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The New York Times, a bastion of censorship and corruption, warns the world that “America Has a Free Speech Problem.”
By Tony Lyons, President, Skyhorse Publishing
In a bold but clearly disingenuous statement from its famed Editorial Board, “a group of opinion journalists whose views are informed by expertise, research, debate, and certain longstanding values,” the New York Times issued a cautionary statement:
“For all the tolerance and enlightenment that modern society claims, Americans are losing hold of a fundamental right as citizens of a free country: the right to speak their minds and voice their opinions in public without fear of being shamed or shunned.”
The Editorial Board pounded the point home:
“People should be able to put forward viewpoints, ask questions and make mistakes, and take unpopular but good-faith positions on issues that society is still working through—all without fearing cancellation…Freedom of speech requires not just a commitment to openness and tolerance in the abstract. It demands conscientiousness…We believe it isn’t enough for Americans to just believe in the rights of others to speak freely; they should also find ways to actively support and protect those rights.”
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“Despite all the lying, or maybe in reaction to it,” Tucker Carlson wrote, “Robert F. Kennedy Jr. is becoming a legitimate folk hero.”
He is a folk hero because he stood up, grabbed a bullhorn, and spoke truth to power. He’s risked everything and lost a lot. He’s realized that you either care about justice or you care about personal consequences. And for him there have been many.
After suppressing freedom of speech for two years, after defending a specific, myopic and harmful narrative, the Editorial Board of the New York Times decided it was the perfect time to take a strong stance against censorship and cancel culture.
The irony of the most powerful and impactful violator of First Amendment rights lamenting the lack of free speech and offering up ideas to protect the rights of Americans was palpable, inescapable, and despicable.
https://rwmalonemd.substack.com/p/mendacious-new-york-times-warning
American Conversations Hosts Christine Dolan and L Todd Wood speak with Tony Lyons of Skyhorse Publishing and medical freedom activist Sofia Karstens who tell the story behind Robert F Kennedy's book 'The Real Anthony Fauci'.
https://rumble.com/vuoh41-episode-3-the-authors-the-story-behind-robert-f-kennedys-book-the-real-anth.html
“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/
Vaccine: Micro Blood Clots in D-dimer tests??
https://rumble.com/vv70q7-emergency-medicine-doctor-shows-micro-blood-clots-in-d-dimer-tests.html
And just like that the FDA keeps pushing vaccines!!
FDA authorizes second COVID booster shot for all Americans over the age of 50
NEWS SARAH TAYLOR
March 29, 2022
https://www.theblaze.com/news/fda-authorizes-second-covid-booster-shot-for-all-americans-over-the-age-of-50
983,166 Americans have died of Covid-19 since early 2020. 907 Americans died yesterday —- 37,461 Canadians have died of Covid-19 since early 2020. 13 Canadians died today.
WE KNOW that RLF-100 (Zyesami, Aviptadil) would have saved, yes saved, the strong majority of these people if the FDA and Health Canada were doing what we pay them to do, truly operating in the People's best interests, that is, SAVING LIVES!!! WE KNOW that our perfect nature based remedy is both safe and effective. We know our "drug" is being suppressed by the FDA to allow vaccines to do their job - prevent Covid-19. The problem is the vaccines do not kill the disease once it is in the human body. RLF-100 not only kills the virus but also heals the ravaged lungs. It brings patients on their death beds back to life aggressively within several days of treatment and back home with a week or two.
Vaccines cannot do what RLF-100 can do. SO, THEY ARE NOT IN COMPETITION. SO, WHY ARE THE FDA AND HEALTH CANADA ACTING AS IF THEY ARE??? Vaccines helps to prevent catching the virus. Relief-100 kills the virus that has already invaded the body. Perfect teammates - Big Pharma and Relief Therapeutics together saving the world.
So what is it FDA, Health Canada are you under staffed? Do you understand the problem? Are you not capable of making a decision that your followers, we the People, all consider a no-brainer? It seem to us, the 99%, that those of you who are doctors are in violation of the Hippocratic Oath by holding back on a known drug and the only drug, that cures a known disease that has killed millions of people worldwide and continues to do so. You could lose your right to practice. Did you consider that?
~ posted by Reg, Y@h00 RLFTF finance conversations
March 3, 2022
Robert M. Califf, M.D.
Commissioner
U.S. Food and Drug Administration
Anthony S. Fauci, M.D.
Director
National Institute of Allergy and Infectious Diseases
Dear Dr. Califf and Dr. Fauci:
We are writing regarding a recent report of a physician practicing in Texas who has used a treatment—ZYESAMI—under the Right to Try Act to save COVID-19 patients’ lives.[1] Our understanding is the drug manufacturer, NRx Pharmaceuticals, applied for three Emergency Use Authorization’s (EUA) with the Food and Drug Administration (FDA) for ZYESAMI. NRx submitted its most recent EUA application on January 4, 2022 but the FDA has not yet granted this authorization. However, we are told the FDA refuses to review the data until the completion of clinical trials later this year.[2] We write to request information on the FDA’s review of ZYESAMI, as well as other information about treatment options for Americans suffering from COVID-19.
According to the physician, more than 20 patients suffering respiratory failure from COVID-19 received ZYESAMI as authorized under Right to Try.[3] At the end of the letter, we included the stories of three individuals that credit ZYESAMI with saving their lives. It is our understanding the patients received ZYESAMI after prior administration of remdesivir did not improve the patients’ conditions.[4] All the patients were at the very end stage of COVID and were not expected to recover. Upon receiving ZYESAMI, no serious adverse events associated with use were reported and 16 of the 20 patients left the hospital.[5] According to the physician, patients with ARDS normally have a 40 percent mortality rate.[6] With ZYESAMI, the mortality rate decreased to roughly 10 percent.[7]
We are grateful to hear of patients successfully receiving lifesaving treatment under Right to Try. However, we are concerned that the FDA, National Institute of Allergy and Infectious Diseases (NIAID) and other public health agencies are not doing all they can to make this promising treatment available to Americans suffering from COVID-19. Almost a year ago, Dr. Fauci touted ZYESAMI as a promising treatment for COVID-19.[8] However, 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.[9]
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.
