But what Big Pharma really hates is its ability to treat infections that antibiotics and antivirals can’t.
Like ivermectin, this forbidden remedy belongs in everyone’s medicine cabinet.
🧵 THREAD
The information in this thread comes from the work of medical researcher @MidwesternDoc. For all the sources and details, read the full report below. midwesterndoctor.com/p/dmso-transfo…
In the 1960s–80s, pharmaceutical companies poured money into DMSO research, and the results were jaw-dropping.
They found DMSO to be effective on viruses, bacteria, fungi, and parasites—with a safety profile better than many over the counter drugs.
The evidence was piling up. The FDA slammed on the brakes. Most medical research was banned.
Why would the FDA ban research on something that was proving so effective?
Approving DMSO meant opening the floodgates for countless new drug applications, undermining Big Pharma’s existing patents.
Congress actually protested. Patients pleaded. Researchers fought back.
But the FDA’s call held, and an entire generation of doctors never learned what this compound could do.
What makes DMSO unique is its combination of powers.
It sounds too good to be true… but believe me—it’s all true!
DMSO:
• Kills or disables microbes without harming human cells
• Removes antibiotic resistance in “superbugs”
• Transports drugs deep into bone, nerves, and organs
• Boosts circulation so the immune system can reach infected areas
• Protects cells from bacterial toxins and drug side effects
This isn’t just another drug—it’s a multi-tool that could reshape medicine, especially for the hardest infections to treat.
@MidwesternDoc Herpes and shingles are among the most well-studied viral uses of DMSO.
For a host of reasons, shingles cases are on the rise. If you or someone you know is at risk, check out the full article from @MidwesternDoc now.
When applied early, patients never developed post-herpetic neuralgia—the debilitating nerve pain that can last weeks, months, or even a lifetime.
DMSO works alone but is even more effective when combined with antivirals like IDU or acyclovir, delivering them directly into tissues where they normally can’t penetrate on their own.
We’re talking faster healing, less pain, and fewer recurrences—results the FDA knew about over 40 years ago! But even today, if you’re diagnosed with shingles, you’re given an oral antiviral and sent on your way.
Everyone needs DMSO in their medicine cabinet.
Shingles pain… gone in two days! Outbreaks healed in a third of the usual time. Nerve damage prevented entirely.
What more is there to say?!
Multiple randomized trials from decades ago back it all up.
Yet in North America, the best topical combo (DMSO + IDU) is still unavailable.
England and Ireland approved it in the 1970s. The US? Nope.
Ask anyone who has been diagnosed with shingles recently… Did the treatment from their mainstream doctor even help? Probably not.
Herpes simplex? Same story!
Multiple studies show DMSO plus IDU or acyclovir dramatically shortens outbreaks, reduces recurrences, and even works for stubborn cases on the genitals, face, or fingers.
Some trials found no recurrences for six months in patients treated with DMSO combos. The control group averaged nearly two recurrences in that time!
Even low concentrations of DMSO can stop viral replication by hitting multiple stages of the virus’s life cycle.
DMSO’s bacterial applications are just as impressive.
DMSO directly damages bacteria, can dissolve them, or just interfere with their metabolism. Most importantly, it removes their defenses—making resistant bacteria sensitive to antibiotics again.
That’s great news. The risk of resistant bacteria continues to rise due to the overuse of antibiotics. DMSO is a solution!
In Tuberculosis research, 5% DMSO made resistant strains up to 200 times more sensitive to streptomycin. In some cases, just a single dose restored antibiotic effectiveness.
For infections within bone, joints, or poorly supplied tissues, DMSO can deliver the antibiotic right where it’s needed—without the toxicity of massive systemic doses.
It sounds like a miracle, doesn’t it?
Imagine if hospitals could take a limb-threatening infection, resistant to every drug on the shelf, and turn it into one that responds to standard antibiotics again.
That’s exactly what DMSO has done in both lab studies and real-world cases!
Just think about the number of people who have needlessly suffered because DMSO isn’t the go to course of action? Despite the medical industry knowing it works…
DMSO has been a miracle worker for ENT and dental infections.
Doctors have used it to shrink inflamed eardrums—within 15 minutes! DMSO has open blocked sinuses in minutes and rapidly cleared up stubborn tonsillitis.
Dentists have applied it after extractions or deep restorations to stop pain even before it starts. Periodontal disease, pulpitis, and abscesses have all responded to DMSO—especially when paired with antibiotics.
In one study, gum disease patients had total elimination of pain and bleeding after just a handful of treatments.
