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PW, definitely cool! Did the assertive poster share his letter to Congressman Posey? It would be likely a more effective campaign to reach out to the U.S. Congress if we were to model a letter after his. Thanks in advance!
Scientific Fraud and the CDC —- ‘These are the people that are entrusted to tell us the truth'
Dr. Cole and I sat down with Art Moore in Washington State on Monday to talk about the CDC covering up data, scientific fraud and what comes next. The video is linked above. But for those who prefer to read, the full transcript of the conversation is below.
Note: the above link is not being allowed to be forwarded by T-mobile and probably other cell phone services. Evidently speaking about censorship and scientific fraud is considered too dangerous by our government.
https://rwmalonemd.substack.com/p/scientific-fraud-and-the-cdc
The senate hearing – where Fauci called Marshall a "moran" – was Fauci's last prominent public event.
So, we’ve been hard at work to break down everything you need to know about Dr. Anthony Fauci and his finances. And now it's all in one place...
We’re excited to share our newest 20-page Oversight Report – just published this week – INVESTIGATING FAUCI’S FINANCES – free to download right now.
Here are just a few of our findings highlighted in the report:
When Dr. Fauci retires, he’ll collect a more than $355,000 annual retirement package – the largest federal pension in history.
The Fauci household’s net worth rivals $11 million.
Dr. Fauci’s wife, Christine Grady out-earned the Vice President – as the chief bio-ethicist at the National Institutes of Health making $238,970 in 2021.
Fauci collected a $1 million prize for "speaking truth to power" during the Trump years.
As you’ll see in the report, Fauci represents the elite administrative state.
But Fauci forgot that bureaucrats work for the people.
Here is the oversight report that Fauci doesn't want you to read!
https://mailchi.mp/3c9672eadab4/35b-from-us-taxpayers-funded-world-health-organization-58867?e=84fec57504
“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/
I recommend both of those abridged versions of the interviews for those (like me) who just cannot stomach the full interviews. I strongly recommend that you read Mr. Harrington’s succinct summary, particularly including the following three paragraphs, which nicely summarize my feelings about the situation.
“All those moves to censor and professionally destroy those who had opinions different from the CDC, actions rooted precisely in the presumption that science is, in fact, black and white, and that those who get it wrong need to be professionally punished, well, that’s all a figment of your primitive imagination.
Or as Harold Pinter put it in his Nobel Prize speech when referring to the US penchant for wantonly destroying other cultures, “It never happened. Nothing ever happened. Even while it was happening it wasn’t happening. It didn’t matter. It was of no interest.”
So yes, excessive psychic detachment turns fellow human beings into self-referential objects or our own minds can be rather problematic. Indeed, I think, though I can’t be sure, that psychologists even have a term for it: psychopathy.”
Bill Gates, Klaus Schwab, Anthony Fauci, Rochelle Walensky , Paul Offit, Janet Woodcock, Rick Bright, Jessica Cecil and her Trusted News Initiative. Don’t forget these names. They should live in infamy. And they all share a common personality profile.
https://rwmalonemd.substack.com/p/how-does-it-feel-to-be-vindicated
The “I am science” crowd!!
https://rumble.com/vrof7e-fascist-psychopath-justin-trudeau-calls-the-unvaccinated-racist-and-misogyn.html
Big government and big business are managing, badly.
https://rumble.com/vrx66v-errthink-the-world-is-run-by-psychopaths-youre-right-watch-this.html
Will psychos stop anyone with a dissenting opinion?
https://rumble.com/vpqbqe-if-you-ever-wondered-how-a-psychopath-speaks-here-it-is.html
They were against a federal mandate before they were for it. Believe as I say not as I do!
https://rumble.com/vsb5u9-these-global-controlling-demonic-psychopaths-are-lying-to-us-100-proof-.html
I wonder how much of what Jon did was conceived in his mind and how much was conceived in the minds of irrational Hanimals?? How much do Hanimals have at stake in Zyesami’s future?? How much do investors have at stake in Zyesami’s future?? Weird how that works!
This is an example of a lawsuit, by private institutions, against the heads of the FDA, HHS and the Biomedical Advanced Research and Development Authority (BARDA) in 2020.
The Association of American Physicians and Surgeons (AAPS) has filed a lawsuit against the heads of the FDA, HHS and the Biomedical Advanced Research and Development Authority (BARDA) over what they call “irrational interference” to limit the use of hydroxychloroquine (HCQ) for treating COVID-19 patients.
https://www.fdanews.com/articles/197519-doctors-sue-fda-hhs-over-hydroxychloroquine-restrictions
Is ZYESAMI in a NIH jail? How can we get a “get out of jail card”, a U.S. Senate subcommittee???
