featured in a document called the “Global Agenda Council on Population Growth 2012-2014”. This Agenda mentions that “the Council is developing tailored policy briefs for the governments of three countries – Nigeria, Rwanda and Pakistan – that are undergoing important demographic transformations and may be able to realise a positive “population dividend” in the coming decades” As public interest has grown more aware about the plans of these elite organisations, they seem to have gradually become more and more careful with public statements about population, since it draws too much attention. One wonders what closed door sessions look like nowadays. I'm going to finish up here. I have planned threads coming up that will link into this As we can see in the posts above. There has been a definite campaign against population growth, especially in non-Western countries, funded by both nongovernmental organisations and governments in other key areas. And one thing seems to be clear, much of the fear against population growth seems to be directed towards non Western Countries The Rockefellers, Population Council, Klaus Schwab's World Economic Forum, Bill Gates, The World Health Organisation, to name a few, have all been instrumental in shaping the Population Extinctionist Movement, which Elon Musk is now calling out as a total scam And let's not forget, the World Health Organisation, largely influenced by Bill Gates, has given itself complete immunity should it be moving us all in the wrong direction. It's written into their charter

Humanspective
Posted - January 23, 2025 at 8:26 PM
Saved - January 24, 2025 at 1:43 AM
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I came across some alarming information regarding a potential link between mRNA COVID vaccines and an increase in colon cancer. Kevin McKernan presented findings showing "Pfizer-like" plasmids in a colon cancer biopsy from someone who received four doses of the vaccine. Dr. Sabine Hazan has also discussed how mRNA vaccines may harm Bifidobacteria in the colon. Additionally, a Pfizer board member acknowledged the rise in colon cancer on CNBC. While correlation does not imply causation, these connections warrant serious consideration. What are your thoughts?

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MUST WATCH. Pfizer board member admits to rise in Colon Cancer, revealing a stunning connection of research. NEW information revealing itself in real time. [@Kevin_McKernan] and Dr Sabine Hazan's research on mRNA covid vaccines intersect with what Pfizer Board member Scott Gottlieb just ADMITTED on CNBC. The rise in Colon Cancer. 3 x clips highlighting a disturbing connection: 1. Kevin McKernan: In a recent presentation on CHD, he presented scientific research about "Pfizer like" plasmids found in a Colon Cancer biopsy of a person (who passed away) that had 4 x Pfizer mRNA covid vaccines. 2. [@SabinehazanMD] has presented on multiple occasions, research relating to how mRNA vaccines "k*ll the Bifidobacteria", which is primarily found in the Colon. 3. Pfizer executive admits now on Mainstream Media that there is a RISE IN COLON CANCER. Correlation is not causation, but these are very interesting connections of research and should NOT be ignored. What do you think is going on here?

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Many people are questioning the potential links between COVID and the COVID vaccine to rising cancer rates. While some cancers, like colon cancer, are increasing, especially among younger individuals, the reasons remain unclear. There are theories suggesting that changes in the US diet may be a contributing factor, but further research is needed to understand these trends fully.
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Speaker 0: You know where I'm going with this. A lot of people point to COVID and maybe even the COVID vaccine because they don't know. What is it? Speaker 1: Yeah. Look. We don't know is the answer. Some cancers are going up. You're right. Colon cancer in particular, the incidence has been going up particularly in young people. 30. Yep. Speaker 0: Right. Speaker 1: So we don't understand that. Some people believe it's related to changes in the US diet.
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We received four Pfizer vaccines, and the one we sequenced is different from any previously analyzed. This may be an earlier version that Pfizer modified later. The vaccine contains a common plasmid used in coronavirus research, which raises questions about its origin. While Pfizer is the likely source, it's possible it leaked from a lab. We found similarities and differences in the components of the vaccines. The contamination hypothesis is unlikely since the plasmids have never been handled in our labs, and formalin fixation prevents spike protein production. Pfizer could have multiple undisclosed plasmids, which would be concerning, especially since we found one in a colon cancer sample that produces spike protein at high levels, indicating it could be replication competent and potentially transmissible. Transmissible cancer is a significant issue.
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Speaker 0: We don't exactly know where this came from. We know we got 4 Pfizer vaccines. This is different than any other vaccine we've sequenced from them, but we've only sequenced 2 Pfizer lots to date ever. So they could have multiple versions out there. This could maybe be their first version of this that hit Germany early and they changed to get rid of the CMD promoter later. But, if you want to line these up to other vaccines, so the one on the left is what is actually BNT162b2. This is something that's never been described before. It has that red box at CMV promoter, but it is a backbone that's a commonly used plasmid in the field. When people want to study coronaviruses, they plug spike protein into this thing or the sequence to look for how the variance change. You may have heard alpha, delta, omega, well they're always categorizing these variants of concern by taking the spike they find in nature, throwing it into that backbone and saying how does it behave differently in mammalian cells. So this PC, this little thing is known as pcdna3, this plasmid is all over the country in terms of research laboratories. So we can't entirely pin this on Pfizer, although it's probably the most likely place where it came from. It was injected. It could in fact, have leaked from a laboratory doing that type of work. This just shows you the kind of the parts and the components that are the same and different between the 2 different flavors of these things that we have found. But as I mentioned before the first hypothesis they're gonna come at us is saying you guys contaminated this again. Right? Well the reason why that doesn't fit is we've never handled those plasmids in our life before. Neither lab has ever seen those and you can't take a plasmid and put it onto formalin fixed tissue and get it to make spike protein because that formalin fixation is kind of like carbon freezing Han Solo. The cells just don't are not translationally active after you've done that. So you can't put a plasmid on formalin fixed tissue and get spike to show up. This person has spike IHC that means they were translationally competent when the plasmid was there they had to be alive. So I don't think that's the answer, but you'll see that in the next fact check I'm sure. So Pfizer could have more than 1 plasmid out in the marketplace that would be a huge shock because they have never disclosed it to anybody, that'd be a problem. And they have one that's much more dangerous. This is being we're finding this in a colon cancer sample and it's making spike protein as a very high copy number, which means it is replication competent, which means it could be transmissible. Transmissible cancer is really not something we want in the world.
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A top gastroenterologist treated a colleague who became debilitated after vaccination. An examination of her microbiome revealed zero bifidobacteria and actinobacteria. This raised questions about whether the vaccine or spike protein affected her gut microbiome. Similar findings were observed in other vaccine-injured patients, all showing zero bifidobacteria. One patient’s count dropped from one million to zero. This suggests the spike protein, possibly combined with nanoparticles and other contaminants, may enter the bloodstream and affect the gut microbiome, leading to conditions like leaky gut. The implications of these findings remain unpublishable and largely ignored by the medical community.
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Speaker 0: My colleague, you know, gastroenterologist at Cedars Sinai in Santa Monica, top of her game, treated like half the celebrities in in in Beverly Hills. This woman gets vaccinated, all of a sudden is debilitated. Okay? She went to the top neurologist at UCLA. He called me and said, can you look at her microbiome? When I saw she had 0 bifidobacteria, 0 actinobacteria, I was like, okay, well, did the vaccine do this? Did the spike protein create a bacteriophage and kill the bifidobacteria? Let me see more. Then I started looking at the kid that was paraplegic and her brother. Again, the kid had 0 actinobacteria phylum, 0 bifidobacteria. Her brother had some bifidobacteria. He got the placebo. Then I started looking at more vaccine injured. None of this can be published, by the way. Nobody wants to hear about it. We have hundreds of patients that are vaccine injured that volunteered for my study that actually, you know, sponsored or helped us with funds to see their microbiome. Okay? And all of them have 0 bifidobacteria. So when you look at those patients that have 0 bifidobacteria and you look at my data where it was before and after, you have one guy that was like at a 1,000,000 bif and drops to 0, you know, and then persists in dropping. Okay? You have to ask yourself, is the spike protein creating a bacteriophage? Is that spike protein and remember, it's not just the spike protein. It's the spike protein with the nanoparticle. It's the spike protein with the contamination. It's the plasmid. It's all that. Is that going into the blood, into the circulation, into the lymphatics, into the nerves, into the colon and landing there and now utilizing the properties or other microbes in the microbiome space in the gut and reproducing and now you have a leaky gut and now all these microbes are passing. Right? Is that being created in the gut? Right? Are you create are you having a spike enter the blood, going to the colon, utilizing properties of other microbes, reinforcing that spike. Right? Or even that spike triggering another virus, triggering another bacteria. No. We don't
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Posted - January 14, 2025 at 9:17 PM
Saved - January 15, 2025 at 12:10 PM
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I learned from Kevin McKernan that Pfizer altered the manufacturing process for their COVID mRNA vaccines. This change means the vaccines most people received never underwent clinical trials, as they tested one formulation on a small group before using a different one globally.

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The "Bait and Switch", brought to you by Pfizer Kevin McKernan points out Pfizer changed the manufacturing process for their covid mRNA vaccines, which means: "the vaccines [everyone] took [using process 2] never went through a clinical trial." Pfizer tested one formulation on a small group, then targeted the entire Planet with another formulation.

