reSee.it - Related Post Feed

@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…

@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.

@GalG____ - Gal.G, Adv 🇮🇱

מאמר מדעי חדש טוען להוכחת קשר בין התרופה של מרק מולנופיראביר לבין יצירת מוטציות גנטיות (וריאנטים) בנגיף הקוביד (ר׳ ציוץ משותף כאן למטה), עכשיו זה כבר לא חשש אלא מציאות. הטענה הזו מסתבר לא חדשה והועלתה לראשונה ע״י האימונולוג וה- whistleblower ריק ברייט, אשר הוסר באפריל 2020 מתפקידו כראש BARDA (הרשות למחקר ופיתוח ביורפואי מתקדם - שהיתה אחראית על העברת סבסוד ציבורי לפיתוח אמצעי הגנה מפני טרור ביולוגי ומגפות). במאי הוא החל לתת את עדותו. https://science.org/content/article/emails-offer-look-whistleblower-charges-cronyism-behind-potential-covid-19-drug ברייט טען שהוא פוטר כי סירב לדרישות הממשל הפדרלי (של טראמפ) להאיץ סבסוד לחברת התרופות שיצרה את מולנופיראביר בין היתר בטענה שהמוצר הזה מסוכן, לא עבר ניסוי קליני בבני אדם, והמחקר בבעלי חיים הביא לתוצאות קשות מאד של פגמים בצאצאים. עוד הוא הצביע על הסכנה בתרופה הזו בהיותה ״מוטגנת״ מדי - דהיינו החשש שתיצור מוטציות חדשות לנגיף עצמו בשל אופי פעולתה הביולוגי - מולנופיראוויר היא קדם-תרופה, המיועדת ליצור טעויות בקוד הגנטי של וירוס SARS-CoV-2, ובכך למנוע את המשך שכפולו. הטעויות בקוד הגנטי של הוירוס יוצרות גם מוטציות מסתבר - והמחקר שפורסם היום (ר׳ לעיל) מבקש להוכיח זאת. מולנופיראוויר פועלת באופן דומה לתקופה לקוביד של פייזר - פקסלוביד, ושתיהן היו אמורות להיות הבשורה שתחליף את רמדסביר של גיליאד. זה גאוני באופן מרושע ממש לייצר מוצר (מוצר 1- תרופה מוטגנית) שמגביר ומאריך משך ״מגפה״ לנגיף שיכל כנראה להיעלם מעצמו תוך זמן קצר, רק כדי להציג מוצר שקוצר את רווחי המגפה ויוצר תלות ממושכת בו + סולל דרך לעולם ביוטכנולוגי חדש של מוצרים רבים נוספים שנחסמו אתית (מוצר 2- ״חיסון״ mRNA) ואז גם להשלים באמצעות מוצרים לתופעות הלוואי החמורות והמוכחשות של מוצר 2 (מוצר 3- טיפולים בכרישיות, בלב, בסרטן ועוד נרכשו ע״י פייזר, מודרנה ותאגידי הפארם הגדולים מראשית פרוייקט ה״חיסונים״) האם הגילויים שעלו מהתלונות של ברייט על התערבות פקידי ממשל וגורמים ב- HHS לקדם תרופה מסוכנת על פניו חסמו אותה? החברה הקטנה שפיתחה את מולנופיראוויר נרכשה לבסוף ע״י חברת מרק בנובמבר 2021 אושרה לשימוש בבריטניה בדצמבר 2021 - קיבלה אישור EUA מה- FDA בינואר 2022 - אישור חירום ממשרד הבריאות הישראלי אישור ה- FDA ניתן תחת סייגים וחששות רבים. מצד אחד הפיתוי היה שהתרופה יכולה להלקח גם בכדור בבית ולכן תפחית אשפוזים ועומס במערכת הבריאות (לפי טענת היצרן) מצד שני חששות לפגמים קשים בעוברים ויצירת מוטציות שיאריכו את משך ״המגפה״ הרתיעו את חברי הועדה שבסוף הצביעו בעד אישור 13 ל-11. הממליצים הציעו שהתרופה תנתן בעיקר ללא מחוסנים שהם ״בעלי סיכון האשפוז החמור ביותר״ https://cnbc.com/2021/11/30/fda-advisory-panel-narrowly-endorses-mercks-oral-covid-treatment-pill-despite-reduced-efficacy.html בלתי נתפס אבל - בישראל פורסם כי משרד הבריאות אישר את 2 התרופות האלו ואף רכש מלאים שלהן בינואר 2022. https://haaretz.co.il/health/corona/2022-01-02/ty-article/.premium/0000017f-f56d-d318-afff-f76fad9f0000 ״מולנופירביר מיועדת לבני 18 ומעלה שסובלים מתסמיני קורונה קלים עד בינוניים, בעלי גורם סיכון אחד לפחות לאשפוז או לתמותה ושחלופות טיפוליות אחרות אינן מתאימות להם.״ הכתבה הנ״ל מפרטת בקצרה בסופה חששות מסויימים שעלו בדיון ב- FDA אך לא מדגישה את הסיכון הקיצוני שהיא עלולה לגרום למטופליה (מומים וכו) וחמור מכך לחברה שסביבם באמצעות יצירת מוטציות לנגיף.

