Blood clots jab or meth shot, is the end result pretty much the same??

https://www.theblaze.com/news/ed-buck-sentenced-prison-drugs

The clot jabs are definitely deadly!

https://rumble.com/v10f1zl-robert-kennedy-jr-pfizers-own-data-shows-this-is-the-deadliest-vaccine-ever.html

Redacted??? Where have seen that before?

https://dailyclout.io/dr-naomi-wolf-on-pfizer-they-hid-they-concealed-they-redacted/

A little-known safe, and potentially life-saving drug for treating patients with severe, late-stage COVID, was purposefully ignored by U.S. health officials, and a group of Congressional Republicans led by Wisconsin Senator Ron Johnson are demanding to know why.

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

Good Stick, may God help us because I don’t think this will be as “quick” as rebooting my PC!

Good Stick, I’ll be watching this later today. Thank you!

PW, please post link(s) to sources/scientists claiming the vaccine lots are clean and pure as the white driven snow.

CONFIRMED! Graphene Oxide Main Ingredient In Covid Shots </header>

By Dr. Ariyana Love, ND

A former Pfizer employee and current analyst for the pharmaceutical and medical device industries, came forward with indisputable documentation proving that GRAPHENE OXIDE NANOPARTICLES is the key ingredient in Biotech’s Covid-19 serums.

This means that an unapproved industrial poison is being dishonestly marketed as “vaccines” and injected into children’s veins.

In her must-watch interview with Stew Peter’s on July 28th, Kingston reveals how graphene oxide was hidden under a trade secret. It was therefore not recorded in Biotech’s patent filing as an ingredient in the Covid-19 serums. It was also not disclosed to the public Kingston explains, because it was not required due to it being the registered intellectual property of the pharmaceutical cartel.

Source: https://ambassadorlove.wordpress.com/2021/08/09/confirmed-graphene-oxide-main-ingredient-in-covid-shots/

PW, we need to oust these psychos from the shadows, where they operate, into the light. They’ve done enough damage!

Opinion: 55 years to fulfill a records request? Clearly, the FDA needs serious reform of its data-sharing practices.

https://www.washingtonpost.com/opinions/2021/12/13/55-years-fulfill-records-request-clearly-fda-needs-serious-reform-its-data-sharing-practices/

In my view, that is about to change once Elon Musk gains control over Tweeetr and makes it the peoples public square, no censure!! All other social media or media forms we’ll have their hands full!! No, no ‘good luck wishes’ for those that will try to stop freedom of free speech.

Musk backing off Twitter board opens door to hostile takeover

https://www.cnbc.com/2022/04/11/musk-backing-off-twitter-board-opens-door-to-hostile-takeover.html

In this video, Dr. Naomi Wolf discusses the Volunteer War Room Posse’s raised concerns over the latest batch of Pfizer FDA POIA documents.

Within these documents, we find toxic ingredients within the injection material as well as the allergen Polyethylene Glycol (PEG), which was not disclosed. These ingredients could very well have been the cause of the many adverse reactions experienced by formerly healthy individuals after they received the injections.

https://rumble.com/v1048z7-volunteer-war-room-posse-raise-concerns-over-the-latest-batch-of-pfizer-fda.html

Hindsight has finally arrived, and while still very murky, the fog of Covid is beginning to clear. As a flood of Pfizer documents is released from the FDA, we’ll learn in more detail how 2021 unfolded, who knew what when, and how harmful the vaccines actually are.

The DailyClout/WarRoom Pfizer Document Review team of analysts from medical, statistics, pharmaceutical research, and medical fraud backgrounds, organized by Dr Naomi Wolf, Project Manager Amy Kelly, and the team at DailyClout are studying the documents and sharing their findings with the public as quickly and accurately as possible. There will be a full interim report released in the coming weeks, and they’re also managing to publicize important pieces of information as they emerge. It seems that Pfizer has a recurring theme of keeping highly relevant data to themselves, only to reluctantly publicize it months later. As a quick reminder, they also colluded with the FDA in a failed attempt to continue to conceal this data for our lifetimes.

https://dailyclout.io/pfizer-failed-to-inform-us-about-these-vaccine-health-risks/

JUST IMAGINE INFORMATION LIKE THIS POSTED TO THE MILLIONS IN TWEETR! WE’LL HEAR A SHOUT FOR FREEDOM OF SPEECH AND AVIPTADIL, THE LIKES THE PEOPLE HAVE NEVER HEARD BEFORE!!

The Republicans noted in the letter that Fauci actually touted ZYESAMI as a promising treatment for COVID-19 almost a year ago, but refused to make it widely available until clinical trials were completed.

“The drug remains largely unavailable, and we are told FDA refuses to review the data of NRx’s EUA until the National Institute of Health (NIH) completes clinical trials of ZYESAMI later this year,” they wrote.

Two years into a pandemic and with a death toll exceeding a reported 900,000 Americans, it is unacceptable that the FDA and NIAID are needlessly delaying a treatment for late-stage COVID-19 with a remarkable track record of success. This bureaucratic dragging of your feet appears in stark contrast to the expedited review of other treatments like remdesivir, Molnupiravir, Paxlovid and the COVID-19 vaccines. The FDA’s disparate review processes for different treatments that appears to favor large manufacturers is troubling.

In an interview with Horowitz, Dr. Flavio Cadegiani, a Brazilian endocrinologist who has treated 2,400 COVID patients without losing a single one, explained how the drug fights the virus.

“Aviptadil is a drug that mimics vasoactive intestinal polypeptide (VIP), however, with prolonged effects, compared to the endogenous (produced by the body) VIP,” he said. “VIP and aviptadil act in a type of lung cell called alveolar type II (AT-2), that, although representing just as few as 5% of the cells in the lungs, are largely responsible for oxygen transfer and inhibition of dysfunctional hyper inflammatory reaction and cytokine storm, through the inhibition of the activity of one of the main triggers of these reactions, called NMDA-induced caspase-3.”

Dr. Cadegiani noted that “to date, there is no other molecule capable of working at late stage against COVID-19, and at the same not causing immunosuppression.”

He also believes aviptadil blocks the IL-6, the most dangerous cytokine at the center of the pulmonary dysfunction related to COVID-19. “The importance is that IL-6 is the cytokine that is not effectively blocked by glucocorticoids, even in very high doses. Thus, aviptadil/VIP could confer additional protection when we most need and when we have the fewest resources for.”

He went further to suggest that it is downright malpractice for hospitals not to try this drug at late stage, given the absence of alternatives. “Due to the absence of therapeutic alternatives targeting AT-2 and IL-6, and given the already well-established safety profile, its approval goes beyond the attempt-to-try principle, since it is highly plausible and likely that it works. Therefore, instead of an action of attempt-to-try when giving aviptadil, not providing it when patients fail to respond to other therapies can be considered a medical negligence, from a bioethical perspective.”

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

For the first time ever to come out of our country, Australian scientists have made contact with Zeee Media to provide evidence of their findings of nanotechnology in the COVID-19 Vaccines.

Their identity is being protected so they can continue doing their important research behind the scenes in Australia, a country under extreme medical tyranny where professionals like this are terrified of speaking out, lest they be raided, lose their jobs, or worse.

Please share this broadcast with everyone that you know. People must be aware of what has been injected into their bodies.

https://rumble.com/vzjlyb-exclusive-australian-whistleblower-scientists-provide-evidence-of-nanotech-.html

I’m afraid not every harm done by the vaxx lot will be fixed by our amazing peptide or, will it???