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Many are surprised to learn that the vaccines did not undergo traditional clinical trials. Initially, they were manufactured using PCR for 44,000 people, but when scaling up, the process was deemed too costly and was replaced with DNA from E. Coli, which also introduced endotoxins. In pharmaceutical manufacturing, the process is crucial; changing it typically requires new trials. The EMA requested a new trial with 252 patients, but the data was never provided, and it was considered too late since vaccinations had already begun. Thus, the rationale for conducting the trial became irrelevant.
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Speaker 0: What most people are shocked to find out is that the vaccines that you took never went through a clinical trial. They did a big bay and switch. They actually manufactured these vaccines using PCR. They could do that for 44,000 people. When they had to actually scale this up for production, they decided that step was too expensive. They ripped it out. And they used the DNA coming straight out of E. Coli. That comes along with some endotoxin and all this other DNA that we're gonna speak about. Normally, in any pharmaceutical manufacturing process, the process is the product. You change the process, you go through the trial again. And in fact, the EMA had asked them to go through another trial with 252 patients, and they never delivered the data and they decided it was too late to matter because they had already injected everybody. So what was the point of doing that trial on the vaccine they never really did a trial on?
Humanspective
Posted - November 25, 2024 at 2:01 AM
Saved - November 25, 2024 at 3:16 PM
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I can't believe what just happened. Senator Canavan pressed the ACMA on why Pornhub isn't covered by the Social Media Minimum Age Bill if YouTube is. The ACMA argued that Pornhub doesn't serve the same purpose as social media, stating it lacks characteristics of online social interaction. Canavan challenged this, pointing out the inconsistency in the law's application. The ACMA's admission that Pornhub is excluded while aiming to protect children is astonishing and raises questions about the clarity of the legislation.

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You're not going to believe this. [@mattjcan] just got them to admit that Pornhub won't fall under the restrictions provided for by (63C) of the Social Media Minimum Age Bill: Senator Canavan: "If Youtube is covered [why isn't Pornhub] covered? [so] show me in the law where [Pornhub] is excluded" Senator Matt Canavan: If YouTube is categorized or covered by 63C, returning to Senator Roberts' question, is Pornhub covered? Why wouldn't it be? It's just explicit material, but yes, it's covered, isn't it? ACMA Representative, James Chrishold: No, the first thing of 63C, 1(a), is that the platform's sole or significant purpose is to enable online social interaction. Senator Canavan: But if YouTube's covered, as a video sharing service for non-explicit content, why wouldn't Pornhub be covered? Is Pornhub covered? I ACMA: I think they have very different purposes, yes. Can you explain that to me? ACMA "Sorry, I... I think this is under the definition; we wouldn't see Pornhub as falling within the scope. It's not seen as a social media platform. Senator Canavan: Just explain to me in simple terms how it would work if YouTube is covered: how would another video sharing service with mainly explicit material not be covered? ACMA: So again, Senator, it comes back to the commitment that the government's already made in relation to... Senator Canavan: No, no, I'm not asking for a commitment; I'm asking about the law. We've got to pass the law, not make government commitments. So, in the law, how are these two services different? ACMA: I think YouTube and Pornhub are completely different. Senator Canavan: I agree with that, but how are they differently defined in the law? Because well, Pornhub is a site for accessing pornography, which children are not permitted to access. Okay, show me in the law where that is excluded. ACMA: Well, yeah, it comes back to the evidence before about how Pornhub is subject to a suite of other rules and regulations, and also, it's not seen as a digital platform as part of this bill. The evidence is that we don't see it as having the characteristics of social interaction. It's a site for... I don't speak from any experience" Senator Canavan: I'm trying to understand here; it's very vague and unclear to any reasonable person about what's in and what's out. Not sure if Senator Canavan intended a pun there, but this is an astounding admission from ACMA. Especially when the purpose of the legislation is to supposedly protect children

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If YouTube is covered under the law, why wouldn't Pornhub be? Both are video-sharing platforms, but they serve different purposes. Pornhub is primarily for accessing pornography, which is restricted for children. The law distinguishes between platforms based on their commitment to enabling online social interaction. While YouTube facilitates social interaction, Pornhub does not fit that definition. The evidence suggests that Pornhub lacks the characteristics of a social interaction platform, which is why it may not be included under the same regulations. This distinction remains unclear and vague to many.
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Speaker 0: If if YouTube's correct click cat categorized or covered by 63 c, returning to Senator Roberts question, what is Pornhub cat covered by it? Why wouldn't it be? It's just it's just explicit material, but it's Speaker 1: Yeah. Yeah. It's covered. Yeah. Speaker 0: The the so it is covered. Speaker 2: The first thing of 60 63 c one a is that the platform sole or significant purpose is to enable online social interaction. Speaker 0: But if YouTube's covered, I mean, as a video sharing for non explicit content video content, why wouldn't Pornhub be covered? Is Pornhub covered? Speaker 2: I think they have very different purposes. Speaker 1: Yeah. What Speaker 0: what explain that to me. Fuck you. Sorry. I I I think this is Speaker 1: Under the definition, we wouldn't see Pornhub as falling within, scope. It's not it's not How Speaker 0: just explain to me in simple terms how it would if YouTube is covered, how would another video sharing service with explicit material, admittedly, not be covered? Speaker 1: So again, Senator, it comes back to the the the commitment that the government's already made in relation Speaker 0: No. No. I'm not asking for a commitment. I'm asking in the law. We gotta pass the law, not government's commitments. So in the law, how are these two services different? Speaker 1: I think the 2 and Pornhub are completely different. Speaker 0: I I agree with that but how are they differently defined in the law? Speaker 1: Well, Pornhub is a site for accessing pornography which children are not permitted decades. Speaker 0: Show me in the law where that is excluded. Speaker 1: Well, it comes back to the evidence before about how Pornhub is subject to a suite of other rules and regulations. Speaker 0: Again, is that in the law? Is that something? Speaker 1: Not in in and I just wanna sort of go through this very carefully. There's a question of whether Pornhub is treated as a digital platform as part of this, this this bill. And the evidence is that we don't see it as having the characteristics of social interaction. Of social interaction. It's a it's a it's a site for I don't speak from any experiences. Well, I'm But I'm just the evidence you cite. You're trying to understand here. Speaker 0: I do very It's not a Speaker 1: site that's forcing you to take Speaker 2: a while. Speaker 0: This is very vague and unclear to, I think, of any reasonable person about what what's in and out.
Humanspective
Posted - September 13, 2024 at 7:25 AM
Saved - November 20, 2024 at 11:35 AM
reSee.it AI Summary
I shared a series of posts highlighting the controversial views of Nobel Prize winner Luc Montagnier and other scientists regarding the origins of the coronavirus. Montagnier asserts that the virus was manipulated, containing sequences similar to HIV, which he believes indicates it is not natural. Professors Angus Dalgleish and Nikolai Petrovski also faced challenges publishing their findings that suggest the virus was engineered and perfectly adapted to human receptors. Their research faced censorship, raising concerns about the integrity of scientific discourse during the pandemic.

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🧵THE BROADCAST MISSED BY THE WORLD - THREAD. Nobel Prize Winner Luc Montagnier features in this EPIC REVIVED CLIP (IN FULL) that has to be watched. All anyone had to do was watch this broadcast...and it might have clarified EVERYTHING right from the start, about the true nature of where the coronavirus came from Instead, pharmaceutical industries, defence and government agencies silenced dissent and prevented or slowed down the progress of other scientists validating similar research findings Scientists in India were pressured to RETRACT papers, whilst other experts in their fields, Professor Nikolai Petrovski and Professor Angus Dalgleish, were also trying to get similar research about the origins of the virus published, in the United Kingdom and Australia All corners of the Globe were met with pushback from the institutions that guarded the publishing arena, which all amounted to a mass censorship of scientific research and further division in the scientific community If you have 37 x minutes of time, this is an EPIC MUST WATCH, with more backup research in THREAD

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"INDEED, THERE WAS A MANIPULATION DONE ON THIS VIRUS" - Luc Montagnier - Nobel Prize winner for HIV research, 2008 "Someone added on top of that some sequences including HIV, the virus for AIDS [and] it is NOT natural [and] it was the job of a professional"