To better understand the FDA’s decisions regarding an EUA for ZYESAMI, we respectfully request the following information:
1. Please provide a timeline of FDA and NIAID actions to review ZYESAMI as an emergency treatment for COVID-19.
2. Please provide documentation of any communications between FDA or NIAID and physicians or hospitals that are utilizing ZYESAMI under Right to Try.
3. Has the FDA ever accepted the data of ongoing clinical trials when issuing an EUA for a treatment for COVID-19? If so, please provide the treatment and its EUA.
4. Please explain why the FDA refuses to review ZYESAMI data until completion of a clinical trial.
5. For COVID patients that received remdesivir and steroids but did not recover, what is the FDA and NIAID’s current treatment recommendation?
Please provide this material as soon as possible but no later than 5:00 p.m. on March 17, 2022. Thank you for your attention to this urgent matter.
Did we/the people requesting responses ever get a response from these two bafoons?
~ posted by Sea Ulls, Y@h00 RLFTF finance conversations
Amy2 hours ago
You’re awesome Thomas!! People like you really can change the world!
Reply1
Brenda
Brenda4 hours ago
Awesome...thank you Thomas!
Reply
GeraldS
GeraldS13 hours ago
Tanks Thomas! You de man!
Reply2
Priviledged
Priviledged17 hours ago
@Thomas Impressive indeed. Did that go out this morning?
Reply92
Bogo
Bogo17 hours ago
Nice Job! Thank you!
Reply10
JohnnyD
JohnnyD17 hours ago
@Zaran ohhhhh they saw it…this Letter is the best news in months! Well done, Thomas!!!
Reply12
Brian A
Brian A17 hours ago
VERY well done, Thomas! Thank you for submitting that letter. And Yes, a lot of people read those letters, including some who are very influential.
I’ve been posting things like this to Twit “ter” too, and I was surprised to find someone with an FDA Twitter handle responded with a “Like.”
Honestly, I can’t imagine how people with a shred of decency, honor, ethics, and morality can idly standby at the FDA and permit this “slow-walk” to continue.
All we can do is continue to get the word out to as many people as possible. I think that’s probably more than half the battle…we’re relatively unknown to the majority of people…anywhere. So, we have to make ourselves known. At the FDA’s current pace, it’s pretty obvious there are Big interests who don’t want “VIP” to cross the lips of those who can get this across the Finish Line to help put an end to all of this needless suffering.
Again, Well Done!
Is there anything better than the original Zyesami/Aviptadil??? How can the people find out if they are not allowed to try it??? The world understands English, does the FDA/NIH???
PW, the people should and are clamoring for the best therapeutic for the times, Zyesami/Aviptadil
In our current roles as U.S. surgeon general and chief science officer for the U.S. Covid-19 Response, we have helped coordinate the United States’ fight against the coronavirus. Until recently, we’ve had the funding to make sure that there will be enough vaccines and antiviral drugs to meet the nation’s needs. Now, for the first time, we cannot order enough vaccines to provide boosters for all Americans if a fourth dose is deemed necessary in the fall. If we need variant-specific vaccines, we will not have the funds to secure them, deliver them or administer them.
https://www.nytimes.com/2022/03/29/opinion/covid-funding-america.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/
Ms Pegs1, I thought so too. The letter was posted by Thomas at Y@h00 RLFTF finance conversations. Everyone interested in the outcome of ZYESAMI clinical trials should write a letter to the FDA/NIH to complain about the clinical trials of vaccines vs clinical trials of therapeutics. It has been disgraceful to say the least.
The New York Times just published my letter in response to an article, "What could happen if there's no more Covid-19 funding".
In a controlled clinical trial at Houston Methodist Hospital, a drug named Aviptadil, the "vip" part of the name stands for "vaso-intestinal peptide, has proven to be remarkably effective in treating critically ill Covid 19 patients.
Patients treated with intravenous Aviptadil-VIP were followed for at least 60 days after ICU admission. They were compared with 24 individuals with comparable COVID-19 and co-morbidities, who received only standard-of-care treatment. Of the 21 patients treated with Aviptadil, 19 survived to day 28, 17 survived to day 60 compared to only five survivors of the 24 individuals in the standard-therapy group (81% vs. 21%; p < 0.0001). Improved radiographic appearance was seen in both lungs of 17 VIP treated patients but only one lung of two VIP treated patients who subsequently died. Four out of five patients treated with Aviptadil on Extracorporeal Membrane Oxygenation were successfully de-cannulated and survived. In comparison, only three out of 13 standard-therapy patients survived.
Initial release of the data revealed increased survival rates that correlated to a significant reduction in plasma IL-6 and improved lung-surfactant production.", has shown to be effective.
Currently in the TESICO trial in the USA, Aviptadil, produced by Relief Therapeutics with their partner NeuroRx, also needs continued funding for this trial.
Does anyone read those letters?
~ Posted by Thomas, Y@h00 RLFTG
When is mRNA not really mRNA? ———
What is pseudouridine, why is it being injected into you, and why should you care
https://rwmalonemd.substack.com/p/when-is-mrna-not-really-mrna
“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.”
.
.
.
