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Saved - October 3, 2023 at 10:40 AM
reSee.it AI Summary
Dr. Robert Malone, in an interview with Joe Rogan, revealed his involvement in researching the Wuhan virus. He received a call from a CIA agent, Michael Callahan, who alerted him about the virus. Malone then focused on developing a protease inhibitor for the virus. He later discovered that Famotidine (Pepcid) could be repurposed as a treatment. Callahan, known for his work in government-funded drug research, collaborated on the project. The CIA agent had access to over 6000 patient records in Wuhan. The connection between the CIA and the virus remains unclear.

@CanariesBlue - Blue Canaries

1. Dr. Robert Malone talked about his "origin" story about 20 minutes into his interview w Joe Rogan. He stated, "There is a CIA agent that I have co-published with in the past named Michael Callahan. He was in Wuhan in the 4th quarter of 2019..."

@CanariesBlue - Blue Canaries

2. cont. "He called me from Wuhan on January 4. I was currently managing a team that was focusing on drug discovery for Gamma Phosphate Poisoning or (?) Nerve Agents for DTRA -- Defense Threat Reduction Agency, involving high performing computing and biorobot screening..."

@CanariesBlue - Blue Canaries

3. cont. "Um, high end stuff. And, he told me, Robert, you gotta get your team spun up because we have a problem with this new virus -- worked with him through prior outbreaks. Um, so, it was then that I turned my attention to this. Started modeling a key protein, a Protease..."

@CanariesBlue - Blue Canaries

4. cont. "inhibitor of this virus when the sequence was released on January 11, as the Wuhan Seafood Market Virus and I have been going pretty much non-stop ever since, with that point with drug repurposing. Um, so, I'm the one that originally discovered Flomatadine as..."

@CanariesBlue - Blue Canaries

5. cont. "an agent. umm, because I was self-treating myself after I got infected (Feb 2020) with agents that we identified through the computer modeling." What is Flomatadine? It is Pepcid

@CanariesBlue - Blue Canaries

6. I found this study in a publication that has both Robert Malone and Michael Callahan as authors.

@CanariesBlue - Blue Canaries

7. More on the CIA agent... "His biggest mission: Create a government-funded drug research and production capability focused strictly on national priorities, such as defense and pandemic preparedness, rather than profits." https://www.uab.edu/medicine/magazine/winter-2013/alumni-profile-michael-callahan

The War on Bugs - Medicine Magazine | UAB The University of Alabama at Birmingham,UAB uab.edu

@CanariesBlue - Blue Canaries

8. More info about the Famotidine project. "They were collaborating with scientists working for a US Department of Defense project called DOMANE." https://cen.acs.org/pharmaceuticals/Pepcid-treat-COVID-19/98/i25

404 Page Not Found | Chemical & Engineering News cen.acs.org

@CanariesBlue - Blue Canaries

9. "Famotidine was one of a few drugs that appeared to interact with the protease in the computational studies, says Robert Malone, a physician and consultant who is on the DOMANE team."

@CanariesBlue - Blue Canaries

10. Another article on Michael Callahan from July 2021. https://deathship.wordpress.com/2021/08/20/darpas-man-in-wuhan/

DARPA’s Man in Wuhan Michael Callahan’s career began in USAID and in the bioweapons labs of the former Soviet Union, advancing the agenda of the global bioweapons and pharmaceutical cartels. He would take what he learned there to execute a massive expansion of DARPA’s biodefense portfolio and today finds himself squarely in the center of the origins of the… deathship.wordpress.com

@CanariesBlue - Blue Canaries

11. "This insight originally derived from the analysis of Dr. Robert Malone and team associated with the U.S. government research contracts as well as observations of a prominent physician and research named Dr. Michael Callahan..." https://trialsitenews.com/famotidine-leads-to-improved-covid-19-patient-outcomes-based-on-retrospective-case-series-led-by-cold-spring-harbor-laboratory/

Famotidine Leads to Improved COVID-19 Patient Outcomes based on Retrospective Case Series Led by Cold Spring Harbor Laboratory Transparent coverage of clinical research trialsitenews.com

@CanariesBlue - Blue Canaries

12. "... after his analysis of over 6,000 patient records at the Wuhan pandemic epicenter." The CIA agent was in Wuhan and had early access to over 6,000 patient records. So, WAS it a CIA Operation? We may not know in this lifetime.

@CanariesBlue - Blue Canaries

13. However, I can think of no better name than: Operation MFP - Mass Formation Psychosis It just wreaks of something that the 3letter gov agency would create. js.

@CanariesBlue - Blue Canaries

@threader please unroll

Saved - August 19, 2023 at 9:32 PM

@AMK_PhD - Ahmad M Khalil 🇺🇸

The #Covid19 drug that was being pushed by Peter Hotez has now been shown to drive the emergence of new variants! It’s a big scandal & fraud!

@TheChiefNerd - Chief Nerd

🚨 New Research Finds Merck’s COVID-19 Antiviral Molnupiravir Drives Viral Mutations “Molnupiravir, an antiviral medication that has been widely used against SARS-CoV-2, acts by inducing mutations in the virus genome during replication. Here we show that SARS-CoV-2 sequencing…

Saved - August 21, 2023 at 3:42 AM
reSee.it AI Summary
The pandemic was intentional mass murder, a power and land grab. Perpetrators like DARPA, DTRA, USAID, HHS, and US DOS are involved in illicit biowarfare research. Labs were expanded after Amerithrax scare. Work was outsourced to Africa, Asia, and Eastern Europe. CIA assets like Peter Daszak, Nathan Wolfe, and Karen Saylors are connected to Epstein and Maxwell. Hunter Biden funded Metabiota. Lab leak cover-up by Fauci and associates. COVID vaccines ordered by DOD, not regulated as drugs. Pfizer fraud. Ineffective treatments. mRNA vaccines have risks. Disturbing connections between vaccine and neurowarfare research. Governments pursuing neurowarfare tech for population control. Democidal attack, killing millions.

@NameIsSpartacus - WeAreIceni

The pandemic wasn't a lab accident. It was intentional mass murder, a power grab, a land grab, and so on, and the perpetrators are still out there, walking free. DARPA, DTRA, USAID, HHS, and the US DOS are all involved in illicit biowarfare research spun off from the Nunn-Lugar CTR program and euphemistically characterized as "biodefense". They massively expanded BSL-3 and BSL-4 lab capacity in the US throughout the 2000s after the false flag Amerithrax scare following 9/11. These labs came under scrutiny from watchdog organizations like Edward Hammond's Sunshine Project. To avoid scrutiny and FOIAs of these labs, they decided to outsource all the work abroad by paying "virus-hunter" middlemen like Peter Daszak and Nathan Wolfe to subcontract grants to biolabs in Africa, Asia, Eastern Europe, et cetera. Peter Daszak (EcoHealth Alliance), Nathan Wolfe (Metabiota), and Karen Saylors (Labyrinth Global Health) are all likely CIA assets, and Nathan Wolfe in particular has known connections to Jeffrey Epstein, Ghislaine Maxwell, and Boris Nikolic. Not only was Nathan Wolfe on DARPA's Defense Science Research Council and EcoHealth Alliance's editorial board, he was also a founding member of Ghislaine Maxwell's fake TerraMar charity, a fact that can be easily confirmed by viewing the earliest snapshot of their site on the Wayback Machine. Hunter Biden funded Metabiota through his investment firm, Rosemont Seneca. There was a 2014 federal funding moratorium on SARS and influenza GOF research in the US, and this was ignored and the work promptly outsourced to Wuhan, with Ralph Baric and Shi Zhengli publishing a paper the very next year. Peter Daszak was trying to impress upon people the need for "medical countermeasures" such as a "pan-coronavirus or pan-influenza vaccine" back in 2015. Peter Daszak and EcoHealth Alliance were actually given a contract by the DHS a few years before the outbreak to establish something called the "Ground Truth Network", a group of subject matter experts enlisted to "contextualize biological events". Peter Daszak was one of the WHO investigators on the ground in Wuhan after the outbreak, and one of the authors of the Lancet's Lab Leak Letter decrying the notion of a lab leak as a "conspiracy theory", both of which are massive conflicts of interest. Anthony Fauci, Jeremy Farrar, Francis Collins, and other associates of theirs, knowingly engaged in a coverup, suppressing the idea of a lab leak. Anthony Fauci knowingly lied under oath before Congress about the NIH funding GOF research. NIH and Moderna co-own the patents to mRNA-1273. Moderna is basically a DARPA front company and have received lucrative biodefense contracts from them for a whole decade (see also, ADEPT: PROTECT and the mRNA-1944 monoclonal antibody prodrug against Chikungunya). DRASTIC Research dug up something called DEFUSE, which was a grant proposal from EcoHealth Alliance to DARPA to develop something very similar-looking to SARS-CoV-2 Spike. DARPA rejected the proposal because it constituted dangerous GOF research, but this doesn't mean that the research wasn't actually done. It is common for researchers to conduct experiments before they actually receive any grant funding. The COVID-19 vaccines were ordered by the US DOD under an Other Transaction Authority as a "prototype to demonstrate mass production" or a "medical countermeasure", and are not legally regulated as any kind of pharmaceutical drug. In fact, the FDA's EUAs for the vaccines were fraudulent; there was nothing for them to approve or reject, since it isn't legally a drug. The COVID-19 vaccines are not actually being manufactured by Pfizer, Moderna, J&J, etc., but by DOD contractors like National Resilience and Emergent BioSolutions. The vaccine is a DOD product that the pharmaceutical companies have rubber-stamped as belonging to them. Brook Jackson, who helped run the trials Ventavia conducted for Pfizer, noticed many discrepancies in the data-collection process, and was fired from her job for whistleblowing. In a subsequent court case, Pfizer admitted there was fraud, but insisted that the government wasn't harmed by the fraud because they were in on it. The clinical trials that tested the efficacy of HCQ and Ivermectin and found them ineffective also found Kaletra and Remdesivir ineffective for the same reason, particularly because they were dosing people with late, futile antiviral treatments long after their viral loads had peaked and declined. COVID-19's clinical course is such that viral load peaks the second day after symptoms, and is almost nonexistent after 10 days. Most of the people receiving antivirals didn't get them until over a week after they became symptomatic, which is around when the hyperinflammation phase starts. Pfizer's Paxlovid was given a head start; they started treating people with it as early as possible, which increased its apparent effectiveness on paper. mRNA/Viral Vector vaccines induce your own cells to produce and display whole Spike proteins on their surfaces, which tells the immune system to come and kill those cells. If the transfected cells happen to be heart muscle tissue, you end up with permanent heart scarring and a reduced life expectancy. There are a number of disturbing connections between people engaged in vaccine research for the DOD, and people engaged in neurowarfare/BCI research. DARPA are hard at work developing a nanotech-based, craniotomy-free BCI that involves transfecting people's brain cells with nanoparticles that stimulate neurons by receiving wireless energy through the skull. There are bioethicists and policy analysts like James Giordano, Charles Morgan, Armin Krishnan, Jonathan Moreno, etc., who are openly speculating on governments pursuing neurowarfare tech specifically to pacify their own civilian populations in the event of economic upheaval and resource shortages. This was a democidal attack by our governments against their own citizens, which has so far killed tens of millions of innocent people, just as planned.

Saved - August 22, 2023 at 4:09 PM
reSee.it AI Summary
The FDA issued an Emergency Use Authorization for GOHIBIC vilobelimab, similar to Remdesivir. The authorization was based on a public health emergency declaration due to COVID-19. However, the emergency supposedly ended on May 11th, 2023. Questions arise about the FDA's authority and the safety of this unapproved drug. Doctors should research before following this narrative. The drug is for emergency use only. The FDA's actions may be influenced by financial incentives. Stay informed and share this thread. NIH also mentions vilobelimab.

@realdefender45 - Defender of the Republic 🇺🇸

Thread: ⚠️WARNING⚠️ Please share so we can stop this before it begins. As of April 4th 2023 the FDA issued an Emergency Use Authorization for GOHIBIC (vilobelimab) the cousin to Remdesivir. Do not be fooled by the bait and switch, this is just as dangerous. https://federalregister.gov/documents/2023/06/05/2023-11852/authorization-of-emergency-use-of-a-drug-product-during-the-covid-19-pandemic-availability

@realdefender45 - Defender of the Republic 🇺🇸

According to the document, “The Authorization follows the February 4, 2020, determination by the Secretary of Health and Human Services (HHS), as amended on March 15, 2023, that there is a public health emergency, or a significant potential for a public health emergency, that affects, or has a significant potential to affect national security or the health and security of U.S. citizens living abroad and that involves a novel (new) coronavirus. The virus, now named SARS–CoV–2, causes the illness COVID–19. On the basis of such determination, the Secretary of HHS declared on March 27, 2020, that circumstances exist justifying the authorization of emergency use of drugs and biological products during the COVID–19 pandemic, pursuant to the FD&C Act, subject to the terms of any authorization issued under that section.”

@realdefender45 - Defender of the Republic 🇺🇸

How can the basis of an emergency be declared for an emergency declared on March 27th 2020 when as you can see here, the supposed “public emergency” ended on May 11th 2023 https://www.cdc.gov/coronavirus/2019-ncov/your-health/end-of-phe.html

COVID-19 and Your Health COVID-19 cdc.gov

@realdefender45 - Defender of the Republic 🇺🇸

Could this have been yet another lie? https://www.hhs.gov/about/news/2023/05/11/hhs-secretary-xavier-becerra-statement-on-end-of-the-covid-19-public-health-emergency.html

HHS Secretary Xavier Becerra Statement on End of the COVID-19 Public Health Emergency Thanks to the Biden-Harris Administration's whole-of-government approach to combatting COVID-19, our country is in a better place hhs.gov

@realdefender45 - Defender of the Republic 🇺🇸

Even the WHO declared an end to the Global “Public Health Emergency” days before the United States did

@realdefender45 - Defender of the Republic 🇺🇸

Is the FDA overstepping it’s authority to authorize the use of an unapproved potentially very dangerous drug for experimental use without an emergency being declared?

@realdefender45 - Defender of the Republic 🇺🇸

Read it for yourself here: https://www.fda.gov/medical-devices/covid-19-emergency-use-authorizations-medical-devices/faqs-emergency-use-authorizations-euas-medical-devices-related-covid-19#:~:text=The%20FDA%20can%20use%20its,life%2Dthreatening%20diseases%20when%20certain

FAQs on Emergency Use Authorizations (EUAs) for Devices - COVID-19 Answers to frequently asked questions about emergency use authorizations (EUAs) issued by the FDA related to COVID-19. fda.gov

@realdefender45 - Defender of the Republic 🇺🇸

You can see here that the drug is emergency use only. I ask that doctors please do your homework before following this narrative. Here’s a link to this drug: https://go.drugbank.com/drugs/DB16416

Vilobelimab: Uses, Interactions, Mechanism of Action | DrugBank Online Vilobelimab is an antibody directed against anti-human complement factor 5a is used to treat COVID-19 in adults for emergency use. go.drugbank.com

@realdefender45 - Defender of the Republic 🇺🇸

Maybe it’s the $50 million dollars InflaRx received from the German government that encouraged the FDA to break the rules.

@realdefender45 - Defender of the Republic 🇺🇸

Do you see it yet? 👀 please share this thread 🙏🏽 we see everything they are doing and we will not allow it any longer.

@realdefender45 - Defender of the Republic 🇺🇸

Already on the NIH website: https://search.nih.gov/search?utf8=%E2%9C%93&affiliate=nih&query=Vilobelimab+IFX-1&commit=Search

vilobelimab ifx-1 - National Institutes of Health Search Results search.nih.gov
Saved - November 2, 2023 at 5:25 PM
reSee.it AI Summary
Ivermectin, a versatile medication, offers numerous benefits. It inhibits flu and RSV viral replication, reduces inflammation, improves the gut microbiome, aids athletic performance, and possesses anti-cancer properties. Moreover, it revolutionized veterinary medicine and is safe and affordable. In comparison, Molnupiravir falls short in COVID-19 treatment. Ivermectin shows a 62% improvement with 99 studies and costs $1 per pill, while Molnupiravir only shows a 15% improvement with 34 studies and costs $707 per pill. Ivermectin's potential has been undermined due to its threat to the lucrative vaccine industry. Its effectiveness had to be discredited to protect the $200 billion vaccine enterprise.

@VigilantFox - The Vigilant Fox 🦊

6 Secrets of Ivermectin: The Medication That Keeps on Giving #1 - It inhibits flu and RSV viral replication, which is why it’s included in the FLCCC flu and RSV protocols. #2 - It reduces inflammation throughout the body. #3 - Improves the gastrointestinal microbiome by boosting levels of the probiotic Bifidobacterium. #4 - It revolutionized veterinary medicine and arguably stabilized the world’s food supply. #5 - May help with athletic and sports performance by boosting cellular energy output in the heart. #6 - It has profound anti-cancer properties. Best of all, Ivermectin is incredibly safe and cheap. When you compare Molnupiravir and Ivermectin head-to-head in the context of COVID-19, you can see what a disgraceful, overpriced stink-bomb Molnupiravir actually is: Ivermectin: 62% improvement, 99 studies, $1 per pill Merck’s Show Pony: 15% improvement, 34 studies, $707 per pill This information was gathered from an article written by @MDMichaelTurner (give him a follow). Read the full in-depth article in the comment below:

@VigilantFox - The Vigilant Fox 🦊

ARTICLE: 6 Secrets of Ivermectin - The Medication That Keeps on Giving https://vigilantnews.com/post/6-secrets-of-ivermectin-the-medication-that-keeps-on-giving

6 Secrets of Ivermectin: The Medication That Keeps on Giving vigilantnews.com

@VigilantFox - The Vigilant Fox 🦊

Related Articles: Ivermectin: The Untold Story of a 'Miracle Drug' https://www.theepochtimes.com/epochtv/the-untold-story-of-a-miracle-drug-4952578?utm_source=partner&utm_campaign=vigilantf&src_src=partner&src_cmp=vigilantf

The Untold Story of a 'Miracle Drug' theepochtimes.com

@VigilantFox - The Vigilant Fox 🦊

Lessons from Ivermectin: Why Stockpiling Life-Saving Drugs Is More Important Than Ever https://vigilantnews.com/post/lessons-from-ivermectin-why-stockpiling-life-saving-drugs-is-more-important-than-ever

Lessons from Ivermectin: Why Stockpiling Life-Saving Drugs Is More Important Than Ever Ivermectin, a Nobel-Prize-winning human medicine, is often touted as "one of the safest and most effective medicines of this era." Leading doctors believe this drug could have potentially curbed the pandemic at its outset. vigilantnews.com

@VigilantFox - The Vigilant Fox 🦊

Can You Overdose on Ivermectin? Dr. Pierre Kory's Answer Will Shock You https://vigilantnews.com/post/can-you-overdose-on-ivermectin-dr-pierre-korys-answer-will-shock-you

Can You Overdose on Ivermectin? Dr. Pierre Kory's Answer Will Shock You "One of the safest drugs in history." vigilantnews.com

@VigilantFox - The Vigilant Fox 🦊

Ivermectin, the drug once labeled “horse de-wormer,” is now showing 15 anti-cancer mechanisms of action. https://vigilantnews.com/post/can-ivermectin-treat-turbo-cancers-9-ivermectin-papers-reviewed

Can Ivermectin Treat Cancer? - 9 Papers Reviewed Oncologist and cancer researcher Dr. William Makis uncovers what Big Pharma doesn't want you to know about ivermectin's anti-cancer mechanisms. vigilantnews.com

@VigilantFox - The Vigilant Fox 🦊

RFK Jr. Reveals Why Ivermectin Had to Be Destroyed Ivermectin is often recognized – 2nd to penicillin – for having the greatest impact on human health. And its discovery won the Nobel Prize in 2015. But its existence threatened a $200 billion vaccine enterprise. “The Federal Emergency Use Authorization Statute says that you cannot issue an emergency use authorization to a vaccine if there is an existing medication that has been approved for any purpose that is demonstrated effective against the target illness,” explained Kennedy. “So they had to destroy ivermectin and hydroxychloroquine and discredit it. And they had to tell everybody it’s not effective. Because if they had acknowledged that it’s effective in anybody, the whole $200 billion vaccine enterprise would have collapsed.”