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Il y a eu une manipulation du virus, avec des séquences ajoutées, notamment du VIH. Ce n'est pas un processus naturel, mais le résultat d'un travail minutieux de biologistes moléculaires. Les raisons de cette manipulation ne sont pas claires, mais il est possible qu'il s'agisse d'une tentative de créer un vaccin contre le sida en intégrant des séquences du VIH dans le coronavirus. Le matériel génétique du virus contient des segments de VIH qui pourraient modifier des sites antigéniques, permettant ainsi de modifier la protéine pour un vaccin. Bien que des rumeurs sur une origine humaine aient circulé, elles ont été largement réfutées, mais il existe une volonté d'étouffer ces recherches, comme l'a montré un groupe de chercheurs indiens qui a été contraint de se rétracter. --- There has been manipulation of the virus, with sequences added, including from HIV. This is not a natural process but the result of meticulous work by molecular biologists. The reasons for this manipulation are unclear, but it may involve an attempt to create an AIDS vaccine by integrating HIV sequences into the coronavirus. The virus's genetic material contains segments of HIV that could modify antigenic sites, allowing for changes to the protein for a vaccine. Although rumors of a human origin circulated, they have been largely refuted, yet there is a desire to suppress this research, as evidenced by a group of Indian researchers who were forced to retract their findings.
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Speaker 0: Et vous êtes arrivé à certaines conclusions. Speaker 1: Alors d'ailleurs vous arrivez à la conclusion qu'effectivement il y avait eu une manipulation au sujet de ce virus. C'est-à-dire bien qu'une partie, je ne dis pas le total, n'est-ce pas, mais il y a un modèle qui est évidemment le virus classique, et là c'était un modèle surtout venant de la chauve-souris, mais ce modèle on a par-dessus ajouté des séquences notamment du VIH, le virus du SIDA. Speaker 0: Mais quand vous dites on a ajouté qui a ajouté Speaker 1: Ah moi je ne sais pas. Speaker 0: Et c'est pas naturel c'est ce que vous voulez dire Speaker 1: Non, ce n'est pas naturel, c'était un travail de professionnel, un travail de de biologiste moléculaire. C'est un travail très minutieux, on peut dire d'horloger, on peut dire Dans quel bout des séquences. Dans quel but Dans quel but ça, ce n'est pas, n'est pas clair. Moi je ne je l'expose si vous voulez. Mon mon travail c'est d'exposer des faits, c'est tout. Je n'accuse personne, je ne sais pas qui a fait ça et pourquoi. La possibilité c'est peut-être que ils ont voulu faire ils, enfin ils on ne sait pas, on a voulu faire un vaccin contre le sida. Donc on a pris des petites séquences du virus et on les a installés dans la séquence plus grande du coronavirus. Speaker 0: Alors je ne suis pas sûr de je ne suis pas sûr de comprendre tout ce que vous dites. C'est-à-dire que dans ce virus, il y a une part de VIH Speaker 1: Voilà, c'est ça. Le le le le matériel génétique du virus est un long ruban d'ARN, n'est-ce pas Comme de l'ADN, c'est de l'ARN. Et dans ce dans ce ce long ruban, à une certaine place, on a fixé des séquences petites de VIH. Mais ces séquences petites ne sont pas petites pour ne rien vouloir dire. Elles ont la possibilité de modifier par exemple ce qu'on appelle des sites antigéniques, c'est-à-dire si on veut faire un vaccin, on peut très bien modifier la protéine qui est exposée pour le vaccin par une petite séquence venant d'un autre virus. JLM Vous Speaker 0: êtes certain Speaker 2: de ça parce qu'on a dit que le bruit a couru que c'était d'une origine humaine finalement et ça a été ensuite réfuté par la plupart des autorités scientifiques quand même. Speaker 1: Il y a quand même une volonté d'étouffement si vous voulez. Les travaux, nous ne sommes pas les premiers. Un groupe de chercheurs indiens très très renommé avaient publié de la même chose, on les aura forcés à rétracter.

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DR MONTAGNIER GOT THE NOBEL PRIZE FOR IDENTIFYING HIV - So if there's anybody on Planet Earth, who ought to be able to tell that HIV exists in this Spike Protein...that's the man" Richard Fleming PhD discusses Luc Montagnier's paper on how HIV "inserts" were found in the coronavirus spike protein "Mutation occur 1 x nucleotide at a time, not 12...OK, THAT'S AN INSERT"......."THAT DOESN'T HAPPEN"

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This complex diagram highlights the presence of HIV in the spike protein, as identified by Luc Montagnier, a renowned virologist and Nobel Prize winner for discovering HIV. Montagnier found 18 RNA fragments matching HIV and SIV, indicating significant similarities. Notably, the PRRA insertion consists of 4 amino acids, requiring 12 nucleotides, which is atypical for mutations that occur one nucleotide at a time. Additionally, a 590 amino acid insert corresponds to 1,770 nucleotide bases matching HIV-1, raising questions about its classification as a mutation. The evidence presented underscores the substantial connection between HIV and the spike protein, suggesting a deeper investigation into this relationship is warranted.
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Speaker 0: This looks awfully complex, doesn't it? And if it does, that's good because every one of these red arrows shows HIV in the spike protein. This work comes from Luc Montagnier. Doctor. Montagnier is the premier virologist in Paris, France. Doctor. Montagnier got the Nobel Prize for identifying HIV. So, if there's anybody on planet Earth who ought to be able to tell you that HIV exists in this spike protein, that's the man and oh, look, where he used to be professor and chair at, that's been deleted from the Internet as well. That's the same place that Zeng Li presented and now got wiped off the face of the Internet and off the face of the planet. Doctor. Montigny identified 18 RNA fragments that match HIV and SIV. This is Simian or monkey, Grade 8 immune deficiency virus. If you look at it, remember I told you about PRRA, that's 4 amino acids and every amino acid requires 3 nucleotides, that's 12, right, 12 nucleotides. Mutations occur 1 nucleotide at a time, not 12, okay. That's an insert. If you think that's bad, look at the HIV insert, 5 90 amino acids are 17 70 nucleotide bases that match HIV-one. Now, understanding that mutations occur 1 nucleotide at a time, scientifically, I'd like somebody to justify to me how that's possibly a mutation. That doesn't happen. This is the man who defines it. Every one of these red arrows and every one of these are the nucleotides that match HIV. That's why there is so much out there. It's like the funding. It's not one. It's not just a little. It's a lot.

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Retracted Paper that Luc Montagnier cites, saying the publisher was pressured - "Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag" - 9 x authors https://www.researchgate.net/publication/338957445_Uncanny_similarity_of_unique_inserts_in_the_2019-nCoV_spike_protein_to_HIV-1_gp120_and_Gag ABSTRACT READS: "We are currently witnessing a major epidemic caused by the 2019 novel coronavirus (2019- nCoV). The evolution of 2019-nCoV remains elusive. We found 4 insertions in the spike glycoprotein (S) which are unique to the 2019-nCoV and are not present in other coronaviruses. Importantly, amino acid residues in all the 4 inserts have identity or similarity to those in the HIV-1 gp120 or HIV-1 Gag. Interestingly, despite the inserts being discontinuous on the primary amino acid sequence, 3D-modelling of the 2019-nCoV suggests that they converge to constitute the receptor binding site. The finding of 4 unique inserts in the 2019-nCoV, all of which have identity /similarity to amino acid residues in key structural proteins of HIV-1 is unlikely to be fortuitous in nature. This work provides yet unknown insights on 2019-nCoV and sheds light on the evolution and pathogenicity of this virus with important implications for diagnosis of this virus"

ResearchGate - Temporarily Unavailable researchgate.net

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I WAS FIRST TO PICK UP IT HAD ESCAPED FROM A LAB - Professor Angus Dalgleish His research was accepted by a Biophysics journal, which understood exactly the point he was making, about how the actual "CHARGE was affected [which] would NEVER EVER occur in normal evolution" ◻️"I was first to pick up it had escaped from a lab" ◻️"It had 6 x insertions round it, we thought THEY NEED TO KNOW THIS" ◻️"We submitted it and it went to cabinet [and] they chose to ignore it" ◻️"It altered the charge and the whole infectivity" Professor Dalgleish said he sent all this scientific research to the top journals, because it was important to know for future modelling of vaccines. He sent it to: Nature Science Virology Lancet "And we got the same reply back [saying] we've nothing against the science, but it is not in the public interest to publish your paper" Professor Nikolai Petrovski, vaccine inventor in Australia, also went through the same thing when he was trying to publish research about the virus being perfectly adapted to Human ACE2 receptors

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I've lost faith in journals. When we first identified the virus with six insertions, we believed it was crucial information for vaccine development. Despite submitting our findings to major journals like Nature and Lancet, we received responses stating it wasn't in the public interest to publish. They should have engaged with us for evidence, but instead, they dismissed it. Molecular biologists suggested it could be random mutation, but that wasn't the case. Eventually, a biophysics journal published our work, recognizing that the alterations in charge and infectivity wouldn't occur through normal evolution. We shared our findings, but there was no willingness for open discussion.
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Speaker 0: I've really lost my faith in the journals. I mean, when I was were the first to pick up the the virus, to escape from the lab because it had 6 insertions around it, we thought, but they need to know this. It's important because if you don't take notice of that, you'll end up with a bad vaccine. We submitted it, and it went to cabinet, and everybody, they've all seen it. They can't deny it, what have you, but they chose to ignore it. And then we sent it to Nature Science Virology Lancet, and we got the same reply back. Really eerie. It said, we've nothing against the science, but it is not in the public interest of to publish your paper. They should have called me in about that and say, here, where's the evidence for these things? Because we were able to translate it. Molecular biologists go, oh, it could be a random mutation, this, that, and the other. No. This wasn't, and the the journal that published it in the end was a biophysics one. So it understood the point we were making, that it altered the charge and the whole infectivity, and this would never ever occur in normal evolution. Because once it got to one stage, it would be kicked out. It would never get to the point where it was so highly charged. And we discussed this, put it all out there, and nobody wanted to, enter any arm, discussion.

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Professor Nikolai Petrovski, vaccine inventor in South Australia, just a few weeks into the Pandemic, new confidently that the virus was probably man made Nikolai Petrovski discusses how in "The first few week of 2020, when the viral sequence was first released" he was only "modelling the virus to build a vaccine" Professor Nikolai Petrovski said - "If it's come from an animal source, then there should be an animal out there who's ACE2 binds better to the virus than Human ACE2, [but] rather than finding some exotic animal at the top of the list, we found Humans"[and it was] so well human adapted. "It took a long time to get published, because the narrative was, that [it] was not an acceptable question to be asking."

