MD, PhD in Global Health / Healthy Longevity / Member of International Scientific Community for Humanitarian Causes. #Longevity

I am thrilled my LNPs as a 5-body problem helped people. But there was some confusion about my last post. The five-track map as a claim about harm. It's not. It's a road map, not a crash report. Biodistribution (where things go) is a different question from pharmacodynamics (what they do when they get there). New post: the same five tracks, as a city road map. See my field guide in the next tweet.
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Paloma Franceschi retweeted
The WHO was established in 1948. For the entire duration of Biopreparat, including the Sverdlovsk anthrax attacks and Aralsk-7 smallpox incident, the Soviets did not report their bioweapons convention treaty violations nor information on BW leaks to WHO
Question: The US has retreated from intl health organizations. Are we equipped to respond to outbreaks like this in Russia and share information accurately? @celinegounder “This is part of the problem because we withdrew from W.H.O. We don't have the access to some of the information that W.H.O. shares out to what we call focal points in different countries.”
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Our study suggests a potential association between prenatal exposure to COVID-19 spike protein and neurodevelopmental problems, such as ASD. #LongCOVID These findings highlight the importance of further research into the potential effects of the COVID-19 virus on embryonic and fetal development and the potential long-term consequences for neurodevelopment.
Replying to @dbdugger
Epub 2023 Oct 27. Prenatal SARS-CoV-2 Spike Protein Exposure Induces Autism-Like Neurobehavioral Changes in Male Neonatal Rats pubmed.ncbi.nlm.nih.gov/3788…
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This review covers potential paths for SARS-CoV-2 infection of the brain. Among these putative processes, ferroptosis may contribute to the etiology of COVID-19-associated Parkinson Disease potentially providing therapeutic methods. via @dbdugger nature.com/articles/s41420-0…
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U.S. government deployed plague-linked raccoonpox vaccines before the 2009 and 2020 pandemics and plans more in 2027, according to @JonFleetwood. A DEFUSE-linked program that is now mass-producing a bat 🦇 vaccine and developing “hands-off, mass delivery” by spray. 🦝🦝 🧵
U.S. Gov’t Deployed Plague-Linked Raccoonpox Vaccines Before 2009 and 2020 Pandemics, Plans More in 2027 DEFUSE-linked program is now mass-producing its bat vaccine while developing “hands-off, mass delivery” by spray.
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Woke Plague
Calling it the 'Black Plague' is just as racist as the 'China virus'. White Russian cocktails don't allow you to call it the White Plague either. If you don't refer to it as a 'Plague of Color', you'll be canceled. In times like this it's imperative we get our micro-aggression, victimhood, and privilege rules locked down.
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Paloma Franceschi retweeted
Just letting y'all know that they are trying to blame mice for spreading plague but we don't have it. It's the other rodents. Blame them.
Replying to @CDCgov @SenRandPaul
SHUT THE FUCK UP WE’RE NOT DOING THIS AGAIN
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Paloma Franceschi retweeted
Why mRNA 💉s Will Never Work #ItsTheLNPsStupid
Go Where U Wanna Go ~ I Get Around (It doesn't stay in the deltoid!) 🧵🧵s on the bio distribution of the C0VID 💉 LNPs. keep showing replies
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Paloma Franceschi retweeted
The Real World Data scandal (where pharma linked entities manufacture health data) meets the RECOVERY study (where COVID patients were subjected to a 30% death rate in order to sell a narrative). IQVIA is one of the major players in synthetic health data, and they can make it up as they go along. If it sells drugs for their pharma clients, they make a lot of money. That is how the racket works. People died on the RECOVERY trial who should never have died. Lots of them. @jeffreytucker @MaryanneDemasi @RWMaloneMD @JesslovesMJK @Fynnderella1 @open_vaet
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Paloma Franceschi retweeted
Replying to @JoshWalkos
Emerging Viruses: AIDS & Ebola; Horowitz. 1996.