@theosanderson - Theo Sanderson

📄 📄 Our molnupiravir work is now out after peer-review! We definitively demonstrate that molnupiravir has resulted in viable SARS-CoV-2 viruses with significant numbers of mutations, in some cases with onwards transmission of mutated viruses. https://www.nature.com/articles/s41586-023-06649-6

A molnupiravir-associated mutational signature in global SARS-CoV-2 genomes - Nature Molnupiravir, an antiviral medication that has been widely used against SARS-CoV-2, acts by inducing mutations in the virus genome during replication. Most random mutations are likely to be deleterious to the virus, and many will be lethal, and so molnupiravir-induced elevated mutation rates reduce viral load1,2. However, if some patients treated with molnupiravir do not fully clear SARS-CoV-2 infections, there could be the potential for onward transmission of molnupiravir-mutated viruses. Here we show that SARS-CoV-2 sequencing databases contain extensive evidence of molnupiravir mutagenesis. Using a systematic approach, we find that a specific class of long phylogenetic branches, distinguished by a high proportion of G-to-A and C-to-T mutations, appear almost exclusively in sequences from 2022, after the introduction of molnupiravir treatment, and in countries and age-groups with widespread usage of the drug. We identify a mutational spectrum, with preferred nucleotide contexts, from viruses in patients known to have been treated with molnupiravir and show that its signature matches that seen in these long branches, in some cases with onwards transmission of molnupiravir-derived lineages. Finally, we analyse treatment records to confirm a direct association between these high G-to-A branches and the use of molnupiravir. nature.com