“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/
Meanwhile, back at the ranch, what has happened to Dr. Anthony Fauci? Last we heard from him was when he was prominently featured on the Woke A_F podcast , which was immediately criticized for spreading vaccine misinformation. Well, he was able to overcome a Senate attempt to break up his empire, with help from Uniparty members from both sides of the aisle. And the religiously masked Dr. Fauci is now back to peddling more dark visions of impending COVID-19 disaster.
“Dr. Anthony Fauci this week said that it is “likely we’re not done” with the Chinese coronavirus “when it comes to vaccines,” leaving the door open for even more jabs into the future, which he said remains uncertain.
While recent polling data shows Americans finally moving past the virus and returning to behaviors aligning with their lives pre-pandemic, Fauci is not deeming anything over.
When asked about coronavirus vaccinations, Fauci (uncharacteristically) said they “don’t know” what will come next.
“It is likely that we’re not done with this when it comes to vaccines,” he told CNBC, adding that “everybody wants to return to normal, everybody wants to put the virus behind us in the rearview mirror, which is, I think, what we should aspire to.” However, his attitude seemed less than optimistic as he said metrics fell in the right direction for other variants before the situation went south.”
Inexplicably, his timing is precisely aligned with the lobbying with FDA and the HHS for yet more vaccine boosters (fourth dose – is this really a vaccine by the commonly understood definition?) by the CEOs of Moderna and Pfizer. Some might see this as evidence supporting Racketeer Influenced and Corrupt Organizations Act (RICO) charges. Of course, I am not a lawyer, and not qualified to opine on such matters.
https://rwmalonemd.substack.com/p/the-great-pivot-of-spring-2022-v
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
Dead end Bill???
https://rumble.com/vxcy0k-never-seen-before-bill-gates-repeatedly-tells-trump-not-to-study-ill-effect.html
Relief Therapeutics’ Wholly Owned Subsidiary, APR Applied Pharma Research, Reports In Vivo Data Published in the Peer Reviewed, International Journal of Molecular Sciences, Indicating Prolonged Release of Amino Acids Using Its Physiomimic™ Technology May Have Benefits for the Treatment of PKU
https://relieftherapeutics.com/news-and-events
What can AVIPTADIL do for you???
VIP stimulates contractility in the heart, causes vasodilation, increases glycogenolysis, lowers arterial blood pressure and relaxes the smooth muscle of trachea, stomach and gallbladder. In humans, the vasoactive intestinal peptide is encoded by the VIP gene. ~ Wiki
CDC on Alzheimer’s —-Key Facts
Alzheimer’s disease is not a normal part of aging.
6.2 million Americans are estimated to be living with Alzheimer’s disease in 2021.
Symptoms usually begin after age 60, but Alzheimer’s disease likely starts a decade or more before problems first appear.
Risk factors include aging, diabetes, high blood pressure (hypertension), smoking cigarettes, and a family history of dementia.
Alzheimer’s death rates increased 33% from 1999 to 2019.
An estimated two-thirds of those who die of dementia do so in nursing homes, compared with 20% of people with cancer and 28% of people dying from all other conditions
In 2020, more than 11 million Americans provided an estimated 15.3 billion hours of unpaid care, a contribution to the nation valued at $257 billion.
Currently, there is no cure. There are pharmaceutical and behavioral interventions for managing symptoms.
Persons with dementia, their families and caregivers can benefit from care planning.
https://www.cdc.gov/dotw/alzheimers/index.html
VIP injected intracerebroventricularly or delivered intranasally prevented impairments in spatial learning and memory associated with cholinergic blockade. These studies suggest both an unusual therapeutic strategy for treatment of Alzheimer deficiencies and a means for noninvasive peptide administration to the brain.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC40251/
“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/
Vaccine: Micro Blood Clots in D-dimer tests??
https://rumble.com/vv70q7-emergency-medicine-doctor-shows-micro-blood-clots-in-d-dimer-tests.html
Consequences??
https://rumble.com/vyddo9-cruz-asked-if-hell-vote-for-ketanji-brown-jackson.-he-answers-bluntly..html
Consequences??
https://rumble.com/vyi2nc-ketanji-brown-jackson-implies-old-laws-are-unfair-for-some-sex-offenders.html
Consequences??
https://rumble.com/vnhb19-where-are-the-feds-sending-the-illegals-todd-bensman-with-sebastian-gorka-o.html
Consequences??
https://rumble.com/vwdzx3-republican-opponent-to-ilhan-omar-drops-new-ad-and-its-devastating.html
Consequences??
https://rumble.com/vnjaul-trump-tears-into-ilhan-omar-she-married-her-own-brother.html
Consequences??
https://rumble.com/vvktu6-royce-white-for-congress..html
Consequences??
https://rumble.com/vy8vih-steve-bannon-gives-royce-white-a-shoutout.html
Consequences??
https://rumble.com/vyjtws-biden-tells-us-troops-theyre-going-to-ukraine-white-house-panics.html
Consequences??
https://rumble.com/vyfs4r-victor-davis-hanson-on-why-the-architect-of-globalism-larry-fink-is-changin.html
Friday Funnies —- “Laugh and the world laughs with you, snore and you sleep alone.”
https://rwmalonemd.substack.com/p/friday-funnies-06c
Catastrophic consequences??
https://rumble.com/vx0mvh-stolen-elections-have-consequences-trump-ad-torches-biden.html
Capitol police on January 6…
https://rumble.com/vh52u9-watch-u.s.-capitol-police-gave-protesters-ok-to-enter-capitol.html
Ted Cruz went ballistic over “Right to Try” drug with a group of fellow Republicans
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Worst of all, in a move seemingly aimed at preventing key competition for the Biden administration’s preferred Big Pharma pals, government bureaucrats are refusing Americans their right to access life-saving medication under the federal Right to Try Act.