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Paloma Franceschi retweeted
This just in. Unreal. Reports Russian lab leak allegedly claims second life, four countries shut borders news.com.au/lifestyle/health…
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Paloma Franceschi retweeted
🚨 The only verified method of removing the rubbery white #CalimariClots which are found in the bodies of live and 💀 people after 💉 with mRNA 💉s. @r_hirschman These clots are formed when the lipid nanoparticles and the polyethylene glycol of the LNP shell escape the deltoid through the surrounding capillaries, enter the 🩸 stream and bond with plasma proteins to form clots. The mRNA then releases its spike protein payload. Spike is cleaved and produces the prion-like S1 subunit causing amyloid fibrin clots to form around it, and degradation of the endothelial layers producing the spike. The clot constructs and endothelial debris aggregate into #microclots and then larger macroclots which slowly fill the vasculature, taking the shape of the vessels themselves. Lab testing has shown the clots to be the tensile strength of EPDM rubber (weather stripping). @GregGr67545 @DanSantiag49091 There are no food-grade safe products to dissolve them. even nattokinase cannot do so. Removal by filtering the 🩸 with apheresis, is the only available option. One 🏥 in the world showing some success doing so is in 🇯🇵 , at considerable patient expense. #EdogawaMcCairnProtocol The other is 👇
Now there's Three separate therapies and filtration columns We've found that DARPA and the US Military have access to use Be We Don't... Three separate therapies and medical devices filtration columns. The Fourth is what's being used in Japan Nearly identical to all of these in design, use and effects. And We can't use the Japanese columns here * either * Just thought you'd like to know
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Self-amplifying RNA vaccines is coming soon.
Governments and militaries are already developing over 21 PLAGUE VACCINES. Self-amplifying RNA (UK) mRNA (Israel) DNA (U.S.) Viral Vector (UK, U.S.) Bacterial Vector (U.S.) Subunit (U.S., UK, China) Live-Attenuated (Russia, China, U.S.) I won't be taking any of them.
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Replying to @ABridgen
The evil part, the unforgivable part, is that they created that deadly virus and released it to the public, expecting at least as many deaths as they first projected, and then claim to be heroes for selling you a vaccine they believed would work. Luckily for us, our mucosal immune system saved most of us. Anything that could increase its efficiency was silenced. Like HCQ and vitamin D. It was evil; too many doctors went along. x.com/GauteNilsen/status/169…
1/3 Once you understand how natural immunity against airborne viruses is created you will never want an injection again. Did you know that immunity against airborne viruses is created in your gut? Peyers patches.
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Paloma Franceschi retweeted
I support this. Even though Andersen said unsavory things about my own work, I believe science is made better if we bring people together in professional venues to discuss different views respectfully. Everyone’s better than their worst moment. Let’s get back to science
Last year, as part of a comprehensive review of NIH’s intramural policies, I announced that NIH was adopting an updated agency-wide framework to embed principles of academic freedom within our Intramural Research Program. This framework recognizes that intramural researchers must be free to share their scientific viewpoints and to communicate their scientific findings through manuscripts, presentations, media interviews, and so on. This includes hosting outside lecturers for events focused on their scientific work. Today, NIH reaffirms this commitment to academic freedom as members of the intramural research community host Kristian G. Andersen, MPhil, PhD, as a guest lecturer. Dr. Andersen is a co-author of a March 2020 paper published in Nature Medicine titled “The proximal origin of SARS-CoV-2.” The paper’s authors assert: “Our analyses clearly show that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus.” They further write that “we do not believe that any type of laboratory-based scenario is plausible.” The paper was cited extensively by members of the media, social media companies, and government officials to refute or suppress lab-origin hypotheses and to discredit anyone who publicly dissented from the dominant natural-origins narrative. As then-NIH Director Dr. Francis Collins wrote, “this study leaves little room to refute a natural origin for COVID-19.” Yet before and after the paper’s publication, Dr. Andersen himself expressed substantially more uncertainty. In January, he wrote in an email that some features of the virus “(potentially) look engineered.” One month after the paper’s publication, he wrote privately that he was not fully convinced that every lab-based scenario could be ruled out. In January 2025, the Central Intelligence Agency released the results of an assessment conducted during the Biden administration that found a “research-related origin” of SARS-CoV-2 was “more likely than a natural origin,” while assessing both theories as plausible. Given the evidence I’ve seen, I think the preponderance of evidence supports the theory that the virus leaked from a lab. I am keenly aware that no hypothesis about the origins of SARS-CoV-2 has been conclusively proven. When it comes to open scientific questions like this, our ability to pursue truth depends on our freedom to explore various hypotheses, weigh all available evidence, and deliberate openly. This freedom was denied to many scientists during the pandemic. 𝗜 𝗮𝗺 𝗽𝗹𝗲𝗮𝘀𝗲𝗱 𝘁𝗵𝗮𝘁 𝗮𝗹𝗹 𝗡𝗜𝗛 𝘀𝗰𝗶𝗲𝗻𝘁𝗶𝘀𝘁𝘀 𝗮𝗻𝗱 𝘁𝗵𝗲𝗶𝗿 𝗴𝘂𝗲𝘀𝘁𝘀—𝗻𝗼 𝗺𝗮𝘁𝘁𝗲𝗿 𝘄𝗵𝗮𝘁 𝘁𝗵𝗲𝘆 𝘁𝗵𝗶𝗻𝗸 𝗮𝗯𝗼𝘂𝘁 𝘁𝗵𝗲 𝗼𝗿𝗶𝗴𝗶𝗻𝘀 𝗼𝗳 𝗦𝗔𝗥𝗦-𝗖𝗼𝗩-𝟮—𝗲𝗻𝗷𝗼𝘆 𝗶𝘁 𝗻𝗼𝘄.