The messenger RNA (mRNA) from Pfizer’s COVID vaccine is able to enter human liver cells and is converted into DNA, according to Swedish researchers at Lund University.
The researchers found that when the mRNA vaccine enters the human liver cells, it triggers the cell’s DNA, which is inside the nucleus, to increase the production of the LINE-1 gene expression to make mRNA.
The mRNA then leaves the nucleus and enters the cell’s cytoplasm, where it translates into LINE-1 protein. A segment of the protein called the open reading frame-1, or ORF-1, then goes back into the nucleus, where it attaches to the vaccine’s mRNA and reverse transcribes into spike DNA.
Reverse transcription is when DNA is made from RNA, whereas the normal transcription process involves a portion of the DNA serving as a template to make an mRNA molecule inside the nucleus.
https://citizenfreepress.com/column-1/bombshell-study-pfizer-vaccine-goes-into-liver-cells-and-is-converted-to-dna/
No, I don’t believe in government angels or gene-editing angels.
Somatic gene therapies, which involve modifying a patient's DNA to treat or cure a disease, have been successfully used to address HIV, sickle-cell disease and transthyretin amyloidosis. The technique could also vastly improve treatment for a variety of cancers. Jul 12, 2021 ~ who.int
https://rumble.com/vwxob3-joe-allen-in-studio-talks-gene-editing-and-biolabs-in-ukraine.html
Let ZYESAMI/AVIPTADIL/RLF-100 handle health conditions, now!
Treatment with an inhaled formulation of synthetic vasoactive intestinal peptide (Aviptadil, Bachem) was initiated, at a dose of 70 µg three times daily, as an alternative treatment to avoid glucocorticoid-related side effects and systemic immunosuppression. Vasoactive intestinal peptide has been shown to dampen type 1 helper T cell (Th1) responses by inhibiting effector T cells and boosting regulatory T cells through its G-protein–coupled receptors (VPAC1 and VPAC2). Its inhaled application in sarcoidosis increases alveolar regulatory T cells and reduces proinflammatory cytokines, resulting in clinical improvement.4
Treatment with inhaled vasoactive intestinal peptide resulted in clinical and radiologic improvement in the lungs (Figure 1B). Analysis of BAL fluid showed reduced alveolar lymphocytosis with reduced CD28 expression and increased regulatory T cells. Spontaneous and lipopolysaccharide-induced release of tumor necrosis factor, reflecting the inflammatory alveolar milieu, were dampened during treatment. Vasoactive intestinal peptide was not associated with toxic effects and did not influence lymphocyte subtypes in peripheral blood (Table S1). Eight weeks after cessation of the treatment, the patient had systemic nonpulmonary progression of melanoma disease.
Our findings support inhaled vasoactive intestinal peptide as a local therapy to reduce the alveolar inflammation found in patients with immune checkpoint inhibitor pneumonitis. Whether this therapy has an influence on tumor progression cannot be determined on the basis of this case. However, further studies are indicated to investigate whether vasoactive intestinal peptide may be a therapeutic option for immune checkpoint inhibitor pneumonitis.
https://www.nejm.org/doi/full/10.1056/NEJMc2000343
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/
Truth is unfolding.....Please see below statement from todays NRX 8-K filing.
"In light of the Company’s strategic focus and the ongoing hostilities in Eastern Europe, and following recent changes in the Ministry of Health in the nation of Georgia, the Company at this time will not be pursuing opportunities in Georgia (which neighbors Russia and Ukraine), elsewhere in the Caucasus region or Europe. In addition, the Board has determined that it could not confirm the current status or effectiveness of the authorization for emergency use of the Company’s COVID-19 therapeutic drug ZYESAMI® in Georgia. Although the Company engaged in an initial training of physicians, to date, the Company has not sold any doses of ZYESAMI® in Georgia. At this time, the Company has ceased efforts to pursue further regulatory drug interactions in Georgia or to conduct clinical trials there."
~ Posted by Newbie, Y@h00 RLFTF finance conversations
https://ir.nrxpharma.com/sec-filings/all-sec-filings/content/0000950142-22-000983/0000950142-22-000983.pdf
JJ and NRXP got a license from SUNY and somehow found out a huge benefactor in the NIH. They definitely own that mess! Reminds me of the socialist/Marxist democrat and his shovel-ready projects. Know a jackasset, know them all!
