COVID-19 / Malicious Medical Quackery
[Ed.: FEAR YOUR DOCTOR! Medicine is a disgraced profession. They cannot (and must not) be trusted any longer!
Cultivate Nosocomephobia and iatrophobia. Spread ‘vaccine hesitancy’! How Bad is My Batch?
If you know someone injured by the jabs, direct them to humanitysuit.com to become a plaintiff. Another great legal recourse is: Freedom Council https://freedomcounsel.org
How Bad is My Batch? Enter your batch number(s) and find out. Then take action and purge yourself of this shit to the extent possible. It’s do-able!]

DIED SUDDENLY: Official Documentary Film [1:17:21]
https://www.thegatewaypundit.com/2025/06/liver-injuries-reportedly-rise-common-fda-approved-meds/
BREAKING: FDA Goes Rogue — Approves Moderna’s Next-Gen COVID-19 mRNA Injection Without Placebo-Controlled Trial NICOLAS HULSCHER, MPH
This move directly contradicts a recent HHS statement: “All new vaccines will undergo safety testing in placebo-controlled trials prior to licensure — a radical departure from past practices.”
MAY 31, 2025
The FDA has officially gone rogue.
It just approved Moderna’s newest COVID-19 mRNA shot—mNEXSPIKE—without a single placebo-controlled trial, directly contradicting recent public assurances from HHS that “all new vaccines will undergo safety testing in placebo-controlled trials prior to licensure.”

However, this authorization appears to align with their so-called “evidence-based approach to COVID-19 vaccination” published in NEJM —a policy that permits the continuation of mass experimentation on many Americans without clinical proof of benefit:
FDA Unveils New Plan to Limit COVID-19 Vaccine Use — Keeps Deadly Program Alive NICOLAS HULSCHER, MPH
MAY 20
According to Moderna:
The U.S. Food and Drug Administration (FDA) has approved mNEXSPIKE® (mRNA-1283), a new vaccine against COVID-19, for use in all adults 65 and older, as well as individuals aged 12-64 years with at least one or more underlying risk factor as defined by the Centers for Disease Control and Prevention (CDC).
The FDA’s approval of mNEXSPIKE is based on results from a randomized, observer-blind, active-controlled Phase 3 clinical trial (ClinicalTrials.gov Identifier: NCT05815498), which enrolled approximately 11,400 participants aged 12 years and older. The primary efficacy objective in this study was to demonstrate the non-inferior vaccine efficacy against COVID-19 starting 14 days after mNEXSPIKE compared to that after the comparator vaccine, mRNA-1273 (Spikevax®), Moderna’s original COVID-19 vaccine.
Moderna expects to have mNEXSPIKE available for eligible populations in the U.S. for the 2025-2026 respiratory virus season, alongside Spikevax and mRESVIA®, the Company’s approved respiratory syncytial virus (RSV) vaccine.
Most concerning is that the package insert for mNEXSPIKE reports a 2.7% serious adverse event rate. That means approximately 1 in every 37 people who receive the shot may suffer a life-threatening injury, hospitalization, or death.
And then there’s the name itself.