Not even one Right to Try Act-related medication has been approved to treat COVID, which would officially allow patients to use drugs that are generally safe to fight the virus.
While they aren’t likely to turn anyone into a billionaire, they have incredible potential to save lives.
https://culturewatchnews.com/ted-cruz-went-ballistic-over-right-to-try-drug-with-a-group-of-fellow-republicans/
Catastrophic consequences??
https://rumble.com/vpowow-senator-warren-gets-desperate-trying-to-explain-bidens-high-gas-prices.html
Look at the last LinkedIn post form today of Relief Therapeutics at the 2022 Annual Clinical Genetics Meeting in Nashville… Look at the photo of the crew - look at right upper part of the the GOLIKE billboard - it writes on a blue background (GOLIKE) “US LAUNCH COMING”
https://www.linkedin.com/posts/relief-therapeutics-holding-sa_acmgmtg22-pku-pkugolike-activity-6912769535225827328-L2Zm
~ posted by IG, Y@h00 RLFTF finance conversations
Catastrophic consequences??
https://rumble.com/vyj2mm-she-cannot-define-what-a-woman-is.html
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/
Elections have consequences. Stolen elections have catastrophic consequences!!
https://rumble.com/vul23q-episode-26-stealing-elections-feat.-rep.-marjorie-taylor-greene-firebrand-w.html
“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.”
.
.
.
“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/
Meanwhile, back at the ranch, what has happened to Dr. Anthony Fauci? Last we heard from him was when he was prominently featured on the Woke A_F podcast , which was immediately criticized for spreading vaccine misinformation. Well, he was able to overcome a Senate attempt to break up his empire, with help from Uniparty members from both sides of the aisle. And the religiously masked Dr. Fauci is now back to peddling more dark visions of impending COVID-19 disaster.
“Dr. Anthony Fauci this week said that it is “likely we’re not done” with the Chinese coronavirus “when it comes to vaccines,” leaving the door open for even more jabs into the future, which he said remains uncertain.
While recent polling data shows Americans finally moving past the virus and returning to behaviors aligning with their lives pre-pandemic, Fauci is not deeming anything over.
When asked about coronavirus vaccinations, Fauci (uncharacteristically) said they “don’t know” what will come next.
“It is likely that we’re not done with this when it comes to vaccines,” he told CNBC, adding that “everybody wants to return to normal, everybody wants to put the virus behind us in the rearview mirror, which is, I think, what we should aspire to.” However, his attitude seemed less than optimistic as he said metrics fell in the right direction for other variants before the situation went south.”
Inexplicably, his timing is precisely aligned with the lobbying with FDA and the HHS for yet more vaccine boosters (fourth dose – is this really a vaccine by the commonly understood definition?) by the CEOs of Moderna and Pfizer. Some might see this as evidence supporting Racketeer Influenced and Corrupt Organizations Act (RICO) charges. Of course, I am not a lawyer, and not qualified to opine on such matters.
https://rwmalonemd.substack.com/p/the-great-pivot-of-spring-2022-v
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
Dead end Bill???
https://rumble.com/vxcy0k-never-seen-before-bill-gates-repeatedly-tells-trump-not-to-study-ill-effect.html
Top Secret Pfizer Documents Leaked: Pfizer Knew That Vaxx Would Kill Thousands…???
https://rumble.com/vwglmp-top-secret-pfizer-documents-leaked-pfizer-knew-that-vaxx-would-kill-thousan.html
Journal of Leukocyte Biology
Early View
ARTICLE - COVID-19 AND RELATED TOPICS
VIP plasma levels associate with survival in severe COVID-19 patients, correlating with protective effects in SARS-CoV-2-infected cells
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First published: 24 March 2022
https://doi.org/10.1002/JLB.5COVA1121-626R
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Our findings support and encourage clinical trials with VIP in COVID-19 patients, which are in progress with intravenous 38 and inhaled 39, 40 formulations and are expected to be disclosed throughout this year. An initial release of the data, as preprint, shows an increase in survival rates and reduction of IL-6 levels on those who received intravenous AVIPTADIL (VIP) 62. Our present data may substantiate additional larger trials with VIP, an overlooked molecule associated with antiviral, anti-inflammatory, and enhanced survival activities.
https://jlb.onlinelibrary.wiley.com/doi/10.1002/JLB.5COVA1121-626R
~ posted by IG, Y@h00 RLFTF finance conversations
Did the FDA know about crimes of extraordinary scale???
https://rumble.com/vx6yvt-161-lawyers-working-on-pfizers-crimes-of-extraordinary-scale.html
JK, not 1:10 but yes to 1:7. We are still in the clutches of the NIH and the FDA, as of 3/17/2022, is in contempt of the US Congress.
Contempt of Congress is the act of obstructing the work of the United States Congress or one of its committees. Historically, the bribery of a U.S. senator or U.S. representative was considered contempt of Congress. ~ wiki
Seems to me the FDA is in contempt of the U.S. Congress or are they in Federal Court, again???
https://www.reuters.com/legal/government/wait-what-fda-wants-55-years-process-foia-request-over-vaccine-data-2021-11-18/
I agree, we are in a political war.
We need RLF-100/ZYESAMI/AVIPTADIL now!!
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.
To better understand the FDA’s decisions regarding an EUA for ZYESAMI, we respectfully request the following information:
1. Please provide a timeline of FDA and NIAID actions to review ZYESAMI as an emergency treatment for COVID-19.
2. Please provide documentation of any communications between FDA or NIAID and physicians or hospitals that are utilizing ZYESAMI under Right to Try.