Video Transcript AI Summary
The speaker discusses a CNN segment where they portrayed him as taking horse medication. He believes this is evidence of a conspiracy, as the medication in question, Ivermectin, is commonly used in humans and has even won a Nobel Prize for its efficacy. He suggests that Ivermectin and hydroxychloroquine were discredited to protect the vaccine industry, as federal law prohibits emergency use authorization for vaccines if there are existing effective medications. Acknowledging the effectiveness of these medications would have undermined the multi-billion dollar vaccine industry.
Full Transcript
Speaker 0: I saw the CNN thing where they made my face yellow and said I was taking horse medication, which is that the most the to say that and repeat that over and over again is such a clear indication that they conspired. It's such a because it's this it's uniform. Farm. It's horse dewormer, uniform, a medication that's used far more often in human beings. It's been prescribed to Speaker 1: for Bill billions. Speaker 0: Yeah. It's insane. And the fact that Speaker 1: And won the Nobel Prize for for efficacy in humans. Speaker 0: Yeah. In humans. Yeah. It was wild. It was just wild. Speaker 1: They had to do it. They had to discredit Ivermectin because, you know, Because there's a federal law the federal law the emergency use authorization statute says that you cannot issue You you cannot issue an emergency use authorization to a vaccine if there is an existing medication that has been approved for any purpose that had that is demonstrated effective against the target illness. So they had to destroy Ivermectin and hydroxychloroquine and discredit it, and they had to tell everybody it's not effective. Because if they had acknowledged that it's effective in anybody, the whole $200,000,000,000 vaccine enterprise would have collapsed.

@VigilantFox - The Vigilant Fox 🦊

Ivermectin: The Truth - by legendary filmmaker Mikki Willis (@Plandemic3Movie). https://t.co/fKvLzszaIw

Video Transcript AI Summary
The video discusses the controversy surrounding the use of Ivermectin as a treatment for COVID-19. While some claim it is a safe and effective medicine, others argue that it is a horse dewormer with no clinical evidence of its efficacy. The video highlights the smear campaign against Ivermectin and suggests that powerful forces, including pharmaceutical companies, may be suppressing its use. It also mentions the positive results seen in countries like India and Peru where Ivermectin was used as part of a multi-drug approach. The video raises concerns about the influence of pharmaceutical companies on the media and the manipulation of clinical studies. Overall, it presents Ivermectin as a potentially effective treatment that has been unfairly maligned.
Full Transcript
Speaker 0: Of all the harmful misinformation spread over the past couple of years, one of the most disturbing false narratives was targeted at the Nobel Prize winning human medicine, Ivermectin. What you're about to see will reveal the motive behind the smear campaign against one of the safest and most effective medicines of this era. A medicine that, according to the numerous top scientists I've interviewed this year, could have ended the pandemic before it began. Speaker 1: So things are clearly bad, but they're being made even worse by people who have refused to take the vaccine and instead are swallowing horse paste. Speaker 2: Horse dewormer. There's no clinical evidence that indicates that this works. Speaker 3: It goes beyond that. We actually know that It doesn't work. Speaker 4: Ivermectin is ineffective against COVID, but could put you in a coma. Speaker 2: It can kill you. Speaker 4: It can kill you. Speaker 5: Turns out I got COVID. So we immediately threw the kitchen sink at it. All kinds of meds, monoclonal antibodies, Ivermectin. Speaker 6: One of those drugs he mentioned, Ivermectin, is something more often used to deworm horses. Speaker 7: We should Speaker 5: talk about that. That bothered you. It should bother you too. They're lying at your network about people taking human drugs versus drugs for the veterinary. Speaker 6: Calling it a horse to wormer is not a flattering thing. Speaker 8: I get that. Speaker 5: It's a lie. Speaker 8: They they shouldn't have said Speaker 9: Why did they Speaker 5: do that? I don't know. You're the medical guy over there. Speaker 6: Ivermectin can be a very effective medication. Speaker 8: You are more likely to die from taking Tylenol than Ivermectin, yet the FDA calls this a dangerous Horse deworming medicine. Speaker 10: What initially led this was an FDA Twitter account that use the term y'all to express denigration of Ivermectin as a horse drug. I have horses. The truth is that the dose that's used for horses by body weight is the same dose that's recommended for humans, But it's formulated and manufactured to a quality standard that's very different. Speaker 6: Lots of medicines are used in both animals and humans. So it's not a sufficient argument Somebody to say, it's a horse dewormer. Speaker 11: Yesterday, the CDC put out a national advisory on this warning the whole country against taking this Drug Ivermectin formulated for horses and cows and sheep. Speaker 12: With that, memo fired to every doctor, then Suddenly, me and all my early treatment colleagues around the country, we were faced with problems like we'd never had before. Speaker 4: I work as an emergency room doctor. And And not only an emergency room doctor, I teach advanced trauma life support, a course to other doctors that wanna work in the emergency room on how to stabilize patients. We were being told there's nothing you can do. Just wait for Fauci and the FDA to acknowledge a vaccine that they were gonna create, and there's no treatment, they said. Why would you want to decrease access to quality, life saving, measures for people who are fighting a worldwide pandemic? Speaker 9: So it was the first time in history that we ever saw a doctor who could be prosecuted for using a generic, Safe and effective drug for the application that doctor thought was appropriate. Speaker 12: My group of 5, the core 5 of us ICU doctors, Collectively, we're some of the most highly published doctors in the history of critical care medicine. Paul Maric is the most published practicing intensivist in the world. Speaker 9: As we sit here today, I'm the most published person in my field in history. But when COVID nineteen hit, my clinical and academic world was turned upside down. Speaker 13: Twitter, in its wisdom, has decided to suspend the account of doctor Robert Malone. Now Robert Malone happens to be the inventor of the mRNA technology of making vaccines. His Twitter account has been suspended because he was allegedly spreading Misinformation on COVID nineteen vaccines. Let that sink in. Speaker 12: We have made contributions to our field for decades. So when we find ourselves, like, dismissed, you know, and they'll do that to anyone. You're suddenly fringe. Speaker 2: Touted as a miracle prevention and cure by far right commentators and anti vaxxers. Speaker 10: I'm not, although I've been characterized as a Right wing Proud Boy, this is a bipartisan issue, and the physicians represented here are truly a bipartisan group. Speaker 12: Our lives started going sideways professionally. Right. Paul started getting numerous complaints against him that he's never had in his career. Speaker 8: For the first time in my entire career, I could not be a doctor. I had to stand by idly. I had to stand by idly watching these people Die. Speaker 14: From the FDA, emergency use authorization of medical products and related Authorities. For the FDA to issue an emergency use authorization, there must be no adequate approved and available alternative to the candidate product for diagnosing, Preventing or treating the disease or condition. If Ivermectin were an effective treatment, the vaccines never would have gotten emergency use authorization in the US. Speaker 10: If a viable therapeutic strategy existed for outpatients, then the logic supporting universal vaccination with largely experimental products, is no longer supportable. Speaker 12: The war on Ivermectin is waged by very powerful Full forces with a lot of money. I mean, public health was built on a obsessive global vaccination policy, which Ivermectin would have threatened. Speaker 11: We've got Pfizer's Q3 earnings. Revenue, they're projecting to be 98 To $102,000,000,000. Pfizer, Speaker 15: BioNTech, and Moderna. Do you know how much profit they made from these shots? $1,000 every second from Wuhan virus vaccines. Speaker 12: You're talking about 100 of 1,000,000,000 of dollars in geopolitical implications That would be significantly affected if the people had access to a safe and widely available medicine. Speaker 16: This is an incredibly cheap drug. It's off license. It's generic. It can be manufactured in huge amounts in India. Remarkably low cost. Speaker 14: Merck's patent on Ivermectin expired in 1996. In 2021, Merck released a statement claiming that Ivermectin was not an effective Treatment against COVID nineteen and bizarrely claimed, quote, a concerning lack of safety data in the majority of studies. It was plenty safe for Merck to distribute widely when it was still under patent, But now they're claiming the safety record is insufficient. Speaker 10: Folks need to understand that just because there is an article out there that asserts that something is false recognize that those are paid. Speaker 7: Every major media outlet in the United States shares at least 1 board member with at least 1 drug company. Let me put it in perspective for you. These board members wake up, they go to a meeting at Merck or Pfizer, and then they have their driver take them over to a meeting with NBC to decide what kind of Programming that network is gonna air. They can't be honest and objective about big pharma because big pharma pays their bills. Speaker 17: In fact, one analysis claimed 9 out of the top 10 drugmakers spent more on marketing than they did on research. Speaker 18: CNN tonight, Brought to you by Pfizer. Brought to you by Pfizer. Brought to you by Pfizer. Brought to you by Pfizer. Brought to you by Pfizer. Brought to you by Pfizer. Speaker 0: Brought to Speaker 8: you by Pfizer. Speaker 18: Brought to you by Fiserv Royal Wedding is brought to you by brought to you by Fiserv. Fiserv. Speaker 19: If asked the question, Did you know how much influence your former employer had on big media and so on? I have no idea. It is clear that the pharmaceutical industry has has a great deal of sway on what goes on. If you can shape the message, then you can shape the world, and that's what they've done. Speaker 13: When was Speaker 9: the last time you turned on the news and ever got an update about how the rest of the world is handling COVID? Speaker 12: A group of South African doctors has launched an urgent court Cajun. They are seeking easier access to Ivermectin. Speaker 20: Globally, at least 5 countries want to use Ivermectin to treat COVID nineteen, Including India and Argentina. There are numerous concrete tests in medical journals around the world that Ivermectin Does work. Speaker 9: The earliest reports we had, one of them we had in Peru, where they got into a good mode of using multidrug Treatment with an Ivermectin based approach that they were crushing their curves. Speaker 2: And the president of the Tokyo Medical Association announced to all doctors during a summer surge That they should use Ivermectin in the treatment. Within weeks, the hospitalization rates reported out of Japan Were lower than at any other time in the pandemic. Speaker 9: The real proof positive came when COVID-nineteen really hit hard in Mexico City. They finally, after lots of struggle, came with an Ivermectin based multi drug approach, and literally cleared out the hospitals. And then we had reports all the way through that various states in India. Speaker 21: In India, the government has been widely promoting the use of Ivermectin. State leaders have just declared that Uttar Pradesh is now officially COVID free. A region with nearly as many people as the entire United States is totally COVID free. Speaker 12: The miracle success of Uttar Pradesh, not one mention of Ivermectin being used. Speaker 22: In the countries that it has been used, in the countries where the studies are, the results are not good. They are overwhelming. They are well over 90% success rate. Speaker 12: In the Speaker 2: United States, it's a horse dewormer. It's horse based, and only the illiterate, ignorant, and and or unvaccinated use it. Speaker 10: The key paradox Is if you look at the mortality rate in the United States, one of the most highly funded medical care systems in the world, And what we find is the mortality in the United States is among the worst in the world. Speaker 2: If you look at these innumerable failed policies, there's only one way to understand them. They are literally written by pharmaceutical companies. They can design trials to fail to disprove the use of cheap medicines, And they can make things appear that they don't work. Speaker 10: I sit as a nonvoting member of the active committee for drugs with NIH. I've seen the dynamics of what are going on with all those trials, which most of which have failed. Unfortunately, it's imminently possible to manipulate the outcomes of a clinical study. If you want a study to fail, that's dead easy. Speaker 12: Now, their 4th quote unquote negative study of Ivermectin in a major medical journal, and each time is a media frenzy. Speaker 3: There was a systematic review looking at Randomized controlled trials that have been done, and they found that there was no benefit for Ivermectin in reducing mortality, death to COVID nineteen, No reduction in symptoms or duration of symptoms for COVID nineteen, so it does not work. Speaker 19: People need to understand that academics Have been threatened with losing their position and threatened with getting no further research grants If they speak out against the narrative, guess why that is? 2 thirds of the world's non commercial biological research is funded by just 3 bodies. The Wellcome Trust in the UK, the NIH, And specifically the NIAID under Tony Fauci and the Bill and Melinda Gates Foundation. Speaker 10: There's this pattern that is consistent with A concerted effort to mislead the public by withholding information using modern technology, media, censorship, really, let's call it what it is, thought control. Speaker 23: He could actually control, Exactly what people think. And that is the that is our job. Yeah. Speaker 12: Whenever you have clear cut evidence that a drug works, You have an ethical obligation to immediately let the people know so that they could have access. Speaker 6: What are you telling people is the Is the optimal profile. Speaker 24: I want a pill, orally administered, single pill Given for 7 to 10 days, little drug drug interaction and low toxicity. Give me that, and I'll be really happy. Speaker 21: Ivermectin has been used safely for decades, has no known drug interactions, won a Nobel Prize for its success treating humans, And is on the WHO's list of the safest, most effective medicines in the entire world. Speaker 10: And it showed an 86% effectiveness to Prevent people from contracting COVID. Speaker 6: Ivermectin has been used over 4,000,000,000 times and it's used for a wide variety of treatments. Ivermectin has been shown Speaker 21: known to possess different anti inflammation, antiviral, and antitumor properties. Speaker 3: Clinical studies abroad suggest It works. Speaker 13: All the studies show that it does have a positive effect. Speaker 22: That is the thing about Ivermectin. It's not good. It's great. Speaker 12: I have never seen an evidence base This large with 81 controlled trials, 10 years of in vitro studies in the lab against a dozen RNA viruses, All showing that Ivermectin stops replication. It literally is, in my mind, the single greatest public health achievement in our history of affection control in the world.
Saved - December 25, 2023 at 2:14 PM
reSee.it AI Summary
PAXLOVID promotes viral mutations and can lead to rebound infections. This could result in increased demand for booster shots.

@DecentFiJC - Jonathan

PAXLOVID was designed to foster viral mutations within COVID-infected hosts, having poor viral clearance leading to in vivo directed evolution. And then followed by common subsequent “rebound/relapse infection” being reported among patients. More “mutant viral strains” means more “booster jabs” they can potentially sell to the masses.

@Amy31129057 - QuestionIt

Were they wrong about Molnupiravir? Molnupiravir was originally developed to treat influenza at Emory University by the university's drug innovation company, Drug Innovation Ventures at Emory (DRIVE), but was reportedly abandoned for mutagenicity concerns when used in Covid patients. Molnupiravir, sold under the brand name Lagevrio, is an antiviral medication that inhibits the replication of certain RNA viruses. It was used to treat COVID-19 in those infected by SARS-CoV-2. It is taken by mouth. For several years, Emory scientists had been working on EIDD-2801, a drug candidate with potential as a treatment for several highly infectious and worrisome viral diseases, including influenza and Venezuelan Equine Encephalitis virus, some of which are biodefense threats. When the pandemic began, the team quickly turned its attention to developing EIDD-2801 as a treatment for COVID-19. DRIVE licensed EIDD-2801, now known as molnupiravir, to Ridgeback Biotherapeutics in 2020, which conducted the first human clinical trials and then partnered with Merck. In October 2021 the UK government announced the procurement of 480 000 courses of molnupiravir (as well as 250 000 courses of the Pfizer antiviral Paxlovid (nirmatrelvir)). Guess who they went with.... PAXLOVID. 😏 https://en.wikipedia.org/wiki/Molnupiravir https://drugdiscovery.emory.edu/molnupiravir/index.html https://www.bmj.com/content/377/bmj.o926

Molnupiravir - Wikipedia en.wikipedia.org
About Molnupiravir | Emory University | Atlanta GA drugdiscovery.emory.edu
Covid-19: What is the evidence for the antiviral molnupiravir? Merck’s drug was originally claimed to halve hospital admissions and deaths in people with covid-19, leading some governments to stockpile it as the pandemic continued. Andy Extance looks at the published evidence for its effectiveness Molnupiravir (marketed as Lagevrio) is an antiviral drug, slightly modified from a compound known as NHC (β-d-N4-hydroxycytidine) that a team at Emory University in Atlanta, Georgia, first described in 2003.1 It is available as hard capsules that are swallowed and absorbed from the gut so is easy to take at home. That contrasts with some other covid-19 drugs such as the monoclonal antibody tocilizumab or the antiviral remdesivir, which must be administered by intravenous infusion in hospitals. In October 2021 the UK government announced the procurement of 480 000 courses of molnupiravir (as well as 250 000 courses of the Pfizer antiviral Paxlovid (nirmatrelvir)). Molnupiravir had been due to enter clinical trials against influenza, but during the pandemic Emory University struck a deal with the biotechnology company Ridgeback Biotherapeutics to test it as a treatment for covid-19.2 Ridgeback then partnered with the pharmaceutical giant Merck in May 2020 for clinical trials and scale-up.3 Antiviral drugs for acute respiratory infections need to be used as early as possible after infection if they are to help prevent disease progression, hospital admissions, and deaths. This normally means within three days, but the drug may still be beneficial up to five days after onset of symptoms. The current advice is to give 800 mg of molnupiravir (four 200 mg tablets) every 12 hours for five days, within five days of symptom onset.4 Like many antivirals, its chemical structure resembles the nucleotide bases that link together to make the long RNA chains that are a virus’s genetic material. After ingestion, molnupiravir breaks down to … bmj.com
Saved - March 20, 2024 at 8:24 AM
reSee.it AI Summary
Post 1: After treatment, patients showed a high number of low-frequency mutations in the virus, some of which became fixed. The drug used can enhance viral evolution in immunocompromised patients, leading to new variants and prolonging the pandemic. Post 2: No information provided.

@kacdnp91 - Kelly DNP🐭Functional/Integrative Med

Within days of treatment, we detected a large number of low-frequency mutations in patients and that these new mutations could persist and, in some cases, were fixed in the virus population. All patients treated with the drug accrued new mutations in the spike protein of the virus, including non-synonymous mutations that altered the amino acid sequence. Our study demonstrates that this commonly used antiviral can ‘supercharge’ viral evolution in immunocompromised patients, potentially generating new variants and prolonging the pandemic.

@kacdnp91 - Kelly DNP🐭Functional/Integrative Med

https://www.medrxiv.org/content/10.1101/2022.12.21.22283811v1 @Fynnderella1

Antiviral treatments lead to the rapid accrual of hundreds of SARS-CoV-2 mutations in immunocompromised patients medRxiv - The Preprint Server for Health Sciences medrxiv.org
Saved - April 4, 2024 at 1:30 PM
reSee.it AI Summary
In a series of posts, it is revealed through FOIA documents that Ralph Baric discussed experiments with the coronavirus and bats in March 2018. EcoHealth Alliance lied about not receiving DARPA funding for COVID research. Ralph Baric, known as the "Coronavirus Hunter," endorsed Remdesivir, a drug with a high mortality rate, before it was widely used. Baric also mentioned the early termination of Remdesivir trials, similar to the situation with AZT for HIV.

@CovidMemo - Covid Memo

🛑WOW. What were you doing on March 5, 2018? A few were planting the seeds on the gain of function research that turned into the Wuhan lab leak... 🔥🔥Brand new FOIA documents show the VERY first emails in March 2018 where Ralph Baric discusses experiments with the coronavirus and bats. 💥March 5: Peter Daszak makes an email introduction stating that Ralph Baric is working on nanoparticles. 💥March 7: Ralph Baric is asked about SARS-CoV spike glycoproteins he is developing "with respect to the DARPA grant" 💥March 15: Baric states...he was planning on testing what he could in mice, "nanoparticles no problem" he states, but that he understood RCN doesn't work well in mice. "I have no bat colony, no way for me to do the experiment-which I definitely think needs to be done or we have no credibility. My understanding another bat colony exists in China, but not sure who is doing what. " ✅FOIA link with all emails below...