A little-known safe, and potentially life-saving drug for treating patients with severe, late-stage COVID, was purposefully ignored by U.S. health officials, and a group of Congressional Republicans led by Wisconsin Senator Ron Johnson are demanding to know why.

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

Wayne Allyn Root, host of the Wayne Allyn Root Show, gives The Real Story on why the Biden border crisis is becoming a super spreader event for Covid-19.

https://rumble.com/vkgh9x-the-real-story-oan-fed-up-with-fauci-with-wayne-allyn-root.html

Tony “the groundhog from Brooklyn“ shows up his face from time to time. Did he fail? That is the excuse to have another voter mass mailing for the coming congressional elections, more electoral fraud and more stolen elections, yes?

Did Tony meet the psycho???

https://rumble.com/v10baw1-live-better-than-god-yuval-noah-harari.html

Sunday Strip

Own nothing, be happy!

https://rwmalonemd.substack.com/p/sunday-strip-55d

Dr. Naomi Wolf on Pfizer: “They hid. They concealed. They redacted.”

April 5, 2022 • by Bannon's War Room on Rumble

Dr. Naomi Wolf discusses the war on children and on Western values. Forcing children to wear masks is abusive because new studies show that this prevents them from developing normal facial recognition and the practice has a now-measurable effect on their IQ levels.

With all the new information surfacing from the WarRoom/DailyClout volunteers regarding the formerly secret Pfizer documents, and with attorney Stevan Looney’s new essay on the redacted documents in the secret Pfizer tranche now published on DailyClout.io, it is becoming clear that informed consent before receiving the vaccine was never even possible.

Bombshell: in order to process just the paperwork from the “large number of adverse events” — Pfizer’s own words — Pfizer had to hire 2,400 new, full-time employees and the company proudly informed the FDA of these thousands of new hires to grapple with the flood of adverse events they saw as early as February 28, 2021. Yet they did not disclose these adverse events to the public and neither did the FDA.

https://dailyclout.io/dr-naomi-wolf-on-pfizer-they-hid-they-concealed-they-redacted/

ZYESAMI/AVIPTADIL held back???

In a letter to NIAID Director Anthony Fauci and FDA Commissioner Robert Califf, Sen. Ron Johnson (R-Wis.) demanded to know why public health officials ignored three Emergency Use Authorization (EUA) requests from the drug manufacturer, NRx Pharmaceuticals, and refused to review data on ZYESAMI’s efficacy against COVID. The letter, co-authored by Sen. Ted Cruz (R-Texas) and Reps. Andy Biggs (R-Ariz.) and Chip Roy (R-Fla.), cited a physician who treated more than 20 patients who were suffering respiratory failure from COVID-19, and received ZYESAMI as authorized under Right to Try.

“It is our understanding the patients received ZYESAMI after prior administration of remdesivir did not improve the patients’ conditions. All the patients were at the very end stage of COVID and were not expected to recover,” the Republicans wrote.

‘Upon receiving ZYESAMI, no serious adverse events associated with use were reported and 16 of the 20 patients left the hospital. According to the physician, patients with ARDS normally have a 40 percent mortality rate. With ZYESAMI, the mortality rate decreased to roughly 10 percent.’

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

VACCINE GOLD RUSH???

https://rumble.com/vxr1e3-vaccine-gold-rush-do-you-trust-gates.html

Blood clots

Like the drug regulatory authorities in other countries, the Danish Medicines Agency has received reports of blood clots in the time after vaccination.

At this time, the Danish Medicines Agency does not suspect the vaccine to cause side effects in the form of blood clots. Blood clots can be explained by several other factors such as the person’s health conditions, including other diseases and medication taken. In addition, the needle prick itself from the vaccine jab may – even when administered correctly – in rare cases cause blood clots. So, blood clots can occur in the time after vaccination without being related to the vaccine.

The reports of blood clots are monitored closely in a collaboration between the Danish Medicines Agency, the European Medicines Agency (EMA) and the other drug regulatory authorities in Europe. >>>

Bill Maher cheers on Elon Musk joining Twitt[er]: He wants to fix social media's 'control' of free speech

https://www.foxnews.com/media/bill-maher-elon-musk-twitter

“The drug remains largely unavailable, and we are told FDA refuses to review the data of NRx’s EUA until the National Institute of Health (NIH) completes clinical trials of ZYESAMI later this year,” they wrote.

“Two years into a pandemic and with a death toll exceeding a reported 900,000 Americans, it is unacceptable that the FDA and NIAID are needlessly delaying a treatment for late-stage COVID-19 with a remarkable track record of success. This bureaucratic dragging of your feet appears in stark contrast to the expedited review of other treatments like remdesivir, Molnupiravir, Paxlovid and the COVID-19 vaccines. The FDA’s disparate review processes for different treatments that appears to favor large manufacturers is troubling.”

In an interview with Horowitz, Dr. Flavio Cadegiani, a Brazilian endocrinologist who has treated 2,400 COVID patients without losing a single one, explained how the drug fights the virus.

“Aviptadil is a drug that mimics vasoactive intestinal polypeptide (VIP), however, with prolonged effects, compared to the endogenous (produced by the body) VIP,” he said. “VIP and aviptadil act in a type of lung cell called alveolar type II (AT-2), that, although representing just as few as 5% of the cells in the lungs, are largely responsible for oxygen transfer and inhibition of dysfunctional hyper inflammatory reaction and cytokine storm, through the inhibition of the activity of one of the main triggers of these reactions, called NMDA-induced caspase-3.”

Dr. Cadegiani noted that “to date, there is no other molecule capable of working at late stage against COVID-19, and at the same not causing immunosuppression.”

He also believes aviptadil blocks the IL-6, the most dangerous cytokine at the center of the pulmonary dysfunction related to COVID-19. “The importance is that IL-6 is the cytokine that is not effectively blocked by glucocorticoids, even in very high doses. Thus, aviptadil/VIP could confer additional protection when we most need and when we have the fewest resources for.”

He went further to suggest that it is downright malpractice for hospitals not to try this drug at late stage, given the absence of alternatives. “Due to the absence of therapeutic alternatives targeting AT-2 and IL-6, and given the already well-established safety profile, its approval goes beyond the attempt-to-try principle, since it is highly plausible and likely that it works. Therefore, instead of an action of attempt-to-try when giving aviptadil, not providing it when patients fail to respond to other therapies can be considered a medical negligence, from a bioethical perspective.”