3. Has the FDA ever accepted the data of ongoing clinical trials when issuing an EUA for a treatment for COVID-19? If so, please provide the treatment and its EUA.
4. Please explain why the FDA refuses to review ZYESAMI data until completion of a clinical trial.
5. For COVID patients that received remdesivir and steroids but did not recover, what is the FDA and NIAID’s current treatment recommendation?
Please provide this material as soon as possible but no later than 5:00 p.m. on March 17, 2022. Thank you for your attention to this urgent matter.
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/
Where are the fact-checkers on the Republicans/ZYESAMI story???
https://rumble.com/vxxeoh-march-20-2022.html
Of course, the government’s help went far beyond mere approval.
Joe Biden went on wild spending sprees purchasing vaccines for the entire population of the United States — in some cases before the Food and Drug Administration (FDA) even approved the drugs in question for emergency use.
https://rumble.com/vwglmp-top-secret-pfizer-documents-leaked-pfizer-knew-that-vaxx-would-kill-thousan.html
https://rumble.com/vkgelv-how-to-speak-bidenese.html
Oooh Christopher Wick left Alexion Pharmaceuticals, a subsidiary of AstraZeneca, for this newly created positon! I'm wondering if this is a sign of a new partnership with Big Pharma? ??????
Also, glad to see the uplisting seems to be going smoothly so far!
~ posted by Major, Y@h00 RLFTF finance conversations
Geneva, Switzerland, March 21, 2022 – RELIEF THERAPEUTICS Holding SA (SIX: RLF, OTCQB: RLFTF, RLFTY) (“Relief”), a biopharmaceutical company seeking to provide patients therapeutic relief from serious diseases with high unmet need, today announced the appointment of Christopher Wick to the newly created position of Senior Director, Head of U.S. Sales. In this position, Mr. Wick will be responsible for building out and leading the company’s U.S. sales team.
“The expansion of our pipeline and commercialized product portfolio, garnered as a result of our collaboration with Acer Therapeutics and the strategic acquisition, last year, of APR Applied Pharma Research SA, have allowed us to proactively plan for U.S. market penetration, initially, for APR’s currently marketed flagship PKU GOLIKE® to treat phenylketonuria and the potential launch of ACER-001 to treat Urea Cycle Disorders, which has a Prescription Drug User Fee Act (PDUFA) target action date of June 5, 2022 ,” stated Raghuram (Ram) Selvaraju, Chairman of Relief. “In this new position, Christopher will work closely with our Head of U.S. Commercial Operations, Anthony Kim, to build our capabilities in this all important market, in order to ensure our commercial success. His highly impressive background, punctuated by extraordinary sales success during more than 20 years at ‘big pharma,’ including with Alexion Pharmaceuticals, GlaxoSmithKline and Novartis, makes Christopher a highly coveted addition to our team.”
Prior to joining Relief, Mr. Wick was, since 2018, Regional Sales Director for Alexion Pharmaceuticals, Inc., where he developed and led two high performing Excellence Award winning teams which achieved best in the nation sales for two product launches of Soliris®, for the treatment of neuromyelitis optica spectrum disorder (NOSD) and generalized myasthenia gravis (gMG). Earlier, from 2015 to 2018, he served as the company’s Southwest Regional Account Manager, where he cultivated a regional key opinion leader physician network while launching two of Alexion’s enzyme replacement therapies for ultra-rare disease.
From 2007 until 2015, Mr. Wick served in positions of increasing responsibility at GlaxoSmithKline, most recently, from 2012 to 2015, as Southwest Health Systems Account Manager helping to ensure early adoption of the company’s launch products as well as the entire pharmaceutical and biologic portfolio. In that role, he was responsible for Hospital System contracts, and collaborating with GlaxoSmithKline’s largest and most complex accounts in the Integrated Delivery Networks (IDN) and Hospital Customer Segment.
Earlier, from 1999 until 2007, Mr. Wick was an Executive Account Manager at Novartis. While there, he contributed to both Specialty and Hospital Sales, served as a National Training Leader and Regional Trainer and consistently achieved a top 15% sales ranking.
Mr. Wick attended Purdue University and earned a Bachelor of Arts in Business Administration from New Mexico State University.
Ted Cruz went ballistic over “Right to Try” drug with a group of fellow Republicans
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Worst of all, in a move seemingly aimed at preventing key competition for the Biden administration’s preferred Big Pharma pals, government bureaucrats are refusing Americans their right to access life-saving medication under the federal Right to Try Act.
Not even one Right to Try Act-related medication has been approved to treat COVID, which would officially allow patients to use drugs that are generally safe to fight the virus.
While they aren’t likely to turn anyone into a billionaire, they have incredible potential to save lives.
https://culturewatchnews.com/ted-cruz-went-ballistic-over-right-to-try-drug-with-a-group-of-fellow-republicans/
Free speech is over-rated...so be happy! <sarcasm>
https://rwmalonemd.substack.com/p/sunday-strip-0e8
After Russell Brand is attacked by big media, Elon Musk and Jordan Peterson defend the comedian
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"In Brand's world, there should be room for 'alternative opinions' such as Rogan's. Maybe the 'mainstream media' are just jealous that Rogan is so successful, Brand suggested," the article noted, and then admitted, "Maybe we're jealous because Rogan's viewers trust him."
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"With so many mainstream media companies saying @rustyrockets [Russell Brand] is crazy/dangerous, I watched some of his videos," Musk wrote on Twitter in a reply to The Independent. "Ironically, he seemed more balanced & insightful than those condemning him! The groupthink among major media companies is more troubling. There should be more dissent."
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Jordan Peterson also defended Brand by saying, "An appalling union of large corporations, media agencies and government. What did Mussolini call that again?"
