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Defending Health, Life and Liberty🇺🇸 Natural News is a science-based natural health advocacy organization led by activist-turned-scientist Mike Adams, the Health Ranger. https://t.me/NaturalNewsChat
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As The Defender previously reported, Dr. Ben Edwards attempted to get the Texas Department of State Health Services (DSHS) to issue a statement on budesonide as a possible treatment for respiratory issues following a measles infection. However, the state's medical director, Dr. Scott Milton, stated that the DSHS's only recommendation for measles was the MMR vaccine, and he did not believe the health authorities would "go for" promoting budesonide.
Lyla's recovery is a beacon of hope in a landscape of medical uncertainty and systemic failures. Her story raises important questions about the state of our healthcare system and the need for a more open-minded, patient-centered approach to treatment. As we continue to face the challenges of infectious diseases, it is crucial that we learn from cases like Lyla's and advocate for better, more accessible treatments.
In the words of Dr. Bartlett, "We need to be open to all the tools in the toolbox." This sentiment echoes the growing awareness and demand for a more comprehensive approach to healthcare, one that prioritizes patient well-being and embraces a wider range of treatment options.
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This system is a stark contrast to other industries. If a defective car or medical device causes harm, manufacturers are held accountable in court. Yet, if a vaccine causes seizures, brain damage, or death, the manufacturer faces no liability. The financial burden of compensating victims falls on a government-managed fund, financed by a 75-cent excise tax on each vaccine dose. Essentially, the public—not the industry—pays for the harm caused by vaccines.
The VICP system is not a safeguard for children; it’s a liability shield for corporations. By shielding manufacturers from lawsuits, the NCVIA removed a critical incentive for ensuring vaccine safety and efficacy.
The lack of safety standards: A dangerous loophole
Vaccines are not held to the same safety standards as other pharmaceutical products. Most vaccines bypass rigorous, long-term, placebo-controlled clinical trials, relying instead on inadequate safety studies with alarmingly short follow-up periods. For example, Sanofi’s IPOL polio vaccine was licensed based on trials that monitored safety for only three days after injection—grossly insufficient to detect serious adverse effects or long-term risks.
The absence of true inert placebos in vaccine trials further exacerbates this issue. Instead, new vaccines are often tested against existing vaccines or their adjuvants, making it nearly impossible to identify safety concerns. This lack of proper scientific rigor undermines the integrity of vaccine safety research and leaves children at risk.
The Vaccine Injury Compensation Program’s flawed design also discourages transparency. By funneling claims into a government-controlled system with minimal payouts, the vaccine industry avoids the scrutiny that comes with legal action. This shields them from public scrutiny and accountability while perpetuating a cycle of harm and injustice.
Should the system be reformed or dismantled altogether?
Critics argue that repealing the NCVIA would dismantle the VICP, leaving vaccine-injured families without recourse. However, a hybrid system is possible—one that preserves the VICP for those who prefer it while allowing direct legal action against manufacturers. This approach would reintroduce accountability, forcing vaccine companies to prioritize safety over profits.
Robert F. Kennedy Jr. has emerged as a leading voice in this movement, advocating for stricter safety standards and legal reforms. As the head of the U.S. Department of Health and Human Services, Kennedy is in a unique position to push for legislative changes. His long-standing criticism of the vaccine industry’s lack of transparency and accountability makes him a bold advocate for reform.
Kennedy has called for vaccines to be held to the same safety standards as other pharmaceutical products, including long-term, placebo-controlled trials. This would ensure that vaccines are proven safe before being mandated for widespread use.
The National Childhood Vaccine Injury Act of 1986 was a grave mistake that must be corrected, the scientific dictatorship disbanded. It’s time to end the protectionist policies that prioritize industry profits over child safety. Holding vaccine manufacturers accountable, enforcing rigorous safety standards, and restoring justice for vaccine-injured families are matters of urgent moral and public health importance.
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For years, Dr. Bhattacharya has been at the forefront of this battle. As a critic of pandemic-era restrictions, he co-authored the “Great Barrington Declaration,” which advocated for focused protection of vulnerable populations rather than broad lockdowns. His efforts have been met with significant resistance, including censorship and personal attacks.