@MidwesternDoc The before-and-after examples of what DMSO has done will blow your mind.
And if all of that wasn’t mind blowing enough—surgical and critical care uses might be the most dramatic.
DMSO speeds wound healing, prevents infection, and can replace the need for invasive procedures. Case reports describe deep fungal infections, scalp abscesses, and chronic osteomyelitis resolving without surgery.
One doctor saved his own contaminated foot wound from infection and cut healing time in half just by applying DMSO along the edges.
For burn units and trauma centers, this could be standard of care—if it weren’t buried.
Fungal infections are notoriously hard to treat—especially in nails, skin, and the eyes.
DMSO enhances antifungal drug penetration so well that in one veterinary study, severe ringworm cleared in under a week—instead of a month.
It can carry drugs like ketoconazole or amphotericin B into the brain or cornea, places most antifungals can’t reach. That opens the door to treating life-threatening systemic fungal infections that are currently almost impossible to cure.
DMSO helps with parasitic infections, too.
Topical DMSO plus anti-parasitic drugs has cured hookworm skin infections and deep tissue parasites that standard treatments can’t reach.
Its real power lies in carrying the drug directly to where the parasite hides—whether in the liver, muscles, or joints.
Even in stubborn liver cysts from tapeworm infections, surgical teams have used a DMSO mix to prevent spread and recurrence.
@MidwesternDoc Most of this research proving DMSO’s effectiveness is decades old. It’s peer-reviewed, documented, and replicated.
But it’s been purposefully kept out of your doctor’s toolkit.
The miracle solvent has saved cats from near-certain death due to panleukopenia, reversed deadly equine herpes cases, and treated bovine mastitis that was resistant to every antibiotic tried.
Farmers and vets have successfully and routinely used it for decades—while human patients are told it’s “unproven” and “dangerous.”
Lung and abdominal infections, meningitis, sepsis, osteomyelitis—there are published case series on all of them.
The list is endless.
Neonates with life-threatening pneumonia recovered in days. Patients with destructive TB cavities in their lungs healed. Chronic peritonitis resolved without repeat surgeries.
In sepsis, DMSO improved survival even when bacteria were antibiotic-resistant.
@MidwesternDoc If one compound could kill superbugs, deliver drugs deep into tissue, and neutralize toxins—without harming you—would you want to know about it?
Why on earth don’t we have DMSO in every hospital, clinic, and pharmacy?
It’s shocking and maddening.
And it’s all because of the exact same reason other low-cost, multi-use therapies get sidelined: no patent monopoly, no billion-dollar profit margin—and a regulatory system that protects those margins.
Meanwhile, millions suffer or die from ailments that DMSO could treat.
@MidwesternDoc It’s time to take back control of our health. Get all the details on how to dose and apply DMSO in the full article from @MidwesternDoc.
While it sounds a bit like it might be, DMSO isn’t magic. It’s science. And we’ve had it for 60 years.
DMSO generally works best when used early, in the right concentration, and when paired with other antimicrobials it can deliver to the heart of an infection.
Its safety record is stronger than most drugs on the market. The real danger is leaving it in the shadows.
@MidwesternDoc Thanks for reading! This information was based on a report originally published by @MidwesternDoc. Key details were streamlined and editorialized for clarity and impact. Read the original report here. midwesterndoctor.com/p/dmso-transfo…
@MidwesternDoc For a deeper dive into what modern medicine has overlooked—or intentionally buried—check out these other eye-opening reports by @MidwesternDoc:
REPORT: The NIH is now funding research into ivermectin as a cancer treatment.
Yes, the same drug they mocked as “horse paste” is now being seriously studied—for its ability to kill cancer cells.
On February 10, the NIH confirmed it’s funding preclinical trials on ivermectin’s anti-cancer properties. Dr. Anthony Letai, head of the National Cancer Institute, said there’s “enough interest” and “enough reports” to take it seriously. Studies are already underway, with results expected in just a few months.
This follows 2024 and 2025 reviews by U.S. scientists showing signs that ivermectin can inhibit tumors. The NIH is now backing that research, pointing to ivermectin’s Nobel Prize-winning legacy and its decades of safe, FDA-approved use in humans.
But instead of welcoming a promising, low-cost treatment, the media doubled down. Outlets like MedPage Today rushed to dismiss the story as “right-wing hype,” ignoring the science and smearing anyone who dared to ask questions.
Why attack a drug that could save lives—unless the real threat is to their bottom line?
If ivermectin works, it won’t just save lives. It’ll shatter the system built to suppress it.