H-U-G-E!!
Thank you PW! I did not see your post in time to stop my repost. I noticed yours is directly from FB while my repost is a repost of poster Christian, Y@h00 finance RLFTF conversation. Poster Christian repost was obviously edited.
From Dr Joey (Facebook):
Good Morning Everyone,
Just a quick update from Washington, these next two weeks are going to be HUGE regarding aviptadil. The Repubs are mounting a full attack on NIAID division of NIH and demanding answers from Dr. Fauci specifically about our drug! They will be giving him a deadline to respond regarding why ZYESAMI has not already been approved. Deadline is most likely set for the next two weeks.
They are also considering not signing for any more COVID funding to be approved until we get answers about this. I'll keep y'all informed about the developments. For added background, This was part of the reason the Dems had to remove the request for additional COVID (vaccine) funding from the recent Ukraine financial aid bill that just got approved.The Rebubs want an update on more COVID therapeutics first! They are telling Fauci it is time to stop focusing on vaccines now and approve more therapeutics... and trust me, they are using ZYESAMI as their flagship example of one that is ready for approval but has been ignored by both Dr Califf ( FDA) and by Fauci (NIAID).
~ posted by Christian, Y@h00/finance RLFTF conversation
Correction: ~ Posted by Newbie, Y@h00 NRXP (not RLFTF) finance conversations
Truth is unfolding.....Please see below statement from todays NRX 8-K filing.
"In light of the Company’s strategic focus and the ongoing hostilities in Eastern Europe, and following recent changes in the Ministry of Health in the nation of Georgia, the Company at this time will not be pursuing opportunities in Georgia (which neighbors Russia and Ukraine), elsewhere in the Caucasus region or Europe. In addition, the Board has determined that it could not confirm the current status or effectiveness of the authorization for emergency use of the Company’s COVID-19 therapeutic drug ZYESAMI® in Georgia. Although the Company engaged in an initial training of physicians, to date, the Company has not sold any doses of ZYESAMI® in Georgia. At this time, the Company has ceased efforts to pursue further regulatory drug interactions in Georgia or to conduct clinical trials there."
~ Posted by Newbie, Y@h00 RLFTF finance conversations
https://ir.nrxpharma.com/sec-filings/all-sec-filings/content/0000950142-22-000983/0000950142-22-000983.pdf
REPLY:
I knew it! They're now skirting the actual truth to cover the mess JJ placed them in! In the days to come more and more will be forthcoming including JJ's notice of retirement!
~ Posted by RR
A Prayer for Relief
Plaintiffs respectfully request relief as follows:
a. An award of damages in an amount exceeding $500,000 to be determined at trial;
b. An award of punitive damages;
c. An order compelling Defendants to perform under the Collaboration Agreement
including, among other relief:
i. An order enforcing the territorial limits of the Collaboration Agreement and prohibiting Defendants from engaging in any commercialization efforts for aviptadil in any country other than the United States, Canada, or Israel;
ii. An order enforcing the territorial limits of the Collaboration Agreement and prohibiting Defendants from engaging in any commercialization efforts for BriLife;
iii. An order requiring Defendants to submit detailed budget proposals for any clinical trials related to the Collaboration Agreement to Relief's Board of Directors;
iv. An order prohibiting Defendants from entering into third party agreements without Relief's consent as required by Section 5 of the Collaboration Agreement;
v. An order compelling Defendants to allow Plaintiffs access to, and an audit of, Defendants' books and financial records as set forth in Exhibit D;
vi. An order compelling Defendants to share information and collaborate with Relief as required by Section 7 of the Collaboration Agreement;
vii. An order compelling Defendants to produce any and all information licensed from SUNY Stonybrook to Relief; and,
viii. An order specifically enforcing the exclusivity provisions of the Collaboration Agreement;
d. A declaration that the Collaboration Agreement provides Relief with the right to access any and all data related to clinical trials of aviptadil in the United States that have been conducted by, in collaboration with, or at the direction of, NeuroRx and/or its affiliates;
e. An accounting;
f. An award of Relief's costs and attorney's fees;
g. An award of pre-judgment and post-judgment interest on the foregoing sums at the highest rate permitted by law; and,
h. Any further and additional relief that the Court deems just and proper.
Jury Trial Demand
Plaintiffs request a jury trial on all issue so triable.