@JamesCTobias - Jimmy Tobias

A few FOIA documents that I received from USGS today re: DEFUSE, etc: https://www.documentcloud.org/documents/24529444-2024-000075__2024-000076_-_combined_records_redacted

2024-000075__2024-000076_-_Combined_Records_Redacted documentcloud.org

@CovidMemo - Covid Memo

This was also revealed in the latest FOIA docs... Will anyone be asked to testify??

@AGHuff - Andrew G. Huff, PhD, MS 🇺🇸

🚨🚨🚨🚨🚨🚨🚨 EcoHealth Alliance claimed that they didn’t make COVID in a lab because “they had not received the DARPA funding.” These FOIA documents prove that EcoHealth Alliance lied and they engineered COVID in a lab even though they had not received the DARPA funding.

@CovidMemo - Covid Memo

Two years later, in May of 2020, while NYC is getting hit hard with Covid deaths, Ralph Baric speaks on coronavirus research. "Put the 2019 pandemic in perspective...when you look at 7 human coronaviruses that have emerged over the last 800 years, 7 of them came from bats." He is asked... 🛑How is it possible to safely study a dangerous virus? Timestamp: 10:54 🔥🔥Listen: https://www.wunc.org/health/2020-05-25/meet-the-coronavirus-hunter-ralph-baric

Meet 'The Coronavirus Hunter' Ralph Baric The coronavirus that causes COVID-19 took most of the world by surprise — but not Ralph Baric. He is an epidemiologist at UNC-Chapel Hill who has been… wunc.org

@CovidMemo - Covid Memo

🔥🔥 Directly after Baric makes that statement above...the announcer comes on... "Today we are sharing an interview of Ralph Baric, who has been called the Coronavirus Hunter.... He is a key member of the team bringing Remdesivir to fight against Covid-19." 🔥🔥 Note: This was one month before the White House signed on Gilead's Remdesivir. History: Remdesivir had a 53% kill rate. It was so deadly, the WHO pulled it in their treatment of Ebola in 2018. So as the pandemic spreads, he speaks on coronavirus research in tandem with his endorsement of a highly profitable, yet dangerous drug 🤔🤔

@VigilantFox - The Vigilant Fox 🦊

Premeditated Murder: They Knew Remdesivir Would KiII, and They Did It Anyway Prior to COVID, Ralph Baric's and Tony Fauci's pet drug, Remdesivir, had a 53% mortality rate in clinical trials done in Africa. "53% mortality if you got Remdesivir!" stressed Dr. David Martin. "There is no such thing as a 53% lethality of anything nature does ... and that's what we chose to use in COVID." @DrDMartinWorld, @rustyrockets

Video Transcript AI Summary
In 2011, 2012, and 2014, publications revealed that pseudouridine in mRNA shots could cause rapid cancers. Remdesivir, with a 53% mortality rate, was chosen by the FDA for COVID treatment despite being deemed unethical by the World Health Organization due to high death rates in Africa. This lethal drug was administered regardless of viral load, resulting in unnecessary deaths.
Full Transcript
Speaker 0: Is there any way we could have deciphered that maybe cardiovascular problems were going to happen? Is there any data that shows that by 2011, 2012, and then again in 2014, publications showed that the pseudouridine that was being used in the mRNA shots was a pro oncologic, protumor generator technology. Did we know that it was going to kill people with rapid cancers? Of course, we did because we knew that it was published just like we knew in 2018 that Ralph Baric's remdesivir had a 53% lethality in clinical trials done in if you wanna call them clinical trials, I call them biological torture trials done in Africa. 53% mortality if you got remdesivir, and yet that was chosen by the FDA as the drug of choice to to use when people were hospitalized with COVID. These things Russell, a 53% mortality exceeds any lethal agent we know in nature. There is no such thing as a 53% lethality of anything nature does, but we were able to inject that into people with impunity. And the publication on that, let's get really clear on that, the publication of that data, the 53% mortality data, that publication was the World Health Organization's own clinical trials where they, in their own discretion, determined that it was unethical to inject Africans with this stuff because 53% of them were dying. And in the paper, it's important to point out, it said regardless of viral load. Russell, let's unpack for the common listener what the heck that means. That means we were killing people who didn't even have Ebola, who didn't even have another disease. Regardless of viral reload means we were killing people because we were injecting them with an agent we knew was toxic, and that's what we chose to use in COVID.

@CovidMemo - Covid Memo

🛑Baric says in this same interview (May 2020) ... Timestamp Remdesivir: 29:24 ..."they stopped the trials of Remdesivir early because it was WORKING so well..." Uh, huh.... Sound familiar? 🤔 Not Fauci's first rodeo... 💥Fauci, the FDA & AZT for HIV. Printed in Time: "After 16 weeks, Burroughs Wellcome announced that they were stopping the trial because there was strong evidence that the compound appeared to be working. The company reasoned that it wouldn’t be ethical to continue the trial and deprive one group of a potentially life-saving treatment." https://time.com/4705809/first-aids-drug-azt/

The Story Behind the First AIDS Drug, Approved 30 Years Ago The first AIDS drug was approved on March 19, 1987—but getting there was by no means easy. Here's the story behind the treatment. time.com
Saved - April 19, 2024 at 1:16 AM
reSee.it AI Summary
Ivermectin has several benefits, including inhibiting flu and RSV viral replication, reducing inflammation, improving the gastrointestinal microbiome, revolutionizing veterinary medicine, potentially enhancing athletic performance, and having anti-cancer properties. It is also safe and affordable. In comparison, Molnupiravir is expensive and less effective against COVID-19. For more details, read the full article by @MDMichaelTurner.

@VigilantFox - The Vigilant Fox 🦊

6 Secrets of Ivermectin: The Medication That Keeps on Giving #1 - It inhibits flu and RSV viral replication, which is why it’s included in the FLCCC flu and RSV protocols. #2 - It reduces inflammation throughout the body. #3 - Improves the gastrointestinal microbiome by boosting levels of the probiotic Bifidobacterium. #4 - It revolutionized veterinary medicine and arguably stabilized the world’s food supply. #5 - May help with athletic and sports performance by boosting cellular energy output in the heart. #6 - It has profound anti-cancer properties. Best of all, Ivermectin is incredibly safe and cheap. When you compare Molnupiravir and Ivermectin head-to-head in the context of COVID-19, you can see what a disgraceful, overpriced stink-bomb Molnupiravir actually is: Ivermectin: 62% improvement, 99 studies, $1 per pill Merck’s Show Pony: 15% improvement, 34 studies, $707 per pill This information was gathered from an article written by @MDMichaelTurner (give him a follow). Read the full in-depth article in the comment below:

Saved - May 20, 2024 at 8:54 PM
reSee.it AI Summary
Many TV doctors have been caught receiving payments from pharmaceutical companies involved in Covid treatments and tests. Dr. Sarah Jarvis received payments from AstraZeneca and Merck & Dohme while promoting vaccination and exaggerating Covid risks. Dr. Amir Khan was paid by Teva while promoting Covid tests. Dr. Hilary Jones received payments from Merck & Dohme while exaggerating Covid dangers. The conflicts of interest should have been disclosed, and it raises questions about the credibility of these doctors and the media's role in promoting their interests.

@StarkNakedBrief - The Stark Naked Brief.

It's not been a good month for our "impartial" TV doctors... Many were caught encouraging vaccination while receiving direct payments from C jab manufacturers. What you might not know is that others have been paid by companies that made Covid treatments and tests. Thread 🧵

@StarkNakedBrief - The Stark Naked Brief.

1. Dr Sarah Jarvis is a GP and broadcaster. Sarah has been the resident doctor for the Jeremy Vine show on BBC Radio 2 for the last 16 years. She has presented on the BBC’s One Show for the last 10 years, and on Good Morning Britain on ITV.

@StarkNakedBrief - The Stark Naked Brief.

In 2022, during a segment on ITV News, Jarvis told viewers it is important that “young people are vaccinated because they can pass it on to older and vulnerable people...”. By then, dozens of studies and the government’s own data conclusively proved the vaccine did not prevent transmission.

Video Transcript AI Summary
Children aged 5 to 11 can now get the COVID vaccine to protect older and vulnerable individuals. The vaccine has low side effects, with only a few cases of heart inflammation out of millions vaccinated in the US. Getting COVID poses a higher risk of heart inflammation than the vaccine. Vaccinating kids can reduce school disruptions and help safeguard older people.
Full Transcript
Speaker 0: And 5 to 11 year olds can now, receive the COVID vaccination. What is your reaction to that? Is that, the the way forwards? Speaker 1: I think it is important that young people are vaccinated because they can pass it on particularly to older and really vulnerable people. We know that the vaccine has a very, very low instance of side effects. Myocardial inflammation of heart muscle is the one that everyone was worried about, but we've now had millions of children. In fact, in the US, 8,700,000 children aged 5 to 11 got the vaccine, and there were only 11 cases of inflammation of the heart muscle, most of them very mild. And, of course, you can get that same into inflammation more commonly if you get COVID than if you have the virus. So I think it will reduce the time of school for children, and I'm really hoping that it will be a way of keeping older, more vulnerable people safe. Speaker 0: Doctor Sarah Jarvis, appreciate your time. Thank you.

@StarkNakedBrief - The Stark Naked Brief.

ABPI’s disclosure records show that Jarvis took home an impressive £39,602.00 in contracted service fees and expenses from pharmaceutical companies in 2022. AZ paid her £4,440.83. ITV did not disclose Jarvis’s conflicts

@StarkNakedBrief - The Stark Naked Brief.

Jarvis would also routinely talk up the risks Covid posed. Her warnings coincided with the approval of Merck & Dohme's Covid antiviral drug Molnupiravir, who naturally stood to profit from Covid alarmism as their product was designed to reduce hospitalisations. (It failed)

Video Transcript AI Summary
COVID spreads quickly in crowds, especially as winter approaches and people spend more time indoors with less ventilation. Seeing friends, colleagues, and family also increases the risk of transmission.
Full Transcript
Speaker 0: We know COVID is spreading really fast, and we also know COVID loves a crowd. As the winter nights draw in, it makes it easier for it to spread. We're spending more time indoors with less ventilation, and we're also seeing more of friends, colleagues, and family. All of those make it much easier for COVID.

@StarkNakedBrief - The Stark Naked Brief.

Merck & Dohme paid her a further £1,400.00 in 2020, £1,662.50 in 2021, and £1,680.00 in 2022. Curiously, Jarvis also peer-reviewed a paper attesting to Molnupiravir’s effectiveness in 2022 for Patient but it omitted any reference to her conflict.

@StarkNakedBrief - The Stark Naked Brief.

2. Dr Amir Khan, a full-time GP and best-selling author working in inner city Bradford, is a resident doctor for ITV’s Lorraine and Good Morning Britain.

@StarkNakedBrief - The Stark Naked Brief.

In March 2021, Khan partnered directly with the DHSC and NHS. This involved the presentation of a series of videos in which he promoted the use of Covid tests (both PCR and LFT). In July 2021, he stated that people should conduct these tests “twice a week”.

Video Transcript AI Summary
Test twice weekly, get a PCR test if symptomatic, wash hands, wear a mask in crowds, use NHS COVID 19 app to check-in.
Full Transcript
Speaker 0: But there are simple things we can do to help reduce the spread. It's really important to keep testing twice a week, And if you have symptoms, however mild, take a PCR test. Keep washing those hands and wear a face covering in crowded places. Use the NHS COVID 19 app to check-in.

@StarkNakedBrief - The Stark Naked Brief.

ABPI’s database shows that Teva, a multinational pharmaceutical company that purveys in manufacturing services, paid Khan £3,400.00 in 2021. According to Teva UK’s website, the company “assisted the UK’s COVID-19 testing program” with the NHS.

@StarkNakedBrief - The Stark Naked Brief.

Specifically, they worked to “repurpose sodium chloride saline solution… to help with mass testing”. Khan encouraged use of a product that was made by a company paying him - on government promotions. His conflict was not disclosed.

@StarkNakedBrief - The Stark Naked Brief.

Experts have criticised both PCR and LFT tests, claiming that they're ineffective due to false positives. In 2021, a Cochrane review of 64 studies found LFTs picked up more false than real positives when infection rates were low in the community.

@StarkNakedBrief - The Stark Naked Brief.

3. Dr Hilary Jones is a GP, TV presenter, medical broadcaster, and author. He currently works as the Health Editor of ITV’s Breakfast show.

@StarkNakedBrief - The Stark Naked Brief.

In October 2020, Jones featured on ITV’s This Morning stressing that Covid was so serious it constituted “the biggest threat to public health for so many decades”. Frequently, he exaggerated the dangers of Covid, particularly if people did not take certain treatments.

@StarkNakedBrief - The Stark Naked Brief.

According to ABPI’s database, Covid antiviral manufacturer Merck & Dohme paid Jones a whopping £24,380.00 in 2020 and an additional £5,000.00 in 2021. He purveyed in Covid alarmism while being paid by a company that stood to financially benefit from such alarmism.

@StarkNakedBrief - The Stark Naked Brief.

Research found that Merck's Molnupiravir makes “no significant difference” to hospitalisation or death rates. Less than 2% of the 2.23 million courses of the drug procured by the Department of Health have ever been prescribed to patients.

@StarkNakedBrief - The Stark Naked Brief.

4. To recap, it is impossible to know what exactly these companies paid Jarvis, Khan, and Jones for. We haven't seen the contracts. Sometimes these docs directly and publicly endorsed products made by companies that were paying them.

@StarkNakedBrief - The Stark Naked Brief.

Sometimes they overstated Covid risks, which benefited the companies financially involved in the Covid response who were also paying them. Investigations have shown that both the media and government purposely exaggerated the danger of Covid to increase public compliance.

@StarkNakedBrief - The Stark Naked Brief.

Is it that much of a jump to consider that doctors might do similar to help these companies? What's clear is that the govt/media should have disclosed these conflicts or these docs should have recused themselves on ethical grounds.

@StarkNakedBrief - The Stark Naked Brief.

@LeilaniDowding @Lewis_Brackpool @TheRustler83 @BGatesIsaPyscho @Johnincarlisle @ABridgen @beverleyturner @FatEmperor @dystopian_DU @Resist_05 @PWestoff @LozzaFox @mattletiss7 @DuttyMonkey_

@StarkNakedBrief - The Stark Naked Brief.

@LeilaniDowding @Lewis_Brackpool @TheRustler83 @BGatesIsaPyscho @Johnincarlisle @ABridgen @beverleyturner @FatEmperor @dystopian_DU @Resist_05 @PWestoff @LozzaFox @mattletiss7 @DuttyMonkey_ If you appreciate this kind of info... I post reports at https://news.starknakedbrief.co.uk/ The media should be doing this shit but they too have a financial interest not to.

The Stark Naked Brief. | JJ Starky | Substack Concise, investigative reports on the defining political issues of our time. Showing rather than telling. Former political strategist. Part-time citizen journalist. Based in 🇬🇧. Click to read "The Stark Naked Brief.", by JJ Starky, a Substack publication with hundreds of subscribers. news.starknakedbrief.co.uk
Saved - October 17, 2024 at 7:00 PM
reSee.it AI Summary
I shared alarming findings from "The Remdesivir Papers," revealing that 64% of 941 service members who died of or with COVID from March 2020 to March 2024 were treated with remdesivir. This data, sourced from a military whistleblower, raises questions about the transparency of clinical trials, particularly those sponsored by the NIAID and the military. Despite some trials showing minimal benefits, significant methodological concerns persist. Additionally, there's ongoing evidence in peer-reviewed literature indicating remdesivir's toxicity.

@SenseReceptor - Sense Receptor

WOW! Military whistleblower data shows that 64% of the 941 service members who died of/with COVID in military treatment facilities/other civilian facilities between March 2020 and March 2024 were "treated" with remdesivir. (1/5) Brad Miller (@BradMiller1010), a former Battalion Commander in the U.S. Army, describes for Michael Nevradakis of Children's Health Defense (@ChildrensHD) some disturbing facts revealed by "The Remdesivir Papers"—a document assembled by an anonymous U.S. military whistleblower (known by the pseudonym Daniel LeMay) and investigative journalist J.M. Phelps (@JMPhelpsLC). The document divulges data derived from the Department of Defense Joint Trauma System (JTS) that's not otherwise not available to the public. The Remdesivir Papers asks the question: "Are U.S. military treatment facilities and others hiding, or manipulating, the deadly results of clinical trials and more surrounding the controversial drug [remdesivir] purported to be a treatment for COVID-19?" In this clip, Miller notes that the NIAID—that is, the National Institutes of Allergies and Infectious Diseases (the government agency that Anthony Fauci used to head)—sponsored four trials for remdesivir—an antiviral drug patented by the pharma giant Gilead—which found the drug "resulted in a minimal positive effect on instances of all-cause mortality and serious adverse side events when compared to the administration of a placebo" (quote from The Remdesivir Papers) despite "significant methodological questions that we might ask ourselves about the conduct of the trials" (Miller's wording). A fifth trial, however, was conducted by Fort Detrick’s U.S. Army Medical Materiel Development Activity (USAMMDA) in conjunction with Gilead. "Headquartered in Foster City, California, Gilead agreed to provide remdesivir for the treatment of DOD personnel exposed to severe acute respiratory syndrome coronavirus (SARS-CoV-2), the causative viral pathogen of COVID-19," The Remdesivir Papers notes. Note that while Miller says that "of those 941 individuals that were administered remdesivir, 601 of them died," The Remdesivir Papers states something slightly different: it evinces data that 64% of the 941 service members who died of/with COVID in military treatment facilities/other civilian facilities between March 2020 and March 2024 were "treated" with remdesivir. Meaning not all 941 service members were administered remdesivir. Despite this caveat, it is still extraordinary—and extraordinarily disturbing—that of the 941 service members who (supposedly) died of/with COVID between March 2020 and March 2024, 64% were given remdesivir. Partial transcription of clip: "Now in addition to those four trials that were sponsored by NIAID, there is a fifth trial that is mentioned in the remdesivir papers, but this one was sponsored by the military, specifically a unit out of Fort Detrick, Maryland that is known as the US Army Medical Research and Development Command. It sponsored a trial. We know that that trial was conducted. However, there is no information that is publicly available about the findings of that clinical trial. "So we might ask ourselves, why? So we have these four trials from NIAID. They appear to present remdesivir in at least a minimally positive light, but there seem to be some significant methodological questions that we might ask ourselves about the conduct of the trials. So we take those four trials. We then look at them alongside this fifth trial sponsored by a military unit, and yet there's no publicly available data. Why? "Now in addition to all of that, with these five trials, we then have information that comes directly from a military whistleblower who presents information that tells us that over a four-year period from March of 2020 to March of 2024, a significant number of people in the wider military community were administered remdesivir. And of those 941 individuals that were administered remdesivir, 601 of them died. That's a, uh, that's a death rate of 64%. "So what caused their deaths? Was it the remdesivir directly? Were there other factors? Should we know? Should we at least be asking questions? And can we trust the fact that the DOD has not been forthcoming with this information?"

