Health
Mel Gibson Drops Two Medical Bombshells on the Joe Rogan Podcast

From The Vigilant Fox
Being familiar with alternative cancer therapies, Rogan concluded Gibson was talking about antiparasitic drugs Ivermectin and Fenbendazole, which Gibson confirmed with a nod.
In the final hour of episode #2254 of The Joe Rogan Experience, actor Mel Gibson shared two shocking medical experiences that defy mainstream knowledge.
It all started the moment Anthony Fauci’s name lept out of Gibson’s mouth.
“I don’t know why Fauci’s still walking around… or at least free,” Gibson remarked before revealing that he had “road rage” after listening to RFK Jr.’s book about Anthony Fauci.
Piling on, Joe Rogan quickly dismantled any doubts about the book’s accuracy, arguing that if it were full of lies, RFK Jr. would have been sued into the ground and publicly humiliated.
“First of all, people that don’t believe it. How come RFK Jr. didn’t get sued? How come there’s no lawsuits? If there were lies, there would be lawsuits. You’d be publicly humiliated,” Rogan pointed out.
“That book is an accurate depiction of what Anthony Fauci did during the AIDS crisis, which probably was an AZT crisis. It wasn’t an AIDS crisis.”
The first bombshell dropped when Gibson shared that he “couldn’t walk for three months” after taking Fauci’s pet drug for COVID.
“[Remdesivir] kills you. I found out that afterward. And that’s why I wonder about Fauci,” Gibson said.
“Remdesivir is so lethal it got nicknamed ‘Run Death Is Near’ after it started killing thousands of COVID patients in the hospital,” Stella Paul wrote in a previous report.
“The experts claimed that remdesivir would stop COVID; instead, it stopped kidney function, then blasted the liver and other organs.”
Unfortunately, Gibson’s gardener wasn’t as fortunate. After reportedly receiving the kidney-toxic treatment, he tragically passed away.
“I knew the guy for 20 years, and we both went to the same hospital, and he died, and I didn’t,” Gibson lamented. “I think we both got remdesivir, which is not good.”
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The most jaw-dropping moment happened when Gibson made a statement that could threaten the entire cancer industry.
Gibson revealed that he has three friends who had “stage four cancer,” and now “all three of them don’t have cancer right now at all.”
“And they had some serious stuff going on,” Gibson added.
Rogan asked, “What did they take?”—to which Gibson hesitantly replied, “They took what you’ve heard they’ve taken.”
Being familiar with alternative cancer therapies, Rogan concluded Gibson was talking about antiparasitic drugs Ivermectin and Fenbendazole, which Gibson confirmed with a nod.
Corroborating what Gibson reported to Rogan, cancer surgeon Dr. Kathleen Ruddy revealed to The Epoch Times last year that she has seen several late-stage cancer patients make dramatic recoveries after taking Ivermectin.
One patient had a grim future, and then something remarkable happened. This man had stage four prostate cancer and tried all the conventional protocols before doctors told him that there was nothing they could do.
Then, he started taking ivermectin…
Within six months, the metastatic lesions began to disappear, and in less than a year, “he was out dancing for four hours” three nights per week, according to Dr. Ruddy.
A similar scenario unfolded for another man named Eddie. He was also in bad shape.
Eddie was diagnosed with two unresectable esophageal tumors that surgeons wouldn’t go near. He was a smoker, couldn’t swallow, and had lost 40 pounds in a year and a half.
“Within a couple of weeks, he sounded stronger. He could swallow. He had gained six pounds. His voice was better,” reported Dr. Ruddy.
Several weeks later, Dr. Ruddy said to Eddie, “You need to get a scan.”
Guess what happened?
“We got the scan. No tumors. Gone. Gone. The problem was that he had sold his fishing boat. That was the biggest problem. He was getting better. His tumor was gone. Now he’s got to buy another fishing boat … I was like, ‘Well, now, that’s interesting.’”
Recently, anecdotal reports have also praised Fenbendazole as a potentially miraculous anti-cancer drug.
It reportedly works by destabilizing microtubules, the structures that help cancer cells divide and grow.
By disrupting this process, Fenbendazole is believed to effectively halt cancer cell division and slow or stop tumor growth.
A case series published in 2020 documented three cancer patients who experienced complete remission after taking Fenbendazole.
“FBZ (Fenbendazole) appears to be a potentially safe and effective antineoplastic agent that can be repurposed for human use in treating genitourinary malignancies.’”
Adding to the growing evidence in support of Fendendazole’s use case against cancer, an Oklahoma man credited his miraculous cancer recovery to the pet med after overcoming terminal small cell lung cancer, defying a less than 1% survival rate and leaving doctors baffled.
EDMOND, Okla. — When you tell someone a medicine for dogs cured your cancer, you better be ready for some skeptics, but Joe Tippens says it saved his life, and the lives of others.
Now, even cancer researchers are open to the possibility it might be true.
“My stomach, my neck, my liver, my pancreas, my bladder, my bones — it was everywhere,” Tippens said.
