Replies to post #44076 on Relief Therapeutics Holding AG (RLFTF)

[Joe Kaplan]

Good Stuff From ..Lt.Francis 12 hours ago over on another y blog
Hi All,

MORAL BOOST TIME:

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

Start at page 34, after pg 74 it gets a little tedious.
Note Ms.Davidson on the FDA panel refer to Aviptadil as a seemingly Miracle drug on page 63.
She's referring to VIP/Aviptadil's use in Neuro degenerative disease such as Alzheimer's and Parkinson's ( pg 52-54 ).
A Dr. Shoemaker who has treated 1700 patients over 8 years tells the FDA panel that Aviptadil is a " Magic Bullet " for Pulmonary Hypertension and the treatment of MOLD sickness in humans.
This is all before COVID in 2016 . It is an interesting read for sure, and speaks to the many possibilities of this Drug when it gets NDA.
This report records a failed attempt by a competitor at some Authorization from the FDA, but the claims being made were pretty encouraging.
It's only a matter of time.
Some indications for neuro diseases will take a few years, but my grand-kids aren't going anywhere, and will be thanking me for their college educations after I'm gone.

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

Lt. F
GLTU- GLTA

[changes_iv]

Thank you JK, likewise!

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

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

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

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

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

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

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

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

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

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

[changes_iv]

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

March 17, 2022 • by Zoe Wilson

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

REMEMBER THIS??

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

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

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

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