Video Transcript AI Summary
A fifth Remdesivir trial, sponsored by the US Army Medical Research and Development Command out of Fort Detrick, Maryland, has no publicly available findings. This is in contrast to four NIAID-sponsored trials that present Remdesivir in a minimally positive light, despite methodological questions. A military whistleblower revealed that, from March 2020 to March 2024, 941 people in the wider military community were administered Remdesivir, and 601 of them died, representing a 64% death rate. The cause of these deaths is unknown, and it is unclear if Remdesivir was a factor. Questions are raised about the Department of Defense's transparency regarding this information.
Full Transcript
Speaker 0: Sponsored by NIAID, there is a 5th trial that is mentioned in the Remdesivir papers, but this one was sponsored by the military, specifically a unit out of Fort Detrick, Maryland that is known as the US Army Medical Research and Development Command. It sponsored a trial. We know that that trial was conducted. However, there is no information that is publicly available about the findings of that clinical trial. So we might ask ourselves, why? So we have these four trials from NIAID. They appear to present remdesivir in at least a minimally positive light, but there seem to be some significant methodological questions that we might ask ourselves about the conduct of the trials. So we take those 4 trials. We then look at them alongside this 5th trial sponsored by a military unit, and yet there's no publicly available data. Why? Now in addition to all of that, with these five trials, we then have information that comes directly from a military whistleblower who presents information that tells us that over a 4 year period from March of 2020 to March of 2024, a significant number of people in the wider military community were administered remdesivir. And of those 941 individuals that were administered remdesivir, 601 of them died. That's a, that's a death rate of 64%. So what caused their deaths? Was it the remdesivir directly? Were there other factors? Should we know? Should we at least be asking questions, and can we trust the fact that DOD has not been forthcoming with this information? So we have this

@SenseReceptor - Sense Receptor

@BradMiller1010 Link to the article describing The Remdesivir Papers, written by J.M. Phelps, who assembled the whistleblowing document in conjunction with the anonymous military whistleblower: https://www.thegatewaypundit.com/2024/10/remdesivir-papers-did-service-members-deserve-die/

The Remdesivir Papers: Did Service Members Deserve to Die? | The Gateway Pundit | by J.M. Phelps           Writing for American Thinker, author Stella Paul once said, “Remdesivir may be the most despised drug in American history, earning the nickname ‘Run Death Is Near’ for its lethal record during COVID.” The Remdesivir Papers captures the essence of her statement for service members and veterans across the country. thegatewaypundit.com

@SenseReceptor - Sense Receptor

@BradMiller1010 Note that there has been robust evidence in the peer-reviewed literature since at least mid-2020 that remdesivir is poisonous. (Really, earlier because remdesivir failed as a drug to treat ebola before failing to treat COVID). List of studies: https://sensereceptornews.com/?p=4565

Running List of (15) Studies Showing Remdesivir Is Harmful and Not Effective – Sense Receptor News sensereceptornews.com

@SenseReceptor - Sense Receptor

@BradMiller1010 Full CHD interview with Miller: https://rumble.com/v5iwlnx-remdesivir-papers-drug-used-to-treat-service-members-led-to-death.html?e9s=src_v1_upp

Remdesivir Papers: Drug Used to Treat Service Members Led to Death What has been revealed in the “Remdesivir Papers” will shock you to the core. This compilation of documents, released by a military whistleblower, contains damning information on the hundreds of death rumble.com

@SenseReceptor - Sense Receptor

@BradMiller1010 Addendum: missing key screenshot from The Remdesivir Papers document... https://t.co/NSB9dmKgtq

Saved - December 7, 2024 at 5:52 PM
reSee.it AI Summary
In early 2020, I explored the contrasting efficacy of Remdesivir and Chloroquine against COVID-19. Chinese trials indicated Chloroquine was more effective, safe, and affordable, while Remdesivir was harmful and nephrotoxic, significantly increasing fatality rates. Despite this, key health officials pushed Remdesivir and sidelined Chloroquine. I highlighted connections between influential figures in healthcare and financial interests, suggesting a coordinated agenda that prioritizes profit over patient safety. The implications of these actions raise serious ethical concerns.

@DecentBackup - BackupDecentFiJC

GILEAD, UNITEDHEALTH & the (SINISTER) BUSINESS of MEDICINE — MANUFACTURING MORBIDITY & MORTALITY 💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥 By FEBRUARY 2020, the Chinese had already conducted IN VITRO side-by-side trials of two known ANTIVIRALS, testing their comparative efficacies against the COVID-19 “novel” coronavirus. ✅REMDESIVIR (GS 5734) *Made by Gilead Sciences. ✅CHLOROQUINE 💥RESULTS: While they determined both to be effective at viral inhibition, they noted CHLOROQUINE, given ORALLY, was widely bioavailable, fast-acting and demonstrated markedly higher levels of viral inhibition at pre-entry, entry and post-entry stages of viral infection. *In addition to that, they noted CHLOROQUINE acts as an IMMUNOMODULATOR in vivo, which should only further synergize its already demonstrable in vitro efficacy in live COVID patients. *Further, they went out of their way to make mention that CHLOROQUINE was CHEAP, SAFE & had a 70-YR TRACK-RECORD of SAFETY/EFFICACY behind it. *Remdesivir was shown to be functionally effective post-entry, albeit less effective than CHLOROQUINE at the same stage, which is in alignment with its mechanism of action and its IV administration. *NOTE: If you’re reading this, and you’re already starting to question the motives behind their unwavering commitment to restricting CHLOROQUINE usage and insisting on REMDESIVIR, good. You’re one of the few remaining who still has some common fucking sense. Congrats. 💥CONCLUSION: Although it may seem like a no-brainer to most of us already, the Chinese recommended that both drugs be earmarked to move onto the next step in therapeutic research — IN VIVO testing for SARS-COV-2 inhibition. *Cool. I have no problems with that and it’s necessary that we be fair and thorough to both agents.

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PS: Not only is remdesivir NOT effective, it’s nephrotoxic, likely hepatotoxic and actually INCREASED CFR. Fuck him. And fuck the people paying him to spew this murderous nonsense too. Their day is coming soon, rest assured.✌️ https://t.co/uJX9avhcpF

@DecentBackup - BackupDecentFiJC

MARCH 8, 2020: That was the day ANTHONY FAUCI, DEBORAH BIRX, ROBERT REDFIELD (CDC) and a few other CDC goons received the email below. It was a status report on the clinical trial results the CHINESE (and other countries) had seen from IN VIVO use of REMDESIVIR for the treatment of SARS-COV-2. (As you can see, the results were disastrous.) 💥RESULTS: REMDESIVIR (GILEAD) was not only INEFFECTIVE at treating COVID-19, it was ALARMINGLY HARMFUL for patient outcomes. *In fact, REMDESIVIR demonstrated an INCREASE in CASE FATALITY RATE (CFR) of 3,500%-4,000%!!! (That’s euthanasia/eugenics/murder, folks.) *NOTE: Many COVID PATIENT FATALITIES were largely a byproduct of a mortal cascade as a result of ACUTE RENAL DAMAGE/FAILURE. (Because again, Remdesivir is NEPHROTOXIC.) So… I know what you’re thinking — Why the FUCK did they INSIST on giving REMDESIVIR to COVID PATIENTS in HOSPITALS, while also DOING EVERYTHING IN THEIR JEW POWER to PREVENT ANYONE from USING HCQ (or IVM)? That’s an EXCELLENT question, my friends! And bet your ass, we’re damn sure going to answer it. But before we do that, aren’t you the LEAST bit curious to know how CHLOROQUINE (and HCQ) had been doing in those same CLINICAL TRIALS for the treatment of SARS-COV-2? Let’s check out the next post & see, shall we…

@DecentBackup - BackupDecentFiJC

MARCH 16, 2020 (8 DAYS LATER): You guys are gonna get a REAL kick outta THIS one… 💥RESULTS: “These research papers show GREAT ANTIVIRAL PROMISE for BOTH HYDROXYCHLOROQUINE and CHLOROQUINE. The Chinese have started using them. SO SHOULD WE… …UNLIKE VACCINES and COSTLY NEW ANTIVIRALS, Hydroxychloroquine and Chloroquine are GENERALLY SAFE, VERY WELL-TESTED, CHEAP and READILY AVAILABLE TODAY. They could be a REAL GAME CHANGER. Please PUBLISH AND DISSEMINATE.” Huh. Weird. You know, it’s a real shame none of us knew THESE emails even fucking existed until just a couple of months ago. A REAL shame.

@DecentBackup - BackupDecentFiJC

PALANTIR: You’re supposedly a repository juggernaut of quantum-level data collation and predictive analytics, armed with AI and Alex Karp (Gilman Louie) algorithms. And yet, when tasked with optimizing America’s COVID response, I knew more about COVID than PALANTIR. Why is that? https://t.co/Uw4W0UPBJn

@DecentBackup - BackupDecentFiJC

*MUCH more is on the way in just a bit, but before I go, here’s a little preview of where this f’ing nightmare is headed, folks. 💥💥💥💥💥💥💥💥💥💥💥💥💥 ANTHONY WELTERS & LARRY RENFRO 💥💥💥💥💥💥💥💥💥💥💥💥💥 ✅GILEAD (Remdesivir… KILL KIDNEYS) ✅SOMATUS INC. (SELL KIDNEYS) ✅OPTUM VENTURES (UnitedHealth) Is it beginning to sink in yet? *No matter how much you think you hate these people, I assure you, it’s not nearly enough.😒🤬

@DecentBackup - BackupDecentFiJC

Guess who else fought to shelve HCQ, while PUSHING REMDESIVIR to the forefront… THIS FA***T. ✅ANDY SLAVITT *BIDEN WH, Senior Advisor for COVID Response *OBAMA WH, Head of Medicare & Medicaid *UNITED STATES OF CARE, Founder & Chair Emeritus *BIPARTISAN POLICY CENTER, Co-Chair of Nat’l Initiative on the Future of Healthcare 💥CLIFFS: ANDY SLAVITT is a SERIES B INVESTOR in SOMATUS, at the SAME FUCKING TIME he was acting as the PRESIDENT’S SENIOR ADVISOR on COVID RESPONSE. (These criminal Jews have got to go.🤦🏻‍♂️)

@DonnaLeist - Donna Leist

@DecentBackup Guess who fought to shelf HCQ https://t.co/2lI8f3sVfm

@DecentBackup - BackupDecentFiJC

Here’s ANDY SLAVITT in his natural habitat.🤣 https://t.co/cKbc9yfIg1

@DecentBackup - BackupDecentFiJC

💥SOMATUS: If this all still sounds like just a Cohencidence™️, check out THESE factoids. *Founded in 2015/2016 by former OBAMA ADMINISTRATION OFFICIALS, right before DJT won the 2016 PRESIDENTIAL ELECTION against HILLARY CLINTON. “Innovative Kidney Care Company works with Health Systems and Payers to enable VALUE-BASED CARE for CKD and END-STAGE RENAL DISEASE (ESRD).” (It almost sounds like they planned on having a surge of people/customers presenting with LATE-STAGE KIDNEY DISEASE. Weird.) ✅DR. IKENNA OKEZIE SOMATUS, Co-Founder & CEO DAVITA, Group Vice President MCKINSEY & CO ✅TONY WELTERS SOMATUS, Co-Founder & Chairman UNITEDHEALTH GROUP, EVP of Public & Senior Markets Group *TONY WELTERS runs shit at NYU, NYU LAW and NYU LANGONE MED CTR, while also serving as DIRECTOR for CARLYLE GROUP (RUBENSTEIN/DUKEU), LOEWS CORP (TISCH/UJA) and LEAD DIRECTOR for GILEAD (Remdesivir). *LARRY FINK (BLACKROCK) is CO-CHAIRMAN of NYU LANGONE MED CTR. 💥Now ask yourself, why do NYU LANGONE MED CTR, CARLYLE GROUP, RUBENSTEIN, DUKE UNIVERSITY, LOEWS CORP, TISCH and UJA all sound so familiar?🤔

@DecentBackup - BackupDecentFiJC

JEWISH COMMUNAL FUND (Mossad slush) 💥💥💥💥💥💥💥💥💥💥💥💥💥💥 JCF was created in 1972 by a group of UJA-FEDERATION (Mossad) executives and former Presidents, largely to serve the best interests of… you guessed it… UJA-FEDERATION (Mossad) and GLOBAL JEWRY. 👺ANDREW TISCH: The CO-CHAIRMAN of LOEWS CORP and a TRUSTEE and FORMER PRESIDENT of JEWISH COMMUNAL FUND. His WIFE, ANNE RUBENSTEIN TISCH, is also a TRUSTEE of JCF and a TRUSTEE of SESAME WORKSHOP. 👺JAMES TISCH: The CEO of LOEWS CORP and BROTHER of ANDREW TISCH who was CHAIRMAN of UJA-FEDERATION during 9/11. The CHAIRMAN of UJA-FEDERATION IMMEDIATELY PRECEDING him was LARRY SILVERSTEIN. APRIL 2019: JAMES TISCH and RICHARD FRIEDMAN (Goldman Sachs) were named CO-CHAIRMEN of the MOUNT SINAI HOSPITAL/HEALTH SYSTEM. MOUNT SINAI receives metric FUCK TONS of funding from DANIEL/MARGARET LOEB (ECOHEALTH ALLIANCE/SUCCESS ACADEMIES/Third Point/Bitwise) and HENRY/MARIE-JOSÉE KRAVIS (KKR/BILDERBERG/SLOAN-KETTERING/Bitwise). 👺JESSICA TISCH: She’s the DAUGHTER of JAMES TISCH (and MERRYL TISCH) who was Cohencidentally™️ JUST APPOINTED NYPD POLICE COMMISSIONER on NOVEMBER 25, 2024. If it’s STILL unclear as to who these people really are or what they’re about, just look at where they send the lion’s share of their money. *Top COMMUNITY ORGANIZATION supported in terms of the TOTAL # of GRANTS and TOTAL DOLLAR AMOUNTS: 👺UJA-FEDERATION (Mossad) *Top GENERAL EDUCATION organizations supported in terms of… TOTAL # of GRANTS: 👺COLUMBIA UNIVERSITY 👺NEW YORK UNIVERSITY (NYU) TOTAL DOLLAR AMOUNTS: 👺BROWN UNIVERSITY 👺JOHNS HOPKINS UNIVERSITY *Top HEALTH ORGANIZATIONS supported in terms of… TOTAL # of GRANTS: 👺SBH COMMUNITY SERVICE NETWORK 👺MEMORIAL SLOAN-KETTERING CANCER CTR TOTAL DOLLAR AMOUNTS: 👺NYU LANGONE HOSPITALS 👺DUKE UNIVERSITY HEALTH SYSTEMS *Gosh, there sure does appear to be tons of current/former UJA-FEDERATION KEY EXECUTIVES on the BOARD of NYU LANGONE, where LARRY FINK is currently CO-CHAIRMAN. Hey, there’s LARRY FUCKING SILVERSTEIN!🤦🏻‍♂️ BONUS FUN FACT: The Top JEWISH EDUCATION ORGANIZATION JCF supports in terms of TOTAL DOLLAR AMOUNTS is… 👺SALANTER AKIBA RIVERDALE ACADEMY *The ASSOCIATE PRINCIPAL of SAR ACADEMY was recently arrested for PRODUCTION OF CHILD PORNOGRAPHY.

@DecentBackup - BackupDecentFiJC

See if you recognize any of THESE people from the MOUNT SINAI HOSPITAL/HEALTH network and JEWISH COMMUNAL FUND. NOTABLE FACTOIDS: 👺JAMES TISCH: He is the past CHAIRMAN of JEWISH AGENCY FOR ISRAEL (Israeli intelligence), has the NYPL named after him, is a member of the CFR and serves on the EXECUTIVE COMMITTEE of the PARTNERSHIP FOR NYC. 👺RICHARD FRIEDMAN: In addition to being CO-CHAIRMAN of the BOARD OF TRUSTEES and CHAIRMAN of the DEVELOPMENT COMMITTEE of MOUNT SINAI HEALTH SYSTEM, and CHAIRMAN of GOLDMAN SACHS ASSET MANAGEMENT, he’s also SENIOR FELLOW and SECRETARY OF THE CORPORATION of… BROWN UNIVERSITY. 👺LEON BLACK: The CO-FOUNDER & FORMER CHAIRMAN of APOLLO GLOBAL MANAGEMENT, and LONG-TIME JEFFREY EPSTEIN ASSOCIATE, is also a TRUSTEE of MOUNT SINAI HOSPITAL. He serves on the BOARD OF DIRECTORS for the PARTNERSHIP FOR NYC. *NOTE: I keep seeing this “PARTNERSHIP FOR NYC” organization popping up wherever there’s JEW FUCKERY AFOOT. It’s almost like these JEWS are serving a coordinated agenda WITHIN NYC and the UNITED STATES that runs antithetical to the best interests of AMERICA and her citizens. Weird. But who on EARTH could be running the show at the PARTNERSHIP FOR NYC?🤔🤔🤔

@DecentBackup - BackupDecentFiJC

MOUNT SINAI: *SVIDER BC Partners *GOGEL CD&R *TISCH Loews, UJA *BLACK, HARRIS, ROWAN Apollo, UJA *LOEB Third Point, EcoHealth Alliance *FRIEDMAN Goldman Sachs *KRAVIS KKR, Bilderberg *BERNIKOW K2, UBS, UJA *NEARY Warburg Pincus *GALIANO Blackstone, Anthos *GOTTLIEB FDA https://t.co/1VNilRq81R

@DecentBackup - BackupDecentFiJC

Please allow me to RE-INTRODUCE you all to the TOP MOSSAD/GCHQ SPY in the UNITED STATES. 👺JERRY SPEYER CHAIRMAN EMERITUS *Partnership for NYC *Columbia University *Tishman Speyer CHAIRMAN *New York Presbyterian Hospital (Cleveland Clinic, Weill Cornell, NYU, etc.) *His son, ROB SPEYER, is CO-CHAIRMAN of the PARTNERSHIP FOR NYC with ALBERT BOURLA. *His wife, KATHERINE FARLEY, is CO-CHAIR of the INTERNATIONAL RESCUE COMMITTEE (IRC), which is (almost CERTAINLY) involved in KID TRAFFICKING. She’s also a TRUSTEE of SUCCESS ACADEMIES, which is CHAIRED by DANIEL LOEB (Margaret Loeb, EcoHealth) and chock FULL of UJA-FEDERATION assets/executives. FARLEY is also extremely close with JOSEPH & CLARA TSAI (ALIBABA) and the absolutely ILLEGITIMATE GOVERNOR OF NY, KATHY HOCHUL.

@DecentBackup - BackupDecentFiJC

💥REMDESIVIR: It’s time you Mossad/CIA/GCHQ bioterrorists paid the piper for your coordinated mass murder scheme. ✅BREAKTHROUGH PROPERTIES A joint venture established JULY 2019 between… 💥BELLCO CAPITAL Arie Belldegrun Family Office 💥TISHMAN SPEYER Jerry Speyer, Rob Speyer https://t.co/af0OSfc6js

@DecentBackup - BackupDecentFiJC

Here’s what JERRY SPEYER, KATHERINE FARLEY, GILEAD, DANIEL LOEB, the TISCH FAMILY and UJA-FEDERATION and have REALLY been up to, folks. *NOTE: It’s also worth mentioning that KATHERINE FARLEY has been a TRUSTEE of ROCKEFELLER UNIVERSITY since 2015, serves as the CHAIRMAN of its NOMINATING AND GOVERNANCE COMMITTEE and sits on its EXECUTIVE COMMITTEE.

@DecentBackup - BackupDecentFiJC

@KimWexlerMAJD @frankgaffney International Rescue Committee (IRC) is one that gets more overlooked than any other, while also being the most dangerous, imo. KATHERINE FARLEY, CO-CHAIR of IRC, is JERRY SPEYER’S WIFE. The TISCH family (Loews/UJA) & GOLDMAN SACHS (Atlantic Council) are also heavily involved. https://t.co/L9drdQIZye

@DecentBackup - BackupDecentFiJC

SPOILERS: If you’re sitting there wondering how the fuck could the people at GILEAD be so callous, and have such a total disregard for HUMAN LIFE, that they and their investors would ever KNOWINGLY HARM PATIENTS and/or WILLINGLY GO ALONG with a CONSPIRACY TO COMMIT HOSPITAL GENOCIDE with their drug, REMDESIVIR, welp… I can give you ~$1,300,000,000 reasons why.🤬

Saved - December 8, 2024 at 5:46 PM
reSee.it AI Summary
I shared insights on the development and trials of Remdesivir, highlighting its origins in 2009 and collaborations with NIH and CDC starting in 2013. I discussed its testing against Ebola and MERS-CoV, and the subsequent trials for COVID-19, particularly the ACTT trial that led to its Emergency Use Authorization in May 2020. I expressed concerns about the FDA's actions, suggesting they were preemptive measures to avoid liability, and pointed out that oral chloroquine was more effective than Remdesivir for COVID treatment. I emphasized the significance of these findings for accountability in the distribution of COVID treatments.

