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]
Moderna’s mDEATHSPIKE, mRNA-Induced Autism, and the ACIP Reset NICOLAS HULSCHER, MPH
Epidemiologist Nicolas Hulscher on Malta’s National TV
JUN 11, 2025
Yesterday, I sat down with Stephanie Chircop on Bejnietna, her long-running program on Malta’s national TV station, NET News. In our rapid-fire conversation, I outlined the current mRNA injection situation in the United States—and why I believe it’s a public health emergency.
Here’s a quick summary:
- mRNA injections deliver modified genetic code inside lipid nanoparticles that travel to every organ system, instructing your cells to manufacture a toxic, non-human spike protein.
Disease X: Wayne Allen Root Interviews Dr. Corsi [8:35] JEROME R. CORSI, PH.D.
Medical Martial Law is on the horizon…globalist plan in motion for decades coming soon, with God’s help we can defeat it in its tracks.
JUN 11, 2025 – Many despicable politicians have followed the slogan “never let a good crisis go to waste.” We witnessed that most recently with the Globalist Left’s COVID power grab within and outside of the U.S. Now, the WEF, WHO other globalists and fellow statists are looking to weaponize “Disease X” against the free world. Dr. Jerome Corsi takes a deep dive into what’s happening on today’s The Truth Central.
MRNA, GENE THERAPIES AND BIOMANUFACTURING FRAUD SASHA LATYPOVA
Arcturus self-amplifying RNA: US approval expected this year.
saRNA platform Kostaive is already approved in Europe and Japan and is being tested in the US now.
JUN 11, 2025
Founded in 2013 and based in San Diego, California, Arcturus Therapeutics Holdings Inc. (NASDAQ:ARCT) is a commercial mRNA medicines and vaccines company with enabling technologies:
- LUNAR® lipid-mediated delivery;
- STARR® mRNA technology (sa-mRNA);
- mRNA drug substance and drug product manufacturing.
Arcturus KOSTAIVE, a self-amplifying messenger RNA (sa-mRNA) COVID vaccine platform is now approved in the EU and Japan. The approval in the United Kingdom is anticipated in Q2 2025, followed by a U.S. BLA filing expected in Q3 2025.
Self-amplifying mRNA vaccine program:
In April 2025, Arcturus received U.S. FDA Fast Track Designation for ARCT-2304, an sa-mRNA vaccine candidate for Pandemic Influenza A Virus H5N1. Arcturus states that its self-amplifying mRNA injection program is 100% funded with federal funds from the Department of Health and Human Services; Administration for Strategic Preparedness and Response; Biomedical Advanced Research and Development Authority (BARDA), under contract number 75A50122C0007. The total amount is $63M of which approx. $24M has been spent to date. In its shareholder disclosures, Arcturus states that:
[Using these funds], Arcturus has completed the recruitment of 212 adults in Phase 1 (132 participants 18-59 years old; 80 participants over 60 years old) for the randomized and claimed as placebo-controlled Phase 1 trial (NCT06602531), which is being conducted at multiple sites in the U.S. and the company expects interim Phase 1 data in H2 2025.
About that “placebo-controlled” statement above. In the new age of gold standard, evidence based, fully transparent, make-America-healthy, imagine-if-it-were-Kamala!!(TM) “good”-FDA, the “placebo-controlled” vaccine study means they are using a, drumroll….
“placebo vaccine”!
Thank you MAHA-FDA! Imagine if those bad Democrats were in power. Phew, did we doge a bullet in Butler, PA or what…
Here is my typical dialogue with MAH-Anons on this topic:
- Me: the study was designed, submitted to and accepted as sufficient design for a US approval by the “bad” FDA run by the bad Democrats in September of 2024.
- MAH-Anons: shut up already and stop splintering the movement!
- Me: this study design is fully compliant with the new FDA policy for “pandemic emergency” mRNA vaccines pre-written during Biden Administration and presented as the work of Dr. Makary (FDA Commissioner) and Dr. Prasad (head of CBER FDA), which does not require any placebo controlled or long term safety studies for shots deployed on the “vulnerable” groups, including children and pregnant women!
- MAH-Anons: it was the best RFK Jr could do to fight BigPharma, baby steps!!!
Maybe I am being unfair to the new, good-FDA. Turns out, Arcturus recently published data for KOSTAIVE self-amplifying mRNA covid vaccine, with a 12-month follow-up from the pivotal clinical study in Vietnam (NCT05012943), which had 17,582 participants and even allegedly had a “true saline placebo, I swear!” control.
Let’s review this published paper.
Study Design:
5 Evidence-Based Approaches to Healing from Vaccine Injury [26:55] NICOLAS HULSCHER, MPH
From myocarditis to turbo cancer, emerging research offers hope for the millions injured by mRNA shots.
JUN 09, 2025
Millions of people injured by mRNA injections have been completely abandoned by our public health agencies. In the absence of meaningful support, it is critically important to identify and advance safe, evidence-based strategies to aid recovery. At the McCullough Foundation, ongoing research has highlighted the following key interventions:
RFK Jr. pushes mRNA shot. He must go! DR. PETER AND GINGER BREGGIN
Dr. Peter and Ginger Breggin radio show about the world’s most prominent advocate for vaccine safety, who has now committed himself to promoting Moderna’s latest version of the mRNA Covid jab.