@dezzie_rezzie - Destiny Rezendes

Data Dump No. 2 * I was so pleased that everyone loved the last data-dump that I've decided to make this a bi-monthly post. This set, like the prior & all future data dumps will be broad spectrum topics of high interest Thank you & Enjoy* --------------------------------------------------------- From Defense Daily on 5/11/2010 titled "BioWatch Program Expects to Begin Gen-3 Testing Shortly." - Discussing one of the longest running disease surveillance apparatuses in the US. Ran by DHS's CWMD & contracting the 3rd & current system called BioWatch Gen-3 to DHS's Office of health affairs. - "two companies developing a new generation of biological detectors, the Department of Homeland Security (DHS) expects to take initial deliveries of the assay technology within the next few weeks" Link: https://defensedaily.com/biowatch-program-expects-to-begin-gen-3-testing-shortly-2/homeland-security/ - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Biodefense: DHS Exploring New Methods to Replace BioWatch and Could Benefit from Additional Guidance [May 20 2021] All about the new platform to add to BioWatch at DHS called the Biological Detection for the 21st Century (BD210) and relays BioWatch's purpose which is to "detection of an aerosolized attack involving a biological agent" Link: https://gao.gov/products/gao-21-292 - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Documents released by the CIA in in 1996 despite being scheduled for release in 1994 which were classified since it was written in 1972 titled; "Intelligence Implications of Disease." The report shows you that the disease surveillance apparatuses are born within the US Intelligence Community starting with Project IMPACT then Project Blackflag. It states: "Project IMPACT went global in the summer of 1968 when a new strain of influenza rolled out of China and within a short period of time affected one out of every four persons in the world.... At this time a unique opportunity was available to review statistical data on influenza (a program to computerize disease information to derive trends, cycles & predictions had already been initiated under a CIA Project called BLACKFLAG);the current epidemic in Hong Kong was causing the highest incidence since the first Asian Type A2 epidemic of 1957" LINK: https://cia.gov/readingroom/docs/intelligence_im.pdf -------------------------------------------------------- Pre-draft proposal for a European Partnership under Horizon Europe One Health Antimicrobial Resistance- 9 February 2022 States that the reports objective is: "Contribute to achieving the objectives of the European One Health Action Plan" & "Connect, merge and align dissemination of outputs with other initiatives to support evidence-based policy in whole One Health domain." *The OneHealth Initiative is a Bill Gates + EcoHealth Alliance+ Global Virome Project globalist agenda LINK: https://research-and-innovation.ec.europa.eu/system/files/2022-02/ec_rtd_he-partnerships-onehealth-amr.pdf -------------------------------------------------------- This one is a mind-blowing database called VaxPal by the Medicines Patent Pool [MPP] that provides the patent status for COVID-19 vaccines worldwide! Here you can search and export the data of all C19 patents, the product name, vaccine type, manufacturer and patent descriptions. LINK: https://vaxpal.org/?originator%5B%5D=Pfizer&page=2… ------------------------------------------------------- The full lawsuit in PDF downloadable file of Moderna v. Pfizer that was filed 12/05/2022 at the US district court for Massachusetts. This lawsuit's premise is based on the allegations that Pfizer had copied/stolen the Covid-19 mRNA vaccine technology from Moderna. The lawsuit drags dirt on both companies and the history of these particular vaccines. Pfizer in the document states: "Moderna’s effort to write other scientists out of the history books is particularly egregious with respect to Drs. Katalin Karikó & Drew Weissman of the University of Pennsylvania. Drs. Karikó & Weissman made foundational discoveries that overcame critical problems plaguing the use of mRNA in drugs before Moderna was even founded. Exs. 1, 22; see also Ex. 26. In particular, Drs. Karikó and Weissman discovered that by replacing a particular component of mRNA—the nucleoside “uracil”—with naturally occurring uracil variants including “pseudouridine” and “1-methyl-pseudouridine”), and by using particular techniques to purify mRNA" & "Pfizer and BioNTech’s vaccine and Moderna’s vaccine use different lipid nanoparticles- Even the lipid nanoparticles in Moderna’s own vaccine rely on third-party technology. Dr. Robert Langer, an MIT professor, Moderna board member, and founder of numerous biotech companies, purportedly told Moderna’s CEO, Stéphane Bancel, “that Moderna was too underfunded and small to create its own delivery system.” Ex. 14 at 3–4" Furthermore, Pfizer claims that Moderna isn't a genuine pharmaceutical company and essentially claims that they are total frauds calling into question the claims made by Moderna that "Moderna is developing medicines that could treat and prevent a wide range of diseases... like influenza, HIV, autoimmune, cardiovascular diseases & rare forms of cancer" Leaving Moderna to have to admit this statement made in the case: "Defendants admit that publicly available sources suggest Moderna had no commercial products in 2011-2016." LINK: https://blog.petrieflom.law.harvard.edu/wp-content/uploads/2023/01/Pfizer-reply-moderna.pdf ------------------------------------------------- Licensing Agreement for COVID-19 Oral Antiviral Treatment Candidate to Expand Access in Low- and Middle-Income Countries November 16, 2021 This document shows the collaboration between Pfizer, GSK, and the Medicine Patent Pool [MPP] for the announcement of: "the signing of a voluntary license agreement for Pfizer’s COVID-19 oral antiviral treatment candidate PF-07321332, which is administered in combination with low dose ritonavir (PF-07321332; ritonavir). The agreement will enable MPP to facilitate additional production and distribution of the investigational antiviral, pending regulatory authorization or approval, by granting sub-licenses to qualified generic medicine manufacturers, with the goal of facilitating greater access to the global population LINK: https://pfizer.com/print/pdf/node/544186 ----------------------------------------------------- Press release from the UK government in 2022 declaring a 10-year-partnership with Moderna in major boost for vaccines and research. The article states: "Moderna to invest in mRNA research and development (R&D) in the UK, and build a state-of-the-art vaccine manufacturing centre with the ability to produce up to 250 million vaccines a year." through the Department of Health & Social Care LINK: https://gov.uk/government/news/uk-cements-10-year-partnership-with-moderna-in-major-boost-for-vaccines-and-research --------------------------------------------- Air Force Research Laboratory Report published in September 2020 [compiled 2018-2019] titled: Operations Security for Emerging Biotechnology Applications "We sought to establish a balanced multidimensional systems analysis process that could be applied by both military and civilian institutions involved in biomedical data procurement, storage, and use. First, we conducted a comprehensive analysis of current legislative requirements for biomedical data security, real-world biomedical research workflows, and likelihood of novel attacks against biomedical data. " It further goes into the implementation of the BioOPSEC framework which is adapted from the military OPSEC LINK: https://apps.dtic.mil/sti/pdfs/AD1121263.pdf ----------------------------------------------------- The pdf file for a eerily predictive book by Mark Honigsbaum called "The Pandemic Century: One hundred years of panic hysteria and hubris." First published in the United Kingdom in 2019, the book descriptions reads as follows; "Although the book was written before the COVID-19 pandemic, Honigsbaum includes a new chapter on this ongoing global health crisis, providing insights into its origins, spread, and societal impacts" LINK: https://openaccess.city.ac.uk/id/eprint/23272/1/The%20Pandemic%20Century-ver3.pdf… ------------------------------------------------- 2022 USMC article titled: Operation Warp Speed and the Countermeasures Acceleration Group—A Twenty-first Century Manhattan Project by John E. Hall SES; Lieutenant Colonel Nate Packard; and the Countermeasures Acceleration Group (CAG) Team. "On 15 May 2020, Operation Warp Speed, later renamed the HHS-DOD COVID-19 Countermeasures Acceleration Group (CAG), was a collaboration between the Department of Health and Human Services, the Department of Defense (DOD), and the private sector to accelerate development, production, and distribution of effective vaccines and therapeutics to counter COVID-19 for the American people." LINK: https://usmcu.edu/Outreach/Marine-Corps-University-Press/MCU-Journal/JAMS-vol-13-no-1/Operation-Warp-Speed/ ----------------------------------------------------- 1992 study submitted before the National Academy of Sciences of the USA titled: Magnetite bio-mineralization in the human brain. The report details the detection of ferromagnetic materials (Fe204) that is precipitated biochemically by bacteria usually in animals but in this report claims is found in the human brain. The study further looks into this phenomena and the potential capabilities. The report states: " Using an ultrasensitive superconducting magnetometer in a clean-lab environment, we have detected the presence of ferromagnetic material in a variety of tissues from the human brain....Biogenic magnetite in the human brain may account for high-field saturation effects...and, perhaps, for a variety of biological effects of low-frequency magnetic fields." LINK: https://europepmc.org/article/PMC/49775 ----------------------------------------------------- The press release from 2013 about a pandemic partnership between JP Morgan Chase and the Bill & Melinda Gates Foundation announcing set their efforts to set up a Big Pharma-backed investment fund. This effort is what we now know to be the Global Health Investment Fund (GHIF). The article reads: "GlaxoSmithKline ($GSK), Merck ($MRK) and Pfizer's foundation are among the investors in the fund, which will back late-stage development of technologies to fight disease in low-income countries. Having raised $94 million from its initial backers, the GHIF will now start trying to give vaccines and other technologies the financial clout to navigate Phase III trials." & ""We found a remarkable pipeline of global health innovations--with as many as 200 new products currently under development through philanthropic, governmental and pharmaceutical industry resources--but lacking capital sufficient to bring them to market," JPMorgan Chase's head of corporate responsibility Peter Scher told ONE, an advocacy organization." *Note ONE is a OneHealth parent entity. Also this later is joined by the GHIC Global Health Investment Corporation. LINK: https://fiercepharma.com/deals/gsk-merck-and-pfizer-join-jp-morgan-vaccine-investment-fund ------------------------------------------------------- Forbes magazine article form October 20 2020 with the alarmist title: Researchers Warn Some Covid-19 Vaccines Could Increase Risk Of HIV Infection The article begins with saying: "Some of the Covid-19 vaccines currently in development could increase the risk of acquiring HIV, warned a group of researchers in the The Lancet medical journal Monday, potentially leading to an increase in infections as vaccines are rolled out to vulnerable populations around the world." LINK: https://forbes.com/sites/roberthart/2020/10/20/researchers-warn-some-covid-19-vaccines-could-increase-risk-of-hiv-infection/?sh=27b590ed3740… ------------------------------------------------ Another conveniently timed report this one from ASPR [Assistant Secretary for Preparedness and Response] titled; National Health Security Strategy 2019-2022 The report was written in 2019 to "enhance the security of the nation's health in times of crisis" LINK: https://medicalcountermeasures.gov/media/37041/2019_ns.pdf -------------------------------------------------------- The sudden death coroner's report for the post vaccine death of a young Air Force Academy member, Hunter Brown, who was only 21years old. Brown collapsed and was unable to revive in January of 2023. The report is clear as to the cause, an enlarged heart & pulmonary thromboembolism of bilateral lungs. LINK: https://s3.documentcloud.org/documents/23599774/23-00032-ar-accident-1.pdf ------------------------------------------------- That's all for now. I could make a thousand of these and still have more to share! Hope you find something worthwhile in this. Don't forget, you ARE smart enough to make judgements for yourself, your health, and everything else. Read-Learn-Share. Thank you-Destiny