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

Alzheimer's disease (AD) is characterized by extracellular deposits of fibrillar beta-amyloid (Abeta) in the brain, increased microglial-mediated inflammatory reactions in senile plaques, selective neuronal death, and cognitive deficits. The use of agents that limit microglial activation and inflammation in AD has recently emerged as an attractive therapeutic strategy for this disease. The vasoactive intestinal peptide (VIP), a widely distributed neuropeptide, has shown neuroprotective effects in acute brain damage in vivo and potent anti-inflammatory actions in central nervous system. Here, we report that VIP inhibits Abeta-induced neurodegeneration by indirectly inhibiting the production of a wide panel of inflammatory and neurotoxic agents by activated microglia cells. The inhibitory effect of VIP is mediated by blocking signaling through the p38 MAPK, p42/p44 MAPK, and NFkB cascades, the three major transduction pathways involved in the transcription of inflammatory mediators and the production of free radicals by Abeta-activated microglia cells. Based on its neuroprotective action and its efficacy in inhibiting a broad range of inflammatory responses, VIP may provide a novel therapeutic approach to AD.

https://pubmed.ncbi.nlm.nih.gov/18442091/

The global market for Alzheimer’s disease expected to attain $25 billion by 2027, growing at a staggering CAGR of 17.5% over the forecast period, driven by rapidly ageing population, increasing prevalence of AD, coupled with technological advancements in diagnostics and biomarkers.

https://www.ihealthcareanalyst.com/global-alzheimers-disease-market/

Remember Democracy never lasts long. It soon wastes exhausts and murders itself. There never was a Democracy Yet, that did not commit suicide. It is in vain to Say that Democracy is less vain, less proud, less selfish, less ambitious or less avaricious than Aristocracy or Monarchy. ~ From John Adams to John Taylor, 17 December 1814 - Founders Online

Maybe free speech absolutist Elon Musk can help!

https://www.standingforfreedom.com/2022/04/free-speech-absolutist-elon-musk-puts-censorship-on-notice-by-becoming-majority-shareholder-board-member-of-twitter/

Once greater freedom of expression is restored to the Tweetr public square then people will have the opportunity to post challenging points of view like the following:

Pharma-funded mainstream media has convinced millions of Americans that Dr. Anthony Fauci is a hero. He is anything but.

As director of the National Institute of Allergy and Infectious Diseases (NIAID), Dr. Anthony Fauci dispenses $6.1 billion in annual taxpayer-provided funding for scientific research, allowing him to dictate the subject, content, and outcome of scientific health research across the globe. Fauci uses the financial clout at his disposal to wield extraordinary influence over hospitals, universities, journals, and thousands of influential doctors and scientists—whose careers and institutions he has the power to ruin, advance, or reward.

During more than a year of painstaking and meticulous research, Robert F. Kennedy Jr. unearthed a shocking story that obliterates media spin on Dr. Fauci . . . and that will alarm every American—Democrat or Republican—who cares about democracy, our Constitution, and the future of our children’s health.

The Real Anthony Fauci reveals how “America’s Doctor” launched his career during the early AIDS crisis by partnering with pharmaceutical companies to sabotage safe and effective off-patent therapeutic treatments for AIDS. Fauci orchestrated fraudulent studies, and then pressured US Food and Drug Administration (FDA) regulators into approving a deadly chemotherapy treatment he had good reason to know was worthless against AIDS. Fauci repeatedly violated federal laws to allow his Pharma partners to use impoverished and dark-skinned children as lab rats in deadly experiments with toxic AIDS and cancer chemotherapies.

In early 2000, Fauci shook hands with Bill Gates in the library of Gates’ $147 million Seattle mansion, cementing a partnership that would aim to control an increasingly profitable $60 billion global vaccine enterprise with unlimited growth potential. Through funding leverage and carefully cultivated personal relationships with heads of state and leading media and social media institutions, the Pharma-Fauci-Gates alliance exercises dominion over global health policy.

The Real Anthony Fauci details how Fauci, Gates, and their cohorts use their control of media outlets, scientific journals, key government and quasi-governmental agencies, global intelligence agencies, and influential scientists and physicians to flood the public with fearful propaganda about COVID-19 virulence and pathogenesis, and to muzzle debate and ruthlessly censor dissent.

https://rumble.com/vw1m5b-the-real-anthony-fauci-introduction-chapter-two.html

Once the people are at it, why not post…???

In Letter to FDA and NIAID, Ron Johnson Demands to Know Why Promising Late-Stage COVID Drug Was Never Approved

In a letter to NIAID Director Anthony Fauci and FDA Commissioner Robert Califf, Sen. Ron Johnson (R-Wis.) demanded to know why public health officials ignored three Emergency Use Authorization (EUA) requests from the drug manufacturer, NRx Pharmaceuticals, and refused to review data on ZYESAMI’s efficacy against COVID. The letter, co-authored by Sen. Ted Cruz (R-Texas) and Reps. Andy Biggs (R-Ariz.) and Chip Roy (R-Fla.), cited a physician who treated more than 20 patients who were suffering respiratory failure from COVID-19, and received ZYESAMI as authorized under Right to Try.

“It is our understanding the patients received ZYESAMI after prior administration of remdesivir did not improve the patients’ conditions. All the patients were at the very end stage of COVID and were not expected to recover,” the Republicans wrote.

“Upon receiving ZYESAMI, no serious adverse events associated with use were reported and 16 of the 20 patients left the hospital. According to the physician, patients with ARDS normally have a 40 percent mortality rate. With ZYESAMI, the mortality rate decreased to roughly 10 percent.”

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

Former Attorney General of Louisiana, Charles C. Foti, Jr., Esq., a partner at the law firm of Kahn Swick & Foti, LLC (“KSF”), announces that KSF has commenced an investigation into NRx Pharmaceuticals (NasdaqGM: NRXP).

https://www.businesswire.com/news/home/20220408005621/en/NRX-PHARMACEUTICALS-INVESTIGATION-INITIATED-By-Former-Louisiana-Attorney-General-Kahn-Swick-Foti-LLC-Investigates-the-Officers-and-Directors-of-NRx-Pharmaceuticals-Inc.---NRXP

Phenylketonuria??? GOLIKE Metabolics!

Comparisons Between Pfizer’s EUA, Pfizer’s Cumulative Analysis of Post-Authorization Adverse Event Reports, and New Studies Raises Several New Questions

March 17, 2022 • by Zoe Wilson

There was a recent study that was published on January 25, 2022 with data compiled from December 2020 through August 2021.

https://jamanetwork.com/journals/jama/fullarticle/2788346

Individually, heart failure (HF) and Alzheimer Disease (AD) are severe threats to population health, and their potential coexistence is an alarming prospect. In addition to sharing analogous epidemiological and genetic profiles, biochemical characteristics, and common triggers, we recently recognized common molecular and pathological features between the 2 conditions. Whereas cognitive impairment has been linked to HF through perfusion defects, angiopathy, and inflammation, whether patients with AD present with myocardial dysfunction, and if the 2 conditions bear a common pathogenesis as neglected siblings is unknown.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5142757/

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by extracellular deposits of fibrillary ß-amyloid (Aß) plaques in the brain that initiate an inflammatory process resulting in neurodegeneration. The neuronal loss associated with AD results in gross atrophy of affected regions causing a progressive loss of cognitive ability and memory function, ultimately leading to dementia. Growing evidence suggests that vasoactive intestinal peptide (VIP) could be beneficial for various neurodegenerative diseases, including AD.

https://pubmed.ncbi.nlm.nih.gov/30498985/

“FIVE FREEDOMS” – NEWS FEED: 25-Year-Old Develops Myocarditis After Moderna Vaccine, Mother Says Doctors ‘Downplayed’ Connection

In an interview with The Defender, Deborah Brenner said some doctors “were totally against” connecting her son’s heart damage to the COVID vaccine when he suffered an adverse reaction just days after receiving his first dose of the Moderna vaccine. READ Megan Redshaw’s article in The Defender

https://dailyclout.io/?s=Myocarditis+


Op-ed: The Emergency Use Law Should Be Used for Emergencies—Like Now

By Dr. Jacobo Elgozy, DO | Jan 5, 2022
Imagine you have a loved one hospitalized in intensive care facing death from Covid-19. All approved therapeutics were tried. Time has run out and you have been told to prepare for the worst. Your doctor advises there is one last drug to try, a natural protein that has been safely used in early trials and shown signs of effectiveness in rescuing patients from ventilators when all else has failed. The National Institutes of Health is doing a global study to prove its effectiveness.

