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What could AVIPTADIL/RLF-100 do for “the people”?
Vasoactive intestinal peptide (VIP), a peptide produced by immune cells, exerts a wide spectrum of immunological functions that control the homeostasis of the immune system. In the last decade, VIP has been clearly identified as a potent anti-inflammatory factor, both in innate and adaptive immunity.
https://pubmed.ncbi.nlm.nih.gov/16312132/
And the experimental vaccine??
Long COVID and post-vaccine syndrome share a high degree of overlap as the two conditions have both been linked to long-term spike protein presence, and the symptoms are often similar too.
“The core problem in post-vaccine syndrome is chronic ‘immune dysregulation,’” Marik shared at the FLCCC conference.
Spike proteins can cause chronic inflammation. Studies have shown that inflammation can lead to cell stress, damage, and even death. Cells make up tissues, different tissues form organs, and organs are part of our own physiological systems. Therefore spike protein injuries are a systemic syndrome.
Spike proteins trigger chronic inflammation by causing immune dysregulation. Spike proteins enter immune cells, switch off normal immune responses, and trigger pro-inflammatory pathways instead.
https://www.theepochtimes.com/health/spike-protein-disrupting-immune-function-in-millions-after-covid-infection-or-vaccination-heres-how-its-being-treated_4813835.html
Remember the great vaxxer billionaire talk in 2021??
https://rumble.com/vp1anh-bill-gates-admits-it-the-vaccines-only-slightly-reduce-the-transmission-of-.html
It seems the experimental vax was moving at the speed of money, yes??
https://rumble.com/v1nhpkq-eu-parliament-member-rob-roos-asked-a-pfizer-representative-at-a-hearing-if.html
Was the solution ever to get vaccinated??
https://nypost.com/2022/10/25/judge-tosses-nyc-vaccine-mandate-orders-workers-backpay/
Sent from my iPhone
We know Raman spectroscopy could have played a role in development to manufacturing of ZYESAMI/RLF-100/AVIPTADIL
https://link.springer.com/article/10.1007/s00216-021-03727-4
But for the experimental vax??
https://rumble.com/v1jayok-pablo-campra-identified-and-evidenced-the-existence-of-graphene-in-jabs.html
Sent from my iPhone
Do all roads lead to Bill Gates? What does the CIA vice chancellor have to do with a, Plandemic? Did Nobel Dr. Kary Mullis, inventor of the PCR test, say the PCR test should not be used to detect a disease in the body? Did Gates say that in order to solve the overpopulation problem, the people must vaccinate? Did Nobel Dr Luc Montagnier say that toxic graphene oxide has been found in the vaccine?
https://rumble.com/v1n2xmg-the-big-reset-movie-english-version..html
Sandy Hook Elementary School families get awarded nearly a billion $$ from ALEX JONES in a defamation suit. How many billions could be awarded to Anthony in a defamation suit against RFK jr for his tell all movie? Watch the movie for the next five days, free and you decide.
https://rumble.com/v1opfyx-the-real-anthony-fauci-movie.-rfk-jr-the-real-anthony-fauci-movie.html
Was Dr Jacobo Elgozy right about
the FDA and AVIPTADIL ?
https://miamicourant.com/stories/617928153-op-ed-the-emergency-use-law-should-be-used-for-emergencies-like-now
Why were doctors with conflict of interests deciding the fate of AVIPTADIL, investors and the lives of others?
https://rumble.com/vygazl-surprise-members-of-independent-vaxx-safety-monitoring-board-have-severe-co.html
Is the vaccine a Trojan horse?
https://rumble.com/vup1m6-dr-richard-fleming-shows-the-hiv-inserts-to-the-s-spike-protein..html
Was AVIPTADIL stopped by federal agencies so that the vaccine could save lives?
https://rumble.com/v1nwblo-cov-19-injections-horror-security-cameras-new-footage-of-people-collapsing-.html
Sent from my iPhone
Could RLF-100/AVIPTADIL become treatment to the vaccine-injured???
Covid Vaccine Injured Speak Out
Vaccine makers are exempt from liability and the medical community is flummoxed at best. The vaccine injury compensation program has failed, and yet, thousands are suffering Covid vaccine injuries with devastating effects. These stories are censored and the injured are shamed. From navigating the insurance system, to finding doctors willing to treat them, or compassionate family members who believe them to debilitating pain which causes some to wonder if they will wake up in the morning, to be Covid vaccine injured is an inconvenient and sometimes unaccepted truth. We have many who are now one year into their experiences and want to share. They were not given informed consent. They share this that you may be more informed.
https://campaigns.dailyclout.io/campaign/brand/f0f16135-d5d6-4acb-8531-26aa8d73f264
Data doesn't lie: mRNA-vaccines and correlation to all-cause mortality
https://rwmalonemd.substack.com/p/data-doesnt-lie-mrna-vaccines-and
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.
https://rumble.com/vuytvt-the-real-anthony-fauci-introduction-chapter-1-a.html
Why is Anthony Fauci not suing Robert F. Kennedy Jr??
On March 28, 2022, President Biden submitted to Congress his FY 2023 Budget request encompassing all Federal agencies - including a proposed budget of approximately $62.5 billion for the NIH.
https://officeofbudget.od.nih.gov/
What’s the extra taxpayer borrowed money for, to buy what??