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In other news, Republicans and Democrats are backing a bill that opens the door to mandatory Digital ID for every American.
It’s called the “Kids Off Social Media Act.” But it doesn’t just target kids. It targets you.
The bill bans anyone under 13 from having a social media account. Sounds reasonable—until you realize enforcement means scanning your face, checking your ID, or tracking your device… just to prove you’re old enough to speak online.
The bill doesn’t have to say “Digital ID.” The logic demands it. And once those systems are in place, they won’t stop at children. They’ll be used to control what you can say, see, and share.
Multiple states have already declared these laws unconstitutional. So why are Republicans still pushing them?
This is exactly how it started in the UK. Today, people are getting arrested for memes.
Watch @zeeemedia's report before they normalize this—and your freedom to speak anonymously disappears forever.
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Google why we no longer see crippled kids from polio. You’ll get one answer: vaccines.
But Dr. Suzanne Humphries says that’s not what the facts show—and when you dig into the history, the real story is jaw-dropping.
First off, polio never actually disappeared. “Polio is still here. Polio is still alive and well,” Humphries says.
What changed? The definition. Once the vaccine was introduced, the medical establishment redefined what counted as “polio.”
Humphries explains: “Polio is called different things today. Whereas back in the 1940s, 1950s, the criteria for diagnosing polio were completely different to the year that the vaccine was introduced. The playing field, the goalposts—everything was changed… they were able to show a complete cascading drop of paralytic polio simply because of the way they changed the definitions of what polio is and what could cause it.”
Suddenly, cases that would’ve been labeled polio were now called Guillain-Barré syndrome, coxsackievirus, echovirus—or simply chalked up to heavy metal poisoning. “They didn’t have virus, or they had coxsackievirus or echovirus, or they were lead poisoned or mercury poisoned, which was—the mercury and lead were the leading treatments of the day,” she said.
But it gets worse.
The rise of polio, she says, directly mirrored the use of toxic pesticides like DDT. “The tonnage of production of DDT absolutely mirrored the diagnosis for polio.” And even today, “the countries that still make DDT today is where we’re still seeing this paralytic polio situation happen.”
So what about the virus?
Polio virus, according to Humphries, is what’s known as a commensal—a normal virus that lives in most people without causing problems. In fact, “95 to 99% of all polio is asymptomatic.” She described a study of the Javante Indians where “98 to 99% of every person they tested… had evidence of immunity to all three strains of polio.”
When asked where all the paralyzed children were, she recalled: “They were like, ‘We don’t have any of that problem.’”
Humphries also points to a 1916 Rockefeller lab in Manhattan that, in her words, had “the specific stated goal… to try to create the most pathological, neuropathological strain of polio possible.” By injecting monkey brains and human spinal serum into monkeys, “there was a big problem with that, which was released into the public by accident. And the world experienced the worst polio epidemic on record. 25% mortality.”
Bottom line? According to Dr. Humphries, polio didn’t disappear because of vaccines. It disappeared behind a curtain of redefinitions, misdiagnoses, manmade disasters—and a whole lot of propaganda.
And if they went that far to deceive you about the polio vaccine, what else are they lying about? 🧵
Did you know the original smallpox vaccine caused serious injuries—and was often contaminated with pus, bacteria, and fungus?
We’ve been told it saved humanity from a deadly disease, but what if that’s a lie?
Dr. Suzanne Humphries explained to Joe Rogan what happened to children who received the vaccine. They developed large ulcers, high fevers, and widespread infections. With no antibiotics available, treatments were limited to mercury, arsenic, bloodletting, or isolation in dark rooms.
These severe reactions weren’t considered rare. In fact, they were referred to as “a good take.”
What made matters worse was how the vaccine was produced. According to Dr. Humphries, it was made by infecting animals and harvesting the resulting pus.
“They would take pus from other animals, scratch it into the belly of a cow, then take the pus off of the big pimples that would form,” she said. The material—called “pure lymph”—often came from cadavers, horses, or ulcerating cow udders, mixed with glycerin, and scratched into the surface of the skin.
Even decades later, contamination was an issue. “There was more bacteria and fungus in the smallpox vaccines than there was smallpox virus.” One widely used version, Dryvax, was eventually considered so problematic that health authorities ordered all remaining specimens destroyed around 2009.
Living conditions at the time were “a disaster.” Streets were filled with human and animal waste, there was no running water, and sanitation was nearly nonexistent. Poor hygiene and co-infections absolutely made smallpox far more deadly than it might have been otherwise.
Despite all this, the smallpox vaccine is still presented as a flawless triumph.