FDA/NIH let our amazing NEUROPEPTIDE (AVIPTADIL) go free to cure the people!!!

Unfortunately, the Food and Drug Administration will not give Emergency Use Authorization because the medicine showed only a 92 percent chance of being effective, rather than the “magic 95 percent” that is the traditional gold standard for approving drugs.

I was that patient. I contracted Covid while serving on the front lines of a hospital, caring for my own patients. My story has a happy ending only because my lifelong friend, an ICU doctor, moved heaven and earth to cut through the red tape and obtain the medicine for me with the FDA’s permission. I was especially lucky that the medicine was being tested at a nearby hospital and the pharmaceutical company immediately rushed an emergency dose to my bedside. I was as close to death as one can be, treated not only with a ventilator but also with extracorporeal membrane oxygenation (ECMO), which few survive. By the time I got the medicine and began to recover, the hospital was already preparing me for a lung transplant.

https://miamicourant.com/stories/617928153-op-ed-the-emergency-use-law-should-be-used-for-emergencies-like-now

REMEMBER THIS??

Wait what? FDA wants 55 years to process FOIA request over vaccine data

https://www.reuters.com/legal/government/wait-what-fda-wants-55-years-process-foia-request-over-vaccine-data-2021-11-18/

Elon Musk, hurry, free up Tweeter so that the people can propagate news on the adverse effects of COVID-19 vaccines while the promising NEUROPEPTIDE AVIPTADIL has been held back. Jon J, can you help?? Sure, that will be the day!!

https://www.standingforfreedom.com/2022/04/free-speech-absolutist-elon-musk-puts-censorship-on-notice-by-becoming-majority-shareholder-board-member-of-twitter/

Thank you JK, likewise!

I thought a little HOpium would not hurt anyone and I say that because control of the process to drug approval is in the hands of those that are not friends of our amazing peptide!!

Pharma-funded mainstream media has convinced millions of Americans that Dr. Anthony Fauci is a hero. He is anything but.

As director of the National Institute of Allergy and Infectious Diseases (NIAID), Dr. Anthony Fauci dispenses $6.1 billion in annual taxpayer-provided funding for scientific research, allowing him to dictate the subject, content, and outcome of scientific health research across the globe. Fauci uses the financial clout at his disposal to wield extraordinary influence over hospitals, universities, journals, and thousands of influential doctors and scientists—whose careers and institutions he has the power to ruin, advance, or reward.

During more than a year of painstaking and meticulous research, Robert F. Kennedy Jr. unearthed a shocking story that obliterates media spin on Dr. Fauci . . . and that will alarm every American—Democrat or Republican—who cares about democracy, our Constitution, and the future of our children’s health.

The Real Anthony Fauci reveals how “America’s Doctor” launched his career during the early AIDS crisis by partnering with pharmaceutical companies to sabotage safe and effective off-patent therapeutic treatments for AIDS. Fauci orchestrated fraudulent studies, and then pressured US Food and Drug Administration (FDA) regulators into approving a deadly chemotherapy treatment he had good reason to know was worthless against AIDS. Fauci repeatedly violated federal laws to allow his Pharma partners to use impoverished and dark-skinned children as lab rats in deadly experiments with toxic AIDS and cancer chemotherapies.

In early 2000, Fauci shook hands with Bill Gates in the library of Gates’ $147 million Seattle mansion, cementing a partnership that would aim to control an increasingly profitable $60 billion global vaccine enterprise with unlimited growth potential. Through funding leverage and carefully cultivated personal relationships with heads of state and leading media and social media institutions, the Pharma-Fauci-Gates alliance exercises dominion over global health policy.

The Real Anthony Fauci details how Fauci, Gates, and their cohorts use their control of media outlets, scientific journals, key government and quasi-governmental agencies, global intelligence agencies, and influential scientists and physicians to flood the public with fearful propaganda about COVID-19 virulence and pathogenesis, and to muzzle debate and ruthlessly censor dissent.

https://rumble.com/vw1m5b-the-real-anthony-fauci-introduction-chapter-two.html

Rand Paul likens Anthony Fauci to 'mafia don,' shares old video of Fauci praising natural flu immunity as 'most potent vaccination'

https://www.theblaze.com/news/rand-paul-anthony-fauci-immunity-vanity-fair

The final magic bullet…

Hi All,

MORAL BOOST TIME:

https://www.fda.gov/media/102282/download

Start at page 34, after pg 74 it gets a little tedious.

Note Ms.Davidson on the FDA panel refer to Aviptadil as a seemingly Miracle drug on page 63.

She's referring to VIP/Aviptadil's use in Neuro degenerative disease such as Alzheimer's and Parkinson's ( pg 52-54 ).

A Dr. Shoemaker who has treated 1700 patients over 8 years tells the FDA panel that Aviptadil is a " Magic Bullet " for Pulmonary Hypertension and the treatment of MOLD sickness in humans.

This is all before COVID in 2016 . It is an interesting read for sure, and speaks to the many possibilities of this Drug when it gets NDA.

This report records a failed attempt by a competitor at some Authorization from the FDA, but the claims being made were pretty encouraging.

It's only a matter of time.

Some indications for neuro diseases will take a few years, but my grand-kids aren't going anywhere, and will be thanking me for their college educations after I'm gone.

GLT- Everyone that has Faith in RLF-100.
We Know.

Lt. F
GLTU- GLTA

~ Posted by Lt. Francis, Y@h00 RLFTF finance conversations

Thank you Good Stick! Best to you, family and friends!

KEYTRUDA is a medicine that may treat certain cancers by working with your immune system. KEYTRUDA can cause your immune system to attack normal organs and tissues in any area of your body and can affect the way they work. These problems can sometimes become severe or life-threatening and can lead to death. You can have more than one of these problems at the same time. These problems may happen any time during treatment or even after your treatment has ended.

Call or see your health care provider right away if you develop any signs or symptoms of the following problems or if they get worse. These are not all of the signs and symptoms of immune system problems that can happen …kEYTRUDA


——————————————-
Good Stick, you may want to check your physician/specialist regarding the use of NAC (supplement/amino acid)

Lung cancer arises as a focal transformation of chronically injured epithelium with cigarette smoke as one of its well recognized causes. Apart from oxidants, cigarette smoke contains several precarcinogens, and it is surprising that not every heavy smoker becomes a victim of malignant disease. This points to the interindividual variability in susceptibility to carcinogens and there are several lines of evidence that metabolic factors are involved in such variability. Metabolism of carcinogens and also the subsequent multisteps of carcinogenesis are affected by host factors and governed by the balance between opposite forces, such as metabolic activation and detoxification, formation, and scavenging of radicals and DNA damage and repair. This implies that carcinogenic compounds can initiate tumor growth only in amounts saturating detoxification mechanisms. In this context it is well known that glutathione plays a crucial role in the detoxification of xenobiotics. N-acetylcysteine (NAC), an aminothiol and precursor of intracellular cysteine and glutathione, has been shown not only to be an efficient antidote in acetaminophen poisoning but also to possess important chemopreventive properties. In this article, sites and mechanisms of the therapeutic action of NAC are reviewed with special reference to its chemopreventive characteristics.