If the Deep St@te is lying about the vaccine, what else are they lying about???
https://rumble.com/vctp0r-the-truth-about-delusional-renewable-energy-and-democrats-larry-elder.html
Dr. Stefanie Seneff - Senior Research Scientist at the MIT Computer Science and Artificial Intelligence Laboratory
Has published over 170 refereed articles on various subjects related to the intersection of biology and computation. In recent years she is concentrating mainly on the relationship between nutrition and health.
https://rumble.com/v1ddw07-dr.-stefanie-seneff-and-dr.-reiner-fuellmich.html
Unlike the vaccine “Trojan Horse”, RLF-100/AVIPTADIL is very low toxicity!!! If the experimental vaccine went to market as experimental, should RLF-100 get the same treatment and be allowed to market as an experimental therapeutic??? Watch/listen to Dr Vernon Coleman.
Like all qualified medical doctors who have told the truth about covid-19, Dr Vernon Coleman has been repeatedly lied about and libelled on the internet and in the mainstream media. In March 2020, after studying the covid death figures and comparing the death statistics in the UK to that of previous years, Dr Coleman said that the threat of covid-19 had been wildly exaggerated and that there was no pandemic. In that first video, he warned that the pandemic fraud (or hoax) would result in the deaths of many old people (which it did), the introduction of mandatory vaccinations (which appears to be happening) and the disappearance of cash (now a serious threat). As a result of his video, his Wikipedia page was deliberately and dramatically changed by government employees and used to 'monster' him. All his lifetime achievements were removed. Without any evidence or justification he was, among other things, labelled a 'conspiracy theorist' and said to be 'widely discredited'. Google, which works with Wikipedia, reproduced the lies in an attempt to discredit him, so that nobody would believe his warnings. Biographies on www.vernoncoleman.com include references.
https://vernoncoleman.org/
What is considered an experimental vaccine? Did Big Pharma get informed consent from the people subjected to the experimental vaccine?? If not…
Doctors, Nurses Giving the Covid19 Vaccine Will Be Tried as War Criminals. 5.56 to the back of melon - same goes for anyone who coerces/forces you to get injected!
https://rumble.com/v1dl9id-doctors-nurses-giving-the-covid19-vaccine-will-be-tried-as-war-criminals.-5.html
Watch/listen MIT doctor explain everything about the experimental vaccine.
Attorney Reiner Fuellmich “It sterilizes men for good” (he’s speaking of the quackseens)
https://rumble.com/v1ds09f-attorney-reiner-fuellmich-it-sterilizes-men-for-good-hes-speaking-of-the-qu.html
When do they get criminally charged???
More Alarming Data About COVID-19 Vaccine (We Forced MILLIONS Of Women To Take That Drug!)
https://rumble.com/v1doul7-more-alarming-data-about-covid-19-vaccine-we-forced-millions-of-women-to-ta.html
Were we denied so that vaxxes could fly???
Dr. Anthony Fauci made perhaps the most damning confession in the Covid vaccine saga. So far-reaching are the implications of his statement that the interview in which he made it may well prove a turning point in the fight against the vaccine fraud that is being perpetrated on the peoples of the world.
In a November 12 podcast session with the New York Times, Fauci was forced to admit the fact that the vaccines do not reliably protect their recipients from serious Covid or death. …
… Even though Fauci tries to palliate the hard impact of his answer in soft language, the harsh truth behind his words is painfully evident.
Fauci’s words amount to the admission that the vaccinated are getting infected and more and more of them are ending up in hospital where they keep succumbing to Covid at increasing rates.
https://www.johnlocke.org/faucis-admission-places-vaccine-fight-in-new-light/
Boosters for children for what purpose???
https://rumble.com/v18yi38-heated-exchange-between-senate-rand-paul-and-anthony-fauci-on-vaccines-and-.html
One alias anonymous poster said:
I am always amazed at how little consideration is given by all the pushers to the strategies of the main shareholder and virtual majority shareholder GEM. Particularly because it is a hedge fund that is out to make as much profit as possible for itself and its backers (not shareholders of RT). That the main shareholder has the possibilities to get rid of the minority shareholders should be undisputed, otherwise ask the authorities.
Posted by VICLOG, Y@h00 RLFTF finance conversations
Another poster replies…
@VICLOG That makes 40 comments in 2 days, not counting your other accounts. Where are your other accounts anyways? It is even weirder that you are using the same account to comment your posts.
…
@VICLOG, I know you will use your 10+ accounts to report this post no worries. But it is noticeable that you made 29 posts in 1 day with your new account. This would mean you have 50+ posts in about 2 days in a stock you are not holding and spreading miss information about.
Are you ok...?
Posted by Z, Y@h00 RLFTF finance conversations
https://dailyclout.io/dailyclout-and-health-freedom-defense-fund-file-citizen-petition-with-fda-to-halt-covid-injections-for-young-children/
- They're trying to get kids as young as possible to be injected. Problem is the studies published in high quality journals show that the immune system of the COVID vaxxed is screwed up by 'immune imprinting': the system keeps rigidly producing a defense to an old version of a pathogen, which leaves it vulnerable when confronted with a new version of a pathogen.