@DecentBackup - BackupDecentFiJC

https://t.co/QfunQWNqkN

@DecentBackup - BackupDecentFiJC

https://t.co/yq34cxHz4C

@DecentBackup - BackupDecentFiJC

*GILEAD: Originally synthesized the PARENT compound of REMDESIVIR in MARCH 2009, then finally ISOLATED REMDESIVIR in 2013. Later that same year (2013), Gilead had connected and begun collaborating with the NIH & CDC, allowing them to step in and run preclinical trials, testing the antiviral efficacy of REMDESIVIR against EBOLA and CORONAVIRUSES. *2014: USAMRIID (DoD) and GILEAD began collaborating to advance Remdesivir and several of Gilead’s other antivirals, initially testing them against EBOLA (filovirus) and MIDDLE EAST RESPIRATORY SYNDROME VIRUS (MERS-CoV). *2021: By this time, USAMRIID had tested (or planned to test) Remdesivir for its efficacy against MARBURG VIRUS. 💥FUN FACT: EBOLA and MARBURG both cause HEMORRHAGIC FEVER. That’s the one where you bleed from everywhere, including tons of places you’re never supposed to bleed from. *REMDESIVIR EBOLA TRIALS (2016-2019): ✅PREVAIL IV - The Partnership for Research on Ebola Virus in Liberia IV (Phase II Trial) ✅PALM - The Pamoja Tulinde Maisha (PALM), when translated, is “TOGETHER SAVE LIVES” (Phase II & Phase III Trials) *REMDESIVIR COVID-19 TRIAL (February 2020): ✅ACTT - The Adaptive COVID-19 Treatment Trial *FDA would later cite the results of the ACTT trial to FRAUDULENTLY ISSUE GILEAD an EUA for REMDESIVIR to treat “HOSPITALIZED PATIENTS WITH SEVERE COVID” on MAY 1, 2020. 💥IMPORTANT: Note the OVERT specificity here in granting the EUA approval, which is the KEY TELLTALE SIGN of what it really is — a PREEMPTIVE CYA measure being taken by the FDA (and GILEAD) as part of their conspiracy to VIOLATE/DEFRAUD EUA LAWS & REQUIREMENTS. These fa***ts attempted to craft some highly-specific, hypothetical use-case scenario where it could be reasonably-argued that “Remdesivir is/was the ONLY EFFECTIVE/VIABLE COVID TX OPTION AVAILABLE”, which could/would technically justify lawful authorization of the EUA. Thereby, they’d absolve themselves of FUTURE CRIMINAL & CIVIL LIABILITIES (via the EUA), which they knew they’d eventually be facing, once people got wise to their coordinated HOSPITAL MURDER AGENDA… and their playing fucking MARKET MAKER of the KIDNEY/KIDNEY TRANSPLANT RACKET. And they would’ve gotten away with it, had we not found the docs that PROVED ORAL CHLOROQUINE was both EFFECTIVE AND SUPERIOR TO REMDESIVIR for the TREATMENT OF COVID at literally EVERY FUCKING STAGE. (These are spoilers from the future, btw.) *Then in OCTOBER 2020, FDA would also cite the ACTT trial, as well as GILEAD’S own trial “results”, as the basis for granting FULL FDA APPROVAL to GILEAD/REMDESIVIR. THIS factor will be EXTREMELY IMPORTANT for us towards TYING IN and NAILING all the “so-and-so was responsible for distribution of all ‘FDA-APPROVED’ COVID TXS & VACCINES” fa***ts out there who think they’ve already gotten away with the perfect crime too. @dezzie_rezzie

Saved - December 9, 2024 at 7:01 PM
reSee.it AI Summary
In April 2020, every ICU patient at Weill Cornell Medicine was intubated, leading to concerns about the treatment protocols involving Remdesivir and other medications. I highlighted Sanford I. Weill's significant financial contributions to the institution and his controversial role in the 2008 financial crisis. Jessica Bibliowicz, who succeeded him as chair, has been linked to Apollo Global Management and various financial maneuvers since before 9/11. I also pointed out the board members of Weill Cornell Medicine, suggesting a deeper, troubling connection among them.

@DecentBackup - BackupDecentFiJC

WEILL CORNELL MEDICINE 💥💥💥💥💥💥💥💥💥 “At the height of April (2020), every single WEILL CORNELL ICU patient was intubated.” *WCM: Named after SANFORD I. WEILL, the former CHAIRMAN of CITIGROUP and JAMIE DIMON’S MENTOR, who was CHAIRMAN of WEILL CORNELL MEDICINE for 20 YEARS. He now serves as CHAIR EMERITUS of WEILL CORNELL MEDICINE. ✅SANFORD I. WEILL *CITIGROUP, Chairman *WEILL CORNELL MEDICINE, Chair Emeritus *SANFORD WEILL: He and his wife, MOSHE, have given at least $650,000,000 to the WCM UNIVERSITY MEDICAL SCHOOL over the years. He was replaced as WCM CHAIRMAN in 2014 by his DAUGHTER, JESSICA. *SANFORD WEILL: He and CITIGROUP are largely credited as having been one of the MAJOR FACTORS/PLAYERS behind CAUSING the FINANCIAL/HOUSING CRISIS in 2008. AIG was certainly another major factor as well. 💥FUN FACT: If you’ll remember, AIG was one of the LARGEST RECIPIENTS of PAULSON & BERNANKE FEDERAL BAILOUT MONEY. If the names MAURICE GREENBERG, JEFFREY GREENBERG, JULES KROLL, ANDREW TISCH, MARC ROWAN, LEON BLACK & UJA-FEDERATION begin to seem EXTREMELY relevant to THIS plot, you’ll quickly understand why. (Yep, it’s THEM again. It’s ALWAYS them.) *JESSICA BIBLIOWICZ: She is the DAUGHTER of SANFORD WEILL and replaced him as CHAIRMAN of WEILL CORNELL MEDICINE in DECEMBER 2014. ✅JESSICA BIBLIOWICZ *WEILL CORNELL MEDICINE, Chairman *NEW YORK PRESBYTERIAN HOSPITAL, Trustee *APOLLO GLOBAL MANAGEMENT, Board *BRIDGE GROWTH PARTNERS, Senior Advisor *PRUDENTIAL INSURANCE FUNDS, Director/Trustee *NATIONAL FINANCIAL PARTNERS (Apollo), Chairman, President & CEO *JOHN A. LEVIN & CO., President & COO *PRUDENTIAL MUTUAL FUNDS, Director of Sales & Marketing *(SALOMON) SMITH BARNEY MUTUAL FUNDS, Head *ASIA PACIFIC FUND *SOTHEBY’S

@DecentBackup - BackupDecentFiJC

💥REMDESIVIR: I just realized what “compassionate use” meant. It was the drug that triggered the “fatal cascade” of multi-organ failure. They were fucking EUTHANIZING unwitting patients with it. For their organs markets. And that’s why they rushed the EUA through on MAY 1, 2020, because they already had literally THOUSANDS of bodies on their blood-stained hands. But HOW, you ask? 👺They intentionally decreased O2 Sat via RESPIRATORY DEPRESSION by deploying IV benzos or opioids, either at or soon after patient presents to the hospital, justifying the introduction of intubation/ventilation. THEN, once independent lung function is sufficiently decreased, they applied remdesivir to destroy the kidneys. 👺Applying a nephrotoxic agent like Remdesivir in a patient with low O2 Sat, COVID-induced HYPERTENSION and now zero independent lung function, means in basically NO TIME AT ALL, organs will begin shutting down. 👺And once vital organs start shutting down, the kidneys typically win out in the battle against the lungs, liver, brain, etc. for all the shunted blood — this leads to the cascade failure of already severely-weakened organs. *I’m still working out the mechanism for the exact order of operations, but this is what we 100% KNOW they did now. I’ll have it fully ironed out by tomorrow and will share it on here. 👺NOTE: You can SEE the criminal intent via their INSISTENCE on UNIFORMITY of TX for EVERYONE! Whether it’s applying INTUBATION in EVERY SINGLE CASE (NYU/Weill Cornell) and/or APPLYING REMDESIVIR in EVERY SINGLE CASE (Italy) — these are the textbook “protocols” of charlatans with an ulterior directive/mandate, not medical professionals treating patients according to an Hippocratic case-by-case basis. And best of ALL… ✅We can (will) easily prove all of this via subpoenaing patient charts for loved ones, and getting FOIAs for certain hospital networks’ communications with ZIENTS, SLAVITT, GOTTLIEB, CALIFF, FAUCI, etc. ✅UNIVERSITY HOSPITALS where those who were directly involved in protocol/drug development will be our lowest-hanging fruit here — Duke, UNC, Columbia, NYU, Vanderbilt, etc.

@DecentBackup - BackupDecentFiJC

JESSICA BIBLIOWICZ 💥💥💥💥💥💥💥 *One of the most vile, subversive, traitorous operatives that GLOBAL JEWRY has, and whom you’ve never heard of before. Until now. 👺JESSICA BIBLIOWICZ previously served as the PRESIDENT & CEO of NATIONAL FINANCIAL PARTNERS (NFP), a firm FOUNDED with STARTUP CAPITAL from APOLLO GLOBAL MANAGEMENT back in 1999. *CLIFFS: Jessica Bibliowicz has been an operative for Apollo Global Management since BEFORE 9/11. 👺JUNE 2003: BIBLIOWICZ became CHAIRMAN of NFP, then THREE MONTHS LATER, took the company PUBLIC (via IPO) in SEPTEMBER 2003. She continued to serve as CHAIRMAN of NFP until NFP was BOUGHT OUT by MADISON DEARBORN PARTNERS in JUNE 2013. *CLIFFS: The NFP IPO, which happened EXACTLY TWO YEARS AFTER 9/11, was the FIRST payoff. The BUYOUT by MDP, which happened EXACTLY at her 10-YEAR ANNIVERSARY of being named NFP CHAIRMAN, was the SECOND payoff. 👺MARCH 2022: JESSICA BIBLIOWICZ officially joins the BOARD OF DIRECTORS of APOLLO GLOBAL MANAGEMENT. *CLIFFS: Her formally joining the APOLLO GLOBAL MANAGEMENT BOARD OF DIRECTORS in MARCH 2022 is the THIRD payoff. It’s their way of saying “job well done” for helping steward these satanic, genocidal, maniacal JEWS as they carry out a GROTESQUE, yet HIGHLY-COORDINATED plot to COMMIT CRIMES AGAINST HUMANITY, BIOTERRORISM and EUGENICS against AMERICA and the WHITE RACE, and maximize their fucking profits while doing so. *NOTE: I only say “formally” about her joining the Apollo Global Management Board in 2022 because she’s already been on their payroll and working at their behest since 1999.

@DecentBackup - BackupDecentFiJC

✅JERRY SPEYER, Chairman NYPH, Board of Trustees “…every single (NYPH) WEILL CORNELL ICU patient at the height of April was INTUBATED.” 💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥 REMDESIVIR + midazolam + INTUBATION = 💀 💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥 (Just in case you forgot, folks.) https://t.co/BpQjzYFglH

@DecentBackup - BackupDecentFiJC

WCM BOARD OF TRUSTEES 💥💥💥💥💥💥💥💥💥 *See if you recognize any of THESE fa***ts who are all BOARD OF TRUSTEES MEMBERS of WEILL CORNELL MEDICINE. 👺SANFORD I. WEILL, Chair Emeritus 👺JESSICA BIBLIOWICZ, Chair 👺LLOYD BLANKFEIN 👺MAURICE R. GREENBERG 👺JEFFREY W. GREENBERG 👺ANDREW H. TISCH 👺JAMES C. ZELTER 👺HOWARD W. LUTNICK 👺LAURENCE D. BELFER 👺ROBERT A. BELFER, Life Fellow 👺RUPERT MURDOCH, Life Fellow 👺CHELSEA CLINTON 👺DAISY SOROS 👺CHARLOTTE FORD *NOTE: You don’t hate these people enough.🤬

Saved - December 12, 2024 at 8:34 PM
reSee.it AI Summary
I’ve been diving deep into the roles of past FDA commissioners during the pandemic, particularly focusing on Margaret Hamburg. Her connections to various organizations and her history raise significant concerns. I highlighted her involvement with Gilead and Remdesivir, suggesting a troubling narrative of collusion. The posts detail her affiliations with powerful entities and her participation in simulations of biological attacks. I also touched on the FDA's authority in the pandemic response and the implications of misinformation within government agencies. More insights are on the way.

@DecentBackup - BackupDecentFiJC

U.S. FOOD AND DRUG ASSOCIATION (FDA) 💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥 The 4 FDA COMMISSIONERS who led us all the way up to and THROUGH the pandemic are more than meets the eye. Lots more. (In reverse order) ✅MARGARET HAMBURG (05/09-04/15) ✅ROBERT M. CALIFF (02/16-01/17) ✅SCOTT GOTTLIEB (05/17-04/19) ✅STEPHEN M. HAHN (12/19-01/21) ✅ROBER M. CALIFF (02/22-PRESENT)

@DecentBackup - BackupDecentFiJC

*GILEAD: Originally synthesized the PARENT compound of REMDESIVIR in MARCH 2009, then finally ISOLATED REMDESIVIR in 2013. Later that same year (2013), Gilead had connected and begun collaborating with the NIH & CDC, allowing them to step in and run preclinical trials, testing the antiviral efficacy of REMDESIVIR against EBOLA and CORONAVIRUSES. *2014: USAMRIID (DoD) and GILEAD began collaborating to advance Remdesivir and several of Gilead’s other antivirals, initially testing them against EBOLA (filovirus) and MIDDLE EAST RESPIRATORY SYNDROME VIRUS (MERS-CoV). *2021: By this time, USAMRIID had tested (or planned to test) Remdesivir for its efficacy against MARBURG VIRUS. 💥FUN FACT: EBOLA and MARBURG both cause HEMORRHAGIC FEVER. That’s the one where you bleed from everywhere, including tons of places you’re never supposed to bleed from. *REMDESIVIR EBOLA TRIALS (2016-2019): ✅PREVAIL IV - The Partnership for Research on Ebola Virus in Liberia IV (Phase II Trial) ✅PALM - The Pamoja Tulinde Maisha (PALM), when translated, is “TOGETHER SAVE LIVES” (Phase II & Phase III Trials) *REMDESIVIR COVID-19 TRIAL (February 2020): ✅ACTT - The Adaptive COVID-19 Treatment Trial *FDA would later cite the results of the ACTT trial to FRAUDULENTLY ISSUE GILEAD an EUA for REMDESIVIR to treat “HOSPITALIZED PATIENTS WITH SEVERE COVID” on MAY 1, 2020. 💥IMPORTANT: Note the OVERT specificity here in granting the EUA approval, which is the KEY TELLTALE SIGN of what it really is — a PREEMPTIVE CYA measure being taken by the FDA (and GILEAD) as part of their conspiracy to VIOLATE/DEFRAUD EUA LAWS & REQUIREMENTS. These fa***ts attempted to craft some highly-specific, hypothetical use-case scenario where it could be reasonably-argued that “Remdesivir is/was the ONLY EFFECTIVE/VIABLE COVID TX OPTION AVAILABLE”, which could/would technically justify lawful authorization of the EUA. Thereby, they’d absolve themselves of FUTURE CRIMINAL & CIVIL LIABILITIES (via the EUA), which they knew they’d eventually be facing, once people got wise to their coordinated HOSPITAL MURDER AGENDA… and their playing fucking MARKET MAKER of the KIDNEY/KIDNEY TRANSPLANT RACKET. And they would’ve gotten away with it, had we not found the docs that PROVED ORAL CHLOROQUINE was both EFFECTIVE AND SUPERIOR TO REMDESIVIR for the TREATMENT OF COVID at literally EVERY FUCKING STAGE. (These are spoilers from the future, btw.) *Then in OCTOBER 2020, FDA would also cite the ACTT trial, as well as GILEAD’S own trial “results”, as the basis for granting FULL FDA APPROVAL to GILEAD/REMDESIVIR. THIS factor will be EXTREMELY IMPORTANT for us towards TYING IN and NAILING all the “so-and-so was responsible for distribution of all ‘FDA-APPROVED’ COVID TXS & VACCINES” fa***ts out there who think they’ve already gotten away with the perfect crime too. @dezzie_rezzie

@DecentBackup - BackupDecentFiJC

MARGARET HAMBURG (05/09-04/15) 💥💥💥💥💥💥💥💥💥💥💥💥💥 👺SPOILERS: This traitorous CIA/NIH/WELLCOME terrorist needs to be at or near the TOP of EVERYONE’S “COVID MOST WANTED” list. Period. Her BIO & TIMELINE are just STUNNING.🤯 Okie doke. Here we go… *MARGARET HAMBURG: Daughter of DR. DAVID A. HAMBURG, the PRESIDENT EMERITUS of CARNEGIE CORPORATION of NEW YORK, PRESIDENT of the NATIONAL ACADEMY OF MEDICINE and CHAIRMAN of the DEPARTMENT OF PSYCHIATRY & BEHAVIORAL HEALTH at STANFORD UNIVERSITY. 👺SANFORD WEILL: Chairman of CARNEGIE HALL and WEILL CORNELL MEDICAL. *She did her residency at NEW YORK HOSPITAL-CORNELL MEDICAL CENTER. *Worked with ANTHONY FAUCI at NIH during the AIDS “PANDEMIC” disaster. *Was NYC HEALTH COMMISSIONER during the first WTC BOMBING in 1993. 👺Founder of the Biodefense arm of the NUCLEAR THREAT INITIATIVE (NTI). 👺JUNE 2001: Participated in OPERATION DARK WINTER, conducted at ANDREWS AIR FORCE BASE, simulating a global BIOLOGICAL ATTACK by WEAPONIZED SMALLPOX. 😳😳😳😳😳 👺Became FDA COMMISSIONER in 2009, exactly two months after GILEAD SCIENCES successfully isolated the PARENT COMPOUND of REMDESIVIR. Led FDA the entire time GILEAD was working up to its full collaboration with NIH, CDC (2013) and the U.S. ARMY and AMRIID (2014). 👺2015: Appointed FOREIGN SECRETARY of the NATIONAL ACADEMY OF MEDICINE. 👺2018: Participated in CLADE X operation, hosted by JOHNS HOPKINS UNIVERSITY CENTER FOR HEALTH SECURITY, simulating a BIOLOGICAL ATTACK of a WEAPONIZED PARAINFLUENZA, designed to DECREASE THE GLOBAL POPULATION. I shit you, the fuck, not. 🤬🤬🤬🤬🤬 (Noticing™️ a recurring pattern here yet, sports fans? You should be.) 👺2020: Participated in the GRAND CHALLENGE ON CLIMATE CHANGE, HUMAN HEALTH, EQUITY. 🤣🤦🏻‍♂️ *Other notable participants included: 👺JEREMY FARRAR: Wellcome Trust 👺PETER DASZAK: EcoHealth Alliance AND REPS FROM… NIH WELLCOME BURROUGHS (Nancy Andrews) ROCKEFELLER FOUNDATION EXXONMOBIL WHO UNIVERSITY OF HONG KONG (Li Ka-Shing) ROBERT WOOD JOHNSON FOUNDATION NOAA 🤦🏻‍♂️🤬🤦🏻‍♂️🤬🤦🏻‍♂️ 👺MARGARET HAMBURG’S current/former affiliations might as well be a confession: ✅MARGARET A. HAMBURG *PRESIDENT’S INTELLIGENCE ADVISORY BOARD, Vice Chair *INTERACADEMY PARTNERSHIP, Co-President *NUCLEAR THREAT INITIATIVE (NTI), Board *NUCLEAR THREAT INITIATIVE (NTI), Bio Advisory Group *DUKE-NUS MEDICAL SCHOOL, Advisory Board *CENTRAL INTELLIGENCE AGENCY (CIA), Intelligence Science Board *COVID COLLABORATIVE, National Advisory Council *WELLCOME TRUST, Strategic Advisory Board on Vaccines and Drug-Resistant Infections *WORLD ECONOMIC FORUM (WEF), Synthetic Biology *COALITION FOR EPIDEMIC PREPAREDNESS INNOVATIONS (CEPI), Chairman of the Joint Coordinating Group *COUNCIL ON FOREIGN RELATIONS *HARVARD MEDICAL SCHOOL, Board of Fellows *HARVARD UNIVERSITY, Global Advisory Council *ALNYLAM PHARMACEUTICALS, Board *ROCKEFELLER FOUNDATION, Board *ROCKEFELLER UNIVERSITY, Board *BIPARTISAN COMMISSION ON *BIODEFENSE, Commissioner *GAVI ALLIANCE, Board *BILL & MELINDA GATES FOUNDATION, Global Health Scientific Advisory Committee *CENTER FOR STRATEGIC AND INTERNATIONAL STUDIES (CSIS), Commission on Strengthening America’s Health Security *COMMONWEALTH FUND, Board (Please, keep going. Believe it or not, there’s more… LOTS more.)