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Recent computer modeling from early 2020 suggested that the virus might be man-made. Initially, the goal was to design a vaccine, but the modeling revealed that the virus was surprisingly well-adapted to humans, raising questions about its origin. Instead of identifying an exotic animal, the research pointed to humans as the closest match for the virus's ACE2 receptor binding. This unexpected finding led to speculation about whether the virus had adapted in a lab setting or was an accidental release. The research faced challenges in publication due to its divergence from the prevailing narrative. Additionally, the presence of a furin cleavage site in the virus raised further concerns, as it appeared unnatural in the context of viral evolution.
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Speaker 0: So you've had some recent, computer modeling that that uncovered some details about the cleavage fur and cleavage site that, perhaps gave some clues on the origin of the virus. Is that accurate? Speaker 1: So it it it's actually not not new, interestingly. We did this in the the first few weeks, of 2020, you know, when the viral sequence was first released. So we we hadn't even seen the virus in Australia at that time. Early in in the pandemic, in the first sort of weeks, we we modeled the virus, with our computers to to design our vaccine. And that modeling told us the virus almost certainly was a man made virus. But we use supercomputers to model viruses. So when we got this new genetic sequence, we put it into our models. Obviously, we're thinking, can we build a model of virus to make a vaccine? Because remember, we had no idea what this virus was. And and and we were sad about that, but we also thought, well, we could use this model of the virus to to work out where it came from because, you know, we know that it's attaching to this receptor ACE 2, in humans. And, if it's come from an animal source, then we there should be an animal out there whose ACE 2, binds better to the virus than than human ACE 2. So so we innocently set about, yeah, modeling all the different animals, to understand which animal the virus came from. The surprising result of that, rather than finding some, you know, exotic animal at the top of the list, we found humans. Alright. Now that was not the intention of our research, but, you know, having found that, like all scientists, we thought, yeah, you know, we should make this available. People can criticize it. And and then we hit this this roadblock of of, you know, you couldn't publish anything because it wasn't part of the official narrative at at the time. This was just we weren't saying where the virus came from or who made it. We just were saying there are features in this virus that cannot be explained, you know, if it if it arose naturally. We found humans, a not very exotic animal. And, of course, that raised really interesting questions because it said this virus, if if you went by our original thinking, it came must have come from from humans because it's so, well human adapted. That that really had us scratching our heads, how to explain that conundrum. And, of course, you know, one of the possibilities is that was by chance, but it that that seemed highly unlikely, given the stringency of the work we've done. Virus that cannot be explained, you know, if it if it arose naturally. Very innocent we thought. No. If you speak against the official narrative, it's not innocent. You know, you're you're you're considered a terrorist, a public health terrorist. You're a danger to the country. The other explanation is that maybe it had adapted to human cells in some, you know, sense. And then, obviously, then, you know, the the most likely place for that is the laboratory. And so so that did raise the question, was the source of this virus not directly from from an animal? Did it get modified or or somehow was it it, an accidental laboratory release, which we've seen with other viruses in the past. So so it was innocent work, but it took a long, long time to get it published because, you know, the narrative was that that was not an acceptable, question to be asking because we were just asking a question. We weren't trying to tell anyone anything other than here's our research, here's what it shows. You know, the furin cleavage site, which is what you referred to as the other intriguing thing that looked like a smoking gun. Again, I I know that head of the CCC at the time said the same things. Many people have said the same things, but in our modeling, it was it was clear to us that it looked like the Purine cleavage site was not a natural part of this virus.

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SCIENTIFIC PAPER FROM NIKOLAI PETROVSKI - "In silico comparison of SARS-CoV-2 spike protein-ACE2 binding affinities across species and implications for virus origin" https://www.nature.com/articles/s41598-021-92388-5

In silico comparison of SARS-CoV-2 spike protein-ACE2 binding affinities across species and implications for virus origin - Scientific Reports The devastating impact of the COVID-19 pandemic caused by SARS–coronavirus 2 (SARS-CoV-2) has raised important questions about its origins and the mechanism of its transfer to humans. A further question was whether companion or commercial animals could act as SARS-CoV-2 vectors, with early data suggesting susceptibility is species specific. To better understand SARS-CoV-2 species susceptibility, we undertook an in silico structural homology modelling, protein–protein docking, and molecular dynamics simulation study of SARS-CoV-2 spike protein’s ability to bind angiotensin converting enzyme 2 (ACE2) from relevant species. Spike protein exhibited the highest binding to human (h)ACE2 of all the species tested, forming the highest number of hydrogen bonds with hACE2. Interestingly, pangolin ACE2 showed the next highest binding affinity despite having a relatively low sequence homology, whereas the affinity of monkey ACE2 was much lower despite its high sequence similarity to hACE2. These differences highlight the power of a structural versus a sequence-based approach to cross-species analyses. ACE2 species in the upper half of the predicted affinity range (monkey, hamster, dog, ferret, cat) have been shown to be permissive to SARS-CoV-2 infection, supporting a correlation between binding affinity and infection susceptibility. These findings show that the earliest known SARS-CoV-2 isolates were surprisingly well adapted to bind strongly to human ACE2, helping explain its efficient human to human respiratory transmission. This study highlights how in silico structural modelling methods can be used to rapidly generate information on novel viruses to help predict their behaviour and aid in countermeasure development. nature.com

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PROFESSOR DALGLEISH'S RESEARCH PAPER - "IT HAD 6 X INSERTIONS AROUND IT" https://www.semanticscholar.org/paper/The-Evidence-which-Suggests-that-This-Is-No-Evolved-S%C3%B8rensen-Dalgleish/bae0b5f2cae9f55b0f72349e7964989641a2d71d

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"The Discovery of HIV as the Cause of AIDS" - Authors: Robert C. Gallo, M.D., and Luc Montagnier, M.D https://www.nejm.org/doi/full/10.1056/NEJMp038194

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Luc Montagnier - The Nobel Prize in Physiology or Medicine 2008. Born: 18 August 1932, Chabris, France https://www.nobelprize.org/prizes/medicine/2008/montagnier/facts/

The Nobel Prize in Physiology or Medicine 2008 The Nobel Prize in Physiology or Medicine 2008 was divided, one half awarded to Harald zur Hausen "for his discovery of human papilloma viruses causing cervical cancer", the other half jointly to Françoise Barré-Sinoussi and Luc Montagnier "for their discovery of human immunodeficiency virus" nobelprize.org

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Luc Montagnier - Biographical - from "The Nobel Prize" https://www.nobelprize.org/prizes/medicine/2008/montagnier/biographical/ “In 1957, the first description of infectious viral RNA from the tobacco mosaic virus by Fraenkel-Conrat and Gierer and Schramm determined my vocation: to become a virologist using the modern approach of molecular biology.”

The Nobel Prize in Physiology or Medicine 2008 The Nobel Prize in Physiology or Medicine 2008 was divided, one half awarded to Harald zur Hausen "for his discovery of human papilloma viruses causing cervical cancer", the other half jointly to Françoise Barré-Sinoussi and Luc Montagnier "for their discovery of human immunodeficiency virus" nobelprize.org

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THE YEAR 2002 RECORDS GAIN OF FUNCTION RESEARCH "combining an HIV pseudovirus with SARS" (according to Richard Fleming PhD) - @Doctor_I_am_The https://t.co/vPY2NVMT2I

@Doctor_I_am_The - Richard M Fleming, PhD, MD, JD

HIV inserted into SARS viruses - originally in 2002. Gain-of-Function at its best. How did this help humanity? https://t.co/4me0wL8Qil

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Senator Rand Paul discusses here in some parts Nikolai Petrovski's research, done at the begining of the Pandemic, which found the virus was perfectly adapted to bind to Human ACE2 receptors https://t.co/go48wc1LZE "So one of the cool things I have discovered about Covid-19 is, they borrowed Oracle supercomputer, a scientist from Australia and the wanted to see which animal that virus would attach best to....it didn't attach to any animals very well but it attached perfectly to humans. This does not happen, it's almost proof positive that this was manipulated in a lab" "What really was sort of the smoking gun though is we discovered that the way the virus is genetically constructed is virtually identical to a research project from 2018 that had dr. Baric from UNC, dr. Shi from Wuhan and dr. Peter Daszak from New York. They actually applied for money to create something that looks very suspiciously like Covid-19" @RandPaul