But for those who experienced the injuries firsthand, and for those who study its full history, the story isn’t so simple.
“This is the one vaccine that eliminated, eradicated a disease,” Dr. Humphries said sarcastically. “Can you believe that fairytale?”
We’ve all been taught that the smallpox vaccine was one of medicine’s greatest triumphs.
But when you read the actual clinical observations recorded by doctors who lived through its rollout, a far more unsettling picture emerges.
It’s not propaganda, and it’s not hindsight. It’s primary-source medicine.
There’s a reason doctors love pushing vaccines. The more they inject, the more money they make.
The foot traffic alone brings in big money, but there’s another perverse incentive, and once you hear it, it will make you angry.
RFK Jr. explains: “Pediatricians who vaccinate 80-85% of the kids in their office, get these giant bonuses... And that's why they throw you out of the office if you fight back…You'll lose them their bonuses.”
Sadly, these perverse financial incentives aren’t limited to vaccines but across many areas of medicine.
Dig a little deeper, and another disturbing pattern appears. Once you see it, you’re left gobsmacked by just how far the corruption runs beyond money. 🧵
The video below is haunting—not because the doctor in it is malicious, but because she genuinely believes she’s helping.
She’s an MD with a Master’s in Public Health, a Fellow of the American Academy of Pediatrics, and a former leader at Georgetown. Her language is warm. Her intentions seem pure.
Yet this interview perfectly captures how public health has lost its way.
After conquering most deadly contagious diseases, it turned toward chronic illness—and failed.
Instead of questioning why children are getting sicker, it doubled down on vaccinating more, earlier, and without dissent, often dismissing safety concerns as heresy.
Watch this video. Then ask yourself what matters more in modern medicine: children’s outcomes—or institutional certainty.
A lawsuit filed several years ago exposed something far more disturbing than a single act of medical misconduct.
It revealed how, during COVID, core medical ethics quietly collapsed—how consent became optional, coercion was reframed as care, and vulnerable people were treated as obstacles rather than patients.
This isn’t about ideology. It’s about what happens when fear, authority, and institutional pressure override conscience.
The real cause of heart disease has been buried for decades in favor of the lie about cholesterol.
40 million Americans take statins to lower their cholesterol, thinking it’s the best way to protect their hearts.
But what doctors never tell them is that statins interfere with the body’s natural repair system, weakening the very cells that rely on cholesterol to function.
In trying to prevent disease, they’re paradoxically fueling it.
This report exposes what really happens to the body when you take a statin every day.
For years, doctors have been taught that high cholesterol causes heart attacks. They’ve passed the warning along to their patients, and most of us have believed them.
But that idea came from one man: Ancel Keys.
Keys cherry-picked data to make fat and cholesterol look deadly while ignoring the real culprit: sugar.
John Yudkin tried to warn the world that sugar—not fat—was driving heart disease. But no one listened. He was ridiculed, silenced, and erased from history.
In 2015, Scott Adams made a “crazy” prediction that most people thought was impossible.
He said Trump had a 98% chance of becoming president, and he made that call on a single observation.
The winning attribute that made Scott confident in Trump’s victory was his one-of-a-kind persuasion skills.
While political betting markets dismissed Trump’s chances, Adams argued—using his background in persuasion and hypnosis—that Trump was the most psychologically effective candidate in the race and therefore favored to win.
He built a massive following by showing how persuasion, not policy, drives political outcomes.
That insight proved correct. But it also revealed something darker. 🧵
After Trump’s victory, Adams pivoted to punditry—and during COVID, even he struggled to see the truth.
Scott strongly endorsed the vaccines, vaccinated himself, and publicly belittled followers who refused. Many later derisively called him “Clot Adams.”
In January 2023, Adams admitted—on video—that he’d been wrong and that the anti-vaxxers were correct. But he framed it as luck: the right people just happened to distrust the government, while “all the data” supposedly pointed intelligent analysts toward vaccination.
That framing matters. It reveals how even skilled observers of persuasion can mistake marketing consensus for truth—and how the same system that manufactures medical certainty also hides the limits of medicine, until reality forces a reckoning.
Last May, Scott told the world something most people never say out loud until it’s unavoidable: he had terminal, metastatic prostate cancer.
He openly stated he planned to use California’s medically assisted dying to reduce suffering.
He also shut down speculation—saying he had already tried fenbendazole and ivermectin and had no interest in continuing them.
The reaction was explosive.
People weren’t just debating treatment choices—they were watching, in real time, what a protracted, modern death actually looks like.
For many, it shattered comforting abstractions about both cancer and mortality.