https://journal.chestnet.org/article/S0012-3692(16)38220-4/fulltext

The molecular pathways which are regulated by N-Acetyl L-cysteine (NAC) include DNA Repair, Angiogenesis and MYC Signaling. These cellular pathways directly or indirectly regulate specific cancer molecular endpoints like growth, spread and death. Because of this biological regulation – for cancer nutrition, the right choice of supplements like N-Acetyl L-cysteine (NAC) individually or in combination is an important decision to be made. When making decisions on the use of supplement N-Acetyl L-cysteine (NAC) for cancer – do consider all these factors and explanations. Because just as true for cancer treatments – N-Acetyl L-cysteine (NAC) use cannot be a one-size-fits-all decision for all types of cancers.

https://addon.life/2021/08/20/for-which-cancer-types-should-i-avoid-n-acetyl-l-cysteine-nac-supplement/

Agreed!! Did the U.S. Government say the vaccinated couldn’t get COVID-19???

https://rumble.com/v100t3y-watch-jim-jordan-blasts-the-democrats-on-real-problems-facing-americans.html

Is the vaccine industry working against the wellbeing of the people???

The April batch came out earlier this week, and Mr. Stevan Looney, a civil trial and appellate attorney of the DailyClout team, has made a pretty shocking discovery. There was one document that was released on Nov 17, 2021 (Dated Feb 28, 2021) with 2 pieces of redacted information. That document showed up as “re-issued” in the April 1 release, with those 2 missing facts now unredacted:

The total number of BNT162b2 (Pfizer) doses that were shipped worldwide as of Feb 28, 2021 was “approximately 126,212,580”. An important figure to have for any independent scientist or data analyst who’s trying to study the data.
The first 3 months of the vaccine rollout generated a “large number” of adverse events reported to Pfizer. Pfizer hired a number of new employees to manage the incoming flood of reports, and that number was just released. At the end of Feb 2021, they had hired 600 new employees, with the expectation of an additional 1800 joining by the end of June, 2021. A total of 2400 employees were hired in a ~6 month span to deal with an unexpected flow of reports.

https://dailyclout.io/dr-wolfs-army-of-volunteers-is-revealing-the-truth-about-pfizer/

Are governments pushing vaccines???

What’s happening in California is of special concern. It is true that cities like San Francisco and Los Angeles no longer require people to show a vaccine card to get into restaurants, bars, and gyms. But while Californians were at the bar sipping their Sierra Nevada brews and watching Golden State Warriors basketball, the state legislature was busy drafting some of the most draconian vaccine mandates in the country. If these bills become law in the next few weeks, this would set a bad precedent for the rest of the nation.

For example, AB 1993 if passed will mandate that everyone who works in the state — whether as an independent contractor working from home or as an employee at the office — must show proof of COVID vaccination. The State will have the power to determine how many additional booster shots means “fully vaccinated” at any given time, and employers who fail to enforce the mandate will face stiff fines. (Under pressure the authors tabled the bill this week but it’s not dead.) Another of the bills, SB 866 will allow children as young as 12 to be vaccinated without their parent’s knowledge or consent. Senate Bill 871 would mandate that all children in California receive COVID vaccines to attend public or private school, starting from preschool. (Never mind that there is currently not even an EUA COVID vaccine for children under 5 years old, and no approved and licensed COVID vaccine is available for any age person in this country.)

https://rwmalonemd.substack.com/p/its-time-to-rally-in-cali

It’s not public what Dr. Fauci’s salary was last year or this year. (The latest published salary is from FY2020.)

It’s not public what stocks and bonds Dr. Fauci bought and sold in 2020 or 2021, as he influenced Covid policies.

It’s not public what Fauci received – or didn’t receive – in royalties. (There are up to 1,000 current and former NIH scientists receiving royalties.) Each payment could be a potential conflict of interest.

Yes, all this information resides with the National Institutes of Health (NIH), but isn’t “public knowledge,” despite Dr. Fauci’s claims otherwise in his sworn U.S. Senate testimony yesterday.

These facts are known because an organization I lead, OpenTheBooks.com, is suing NIH for production of those records. In fact, NIH admits it holds approximately 1,200 pages relating to Fauci’s financial information and conflict of interest disclosures.

Transparency advocates say that NIH should post these documents online immediately.

https://www.openthebooks.com/forbes-no-faucis-records-arent-available-online-why-wont-nih-immediately-release-them/

Nov 25, 2019: Dr. ANTHONY FAUCI said that he wanted the chance to respond to a brand new pandemic

https://rumble.com/vrtuxr-nov-25-2019-dr.-anthony-fauci-said-that-he-wanted-the-chance-to-respond-to-.html

Bill, can you help???

https://rumble.com/vp10sj-bill-gates-smallpox-germ-games-and-10-15-fewer-people-in-the-world.html

NOVEMBER 13, 2021 EXCLUSIVE! 3 BOMBS DROPPED at Health and Freedom Dr. Judy Mikovits Mikki Willis

https://rumble.com/vp6utd-november-13-20201-exclusive-3-bombs-dr.-judy-mikovits-mikki-willis.html

Can AVIPTADIL help…???



The researchers, who report their findings today in Nature, analyzed human lung tissue to identify the new cells, which they call respiratory airway secretory cells (RASCs). The cells line tiny airway branches, deep in the lungs, near the alveoli structures where oxygen is exchanged for carbon dioxide. The scientists showed that RASCs have stem-cell-like properties enabling them to regenerate other cells that are essential for the normal functioning of alveoli. They also found evidence that cigarette smoking and the common smoking-related ailment called chronic obstructive pulmonary disease (COPD) can disrupt the regenerative functions of RASCs -- hinting that correcting this disruption could be a good way to treat COPD.

"COPD is a devastating and common disease, yet we really don't understand the cellular biology of why or how some patients develop it. Identifying new cell types, in particular new progenitor cells, that are injured in COPD could really accelerate the development of new treatments," said study first author Maria Basil, MD, PhD, an instructor of Pulmonary Medicine.

https://www.sciencedaily.com/releases/2022/04/220401122222.htm

The most abundant neuropeptide in the lung is the vasoactive intestinal peptide (VIP), which is a potent muscle relaxant and has therefore been suggested in the therapy of chronic inflammatory lung diseases, including COPD [15,16]. In experimental conditions, VIP has a positive inotropic and chronotropic effect.

https://www.karger.com/Article/Fulltext/439228

The global asthma and COPD drugs market size was US$ 34522.6 million in 2021. The global asthma and COPD drugs market size is forecast to reach US$ 53049.54 million by 2030, growing at a compound annual growth rate (CAGR) of 4.65% during the forecast period from 2022 to 2030.

https://www.marketwatch.com/press-release/asthma-and-copd-drugs-market-2022-industry-outlook-share-size-opportunities-and-forecast-to-2030-2022-03-25

Bill, just in case you no longer see a 1:20 ROI on vaccines, we have a therapeutic named AVIPTADIL/ZYESAMI/RLF-100 but…

https://rumble.com/vym4h0-bill-gates-nightmare-support-for-non-covid-vaccine-mandates-nose-dives-post.html

…we don’t think AVIPTADIL will for a depopulation strategy!!

https://rumble.com/vp10sj-bill-gates-smallpox-germ-games-and-10-15-fewer-people-in-the-world.html

Science caused COVID-19??

https://rumble.com/vxxqln-theyre-lying-to-you-if-science-caused-covid-whats-next.html

Here is one dated more recently!