Video Transcript AI Summary
Animal viruses that jump to humans often struggle to infect effectively due to their evolution in animals. The first SARS virus in 2003 had a 10% mortality rate but only infected 8,000 people because it didn't adapt well to humans. In contrast, COVID-19 attached perfectly to humans, suggesting possible lab manipulation. Researchers used a supercomputer to find that the virus did not attach well to other animals, indicating it was pre-adapted for humans. Evidence points to a 2018 research project that aimed to create a virus similar to COVID-19. Despite this, obtaining records from the Biden administration has been challenging, even with bipartisan support for transparency. The situation remains frustrating, highlighting the need for further investigation.
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Speaker 0: So the one thing that's universally true about animal viruses that break into the human kingdom, from the animal kingdom to the human kingdom, is they're clunky. They don't infect humans very well because they've evolved and adapted. Natural selection has selected for ones that infect that animal well. And so when they infect humans, they try it many times until they get lucky, and then they get a mutation where it can infect other humans. The best example of this is 2,000 and 2, 2003, when the first SARS virus came out, it had a 10% mortality rate, which is in you know, that's, like, 30 times worse than this the current COVID nineteen we had, but it only infected 8,000 people. Why? It just didn't infect humans very well. When they went back and did testing, they found that it infected civets well and also bats. So one of the cool things that I've discovered about COVID nineteen is they they borrowed Oracle's supercomputer, a scientist from Australia, and they wanted to see which animal that the virus would attach best to. So they tested it with humans and, like dozens of other animals. And lo and behold, it didn't attach to any animals very well. It attached perfectly to humans. This does not happen. It's almost proof positive that this was manipulated in the lab. And what you do in the lab is you actually speed up evolution and you direct evolution because you keep infecting mice that have human lung markers. So it thinks it's infecting a human lung. And you do it over and over again, you get the sickest mouse and the one with the highest viral load, you take that out and you infect the mice again. And each time you pass it through the virus, you get the sickest and the most infected mouse, and you do it again, you're selecting for the worst, the most deadly, the most efficiently. And this is what the scientists found. Alina Chan from MIT, she said it looked pre adapted. And this is what convinced her. What really was sort of the smoking gun though is we discovered that the way the virus is genetically constructed is virtually identical to a research project from 2018 that had Doctor. Barrick from UNC, Doctor. Xi from Wuhan, and Doctor. Peter Daszak from New York, they actually applied for money to create something that looks, very suspiciously like COVID-nineteen. They didn't get the money for it, but almost everybody believes now that doctor Xi in China went ahead and did that project, created that virus, probably to create a vaccine, and probably it was an accident that it leaked out. But we have all of this evidence now, and yet it has been like pulling teeth to get a Democrat anywhere in Congress to sign even a records release. And I tell these people all the time, look, I'm a Republican, but if a Democrat comes to me ever and asks me if I'm the chairman of a committee to sign a records release, I will never turn them down. I can't imagine ever turning down a records release from our government. And yet, I have had to use blocking nominations, blocking legislation, tying things up in order to get them to finally sign letters. And lo and behold, even when I finally got a Democrat to sign letters to get COVID records, the Biden administration won't give it to me. It's not even classified, but they won't give us the records. It's really it's shocking, and your book describes it so well. I really hope everyone in our audience reads it because

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DID NIH FUND GOF RESEARCH AT THE WUHAN INSTITUTE OF VIROLOGY THROUGH ECOHEALTH? Dr. Tabak: “ yes, we did” https://t.co/Htu6fuf0ql

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NIH did fund research at the Wuhan Institute of Virology through ECHO Health, depending on how you define gain of function research. If you refer to the broader term, then yes, it was funded. This type of research occurs in many labs across the country and is not regulated because it does not pose any threat or harm.
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Speaker 0: Doctor Tabak, did NIH fund gain of function research at the Wuhan Institute of Virology through ECHO Health? It depends on your definition of gain of function research. If you're speaking about the generic term, yes, we did, because but this is research. The generic term is research that goes on in many many labs around the country. It is not regulated, and the reason it's not regulated is it poses no threat or harm to anybody.

@Humanspective - Humanspective

"WAS THE WUHAN INSTITUTE CONDUCTING GOF RESEARCH ON [BAT] CORONAVIRUS's?" https://t.co/JRdKvn4nCx Former Director of the U.S. Centers for Disease Control, Dr Robert Redfield - "ABSOLUTELY" Dr Robert Redfield also adds that their is an effort by scientist's to compartmentalise the various forms of gain of function research, saying that he thinks it's all GOF if it's an attempt to increase Pathogenicity - "If I make a nonpathogen pathogenic, that's gain-of-function."

Video Transcript AI Summary
Gain of function research involves modifying a pathogen to enhance its transmissibility or pathogenicity. This definition includes making a nonpathogen pathogenic. Regarding the Wuhan Institute, there is skepticism about whether they were conducting gain of function research on coronaviruses. Gain of function research has not led to any life-saving vaccines or therapeutics, nor has it stopped a pandemic; in fact, it may have contributed to the current pandemic. While supporters of this research believe it could yield benefits, I personally see no tangible advantages in it.
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Speaker 0: In one sentence, can you provide a definition of gain of function research? And I say that because there becomes a little semantics sometimes, I believe, within the scientific community of what is a chimera and what is gain of function? Speaker 1: Yes, I think it's to take a pathogen and try to increase 1 of 2 things or both, to increase its transmissibility or its pathogenicity. I disagree with some of my colleagues at NIH to say the definition is restricted to a pathogen that's already a pathogen. If I make a nonpathogen pathogenic, that's gain of function. Speaker 0: So in your expert opinion, was the Wuhan Institute conducting gain of function research on the coronaviruses? So one other path of questioning for you, Doctor. Redfield. Proponents of this research claim it may result in vaccines or maybe even stop a pandemic. Doctor. Redfield, has gain of function created any life saving vaccines or therapeutics to your knowledge? Speaker 1: Not to my knowledge. Speaker 0: Has gain of function stopped a pandemic in your opinion? Speaker 1: No. On the contrary, I think it probably caused the greatest pandemic our world has seen. Speaker 0: Do you find any tangible benefits to gain of function research at this time? Speaker 1: I personally don't, but I do want to stress, I think the men and women that support it are people of good faith because they truly believe it's going to lead to a potential benefit. I disagree with that assessment.
Humanspective
Posted - October 17, 2024 at 8:14 PM
Saved - October 18, 2024 at 3:30 AM
reSee.it AI Summary
I recently learned that the lead author of a controversial nutrition paper was at Davos promoting the idea that ultra-processed cereals, like Lucky Charms, are healthy. When I questioned him about the study's claims, he became aggressive and defensive, insisting that cereals fortified with vitamins are as good as whole grains. Despite my concerns about his conflicts of interest and the influence of food industry funding on research, he dismissed my questions and even threatened me. This situation highlights how such studies can shape policies that negatively impact children's health.

@Humanspective - Humanspective

Calley Means reveals the lead author of a well known nutrition paper was in Davos marketing to Klaus Schwab's WEF Globalist's, selling the idea ultra processed cereal is healthy. The author rang him up berating him and threatening him to stop advocating for children's health. According to @calleymeans this same report/study basically said "Lucky Charms cereal [was] healthier then eggs"....a report where eggs and free range grass fed steak is discouraged. According to Calley Means, with a study like this you can start getting political and influencing different systems, like education and politics. The result? "They're serving Lucky Charms in schools" [and] "Reeses Pieces Cereal was a recommended item". They are serving children ultra processed foods that dramatically impact metabolic health TRANSCRIPT: "but the the study's author uh called me from Davos he was on a panel actually promoting the study to people around the world about how cereal is healthy..... and he started screaming at me, so he's in the hallways [OF DAVOS] he got my number call me and he started questioning my credentials. "He said you don't know how this works, I said sir not I have one question uh, Cheerios was rated as as better than organic quinoa as a grain are you saying that the grains and cheerios or Lucky Charms are as good as organic quinoa or some like whole natural grain? "he's like yes [Lucky Charms] is as healthy as the as the most natural grain because they fortify it with vitamins and fortify it with other good things which is which is a great advancement and I would absolutely recommend somebody eating Reese's Puffs grains as much as any other whole grain" "And I then I asked him does the fact that you have been paid personal consulting payments not research grants but his conflicts of interest is a laundry list of personal consult personal bribes [from] food companies from an Ozempic distributor.....does this impact your guidance?" "Plus the fact that your school Tufts Nutrition School is majority funded by food companies the food industry spends 11 times more on research than the NIH.... does that impact your judgment?" "He laughed at me and said you don't know how the world works, how dare you ever suggest that that would impact my judgment, this is just the way it works" "So he [then] threatened me and said you know we we know some of the same people at Stanford where we both went and and basically threatened to you know, if I kept rocking the boat that he was gonna talk to some of our mutual acquaintances at Stanford..... which is you know is always always part of the game to threaten club membership if you happen to be advocating for children not poisoning them with added sugar so um yeah it was it was it was it was a educational experience" Eat bugs and cereal otherwise the Globalist's are coming for you