The Biden administration's alleged collusion with social media companies to censor dissenting views on COVID-19 policies, lockdowns, and mask and vaccine mandates has been the subject of multiple lawsuits. In a landmark case, the U.S. Supreme Court acknowledged that Bhattacharya and other plaintiffs were indeed censored, though it remanded the case to the lower court for further proceedings.
Reform and transparency
In his nomination hearings, Bhattacharya committed to changing the culture of censorship at NIH. “Over the last few years, top NIH officials oversaw a culture of cover-up, obfuscation and a lack of tolerance for ideas that differ from theirs,” he said. “Dissent is the very essence of science. I’ll foster a culture where NIH leadership will actively encourage different perspectives.”
He emphasized that scientific progress requires tolerance for a broad range of perspectives. “I want to make sure that all the ranges of hypotheses are supported,” Bhattacharya told committee members. He also highlighted the harms caused by censorship of non-establishment perspectives, including the negative impacts of pandemic-era measures such as lockdowns on child development and the spread of the virus.
The NIH’s recent actions, including the cancellation of grants targeting "vaccine hesitancy," are a significant step in the right direction. However, as Toby Rogers, Ph.D., a scholar at the Brownstone Institute, pointed out, more needs to be done. “Cancelling contracts is a good start. We also need to fire the people responsible, prosecute any criminal actions, repeal any laws or policies that enabled this to happen, and allow the public to access all government records concerning the censorship program.”
The fight for free speech and scientific integrity is far from over, but the NIH’s recent actions under Dr. Bhattacharya’s leadership mark a promising beginning. As the agency continues to reassess its funding practices and promote open scientific discourse, the hope is that it will set a new standard for transparency and accountability in health research.
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"If I was wrong, I would have expected the drug companies whose products I am maligning to have sought and secured a court injunction to stop me repeating these allegations," Dr. Yeadon said. "Neither of those things have ever happened. What has happened instead is that I have been extraordinarily censored and smeared sideways. And I think I offer that to you as strong evidence that I may be 'over the target,' at least in relation to these injectable products that have definitely injured and killed many people."
Dr. Yeadon's testimony adds a layer of complexity to the debate, suggesting that the scientific establishment and media have a role to play in the accountability process. Social media platforms like YouTube and the BBC, for instance, could face legal action for censoring critical voices and suppressing vital information.
The European Court of Justice's ruling marks a pivotal moment in the ongoing saga of the COVID-19 vaccination campaign. It underscores the need for transparency, accountability and a reevaluation of how medical professionals are held responsible for their actions. As the legal and financial implications unfold, the medical landscape may see profound changes, potentially leading to a future where human doctors are no longer the primary providers of healthcare.
For now, the ruling serves as a stark reminder of the potential consequences of rush-to-market medical interventions and the importance of careful, evidence-based decision-making in healthcare.
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World Health Organization in crisis, prepares for DOWNSIZING after U.S. withdrawal and funding problems
The globalist World Health Organization (WHO) is now facing an existential crisis, following funding cuts and U.S. President Donald Trump's announcement that Washington will withdraw from the global health body.
A confidential memo obtained by Reuters reveals that the Geneva-based agency under the United Nations is preparing to slash its budget by 21 percent and reduce its workforce. The memo comes after the U.S. – the WHO's largest donor – formally withdrew under Trump in January. Since then, the WHO has desperately scrambled for alternative funding – including a failed public begging campaign.
The internal WHO memo, dated March 28 was signed by Director-General Tedros Adhanom Ghebreyesus. Tedros bluntly admitted in the document that the organization has "no choice but to reduce the scale of our work and workforce" following the U.S. departure.
According to the memo, the budget for 2026 to 2027 will be cut from an initial $5.3 billion to $4.2 billion. Layoffs are also expected across all levels, including senior leadership in Geneva. The WHO employs 25 percent of its 9,473-strong staff in its Swiss headquarters alone.
Trump justified Washington's withdrawal from the WHO by accusing the global health body of mishandling the Wuhan coronavirus (COVID-19) pandemic and kowtowing to China. The withdrawal, Reuters mentions, has left a staggering $706 million shortfall in the agency's 2024 to 2025 budget.