Tippens said he was told to go home, call hospice and say his goodbyes two years ago.
The doctors were unanimous, he was going to die of small cell lung cancer.
“Once that kind of cancer goes that far afield, the odds of survival are less than 1 percent, and median life expectancy is three months,” Tippens said.
Tippens said he went from 220 pounds to 110.
“I was a skeleton with skin hanging off of it,” he said. “It was difficult.”
But that was January of 2017. Today, Tippens is very much alive and what he credits for his survival has doctors scratching their heads, and the rest of us raising eyebrows.
“About half the people think I’m just crazy,” he said. “And about half the people want to know more and dig deeper.”
Tippens said he received a tip from a veterinarian, of all people. And in his desperation, he turned from people medicine to dog medicine.
Specifically, something you give your dog when it has worms.
“The truth is stranger than fiction, you know?” Tippens said, laughing.
Just three months later, Tippens says, his cancer was gone.
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Courageous Discourse
Europe Had 127,350 Cases of Measles in 2024

By Peter A. McCullough, MD, MPH
US Mainstream Media Maintains Myopic Focus on Less than 1000 Cases
As the measles story in the US continues to unfold with reporting of a few cases here and there come in through mainstream media, I wondered about measles in Europe.
The WHO casually reported that the Europe Region had 127,350 cases in 2024.
According to an analysis by WHO and the United Nations Children’s Fund (UNICEF), 127 350 measles cases were reported in the European Region for 2024, double the number of cases reported for 2023 and the highest number since 1997.
Children under 5 accounted for more than 40% of reported cases in the Region – comprising 53 countries in Europe and central Asia. More than half of the reported cases required hospitalization. A total of 38 deaths have been reported, based on preliminary data received as of 6 March 2025.
Measles cases in the Region have generally been declining since 1997, when some 216 000 were reported, reaching a low of 4440 cases in 2016. However, a resurgence was seen in 2018 and 2019 – with 89 000 and 106 000 cases reported for the 2 years respectively. Following a backsliding in immunization coverage during the COVID-19 pandemic, cases rose significantly again in 2023 and 2024. Vaccination rates in many countries are yet to return to pre-pandemic levels, increasing the risk of outbreaks.
Many regions in Europe have lower rates of measles vaccination than the goal of 95%.
Less than 80% of eligible children in Bosnia and Herzegovina, Montenegro, North Macedonia and Romania were vaccinated with MCV1 in 2023 – far below the 95% coverage rate required to retain herd immunity. In both Bosnia and Herzegovina and Montenegro the coverage rate for MCV1 has remained below 70% and 50% respectively for the past 5 or more years. Romania reported the highest number of cases in the Region for 2024, with 30 692 cases, followed by Kazakhstan with 28 147 cases.
The WHO Report does not mention adjudication of hospitalizations or deaths. Presumably hospitalization of healthy kids is routine for contagion control. So if measles is so common and presumably well-handled by Europe, why is it such a big deal in the United States? Don’t look for Sanjay Gupta or Anderson Cooper to tell you that a similar size region and population handles >100K cases per year without much fanfare.
Peter A. McCullough, MD, MPH
President, McCullough Foundation
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Break The Needle
Why psychedelic therapy is stuck in the waiting room

There is mounting evidence of psychedelics’ effectiveness at treating mental disorders. But researchers face obstacles conducting rigorous studies
In a move that made international headlines, America’s top drug regulator denied approval last year for psychedelic-assisted therapy to treat post-traumatic stress disorder.
In its decision, the U.S. Food and Drug Administration cited concerns about study design and inadequate evidence to assess the benefits and harms of using the drug MDMA.
The decision was a significant setback for psychedelics researchers and veterans’ groups who had been advocating for the therapy to be approved. It is also reflective of a broader challenge faced by researchers keen to validate the therapeutic potential of psychedelics.
“Sometimes I feel like it’s death by 1,000 paper cuts,” said Leah Mayo, a researcher at the University of Calgary.
“If the regulatory burden were a little bit less, that would be helpful,” added Mayo, who holds the Parker Psychedelics Research Chair at the Psychedelic and Cannabinoid Therapeutics Lab. The lab develops new treatments for mental health disorders using psychedelics and cannabinoids.
Sources say the weak research body behind psychedelics is due to a complex interplay of factors. But they would like to see more research conducted to make psychedelics more accessible to people who could benefit from them.
“If you want [psychedelics] to work within existing health-care infrastructure, you have to play by [Canadian research] rules,” said Mayo.
“Therapy has to be reproducible, it has to be evidence-based, it has to be grounded in reality.”
Psychedelics in Canada
Psychedelics are hallucinogenic substances such as psilocybin, MDMA and ketamine that alter people’s perceptions, mood and thought processes. Psychedelic therapy involves the use of psychedelics in guided sessions with therapists to treat mental health conditions.
Psychedelics are generally banned for possession, production and distribution in Canada. However, two per cent of Canadians consumed hallucinogens in 2019, according to the latest Canadian Alcohol and Drugs Survey. Psychedelics are also used in Canada and abroad in unregulated clinics and settings to treat conditions such as substance use disorder, post-traumatic stress disorder (PTSD) and various mental disorders.