JUN 09, 2025
On May 30, 2025, the FDA sent a letter of approval to the pharmaceutical company Moderna to manufacture and sell its new COVID-19 vaccine.1 But even more dismaying, Robert F. Kennedy Jr., the world’s most prominent advocate for vaccine safety, has now gone out on a political limb and committed himself to promoting Moderna’s latest version of the mRNA Covid jab.2 In doing so, Kennedy is supporting the continuation of the world’s most lethal medical or wartime assault on humanity, one that many see as a bioweapons attack on America by the globalists, including Communist China. [continued below]
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There are more than 38,000 reports of death to date to the CDC and FDA from the COVID-19 vaccines. Nothing like this catastrophe has ever before happened in medicine or public health. In addition, there is a deluge of reports and independent studies verifying the almost infinite harms caused by these mRNA vaccines. These harms include infertility, a declining birth rate, multiple harms to infants and mothers, cardiovascular disorders, including myocarditis in children and strokes in adults, tumors, a wide range of neurological and psychiatric disorders, and Acquired Immunodeficiency Syndrome (AIDS), which results in greater susceptibility to infections and cancer. But for every reported death and other serious adverse event, we know that there are more than 100 actual deaths or harms. These “vaccines” are killing and maiming millions in America and millions more around the world.3
Here is Kennedy’s entire defense of his atrocious actions:
Actually, there is nothing “limited” about the approval letter. The letter specifically empowers Moderna to manufacture and distribute the drug. They will go ahead with this before completing any additional studies supposedly promised to Kennedy, which would take years more. Besides, once a drug company has spent multi-millions getting a drug approved, as they have already done, I’ve never seen a company actually complete additional studies that could invalidate their drug. Moderna’s survival is at stake, and drug companies don’t commit economic suicide. And this one has the backing of Bill Gates!
Kennedy has broken many recent promises to get himself into this bizarre situation of betraying his previously voiced ideals. He is approving the Moderna COVID-19 vaccine without so much as a placebo-controlled clinical trial or even a review by the FDA Vaccine Committee. On top of that, pregnant women are not protected as he promised to do. But worst of all, he has never even promised to stop the heavily documented murder of the elderly who are killed by the mRNA covid vaccines at a rate of eight times more than the rest of the population.4
Many of us will remain eternally grateful for RFK Jr’s support for Donald Trump’s election campaign. But now he must resign or be removed.
Kennedy’s acceptance of the FDA’s approval of Moderna’s Covid vaccine is more than sufficient reason to fire him. But in addition, he is also grossly undermining the Trump administration and further threatening the well-being of all our citizens by advocating the use of extremely dangerous neurotoxins, including methylene blue, MDMA or Ecstasy, and psychedelics. Trump’s choice for Surgeon General, based on Kennedy’s recommendation, is devoted to psychedelics! Remember, the brain was not designed to benefit from neurotoxic intrusions, even very small ones. It was instead designed to keep them out by means of the blood-brain barrier and then to fight them on a cellular level if they manage to break in. It’s as if RFK Jr. has become a toxic mole within the America First movement.
For an in-depth scientific analysis and presentation about everything in this synopsis, please read the full article:
RFK Jr. blatantly supports the deadly mRNA COVID shots and must be forced to resign
JUN 6, 2025
Many of us will remain eternally grateful to Robert F. Kennedy Jr., for helping to elect Donald Trump to the Presidency, bringing America First to power in our nation and the world. Now, RFK Jr. must be removed from office immediately, before he can cause further damage!
End Notes
1 May 30, 2025 Approval Letter – MNEXSPIKE
2 Secretary Kennedy on X: “I want to address those of you who have anxieties about @US_FDA’s limited approval of a new mRNA COVID vaccine for high-risk populations. Moderna has agreed to a true placebo-controlled trial of the new vaccine, which is similar to the existing mRNA vaccine but uses a smaller” / X. Actually, there is nothing “limited” about the approval letter. Besides, once a drug has spent multi-millions getting a drug approved, I’ve never seen one fulfill a promise to do studies that could invalidate their drug. Besides, if a study of safety is still needed, it’s ridiculous to put off until after it’s been approved, by which time many could be harmed.
3 New FDA Plans for the Covid Vaccines Will Kill Millions More
4 New FDA Plans for the Covid Vaccines Will Kill Millions More
Deadly Heart Condition Surges 115,100% in Covid mRNA-Vaccinated Frank Bergman
June 8, 2025
A world-renowned immunologist is sounding the alarm after his peer-reviewed research uncovered a devastating surge in a deadly heart condition among people who received Covid mRNA “vaccines.”
Dr. János Szebeni, an internationally recognized European immunologist, issued a stomach-churning warning to the world after confirming that the injections have caused a staggering 115,100% surge in myocarditis.
Myocarditis is a “silent killer” at the center of the sudden deaths crisis that emerged after the Covid injections were rolled out for public use in early 2021.