Peterson is likely referencing this quote: "Fascism should more properly be called corporatism, since it is the merger of state and corporate power." This quote is commonly attributed to Benito Mussolini, but there doesn't seem to be any proof that the Italian fascist leader ever said it.
https://www.theblaze.com/news/russell-brand-elon-musk-jordan-peterson
Get your clot shot, you know its NOT safe, its NOT effective, and its certainly NOT free.
The FOURTH Clot Shot, is proof this is NOT WORKING and we need AVIPTADIL AND OR ZYESAMI. ~ posted by Joe Kaplan @ iHub
https://rumble.com/vxeqvu-pathologist-on-ryan-cole-on-the-mystery-blood-clots.html
We need ZYESAMI/AVIPTADIL/RFL-100 now!!
Dear Dr. Califf and Dr. Fauci:
We are writing regarding a recent report of a physician practicing in Texas who has used a treatment—ZYESAMI—under the Right to Try Act to save COVID-19 patients’ lives.[1] Our understanding is the drug manufacturer, NRx Pharmaceuticals, applied for three Emergency Use Authorization’s (EUA) with the Food and Drug Administration (FDA) for ZYESAMI. NRx submitted its most recent EUA application on January 4, 2022 but the FDA has not yet granted this authorization. However, we are told the FDA refuses to review the data until the completion of clinical trials later this year.[2] We write to request information on the FDA’s review of ZYESAMI, as well as other information about treatment options for Americans suffering from COVID-19.
According to the physician, more than 20 patients suffering respiratory failure from COVID-19 received ZYESAMI as authorized under Right to Try.[3] At the end of the letter, we included the stories of three individuals that credit ZYESAMI with saving their lives. It is our understanding the patients received ZYESAMI after prior administration of remdesivir did not improve the patients’ conditions.[4] All the patients were at the very end stage of COVID and were not expected to recover. Upon receiving ZYESAMI, no serious adverse events associated with use were reported and 16 of the 20 patients left the hospital.[5] According to the physician, patients with ARDS normally have a 40 percent mortality rate.[6] With ZYESAMI, the mortality rate decreased to roughly 10 percent.[7]
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https://www.wispolitics.com/2022/u-s-sen-johnson-leads-colleagues-in-demanding-answers-from-dr-califf-and-dr-fauci/
JK, we seem to be going into another war, instigated by lousy energy/foreign policies, against gangsters of the world like China, Russia, Iran, Afghanistan Taliban, socialist/Marxist democrat Venezuela, you name it, we are up against all that. Our energy policy has driven the oil price beyond USD $80 bbl. and the criminals are getting funding?? The incompetent are funding Ukraine with $14 billion to fend off the Russian invasion while the USA is getting invaded!! No one is going to be paying attention to sociopath/“Moran” Fauci since everyone will be engaged in “survival of the fittest “.
https://rumble.com/vb8pbf-open-borders-makes-you-sick.html
Zyesami (Aviptadil) is a formulation of synthetic human Vasoactive Intestinal Peptide (VIP), which was first discovered in 1970. VIP is known to target the VPAC1 receptor of the alveolar type II (ATII) cell and protect that cell against all manner of injuries, including smoke inhalation, exposure to stomach acid, and exposure to infectious agents. In addition, VIP prevents apoptosis, blocks cytokines, lowers TNFa levels, reverses CD4/CD8 ratio, and reduces cough and dyspnea in nonclinical and clinical studies.
Although first identified in the intestinal tract, VIP is produced throughout the body, primarily concentrated in the lungs. In addition, VIP has been shown in more than hundreds of peer-reviewed studies to have potent anti-inflammatory/anti-cytokine activity in animal models of respiratory distress, acute lung injury, and inflammation says the Company.
Because of its lack of toxicity and low cost of manufacture compared to proprietary biologics, VIP may be uniquely attractive to those focused on global countermeasures against COVID-19, says the Company.
https://www.precisionvaccinations.com/vaccines/zyesami-aviptadil-therapeutic
Right or wrong, it is a response to the mandates jackassery and mainstream media propaganda.
Later, Rep. Joseph Shapiro, a Keene Democrat, warned colleagues that the GOP’s prioritization of individual rights are pushing state public health policy in a single direction.
“We have tipped the scales in terms of privacy, personal liberty and choice, we are not taking into consideration the greater good for the greater number of people,” Schapiro said.
“Yes, we have a lot of bills, we all notice that,” said Republican Rep. Dennis Acton of Newington. “But these were not just brought out of thin air. They are a response to what we feel is the overplaying of a hand by the medical system.”
https://www.nhpr.org/nh-news/2022-03-07/ivermectin-nh-pharmacists-state-legislature
In short, our immune system by and large is incredibly effective at working around the clock to keep a myriad of infections and diseases at bay while simultaneously being able to identify between outside invaders and our own cells and effectively prioritise what to attack and what to protect. However, occasionally, either due to genetic factors or rampant viral infections like COVID-19, our immune system can become overzealous and go rogue - attacking and killing everything in sight, including healthy cells in the body. When that happens it is referred to as a cytokine storm and it may be killing around half of severe COVID-19 patients.
https://www.forbes.com/sites/claryestes/2020/04/16/what-is-the-cytokine-storm-and-why-is-it-so-deadly-for-covid-19-patients/
The vaxx is supposed to help identify/fight off the invader in order to avoid the killing cytokine storm.
Once under attack, one should get the best medical advice and have access to the available arsenal of prescribed medicines, supplements and vitamins.