The WHO's panicked response was epitomized by Maria Van Kerkhove, its technical lead for COVID-19, who took to social media pleading for public donations. Unfortunately, her public fundraiser with an ambitious $1 billion goal raised a paltry $23,000 – proof that global goodwill toward the WHO has evaporated.
China pays pennies, U.S. blows billions
In an executive order signed shortly after taking office in January, Trump condemned the WHO's "unfairly onerous payments" imposed on the U.S. while letting China contribute a fraction of what America did.
While Washington was expected to provide $442 million in voluntary funding for 2024 to 2025, Beijing pledged a mere $2.5 million. Even in mandatory contributions, the disparity was glaring: The U.S. paid $264 million compared to China's $181 million.
The WHO's credibility has been further eroded by its obsequious deference to Beijing during the pandemic. Despite China's obstruction of investigations into COVID-19's origins, WHO officials initially praised China's lockdowns as "the most ambitious, agile and aggressive disease containment effort in history." Later, under Chinese pressure, the agency dismissed the lab-leak theory as "extremely unlikely."
As Van Kerkhove herself admitted to Science magazine in January, China has repeatedly stonewalled requests for information on early cases and lab research. Yet, the WHO continues to shield Beijing from accountability.
The U.S. exit has sent shockwaves through global health programs, particularly those combating HIV, tuberculosis, and other infectious diseases, which relied heavily on American funding. But Trump’s order makes clear that Washington will redirect resources to more accountable partners, bypassing the WHO's inefficiencies.
With its budget imploding and its reputation in tatters, the WHO now faces a reckoning. As the agency scrambles to prioritize its dwindling resources, the world is left questioning whether the WHO – a body that prioritized politics over science – deserves to survive at all.
Watch WHO Director-General Tedros Adhanom Ghebreyesus falsely claiming that the global health body didn't impose medical tyranny during the COVID-19 pandemic in this clip.
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As the world grapples with the aftermath of the COVID-19 scandal, questions linger about the true cost of mass vaccination. Are we poised on the brink of another health catastrophe, or are these concerns mere overblown anxieties? The answer may lie in the data: in the rising cancer rates, the excess deaths, and the lingering disabilities that shadow the vaccinated population.
As Dr. Soon-Shiong aptly put it, "This is existential." The narrative of the COVID-19 scandal is far from over, and the pages of history are yet to be written. One thing is clear: the legacy of this era hinges on our ability to confront the truth, no matter how inconvenient it may be. The COVID-19 scandal has unveiled disturbing levels of medical experimentation, driving medical systems into a state of perpetual fraud and coverups of iatrogenic error.
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Oncologist warns of ‘terrifyingly aggressive’ cancers in children, linked to immune suppression from COVID vaccines
The rise of "turbo cancers" and a medical betrayal
For the first time in modern medical history, children as young as eight are being diagnosed with aggressive colon cancer—a phenomenon so rare it was virtually unheard of before 2021. But now, elite oncologists are breaking ranks, exposing what they call a "global epidemic" of fast-moving cancers directly linked to COVID-19 vaccines. The same medical authorities who once demanded blind faith in these shots have gone eerily silent as the bodies pile up.
Dr. Patrick Soon-Shiong, a pioneering cancer researcher who developed the FDA-approved drug Abraxane, recently dropped a bombshell during an interview with Tucker Carlson. "We have to face reality," he said, bluntly connecting the dots between mRNA vaccines and the surge in deadly cancers. His warning follows a flood of reports from frontline doctors witnessing bizarre, rapid-onset tumors in young patients—cases that defy decades of medical understanding.
Meanwhile, Dr. Angus Dalgleish, a renowned oncologist from the University of London, has called for an outright ban on mRNA vaccines, declaring they have no place in medicine outside of terminal cancer cases. "The fact that mRNA can integrate [into DNA], even if it doesn’t most of the time, makes it unjustifiable to use on young people, especially children," Dalgleish told the Vaccine Safety Research Foundation. His research found mRNA fragments inside tumors, suggesting the shots may be fueling cancer growth.