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The speaker recounts a phone call from the author of a study promoting cereal's health benefits, who allegedly berated the speaker and questioned their credentials. The speaker challenged the author's claim that the grains in cereals like Cheerios and Lucky Charms are as healthy as organic quinoa due to fortification. The speaker questioned whether the author's personal consulting payments from food companies, including an Ozempic distributor, and the funding of Tufts Nutrition School by food companies, influenced his judgment. The author reportedly dismissed the suggestion, stating that food companies largely fund nutrition research. The speaker claims the author then threatened to contact mutual acquaintances at Stanford if the speaker continued to challenge his claims.
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Speaker 0: The study's author called me from Davos. He was on a panel actually promoting this study to people around the world about how cereal's healthy, and he started screaming at me. So he's in the hallways. He got my number, call me, and he started questioning my credentials. He said, you don't know how this works. I said, sir, I have one question. Cheerios was rated as better than organic kin was at grain. Are you saying that the grains in Cheerios or Lucky Charms are as good as organic quinoa or some whole natural grain? He's like, yes, I do. I think that grain in Lucky Charms is as healthy as the as the most natural grain because they fortify it with vitamins and fortify it with other good things, which is which is a great advancement. And I would absolutely recommend somebody eating Reese's Puffs grains, as much as any other whole grain. And I then I asked him, does the fact that you have been paid personal consulting payments, not research grants, but his conflicts of interest is a laundry list of personal consult personal bribes, I consider them, to him from food companies, from, I don't know, Ozempic, distributor. Does this impact your guidance, plus the fact that your school, Tufts Nutrition School, is majority funded, by food companies? The the food industry spends 11 times more on research than the NIH. Does that impact your judgement? He laughed at me and said, you don't know how the world works. How dare you ever suggest that that would impact my judgement? This is just the way it works, that we're funded the majority by food companies. There wouldn't be nutrition research otherwise. And, of course, not. And that's a that's an outlandish implication. So the and he he he then threatened me, and said, you know, we we know some of the same people at Stanford where we both went and and basically threatened to, you know, if I kept rocking the boat that he was gonna talk to some of our mutual acquaintances at Stanford, which is, you know, is always always part of the game to to threaten club membership if you happen to be advocating for children not poison themselves with that and sugar. So, yeah, it it was a it was a it was a educational experience.
sophiadahl1
Posted - October 15, 2024 at 5:03 AM
Saved - October 15, 2024 at 11:06 PM
reSee.it AI Summary
A reminder highlights findings from German pathologist Dr. Arne Burkhardt, who conducted autopsies on patients who died suddenly after vaccination. He reported that the vaccine can cross the blood-brain barrier, leading brain cells to produce spike proteins instead of performing their normal functions. In response, another participant noted the intriguing connection between lipid nanoparticles crossing the blood-brain barrier and the production of spike proteins by brain cells.

@sophiadahl1 - Sophia Dahl

Reminder ‼️ German Patholgists Finds Brain Cells Had Made Spike Protein in Autopsy Examination of “Vaxxed” Patients‼️ German pathologists Dr. Arne Burkhardt presents autopsy results of "Sudden Adult Death" Patients Post-Vax and makes some important discoveries‼️ "The blood brain barrier can be crossed by the vax. And you can see that it's the actual brain cells that produce the spike protein."‼️ “These brain cells are supposed to be actually helping us to think rather than focusing on making the spike protien.”‼️🙏👇 Source and Full Video🔗👇👇 https://odysee.com/@en:a5/Pathology-Conference_Burkhardt_Presentation_EN_20220311:7

Pathology of vaccine deaths and vaccine injuries | After the evidence now first proof https://pathologie-konferenz.de/en/ odysee.com

@Humanspective - Humanspective

@sophiadahl1 Now there's an interesting mechanistic connection. Lipid Nano Particles cross the Blood Brain Barrier and cause brain cells to produce spike protein?

@Humanspective - Humanspective

MODERNA KNEW IN 2017 mRNA TECHNOLOGY WOULD GO TO THE BRAIN. That means it likely crosses the Blood Brain Barrier (BBB) PFIZER VERIFIED MODERNA'S FINDINGS in the bioaccumulation studies, released by FOI from the Australian TGA. Document 6 - "Nonclinical Evaluation Report BNT162b2 [mRNA] COVID-19 vaccine (COMIRNATYTM) - dated January 2021" Pfizer and Moderna both knew it would go to the brain. Were civilian populations warned about that?

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In 2017, Moderna published a paper on an influenza vaccine using lipid nanoparticles. The study showed that in animals tested, the lipid nanoparticle vaccine spread into the brain, bone marrow, liver, spleen, and the muscle site where it was injected.
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Speaker 0: That's not the only page paper you should know about because in 2017, Moderna published a paper using lipid nanoparticles on the influenza vaccine, and it showed then in the animals tested, their lipid nanoparticle vaccine spread into the brain, the bone marrow, the liver, the spleen, and the muscle site where it was injected. 2017, brought to you by Moderna.
Humanspective
Posted - October 15, 2024 at 12:47 AM
Saved - October 15, 2024 at 11:42 AM
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Pfizer faces significant legal challenges as Kris Kobach, Attorney General of Kansas, leads a lawsuit against the company, citing violations of the Kansas Consumer Protection Act. He claims Pfizer misrepresented the safety of its COVID vaccine for pregnant women, despite knowing about risks, including a miscarriage rate exceeding 10% among 458 cases studied as early as February 2021. The lawsuit also criticizes government agencies for continuing to promote the vaccine as safe, amidst growing concerns about contamination in vaccine vials.

@Humanspective - Humanspective

PFIZER IS IN BIG TROUBLE. NEW interview with Kris Kobach, Attorney General for the State of Kansas, who is suing Pfizer, along with 5 x other American States. He mentions they knew 10% of women had miscarriages: "Pfizer was well aware of the many risks to pregnant women and they had information in their possession not only of of causing you know grave problems for pregnant rats but they also had information as early as February 2021 on 458 pregnant women and they knew that there were complications including miscarriages in over 10% of the cases" TRANSCRIPT FOR CLIP: NEWSMAX "You're suing Pfizer for misleading claims on the covid vaccine sir round of applause for you on this what's this about and what's your case" KRIS KOBACK "Well the case is that Pfizer violated the Kansas Consumer Protection Act and by the way all 50 states have some version of a consumer Protection act and while the federal government gave all the vaccine manufacturers immunity from normal tort suits, where someone who's injured would sue the company seeking damages for their injury, the federal government did not give the vaccine manufacturers license to misrepresent or state things that they knew to be false when trying to push their product, and that's what this lawsuit is about" "[Pfizer] made multiple misrepresentations, including saying it was safe for pregnant women, when Pfizer was well aware of the many risks to pregnant women. And they had information in their possession not only of of causing, you know grave problems for pregnant rats, but they also had information as early as February 2021 on 458 pregnant women and they knew that there were complications, including miscarriages in over 10% of the cases..... just think about that a person dies in every miscarriage and yet they proceeded to advertise it as safe for pregnant women". This lawsuit also highlights the amount of ignorance within other government departments, that are still pushing the "safe and effective" narrative on a Global scale. Add on top of the that the more recent accumulating evidence of DNA contamination in Pfizer and Moderna vials, and you have a ticking time bomb for the Pharmaceutical industry

Video Transcript AI Summary
The Kansas Attorney General is suing Pfizer for violating the Kansas Consumer Protection Act by making misleading claims about its COVID-19 vaccine. The suit alleges Pfizer misrepresented the vaccine's safety, particularly for pregnant women. While vaccine manufacturers have immunity from injury lawsuits, they aren't protected from liability for misrepresentation. The Attorney General claims Pfizer advertised the vaccine as safe for pregnant women despite knowing of risks. He states that Pfizer possessed information as early as February 2021 regarding complications, including miscarriages in over 10% of cases, yet still promoted the vaccine as safe for pregnant women. The lawsuit focuses on Pfizer allegedly misrepresenting their product.
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Speaker 0: You're suing Pfizer for misleading claims on the COVID vaccine, sir. Round of applause for you on this. What's this about, and what's your case? Speaker 1: Well, the case is that Pfizer violated the Kansas Consumer Protection Act. And by the way, all 50 states have some version of a Consumer Protection Act. And while the federal government gave all the vaccine manufacturers immunity from normal tort suits where someone who's injured would sue the company seeking damages for their injury, The federal government did not give the vaccine manufacturers license to misrepresent or state things that they knew to be false when trying to push their product. And that's what this lawsuit is about. They made multiple misrepresentations, including saying it was safe for pregnant women when Pfizer was well aware of the many risks to pregnant women, and they had information in their possession, not only of causing, you know, grave problems for pregnant rats, but they also had information as early as February 2021 on 458 pregnant women. And they knew that there were complications, including miscarriages in over 10% of the cases. Just think about that. A person dies in every miscarriage, and yet they proceeded to advertise it as safe for pregnant women. So the lawsuit is about misrepresenting their product. Speaker 0: Yeah. No. That is shocking to me. Well, attorney general Chris Kobach, I really appreciate you doing this, filing that suit and the briefs for the Chevron case. Outstanding work, sir. Appreciate it. Speaker 1: Thank you.
Humanspective
Posted - October 15, 2024 at 12:47 AM
Saved - October 15, 2024 at 6:23 AM
reSee.it AI Summary
Pfizer faces a lawsuit led by Kris Kobach, Attorney General of Kansas, alongside five other states, for allegedly misleading claims about the COVID vaccine's safety for pregnant women. Kobach asserts that Pfizer was aware of significant risks, including a miscarriage rate exceeding 10% among 458 pregnant women studied as early as February 2021. The lawsuit claims Pfizer violated the Kansas Consumer Protection Act by misrepresenting the vaccine's safety, despite having information about potential complications. This situation raises concerns about the broader implications for the pharmaceutical industry.