Dated: October 6, 2021
$NRXP
~ Posted by woodcrest, Y@h00 RLFTF finance conversations
PW, I agree. The credit goes to Wong, Y@h00 RLFTF finance conversations
If you read the 8-k by NRXP it states they will focus on commercialization of Aviptadil in the US. It seems NRXP has relinquished their rights to Israel and Canada to Relief. They also state they are pulling out of Georgia, the surrounding areas and the EU. Those are all Relief's territory. As far as I can tell with the abrupt departure of JJ as CEO Relief is calling the shots and allowing NRXP to still be a part of aviptadil in the states in exchange of certain caveats. 1 being, JJ is out as CEO and 2 is you stop all commercialization activity in Relief's territory. Now we wait to see if there has been a change to the revenue splits between the two companies. This too is speculation but it is speculation based off factual events that have transpired over the last week or so.
Wong, Y@h00 RLFTF finance conversations
https://ir.nrxpharma.com/sec-filings/all-sec-filings/content/0000950142-22-000983/0000950142-22-000983.pdf
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/
What Are the Four Elements of Medical Malpractice?
* Duty: The duty of care owed to patients.
* Dereliction: Or breach of this duty of care.
* Direct cause: Establishing that the breach caused injury to a patient.
* Damages: The economic and noneconomic losses suffered by the patient as a result of their injury or illness.
https://bencrump.com/medical-malpractice/what-are-the-four-elements-of-medical-malpractice/
The second leg of the fraud is less visible to the naked eye but much more powerful. If I wrote this before I retired, I would be called before the Board of my group and told in no uncertain terms to shut up. I might even be assessed a financial penalty with several zeroes after the one. That's a serious impairment of my pursuit of happiness. The reason for my group's dislike is more than the fact that I might be an irritant. They may actually agree with what I have to say. But they simply cannot afford for me to say it. That's right: as a practicing physician in a group, my freedom of speech can become very expensive...to the group.
My group cared for patients of all descriptions, with roughly half of them on Medicare and another batch on Medicaid. Both programs are ultimately managed by the feds, one of the most humorless groups on the planet. They write a whole bunch of rules on how you have to document everything you do. If you didn't document it correctly, it didn't happen, and you won't get paid. But that's not the half of it.
https://www.americanthinker.com/articles/2021/09/why_do_doctors_go_along_with_covid_panic_porn_and_cdc_prescriptions.html
Remember this?
Germany - VIP Given to Cancer Patient, remarkable results
https://www.uniklinik-freiburg.de/presse/pressemitteilungen/detailansicht/2058-hormon-inhalation-stoppt-schwere-nebenwirkung-von-immun-krebstherapie.html?fbclid=IwAR2Wx7usysrBoVl7scw3rVvfBZkMGshtKagJZPBb0xoqGfaYfiR9cE0G_vE
**Translated Version
Freiburg, June 25th, 2020
Hormone Inhalation Stops Serious Side Effect Of Immune Cancer Therapy
Using a novel therapeutic approach, doctors at the University Medical Center in Freiburg succeeded in curing pneumonia in a patient that had occurred as a result of immune cancer therapy / publication in the New England Journal of Medicine
The treatment of cancer patients can no longer be imagined without innovative immunotherapies. However, they also repeatedly lead to life-threatening inflammation of the lungs. Scientists and doctors at the Freiburg University Medical Center have now successfully used a novel therapeutic approach on a patient. The patient had received immunotherapy for melanoma, also known as black skin cancer. However, this triggered severe pneumonia. The doctors decided to give him the intestinal hormone "vasoactive intestinal peptide" (VIP) for inhalation, the use of which is being researched at the Freiburg University Medical Center for similar diseases. The pneumonia completely disappeared within a few weeks, something that had not previously been possible with cortisone. The case report was published on Jan.New England Journal of Medicine published.
"After the patient initially received cortisone, the shortness of breath and coughing quickly returned," reports Dr. Frank Meiß , Senior Consultant in Charge at the Clinic for Dermatology and Venereology at the Freiburg University Hospital. Therefore, it was decided together with the patient to go a new way and give him VIP for inhalation.
The Freiburg doctors and scientists came up with the idea of ??the VIP gift because they were researching new therapeutic approaches for the lung disease sarcoid in several research projects and had already achieved initial successes with VIP. "We chose this experimental therapy because there are similarities between sarcoid and this type of non-bacterial pneumonia," says Dr. Björn Christian Frye , senior physician at the Pneumology Clinic at the University Hospital Freiburg.