He said the mortality rate “trended” towards being better but “has not yet reached statistical significance.”

So, why was the announcement made so soon? Fauci said, “We have an ethical obligation to let people in the placebo group know so they can have access.”

https://www.healthnewsreview.org/2020/04/what-the-public-didnt-hear-about-the-nih-remdesivir-trial/

Tony, how about spreading the love/ethics?? Yes, can we spread the ethics??

The Republicans noted in the letter that Fauci actually touted ZYESAMI as a promising treatment for COVID-19 almost a year ago, but refused to make it widely available until clinical trials were completed.

“The drug remains largely unavailable, and we are told FDA refuses to review the data of NRx’s EUA until the National Institute of Health (NIH) completes clinical trials of ZYESAMI later this year,” they wrote.

Two years into a pandemic and with a death toll exceeding a reported 900,000 Americans, it is unacceptable that the FDA and NIAID are needlessly delaying a treatment for late-stage COVID-19 with a remarkable track record of success. This bureaucratic dragging of your feet appears in stark contrast to the expedited review of other treatments like remdesivir, Molnupiravir, Paxlovid and the COVID-19 vaccines. The FDA’s disparate review processes for different treatments that appears to favor large manufacturers is troubling.

In an interview with Horowitz, Dr. Flavio Cadegiani, a Brazilian endocrinologist who has treated 2,400 COVID patients without losing a single one, explained how the drug fights the virus.

“Aviptadil is a drug that mimics vasoactive intestinal polypeptide (VIP), however, with prolonged effects, compared to the endogenous (produced by the body) VIP,” he said. “VIP and aviptadil act in a type of lung cell called alveolar type II (AT-2), that, although representing just as few as 5% of the cells in the lungs, are largely responsible for oxygen transfer and inhibition of dysfunctional hyper inflammatory reaction and cytokine storm, through the inhibition of the activity of one of the main triggers of these reactions, called NMDA-induced caspase-3.”

Dr. Cadegiani noted that “to date, there is no other molecule capable of working at late stage against COVID-19, and at the same not causing immunosuppression.”

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

Pharma-funded mainstream media has convinced millions of Americans that Dr. Anthony Fauci is a hero. He is anything but.

As director of the National Institute of Allergy and Infectious Diseases (NIAID), Dr. Anthony Fauci dispenses $6.1 billion in annual taxpayer-provided funding for scientific research, allowing him to dictate the subject, content, and outcome of scientific health research across the globe. Fauci uses the financial clout at his disposal to wield extraordinary influence over hospitals, universities, journals, and thousands of influential doctors and scientists—whose careers and institutions he has the power to ruin, advance, or reward.

During more than a year of painstaking and meticulous research, Robert F. Kennedy Jr. unearthed a shocking story that obliterates media spin on Dr. Fauci . . . and that will alarm every American—Democrat or Republican—who cares about democracy, our Constitution, and the future of our children’s health.

The Real Anthony Fauci reveals how “America’s Doctor” launched his career during the early AIDS crisis by partnering with pharmaceutical companies to sabotage safe and effective off-patent therapeutic treatments for AIDS. Fauci orchestrated fraudulent studies, and then pressured US Food and Drug Administration (FDA) regulators into approving a deadly chemotherapy treatment he had good reason to know was worthless against AIDS. Fauci repeatedly violated federal laws to allow his Pharma partners to use impoverished and dark-skinned children as lab rats in deadly experiments with toxic AIDS and cancer chemotherapies.

In early 2000, Fauci shook hands with Bill Gates in the library of Gates’ $147 million Seattle mansion, cementing a partnership that would aim to control an increasingly profitable $60 billion global vaccine enterprise with unlimited growth potential. Through funding leverage and carefully cultivated personal relationships with heads of state and leading media and social media institutions, the Pharma-Fauci-Gates alliance exercises dominion over global health policy.

The Real Anthony Fauci details how Fauci, Gates, and their cohorts use their control of media outlets, scientific journals, key government and quasi-governmental agencies, global intelligence agencies, and influential scientists and physicians to flood the public with fearful propaganda about COVID-19 virulence and pathogenesis, and to muzzle debate and ruthlessly censor dissent.

https://rumble.com/vw1m5b-the-real-anthony-fauci-introduction-chapter-two.html

The scheme of lies, false data, and political divisiveness surrounding Pfizer jabs are finally collapsing. Friday on the Stew Peters Show, Dr. Robert Malone exposes confidential information from Pfizer containing fatal vaccine injuries and lists of extreme adverse events. In the premium interview, Dr. Malone evaluates the data and the consequences of the jabs.

https://rumble.com/vwglmp-top-secret-pfizer-documents-leaked-pfizer-knew-that-vaxx-would-kill-thousan.html

Your mission, Monk44, should you choose to accept it, is to find the latest and greatest news on AVIPTADIL while in the clutches of federal agencies!! Easy, no sweat!!

National Institute of Allergy and Infectious Diseases Director Anthony S. Fauci, MD, said today that data from a multinational randomized control trial showed that Gilead’s investigational antiviral remdesivir “has a clear-cut significant positive effect in diminishing time to recovery” for patients with COVID-19.

https://www.healio.com/news/infectious-disease/20200429/fauci-on-remdesivir-for-covid19-this-will-be-the-standard-of-care

Pharma-funded mainstream media has convinced millions of Americans that Dr. Anthony Fauci is a hero. He is anything but.

As director of the National Institute of Allergy and Infectious Diseases (NIAID), Dr. Anthony Fauci dispenses $6.1 billion in annual taxpayer-provided funding for scientific research, allowing him to dictate the subject, content, and outcome of scientific health research across the globe. Fauci uses the financial clout at his disposal to wield extraordinary influence over hospitals, universities, journals, and thousands of influential doctors and scientists—whose careers and institutions he has the power to ruin, advance, or reward.

During more than a year of painstaking and meticulous research, Robert F. Kennedy Jr. unearthed a shocking story that obliterates media spin on Dr. Fauci . . . and that will alarm every American—Democrat or Republican—who cares about democracy, our Constitution, and the future of our children’s health.

The Real Anthony Fauci reveals how “America’s Doctor” launched his career during the early AIDS crisis by partnering with pharmaceutical companies to sabotage safe and effective off-patent therapeutic treatments for AIDS. Fauci orchestrated fraudulent studies, and then pressured US Food and Drug Administration (FDA) regulators into approving a deadly chemotherapy treatment he had good reason to know was worthless against AIDS. Fauci repeatedly violated federal laws to allow his Pharma partners to use impoverished and dark-skinned children as lab rats in deadly experiments with toxic AIDS and cancer chemotherapies.

In early 2000, Fauci shook hands with Bill Gates in the library of Gates’ $147 million Seattle mansion, cementing a partnership that would aim to control an increasingly profitable $60 billion global vaccine enterprise with unlimited growth potential. Through funding leverage and carefully cultivated personal relationships with heads of state and leading media and social media institutions, the Pharma-Fauci-Gates alliance exercises dominion over global health policy.