The scientist elaborated further, explaining that the mRNA from COVID-19 vaccines has been observed to “incorporate” into cancerous cells.
Dr. Dalgleish highlighted that researchers have identified traces of mRNA within cancerous tumors, noting that this genetic material plays a role in their rapid growth and the aggressive spread of these cancers. He asserted, “Cancer caused by mRNA vaccines is a known outcome.” Dr. Dalgleish issued a cautionary note, emphasizing that mRNA vaccines should not be utilized as a preventive measure against cancer, as they are implicated in its causation.
A manufactured crisis and the silencing of dissent
The timing of these cancers is undeniable. Before 2021, childhood cancers like glioblastoma and advanced colon cancer were statistical anomalies. Now, pediatric oncology wards are filling with cases that progress at terrifying speeds—what doctors now call "turbo cancers." Yet instead of investigating, public health agencies and pharmaceutical giants have doubled down on censorship, smearing dissenting experts as "conspiracy theorists" while quietly updating vaccine injury compensation programs to include cancer claims. The term "turbo cancer" isn't even a recognized medical term, yet doctors continue to report terrifyingly aggressive cancer cases, in adults and young children without a history of medical issues.
The parallels to past medical scandals are chilling. Just as Big Tobacco buried evidence linking smoking to lung cancer for decades, the COVID vaccine pushers—from the FDA to Pfizer—are gaslighting the public while children suffer. "We know [the cancer] is caused by [mRNA vaccines]," Dalgleish stated unequivocally.
History repeats itself when profit outweighs ethics. The same institutions that lied about opioids, asbestos, and Agent Orange are now dismissing vaccine injuries as "anecdotal." But with elite doctors like Soon-Shiong and Dalgleish risking their careers to speak out, how long can the facade hold? As grieving parents demand answers, one question burns: If vaccines are safe, why are the architects of this experiment refusing to debate their critics in the open?
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NIH study, buried for decades, reveals that Flu Shots INCREASE elderly deaths, not prevent them
The study they didn’t want you to see
For decades, public health officials have assured Americans that flu vaccines save lives, particularly among the elderly. Yet buried research reveals a shocking truth: mass vaccination campaigns may have increased mortality rates instead of reducing them. A 2005 National Institutes of Health (NIH) study, later covered up by federal agencies, found no correlation between rising flu shot uptake and declining death rates—despite billions spent on promotion.
In 2006, CBS News investigative reporter Sharyl Attkisson exposed the NIH’s damning findings. The study, published in the Journal of the American Medical Association (JAMA), analyzed 33 years of data (1968–2001) and found that as flu vaccination rates among seniors jumped from 15% to 65%, death rates climbed instead of dropping.
Attkisson interviewed Dr. Thomas Reichert, a co-author of the study, who admitted: "We realized we had incendiary material... We’ve looked at other countries now, and the same is true."
The NIH blocked lead researcher Lone Simonsen from speaking to CBS—a red flag suggesting institutional suppression. The study’s conclusion was unambiguous: flu shots showed no measurable benefit in reducing mortality in any age group.
The flawed science behind flu shot propaganda
For years, observational studies claimed flu vaccines reduced winter deaths by 50%—a statistic now debunked as mathematically impossible. The NIH study revealed:
• Less than 10% of winter deaths in the elderly are flu-related, making a 50% reduction implausible.
• Vaccinated cohorts were inherently healthier—frail seniors were less likely to get shots, skewing results.
• Immune senescence in the elderly renders flu shots ineffective, yet policymakers ignored this biological reality.
Despite this, the CDC doubled down, expanding recommendations to children in 2006—a move critics argue was designed to boost Pharma profits, not public health.
A legacy of medical tyranny
The COVID-19 scandal exposed how corruption and censorship dominate public health. The flu vaccine fraud is no different:
• High-dose flu shots (with 3–4x more antigen) were introduced post-2005 study, increasing side-effect risks.
• No accountability: Officials like Dr. Walter Orenstein (ex-CDC) admitted flu shots failed but kept pushing them.
• Media complicity: Major outlets ignored the NIH study, perpetuating the "safe and effective" myth.