- Another problem is suppression of T- and B-cell responses of the immune system, which leads to more general immunodeficiency (VAIDS). The enormous increase in reports of for instance (reactivation of) shingles, herpes and Epstein-Barr, but also flu after vaccination, confirms this.
https://rumble.com/v1axpj9-dr.-robert-malone-msm-is-propaganda-arm-for-pharma-alarming-explosive-adver.html
What is immune imprinting?
Immune imprinting results from exposure to proteins or other biological structures of viruses, like those found in SARS-CoV-2, that allow the virus to penetrate host cells and cause infection. Jun 13, 2022
https://rumble.com/v1b8fgj-dr.-robert-malone-explains-immune-imprinting.html
The NIH needs more money to do what???
On March 28, 2022, President Biden submitted to Congress his FY 2023 Budget request encompassing all Federal agencies - including a proposed budget of approximately $62.5 billion for the NIH.
https://officeofbudget.od.nih.gov/
More of this???
The bottom line is that the Pfizer Phase 3 trial which was used by NIAID, FDA and CDC to justify the emergency use authorization is pretty much a junk clinical trial which was inappropriately halted long before it even got close to meeting the intended follow up period, did not provide a sufficiently long follow up analysis of vaccination-associated adverse events, and in which the control group was intentionally eliminated. This resulted in basically erasing any opportunity to ever get to the bottom of what the major true risks of the Pfizer mRNA inoculations were. In terms of more minor risks, the study was not powered (not big enough) to evaluate those.
Into the breach, an intrepid group of (mostly) senior academic researchers have stepped forward. The expression “fools rush in where angels fear to tread” comes to mind, in that it has become extremely risky for any academic to question the approved vaccine narrative. But bravely this decidedly un-foolish group has stepped forward.
To my reading, the approach that they have taken with this analysis and report has been to make a good faith effort to perform the analysis of the Phase 3 clinical trials (those are supposed to be the “big, final” clinical trials prior to licensure of a product) which should have been performed by Moderna and Pfizer. Basically, the analysis that the FDA should have done themselves, and also should have forced Moderna and Pfizer to do. If White House Chief of Staff Mark Meadows had not put pressure on the FDA, perhaps it would have done the right thing. But it apparently caved and did not do it’s job, and here we are.
Herein lies the rub. The FDA not only did not do its job, but neither FDA nor Moderna nor Pfizer will release the primary data, which means that no-one else can do it either. As the authors of this recent analysis note in their discussion:
A systematic review and meta-analysis using individual participant data should be undertaken to address questions of harm-benefit in various demographic subgroups. Full transparency of the COVID-19 vaccine clinical trial data is needed to properly evaluate these questions. Unfortunately, well over a year after widespread use of COVID-19 vaccines, participant level data remain inaccessible.
https://rwmalonemd.substack.com/p/pfizer-and-moderna-analysis-re-do
Who do you believe, an aliased anonymous poster …????
DD to win
Folks trying to sugar coat incompetence. Not having the approval of the cite inspection by the FDA is incompetence. Now it will cost more time.
Hard to tell which group of so called experts are bigger clowns. Another embarrassment. ~posted by DD to win, y@h00 RLFTF, finance conversations
Or aliased anonymous posters …????
@immobiliencoin - I told you that we will see rates below 3 centimes before GEM possibly comes into play. With the 52-week low, it should go several times further in the next few weeks.
The PR of today to ADR / Nasdaq is a pure alibi exercise of Mr. Selvaraju and Mr. Weinstein.
There will never be an uplisting. One more chapter in the book of Dr. Ram Selvaraju: Possibilities held out in prospect that could never come close to being realized.
Sue the management for misleading and related price manipulation if you want to see even a part of your money back. Currently, a lot of it is still going into the pockets of the manipulators! ~Posted by VICLOG, y@h00 RLFTF finance conversations
Or a real life MD not hiding behind an alias???
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.
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.
https://miamicourant.com/stories/617928153-op-ed-the-emergency-use-law-should-be-used-for-emergencies-like-now
Or an non aliased investigative lawyer/writer???
Robert F. Kennedy Jr's book is selling like wildfire. The people clearly want to know what he and his team have uncovered about Anthony Fauci, but if one gets their information from mainstream media they probably don't even know the book exists. That's the problem with censorship. It's not just about stifling the truth when it gets out. Censorship often manifests in the prevention of the truth from ever seeing the light of day.
His book, titled "The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public," is an extraordinarily well-researched and properly cited manuscript that reveals some of the most damning facts about the man who is most responsible for pandemic protocols in America. It's fitting as he may also be the man most responsible for the formation of the very disease he's been tasked with fighting... but we'll leave those details for the book itself to describe.
https://rumble.com/vrp7qy-rfk-jr.s-publisher-obliterates-false-logic-driving-censorship-of-book-expos.html
Or a non aliased author and investigative journalist???
In her most provocative book yet, Dr. Naomi Wolf shows how these forces — from Big Tech and Big Pharma to the CCP and our oligarchical elites — seized upon two years of COVID-19 panic in sinister new ways, to not only undermine our Republic but to fundamentally reorient human relations.
Their target is humanity itself. Their end goal is to ensure that our pre-March 2020 world is gone forever. Irretrievable. To be replaced with a world in which all human endeavor-all human joy, all human fellowship, all human advancement, all human culture, all human song, all human drama, all worship, all surprise, all flirtation, all celebration-is behind a digital paywall. A world in which we will all have to ask technology’s permission to be human.