“We had expected an improvement in the pneumonia, but were very positively surprised by the success of the therapy. The inflammation subsided and the patient's shortness of breath disappeared, ”says Prof. Dr. Joachim Müller-Quernheim, Medical Director of the Clinic for Pneumology at the University Medical Center Freiburg. This type of non-bacterial pneumonia, called pneumonitis, occurs in 10 to 20 percent of all patients who have received immune cancer therapy and so far have usually been treated with steroids such as cortisone. However, some of these have severe side effects and the immunotherapy must be discontinued. Instead of cortisone tablets, which only led to short-term improvement but also to side effects, the patient only had to inhale three times a day. There were no side effects under VIP therapy.
In the next step, the Freiburg team is planning a larger clinical study to clarify whether and for which cancer patients with pneumonitis the therapeutic approach could be considered.
Original title of the publication: Vasoactive Intestinal Peptide in Checkpoint Inhibitor – Induced Pneumonitis
DOI: 10.1056 / NEJMc2000343
Link to the study: https://www.nejm.org/doi/10.1056/NEJMc2000343
Contact:
Prof. Dr. Joachim Müller-Quernheim
Medical Director
Clinic for Pneumology
University Hospital Freiburg
Telephone: 0761 270-37060
joachim.mueller-quernheim@uniklinik-freiburg.de
Big Pharma moving to checkpoint inhibitors to fight cancer. We are about to receive a patent to treat checkpoint inhibitor pneumonitis a common occurrence in patients receiving this therapy. Connect the dots. Aviptadil for CIP will be huge.
On Feb. 28, the FDA accepted Bristol Myers Squibb’s application for approval of a new use of blockbuster checkpoint inhibitor Opdivo and said it would make a decision by July 13.
That estimate turned out to be conservative, to say the least. On Friday, just five days after accepting the application, the FDA OK’d it, handing the Big Pharma a landmark approval.
Opdivo can now be used to treat patients with early-stage non-small cell lung cancer prior to receiving surgery to remove their tumor.
~Wong, Y@h00 RLFTF financial conversations
==================================
By acquiring the rights to AdVita’s therapy formulation, Relief also will accelerate and secure RLF-100’s future development as an inhaled therapy for lung diseases, such as pulmonary sarcoidosis, that are associated with COVID-19. Other lung diseases associated with COVID-19, which also could potentially be treated by RLF-100, include checkpoint inhibitor-induced pneumonitis, and acute respiratory distress syndrome (ARDS).
https://sarcoidosisnews.com/2021/01/28/deal-gives-relief-therapeutics-intellectual-rights-potential-sarcoidosis-therapy-rlf-100/
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://roar-assets-auto.rbl.ms/documents/14130/2022-03-03%20Letter%20to%20FDA%20and%20NIAID%20re%20Right%20to%20Try.pdf
Thank you Panton!! Excellent article!!
https://www.theblaze.com/op-ed/horowitz-sen-johnson-calls-out-the-fda-for-not-approving-promising-late-stage-covid-drug
I think we could do so much good if only we were not in the clutches of animals…
Zyesami (Aviptadil) Therapeutic Description 2022
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
After a fabricated pandemic, what else could go wrong???
https://www.zerohedge.com/commodities/russia-recommends-fertilizer-makers-halt-all-exports
Bill, can you help???
Hungary is banning grain exports, its agriculture minister told television channel RTL on Friday. Argentina and Turkey also made moves this week to increase their control over local products. And Moldova, albeit a small shipper, temporarily halted exports of wheat, corn and sugar from this month.
Protectionist measures -- which already picked up in recent years as the Covid-19 pandemic sparked worries about local supplies and high prices -- could spell more bad news for global food trade. The war in Ukraine has brought crop shipments from much of the crucial Black Sea region to a halt, heightening fears of shortages of grain and sunflower oil.
Read: Wheat Mounts Historic Week as War Sparks Deepening Supply Fears
https://finance.yahoo.com/news/governments-step-protect-food-supplies-162829874.html
Maybe Bill can help as he helps himself, yes???
All told, the 2017 acquisition of AgCoA and the 2018 acquisition of the 100 Circles tract in the Horse Heaven Hills of Eastern Washington total an investment in farmland assets of more than $690 million. Janiec’s sources said some of the AgCoA assets were quickly sold off, but according to the Land Report 100 Research Team, an estimated 242,000 acres of farmland remained.