The promotion of flu vaccines among the elderly raises critical questions about the ethics of public health campaigns. Why have health authorities continued to push a practice that has been proven ineffective?
The answer lies in the interplay of institutional bias and financial interests. Public health experts long assumed flu vaccines were effective, ignoring contradictory evidence—assuming, in essence, that their hypotheses were correct simply because they wanted them to be. This wishful thinking has had deadly consequences.
The government’s response to the NIH findings was particularly troubling. Instead of acknowledging the failure of their policies, officials shifted the focus to vaccinating children and others who might come into contact with the elderly—an admission of defeat cloaked in scientific jargon.
The flu vaccine industry, meanwhile, has doubled down on its flawed approach, creating “high-dose” vaccines with significantly higher antigen content and additional adjuvants. While these changes aim to compensate for the vaccines’ ineffectiveness, they also increase the risk of severe side effects.
History repeats itself—from thalidomide to opioids to COVID-19, the same players prioritize profits over lives. The flu vaccine deception mirrors Big Tobacco’s 50-year cover-up of smoking risks: corporations and governments colluding to sell a deadly product under the guise of "protection."
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Ontario judge rules against family of Canadian teen killed by the lethal COVID-19 injection
A judge in Canada's Ontario province has issued a ruling against the family of a teenager killed by the lethal Wuhan coronavirus (COVID-19) injection.
Blacklock's Reporter said on Wednesday, March 26, that Ontario Superior Court Justice Sandra Antoniani was the magistrate behind the decision. "The plaintiff's tragedy is real, but there is no private law duty of care made out," she wrote. "There is no private law duty of care to individual members of the public injured by government core policy decisions in the handling of health emergencies which impact the general population."
The ruling was in relation to a case filed by Dan Hartman, whose 17-year-old son Sean died after getting the COVID-19 injection. The teenager died on Sept. 27, 2021 – almost five weeks after being injected with the Pfizer-BioNTech mRNA COVID-19 shot.
According to the magistrate, Health Canada – the federal health department and defendant in the lawsuit – "deemed that urgent action was necessary" to address the pandemic. She further continued that the department's actions "were aimed at mitigating the health impact of a global pandemic on the Canadian public."
"Imposition of a private duty of care would have a negative impact on the ability of the defendants to prioritize the interests of the entire public, with the distraction of fear over the possibility of harm to individual members of the public, and the risk of litigation and unlimited liability."
Five years after the pandemic, the Canadian government is now washing its hands of any responsibility for the injuries and deaths caused by these experimental shots. Ottawa's sweeping mandates, which pressured millions into taking a barely tested medical intervention, now absolve it of any obligation to those who suffered severe consequences.
Forced to comply, denied compensation
While officials continue to justify their coercive policies as necessary for public health, families like that of Sean are left without justice – their suffering dismissed as collateral damage in the name of pandemic mitigation. Sean's father Dan has been fighting for accountability ever since, only to be met with legal roadblocks and bureaucratic indifference.
The Hartman family's ordeal is far from unique. Canada's Vaccine Injury Support Program (VISP), established in December 2020, was supposed to provide recourse for those harmed by COVID-19 vaccines. Yet, out of 1,859 claims filed, only 103 have been approved – meaning thousands of Canadians alleging vaccine injuries have been left in limbo.
Denied compensation through VISP, Dan had no choice but take the matter to court – filing a separate $35.6 million lawsuit in October 2023. He accused Pfizer of negligence and misrepresentation. The grieving father also accused the New York-based drug giant of concealed the risks of its vaccine, including myocarditis (inflammation of the heart muscle).
Dan's legal counsel Umar Sheikh argued in the filing that Pfizer "concealed the fact the Pfizer-BioNTech COVID-19 vaccination had severe possible risks and outcomes when administered, including but not limited to myocarditis, pericarditis (heart lining inflammation) and death."
According to court documents, an American doctor determined that Sean's death was caused by the Pfizer shot. The 17-year-old received the vaccine under pressure from his local hockey league.
"They said there is no proof the vaccine killed Sean. There’s also no proof that it didn't," Hartman said at the time. expressing frustration with the system's unwillingness to acknowledge the truth.