But we, the people of the world, did not vote to abandon our old systems and destroy our old ways so absolutely they could never be recovered. And Wolf shows how, against overwhelming odds, we still might win.
https://dailyclout.io/product/the-bodies-of-others-the-new-authoritarians-covid-19-and-the-war-against-the-human/
Or a non-aliased CEO & founder of OpenTheBooks.com, a non-profit, nonpartisan government financial watchdog group
By litigating against NIH, OpenTheBooks got the first real glimpse into what’s happening with these royalty payments from Big Pharma, Kennedy said.
“We know that every single year, NIH doles out $32 billion worth of grants, and there are 56,000 entities that receive a grant,” said Andrzejewski. “So tens of billions of dollars of grant-making is going one way.”
https://rumble.com/v1607jr-adam-andrzejewski-taxpayers-in-the-dark-as-nih-scientists-receive-millions-.html
Or a famous investigative journalist that helps the people understand, are vaccines as good as their payloads???
https://rumble.com/vnaz55-mike-wallace-60-minutes-exposes-swine-flu-pandemic-vaccine-fallout-of-1976.html
The US government's Covid adviser, Anthony Fauci, has tested positive for coronavirus.
Aviptadil helps??.
Bad karma ~From Max @ Y@h00 RLFTF finance conversations
https://nypost.com/2022/06/15/dr-anthony-fauci-tests-positive-for-covid-19/
Last year, the National Institutes of Health – Anthony Fauci’s employer – doled out $30 billion in government grants to roughly 56,000 recipients. That largess of taxpayer money buys a lot of favor and clout within the scientific, research, and healthcare industries.
However, in our breaking investigation, we found hundreds of millions of dollars in payments also flow the other way. These are royalty payments from third-party payers (think pharmaceutical companies) back to the NIH and individual NIH scientists.
We estimate that between fiscal years 2010 and 2020, more than $350 million in royalties were paid by third-parties to the agency and NIH scientists – who are credited as co-inventors.
Because those payments enrich the agency and its scientists, each and every royalty payment could be a potential conflict of interest and needs disclosure.
https://openthebooks.substack.com/p/faucis-royalties-and-the-350-million
Robert F. Kennedy, Jr: "He owns stakes, very, very large stakes, [in] almost all the big pharmaceutical companies. Then he gives essentially about a billion dollars to WHO every year, but through Rotary International, through GAVI, through CEPI, and through the Gates Foundation, but the cumulative [funding] is even larger than U.S., which is the second biggest [contributor to WHO]. That gives him control over WHO's policies, so the analysis of WHO [is that] there's nothing that goes through WHO that is not vetted first by the Gates Foundation."
https://rumble.com/v16znzc-a-decade-of-vaccines-bill-gates-strange-meeting-with-fauci-and-his-sadistic.html
Aviptadil, the amazing NEUROPEPTIDE, does not fit the Bill. FDA the gold standard???
https://rumble.com/v16h2z9-watch-bill-gates-push-depopulation-agenda-under-a-humanitarian-mask.html
“In other words: Congress and US Presidents legalized and funded the overthrow of the U.S. Constitution, the U.S. government and the American people, through a massive domestic bioterrorism program relabeled as a public health program, conducted by the HHS Secretary on behalf of the World Health Organization and its financial backers.”
https://dailyclout.io/americans-natural-rights-an-unjust-law-is-no-law-at-all/
Yes, the people need AVIPTADIL/RLF-100
There is mounting evidence that pulmonary arterial hypertension (PAH), asthma and chronic obstructive pulmonary disease (COPD) share important pathological features, including inflammation, smooth muscle contraction and remodeling. No existing drug provides the combined potential advantages of reducing vascular- and bronchial-constriction, and anti-inflammation. Vasoactive intestinal peptide (VIP) is widely expressed throughout the cardiopulmonary system and exerts a variety of biological actions, including potent vascular and airway dilatory actions, potent anti-inflammatory actions, improving blood circulation to the heart and lung, and modulation of airway secretions. VIP has emerged as a promising drug candidate for the treatment of cardiopulmonary disorders such as PAH, asthma, and COPD. ~ Researchgate
Although psychotic depression itself cannot evolve into schizophrenia, when severe depression is untreated or undertreated, it's possible for the resulting distress and side effects to trigger an underlying psychotic disorder, such as schizoaffective disorder.
https://www.brightquest.com/blog/can-psychotic-depression-lead-to-schizophrenia-what-can-you-do-about-it-now/
The prevalence of any anxiety disorder (at syndrome level) in schizophrenia is estimated to be up to 38 %, with social anxiety disorder (SAD) being the most prevalent. Severity of positive symptoms may correlate with severity of anxiety symptoms, but anxiety can occur independently of psychotic symptoms.
https://pubmed.ncbi.nlm.nih.gov/26482261/
Guns??? What do you propose, a government of caring angels???
China established gun control in 1935. From 1948 to 1952, 20 million political dissidents, unable to defend themselves, were rounded up and exterminated.
https://gatguns.com/gun-history/
The gunman who slaughtered 19 kids and two teachers at a Texas elementary school reportedly exhibited increasingly bizarre behavior leading up to the rampage – including cutting up his face with knives just “for fun,” friends said.
https://nypost.com/2022/05/25/details-emerge-on-texas-school-shooter-salvador-ramos-behavior/
A government-pushed vaccine???
https://rumble.com/v12gycf-ouch-excess-mortality-in-israel-plotted-against-vaxx-doses-.html
A government-pushed Remdesivir over a safe and effective Aviptadil???
https://rumble.com/v134ift-infants-to-be-guinea-pigs-as-remdesivir-dangerously-approved-by-fda-without.html
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.