The vaxx can be a a lots Trojan horse.
https://rumble.com/vxumcl-is-this-necessary.html
https://pubmed.ncbi.nlm.nih.gov/34466270/
On the other hand, thanks to the advent of computers and the internet, people know Ivermectin is part of the arsenal of medicines.
https://rumble.com/vnqvjh-cnn-openly-lying-could-cost-lives.html
I use NAC…
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649937/
And glycine…
https://pubmed.ncbi.nlm.nih.gov/33783984/
And or DMG…
https://www.webmd.com/vitamins/ai/ingredientmono-859/dimethylglycine-dmg
Additional questions for Cruz, et. al to ask:
Why has Activ-3b NIH/NIAID trial taken ~1 year to get ~400 patients & ~18 months to get 644 patients?
+ While BP trials fill 1,000 patient trials in less than 1 month.
Can NIH/NIAID help accelerate awareness and enrollments? If not, why not?
+ Why hasn't NIH/NIAID done more to support this trial?
Are severely ill Covid patients a focus for NIH/NIAID? If not, why not?
~ posted by Equalizer, Y@h00 RLFTF finance conversations
INTERESTINGLY, there is a Republican Sponsored Bill pending in the New Hampshire Legislature that if passed would allow Pharmacists, without prescription, to dispense Ivermectin.
“During the pandemic, COVID-19 vaccine skeptics and anti-vaccine activists have latched onto ivermectin, though it has not been approved by the FDA as a treatment for COVID-19, nor is there evidence to support that it can treat the virus.
Supporters of the bill said granting broad access to ivermectin, which is available over-the-counter in some countries and also used in veterinary medicine will allow individuals to make medical choices denied to them by the medical establishment.”
https://www.nhpr.org/nh-news/2022-03-07/ivermectin-nh-pharmacists-state-legislature
https://www.seacoastonline.com/story/news/2022/03/09/ivermectin-could-dispensed-nh-without-prescription-if-bill-passes/9441560002/
Doesn’t this rally a cry and line of action for Relief and NRXP, to seek the same approval, irrespective of EUA, as is being done with Ivermectin. Ivermectin has not received FDA approval for the treatment of Covid, as a the first article mentions.
What storm can be created with this??
Thoughts? Those in New Hampshire ought to reach out to the same Republican Legislators involved in sponsoring the Bill. And outside of New Hampshire, perhaps an avenue of relief from the oppressive regime of the current FDA.
~ posted by BOGO, Y@h00 RLFTF finance conversations
“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.”
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“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/
Meanwhile, back at the ranch, what has happened to Dr. Anthony Fauci? Last we heard from him was when he was prominently featured on the Woke A_F podcast , which was immediately criticized for spreading vaccine misinformation. Well, he was able to overcome a Senate attempt to break up his empire, with help from Uniparty members from both sides of the aisle. And the religiously masked Dr. Fauci is now back to peddling more dark visions of impending COVID-19 disaster.
“Dr. Anthony Fauci this week said that it is “likely we’re not done” with the Chinese coronavirus “when it comes to vaccines,” leaving the door open for even more jabs into the future, which he said remains uncertain.
While recent polling data shows Americans finally moving past the virus and returning to behaviors aligning with their lives pre-pandemic, Fauci is not deeming anything over.
When asked about coronavirus vaccinations, Fauci (uncharacteristically) said they “don’t know” what will come next.
“It is likely that we’re not done with this when it comes to vaccines,” he told CNBC, adding that “everybody wants to return to normal, everybody wants to put the virus behind us in the rearview mirror, which is, I think, what we should aspire to.” However, his attitude seemed less than optimistic as he said metrics fell in the right direction for other variants before the situation went south.”
Inexplicably, his timing is precisely aligned with the lobbying with FDA and the HHS for yet more vaccine boosters (fourth dose – is this really a vaccine by the commonly understood definition?) by the CEOs of Moderna and Pfizer. Some might see this as evidence supporting Racketeer Influenced and Corrupt Organizations Act (RICO) charges. Of course, I am not a lawyer, and not qualified to opine on such matters.
https://rwmalonemd.substack.com/p/the-great-pivot-of-spring-2022-v
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
Dead end Bill???
https://rumble.com/vxcy0k-never-seen-before-bill-gates-repeatedly-tells-trump-not-to-study-ill-effect.html
There are NIHanimals and then there are, DOJanimals???
https://rumble.com/vxlvp3-this-is-going-to-backfire.html
Zaran8 hours ago
NIH MONTHLY REVIEW PROCESS (?); LEUPPI Inhaler trial ending March 2022, NOW! Mediation results (?) Ron and Ted's mystery show-down by 5 PM tomorrow... Lots of possibilities, when a rocket ignites, it is hard to catch up with it.... buy now if you feel positively about this company and it's potential, otherwise you will be looking at a lost opportunity of several hundred percent when it initially pops
the drug does what has been reported, the studies are and have confirmed this, Publicity is beginning to build on
new platforms, yes, we've been battered, we have been beaten, we have been lied to and mis-represented, and as a result...
these are tremendous prices for any investor to make a nod
imho
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Replies
RC1 hour ago
@Zaran You just might be the first one to get this rocket thing right in a long time.
Bullish
Lt. Francis5 hours ago
Right on Zaran. I share your views completely. You have always been a staunch RT supporter.
Great Job!
Sea Change is coming.
GLTU - GLTA
Bobby6 hours ago
@Zaran I'm strapped on very tightly to this rocket
POSTS Y@h00 RLFTF
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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/
It is not enough to have questions, you have to be proactive, reorganize/decentralize a federal government agency, led by unelected officials, and engaged in “irrational interference”!