In Latin, the word “NEX” doesn’t just mean “death.” It refers specifically to violent or unlawful death—murder, execution, or slaughter. Roman legal and military texts used it to describe judicial killings, combat fatalities, and state-ordered executions—as found in the writings of Cicero, Caesar, Virgil, and Suetonius.
mRNA-1283 is Moderna’s next-generation COVID-19 mRNA vaccine, designed to encode the receptor-binding domain (RBD) and N-terminal domain (NTD) of the SARS-CoV-2 spike protein—unlike the original mRNA-1273 vaccine, which encodes the full-length spike protein.
But buried in the FDA’s May 30 approval letter is a concerning admission: the critical placebo-controlled trial that would actually assess the safety and efficacy of this new mRNA injection hasn’t even started yet.
According to the FDA, Moderna is only planning to begin a Phase 4, randomized, observer-blind, placebo-controlled study in adults aged 50–64 years without high-risk conditions on November 30, 2025—with final results not expected until January 2027.
Meanwhile, the trial used to justify this approval—NCT05815498—was not placebo-controlled. Instead, it merely compared mNEXSPIKE to Moderna’s previous COVID-19 shot (mRNA-1273/Spikevax)—a product already linked to serious adverse events and mass death.
This means the FDA fully licensed mNEXSPIKE for broad use without ever having seen placebo-controlled safety data in the exact population now being targeted.
This approval directly contradicts a recent public statement by an HHS spokesperson, who told The Washington Post:
“All new vaccines will undergo safety testing in placebo-controlled trials prior to licensure — a radical departure from past practices.”
BREAKING — RFK Jr. to Require Placebo-Controlled Trials for New Vaccines as FDA Admits “Void of Data” on COVID Boosters NICOLAS HULSCHER, MPH
MAY 1
Based on this extremely disappointing and dangerous development, it can be assumed that the Bio-Pharmaceutical Complex still exerts majority control over our regulatory agencies:
If we truly want to Make America Healthy Again, this global syndicate has to be properly dealt with.
Nicolas Hulscher, MPH Epidemiologist and Foundation Administrator, McCullough Foundation
Please consider following both the McCullough Foundation and my personal account on X (formerly Twitter) for further content.
https://www.thegatewaypundit.com/2025/06/red-alert-doctors-sound-alarm-after-fibrous-clots/
The Medical Miracle They Tried to Erase From History The Vigilant Fox
Three patients were on the brink of death from total lung failure. Then, something incredible happened after they started taking this substance.
JUN 07, 2025
The following information is based on a report originally published by A Midwestern Doctor. Key details have been streamlined and editorialized for clarity and impact. Read the original report here.
This drug reversed a condition that usually ends with a ventilator and a body bag.
Three patients were on the brink of death from total lung failure.
Then they were given intravenous DMSO—and something incredible happened.
Days later, they were breathing freely. One even had completely normal lungs within just a week.
You’ve probably never heard of DMSO—and that’s by design.
Once you see what it can do, you’ll understand why it had to be buried.
Upgrade to paid
The information in this thread comes from the work of medical researcher A Midwestern Doctor. For all the sources and details, read the full 9,000+ word report below.
The Forgotten Side of Medicine
How DMSO Protects and Heals the Internal Organs
7 months ago · 1331 likes · 471 comments · A Midwestern Doctor
DMSO (dimethyl sulfoxide) use exploded in the 1960s as a medical breakthrough.
There were thousands of studies.
There was massive public demand.
And there were miracle recoveries.
But the FDA dropped the hammer—and the pharmaceutical industry buried DMSO.
Why?
Because it worked.
The science is absolutely staggering.
DMSO does the following… and more:
• Reverses strokes
• Repairs heart damage
• Regenerates lung tissue
• Cures GI ulcers
• Protects organs from toxins
• Dissolves kidney and gallstones
All with a remarkably safe profile.
You may have noticed that
A Midwestern Doctor is a huge fan of DMSO—and rightly so. Today, I’m digging into how DMSO can heal our internal organs and sharing some incredible highlights from the article below:
DMSO shields heart cells during and after heart attacks, reduces tissue death, prevents cardiac rupture, and even helps stem cells regenerate heart tissue.
It boosts circulation and can restart weak hearts without even touching heart rhythm.
But Big Pharma said… pass.
Stroke patients have regained motor function—even years later—after using DMSO.
Why? Because DMSO “shocks” dormant cells back to life.
It works best when used immediately after a stroke or brain injury.
Timing is everything—but no one is telling you to use DMSO post-stroke.
DMSO heals ulcers and stops GI bleeding.
Study after study showed it outperformed drugs like cimetidine and prevented ulcer relapse better than anything on the market.
It also treats irritable bowel syndrome, colitis, and bleeding gastritis. Wow!
Studies have shown that DMSO can reverse ARDS (a common COVID killer), protect the lungs from smoke, trauma, shock, and edema, heal pulmonary fibrosis, and even save sheep from fatal smoke inhalation when nebulized.
But here’s the jaw-dropper: In the only human ARDS study, three patients near death were given IV DMSO.
All three patients recovered. One had completely normal lungs in just 7 days. Really.
How was this not global news?!
DMSO even protects the liver—shielding it from alcohol, industrial toxins, anesthetics, cirrhosis, and even surgery.
In one study, terminal cirrhosis patients given oral DMSO and aloe not only lived but improved dramatically.
And they were supposed to be dead within a year.
DMSO has been used to chemically dissolve gallstones.
It even helped rats recover from blocked bile ducts. Normally, that would be a death sentence.
And this is not just a theory. It’s all published research.
DMSO has reversed kidney failure from ischemia, radiation, antibiotics, and mercury.
In one study, every rat with renal failure from artery clamping died—except those given DMSO.
Those rats not only lived, but they recovered!
DMSO protects the pancreas from autoimmune attacks, boosts insulin response, and reduces the need for insulin.
It has also been shown to dramatically relieve pancreatitis—one of the hardest conditions to treat.
And yes, it helps with diabetic nerve pain, too.
DMSO can even cure interstitial cystitis, prostatitis, radiation cystitis, and painful urination.
One doctor reported curing 40 out of 40 bacterial prostatitis cases with antibiotics mixed in DMSO—delivered by catheter.
With zero recurrences.
Zero.
In a Chilean study, 57% of women with blocked fallopian tubes became pregnant after DMSO-based treatments.
Compare that to modern surgery’s 10–30% success rate.
It helps with pelvic pain, endometriosis, and uterine inflammation.
So why does DMSO work for all of these things? It almost sounds too good to be true!
DMSO penetrates deeply, carries other compounds with it, stops inflammation, reduces oxidative stress, preserves ATP production, and brings dying cells back online.
It’s a true regenerative therapy.
That’s why it was banned.
DMSO couldn’t be patented. It was too versatile. Too safe. Too cheap.
So, of course, it threatened billion-dollar pharmaceutical markets.
The only option was for the FDA to turn on it, and the public never knew why.
Interested in trying DMSO yourself? Here are some safety tips:
• Start low: 30–50% topical
• Do a patch test first
• Only use oral if tolerated
• Always dilute in water or aloe
• Use glass containers (not plastic)
• Only apply to clean skin because DMSO pulls in anything it touches
Thanks to
A Midwestern Doctor for working so hard to revive interest in DMSO.
Too many lives are being lost to treatable diseases, and too many people are living in pain when they don’t need to.
The FDA tried to erase DMSO. But the truth is impossible to hide forever.
Thanks for reading! This information was based on a report originally published by A Midwestern Doctor. Key details were streamlined and editorialized for clarity and impact. Read the original report here.