Unfortunately, most Americans are not as fortunate as I was. Each day another 1,400 people die anonymous, lonely deaths in the ICU, isolated from their loved ones when some number could be saved by emergency use medicines. The nation awaits confirmation of a new FDA Commissioner at a perilous time for public health as Covid continues to ravage the world.
Congress passed Emergency Use Authorization to empower the FDA to give doctors, patients, and families access to medicines that “may be effective” when all else has failed. For the first year of the pandemic, EUA decisions were overseen by the Commissioner’s office. Promising therapies were given a chance to show their effectiveness, or lack thereof, for the benefit of patients and families. Some early EUA medicines, such as remdesivir and tocilizumab, went on to prove their benefit in definitive trials and became approved drugs, while others failed and were withdrawn. That sort of trial is exactly what Congress and the American people intended in the face of an unrelenting enemy.
Unfortunately, in the absence of a confirmed FDA Commissioner, EUA decisions have been relegated to the traditional review groups that apply more rigorous measures of safety and effectiveness for permanent new drug approvals. FDA is listening to the voices of statisticians, not to the voices of doctors, patients, and families.
https://miamicourant.com/stories/617928153-op-ed-the-emergency-use-law-should-be-used-for-emergencies-like-now
JK, while we wait for EUA, the hits from big government just keep on coming…
Gilead is at it again, Meryl Nass, M.D. likens FDA collaboration to approve dangerous drug Remdesivir for infants as young as 28 days old to Tamiflu in which Gilead ‘massaged’ data in order to get FDA approval.
“Approval was based on a single trial of 53 children conducted by Gilead”, 3 of which died, she unpacks.
Nass asserts that Remdesivir in general has been used improperly over the last 2 years during a period when the live virus is no longer present in the body.
https://rumble.com/v134ift-infants-to-be-guinea-pigs-as-remdesivir-dangerously-approved-by-fda-without.html
“In a stunning 46-page legal filing2 to the International Criminal Court on December 6 [2021], an intrepid attorney and seven applicants accused Anthony Fauci, Peter Daszak, Melinda Gates, William Gates III, and twelve others of numerous violations of the Nuremberg Code. These included various crimes against humanity and war crimes as defined by the Rome Statutes, Articles 6, 7, 8, 15, 21, and 53.”
In all, the 16 defendants named in the legal filing are:
https://theparadise.ng/will-these-16-people-be-charged-with-genocide/
SARS-CoV2 Spike protein is a toxin
Factcheckers were wrong. People continue to suffer the consequences.
https://rwmalonemd.substack.com/p/sars-cov2-spike-protein-is-a-toxin
Hope is a good thing but…
VIP Restores Natural Killer Cell Activity Depressed by Hepatitis B Surface Antigen
https://www.liebertpub.com/doi/abs/10.1089/vim.1992.5.195?journalCode=vim
One article that so eloquently refuted the possibility of shedding the vaccines also argued that it was improbable for components of the mRNA vaccines to migrate from the injection site to other areas of the body since they would degrade within 24-48 hours. Thus they wouldn’t be able to have any negative effects on women’s reproductive systems. Their concerns were adamantly debunked by the experts in this Reuters article dated April 23, 2021:
https://www.reuters.com/article/factcheck-covid19vaccine-reproductivepro-idUSL1N2MG256
Well, we are now finding out how heartbreakingly untrue the naysayers claims about women’s reproductive health were. The evidence is mounting that not only are components of the vaccines traveling to and collecting in various organs, they also appear to be having devastating effects on pregnant women and their babies.
‘What I’ve Seen in the Last 2 Years Is Unprecedented’: Physician on COVID Vaccine Side Effects on Pregnant Women
https://link.theepochtimes.com/mkt_app/what-ive-seen-in-the-last-two-years-is-unprecedented-physician-on-covid-vaccine-side-effects-on-pregnant-women_4428291.html
The agencies involved in regulating the vaccines were aware of these potential negative impacts. They were negligent in having approved them at all, but particularly recommending them for pregnant women.
Flawed CDC Study Wrongly Concludes COVID Vaccines Safe in Pregnancy
https://link.theepochtimes.com/mkt_app/flawed-cdc-study-wrongly-concludes-covid-vaccines-safe-in-pregnancy_4437106.html
https://dailyclout.io/vaccine-shedding-can-this-be-real-after-all/
Live vaccines contain a little bit of the disease causing pathogen, but so little that it won't lead to severe effects in the vast majority of people. These vaccines are very good at stimulating the immune system, which means you only need one shot to be protected.
Non-live vaccines contain inactivated parts of the pathogen. The advantage of these vaccines is that they can't cause the real disease, even in people with a weak immune system. This is why doctors tend to prefer these kinds of vaccines. A disadvantage is that they are weaker at generating an immune response, which means you need more doses to get an adequate protective effect.
