RUTHFULLY YOURS

https://www.wsj.com/articles/fda-food-and-drug-admin-arg1-d-pegzilarginase-aeglea-biotherapeutics-arginine-deficiency-healthcare-c9e8c21f?mod=opinion_lead_pos6

We’ve spent most of our medical careers investigating and treating rare genetic conditions, including some afflicting only a few dozen Americans. Recently, scientists developed a treatment for one such condition—arginase 1 deficiency, or ARG1-D, which causes the amino acid arginine to accumulate in the blood, harming the brain and causing seizures, stunted growth and intellectual disability. The Food and Drug Administration has refused to consider the therapy. Its decision ignores the best available data and indicates a lack of understanding of rare-disease research.

Discovering treatments for rare diseases is a daunting task. Recruiting even a few dozen people for a clinical trial requires doctors and drug companies to identify a large share of the patient population. And since the market for such therapies is necessarily small, it’s nearly impossible to attract investment. So when news emerged aboutAeglea BioTherapeutics’ ARG1-D therapy pegzilarginase, we could hardly believe it. Pegzilarginase is an enzyme engineered to lower the body’s levels of arginine. The randomized placebo-controlled study of pegzilarginase included 32 patients with ARG1-D.

The results speak for themselves. The amount of arginine present in blood plasma declined by 80% for patients on pegzilarginase. After only six months, 90.5% of patients who received pegzilarginase had normal arginine levels, and this was sustained over time. The data also suggested progressive improvements in motor function compared with a placebo. And most patients tolerated the therapy quite well.

These numbers were jaw-dropping. Which is why the FDA’s decision is incomprehensible.

PIERRE KORY, MD, MPA-https://pierrekorymedicalmusings.com/p/reports-from-the-front-lines-of-the-ef4?utm_source=substack&utm_campaign=post_embed&utm_medium=email

The point of these “Reports From the Front Lines” posts is to bring to life all of the accumulating data of the mRNA vaccine’s toxicity and lethality. I am trying to relate what it is like for those professionals who are “awake” and “on the ground.” I believe the below will well manifest the lived experiences and observations of appropriately trained and concerned citizens during this historic pharmageddon.

In the below, I will share numerous “anecdotes” compiled from my ever-expanding network of contacts, colleagues, confidants, patients etc. I have no reason to believe any of these observations or reports are anything but reflective of their reality/truth. I understand that an anecdote is an anecdote. But a 100 anecdotes.. is a 100 anecdotes. And so on and so forth. You know what you can do with your pharma-conducted randomized controlled trials.

A large number of these observations come from “My Spy On The Inside” who I will call “MSOTI” below. Recall that she is a veteran ER-ICU nurse in a major academic health center. She knows pretty much everyone there; hospitalists, specialists, sub-specialists, nurse managers, blood bank technicians, department directors, IT experts, hospital administration, you name it.

She was very early to catch on to the toxicity and lethality and corruption around the vaccines and has been documenting what she is seeing. In the first 2 posts (here and here) and in what follows is, with her permission and some identifying details removed, a lot of what she has related to me in our text and telephone conversations over the past 18 months.

If the first two posts were not frightening enough, these next ones are a doozy (this is Post 3 and I have three more coming). I transcribed (and lightly edited the medical acronyms) from numerous text conversations that me and MSOTI have had over these last months, but I also included reports from others in my network.

I will start off with the below post from a commenter on my recent Substack which described the plight of the vaccine injured in our current medical system:

https://www.frontpagemag.com/cdc-confessions/

With mysterious new variants allegedly emerging, Joe Biden announces new vaccines “for everybody,” regardless of what they had done in the past. As this news breaks, former Centers for Disease Control director Dr. Robert Redfield reveals that the government health bureaucracy tried to quash discussion about the ineffectiveness of Covid vaccines.

“There was such an attempt to not let anybody get any hint that maybe vaccines weren’t foolproof, which, of course, we now know they have significant limitations,” said the former CDC director, co-founder of the University of Maryland’s Institute of Human Virology and Chief of Infectious Diseases at the University of Maryland School of Medicine.

“My position was just tell the American public the truth. There are side effects to vaccines. Tell them the truth and don’t try to package it.” In similar style, “I think we should really have confidence and not be afraid to debate the issues that we think are in the public’s interest and just tell the public the truth,” said Redfield (pictured above), who had been at odds with the government health establishment before.

In 2021, Redfield told CNN, “I’m of the point of view that I still think the most likely etiology of this pathology in Wuhan was from a laboratory, you know, escaped.” After these statements, as Vanity Fair reported, “death threats flooded his inbox,” some from prominent scientists.

“I was threatened and ostracized because I proposed another hypothesis,” Redfield explained. “I expected it from politicians. I didn’t expect it from science.” The people might expect the FBI, on full alert against “domestic violent extremists,” to investigate death threats against a public official. If any investigation took place, nothing has been reported.

In May of 2021, Joe Biden tasked the intelligence community to “redouble their efforts to collect and analyze information” on the origin of the pandemic.  Despite their efforts, in August Biden lamented that “critical information about the origins of this pandemic exists in the People’s Republic of China,” but China “continues to reject calls for transparency and withhold information.”