Sheikh also mentioned in the lawsuit that Pfizer "owed a duty of care to Sean to accurately inform him of all risks associated with the Pfizer-BioNTech COVID-19 vaccination." Unfortunately, the recent ruling by Antoniani reaffirmed that the drug giant isn't accountable to the Hartman family and others who were injured and killed by its lethal vaccine.
North Carolina Supreme Court rules family can sue over COVID-19 force-vaccination of teen without parental consent
A mother’s constitutional rights were violated when her 14-year-old son was force-vaccinated with the deadliest jab in the universe, the blood-clotting mRNA Covid stab, without her consent, and the North Carolina Supreme Court has ruled in her favor. It’s no wonder the Supreme Court Justices are NOT paid off by Big Pharma to rule in favor of the Vaccine Industrial Complex, since most cases like this one get thrown out of courts and proxied by the fake kangaroo “court” invented by Pharma that uses slush funds to censor vaccine horror stories.
Emily Happel and her teenage son can proceed suing local school board and medical organization responsible for injecting her teen son with deadly spike prions
Happel’s son, Tanner Smith, was illegally force-injected with a deadly Covid-19 spike prion jab, that creates millions of prions in the blood forever. The vaccine industrial complex and all the vaccine fanatic cultists often do this sort of thing on purpose out of spite and for revenge against what they call “anti-vaxxers.” They’ll often say it was on accident or something like that, but that’s just a cover story. Now, they may be paying a hefty price for their insidious acts of medical malpractice, especially if the boy suffers long-term health damage, like most people are suffering now who got the deadly Fauci Flu stabs.
The lower courts, of course, ruled in favor of the Vaccine Industrial Complex, even though administrators never got consent from Tanner’s parents to stab him with known carcinogens and neurotoxins, claiming the PREP Act allows them to jab any kid anytime with experimental “vaccines” without parental consent.
Steven Walker, an attorney representing Happel and her son, told The Epoch Times in an email: “We are very pleased with the Court’s ruling. While we would have, of course, loved to see the battery claim reinstated as well, we believe that the Court decision was very favorable in the main on the case and have no real complaints. “I believe the case is important even outside the issue of the PREP Act in that the Court gave its clearest explanation to date concerning the rights of parents to make medical decisions for their children under the North Carolina constitution,” and Walker continued... “The PREP Act has a purpose, and that purpose is to provide immunity protections in situations when it might be difficult to determine the safety of a countermeasure during a time of crisis. It was never intended to allow the government to trample on the clear constitutional rights of its citizens.”
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Is the vaccine-autism debate reopening? Washington Post sparks controversy with preemptive hit piece on David Geier
On Tuesday, the Washington Post published an article that many are calling a preemptive hit piece on David Geier, a researcher reportedly tapped by the U.S. Department of Health and Human Services (HHS) to lead a study on possible links between vaccines and autism. The Post's piece, which cited anonymous "officials," has sparked significant controversy and raised questions about the credibility and intent of such a study.
A contested appointment
David Geier, an experienced data analyst and expert on thimerosal — a mercury-based preservative used in vaccines — has conducted extensive research on the connections between toxic exposures and autism and other neurodevelopmental disorders. He has published hundreds of peer-reviewed articles on these topics and has analyzed the CDC’s Vaccine Safety Datalink, a nonpublic database with data on over 10 million patients.
However, the Post and other mainstream news outlets have consistently portrayed Geier as a "vaccine skeptic" who has "long promoted false claims about the connection between immunization and autism." This characterization has been aggressively repeated, despite Geier's extensive scientific background and published research.
Historical context: The vaccine-autism debate
The debate over the link between vaccines and autism has a long and contentious history. In 1998, Dr. Andrew Wakefield published a study in The Lancet suggesting a link between the MMR vaccine and autism. This study was later discredited and retracted due to serious ethical violations and methodological flaws. Despite the retraction, skepticism gained significant traction, fueled by the emotional and personal stories of parents whose children developed autism after receiving vaccines.