Currently, most administered vaccines are of the non-live type.
https://rumble.com/v13q9f8-how-vaccines-train-the-immune-system-in-ways-no-one-expected-christine-stab.html
In this interview from 2019, Bill Gates estimates that the $10 billion his funds have invested in vaccines over a 20 year period, has turned into $200 billion of economic benefit. That is a 1900% profit.
For comparison: investing that money in a widely diversified stock market fund (S&P500) would only have yielded a 70% total return (i.e. with dividends reinvested) over the same period.
https://rumble.com/v13dscn-bill-gates-10-billion-vaccine-investments-turned-into-200-billion-economic-.html
Killer Cell Activity Depressed by Hepatitis B Surface Antigen
https://www.liebertpub.com/doi/abs/10.1089/vim.1992.5.195?journalCode=vim
Data safety monitoring boards are crucial, not only because normal people do not have the time, inclination or expertise to comb through hundreds of thousands of pages of data, but also because the data were kept confidential from the general public. Therefore, even truly independent scientists who do have the time, inclination and expertise to comb through the data, have been unable to do so until very recently.
Many calls were made for all the relevant safety data to be made public from the very beginning in accordance with the professed goal of transparency by the government agencies and leaders. However, it has taken many lawsuits and freedom of information requests to pry the data loose from the government's jealous hands.
In the end it comes down to the need for the public to trust people who are inherently untrustworthy, because they have severe conflicts of interest and are True Believers who have an absolute, unassailable belief in the necessity, safety and efficacy of all 'vaccines'.
https://rumble.com/vygazl-surprise-members-of-independent-vaxx-safety-monitoring-board-have-severe-co.html
From Y@h00 Finance Conversations
Edward 15 hours ago
Link to Dr Harris and Fauci conversation posted today..seems promising
IV Aviptadil under Right to Try
Once a drug is in phase 3, we may also make that medicine available under Federal and State Right to Try laws, upon request of patients, families, and the treating physicians, provided our medical consultants concur that our investigational products have a reasonable likelihood of an acceptable risk-benefit for the patient.
At this time, NRx Pharmaceuticals is able to provide limited access, on a case-by-case basis, to its investigational medicine Aviptadil through the Aviptadil Right to Try Program. Patients considered for this program would need to meet the following minimum requirements for access:
—-Patients who have a serious disease or condition and whose life is immediately threatened by this disease or condition.
—-Critical COVID-19 meets this standard.
Patients who have no comparable or satisfactory therapy to treat their disease or condition.
—-Patients who are unable or ineligible to participate in a clinical trial involving Aviptadil
For more information, please contact us at ZyesamiRTT@nrxpharma.com.
The Aviptadil Right to Try Program is subject to drug availability and medical review by NRx Pharmaceuticals. NRx Pharmaceuticals has selected Clinigen to administer the Aviptadil Right to Try Program. All requests for Aviptadil under the Aviptadil Right to Try Program must be made by the patient’s treating physician, by completing this application form:
https://www.nrxpharma.com/right-to-try/
Kevin Street, a man who received his first COVID vaccine, collapsed and was diagnosed with “functional neurological disorder” and advised by doctors not to take his second vaccine. Since taking his first dose, Kevin has been plagued by months of misery and suffering. Despite the advice not to receive a second shot, Kevin has had a difficult time finding a doctor willing to put their name on paperwork to file an adverse reaction report.
FULL REPORT from Tamara Ugolini: https://rebelne.ws/3hMqiFc
https://rumble.com/vk23ha-patient-asserts-sudden-neurological-disorder-caused-by-covid-vaccine.html
Although we have made great strides in uncovering the pathological nature of several disorders of the CNS in recent years, many neurological diseases that affect so many people worldwide have little or no effective treatment options. However, findings from current research have indicated a promising pharmacotherapeutic role for VIP and its receptors for treating several neurological disorders, such as AD, PD, and ASD. In AD and PD, microglia activation stands out as one of the histopathological hallmarks, causing widespread cell death. VIP has shown to be a major neuroprotective factor against this inflammatory response by inhibiting microglia-derived proinflammatory factors. Therefore, this peptide presents good potential as a therapeutic agent for inflammation-induced neurodegenerative disorders of the CNS. Likewise, alterations in VIP have also been associated with other neurological disorders, such as ASD. Although there is currently no cure or effective treatment for ASD, this peptide is worthy of future pharmacotherapeutic exploration and design, as several studies have indicated a strong link between this peptide and ASD. VIP and its receptors are widely distributed throughout the body, demonstrating that this peptide is important for a myriad of biological functions. A greater understanding of VIP, VIP receptor signaling, and their role in neurological pathologies is needed for the development of novel and efficacious therapeutics for the treatment of complex CNS disorders.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967653/
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
Kennedy: Anthony Fauci is the architect of agency capture within the public health agencies.
He has orchestrated the transformation of HHS [U.S. Department of Health and Human Services] from a public health agency to an incubator for pharmaceutical products and a promoter of the Big Pharma agenda.
He’s the J. Edgar Hoover of public health. He’s managed to stay for 50 years in office, I show in my book, not by actually accomplishing any measurable successes in public health — public health has declined dramatically under his regime — but rather by serving the interests of pharmaceutical companies — by helping make this country the most pharmaceutical dependent nation in the world.
We take three times more pharmaceutical drugs than the average in other western nations.
We pay the highest prices for those drugs, and we have by far the worst health outcomes in the entire developed world. We’re 79th in the world in terms of our total health outcomes.