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“We’ve learned a lot over the past two years, but one lesson in particular is that no one person should be deemed “dictator-in-chief.” No one person should have unilateral authority to make decisions for millions of Americans,” said Dr. Paul. “To ensure that ineffective, unscientific lockdowns and mandates are never foisted on the American people ever again, I’ve introduced this amendment to eliminate Dr. Anthony Fauci’s position as Director of the National Institute of Allergy and Infectious Diseases, and divide his power into three separate new institutes. This will create accountability and oversight into a taxpayer funded position that has largely abused its power, and has been responsible for many failures and misinformation during the COVID-19 pandemic.”
https://www.paul.senate.gov/news/dr-rand-paul-introduces-amendment-eliminate-dr-faucis-position-director-niaid
Who really cares???
This is a very good article describing and explaining FDA powers and who “POLICES” the FDA.
Generally, we obviously know the Political Powers who control the FDA. But this is a teaching, going more in depth into the historical and current day mechanisms that may be used. Clearly, Biden’s vaccine policy was the King in the room, as was conformity compliance with BP’s collusion/corruption of the process, on what therapeutics are SOC and get approved.
But here we are now, truly in an amazing position.
We are the only therapeutic left in a Trial run/funded by the NIH after a field of over 600 have been stopped. We, Zyesami/Aviptadil are known to Congress and the Senate, and investigation is being sought as to the Non-Approval. We have dozens of continued institutional share holders. We have Covariants tearing-up China and Germany, by reported news yesterday. We have the Biden policy on the vaccines that foresees/expects all Americans to have to take a Covid vaccine/booster yearly, like the flu. And certainly, we have many of our politicians holding stock in these BP companies looking for returns.
How much power do these Senators/Congressman have over the FDA? Read the paper.
https://dash.harvard.edu/bitstream/handle/1/8852216/Cook.html?sequence=2&isAllowed=y
~ posted by Bogo, Y@h00 RLFTF finance conversations
“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.”
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/
There is another important element in the national vaccine program, which is the requirement to keep the vaccine production facilities up and running. These facilities are producing a biological product; they must be kept in production or the process for re-licensure is onerous, if not impossible. In the case of seasonal flu, one of the justifications for the yearly vaccine is to keep the manufacturing plants running and ready for business in case of a truly severe strain of flu or some other, unknown pathogen become a threat. If those facilities are moth-balled, they can’t be brought back on line quickly. Bet you did not know that. One major reason for pushing annual influenza vaccines is to maintain influenza vaccine manufacturing capacity. The industry term used is “warm base manufacturing”. Of course, this results in a very nice annual “cash cow” for the vaccine industry, one which gets annually milked for a tidy guaranteed profit. The term “rent seeking behavior” applies. The same is true of the various “biodefense” vaccines and products which are maintained in the “strategic national stockpile”. In the context of Smallpox, these include ACAM2000. These products have half lives, which is to say that even though they are (hopefully) not used, they still have to be replaced every few years. Again, nice predictable profit. The corporation “Emergent Biololutions” has become particularly adept at exploiting this “market opportunity”, and has managed to monopolize many of the biodefense-related vaccines and products which the US Government purchases for the Strategic National Stockpile, including ACAM2000.
https://rwmalonemd.substack.com/p/safe-and-effective
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
G-Money7 hours ago
All the recent media coverage mentions zyesami and nrxp. To the casual observer there is nothing that points back to RLFTF. It's not surprising that there's no real price movement. Where's the PR educating/reminding the public that RLFTF is the patent holder of Aviptadil and that nrxp is a contractor?And that RLF-100 is the commercial name for Aviptadil and zyesami is currently just another name for RLF-100? We need to keep our name at the forefront of all things Aviptadil. That takes media relations personell. Don't we have any of those?
Hello All,
~ posted by G-Money, Y@h00 RLFTF finance conversations
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You are still here, and I am still here, in the unbelievable geopolitical world of March 2022.
On the lack of news or PR from Relief Therapeutics.
I have just read @G-Money on my daily morning read of this forum.
Right now I am not worried about the lack of news from Relief because my reading is that mediation is still ongoing. The removal of Dr Javitt as CEO of NRx was the key to any progress and look how long that took - 2 weeks. And it took that long because he is a majority shareholder of NRx and gathering all the evidence to ensure that he stepped down would have needed an incredible amount of external and internal negotiations.
While all this is happening there is no way Relief would issue any PR or address the public perception of Zyesami - their lawyers would have told them not to. I know from experience.
What will also not happen is a PR telling us the full details of the mediation because when it finishes there will be a lot of non-disclosure agreements. We will simply have to put together in our heads a schema of what we think happened from the events that will develop in front of us. Just the little piece of information that told us that NRx will now concentrate on the US market tells us a lot already about one part of the mediation : territory. Relief have won that round already. Going forward we will simply have to do more detective work like that from the events that develop.
Everything so far confirms the trust I have in Relief's management on this crazy affair.
We will be OK, we are OK.
Have a good week all.
~ posted by IlkaS, Y@h00 finance conversations
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https://rumble.com/vq9fsp-plandemic-part-1-dr.-judy-mikovits.html
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Can we get Zyesami out of NIHanimals jail before dollar collapses???
https://eurasiantimes.com/petro-dollar-vs-petro-yuan-is-china-set-to-replace-u-s-as-the-biggest-player-in-m-east-as-ties-grow-with-saudi-arabia/
This is great! Thanks again PW!
Many thanks PW!
If not, I will start my letter to my U.S. Senator/Representative as follows:
1- I will reference March 3, 2022 Letter from Congress to the FDA & Fauci regarding Zyesami:
2- Reference brief description of therapeutic/AVIPTADIL/ZYESAMI/RLF-100
3- Ask congressmen to join colleagues requesting answers from the FDA
& Fauci