@Inversionism - Inversionism

This is how we know that there was malice and forethought during the COVID pandemic. The US government bought up nearly the ENTIRE world supply of remdesivir in mid 2020. Nearly all of it, which is so insane considering what we know now with it's kidney nuking capacity and complete lack of efficacy. Then they took extreme actions towards doctors who were trying cheaper and safer alternative treatments by going as far as removing their license and ability to practice medicine. They even banned doctors from using vitamin C of all things... They only wanted people to use the severely toxic remdesivir because it was a cash cow for pharma at nearly $2000 per course of treatment, in addition to it being great at ensuring COVID mortality was exacerbated to pad the numbers and keep up the narrative of how deadly it was to further sell the vaccine. Idk how anyone can look back on the sequence of actions taken by the government and pharma from early 2020 until now with the continual shilling of boosters, and not see gross levels of malice with forethought. Beginning to end, it was completely anti-human, anti-health, anti-science, and absurdly pro-pharma in every way imaginable. They made billions off the willful harm and death of so many people.

@iluminatibot - illuminatibot

This is how we know that there was malice and forethought during the COVID pandemic. The US government bought up nearly the ENTIRE world supply of remdesivir in mid 2020. Nearly all of it, which is so insane considering what we know now with it's kidney nuking capacity and complete lack of efficacy. Then they took extreme actions towards doctors who were trying cheaper and safer alternative treatments by going as far as removing their license and ability to practice medicine. They even banned doctors from using vitamin C of all things... They only wanted people to use the severely toxic remdesivir because it was a cash cow for pharma at nearly $2000 per course of treatment, in addition to it being great at ensuring COVID mortality was exacerbated to pad the numbers and keep up the narrative of how deadly it was to further sell the vaccine. I don't know how anyone can look back on the sequence of actions taken by the government and pharma from early 2020 until now with the continual shilling of boosters, and not see gross levels of malice with forethought.