This generation of children that has come of age during Tony Fauci’s regime — since 1984 — is the sickest generation in history.
https://rumble.com/vq52ba-robert-kennedy-jr.-warns-fauci-and-gates-using-pandemic-for-totalitarianism.html
What’s next, highly infectious small pox???
https://rumble.com/vp10sj-bill-gates-smallpox-germ-games-and-10-15-fewer-people-in-the-world.html
Dr. Naomi Wolf On The FDA’s Late Release of Vaccine Risks
May 6, 2022 • by Steve Bannon's WarRoom, Rumble
In this video, Dr. Naomi Wolf discusses the late release of information on vaccine adverse events such as life-threatening blood clots. Catch up on what we know about Pfizer, J&J, and more so far.
https://dailyclout.io/dr-naomi-wolf-on-the-fdas-late-release-of-vaccine-risks/
PERHAPS AVIPTADIL CAN HELP
VIP protects us from over-and under-activity of coagulation genes.
https://www.survivingmold.com/save-vip/additional-uses-of-vip
Rochelle, how about a saline placebo instead of the experimental vaccine???
Medical Ethics and Human Rights
These principles, which we know as the Nuremberg Code, included a new, comprehensive, and absolute requirement of informed consent (principle 1), and a new right of the subject to withdraw from participation in an experiment (principle 9).
https://www.nejm.org/doi/full/10.1056/nejm199711133372006
"Never in human history have old people required the young people [to] take risks, make sacrifices, and die to preserve older people. We have a fiduciary duty to our children. Old people sacrifice themselves for children in a moral society, a robust society, and a society that we're proud of. We do not tell children to take risks to preserve old people, and we need to stand up and make a moral choice and an ethical choice for our children."
https://rumble.com/v10hnuq-illegal-under-the-nuremberg-code-rfk-jr-safeguards-the-kidsrefuses-to-let-t.html
Johnson for years—dating back to 2014—led efforts in the U.S. Senate to pass Right to Try legislation, which allows terminally ill patients to try experimental as-of-yet-unapproved medical treatments to try to save their lives.
On his U.S. Senate website, Johnson details the timeline of what eventually led to Congress passing—and then-President Donald Trump signing into law—his Right to Try legislation in the spring of 2018. It started back in 2014, when he met a woman named Trickett Wendler.
https://www.breitbart.com/politics/2022/04/13/exclusive-ron-johnson-hits-wisconsin-airwaves-with-ad-highlighting-right-to-try-life-saving-success/
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/
When governments collude…
Rhode Island Democrats Move to Double State Income Taxes on Unvaccinated Residents
https://dailyclout.io/?s=Rhode+Island+
According to the Blaze’s Daniel Horowitz, the FDA allowed aviptadil to be prescribed to treat patients with Acute respiratory distress syndrome (ARDS) under the “orphan drug designation” way back in 2001. Orphan drugs are pharmaceutical agents that are not profitable because they treat rare medical conditions, and thus require government assistance to produce. They are used to treat life-threatening or chronically debilitating conditions affecting less than 200,000 patients.
Aviptadil was also awarded the orphan drug destination for pulmonary arterial hypertension in 2005, and for pulmonary sarcoidosis in 2021, Horowitz reported. Unfortunately, it has never been fully approved by the FDA.
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/
MIT Scientist Links Covid Vax and Severe Disease
https://rumble.com/vsxgyr-mit-scientist-links-covid-vax-and-severe-disease-5880.html
Neurodegenerative disorders (NDDs) are characterized by neuronal death in the brain. The mechanism of the neuronal death is too complicated to be fully understood, although in many NDDs, aging and neurotoxins are known risk factors. In the central and peripheral nervous system, vasoactive intestinal peptide (VIP), a 28-amino acid neuropeptide, is released to support neuronal survival in both physiological and pathological condition. VIP can inhibit the neurodegeneration induced by the loss of neurons. The indirect protection effect is mainly mediated by glial cells through the production of neurotrophic factor(s) and inhibition of proinflammatory mediators. By remolding the structure and improving the transfer efficiency of VIP, its nerve protective function could be further improved. Its neuroprotective action and efficacy in inhibiting a broad range of inflammatory responses make VIP or related peptides becoming a novel therapeutic method to NDDs. In this review, we aim to summarize the relationship between VIP and NDDs.
https://pubmed.ncbi.nlm.nih.gov/27786097/
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
https://www.precisionvaccinations.com/vaccines/zyesami-aviptadil-therapeutic
Write to the U.S. Congress for approval of AVIPTADIL, now!!
Feeling curious about the Pfizer Document? —- You are not alone. We all are curious.
Abir Ballan, MPH
Are you curious about the Pfizer document that was released by the FDA following the Freedom of Information Act Request and the case brought forward by Public Health and Medical Professionals for Transparency?
Why did it take a court order to release this document that details the reported adverse events following the rollout of the Covid vaccines to the market?
Why was this information withheld from the public?
Did you know that the FDA initially requested 75 years to release the Pfizer data that it reviewed in 108 days to issue full approval for the non-marketed form of the Pfizer Covid-19 vaccine under the name of Comirnaty? (The Pfizer vaccine currently available on the market is still under emergency use authorisation)
https://abirballan.substack.com/p/feeling-curious-about-the-pfizer
An Open Letter to Elon Musk
May 2, 2022 • by Abir Ballan, MPH
Dear Elon,
Congratulations on the acquisition of Twitter. We hope this will help put the world on track to be a better place.