Yet farmland assets aren’t the sole component of the Gateses’ landholdings. In 2017, Cascade Investment bought a “significant stake” in 24,800 acres of transitional land on the western edge of Phoenix, the most populous city in Arizona and the 10th largest metropolitan area in the country. The acreage sits off Interstate 10, and it is poised to be accessible by Interstate 11, a proposed highway that would traverse 5 miles of the 40-square-mile holding. At buildout, the Belmont development will create a brand-new metropolis, one similar in size to the Phoenix suburb of Tempe, home to Arizona State University and almost 200,000 residents. According to The Arizona Republic, Belmont is projected to include up to 80,000 homes; 3,800 acres of industrial, office, and retail space; 3,400 acres of open space; and 470 acres for public schools.
Cascade Investment doubled down on Phoenix transitional land two years later when it made a second major investment by acquiring more than 2,800 acres known as Spurlock Ranch in Buckeye for $25 million.
https://landreport.com/2021/01/bill-gates-americas-top-farmland-owner/
Maybe not…
In 2014 GRAIN published a detailed breakdown of the grants made by the Bill and Melinda Gates Foundation to promote agricultural development in Africa and other parts of the world.1 Our main conclusion then was that the vast majority of those grants were channelled to groups in the US and Europe, not Africa nor other parts of the global South. The funding overwhelmingly went to research institutes rather than farmers. They were also mainly directed at shaping policies to support industrial farming, not smallholders.
Much has happened since then. For starters, Bill and Melinda Gates announced their divorce in May this year, leaving the future of the Foundation and its grant-making in doubt. The news came as Bill Gates himself came under fire for supporting Big Pharma's patent monopoly on COVID-19 vaccines, for effectively preventing people's access across much of the world, and for how he treats - or mistreats - women.2 The Foundation's agenda with agriculture has also been coming under increased scrutiny. A 2020 report from Tufts University concluded that its work in Africa completely failed to meet the objectives that it had set itself.3 The African Centre for Biodiversity published a string of reports denouncing the Gates Foundation for pushing GMOs and other harmful technologies onto Africa.4 Amongst all this, the US Right to Know collective started a “Bill Gates Food Tracker” to monitor the multiple initiatives that Gates is involved in to reshape the global food system.
https://grain.org/en/article/6690-how-the-gates-foundation-is-driving-the-food-system-in-the-wrong-direction
Hold off on the pandemics and famine or we’ll start looking as bad as the CCP…
https://rumble.com/vtgxu3-theyll-be-worse-pandemics-than-this-thanks-bill..html
First Jan 2022, then February 22 and beyond that I do not know.
Vaccine makers have been busy…
https://rumble.com/vva4pv-trudeaus-foundation-owns-40-of-acuity-which-manufactures-mechanic-lipids-fo.html
The price of liberty, eternal vigilance!!!
https://rumble.com/vsgn8d-wow-darpa-confirms-covid-bioweapon-gun-confiscation-covid-prison-camps-and-.html
Head transplants???
https://rumble.com/vt4io2-head-transplants-james-giordano-on-swapping-heads.html
Bill, what is the ROI on vaccine therapy???
Bill Gates says investing in global health organizations aimed at increasing access to vaccines creates a 20-to-1 return. “Helping young children live, get the right nutrition, contribute to their countries — that has payback that goes beyond any typical financial return.” ~ Facebook com
https://rumble.com/vtgxu3-theyll-be-worse-pandemics-than-this-thanks-bill..html
Vaccine therapy??? Vaccines for all???
Years ago…
What caused Robert F. Kennedy Jr asthmatic dystonia???
An increased risk of narcolepsy was found following vaccination with Pandemrix, a monovalent 2009 H1N1 influenza vaccine that was used in several European countries during the H1N1 influenza pandemic. This risk was initially found in Finland, and then other European countries also detected an association.
https://www.cdc.gov/vaccinesafety/concerns/history/narcolepsy-flu.html
Joey cares so much about the strength/resilience of the people!! Does he want vaccine therapy for all???