@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://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

@Amy31129057 - QuestionIt

Good Grief, Pay Attention~ Anti-viral drug backfires: COVID drug linked to viral mutations that spread. Merck's small-molecule molnupiravir linked to mutated viruses that spread in people. (September 26, 2023) According to a new peer-reviewed study in the journal Nature, the anti-viral drug dubbed molnupiravir is linked to specific SARS-CoV-2 mutation signatures that happened to spring up in 2022 when the drug was introduced. The study's authors—led by researchers at the Francis Crick Institute in London and the University of Cambridge—scanned through more than 15 million SARS-CoV-2 genome sequences found in global databases. They picked out unique mutation signatures that closely linked to signatures seen in viruses from patients known to have been treated with molnupiravir. These suspected molnupiravir-linked mutation signatures also matched those seen in viruses examined in a clinical trial of molnupiravir. https://arstechnica.com/health/2023/09/covid-anti-viral-drug-is-actively-helping-sars-cov-2-mutate-and-evolve/

Anti-viral drug backfires: COVID drug linked to viral mutations that spread Merck's small-molecule molnupiravir linked to mutated viruses that spread in people. arstechnica.com

@Amy31129057 - QuestionIt

Question IT! https://x.com/Amy31129057/status/1735456355300045068?s=20

@Amy31129057 - QuestionIt

Please look into this more @RandPaul @RepThomasMassie @SenRonJohnson @Leeshotfury1966 @I_Am_JohnCullen @LmBubba Drug launched at Emory reduces virus that causes COVID-19 to undetectable levels (March 17, 2021) Ridgeback Biotherapeutics~ Ridgeback Biotherapeutics is a Miami-based biotechnology company, primarily known for its involvement in developing a successful COVID-19 medication. Ridgeback is privately owned by hedge fund manager and physician, Wayne Holman (formerly of S.A.C. Capital Advisors) and his wife Wendy Holman. Wendy is the CEO at the company, which refers to itself as a majority woman owned business. In early 2020, Ridgeback purchased an exclusive license for the commercial development of Molnupiravir from Emory University, where the drug was initially developed with $16 million in grants from Federal agencies including the National Institutes of Health. The terms of the deal were undisclosed. Molnupiravir was initially researched as a treatment for influenza, but may have broad spectrum activity against other viruses. Ridgeback was mentioned in a whistleblower complaint from Rick Bright, former director of the Biomedical Advanced Research and Development Authority (BARDA). The complaint alleged that Ridgeback lobbied the government for millions in funding to help develop Molnupiravir. Merck & Co. partnered with Ridgeback to perform clinical trials with Molnupiravir in humans to treat COVID-19. An antiviral drug initially discovered by Emory’s non-profit drug development company DRIVE appears safe and reduces SARS-CoV-2 to undetectable levels in COVID-19 patients after five days of administration, according to data from a Phase II clinical trial in the United States. Molnupiravir, previously known as EIDD-2801, can be provided as a pill in an outpatient setting, which could be a step up in ease of distribution and convenience. Although remdesivir and antiviral monoclonal antibodies have received Emergency Use Authorizations from the FDA, they must be given intravenously or by injection. In addition, drugs like molnupiravir could flexibly tackle SARS-CoV-2 variants, which have emerged as a concern in recent months. "There's still an urgent need for an antiviral drug against SARS-CoV-2 that can be easily produced, transported, stored, and administered," says George Painter, PhD, CEO of DRIVE (Drug Innovation Ventures at Emory) and director of the Emory Institute for Drug Development. When the COVID-19 pandemic began, DRIVE quickly repurposed a broad-spectrum antiviral drug it had been developing against influenza and equine encephalitis. Molnupiravir is being developed further by Merck and its partner Ridgeback Biotherapeutics, a closely held biotechnology company, which licensed the drug from DRIVE last year. All funds for the post-licensing development of EIDD-2801/molnupiravir have been provided by Ridgeback and Merck. In the most recent clinical study, molnupiravir eliminated infectious coronavirus from nose swabs within five days in all of the people taking it. For comparison, a quarter of people receiving placebo still had detectable virus in their nose swabs at day five. Emory physicians were not involved in the clinical trial, which recruited 202 adults with COVID-19 symptoms at outpatient clinics in the United States. The data were presented at the recent Conference on Retroviruses and Opportunistic Infections (CROI). While molnupiravir is proven to interfere with coronavirus replication in infected patients, more data is required to determine whether it can prevent severe illness. Merck and Ridgeback say that more results from the U.S. clinical trial will be shared when they become available, and additional Phase 2 and 2/3 clinical studies are underway. Molnupiravir has also been tested for safety in a clinical trial in the United Kingdom. Molnupiravir works by forcing the viral enzyme that copies SARS-CoV-2’s genetic material to make so many mistakes that the virus can’t replicate. Still, Merck’s comprehensive testing indicates that high doses of the drug are not mutagenic in animals. Emory scientists, in collaboration with top coronavirus experts at other universities, have previously shown that EIDD-2801 is highly effective at interfering with coronavirus replication and transmission in animal models and also in mice implanted with human lung tissue. EIDD-2801 has broad spectrum activity against a number of diseases of public health concern, including influenza, SARS-CoV-1, MERS, chikungunya, Ebola and equine encephalitis. The drug was initially developed with the support of the National Institute of Allergy and Infectious Diseases, the Defense Threat Reduction Agency, and the Georgia Research Alliance's Venture Development program. https://news.emory.edu/stories/2021/03/coronavirus_DRIVE_molnupiravir/index.html https://en.wikipedia.org/wiki/Ridgeback_Biotherapeutics https://www.science.org/content/article/emails-offer-look-whistleblower-charges-cronyism-behind-potential-covid-19-drug https://en.wikipedia.org/wiki/Molnupiravir

Drug launched at Emory reduces virus that causes COVID-19 to undetectable levels | Emory University | Atlanta GA An antiviral drug initially discovered by Emory’s non-profit drug development company DRIVE appears safe and reduces SARS-CoV-2 to undetectable levels in COVID-19 patients after five days of administration, according to data from a Phase II clinical trial. news.emory.edu

Ridgeback biotherapeutics - Wikipedia en.wikipedia.org

Molnupiravir - Wikipedia en.wikipedia.org

@Kevin_McKernan - Kevin McKernan

This is what these Pharma pimps do. Now consider everything you’ve ever been told about generic natural drugs like cannabinoids. It’s all a ruse.