@DecentBackup - BackupDecentFiJC

Here’s some of those receipts from the previous tweet, and a bit more info on her dad, DAVID A. HAMBURG, and a little hint as to what CARNEGIE CORPORATION is all about today. As you can see, this bitch’s bio is nutz.🤣

@DecentBackup - BackupDecentFiJC

NUCLEAR THREAT INITIATIVE 💥💥💥💥💥💥💥💥💥💥 NTI BOARD OF DIRECTORS *At NTI, MARGARET HAMBURG (CIA/Wellcome/Duke-NUS) serves on the NTI BOD alongside… ✅GIDEON FRANK *ISRAELI ATOMIC ENERGY COMMISSION, Director General ✅LUCIANA BORIO *IN-Q-TEL (CIA), Senior Vice President *ARCH VENTURE PARTNERS, Venture Partner *COUNCIL ON FOREIGN RELATIONS, Senior Fellow for Global Health NTI BIO ADVISORY GROUP *At NTI, MARGARET HAMBURG serves on the NTI BIO ADVISORY GROUP alongside… ✅RESHMA SHETTY *GINKGO BIOWORKS (CIA), Co-Founder ✅JEREMY KONYNDYK *USAID OFFICE OF FOREIGN DISASTER ASSISTANCE, Director *CENTER FOR GLOBAL DEVELOPMENT, Senior Policy Fellow ✅JOHN-ERIK STIG HANSEN DENMARK CENTRE FOR BIOSECURITY AND BIOPREPAREDNESS, Director (Denmark, eh?)

@DecentBackup - BackupDecentFiJC

👺NOTE 1: GINKGO BIOWORKS gets tons of funding from IN-Q-TEL (CIA VC) and is PARTNERED with MODERNA for VACCINE PRODUCTION. Its largest shareholder is also the largest shareholder of http://WIX.COM (IDF Unit 8200)… ✅BAILLIE GIFFORD 👺NOTE 2: GINKGO also ties us right back to JERRY SPEYER (NYPH/NYU, PFNYC, MOSSAD/GCHQ) and ARIE BELLDEGRUN (KITE, GILEAD, GINKGO and BELLCO). 👺NOTE 3: USAID is a well-known CIA front led by SAMANTHA POWER that launders money, kids and weapons all over the world. Especially Ukraine. Lol. 👺NOTE 4: DENMARK further ties in WELLCOME TRUST to the CREATION & COVERUP of COVID, and the J6 ENTRAPMENT OPERATION against TRUMP SUPPORTERS. *This is all thanks to SEDITION HUNTER, TOMMY CARSTENSEN (DENMARK), a BIOSTATISTICIAN from the WELLCOME SANGER INSTITUTE in… DENMARK.

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@DecentBackup - BackupDecentFiJC

COUNCIL ON FOREIGN RELATIONS 💥💥💥💥💥💥💥💥💥💥💥💥 “Lessons Learned with Margaret (Peggy) Hamburg” - March 13, 2023 -Presider, Gigi Kwik Gronvall (🤦🏻‍♂️🤬) GRONVALL: “We have a question from the virtual audience.” OPERATOR: “Our next question will come from AMY MAXMEN.” (FUCK Amy Maxmen.🤦🏻‍♂️🤬) MAXMEN Q: “Hi. Thanks a lot. I actually had a follow-up to that question, so that was good timing for me. So about misinformation, so what we saw in this pandemic is that a lot of misinformation actually comes from, you know, within the government. And you saw that at multiple times during the pandemic. I saw just recently that the CDC and the FDA sent a letter to Florida’s surgeon general about sort of the antivaccine misinformation he’s been promoting. Are there any ideas, you know, within the FDA to make sure that it is not kind of falling prey to politicization? 💥You know, like as we saw with HYDROXYCHLOROQUINE?💥 And also moves to make sure that there’s kind of a more one government response in terms of this is—this is what the best science says right now? Because I think that just contributed to so much misinformation and politicization of all sorts of information.” HAMBURG: “Yeah. Well, that does build on the last question in important ways. And I think, you know, first to say that we may have failed during COVID from different venues to really help explain that the response was going to depend on an iterative process of the unfolding experience of the pandemic, ongoing studies of what works and what didn’t, understanding the nature of how the virus is transmitted, asymptomatic transmission, long COVID, what kinds of treatments actually were studied and demonstrated to have benefit, et cetera.” 👺NOTE: As much as you THINK you hate these people, I assure you, it’s not enough. And this is just ONE of the former FDA COMMISSIONERS. Lol.

@DecentBackup - BackupDecentFiJC

*Much more is coming later this evening, after I take myself a well-deserved break. But before I do that, I’ll leave you with something important for you to have for safekeeping. 👺Take a moment to soak in this passage from the NYT regarding the authority of the FDA: “The FDA has been front and center in the FEDERAL GOVERNMENT’S RESPONSE to the CORONAVIRUS PANDEMIC. It has the AUTHORITY to APPROVE COVID VACCINES, TESTS and TREATMENTS…” (That’ll be EXTREMELY integral to the overall plot going forward, sports fans. Cheers.)

Saved - January 1, 2025 at 7:30 PM
reSee.it AI Summary
Happy New Year! It seems like the issues we face are persistent. I’ve been reflecting on the effectiveness of treatments for COVID-19, particularly comparing Remdesivir and Chloroquine. The latter has shown promising results in trials, being cheap, safe, and effective at various stages of infection. It’s concerning to see the push against its use despite its benefits. I also shared thoughts on various organizations and entities involved in healthcare and technology, highlighting the interconnectedness of these fields.

@DecentBackup - BackupDecentFiJC

Happy New Year, gang. This shit isn’t going away. Fa***ts. Sincerely, GoyWonder™️ @elonmusk @DavidSacks @PalantirTech @peterthiel @AnthemBCBS @Loews_Hotels @GileadSciences @McKinsey @BCG @BainandCompany @8vc @UJAfedNY @github @kleinerperkins @anduriltech @Columbia @nyphospital @WeillCornell @jfederations @ClevelandClinic @TPUSA @sethklarman @realDailyWire @AmwayUS @prageru @BlazeMediaPR @Chabad @ClintonFdn @McCainInstitute @ADL @AIPAC @WHU_1893 @luxcapltd @JohnsHopkinsSPH @JohnsHopkins

@DecentBackup - BackupDecentFiJC

GILEAD, UNITEDHEALTH & the (SINISTER) BUSINESS of MEDICINE — MANUFACTURING MORBIDITY & MORTALITY 💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥 By FEBRUARY 2020, the Chinese had already conducted IN VITRO side-by-side trials of two known ANTIVIRALS, testing their comparative efficacies against the COVID-19 “novel” coronavirus. ✅REMDESIVIR (GS 5734) *Made by Gilead Sciences. ✅CHLOROQUINE 💥RESULTS: While they determined both to be effective at viral inhibition, they noted CHLOROQUINE, given ORALLY, was widely bioavailable, fast-acting and demonstrated markedly higher levels of viral inhibition at pre-entry, entry and post-entry stages of viral infection. *In addition to that, they noted CHLOROQUINE acts as an IMMUNOMODULATOR in vivo, which should only further synergize its already demonstrable in vitro efficacy in live COVID patients. *Further, they went out of their way to make mention that CHLOROQUINE was CHEAP, SAFE & had a 70-YR TRACK-RECORD of SAFETY/EFFICACY behind it. *Remdesivir was shown to be functionally effective post-entry, albeit less effective than CHLOROQUINE at the same stage, which is in alignment with its mechanism of action and its IV administration. *NOTE: If you’re reading this, and you’re already starting to question the motives behind their unwavering commitment to restricting CHLOROQUINE usage and insisting on REMDESIVIR, good. You’re one of the few remaining who still has some common fucking sense. Congrats. 💥CONCLUSION: Although it may seem like a no-brainer to most of us already, the Chinese recommended that both drugs be earmarked to move onto the next step in therapeutic research — IN VIVO testing for SARS-COV-2 inhibition. *Cool. I have no problems with that and it’s necessary that we be fair and thorough to both agents.

@DecentBackup - BackupDecentFiJC

@DukeMedSchool @DukeCapPartners @Stanford @bcpartners @apolloglobal @sunmicrosystems @OpenAI @KKR_Co @RANDCorporation @Novartis @illumina @YaleMed @RenTechServices @lightspeedvp @foundersfund @a16z @pmarca @sequoia @khoslaventures @SoftBank @Deloitte @blackstone @TempusAI @US_FDA @HHSGov @BrookingsInst @CFR_org @EcoHealthNYC @JNJNews @genentech @Roche @EliLillyandCo @pfizer @BlueVoyant @Optum @UHC

@DecentBackup - BackupDecentFiJC

@Cognizant @DunBradstreet @IMSHealth @MarshMcLennan @Merck @IBM @Akamai @Google @Tsinghua_Uni @BlackRock @IQVIA_global @BoozAllen @fema @CadmusGroup @RenaissanceREI @OneCarlyle @CommScope @ericsson @WiFiNet @SeaGen_ @23andMe @WaltDisneyCo @Infosys @nyulangone @Temasek @MountSinaiNYC @CedarsSinai

@DecentBackup - BackupDecentFiJC

@JuniperNetworks @Accenture @HP @CiscoSecure @sanofi @tishmanspeyer @TheNewSchool @NewAmerica @TrilateralNA @10xGenomics @Gartner_inc @CSHL @AlibabaGroup @TencentGlobal @Huawei @symantec @Broadcom @FDD @NEDemocracy @UBS @InfoLab41 @Unit42_Intel @AEA @CerberusCapital @Ballardpartners @pentagrp @UCLA @NSAGov @nytimes @CNBC @BNYglobal @Verizon @AOL

@DecentBackup - BackupDecentFiJC

@WellsFargo @HerculesVC @tenethealth @p72vc @26northpartners @ecfs @SARacademy @CDCgov @FocusFinancial @SavetheChildren @careusa @NCCGroupplc @NSOgroup__ @ICGplc @IridiumComm @AspenInstitute @Ripple @solana @coinbase @Mangroves @RayDalio @Lazard @MichaelDell @ethereum @w3c @SymantecGov @Mandiant @DAlperovitch @awscloud @snyksec @Fortinet @Darktrace

@DecentBackup - BackupDecentFiJC

@SemperisTech @silverlake_news @bancosantander @CocaCola @Wendys @TheRTP @JewishAgency @IDF @Ginkgo @moderna_tx @TriatomicCap @PhRMA @GoDaddy @AIGinsurance @krollbondrating @duffandphelps @ThirdPointLLC @LKSF @Harvard @GoHeels @Oracle @SpaceX @Tesla @CatalioCapital @PIIE @DukeKunshan @dukenus @EY_US @mocafiapp @MSKCancerCenter

@DecentBackup - BackupDecentFiJC

@RedCellPartners @epirus @PayPal @CrowdStrike @SentinelOne @QinetiQ @HakluytCompany @GoldmanSachs @JewishCommFund @SesameWorkshop @PaulsonInst @AtlanticCouncil @NATO @Centerviewfin @RobinhoodApp @GCHQ @MOSSADil @CIA @DHSgov @CNASdc @WEAdvisors @Teneo @FordFoundation @MarkleFdn @NIH @wellcometrust @sangerinstitute

@DecentBackup - BackupDecentFiJC

@HCAhealthcare @GrailBio @Freescale @NXP @DXCTechnology @NTI_WMD @WHO @odigo @OtisElevatorCo @McLartyAssoc @AthoraNL @K2Integrity @K2Global @K2GlobalJKroll @PublicisGroupe @thermofisher @Accel @Microsoft @Rackspace @PaloAltoNtwks @solarwinds @Boeing @generaldynamics @BAESystemsInc @jpmorgan @Citi

@DecentBackup - BackupDecentFiJC

@WellsFargo @HerculesVC @tenethealth @p72vc @26northpartners @ecfs @SARacademy @CDCgov @FocusFinancial @SavetheChildren @careusa @NCCGroupplc @NSOgroup__ @ICGplc @IridiumComm @AspenInstitute @Ripple @solana @coinbase @Mangroves @RayDalio @Lazard @MichaelDell @ethereum @w3c @SemperisTech @RedCellPartners @HCAhealthcare @GrailBio @Freescale @NXP @Yahoo @PepsiCo @RigettiCo @nightdragon @IsraelPolicy4m @ManhattanInst @KitePharma @AllogeneTx @SkaddenArps @Clear @Capgemini @ATT @FirstNet @RioTinto @WeizmannScience @usisraelbsf @ARPA_H @BARDA @DARPA

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/

Video Transcript AI Summary
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.
Full Transcript
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

Video Transcript AI Summary
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.
Full Transcript
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.

@Humanspective - Humanspective

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.

Video Transcript AI Summary
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.
Full Transcript
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
Saved - February 3, 2025 at 2:19 PM
reSee.it AI Summary
I reached out to @snaggie1 with a question about the timeline of COVID treatment research. By March 2020, we knew Remdesivir was harmful and that HCQ was safe and effective, yet discussions about HCQ trials continued into September. I questioned why the focus was solely on prophylactic applications when HCQ had shown superiority in various stages of infection. I also shared a thread detailing early antiviral trials that highlighted HCQ's advantages over Remdesivir, emphasizing its safety, efficacy, and low cost. I concluded by urging a fair evaluation of both treatments.

@DecentBackup - BackupDecentFiJC

Btw, since I’ve got you here, @snaggie1, do me a favor and answer a quick question for me: *Thanks to emails sent to Anthony Fauci and his staff directly, we KNEW by March 8, 2020 that Remdesivir was increasing COVID CFR by 35-40x, AND that it was nephrotoxic in an alarming number of patients. *Just EIGHT DAYS LATER, by MARCH 16, 2020, NIH and DUKE (and everyone else) knew that HCQ was not only safe and effective for COVID, but that the countries using HCQ reported ZERO COVID FATALITIES WHATSOEVER! By APRIL, ORAL HCQ was demonstrated to be literally SUPERIOR to REMDESIVIR at all 3 “COVID exposure phases” of clinical testing. 💥QUESTION: Now, given that ALL of the above is irrefutably true, can you please tell me why you’re filming YOUTUBE VIDEOS to discuss the “HERO trials testing for the potential efficacy of HCQ” all the way in LATE SEPTEMBER 2020? (That’s more than 6 fucking months after we’d already had ALL our efficacy questions regarding HCQ answered DEFINITIVELY.) And further, why were you so laser focused SOLELY on testing the “prophylactic application” of HCQ exclusively? What about the EARLY/LATE-stage post-COVID infection phases, where (I remind you) ORAL HCQ was ALSO demonstrated to be markedly superior to (IV) Remdesivir?

@DecentBackup - BackupDecentFiJC

So, let me guess, @DukeMedSchool, @DukeHealth and CTSI are all Jews, Chinese and a smattering of Indians? Much like Duke Kunshan University and DukeNUS, where you helped the CCP create COVID in Wuhan and Singapore, amirite? How many non-Jew Whites are on staff at Duke University Medicine or Duke Health? PS: Did David Lobach come into work today? How about Nancy Andrews and Laurene Sperling?

@DecentBackup - BackupDecentFiJC

@snaggie1, please find the embedded thread below for those very trials I mentioned above. I very much look forward to receiving your EXPERTLY well-reasoned, evidence-based response here. Thank you in advance. “Doc.” https://t.co/sOf4M11Q2i

@DecentBackup - BackupDecentFiJC

GILEAD, UNITEDHEALTH & the (SINISTER) BUSINESS of MEDICINE — MANUFACTURING MORBIDITY & MORTALITY 💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥💥 By FEBRUARY 2020, the Chinese had already conducted IN VITRO side-by-side trials of two known ANTIVIRALS, testing their comparative efficacies against the COVID-19 “novel” coronavirus. ✅REMDESIVIR (GS 5734) *Made by Gilead Sciences. ✅CHLOROQUINE 💥RESULTS: While they determined both to be effective at viral inhibition, they noted CHLOROQUINE, given ORALLY, was widely bioavailable, fast-acting and demonstrated markedly higher levels of viral inhibition at pre-entry, entry and post-entry stages of viral infection. *In addition to that, they noted CHLOROQUINE acts as an IMMUNOMODULATOR in vivo, which should only further synergize its already demonstrable in vitro efficacy in live COVID patients. *Further, they went out of their way to make mention that CHLOROQUINE was CHEAP, SAFE & had a 70-YR TRACK-RECORD of SAFETY/EFFICACY behind it. *Remdesivir was shown to be functionally effective post-entry, albeit less effective than CHLOROQUINE at the same stage, which is in alignment with its mechanism of action and its IV administration. *NOTE: If you’re reading this, and you’re already starting to question the motives behind their unwavering commitment to restricting CHLOROQUINE usage and insisting on REMDESIVIR, good. You’re one of the few remaining who still has some common fucking sense. Congrats. 💥CONCLUSION: Although it may seem like a no-brainer to most of us already, the Chinese recommended that both drugs be earmarked to move onto the next step in therapeutic research — IN VIVO testing for SARS-COV-2 inhibition. *Cool. I have no problems with that and it’s necessary that we be fair and thorough to both agents.

@DecentBackup - BackupDecentFiJC

@snaggie1 YOUTUBE CLIP: https://youtu.be/3fhhvI6THgI?si=wDRRPI67XgG3lq5l

Saved - May 23, 2025 at 6:11 PM
reSee.it AI Summary
I shared concerns about Remdesivir, a drug initially deemed too dangerous for Ebola trials due to its high mortality rate. Despite this, it was the only drug authorized for COVID patients, leading to severe kidney and liver damage. Families affected have labeled it 'Run-Death-Is-Near' due to its lethal effects. The government incentivized hospitals to use it, even after the WHO advised against it. Prominent figures, including RFK Jr., warned about its dangers, yet it continues to be used in hospitals today.