@Humanspective - Humanspective

PFIZER IS IN BIG TROUBLE. NEW interview with Kris Kobach, Attorney General for the State of Kansas, who is suing Pfizer, along with 5 x other American States. He mentions they knew 10% of women had miscarriages: "Pfizer was well aware of the many risks to pregnant women and they had information in their possession not only of of causing you know grave problems for pregnant rats but they also had information as early as February 2021 on 458 pregnant women and they knew that there were complications including miscarriages in over 10% of the cases" TRANSCRIPT FOR CLIP: NEWSMAX "You're suing Pfizer for misleading claims on the covid vaccine sir round of applause for you on this what's this about and what's your case" KRIS KOBACK "Well the case is that Pfizer violated the Kansas Consumer Protection Act and by the way all 50 states have some version of a consumer Protection act and while the federal government gave all the vaccine manufacturers immunity from normal tort suits, where someone who's injured would sue the company seeking damages for their injury, the federal government did not give the vaccine manufacturers license to misrepresent or state things that they knew to be false when trying to push their product, and that's what this lawsuit is about" "[Pfizer] made multiple misrepresentations, including saying it was safe for pregnant women, when Pfizer was well aware of the many risks to pregnant women. And they had information in their possession not only of of causing, you know grave problems for pregnant rats, but they also had information as early as February 2021 on 458 pregnant women and they knew that there were complications, including miscarriages in over 10% of the cases..... just think about that a person dies in every miscarriage and yet they proceeded to advertise it as safe for pregnant women". This lawsuit also highlights the amount of ignorance within other government departments, that are still pushing the "safe and effective" narrative on a Global scale. Add on top of the that the more recent accumulating evidence of DNA contamination in Pfizer and Moderna vials, and you have a ticking time bomb for the Pharmaceutical industry

Humanspective
Posted - October 12, 2024 at 10:51 PM
Saved - October 13, 2024 at 4:25 AM
reSee.it AI Summary
I shared a significant moment in Australia where the Port Hedland Council voted 5-2 to call for an immediate suspension of Pfizer and Moderna COVID-19 vaccines due to alarming levels of DNA contamination. The motion aims to inform all local councils and health practitioners across Australia, urging them to share this critical information with patients. I emphasized the importance of questioning government silence on health risks and expressed hope that this grassroots movement could inspire broader action nationwide and potentially worldwide.

@Humanspective - Humanspective

NEW. HISTORIC MOMENT IN AUSTRALIA. The action that results from this could end up sweeping the World A new motion brought by the Port Hedland Council, in Western Australia, gets a 5-2 majority vote to "Call for an immediate suspension of the Pfizer and Moderna COVID-19 products". Here's some IMPORTANT POINTS of the motion that was passed by majority: ◻️All 537 Local Councils Australia Wide will be notified that they have called for the immediate suspension of covid mRNA vaccine, providing also the evidence and research around DNA contamination ◻️ "That Council forthwith deliver the letter seen at Annexure 1 to the Prime Minister" ◻️ "That Council forthwith circulates to all registered health practitioners and medical clinics operating within the Port Hedland Local Government Area" ◻️Councils will “Circulate to all other Australian Local Government Councils and shires [informing] all Councils and Shires about the findings” ◻️“Council strongly urges to practitioners to share this information with patients contemplating receiving any Pfizer or Moderna Cvoid mRNA vaccines” ◻️The CEO and their delegates contact the Commonwealth Minister for Health and Aged Care, Mark Butler, presenting Dr. Speicher’s Special Council Meeting Agenda” ◻️“The Council request a formal and public response from Minister Butler", the Australian Federal Health Minister These councillors discuss "the seriousness of the matter" around DNA contamination of both Pfizer and Moderna vaccines [which showed] levels 145x higher then levels deemed safe by the TGA. The councillors say there is "Clear scientific evidence that millions of Australians" could be, or have been, exposed to these risks: (4:34) Second Councillor Speaks. Votes FOR. Mentions that the silence from the Government and Health Officials is "QUITE ALARMING" (13:33) This is a Historic Motion (14:49) Nurse with 47 years experience. Votes FOR (16:21) Fourth Councillor votes FOR (16:57) Deputy Mayor. Votes FOR (21:15) Closing Remarks by Cr. Adrian McRae and final Vote. Adrian mentions BRIEF OVERVIEW FROM TRANSCRIPT: "Evidence [shows] levels of synthetic DNA contamination [is] up to 145 times higher [than] the TGA's own safety limits. For those unfamiliar the TGA limits are there for a reason, because synthetic DNA has been shown to integrate into human cells, leading to potential longterm health risks, like cancer genomic instability, vascular thromboses and blood clotting.....as well as immune system disruptions. These findings are alarming, but they are also far from isolated. Independent studies now in Canada, Germany and the US have all confirmed similar levels of contamination. International experts including some of the world's leading oncologists, geneticists, virologists, immunologists, microbiologists, and biochemists have joined forces to warn governments around the world, including our own government, about the dangers these contaminants pose. This is why the honorable Russell Broadbent MP, the Federal Member for Monash, has written multiple letters to the Prime Minister urging an immediate investigation and suspension of these vaccines. Yet the response from our government has been nothing but silence, not a word from the Prime Minister, not a word from the minister of health, despite receiving clear scientific evidence that millions of Australians could be at risk including those folks right here in Port Headland who were forced to take these experimental shots" "Sure health is not in the remit of of local government, but looking after our people most certainly is.....Tonight it was certainly not doing anything other than asking questions.....I would like to think that most of the people here are are not scared to ask questions of our bosses or of our state governments, or federal governments....we're all people no matter, you know, we're all just making our way through and I just think [that] this motion tonight [could] be the ripple that um creates a bigger wave across the country, and perhaps across the world. So there are a lot of people watching this, I know all over the world, pretty much every continent is covered and it's been a honour to talk with you guys about it, and it's an honour to represent you guys on such an issue.... [but] I just hope that everyone votes the right way and [I think] most people here know what the right way is so thank you" This really could be the beginning of a grass roots movement within the smaller government councils, notifying smaller communities Australia wide, pushing the Federal and State governments to take real action

@Humanspective - Humanspective

@_aussie17 @SaiKate108 @KatieGrace2022 @drcole12 @Kevin_McKernan @BroadbentMP @SenatorRennick @MRobertsQLD @roller2426 @risemelb @Carmilla5 @Theblackfemini3 @drmelissamccann @DrJulieSladden @myletrinh123

@Humanspective - Humanspective

@_aussie17 @SaiKate108 @KatieGrace2022 @drcole12 @Kevin_McKernan @BroadbentMP @SenatorRennick @MRobertsQLD @roller2426 @risemelb @Carmilla5 @Theblackfemini3 @drmelissamccann @DrJulieSladden @myletrinh123 Make sure to send/text the link to friends and family to let them know their local council will be receiving this information so they can follow up with them in their own communities 🙏

Humanspective
Posted - April 4, 2024 at 10:18 AM
Saved - October 13, 2024 at 12:15 AM
reSee.it AI Summary
I discussed Robert F. Kennedy's conversation with Joe Rogan about the types of mercury, particularly ethylmercury and methylmercury, and the implications for vaccines. RFK questioned the CDC's stance on mercury in tuna versus flu shots, citing a study by Dr. Thomas Burbacher that showed ethylmercury accumulates in the brains of monkeys. Dr. Paul Offit responded, agreeing on the accumulation but disputing claims of inflammation. I also noted the ongoing use of mercury in dental amalgams despite evidence of its dangers and highlighted the European Parliament's decision to ban toxic mercury uses by 2025.

@Humanspective - Humanspective

Healthy mercury in the body? Short thread 🧵 Robert F Kennedy discussed with Joe Rogan about the different types of Mercury, Ethylmercury vs Methylmercury. He illustrated this discussion using a conversation he says he had with Dr Paul Offit, in regards to how older vaccines were produced. RFK asks: “Why is it that CDC recommends that Pregnant women do not eat Tuna Fish to avoid the mercury, but that CDC is recommending mercury containing flu shots”. According to RFK, Dr. Paul Offit said "There’s a good mercury and theres a bad mercury." According to RFK, speaking to the reasoning behind even using mercury in products: "The NIH admitted that it was an adjuvent, to amplify the immune response." RFK added that "The more toxic the adjuvent the more robust the immune response". Apparently the immune system doesn’t react as powerfully if it’s just a “live virus” without adjuvant. According to RFK (and this makes total sense), vaccine developers always disagreed with Toxicologists, because the Toxicologist would always ask "What is the fate of that in your body?”. RFK dived into some of the studies he discussed with Paul Offit at the time. Apparently, Offit went silent about a very important study that RFK knew about when he asked the question about why they're using mercury in vaccines. It's at this point, Dr Offit sighted the Pichichero study. That's when RFK "caught him in a lie". In the Pichichero study of 2002 (10), they noticed the ethylmercury was excreted very quickly. Pichichero also found that the "Estimated blood half-life of ethylmercury was 7 days" [for] the cohort of 2 - 6 x month old babies (yes you read that right, they got mercury). Then RFK adds that "The NIH actually commissioned a study", to find out the truth of the fate of the different types of mercury. Which is why they enlisted the help of Thomas Burbacher. He basically did the same study (8), but did it with monkeys so that at the end (sadly and unethically) he could k*ll the monkeys. He found that Pajero was RIGHT about one fact. The ethylmercury "was gone from their blood in a week" - RFK. BUT importantly, when he did the Post-mortems, Burbacher found out the reason they couldn't find it in the same places Pajero looked. It was accumulating in the brains of the monkeys.