The mind-blowing discovery was revealed in a sweeping peer-reviewed study by Dr. Szebeni, a professor at Hungary’s Semmelweis University and Sungkyunkwan University and a leading immunotoxicology researcher at SeroScience.
Dr. Szebeni is calling for a critical reevaluation of mRNA injections’ classification as “vaccines.”
Szebeni argues that the shots cannot be considered “vaccines” due to the dramatically expanding profile of adverse events (AE).
He also highlights the underreporting of AEs in official statistics and systemic biological risks inherent to the “vaccine” platform.
The study’s peer-reviewed findings were published in the prestigious journal Pharmaceutics.
Szebeni’s paper challenges both the prevailing regulatory definitions and the assumption that mRNA vaccines pose only minimal safety concerns in healthy populations.
The prominent Hungary-based physician-investigator hypothesizes that adverse events (AEs) linked to mRNA-based Covid “vaccines” are more frequent and severe than initially reported.
As a result of his findings, Prof. Szebeni argues that mRNA “vaccines” must be reclassified as gene therapies.
A distinguished immunologist renowned for his significant contributions to the fields of artificial blood, liposomes, and the complement system, Dr. János Szebeni serves as the director of the Nanomedicine Research and Education Center at Semmelweis University in Budapest, Hungary.
He also holds a full professorship in immunology and biology at the University of Miskolc.
Dr. Szebeni is also the founder, CEO, and lead researcher of SeroScience Ltd.
SeroScience is a company specializing in immunotoxicology services, particularly in predicting and preventing hypersensitivity reactions to intravenous drugs.
During the study, Szebeni tapped into multiple sources of global data, including official government databases.
This is a comprehensive synthesis of published literature, Pfizer post-marketing safety reports, and global vaccination statistics.
The study also analyzed data from the U.S. Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS).
It compares AE incidence in mRNA “vaccines” from Pfizer and Moderna to traditional influenza vaccines.
The study places emphasis on “Brighton-listed” serious AEs.
The Brighton Collaboration created a priority list, endorsed by the World Health Organization (WHO), of potential adverse events relevant to Covid vaccines.
The study also examines plausible mechanisms for AEs, such as immune hyperactivation, autoimmunity, and complement activation.
Dr. Szebeni’s analysis exposed alarming AE ratios and “vaccine” platform risks.
The analysis found that recipients of Covid mRNA “vaccines” experienced AEs at an average of 26 times the rate of flu vaccine recipients.
The study revealed that Covid injections caused a staggering 1152 times higher incidence of myocarditis, a dangerous form of heart inflammation, when compared to the flu shot.
Szebeni’s findings show a 115,100% surge in heart failure among the mRNA-vaccinated.
Myocarditis is the inflammation of the heart muscle (myocardium).
The condition reduces heart function, causing strokes, blood clots, cardiac arrest, or even sudden death.
Myocarditis is described by cardiologists as a “silent killer” as it’s often symptomless, leaving many sufferers unaware that they have it until they suffer a side effect, such as a cardiac arrest, when it’s too late.
According to the CDC, myocarditis is a known side effect of Covid mRNA “vaccines.”
However, myocarditis was just one of the extreme adverse events observed in the study.
Dr. Szebeni listed the most extreme AEs as:
- Myocarditis: 1152x higher incidence
- Thrombosis: 455x higher
- Myocardial infarction: 226x
- Death reports: 218x
- Tachycardia, dyspnea, hypertension: 130–160x higher
Approximately 4–18% of all reported AEs were classified as severe.
A separate reanalysis of the original Pfizer trial data found a 36% higher risk of serious adverse events in the vaccinated arm compared to the placebo.
This finding contradicts earlier safety assurances regarding the injuries.
Notably, only 47% of AE cases in Pfizer’s early safety surveillance had fully recovered within three months.
In addition, the study highlights systemic issues in “vaccine” surveillance, including:
- Inconsistencies in data collection across agencies
- CDC and FDA reliance on voluntary reports (VAERS), estimated to capture fewer than 10% of actual serious AEs
- Pfizer’s use of vague AE categorization and a staggering 1,100+ unique adverse event labels, including over 220 inflammatory or autoimmune-related events
These inconsistencies, Szebeni and his team argue, have delayed recognition of real-world “vaccine” toxicity patterns and obscured the large spikes in serious injuries.
Dr. Szebeni is calling for the reclassification of mRNA injections as “prophylactic immuno-gene therapies,” rather than “vaccines.”
He states that the term reflects the shots’ mechanism of genetic transfection and immune modulation.
Szebeni further argues that persistently disabling AEs meet the criteria for iatrogenic orphan diseases.
As such, they warrant special regulatory recognition and funding for affected individuals.
Szebeni reveals that VAERS data shows that mRNA “vaccines” have killed up to 160,000 Americans.
However, he warns that the figure is likely far higher due to the unreporting that the study exposed in the system.
In addition, global deaths linked to “vaccination” are expected to be far higher again and command a thorough investigation.
READ MORE – Red Alert Issued as Fibrous Clots Found in Young Children of Covid-Vaxxed Mothers
Liver Injuries Reportedly on the Rise: Common, FDA-Approved Meds Linked to Alarming Trend
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.