Throughout the Moderna and Pfizer/BioNTech clinical trials, eight cases of Bell’s palsy — a type of rare, sudden muscle weakness in the face — were reported in total. Four of the cases were in the Pfizer vaccine group, three in the Moderna vaccine group, and one in the Moderna placebo group. The rate of Bell’s palsy incidence in the vaccine clinical trials was less than or equal to the rate of developing the condition in general. While there’s no evidence the cases were caused by the vaccine, they are considered an adverse event and will continue to be reported and monitored as a special interest adverse effect.
https://www.uchicagomedicine.org/forefront/coronavirus-disease-covid-19/what-to-know-about-the-covid-19-vaccine#:~:text=Throughout%20the%20Moderna%20and%20Pfizer,special%20interest%20adverse%20effect.
https://rumble.com/vo0ide-wh-vaccine-rollout-plan-for-5-11-year-olds-nypd-disciplines-maskless-office.html
This [jackassery] didn’t age well…
The Ajinomoto Group commands a dominant share of the global amino acids market in food, feed, pharmaceutical, and other segments. Our advanced production technology and capacity to ensure stable supply of amino acid-based products is the core of our competitive strength.
https://www.ajinomoto.com/innovation/rd/acids
Revenue in healthcare and others —- 239 billion yen ~ 2 billion U.S.
https://www.statista.com/statistics/910865/ajinomoto-sales-by-segment/
Ajinomoto has amino acids/peptides but RLFTF has the 28 amino acid peptide, with the potential to dominate healthcare therapeutics and that includes domination over the vaxx sheet therapies. Are we currently burning cash while in the clutches of the NIH (why $50+ billion annual budget for these animals?) and their cronies?
Duck 73, you may want to add glycine to your investigation of NAC.
The amino acid glycine has a hyperpolarizing effect on airway smooth muscle that is bronchodilatory. Insuring optimal intracellular levels of magnesium may modestly blunt the stimulatory impact of intracellular free calcium on bronchoconstriction. Nutraceutical regimens or functional foods incorporating at least several of these agents may have utility as nutraceutical adjuvants to standard clinical management of asthma.
https://www.dovepress.com/review--nutraceuticals-can-target-asthmatic-bronchoconstriction-nadph--peer-reviewed-fulltext-article-JAA
Glycine complements NAC in raising glutathione tissue levels
https://www.nutraingredients.com/Article/2021/06/28/Review-assesses-nutraceutical-measures-for-asthma-relief
Supplementation with GlyNAC (combination of glycine and N-acetylcysteine as a cysteine precursor) was found to improve/correct cellular glycine, cysteine, and GSH deficiencies; lower OxS; and improve mitochondrial function, inflammation, insulin resistance, endothelial dysfunction, genotoxicity, and multiple aging hallmarks; and improve muscle strength, exercise capacity, cognition, and body composition.
https://pubmed.ncbi.nlm.nih.gov/34587244/
What is AjiPure??? —- AjiPure's amino acid supplements and information from Ajinomoto, the world's #1 amino science company.
The AjiPure Difference
Purity. Safety. Efficacy. With Ajinomoto's AjiPure® amino acids, purity means quality. AjiPure® amino acids are manufactured by Ajinomoto®, the first company to identify, refine and market amino acids. More than 100 years later, as the leading global supplier of pharmaceutical and research-grade amino acids, we exceed industry standards for purity and quality.
http://www.ajipure.com/ajipuredifference/resource
We need AVIPTADIL/Zyesami/RLF-100 yesterday!!!
Best to you, brother and family
Natural immunity refers to the protection people enjoy against the CCP (Chinese Communist Party) virus after recovering from COVID-19.
“When somebody is naturally immune—like they got COVID—they probably have better, like not better, but more antibodies against the virus,” said Nick Carl, one of the scientists.
“So your antibodies are probably better at that point than the vaccination,” he added later.
Chris Croce, another scientist at Pfizer, told an undercover reporter that people are “probably more” protected by natural immunity when compared with vaccination.
“You’re protected most likely for longer since there was a natural response,” he said.
A third scientist who allegedly works for Pfizer, Rahul Khandke, said that employees have had to sit through many seminars where they’re told that getting the company’s vaccine is safer than getting COVID-19 and that they cannot discuss the differences in public.
“Logically though, if you have antibodies built up, you should be able to prove that you have those built up. I don’t know, potentially that doesn’t seem that crazy,” he said.
https://www.theepochtimes.com/pfizer-scientists-in-undercover-videos-say-natural-immunity-likely-better-than-covid-19-vaccination_4034713.html
Hello All,
On Zyesami vs RLF-100.
I just wanted to comment on what I read here over the weekend.
"Zyesami is a new formulation".