The Real Anthony Fauci details how Fauci, Gates, and their cohorts use their control of media outlets, scientific journals, key government and quasi-governmental agencies, global intelligence agencies, and influential scientists and physicians to flood the public with fearful propaganda about COVID-19 virulence and pathogenesis, and to muzzle debate and ruthlessly censor dissent.

https://rumble.com/vw1m5b-the-real-anthony-fauci-introduction-chapter-two.html

Rand Paul likens Anthony Fauci to 'mafia don,' shares old video of Fauci praising natural flu immunity as 'most potent vaccination'

https://www.theblaze.com/news/rand-paul-anthony-fauci-immunity-vanity-fair

I Just Love This! Remdesivir Failed Make Room For RLF!
~ posted by TnT, Y@h00 RLFTF finance conversations

https://www.reuters.com/business/healthcare-pharmaceuticals/gileads-remdesivir-fails-show-benefit-european-trial-no-fetus-risk-seen-with-2022-04-04/

G-Money
12 hours ago
Most of you don't seem to understand that the continued use of the name zyesami undermines our company in the eyes of the world. And also with our court case. That name points back to nrxp and gives the impression that it's their drug. It's not. There is nothing verifying that zyesami is a new formulation of Aviptadil or a more stable version. Nothing.

If you plan to share videos and news reports etc... they need to point back to Relief Therapeutics and RLF-100. We own the formulation. If we don't educate the world on RLF -100 they will falsely believe nrxp is responsible for Aviptadil.

They are facing class action lawsuits, criminal lawsuits, SEC investigation, Dept. Of Justice investigations, and possibly FBI investigation. We don't want to be associated with nrxp.
Less

ReplyReplies (9)205
Sign in to post a reply.
Michael
Michael8 hours ago
@DD to win your understanding of how things work is way off. Gotta block you simpleton.


GeraldS
8 hours ago
Gee. With all due respect are you a lowly share holder (how many million shares at what prices) an insider on the board of directors or a lawyer suing NRXP? 1. The companies have already declared their preference for an amicable settlement so IMHO whatever we call this peptide on a public anonymous discussion board doesn't mean a hill of beans. How about "Soylent Green"?
Less

WONG
8 hours ago
@DD to win Wow, so sensitive. You act as though JJ created Zyesami himself with his at home Mr. Wizard chemistry set. Nephron reformulated the existing formulation. Not JJ. It wasn't even JJ's idea to use aviptadil to treat Covid. Give it up already. How do we even know there is a new formulation?
Bullish

DD to win
9 hours ago
@WONG ZyeSami is the current IV Aviptadil treatment under trials and continues to be the only therapeutic for critical covid patient patients.

Perhaps RLFTF should formulate an adequate IV treatment on their own. That will take over a year or more.

These two companies need to resolve their issues and split the proceeds according to their new CA they are working on.
Less

WONG
9 hours ago
Zyesami is the commercial name for RLF-100 (Aviptadil) in the states if NRXP is still bringing it to market here. We will know when the mediation is over.
Bullish


DD to win
10hours ago
You need to read more and post less misinformation. The CA spells everything out you're missing.

HOID.
11 hours ago
@HOID. I’ve been using all three for the time being. Zyesami RLF-100 Aviptadil.

HOID.
11 hours ago
I have been conflicted on this in my messaging. More so now than ever since the Senators letter mentions Zyesami. That’s the wave I will have to ride for the time being.

James
11 hours ago
You didn’t think about this too hard before posting.

~ posted at Y@h00 RLFTF finance conversations

THE UNTOLD TRUTH….

When Tony followed science…

https://rumble.com/vz8ef3-flashback-to-when-fauci-followed-science-instead-of-money.html

The Republicans noted in the letter that Fauci actually touted ZYESAMI as a promising treatment for COVID-19 almost a year ago, but refused to make it widely available until clinical trials were completed.

“The drug remains largely unavailable, and we are told FDA refuses to review the data of NRx’s EUA until the National Institute of Health (NIH) completes clinical trials of ZYESAMI later this year,” they wrote.

Two years into a pandemic and with a death toll exceeding a reported 900,000 Americans, it is unacceptable that the FDA and NIAID are needlessly delaying a treatment for late-stage COVID-19 with a remarkable track record of success. This bureaucratic dragging of your feet appears in stark contrast to the expedited review of other treatments like remdesivir, Molnupiravir, Paxlovid and the COVID-19 vaccines. The FDA’s disparate review processes for different treatments that appears to favor large manufacturers is troubling.

In an interview with Horowitz, Dr. Flavio Cadegiani, a Brazilian endocrinologist who has treated 2,400 COVID patients without losing a single one, explained how the drug fights the virus.

“Aviptadil is a drug that mimics vasoactive intestinal polypeptide (VIP), however, with prolonged effects, compared to the endogenous (produced by the body) VIP,” he said. “VIP and aviptadil act in a type of lung cell called alveolar type II (AT-2), that, although representing just as few as 5% of the cells in the lungs, are largely responsible for oxygen transfer and inhibition of dysfunctional hyper inflammatory reaction and cytokine storm, through the inhibition of the activity of one of the main triggers of these reactions, called NMDA-induced caspase-3.”

Dr. Cadegiani noted that “to date, there is no other molecule capable of working at late stage against COVID-19, and at the same not causing immunosuppression.”

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

Pharma-funded mainstream media has convinced millions of Americans that Dr. Anthony Fauci is a hero. He is anything but.

As director of the National Institute of Allergy and Infectious Diseases (NIAID), Dr. Anthony Fauci dispenses $6.1 billion in annual taxpayer-provided funding for scientific research, allowing him to dictate the subject, content, and outcome of scientific health research across the globe. Fauci uses the financial clout at his disposal to wield extraordinary influence over hospitals, universities, journals, and thousands of influential doctors and scientists—whose careers and institutions he has the power to ruin, advance, or reward.

During more than a year of painstaking and meticulous research, Robert F. Kennedy Jr. unearthed a shocking story that obliterates media spin on Dr. Fauci . . . and that will alarm every American—Democrat or Republican—who cares about democracy, our Constitution, and the future of our children’s health.

The Real Anthony Fauci reveals how “America’s Doctor” launched his career during the early AIDS crisis by partnering with pharmaceutical companies to sabotage safe and effective off-patent therapeutic treatments for AIDS. Fauci orchestrated fraudulent studies, and then pressured US Food and Drug Administration (FDA) regulators into approving a deadly chemotherapy treatment he had good reason to know was worthless against AIDS. Fauci repeatedly violated federal laws to allow his Pharma partners to use impoverished and dark-skinned children as lab rats in deadly experiments with toxic AIDS and cancer chemotherapies.

In early 2000, Fauci shook hands with Bill Gates in the library of Gates’ $147 million Seattle mansion, cementing a partnership that would aim to control an increasingly profitable $60 billion global vaccine enterprise with unlimited growth potential. Through funding leverage and carefully cultivated personal relationships with heads of state and leading media and social media institutions, the Pharma-Fauci-Gates alliance exercises dominion over global health policy.