“The cat’s out of the bag, and people are using this,” said Zachary Walsh, a professor in the Department of Psychology at the University of British Columbia.
Within Canada, there are three ways for psychedelics to be accessed legally.
The federal health minister can approve their use for medical, scientific or public interest purposes. Health Canada runs a Special Access Program that allows doctors to request the use of unapproved drugs for patients with serious conditions that have not responded to other treatments. And Health Canada can approve psychedelics for use in clinical trials.
Researchers interested in conducting clinical trials involving psychedelics face significant hurdles.
“There’s been a concerted effort — and it’s just fading now — to mischaracterize the risks of these substances,” said Walsh, who has conducted several studies on the therapeutic uses of psychedelics. These include studies on MDMA-assisted therapy for PTSD, and the effects of microdosing psilocybin on stress, anxiety and depression.
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The U.S. government demonized psychedelic substances during its War on Drugs in the 1970s, exaggerating their risks and blocking research into their medical potential. Influenced by this war, Canada adopted similar tough-on-drugs policies and restricted research.
Today, younger researchers are pushing forward.
“New ideas really come into the forefront when the people in charge of the old ideas retire and die,” said Norman Farb, an associate professor in the Department of Psychology at the University of Toronto.
But it remains a challenge to secure funding for psychedelic research. Government funding is limited, and pharmaceutical companies are often hesitant to invest because psychedelic-assisted therapy does not generally fit the traditional pharmaceutical model.
“It’s not something that a pharmaceutical company wants to pay for, because it’s not going to be a classic pharmaceutical,” said Walsh.
As a result, many researchers rely on private donations or venture capital. This makes it difficult to fund large-scale studies, says Farb, who has faced institutional obstacles researching microdosing for treatment-resistant depression.
“No one wants to be that first cautionary tale,” he said. “No one wants to invest a lot of money to do the kind of study that would be transparent if it didn’t work.”
Difficulties in clinical trials
But funding is not the only challenge. Sources also pointed to the difficulty of designing clinical trials for psychedelics.
In particular, it can be difficult to implement a blind trial process, given the potent effects of psychedelics. Double blind trials are the gold standard of clinical trials, where neither the person administering the drug or patient knows if the patient is receiving the active drug or placebo.
Health Canada also requires researchers to meet strict trial criteria, such as demonstrating that the benefits outweigh the risks, that the drug treats an ongoing condition with no other approved treatments, and that the drug’s effects exceed any placebo effect.
It is especially difficult to isolate the effects of psychedelics. Psychotherapy, for example, can play a crucial role in treatment, making it difficult to disentangle the role of therapy from the drugs.
Mayo, of the University of Calgary, worries the demands of clinical trial models are not practical given the limitations of Canada’s health-care system.
“The way we’re writing these clinical trials, it’s not possible within our existing health-care infrastructure,” she said. She cited as one example the expectation that psychiatrists in clinical trials spend eight or more hours with each patient.
Ethical issues
Psychedelics research can also raise ethical concerns, particularly where it involves individuals with pre-existing mental health conditions.
A 2024 study found that people who visited an emergency room after using hallucinogens were at a significantly increased risk of developing schizophrenia — raising concerns that trials could harm vulnerable participants.
Another problem is a lack of standardization in psychedelic therapy. “We haven’t standardized it,” said Mayo. “We don’t even know what people are being taught psychedelic therapy is.”
This concern was underscored in a 2015 clinical trial on MDMA in Canada, where one of the trial participants was subjected to inappropriate physical contact and questioning by two unlicensed therapists.
Mayo advocates for the creation of a regulatory body to standardize therapist training and prevent misconduct.
Others have raised concerns about whether the research exploits Indigenous knowledge or cultural practices.
“There’s no psychedelic science without Indigenous communities,” said Joseph Mays, a doctorate candidate at the University of Saskatchewan.
“Whether it’s medicalized or ceremonial, there’s a direct continuity with Indigenous practices.”
Mays is an advisor to the Indigenous Reciprocity Initiative, which funnels psychedelic investments back to Indigenous communities. He believes those working with psychedelics must incorporate reciprocity into their work.
“If you’re using psychedelics in any way, it only makes sense that you would also have a commitment to fighting for the rights of [Indigenous] communities, which are still lacking basic necessities,” said Mays, suggesting that companies profiting from psychedelic medicine should contribute to Indigenous causes.
Despite these various challenges, sources remained optimistic that psychedelics would eventually be legalized — although not due to their work.
“It’s inevitable,” said Mays. “They’re already widespread, being used underground.”
Farb agrees. “A couple more research studies is not going to change the law,” he said. “Power is going to change the law.”
This article was produced through the Breaking Needles Fellowship Program, which provided a grant to Canadian Affairs, a digital media outlet, to fund journalism exploring addiction and crime in Canada. Articles produced through the Fellowship are co-published by Break The Needle and Canadian Affairs.
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