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“Today, NIH reaffirms this commitment to academic freedom as members of the intramural research community host Kristian G. Andersen, MPhil, PhD, as a guest lecturer. Dr. Andersen is a co-author of a March 2020 paper published in Nature Medicine titled “The proximal origin of SARS-CoV-2.” The paper’s authors assert: “Our analyses clearly show that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus.” They further write that ‘we do not believe that any type of laboratory-based scenario is plausible’.” 👇🏻
Last year, as part of a comprehensive review of NIH’s intramural policies, I announced that NIH was adopting an updated agency-wide framework to embed principles of academic freedom within our Intramural Research Program. This framework recognizes that intramural researchers must be free to share their scientific viewpoints and to communicate their scientific findings through manuscripts, presentations, media interviews, and so on. This includes hosting outside lecturers for events focused on their scientific work. Today, NIH reaffirms this commitment to academic freedom as members of the intramural research community host Kristian G. Andersen, MPhil, PhD, as a guest lecturer. Dr. Andersen is a co-author of a March 2020 paper published in Nature Medicine titled “The proximal origin of SARS-CoV-2.” The paper’s authors assert: “Our analyses clearly show that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus.” They further write that “we do not believe that any type of laboratory-based scenario is plausible.” The paper was cited extensively by members of the media, social media companies, and government officials to refute or suppress lab-origin hypotheses and to discredit anyone who publicly dissented from the dominant natural-origins narrative. As then-NIH Director Dr. Francis Collins wrote, “this study leaves little room to refute a natural origin for COVID-19.” Yet before and after the paper’s publication, Dr. Andersen himself expressed substantially more uncertainty. In January, he wrote in an email that some features of the virus “(potentially) look engineered.” One month after the paper’s publication, he wrote privately that he was not fully convinced that every lab-based scenario could be ruled out. In January 2025, the Central Intelligence Agency released the results of an assessment conducted during the Biden administration that found a “research-related origin” of SARS-CoV-2 was “more likely than a natural origin,” while assessing both theories as plausible. Given the evidence I’ve seen, I think the preponderance of evidence supports the theory that the virus leaked from a lab. I am keenly aware that no hypothesis about the origins of SARS-CoV-2 has been conclusively proven. When it comes to open scientific questions like this, our ability to pursue truth depends on our freedom to explore various hypotheses, weigh all available evidence, and deliberate openly. This freedom was denied to many scientists during the pandemic. 𝗜 𝗮𝗺 𝗽𝗹𝗲𝗮𝘀𝗲𝗱 𝘁𝗵𝗮𝘁 𝗮𝗹𝗹 𝗡𝗜𝗛 𝘀𝗰𝗶𝗲𝗻𝘁𝗶𝘀𝘁𝘀 𝗮𝗻𝗱 𝘁𝗵𝗲𝗶𝗿 𝗴𝘂𝗲𝘀𝘁𝘀—𝗻𝗼 𝗺𝗮𝘁𝘁𝗲𝗿 𝘄𝗵𝗮𝘁 𝘁𝗵𝗲𝘆 𝘁𝗵𝗶𝗻𝗸 𝗮𝗯𝗼𝘂𝘁 𝘁𝗵𝗲 𝗼𝗿𝗶𝗴𝗶𝗻𝘀 𝗼𝗳 𝗦𝗔𝗥𝗦-𝗖𝗼𝗩-𝟮—𝗲𝗻𝗷𝗼𝘆 𝗶𝘁 𝗻𝗼𝘄.
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