@CovidAnalysis - Covid Analysis

PRINCIPLE trial: significantly improved recovery and significantly lower risk of long COVID with ivermectin, even with very late treatment and poor administration. This is despite being the most clearly designed to fail study (compare the treatment delay, population, treatment regimen, and administration with the same group’s molnupiravir trial), and despite the team taking 19 months to get the data “fully cleaned”. The p-values for ivermectin improving sustained recovery, early sustained recovery, alleviation of all symptoms, and sustained alleviation are < 0.0001. Patients in the ivermectin group had significantly better health one year later. The p-value for lower moderate/major symptoms with ivermectin at 12 months is < 0.0000001 (individual symptom results combined). The spin in the paper is incredible. (Compare also with the spin in the group’s recent paper showing increased mutagenesis and viral persistence with molnupiravir, where they recommend longer treatment).

@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

@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 🤔🤔

@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

@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.

@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)

@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”.

@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

@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

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.🤬

@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

@DecentBackup - BackupDecentFiJC

Incorrect. China has been giving its COVID patients HYDROXYCHLOROQUINE and CHLOROQUINE, at ALL levels of infection and severity, since (at LEAST) MARCH 2020. Btw, since you mentioned “LongCovid”, you mentioned how much better China is doing at something than we Americans are and your entire post was a fucking lie, I’m gonna assume you’re Jewish. And since you also have all the classic “Kindness” and “Global citizen” bullshit in your profile, I’m gonna KNOW you’re Jewish. Something that WILL cure LongCovid, however, is preventing Jews from ever being able to hold professional roles of any kind in healthcare, education, research, government or law in this country ever again. Because COVID wouldn’t have existed in the first place without them. Get COMPLETELY fucked.🖕

@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.

Your website, your business, your future｜Wix.com Create your website and grow with confidence. From an intuitive website builder to advanced business solutions & powerful SEO tools—Try Wix for free. wix.com

@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.)

@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

@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

@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

@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

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

@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

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

@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

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

@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.👇)

Authentic | Your Brand New Universe Explore your favorite brands with exclusive access to new drops, promotions and experiences. Shop the latest from Brooks Brothers, Juicy Couture, Lucky Brand, Forever21, Spyder, Volcom, and more. authentic.com

@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

@ValerieAnne1970 - Valerie Anne Smith

PAXLOVID...Pfizer's Approved 'Antiviral' Treatment For Mild COVID Symptoms. It Contains The HIV/AIDS Drug Ritonavir As A 'Booster' To Enhance Paxlovid's 'Other Ingredients.' Package Insert Includes A Black Box Warning: "Paxlovid Leads To Severe Life Threatening Fatal Events." Ingredients in PAXLOVID... Nirmatrelvir--Antiviral drug Ritonavir--HIV/AIDS drug Titanium dioxide Anhydrous dibasic calcium phosphate Copovidone Polysorbate 80 Talc Colloidal silicon dioxide Croscarmellose sodium Lactose monohydrate Microcrystalline cellulose Sodium stearyl fumarate Iron oxide red Polyethylene glycol Paxlovid 'Rebound' Covid Illness...within 2 to 8 days after completing the five-day course of Paxlovid; a rebound of infectious & transmissible COVID Coronavirus is experienced. Paxlovid/Nirmatrelvir Post Marketing Adverse Events... Severe skin reactions: Painful sores or ulcers in the mouth, nose or genital area. Blistering, peeling or loosening of the skin. This includes life-threatening conditions like Stevens-Johnson syndrome & toxic epidermal necrolysis. Internal Organ Reactions: Severe Liver & Kidney damage. Elevated blood sugar leading to Type 2 Diabetes. Elevated blood pressure causing hypertension. Various Frequent Reactions: Altered taste: Many people report a metallic or bitter taste, called "Paxlovid mouth", Diarrhea, Headache, Nausea, Muscle pain, Fatigue. Paxlovid/Ritonavir Post Marketing Adverse Events... Pancreatitis: Symptoms of inflammation of the pancreas include severe abdominal pain that may radiate to the back, nausea & vomiting. Liver Damage & Toxicity: Ritonavir causes liver damage. Signs include yellowing of the skin or eyes (jaundice), dark urine, pale stools, stomach pain, loss of appetite & itching. Heart rhythm changes: This can cause an irregular or fast heartbeat, dizziness, lightheadedness, chest pain & fainting. Metabolic changes: Increases triglyceride levels & raises blood sugar, leading to diabetes. Body fat changes: This is known as lipodystrophy syndrome, causing an accumulation of fat in areas like the neck ("buffalo hump") & stomach. Increased bleeding risk & kidney stone formation. Neurological effects: Patients experience dizziness, headaches & a burning, tingling, or "pins & needles" sensation in the hands, feet, or around the mouth. Taking Into Consideration Of Illness Duration: For all of the side effects from Paxlovid & other antivirals that must be endured...antivirals only shorten flu duration from 5 days to 4 days. Antivirals only shorten the duration of illness by 1 day. Serious Life Threatening Drug Interactions: Ritonavir HIV/Aids drug interacts with & negatively affects 100s of common medications that patients take on a daily basis. This results in life threatening serious adverse events (SAE) & fatalities. Paxlovid Does Not Reduce Hospitalization Or Death As Pfizer Data Reported: "Paxlovid’s effect on COVID-19 hospitalization is four times weaker than the effect originally reported in Pfizer’s 2022 clinical trial." 👇Pfizer PAXLOVID Package Insert👇 https://labeling.pfizer.com/ShowLabeling.aspx?id=19599 👇Adverse Events Of Nirmatrelvir & Ritonavir👇 https://pmc.ncbi.nlm.nih.gov/articles/PMC9786063/ 👇Paxlovid 4X Less Effective Than Pfizer Reported👇 https://www.uclahealth.org/news/release/paxlovids-impact-hospitalization-and-death-covid-vaccinated Speaker: Dr Jeffrey Barke, MD