THIS is a most critical issue. No-one, absolutely no-one, outside NRx or the mind of Dr Javitt, has actually been able to verify this. Not a single person. I have seen numerous post arguing this point when scientists better qualified than the posters don't even know that answer because, exactly, NRx has never released that information to Relief as required by the Collaboration Agreement. For all anyone of us knows, it could very well be that the very reason NRx have broken the CA in not releasing that information is because there is no material difference. I would go further : the very fact that NRx filed only a potential patent for Zyesami, rather than a full patent, is because it allows them not to reveal the formulation. So, until proven, do not even think for one minute that there is a significant patentable difference between Zyesami and the various patents Relief Therapeutics hold.
Second, to add to the above, just look at the picture, at the record of NRx : two failed EUAs for the same reason each time - insufficient numbers. Then the NRX100 and NRX101 products, which themselves were the subject of litigation, have had zero news about them since December 2019. Think about that for a second : I have subscribed to news about NRx since December 2019 and there has been no news about those two products in terms of advancements, trials, results, etc. Zero. And then look at the COVID vaccine : the same slow slow pace of, effectively, insufficient numbers in marginal countries : all the news we ever see are "opinions", vague news about "good for the long term" and then "not so efficient without booster after all", then more "opinions", but actual Trial Data with numbers, numbers, numbers, numbers, is always missing.
So, when you put all those pictures together the very LAST thing to even think is true is that Zyesami is really a materially different and patentable formulation.
Have a good week all.
Ilka, Y@h00 finance RLFTF
JK, BP and Big Government are driving the USA into a socio-economic ditch. What is the government hiding?
https://www.reuters.com/legal/government/wait-what-fda-wants-55-years-process-foia-request-over-vaccine-data-2021-11-18/
I will help you find reality, freeee…
https://rumble.com/vdqwr7-covid-truths-and-near-truths.html
Down on the Bayou: The Battle for health freedom in Baton Rouge.
Over the last three days I took an interesting trip down to Baton Rouge Louisiana with the Children’s Health Defense team on short notice to help Health Freedom Louisiana, the physician and nurses’ advocacy group Louisiana for Medical Freedom, Representative Kathy Edmonston, and Attorney General Jeff Landry by supporting testimony opposing the Louisiana Department of Health (“LDH”- backed by Governor John Bel Edwards) move to mandate the unlicensed and still experimental Pfizer vaccine be taken by Louisiana school children. General belief that I heard from the locals is that this is an attempt by Governor Edwards to curry favor with the Biden administration as he seeks a federal appointment as an exit strategy from the government and great State of Louisiana.
This is an even more radical position than that which has been advanced in the State of California by Governor Gavin Newsom, which state is intending to mandate the Pfizer vaccine be taken by all California school children when and if it becomes licensed. The leading organization opposing that California mandate is The Unity Project (www.uniprojectonline.com), for which I serve as Chief Medical and Regulatory Officer.
https://rwmalonemd.substack.com/p/down-on-the-bayou-the-battle-for
Not in the News: COVID Epidemiology
It is negligent to ignore the vaccinated as a source of transmission when deciding about public health control measures.
An article in Lancet Regional Health EU titled: “The epidemiological relevance of the COVID-19-vaccinated population is increasing” has important aggregated data on the significance of the vaccinated as sources for transmission of SARS-CoV-2 (1).
The article highlights that high COVID-19 vaccination rates have not reduced transmission of SARS-CoV-2 in populations by reducing the number of possible sources for transmission and thereby reduced the burden of COVID-19 disease. Recent data indicates that the epidemiological relevance of COVID-19 vaccinated individuals as a source of transmission is increasing, as there are fewer unvaccinated and more people are naturally immune.
https://rwmalonemd.substack.com/p/not-in-the-news-covid-epidemiology
Bill Gates, Vaccines & Profits
https://rumble.com/vodtir-bill-gates-vaccines-and-profits.html
This doctor said Suramin, an anti cancer drug, is the antidote to the vaxx sheet!! The question is, can you still get a prescription for this 100 year old drug?!?
Of course, I also believe AVIPTADIL is curative therapy!!!
https://rumble.com/vj2bjr-dr-judy-mikovits-there-is-an-antidote....html
On November 15, The Food and Drug Administration (FDA) asked a federal judge to give it until the year 2076 to fully release all of the data and the documents the agency used as the basis for the approval and license of the Pfizer-BioNTech COVID-19 vaccine. Now we know why.
https://techstartups.com/2021/12/02/1200-vaccine-deaths-reported-within-first-90-days-pfizer-vaccine-rollout-according-first-batch-pfizers-confidential-documents-released-fda-following-foia-laws/