The Real Anthony Fauci details how Fauci, Gates, and their cohorts use their control of media outlets, scientific journals, key government and quasi-governmental agencies, global intelligence agencies, and influential scientists and physicians to flood the public with fearful propaganda about COVID-19 virulence and pathogenesis, and to muzzle debate and ruthlessly censor dissent.

https://rumble.com/vw1m5b-the-real-anthony-fauci-introduction-chapter-two.html

The scheme of lies, false data, and political divisiveness surrounding Pfizer jabs are finally collapsing. Friday on the Stew Peters Show, Dr. Robert Malone exposes confidential information from Pfizer containing fatal vaccine injuries and lists of extreme adverse events. In the premium interview, Dr. Malone evaluates the data and the consequences of the jabs.

https://rumble.com/vwglmp-top-secret-pfizer-documents-leaked-pfizer-knew-that-vaxx-would-kill-thousan.html

Friday funnies!!

https://rwmalonemd.substack.com/p/friday-funnies-c7a

Catastrophic consequences??

Nearly a year ago, Dr. Fauci touted ZYESAMI as a promising treatment for COVID-19. However, the drug appears no closer to receiving FDA approval. Meanwhile, treatments including remdesivir, Molnupiravir, Paxlovid and the COVID-19 vaccines were fast tracked to approval.

The members are seeking an explanation for the delayed review process and favoritism shown by federal health agencies for large drug manufacturers.

https://www.wispolitics.com/2022/u-s-sen-johnson-leads-colleagues-in-demanding-answers-from-dr-califf-and-dr-fauci/

The senator wrote, “Based on data from the Defense Medical Epidemiology Database (DMED), Thomas Renz, an attorney who is representing three Department of Defense (DoD) whistleblowers, reported that these whistleblowers found a significant increase in registered diagnoses on DMED for miscarriages, cancer, and many other medical conditions in 2021 compared to a five-year average from 2016-2020. For example, at the roundtable Renz stated that registered diagnoses for neurological issues increased 10 times from a five-year average of 82,000 to 863,000 in 2021.”

Senator Johnson also raised concerns that “some DMED data showing registered diagnoses of myocarditis had been removed from the database.”

The full text of the letter can be found here and below.

Read more coverage regarding the senator’s oversight efforts at The Blaze: Military spokesman claims 5 random years of DOD medical surveillance system were plagued by a giant glitch

https://www.ronjohnson.senate.gov/2022/2/sen-johnson-to-secretary-austin-has-dod-seen-an-increase-in-medical-diagnoses-among-military-personnel

The unexpected finding that the synthetic form of Vasoactive Intestinal Peptide (aviptadil) administered via inhalation was well tolerated and led to dampening of alveolar inflammation, radiological and clinical improvement of pneumonitis resulting from a checkpoint inhibitor therapy for melanoma, was the basis for this issued patent

~ posted by Jan, Y@h00 RLFTF finance conversations

Reply:

"The granting of this Swiss patent for the inhaled version of RLF-100 serves to further strengthen our growing intellectual property portfolio for this highly promising drug candidate" (RAM).

Our little peptide is still a promise and we won't drop it.

~ posted by Franz, Y@h00 RLFTF finance conversations

I think Big Pharma doesn’t like competition and it takes NIHanimals and other Big Gov criminals to make it happen, acquisition of a small competitor(s) for peanuts. When I saw Jon ditching the responsibilities of the CA and going to SUNY, I asked myself whyyyyy?? HOpium made me believe for a while longer but no more!! Robbery in progress???

——————>>>>

The Robert Langer-backed nanoparticle cancer biotech Bind ($BIND), after a decade in the business, looks to be at the end of the road after the company said it was seeking an approval for a “stalking horse” bid today from Pfizer ($PFE).

The company, which in April axed nearly 40% of its staff and filed for bankruptcy just a week later, is set to sell nearly all of its assets in a court-supervised deal to the New York Big Pharma for just under $20 million in cash--with Pfizer also agreeing to take on some of the “contractual liabilities” of the Boston biotech. Bind had raised nearly $100 million during its short life.

https://www.fiercebiotech.com/biotech/bankrupt-biotech-bind-eyes-20-million-sale-to-pfizer

Pharma-funded mainstream media has convinced millions of Americans that Dr. Anthony Fauci is a hero. He is anything but.

As director of the National Institute of Allergy and Infectious Diseases (NIAID), Dr. Anthony Fauci dispenses $6.1 billion in annual taxpayer-provided funding for scientific research, allowing him to dictate the subject, content, and outcome of scientific health research across the globe. Fauci uses the financial clout at his disposal to wield extraordinary influence over hospitals, universities, journals, and thousands of influential doctors and scientists—whose careers and institutions he has the power to ruin, advance, or reward.

During more than a year of painstaking and meticulous research, Robert F. Kennedy Jr. unearthed a shocking story that obliterates media spin on Dr. Fauci . . . and that will alarm every American—Democrat or Republican—who cares about democracy, our Constitution, and the future of our children’s health.

The Real Anthony Fauci reveals how “America’s Doctor” launched his career during the early AIDS crisis by partnering with pharmaceutical companies to sabotage safe and effective off-patent therapeutic treatments for AIDS. Fauci orchestrated fraudulent studies, and then pressured US Food and Drug Administration (FDA) regulators into approving a deadly chemotherapy treatment he had good reason to know was worthless against AIDS. Fauci repeatedly violated federal laws to allow his Pharma partners to use impoverished and dark-skinned children as lab rats in deadly experiments with toxic AIDS and cancer chemotherapies.

In early 2000, Fauci shook hands with Bill Gates in the library of Gates’ $147 million Seattle mansion, cementing a partnership that would aim to control an increasingly profitable $60 billion global vaccine enterprise with unlimited growth potential. Through funding leverage and carefully cultivated personal relationships with heads of state and leading media and social media institutions, the Pharma-Fauci-Gates alliance exercises dominion over global health policy.

The Real Anthony Fauci details how Fauci, Gates, and their cohorts use their control of media outlets, scientific journals, key government and quasi-governmental agencies, global intelligence agencies, and influential scientists and physicians to flood the public with fearful propaganda about COVID-19 virulence and pathogenesis, and to muzzle debate and ruthlessly censor dissent.

https://rumble.com/vw1m5b-the-real-anthony-fauci-introduction-chapter-two.html

As of today the checkpoint inhibitor lung disease patent from Advita is granted (published B1 status) by SwissREG.

~ posted by IG, Y@h00 RLFTF finance conversations

https://www.swissreg.ch/srclient/loadPatDocPdf/A2245C34750A590F2A5A747143F5C2BE30A253F6

The granted Advita patent is THE NEWS OF TODAY!

Everything else was already known to a certain extent.

There are further indications that the dispute with $NRXP will not be settled until after the court hearing on the secondary lawsuits in June or thereafter.

Read RLFTF's comment. Status Quo - Mediation is apparently suspended - apparently both parties are waiting for the rulings in the counterclaim. The rulings will also clarify the status of the parties. I speculate that both parties have deliberately and in collusion suspended mediation pending resolution of the cross-complaint. RLFTF speaks of having hopes to resolve the dispute amicably. But is obviously pushing for a landmark judgment in the counterclaim first. NRX is apparently also waiting for this.

~ posted by AdVita, Y@h00 RLFTF finance conversations

Since Dr Fauci will not be present to testify, who is Dr Fauci???

https://rumble.com/vq9fsp-plandemic-part-1-dr.-judy-mikovits.html

CDC Director, Surgeon General and Others Testify on COVID Response

CDC Director Dr. Rochelle Walensky, U.S. Surgeon General Vivek Murthy, and others testify before the House Select Subcommittee on the Coronavirus Crisis on the federal response to the COVID-19 pandemic.

https://www.c-span.org/video/?519008-1/cdc-director-surgeon-general-testify-covid-response