Adverse Events Associated with Nirmatrelvir/Ritonavir: A Pharmacovigilance Analysis Based on FAERS Nirmatrelvir/ritonavir is approved for the treatment of adults and pediatric patients with mild to moderate COVID-19, but information on adverse events associated with its use is limited. We aim to evaluate adverse events with potential risk for ... pmc.ncbi.nlm.nih.gov

Paxlovid’s impact on hospitalization and death in COVID-vaccinated older adults far weaker than previously thought Paxlovid does not significantly reduce COVID-19 hospitalization and mortality among vaccinated older adults. The study questions the assumption that Paxlovid’s effectiveness in reducing COVID-19 hospitalizations and deaths in unvaccinated adults also applies to vaccinated adults. uclahealth.org

@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

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

@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

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

@ValerieAnne1970 - Valerie Anne Smith

HELICOPTER PILOT WHISTLEBLOWER: TICK AIRDROPS “I work for a private Charter Company in Ontario Canada. We get paid handsomely to AirDrop Ticks every year — this year we dropped MORE and EARLIER. These were DEER TICKS.” This isn’t “nature” — it’s deliberate. Tick-borne Alpha-Gal Syndrome (the meat allergy nightmare) has exploded 9,800% in the US since 2013. Coincidence? Or part of the plan to crash the food supply and control the population? Bill Gates and his cronies have been obsessed with “fixing” humanity through bugs, vaccines, and engineered crises. Now we’re literally being bombed with them. This is biological terrorism from the skies.

@ValerieAnne1970 - Valerie Anne Smith

https://t.co/DSVGBPcunG

@ValerieAnne1970 - Valerie Anne Smith

ALARMING TIMELINE: Bill & Melinda Gates Foundation + Vanderbilt University + Alpha-Gal Syndrome 2012 Bill & Melinda Gates Foundation begins funding Vanderbilt University’s work on Alpha-Gal Syndrome. A condition most people had never even heard of yet. 2013 Bill Gates starts publicly pushing synthetic lab-grown meat as the future — “better for the planet,” he says. 2017 Gates pours serious money into Memphis Meats (now Upside Foods). He’s all-in on fake meat replacing real beef, pork, and lamb. 2012–Present Lone star tick populations explode across the U.S. Hundreds of thousands develop Alpha-Gal Syndrome — a brutal, lifelong allergy to red meat triggered by a single tick bite. Cases keep rising dramatically. 2021–2023 Gates Foundation funds Oxitec’s genetically modified cattle tick projects. Official story: “for livestock protection.” 2024 Vanderbilt ramps up actual development of the Alpha-Gal vaccine. 2025–2026 (NOW) Tick infestations surging. Alpha-Gal cases climbing fast. Gates still aggressively promotes lab-grown meat. The vaccine “fix” is moving forward. The pattern is crystal clear: 1. Fund the “problem” (Alpha-Gal research at Vanderbilt since 2012) 2. Accelerate the crisis on the ground (tick explosion + meat allergy epidemic) 3. Push people off real meat (synthetic meat empire + campaigns) 4. Sell the “solution” (lab meat + the vaccine) Create the crisis → Control the food supply → Profit from the cure. They’re not even hiding it anymore. This isn’t coincidence. This is a timeline.

@ValerieAnne1970 - Valerie Anne Smith

https://www.malone.news/p/declassified-documents-link-us-bioweapons Declassified Documents Show U.S. Bioweapons Program Weaponized Ticks For Lyme Disease.