@ValerieAnne1970 - Valerie Anne Smith

Remdesivir Was Declared Too Deadly & Unethical To Use In African Ebola Trials Because It Had A 53% Kill Rate. Yet, It Was The Only Drug Fauci Allowed To Be Used On COVID Patients In Hospitals. Families Whose Loved Ones Were Killed By Remdesivir Call It 'Run-Death-Is-Near.' Remdesivir kills kidney function, combine that with a ventilator & patients develop pulmonary edema, causing their lungs to fill with fluid & drown to death. Remdesivir kills the liver & causes organ shut down. In the halted Ebola trial, Remdesivir mortality was 53% overall & 85% mortality in those with high viral load. The US Govt BRIBED Hospitals to Administer a Kidney and Liver Toxic Drug with incentives & huge bonuses. Remdesivir is so lethal it got nicknamed ‘Run Death Is Near’ after it started killing thousands of Covid patients in the hospital. Anthony Fauci claimed that Remdesivir would stop Covid; instead, it stopped kidney function, then blasted the liver & other organs. What the US government never told you about Remdesivir is that by November 2020, even the WHO said, "Do not use Remdesivir." But instead, HHS added a 20% bonus on the entire hospital if they administered this liver and kidney-toxic drug. That 20% bonus ended up being a BIG pay day. Before Taking His Role at HHS, RFK Jr. Warned the World also: “Tony Fauci Knew That Remdesivir Would Kill You.” “How does it kill you?” he asked. “Kidney failure, heart failure & all-organ collapse.” “All the doctors said ... ‘We’ve never seen a virus that attacks the kidneys.’ Because it wasn’t the virus; it was the Remdesivir.” Remdesivir is still being used in hospitals today... 👇African Ebola Drug Trials Using Remdesivir👇 https://www.franciskovacevic.com/remdesivir-2019-ebola-trials 👇Kidney Failure From Remdesivir👇 https://www.scielosp.org/article/csp/2021.v37n10/e00077721/#:~:text=Table%201%20describes%20the%20number%20of%20adverse,of%20renal%20adverse%20events%20among%20patients%20with 👇Heart Failure From Remdesivir👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8511861/ 👇Liver Failure From Remdesivir👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8224190/ Speaker: David Martin Video: ForeverSovereign

Video Transcript AI Summary
In 2018, remdesivir was considered unethical for Ebola clinical trials in Africa due to a 53% kill rate, higher than Ebola's typical mortality. Despite this, it was chosen to treat COVID in April and May 2020, with Anthony Fauci and Deborah Burke advocating for its use despite the World Health Organization's ethical concerns. The speaker claims that a conflict of interest exists because the same entities that financially benefit from promoting certain products are declaring the pandemic. These entities are allegedly linked to the Eugenics office at Carnegie Mellon in 1913 and the establishment of the World Health Organization in 1953. The speaker expresses concern about the influence of eugenics on these decisions.
Full Transcript
Speaker 0: Remember that in 02/2018, remdesivir, '1 of my favorite targets, remdesivir was too unethical to put into Ebola clinical trials in Africa because it had a fifty three percent kill rate published in medical journals. Ebola doesn't have a fifty three percent kill rate, but it was chosen in April and May of twenty twenty to be the drug of choice to treat COVID. This drug was too unethical to use in an African clinical trial because it was killing fifty three percent of the people that it was given to. And we had Anthony Fauci, Deborah Burke sitting next to the president going, we need to use remdesivir despite the fact that the World Health Organization said it was unethical to use it. Here's the problem. The problem is as long as the financial interest that dictates what product is going to be promoted is the one making the declaration of the pandemic, we have no possibility for accountability. We have no possibility for justice. And what we do is we allow people who were formed out of the Eugenics office, Carnegie Mellon in 1913, that same group of people that were the same group of people that established the World Health Organization in 1953, that same group of people are the ones who are making this decision. And I don't know how you feel about Eugenics, but I have a problem with it.
Remdesivir December 2019 - Ebola Trials — FRANCIS KOVACEVIC franciskovacevic.com
SciELO - Saúde Pública - Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database scielosp.org
Potential Cardiotoxic Effects of Remdesivir on Cardiovascular System: A Literature Review Corona disease 2019 (COVID-19) pandemic continues to spread around the world with no efficacious treatment. Intravenous remdesivir is the only authorized drug for treatment of COVID-19 disease under an Emergency Use Authorization. Remdesivir is a ... pmc.ncbi.nlm.nih.gov
Hepatic manifestations of COVID-19 and effect of remdesivir on liver function in patients with COVID-19 illness COVID-19 has emerged as a major global health crisis since the first cases were reported in China in December 2019. Remdesivir is the only broad-spectrum antiviral approved by the US Food and Drug Administration to treat hospitalized patients with ... pmc.ncbi.nlm.nih.gov
Saved - June 17, 2025 at 12:07 PM
reSee.it AI Summary
I discuss the controversial use of Remdesivir, a drug initially deemed too dangerous for Ebola trials due to its high mortality rate. Despite this, it became the only drug authorized for COVID patients in hospitals, leading to severe kidney and liver damage. I highlight the alarming nickname it received and the financial incentives hospitals received for its administration. Even after warnings from the WHO, it continued to be used, and recently, it was fast-tracked for pediatric use, raising concerns about its safety for infants and children.

@ValerieAnne1970 - Valerie Anne Smith

Remdesivir Was Declared Too Deadly & Unethical To Use In African Ebola Trials Because It Had A 53% Kill Rate. Yet, It Was The Only Drug Fauci Allowed To Be Used On COVID Patients In Hospitals. Remdesivir Is Still Used Today & It Is Now Being Used On Infants & Children... The drug is so lethal it got nicknamed ‘Run Death Is Near’ after it started killing thousands of Covid patients in the hospital. Remdesivir (Veklury) kills kidney function, combine that with a ventilator & patients develop pulmonary edema, causing their lungs to fill with fluid & drown to death. Remdesivir kills the liver & causes organ shut down. In the halted Ebola trial, Remdesivir mortality was 53% overall & 85% mortality in those with high viral load. The US Govt BRIBED Hospitals to Administer a Kidney & Liver Toxic Drug with incentives & huge bonuses. Anthony Fauci claimed that Remdesivir would stop Covid even though he knew it would cause 1000s of deaths. Remdesivir (Veklury) never stopped Covid...instead, it stopped kidney function, then it fatally stopped the liver & heart. What the US government never told you about Remdesivir is that by November 2020, even the World Health Organization (WHO) stated, "Do not use Remdesivir." But instead of heading this warning, the NIH & HHS added a 20% bonus on the entire hospital if they administered this liver, kidney & heart-toxic drug. That 20% bonus ended up being a BIG pay day. There has never been a virus that attacks the kidneys...because it wasn't the COVID virus attacking the kidneys...it was the Remdesivir. Remdesivir is still being used in hospitals today...and now Remdesivir (Veklury) is approved for use in infants. Specifically, the Food & Drug Administration (FDA) expanded its approval of remdesivir to include pediatric patients 28 days of age & older. Remdesivir (Veklury) is the ONLY approved treatment for hospitalized or non-hospitalized children that have mild-to-moderate COVID-19 & a positive PCR test. It historically takes 6 to 10 years for a drug approved for adults to receive pediatric labeling. Remdesivir was fast tracked & approved for use in pediatric patients, including neonates, all within 3 years of approval for use in adults & adolescents. 👇African Ebola Drug Trials Using Remdesivir👇 https://www.franciskovacevic.com/remdesivir-2019-ebola-trials 👇Kidney Failure From Remdesivir👇 https://www.scielosp.org/article/csp/2021.v37n10/e00077721/#:~:text=Table%201%20describes%20the%20number%20of%20adverse,of%20renal%20adverse%20events%20among%20patients%20with 👇Heart Failure From Remdesivir👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8511861/ 👇Liver Failure From Remdesivir👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8224190/ Speaker: Dr Bryan Ardis

Video Transcript AI Summary
Since May 2020, remdesivir may result in at least 30% death in hospitalized patients who receive it for five to ten days. CMS data for Medicare patients in New York showed 26.9% of those who received remdesivir died. In October 2020, the cardiovascular toxicology journal found remdesivir causes death of heart cells, is cardiotoxic, and can lead to cardiac arrest. Despite this, in December 2020, the NIH, with Anthony Fauci, updated guidelines listing remdesivir as the only FDA-approved drug for hospitalized Americans, even though the WHO published data in April of last year that it increases acute kidney failure compared to other drugs used to treat COVID-19. As of January 21st of this year, the FDA extended emergency use authorization, making remdesivir the only authorized medication that can be administered intravenously to newborns to 18-year-olds for COVID-19.
Full Transcript
Speaker 0: Proven to kill lives. I said since May 2020, remdesivir will result with at least thirty percent deaths of everyone who receives that drug in a hospital for five to ten days. I got Thomas Rince to pull the CMS data. You know, for the state of New York, I decided to run-in New York. I wanted to know Medicare aged patients. What's the percentage of death of those who received remdesivir for its five day protocol? Twenty six point nine percent of them died. And do you know right now that remdesivir as of October 2020 was found by the cardiovascular toxicology journal that it actually causes death of heart cells and is cardiotoxic and can lead to cardiac arrest. That was in October. December 16, your FDA I'm sorry. Your NIH with Anthony Fauci there decided to update now all guidelines for treatment drugs allowed and approved for COVID nineteen Americans. Guess what's the only listed drug FDA approved for hospitalized Americans? Remdesivir. When it is published by the World Health Organization to cause increased acute kidney failure compared to all other drugs being used in the world when treating COVID nineteen. And that was published in April of last year. So you have kidney failure, liver failure, now heart failure being caused by remdesivir published to do so. Two months later, your NIH, the FDA, still sits back and goes, this is the only approved drug for hospitalized COVID nineteen patients. You know what's more disgusting? January twenty first of this year, the FDA extended an emergency use authorization and said there's now only one authorized medication that can be pumped into the veins of all newborns in this country to 18 year old pediatric age ranged children, starting with seven pound newborns. Guess what the only authorized drug to treat COVID nineteen children is now? In hospitals and outside. Remdesivir.
Remdesivir December 2019 - Ebola Trials — FRANCIS KOVACEVIC franciskovacevic.com
SciELO - Saúde Pública - Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database scielosp.org
Potential Cardiotoxic Effects of Remdesivir on Cardiovascular System: A Literature Review Corona disease 2019 (COVID-19) pandemic continues to spread around the world with no efficacious treatment. Intravenous remdesivir is the only authorized drug for treatment of COVID-19 disease under an Emergency Use Authorization. Remdesivir is a ... pmc.ncbi.nlm.nih.gov
Hepatic manifestations of COVID-19 and effect of remdesivir on liver function in patients with COVID-19 illness COVID-19 has emerged as a major global health crisis since the first cases were reported in China in December 2019. Remdesivir is the only broad-spectrum antiviral approved by the US Food and Drug Administration to treat hospitalized patients with ... pmc.ncbi.nlm.nih.gov
Saved - July 15, 2025 at 7:17 PM
reSee.it AI Summary
I discussed the controversial use of Remdesivir, a drug initially deemed too dangerous for Ebola trials due to its high mortality rate. Despite this, it became the only drug approved for COVID patients in hospitals, leading to severe organ damage and death. The government incentivized hospitals to use it, ignoring warnings from the WHO. Now, Remdesivir is approved for infants, a rapid approval process that typically takes years. I highlighted the alarming implications of its continued use and the potential risks to vulnerable populations.

@ValerieAnne1970 - Valerie Anne Smith

Remdesivir Was Declared Too Deadly & Too Unethical To Use In African Ebola Trials Because It Had A 53% Kill Rate. Yet, It Was The Only Drug Fauci Allowed To Be Used On COVID Patients In Hospitals. Remdesivir Is Still Used Today & It Is Now Being Used On Infants & Children... The drug is so lethal it got nicknamed ‘Run Death Is Near’ after it started killing thousands of Covid patients in the hospital. Remdesivir (Veklury) kills kidney function, combine that with a ventilator & patients develop pulmonary edema, causing their lungs to fill with fluid & drown to death. Remdesivir kills the liver & causes organ shut down. In the halted Ebola trial, Remdesivir mortality was 53% overall & 85% mortality in those with high viral load. The US Govt BRIBED Hospitals to Administer a Kidney & Liver Toxic Drug with incentives & huge bonuses. Anthony Fauci claimed that Remdesivir would stop Covid even though he knew it would cause 1000s of deaths. Remdesivir (Veklury) never stopped Covid...instead, it stopped kidney function, then it fatally stopped the liver & heart. What the US government never told you about Remdesivir is that by November 2020, even the World Health Organization (WHO) stated, "Do not use Remdesivir." But instead of heading this warning, the NIH & HHS added a 20% bonus on the entire hospital if they administered this liver, kidney & heart-toxic drug. That 20% bonus ended up being a BIG pay day. There has never been a virus that attacks the kidneys...because it wasn't the COVID virus attacking the kidneys...it was the Remdesivir. Remdesivir is still being used in hospitals today...and now Remdesivir (Veklury) is approved for use in infants. Specifically, the Food & Drug Administration (FDA) expanded its approval of remdesivir to include pediatric patients 28 days of age & older. Remdesivir (Veklury) is the ONLY approved treatment for hospitalized or non-hospitalized children that have mild-to-moderate COVID-19 & a positive PCR test. It historically takes 6 to 10 years for a drug approved for adults to receive pediatric labeling. Remdesivir was fast tracked & approved for use in pediatric patients, including neonates, all within 3 years of approval for use in adults & adolescents. 👇African Ebola Drug Trials Using Remdesivir👇 https://www.franciskovacevic.com/remdesivir-2019-ebola-trials 👇Kidney Failure From Remdesivir👇 https://www.scielosp.org/article/csp/2021.v37n10/e00077721/#:~:text=Table%201%20describes%20the%20number%20of%20adverse,of%20renal%20adverse%20events%20among%20patients%20with 👇Heart Failure From Remdesivir👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8511861/ 👇Liver Failure From Remdesivir👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8224190/ Speaker: @DrBryanArdis Podcast: @elisabethicarson

Video Transcript AI Summary
An experimental drug called remdesivir will be responsible for people's deaths. People diagnosed with COVID-19 in the hospital died between day one and day nine, specifically on day nine of a ten-day remdesivir treatment. Dr. Anthony Fauci claimed in May 2020 that remdesivir was found safe and effective in a drug trial in Africa a year earlier (02/2019), and hyperlinked the study in a memo to hospitals. However, in that trial, remdesivir killed 53% of people, and the safety board suspended its use at month six, deeming it too deadly and toxic for Ebola patients. Dr. Anthony Fauci and his department at the NIH funded the Ebola trial in Africa in 02/2019. Therefore, Fauci lied to Congress and the American people by claiming the drug was safe and effective against Ebola, when the safety board had deemed it too deadly and pulled it from the trial.
Full Transcript
Speaker 0: Warned the world that there is an experimental drug called remdesivir that will be responsible for their death. Yeah. I explained the entire way in which everyone with COVID nineteen being diagnosed in the hospital, how they died between day one and day nine. Everybody died that died died on day nine of a ten day treatment with remdesivir. Yeah. They called it an antiviral drug. Doctor Anthony Fauci claimed in May of twenty twenty, it was found safe and effective in a drug trial in Africa a year earlier in 02/2019. And he hyperlinked the study in his memo to all hospitals. I happened to be retired. I opened the link to read the study about this drug I'd never heard of. And imagine my shock that in that trial in Africa, a year before COVID, it killed fifty three percent of all people they gave it to. And the safety board for the trial had suspended the use of remdesivir in that trial at month six and notified the funders that this drug is too deadly and too toxic. We're not using it anymore against Ebola patients. Guess who I discovered in that research study was the funder of that Ebola trial in Africa in 02/2019. Who? Doctor Anthony Fauci and his department at the NIH. Ugh. So he lied to the entire congress, lied to the entire American people, and told you that drug was found safe and effective against Ebola when in fact, the independent safety board deemed it too deadly, too toxic, and it pulled it from the trial. America should be furious.
Remdesivir December 2019 - Ebola Trials — FRANCIS KOVACEVIC franciskovacevic.com
SciELO - Saúde Pública - Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database scielosp.org
Potential Cardiotoxic Effects of Remdesivir on Cardiovascular System: A Literature Review Corona disease 2019 (COVID-19) pandemic continues to spread around the world with no efficacious treatment. Intravenous remdesivir is the only authorized drug for treatment of COVID-19 disease under an Emergency Use Authorization. Remdesivir is a ... pmc.ncbi.nlm.nih.gov
Hepatic manifestations of COVID-19 and effect of remdesivir on liver function in patients with COVID-19 illness COVID-19 has emerged as a major global health crisis since the first cases were reported in China in December 2019. Remdesivir is the only broad-spectrum antiviral approved by the US Food and Drug Administration to treat hospitalized patients with ... pmc.ncbi.nlm.nih.gov
Saved - August 6, 2025 at 8:23 PM
reSee.it AI Summary
The conversation centers on allegations against Zachary Goldberg, CTO of AutoLotto, who is accused of manipulating lottery payouts and having ties to various controversial figures and organizations. The discussion highlights Goldberg's alleged connections to financial misconduct, including interest-free loans to AutoLotto and associations with entities like Thermo Fisher and Temasek. The participants express strong criticism of Goldberg and other individuals involved, linking them to broader conspiracies and unethical practices, particularly regarding COVID-19 and financial dealings.

@DickAlupinya247 - Richard Allupinya

Imagine thinking Americans will just have to “learn to live” with this bullshit going forward, instead of throwing them TF out and killing them if necessary.👇🤣

@DickAlupinya247 - Richard Allupinya

But Israel is going away tho. There’s no scenario where America continues to exist and Americans allow traitorous Jews to help Israel turn America into a vassal and completely subjugate hundreds of millions of Americans. They wrongly assume Israel and Jews are the only ones capable of violence or are willing to use it for self-preservation.

@AFpost - AF Post

Mike Cernovich argued that since Israel “isn’t going away,” Trump supporters should focus on pressuring pro-Israel figures to support their causes more strongly, rather than voting them out of office. Follow: @AFpost

@DickAlupinya247 - Richard Allupinya

*Zachary Goldberg, CTO of AutoLotto* 🚨REMINDER: ZACHARY GOLDBERG, who believes “AMERICA is a WHORE OF A NATION whose people are MADE TO BE RAPED”, designed the http://Lottery.com software to rig lotto payouts and send the massive TAXPAYER-FUNDED WINNINGS to their (JEWS’) desired “winners”… which are often times just their colleagues and merc operatives. *allegedly* 👺VADIM KAMISSAROV CEO of AutoLotto *KAMISSAROV is/was the CEO of the TRIDENT ACQUISITIONS CORP (TDAC) that merged with and acquired AUTOLOTTO INC., making AutoLotto Inc. a wholly-owned subsidiary of TDAC, which was then RENAMED to http://LOTTERY.COM just prior to the completion of the merger. “FOUNDER HOLDERS” of AUTOLOTTO: 👺VADIM KAMISSAROV 👺ILYA PONOMAREV 👺MARAT ROSENBERG (Yes, they are.) *KAMISSAROV was arrested by the FBI and indicted on or about FEBRUARY 20, 2025, on charges of SECURITIES FRAUD, OBSTRUCTION OF JUSTICE, making FALSE/MISLEADING STATEMENTS about the financial health of the company and had *allegedly* conducted roughly $9,000,000-worth of FAKE TRANSACTIONS under an alias (“Vlad”) he often used. *KAMISSAROV even provided INTEREST-FREE LOANS to AUTOLOTTO, using companies HE OWNED and companies who were CORPORATE AFFILIATES of AUTOLOTTO. VIKTORIA GROUP, LLC. (Dec. 2019) *Kamissarov = Owner, President & CFO *Loaned AutoLotto $180,000 to meet working capital requirements. ✅LOAN PAID OFF VK CONSULTING, LLC. (Jan. 2020) *Kamissarov = Owner *Loaned AutoLotto $425,000 to meet working capital requirements. ✅LOAN PAID OFF BGV GROUP, LTD. (Feb. 2020) *Corporate Affiliate of AutoLotto *Loaned AutoLotto $800,000, $1,500,000 and $1,000,000, respectively, totaling $3,400,000. ❌LOAN STILL DUE “CORPORATE AFFILIATE” (Nov. 2020) *Loaned AutoLotto $1,100,000 to meet working capital requirements. VK CONSULTING, LLC. (May 2021) *Loaned AutoLotto $425,000 to meet working capital requirements. VIKTORIA GROUP, LLC. (Aug 30- Sept 9, 2021) *Loaned AutoLotto $492,000 to meet working capital requirements. ⚠️ONLY $112,000 PAID BACK 🚨NOTE: It must be nice as fuck to give yourselves INTEREST-FREE LOANS without legal recourse, but still get to CHARGE 20-30% INTEREST on loans to AMERICAN GOYIM… all while you give yourselves ~95% of U.S. FEDERAL GOVERNMENT GRANTS to fund so many of your “goyim destroying NONPROFITS” and cover costs of your PRIVATE SECURITY DETAIL… also paid for by… AMERICAN GOY TAXPAYERS. (Yes, I hate so much about the things you Jews choose to be. This’ll be your undoing.)