You stated that “Free speech is the bedrock of a functioning democracy and Twitter is the digital town square where matters vital to the future of humanity are debated…”
https://dailyclout.io/an-open-letter-to-elon-musk/
Ms Pegs1, we can only patiently wait but at the same time we must also fight the corrupt government agencies as you do by writing to the US Congress and posting in forums where constitutional freedom of speech, the peoples constitutional rights are still respected! Many thanks to Elon Musk for what he has done with Tweeter (my spelling) and freedom of expression.
https://rumble.com/v10zdey-while-defending-free-speech-musk-describes-twitter-as-an-arena-and-a-warzon.html
The Tweeter investors defended their property, sold at a premium and won!! The people prevailed over the purveyors of equality in poverty and disease!!
https://rumble.com/v12jmus-project-veritas-leaks-audio-from-internal-twitter-meeting-after-elon-musk-t.html
SARS-CoV-2 vaccination can elicit a CD8 T-cell dominant hepatitis
https://www.sciencedirect.com/science/article/pii/S0168827822002343
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.
ZYESAMI (off-patent aviptadil) has shown promise as a treatment for COVID patients who are suffering with severe lung inflammation following an excessive immune response known as a “cytokine storm.” The drug is available through the “Right to Try” law—passed by Congress in 2018—but the Food and Drug Administration (FDA), and National Institute of Allergy and Infectious Diseases (NIAID) have failed to recommend it, so it remains largely unknown as a treatment option.
Unlike repurposed drugs like Hydroxychloroquine, and Ivermectin, before the pandemic, Aviptadil already had a track record for treating pulmonary inflammation conditions.
https://thejewishvoice.com/2022/03/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/
A Pilot who went for his first yearly physical after receiving his vaccine was told he now has a heart condition – after 20 years of perfect health.
https://dailyclout.io/adverse-events-heavy-landing-pilot-in-perfect-health-until-vaccine/
In a letter to the FDA, Senators Ron Johnson, Ted Cruz, with Congressman Andy Biggs and Chip Roy, demanded the agency explain why they were dragging their feet on approving the drug ZYESAMI for treating COVID. For some context, it is a late-stage treatment that has anecdotally pulled people from death’s door. Even Dr. Fauci had some positive things to say, which is a miracle since he does not appear to own stock in the company that produces it.
Over 900,000 people (about half the population of Idaho) have died from COVID. Even if you pull out the “with COVID” group from that number, it will still be many people. Yet the protocols are still the same in the hospital, Remdesivir plus ventilator. Even with everything we have learned from courageous doctors worldwide literally trying everything, the only thing that has changed has been the almost cultish adherence to the experimental vaccines.
Early treatments that have undergone rigorous study were ignored. Natural immunity is discounted and forgotten. Why won’t the FDA do everything it can to correct the error of its ways and get aggressive about trying anything and everything that looks promising? The masks are coming off in all states. What is there to lose? Even the CDC (Center for Disease Control) director Walensky is starting to backpedal on the vaccines to save face and reframe her position in the crisis.
https://capitalhillnews.com/johnson-cruz-biggs-and-roy-slam-the-fda-for-delaying-possible-covid-treatment/
Former BlackRock Fund Manager Edward Dowd Reveals Wall Street Now Paying Attention to the ‘Trust the Science’ Fraud
https://dailyclout.io/blackrocks-edward-dowd-reveals-wall-street-now-paying-attention-to-the-trust-the-science-fraud/
EUAs for Big PHARMA’s Remdesivir, COVID vaccines, Mulnupiravir, & Paxlovid. What about Zyesami, a drug that is saving lives through Right to Try? What does
@FDA @NIH have against drugs that save lives?
They must answer 4 members of Congress’ questions.
EUAs for Big PHARMA’s Remdesivir, COVID vaccines, Mulnupiravir, & Paxlovid. What about Zyesami, a drug that is saving lives through Right to Try? What does @FDA @NIH have against drugs that save lives?
— Senator Ron Johnson (@SenRonJohnson) March 23, 2022
They must answer 4 members of Congress’ questions.https://t.co/EPvmQmCkWQ
When government legislates prices…
Price controls adverse effects on innovation
Price controls lead to rationing, yes???
How are government price controls going to help the people, our company, our stock price???
This bill, H.R. 3, would give the federal bureaucracy unprecedented power to set prices for prescription drugs. Rather than pursuing this measure, Congress should work toward common-sense reforms that have broad support and will ensure continued access to life-saving and life-enhancing medications.
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For example, in Canada, where a government board determines drug prices, patients only have access to half of new drugs. In contrast, US patients have access to 89 percent of new drugs.
Similarly, European Union countries with price controls have experienced worsening drug shortages. The low prices limit production of the drug and what is available for patients. According to a 2019 report, in France, “The number of drugs reported as scarce in the country increased 20-fold between 2008 and 2018, according to the country’s drugs regulator — and is predicted to rise by a further 60 percent this year.” In Italy, some cancer patients struggle to access medications. In Poland, the shortage of neurological drugs rose to an “unprecedented scale.”
https://nypost.com/2021/07/10/drug-prices-set-by-washington-would-be-a-disaster-for-health-care/