@ValerieAnne1970 - Valerie Anne Smith

https://www.gatesfoundation.org/about/committed-grants/2023/04/inv-045130 $7.6 Million To Develop Bioengineered GMO Tick:

@ValerieAnne1970 - Valerie Anne Smith

Pfizer's PAXLOVID...'Approved' Antiviral Treatment For COVID Contains The HIV/AIDS Drug Ritonavir. Package Insert Includes A Black Box Warning: "Paxlovid Leads To Severe Life Threatening Fatal Events." Ingredients in PAXLOVID: Nirmatrelvir--Antiviral drug Ritonavir--HIV/AIDS drug Titanium dioxide Copovidone Polysorbate 80 Talc Silicon dioxide Iron oxide red Polyethylene glycol Paxlovid 'Rebound' Covid Illness...within 2 to 8 days after completing the five-day course of Paxlovid; a rebound of infectious & transmissible COVID is experienced. Paxlovid Post Marketing Adverse Events... Severe skin reactions: Mouth, nose & genital ulcers. Stevens-Johnson syndrome & toxic epidermal necrolysis. Internal Organ Reactions: Severe Liver & Kidney damage. Elevated blood sugar leading to Type 2 Diabetes. Elevated blood pressure causing hypertension, Pancreatitis, Heart rhythm changes. Neurological effects: Patients experience dizziness, headaches & a burning, tingling, or "pins & needles" sensation in the hands, feet, or around the mouth. Efficacy: Paxlovid only shortens flu duration from 5 days to 4 days. Antivirals only shorten the duration of illness by 1 day. Serious Life Threatening Drug Interactions: Ritonavir HIV/Aids drug interacts with & negatively affects 100s of common medications that patients take on a daily basis. This results in life threatening serious adverse events (SAE) & fatalities. Paxlovid Does Not Reduce Hospitalization Or Death As Pfizer Falsely Reported: "Paxlovid’s effect on COVID-19 hospitalization is 4X less effective than originally reported in Pfizer’s 2022 clinical trial."

@ValerieAnne1970 - Valerie Anne Smith

CDC Whistleblower's Secret Recording: "We Buried the Data on MMR & Autism, I'm Completely Ashamed." Dr. Brian Hooker secretly recorded a senior CDC scientist, Dr. William Thompson, who made a shocking admission. On those recordings, Dr. Thompson freely confessed to a massive cover-up. He admitted that he and his senior associates at the CDC had buried the damning data showing a statistical link between the MMR vaccine and autism. Thompson stated, "Thimerosal causes autism-like features." He expressed profound shame, saying, "I'm completely ashamed of what I did. The higher-ups wanted to do certain things and I went along with it." He named senior officials—Colleen Boyle, Frank DeStefano, Marceline Moulton—as participants. At the helm was Dr. Julie Gerberding, who later became president of Merck Vaccine. This is not a theory. It is a confession from a lead CDC co-author on the pivotal studies used to deny any link. The man inside the machine admitted the fraud. The public deserves the truth. The victims deserve justice.

@ValerieAnne1970 - Valerie Anne Smith

Dr. Sherri Tenpenny: "Health CANNOT come through a NEEDLE... you cannot INJECT Health. You don't NEED to be VACCINATED." "Doctor's don't know what's best for you just because they have a title & wear a white coat." "Injecting a virus, bacteria & chemicals is not health." Inside vaccines: Aluminum • Formaldehyde • Glutaraldehyde • Polysorbate 80 • Triton X-100 • SV40 • Neomycin, Polymyxin B, Streptomycin (antibiotics) • 2-Phenoxyethanol • Sodium Deoxycholate • Squalene (MF59) • Monosodium Glutamate (MSG) • Gelatin (from mRNA vaccinated pigs) • Egg proteins • Bovine calf serum / Fetal Bovine Serum • and more. Animal organs & cell lines used: - Monkey kidney cells (Vero cells) - Chicken embryo cultures - Dog kidney cells (MDCK oncogenic) - Bovine (cow) extracts, casein, serum - Chinese hamster ovary (CHO) - Fall armyworm ovary cells (Sf9 insect cells) — yes, ovaries from the fall armyworm moth! Many are still grown in **aborted baby organs** — lungs, kidneys, retinas from 3-month-old fetuses (WALVAX-2, HEK-293, MRC-5, WI-38). They’re STILL harvesting fresh fetal tissue to keep the lines going. Doctors in white coats don’t own your body. Real health comes from **nature, real food, sunshine** — NOT a syringe full of toxins, animal organs, insect ovaries, and foreign human tissue. Health is **NOT** injectable.

@Inversionism - Inversionism

This is how we know that there was malice and forethought during the COVID pandemic. The US government bought up nearly the ENTIRE world supply of remdesivir in mid 2020. Nearly all of it, which is so insane considering what we know now with it's kidney nuking capacity and complete lack of efficacy. Then they took extreme actions towards doctors who were trying cheaper and safer alternative treatments by going as far as removing their license and ability to practice medicine. They even banned doctors from using vitamin C of all things... They only wanted people to use the severely toxic remdesivir because it was a cash cow for pharma at nearly $2000 per course of treatment, in addition to it being great at ensuring COVID mortality was exacerbated to pad the numbers and keep up the narrative of how deadly it was to further sell the vaccine. Idk how anyone can look back on the sequence of actions taken by the government and pharma from early 2020 until now with the continual shilling of boosters, and not see gross levels of malice with forethought. Beginning to end, it was completely anti-human, anti-health, anti-science, and absurdly pro-pharma in every way imaginable. They made billions off the willful harm and death of so many people.