@Humanspective - Humanspective

As @TheChiefNerd also covered, Dr Paul Offit published a response to RFK's on his substack (11), providing a counter story to the evidence Kennedy provided. One of the most interesting statements Dr Paul Offit makes is: “it was not surprising that Thomas Burbacher found trace quantities of ethylmercury in the brain of infant monkeys injected with thimerosal, which can cross cell membranes”. He's actually agreeing with RFK. However he disagrees on RFK stating that it was "causing severe inflammation". - Robert F Kennedy. Offit also said “First, I have never worked for a pharmaceutical company”. This confuses me. According to Dr Paul Offit's very own Published article in the New England Journal of Medicine on September 27, 2007 (13), he declares at the end of the article that: “Dr. Offit reports serving on the scientific advisory board of Merck and being the coinventor of the bovine–human reassortant rotavirus vaccine RotaTeq, on which he holds a patent.”. And then Dr Offit also calls out RFK's claim "You need to talk to Paul Offit. Paul Offit made a $186 million deal with Merck", as a complete lie. I did find one story in relation to this from CBS. That article By Sharyl Attkisson on July 25, 2008 stated that: "Offit holds in a $1.5 million dollar research chair at Children's Hospital, funded by Merck. He holds the patent on an anti-diarrhea vaccine he developed with Merck, Rotateq, which has prevented thousands of hospitalizations. And future royalties for the vaccine were just sold for $182 million cash. Dr. Offit's share of vaccine profits? Unknown”. So what does that all mean? Is there a connection with Merck somehow? So the only point of contention in the monkey study is whether or not mercury causes inflammation in the brain. Both RFK and Offit agree on the point that it was accumulating in the brains of the monkeys. That's an important point because according to RFK, Paul was relying on the Pichichero study of 2002 (10), saying that the ethylmercury was excreted very quickly. Important to note, that when "The Chief Nerd" covered this, he cites a toxicology study stating - “These findings showed that both thimerosal and aluminum can change oxidant/antioxidant status, cause DNA damage, alter dopamine and DAT levels". Interesting, becuase I also found another related article (17) stating that: "When applied at non-toxic concentrations, methylmercury, the most common environmental form of mercury, becomes neurotoxic under pro-oxidant conditions. Furthermore, lead and mercury induce glial cell reactivity, a hallmark of brain inflammation". But it's actually the remarks made by RFK about the accumulation of Mercury for that monkey study, which reminded me of another big topic related to Mercury exposure. That actually led me to recent News that doesn't seem to getting much mainstream media attention.

@Humanspective - Humanspective

Remember the "Smoking Teeth" video? 17 x years ago this was published on Youtube showing the release of mercury vapours from mercury amalgam fillings. https://t.co/KhMO7KrNKy

Video Transcript AI Summary
The International Academy of Oral Medicine and Toxicology is concerned about manufacturers' and dental trade associations' safety claims, which they say contradict peer-reviewed scientific evidence. They believe the precautionary principle necessitates action when potential harm exists, regardless of absolute proof. Mercury vapor is shown emanating from a 25-year-old silver amalgam filling, even when submerged in body-temperature water or lightly rubbed. The amount of mercury released is claimed to be over 1,000 times the EPA's safe level for air. Mercury vapor is also released when the filling's temperature is raised to 110 degrees. The World Health Organization acknowledged in 1991 that dental fillings are the primary source of human mercury exposure. This is presented as a concern for those wanting healthy children.
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Speaker 0: The International Academy of Oral Medicine and Toxicology is extremely concerned about the anecdotal claims of safety by manufacturers and dental trade associations. They are at variance with the published, peer reviewed scientific evidence to the contrary. The precautionary principle requires action once the possibility of harm exists. It does not require proof beyond a shadow of a doubt that in the case of heavy metal and xenobiotic exposure is both nearly impossible and unnecessary in our opinion. What you're seeing is mercury vapor coming off a 25 year old silver amalgam filling in an extracted tooth. The background is a phosphorescent screen. The mercury vapor absorbs the fluorescent light and you can see it as a shadow on the screen. This is mercury coming off a filling that was dipped in water that's the same temperature as the human body. This is a filling that was rubbed with a pencil eraser for just a few seconds. Like going to the hygienist and having her clean your teeth. These are not small amounts of mercury. If you can see it, it's more than 1,000 times higher than the Environmental Protection Agency will allow for the air that we breathe. What about the last time you went to the dentist and they drilled on your tooth? Here is the mercury vapor every time you raise the temperature to 110 degrees. In 1991, the World Health Organization acknowledged that the predominant source of human exposure to mercury is from your fillings. That should be of concern to anyone wanting to have healthy children.

@Humanspective - Humanspective

This video was published on Jan 2016. Once again showing how "mercury vapour" is released. Don't you think it's interesting that after 17 x years (since the smoking teeth video), so many dentists are still using amalgam fillings and the whole industry seems to be plodding along and ignoring this information?

Video Transcript AI Summary
A visualization box was constructed using common hardware store materials to demonstrate mercury vapor release from dental amalgam. The experiment aims to show that significant mercury vapor is released during mixing and packing of amalgam, contrary to the common teaching in dental schools that mercury is trapped within the amalgam matrix. The experiment also visualizes mercury vapor released during the removal of set amalgam fillings with a high-speed dental drill. This demonstrates that drilling amalgam fillings exposes patients, dentists, and dental technicians to substantial amounts of mercury vapor, even more than previously imagined. Measurements reached 24,183 micrograms per cubic meter, which are levels described as unprecedented.
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Speaker 0: We just finished constructing our, visualization box, which is made out of everyday materials that you can get in any hardware store. Typically, in most dental schools, it's been taught that the mercury is trapped within the matrix of the amalgam. And so therefore, we're trying to visualize here and prove the fact that there's a significant amount that comes off during the mixing, during the packing, and then we'd have some teeth with the amalgam that's been set for a while, and we're gonna be removing that with a high speed dental drill in order to visualize how much vapor comes off during that procedure as well. Speaker 1: The American Dental Association has made the argument that mercury is fixed in the amalgam fillings and it doesn't come out easily. And what this research that we're doing here visually shows is that when you drill on an amalgam filling that dramatically exposes the patient and the dentist and the dental technician to huge amounts of mercury vapor that enters the body. It's even worse than what they imagined. 24183 micrograms per cubic meter, and, I've never seen levels of mercury this high.

@Humanspective - Humanspective

MEDIA SILENCE. New PRESS RELEASE. THE EUROPEAN PARLIAMENT and the European Council reach an "agreement to ban all remaining intentional uses of toxic mercury in the EU [to] further protect Europeans from toxic mercury". "European Parliament and the Council on the Commission's proposal for a revision of the Mercury Regulation. Given the availability of alternatives, the revised Mercury Regulation will prohibit the last intentional remaining uses of mercury in the EU. By prohibiting the use of dental amalgam as of 1 January 2025 and by introducing a prohibition to manufacture, import and export of certain mercury-containing lamps, this revised regulation will further protect Europeans from toxic mercury". Source: European Commission - 8th February 2024.

Humanspective
Posted - July 11, 2024 at 7:29 AM
Saved - September 28, 2024 at 1:51 PM
reSee.it AI Summary
I’ve noticed a growing number of whistleblowers eager to expose the truth, yet many fear becoming victims like Brandy Vaughan, who faced severe intimidation after leaving Merck. Andrew Wakefield recently highlighted alarming evidence from Merck's court documents, revealing threats against dissenting doctors. Vaughan documented her own terrifying experiences, including a break-in, tampered security systems, and unsettling messages left in her home. These incidents raise serious concerns about the safety of those challenging the pharmaceutical industry, especially in light of her untimely death.

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💥More whistleblowers want to reveal the truth, but they don't want to be "Brandy Vaughan'dised". Brandy Vaughan worked for Merck before being fired and becoming a whistleblower against Big Pharma. Here is a video where she documented some disturbing things Makes you wonder, how many people feel threatened to speak up and challenge the Pharmaceutical industry? Recently, Andrew Wakefield (who was also destroyed for challenging Big Pharma and the immunisation industry), talked about some intriguing and concerning evidence uncovered during court discovery, during a case against Merck for VIOXX. Internal letters/emails found from employees, regarding how to "deal" with DR's that spoke out mentioned: ◻️‘We may have to seek them out and destroy them where they live’ - Andrew Wakefield discussing Merck court discovery docs That story fits in perfectly here. In this documented video by the late Brandy Vaughan, she goes through all the super creepy and intimidating behaviour she has had to deal with at her own house since being fired from Merck ◻️Some seriously concerning intimidation allegations documented in this video by the late Brandy Vaughan: (1:00) - Installed a $3000 alarm system after initial break in. But then they disarmed the alarm system with the master code which nobody had except her (1:27) Documents the evidence the alarm company found about the home intrusion (2:30) Security experts mention how these might be intimidation tactics and that the whole house is probably bugged (4:10) Laptop was moved from hiding spot and placed in the middle of the kitchen floor, with a message (5:45) They returned to find a ladder taken from the garage and placed right out front a window (7:55) She finds a Duck Statue out the back patio are after she's been making provate phone calls about feeling like "a sitting duck" 🤯 This is all before she died suddenly, reportedly from Natural causes 🧐

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