Lottery.com Lottery.com is the internet's top source for official lottery results, numbers, games, jackpots, winners and news. lottery.com
Lottery.com Lottery.com is the internet's top source for official lottery results, numbers, games, jackpots, winners and news. lottery.com

@DickAlupinya247 - Richard Allupinya

But that’s not ALL, sports fans… It appears at first glance that our good buddy, ZACHARY GOLDBERG, has had his hands in some OTHER treasonous JEW FUCKERY. What could I POSSIBLY be referring to, you ask? Welp. A couple things: 1. THIS Zachary S. Goldberg from LOS ANGELES, CA is a business associate of: 👺ALEXEY KOMISSAROUK *IDF, Software Developer *MASTERCLASS, Head of Growth Engineering *OPENDOOR, Growth Experience Manager *HACKER PARADISE, Founder NOTE: Hacker Paradise is affiliated with one other legal entity — DESTINATION PARADISE PTY. LTD. in SINGAPORE. The bio on Destination Paradise Pty. LTD. describes it as a “Singaporean company focused on business events, relationship marketing and executive concierge services.” (Flying, wining & dining business execs.) SINGAPORE, eh? Sounds so familiar.🤔 I’m sure it’s nothing. We’ll forget about those pertinent details that’ll never be important again and just move on to #2. So, what’s #2, you ask? Welp. 2. Did you Notice™️ THIS Zachary S. Goldberg from LOS ANGELES, CA has a “http://MAIL.HOUSE.GOV” EMAIL ADDRESS, which is the OFFICIAL EMAIL DOMAIN for the U.S. HOUSE OF REPRESENTATIVES?! Or that he also has an “http://AUTHENTIC.COM” EMAIL ADDRESS as well? (😳🤯) Yep. Shit’s potentially getting UGLY for our friend, ZACHARY GOLDBERG, who says “AMERICA is a WHORE OF A NATION whose CITIZENS were MADE TO BE RAPED.” (Continued on next post.👇)

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@DickAlupinya247 - Richard Allupinya

Here’s a closer zoom in on those email addresses, as well as his potential connections to TEMASEK and THERMO FISHER. *TEMASEK is WHOLLY-OWNED by the SINGAPORE MINISTRY of FINANCE and is the 9TH-LARGEST STATE INVESTOR. ($173,000,000,000 in total AUM) *ZACHARY GOLDBERG is also the “ASSOCIATE CORPORATE COUNSEL” at THERMO FISHER and is based in RALEIGH, NC (Research Triangle Park/Duke University), according to his LINKEDIN page. However, ZACHARY GOLDBERG is listed elsewhere (Zoom Info) as working for THERMO FISHER up in WALTHAM (BOSTON), MA as well. Hmmm. Who knows. Perhaps ZACHARY GOLDBERG works in BOSTON, MA AND in RALEIGH-DURHAM, NC in RESEARCH TRIANGLE for THERMO FISHER, folks. And why does any of THAT matter, you ask? Welp. 💥TEMASEK is one of the MAJOR SHAREHOLDERS of AUTHENTIC BRANDS GROUP, which was FOUNDED by CHAIRMAN & CEO, JAMIE SALTER. 💥QATAR INVESTMENT AUTHORITY is ANOTHER MAJOR SHAREHOLDER of the AUTHENTIC BRANDS GROUP. (NOTE: I love how RICHARD GOLDBERG of AUTHENTIC BRANDS GROUP in NEW YORK, NY speaks HEBREW too lol. Nbd.) OTHER KEY AUTHENTIC INVESTORS: 💥CVC CAPITAL 💥GENERAL ATLANTIC 💥BROOKFIELD MANAGEMENT 💥LION CAPITAL 💥OAKTREE 💥JASPER RIDGE PARTNERS (“Ridge” PE) 💥GIC (Yes, they’re all OVERWHELMINGLY Jewish.) Is there anything ELSE you need to know about TEMASEK? Yep. In MAY of 2014, TEMASEK, aka, the GOVERNMENT OF SINGAPORE, dumped $634,000,000 into THERMO FISHER and over $400,000,000 into GILEAD SCIENCES… which is the SAME YEAR the DEPARTMENT OF DEFENSE (DOD) began working DIRECTLY with GILEAD SCIENCES on REMDESIVIR testing and USAMRIID. (Continued)

@DickAlupinya247 - Richard Allupinya

Oh, btw… allow me to introduce you all to the LEAD DIRECTOR of THERMO FISHER (SCOTT SPERLING) and the CHAIRMAN of CJP, aka… “BOSTON MOSSAD” (LAURENE SPERLING). Thermo Fisher was kind enough to provide the GLOBAL PLANDEMIC with all the PCR tests one world could ever fucking need. Huge shoutout to TF!!! 🚨PS: Laurene Sperling is also the CHAIRMAN of the BOARD OF TRUSTEES of DUKE UNIVERSITY in RALEIGH-DURHAM, NC, and sits on the ADVISORY BOARD of DUKE KUNSHAN UNIVERSITY in WUHAN, CHINA. Ohhhhh. BOSTON AND RALEIGH-DURHAM. I get it now. THAT makes sense. (Fuck you, Zachary Goldberg.🖕)

@DickAlupinya247 - Richard Allupinya

Oh look, here’s DUKENUS, the PARTNERSHIP UNIVERSITY that DUKE UNIVERSITY has with the NATIONAL UNIVERSITY OF SINGAPORE (NUS). “SYMPOSIUM ON EMERGING INFECTIOUS DISEASES” 👺RALPH BARIC (UNC) - One of Fauci’s most KEY co-conspirators in the coverup of the origins of COVID-19. 👺SUSANNA NAGGIE (Duke University School of Medicine) - The murderous Vice Dean for Clinical and Translational Research at Duke University and Director of Duke CTSI who deliberately SABOTAGED the fucking HERO-HCQ TRIALS and let TENS OF THOUSANDS OF AMERICAN COVID PATIENTS DIE. All so the JEWISH GILEAD SCIENCES/UJA/LOEWS/MOUNT SINAI/APOLLO/MCKINSEY & CO./SOMATUS (MOSSAD) MURDERERS could get their god damned EUA “LICENSE TO KILL”. And so PALANTIR, GINKGO BIOWORKS (BAILLIE GIFFORD) and MODERNA (CIA/NTI/ISRAEL) could fulfill their fucking VACCINES CONTRACTS. Yes, NAGGIE is a fucking JEW, btw. (If it pisses you off that I’m Noticing™️ how all these fucking monsters are JEWS, well… fuck you too, I guess.🖕🤬) “Duke-NUS was one of the first institutions in the world to ISOLATE the SARS-CoV-2 virus…” (Yeah, I bet you fucking were.)

@DickAlupinya247 - Richard Allupinya

*SUSANNA NAGGIE* I hope you never have another peaceful night’s sleep for as long as you live. The same goes for your whole family too, you genocidal cunt. https://t.co/CoF4ZLKxDD

@DickAlupinya247 - Richard Allupinya

I’m gonna make you eat these fucking words one day soon, you vile piece of shit.🫡 https://t.co/YxgDL9upWL

@DickAlupinya247 - Richard Allupinya

*ALEXEY KOMISSAROUK* Hacker Paradise & Destination Paradise Pty LTD https://t.co/cpJtOA6fGH

@DickAlupinya247 - Richard Allupinya

MASSIVE PROPS to Vril, @UnclFuhrious and @CagedLionPhilos for the support on the receipts on the Zachary Goldberg saga!🔥 https://t.co/vJpbYraWHR

@UncleFuhrious - Wolfsschanze

@DickAlupinya247 @virilnews https://t.co/myQSX4ZXH6

@DickAlupinya247 - Richard Allupinya

@CagedLionPhilos Zach Goldberg is the gift that keeps on giving.🤣 https://t.co/CMGZJTEdfS

Saved - October 25, 2025 at 6:35 AM
reSee.it AI Summary
I state that Remdesivir was deemed unethical for Ebola trials in Africa due to a 53% kill rate, and the government selected it as the “drug of choice” for Covid. It’s still prescribed and recently approved for newborns under 28 days and at least 3 lbs. The pediatric trial had 58 hospitalized infants over 10 days. Remdesivir is linked to AKI, various heart issues, and liver toxicity, potentially leading to edema and death; sources include the Veklury package insert and related studies.

@ValerieAnne1970 - Valerie Anne Smith

"Remdesivir Was Too Unethical To Put Into Ebola Clinical Trials In Africa Because It Had A 53% Kill Rate." Dr David Martin, PhD "The Gov't Chose Remdesivir That Kills 53% Of People...As The 'Drug Of Choice' For Covid." Still Prescribed Today & Now Approved For Newborn Infants. Remdesivir, under the brand name Veklury, is still the 1st line treatment in hospitals & outpatient clinics for the treatment of Covid. Previously for ages 12 & up, the CDC & FDA have recently approved Remdesivir for infants less than 28 days old & it is now being marketed as treatment for newborns who weight at least 3 lbs. The pediatric 'safety' clinical trial that brought the updated inclusion of newborns was based on 58 hospitalized infants who were injected with Remdesivir & monitored for only 10 days. Remdesivir (Veklury) Toxicity Across All Age Groups For Multi Organ Failure Of Kidneys, Heart & Liver... Kidneys: Patients treated with Remdesivir (Veklury) suffered 2.81X greater AKI Acute Kidney Injury & subsequent permanent renal damage. Heart: Continuous cardiac monitoring is recommended for those receiving remdesivir because it has been documented to cause... Sinus bradycardia (slow heart rate) T-wave abnormalities Prolonged QT interval Ventricular fibrillation Cardiac arrest Heart block Torsade de pointes, a fatal arrhythmia Liver: On a cellular level, remdesivir has been demonstrated to be toxic to human hepatocytes, causing drug induced permanent liver damage. Combine this damage with being placed on a ventilator & patients quickly develop pulmonary edema, causing their lungs to fill with fluid & drown to death. Loved ones lost their lives while hospitals brought in millions of dollars of profit from government incentive programs & huge payments for each patient, each treatment & each diagnosis. 👇Remdesivir (Veklury) Package Insert👇 https://www.gilead.com/-/media/files/pdfs/medicines/covid-19/veklury/veklury_pi.pdf 👇Remdesivir Causes Kidney Failure👇 https://www.scielosp.org/article/csp/2021.v37n10/e00077721/#:~:text=Table%201%20describes%20the%20number%20of%20adverse,of%20renal%20adverse%20events%20among%20patients%20with 👇Remdesivir Causes Heart Failure👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8511861/ 👇Remdesivir Causes Liver Failure👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8224190/ Speaker: Dr David E Martin, Phd Video: @foreversovereign

Video Transcript AI Summary
Speaker 0: Remember that in 02/2018, remdesivir, one of my favorite targets, remdesivir was too unethical to put into Ebola clinical trials in Africa because it had a fifty three percent kill rate published in medical journals. Ebola doesn't have a fifty three percent kill rate, but it was chosen in April and May 2020 to be the drug of choice to treat COVID. This drug was too unethical to use in an African clinical trial because it was killing fifty three percent of the people that it was given to. And we had Anthony Fauci, Deborah Burke sitting next to the president going, we need to use remdesivir despite the fact that the World Health Organization said it was unethical to use it. Here's the problem. The problem is as long as the financial interest that dictates what product is going to be promoted is the one making the declaration of the pandemic, We have no possibility for accountability. We have no possibility for justice. And what we do is we allow people who were formed out of the Eugenics office, Carnegie Mellon in 1913, that same group of people that were the same group of people that established the World Health Organization in 1953, that same group of people are the ones who are making this decision. And I don't know how you feel about Eugenics, but I have a problem with it.
Full Transcript
Speaker 0: Remember that in 02/2018, remdesivir, one of my favorite targets, remdesivir was too unethical to put into Ebola clinical trials in Africa because it had a fifty three percent kill rate published in medical journals. Ebola doesn't have a fifty three percent kill rate, but it was chosen in April and May 2020 to be the drug of choice to treat COVID. This drug was too unethical to use in an African clinical trial because it was killing fifty three percent of the people that it was given to. And we had Anthony Fauci, Deborah Burke sitting next to the president going, we need to use remdesivir despite the fact that the World Health Organization said it was unethical to use it. Here's the problem. The problem is as long as the financial interest that dictates what product is going to be promoted is the one making the declaration of the pandemic, We have no possibility for accountability. We have no possibility for justice. And what we do is we allow people who were formed out of the Eugenics office, Carnegie Mellon in 1913, that same group of people that were the same group of people that established the World Health Organization in 1953, that same group of people are the ones who are making this decision. And I don't know how you feel about Eugenics, but I have a problem with it.
SciELO - Saúde Pública - Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database scielosp.org
Potential Cardiotoxic Effects of Remdesivir on Cardiovascular System: A Literature Review Corona disease 2019 (COVID-19) pandemic continues to spread around the world with no efficacious treatment. Intravenous remdesivir is the only authorized drug for treatment of COVID-19 disease under an Emergency Use Authorization. Remdesivir is a ... pmc.ncbi.nlm.nih.gov
Hepatic manifestations of COVID-19 and effect of remdesivir on liver function in patients with COVID-19 illness COVID-19 has emerged as a major global health crisis since the first cases were reported in China in December 2019. Remdesivir is the only broad-spectrum antiviral approved by the US Food and Drug Administration to treat hospitalized patients with ... pmc.ncbi.nlm.nih.gov
Saved - December 11, 2025 at 9:24 PM
reSee.it AI Summary
I report that in the halted Ebola trial, Remdesivir had 53% overall mortality and 85% with high viral load; the DSMB stopped the study. Fauci allegedly pushed Remdesivir as COVID treatment, leading to FDA approval from insiders. The drug is claimed to cause multi-organ failure—kidney injury, liver toxicity, and cardiac issues—raising costs as hospitals profit from testing, admissions, Remdesivir use, and ventilation.

@ValerieAnne1970 - Valerie Anne Smith

"There Were 4 Drugs That Were Being Tested For Ebola...Remdesivir Killed More People Than Placebo" Dr Paul Marik, MD "The Data Safety Monitoring Board Actually Stopped The Study" "53% Of The Patients Died In The Failed Ebola Trial" Remdesivir Was Fauci's 'Covid Drug Of Choice' In the halted Ebola trial, Remdesivir mortality was 53% overall & 85% mortality in those with high viral load. Fauci took the failed Ebola drug, Remdesivir (Veklury), & made it the mandatory treatment as an unelected bureaucrat to be used at every hospital for the treatment of COVID in the United States. Not only does the drug not cure COVID it kills people by causing multi organ failure, yet the FDA approved the drug based on expert opinions from Big Pharma industry insiders who used to work at the CDC & FDA. Remdesivir (Veklury) continues to be used in hospitals today as 1st line treatment across ALL age groups. Recently FDA & CDC approved to be used for the treatment in neonate newborns, less than 28 days old, weighing at least 3 lbs. All of the doctors, nurses & hospitals know at this point...Nurses even coined Remdesivir's nickname 'Run...Death...Is...Near.' Hospital administration continues on. Their bosses make more money when patients with organ failure hit the ICU. It is well known that Remdesivir does not work for COVID or any other illness & is in fact a death sentence to the majority of the people it's given to. Remdesivir Causes Multi Organ Failure By Harming The Kidneys, Liver & Heart... Kidney Damage...Those treated with Remdesivir (Veklury) suffered 2.8X times greater Acute Kidney Injury (AKI) & subsequent permanent renal damage. Liver Damage...Remdesivir, on a cellular level, has been demonstrated to be toxic to human hepatocytes, causing drug induced permanent liver damage. Heart Damage...Continuous cardiac monitoring is recommended for those receiving remdesivir because of documented cases of Cardiac arrest, Heart block, Torsade de pointes (fatal arrhythmia), Sinus bradycardia (slow heart rate), T-wave abnormalities, Prolonged QT interval, Ventricular fibrillation Hospitals murdered COVID patients. The more they kill, the more money they make. When the hospitals test for COVID, they get paid more. When they admit patients for COVID, they get paid more. When they put people on Remdesivir, they get paid more. And when they put loved ones on a ventilator, they get paid more. 👇2019 Ebola Drug Trial Research Documents👇 https://www.franciskovacevic.com/remdesivir-2019-ebola-trials 👇Remdesivir (Veklury) Package Insert👇 https://www.gilead.com/-/media/files/pdfs/medicines/covid-19/veklury/veklury_pi.pdf 👇Remdesivir Causes Kidney Failure👇 https://www.scielosp.org/article/csp/2021.v37n10/e00077721/#:~:text=Table%201%20describes%20the%20number%20of%20adverse,of%20renal%20adverse%20events%20among%20patients%20with 👇Remdesivir Causes Heart Failure👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC8511861/ Video: Vaxxed 3: Authorized To Kill Documentary Credit: @ChildrensHD

Video Transcript AI Summary
Speaker 0: There were four drugs that were being tested for Ebola. Remdesivir killed more people than placebo, and the data safety monitoring board had actually stopped the study where literally fifty three percent of Speaker 1: the patients died in the failed Ebola trial and was repurposed. It was a failed Ebola drug because it caused more harm than good in Ebola trials. It was still unpatent. It was Tony Fauci's drug of choice. The majority of hospital deaths were actually caused by Anthony Fauci because his NIH put out protocols that if the hospital systems adhered to, they got bonuses, big bonuses, lots of money, $3,000 per for putting an IV in of remdesivir. Boom. $3,000. But guess what? On top of the entire hospital stay, a 20% bonus, that could be hundreds of thousands of dollars. Speaker 0: The data was so overwhelming that remdesivir killed patients more so than placebo. The drug had to be stopped, and this was published in the New England Journal in the 2019. Speaker 2: What happened during COVID could not have happened without propaganda and censorship. And how do we overcome that propaganda and censorship? It's primarily through people not being willing to shut up.
Full Transcript
Speaker 0: There were four drugs that were being tested for Ebola. Remdesivir killed more people than placebo, and the data safety monitoring board had actually stopped the study where literally fifty three percent of Speaker 1: the patients died in the failed Ebola trial and was repurposed. It was a failed Ebola drug because it caused more harm than good in Ebola trials. It was still unpatent. It was Tony Fauci's drug of choice. The majority of hospital deaths were actually caused by Anthony Fauci because his NIH put out protocols that if the hospital systems adhered to, they got bonuses, big bonuses, lots of money, $3,000 per for putting an IV in of remdesivir. Boom. $3,000. But guess what? On top of the entire hospital stay, a 20% bonus, that could be hundreds of thousands of dollars. Speaker 0: The data was so overwhelming that remdesivir killed patients more so than placebo. The drug had to be stopped, and this was published in the New England Journal in the 2019. Speaker 2: What happened during COVID could not have happened without propaganda and censorship. And how do we overcome that propaganda and censorship? It's primarily through people not being willing to shut up.
Remdesivir December 2019 - Ebola Trials — FRANCIS KOVACEVIC franciskovacevic.com
SciELO - Saúde Pública - Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database Potential kidney damage associated with the use of remdesivir for COVID-19: analysis of a pharmacovigilance database scielosp.org
Potential Cardiotoxic Effects of Remdesivir on Cardiovascular System: A Literature Review Corona disease 2019 (COVID-19) pandemic continues to spread around the world with no efficacious treatment. Intravenous remdesivir is the only authorized drug for treatment of COVID-19 disease under an Emergency Use Authorization. Remdesivir is a ... pmc.ncbi.nlm.nih.gov
Saved - June 13, 2026 at 8:53 PM
reSee.it AI Summary
I’m calling this TREASON: a Pentagon admission says the US and China created Covid, engineers allegedly knew masks don’t work, and mRNA vaccines are basically poison—crimes that I say justify an overthrow of the United States Government.

@Jason_Jorjani - Jason Reza Jorjani

Pentagon admission that the US created Covid TOGETHER WITH CHINA, that the virus engineers knew masks don't work, and that the mRNA vaccines are basically poison. This is TREASON and one of many crimes that justify and necessitate an overthrow of the United States Government. https://t.co/8pGTwjUzzl

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