The CDC and the scientific community have repeatedly emphasized that numerous studies have found no causal link between vaccines and autism. However, the issue remains a hot-button topic, with passionate advocates on both sides. Geier’s appointment to lead an HHS study on this topic has reignited the debate, with many expressing concerns about the objectivity and potential biases of the research.
Critics and concerns
Critics of the appointment, including former CDC officials and prominent public health experts, have raised several concerns. Dr. Richard Besser, president of the Robert Wood Johnson Foundation and a former acting CDC director, called Geier a "deeply irresponsible choice" due to his "no medical degree and a long history of pushing discredited theories about vaccines and autism."
"A growing measles outbreak is spreading in at least three states: Texas, Oklahoma and New Mexico. As of Wednesday, 377 cases had been confirmed in those states—the vast majority in unvaccinated children in Texas. It’s the largest measles outbreak in the U.S. since 2019. Two people have died, including a 6-year-old girl," Besser stated. "In this context, it is particularly concerning to see resources and attention diverted to rehashing a question that has already been answered."
A call for transparency and credibility
The controversy surrounding Geier's potential role in the study highlights the broader debate over scientific integrity and public trust. Advocates for robust, unbiased research emphasize the need for transparent and credible studies that can provide clear answers to important public health questions.
As of press time, neither the HHS nor Geier had responded to requests for comment. However, the appointment remains a subject of intense scrutiny and debate, with many watching closely to see how this story will unfold.
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Aluminum, mercury, and the allergy epidemic
Vaccines aren’t just ineffective—they’re immune disruptors. Aluminum, added to provoke stronger reactions, skews the immune system toward allergies. "If a baby eats peanuts around vaccination, their body may tag it as a threat," Humphries warned. When immune responsive cells attack the injection site, aluminum cations from the vaccine are up-taken into the cytoplasm of the immune responsive cells. These aluminum salts are then carried throughout the body, and sometimes across the blood brain barrier, where they cause inflammation. The aluminum cations are then released in unpredictable places throughout the body.
Then there’s mercury. "If a mercury-containing vaccine spills, HAZMAT teams are called," she said. "Yet we inject it into infants." Vaccine production relies on diseased animal tissue (monkey kidneys, cow pus) bathed in antibiotics, heavy metals, and fetal bovine serum.
Somehow "mercury is only ‘safe’ in vaccines, dental fillings, and toxic waste dumps," Humphries quipped, exposing the hypocrisy of vaccine science and toxicology.
Breast milk is the key to child’s immune system
Breast milk is a powerhouse of immunity, offering infants vital protection against infections and diseases. It contains antibodies, primarily secretory immunoglobulin A (IgA), which coat the baby’s mucous membranes, blocking pathogens from entering the body. White blood cells in breast milk further bolster immunity by attacking harmful bacteria and viruses. Additionally, breast milk provides oligosaccharides, which act as prebiotics, nourishing beneficial gut bacteria and preventing harmful microbes from thriving. Lactoferrin, another key component, binds to iron, inhibiting bacterial growth, while lysozyme enzymes break down harmful bacteria. Cytokines and growth factors in breast milk regulate immune responses, reducing inflammation and promoting tissue repair. Colostrum, the first milk, is especially rich in these protective elements. By breastfeeding, mothers also pass on immunity to pathogens they’ve encountered, ensuring dynamic, tailored protection. This natural immunization helps infants build a robust immune system, reducing risks of infections, allergies, and chronic conditions. Treatments such as lyposomal vitamin C and vitamin D supplements are safe to give to children during infectious disease, too.
Humphries’ work dismantles the profit-driven mythology of modern medicine. Polio didn’t vanish because of vaccines—it was redefined. Diseases didn’t decline due to shots—but sanitation and nutrition.
As she told Rogan: "Science isn’t settled—it’s questioned. Until we confront inconvenient truths, we’ll keep trading short-term gains for long-term harm."
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Ending a reckless genetic experiment that should have never been approved in the first place
The so-called "COVID vaccines" were never vaccines—they were unproven, reckless genetic experiments forced upon the public under the guise of emergency use. These mRNA-based injections, fraudulently marketed as life-saving, were in fact biological weapons that corrupted human cellular machinery, forcing cells to produce a foreign, toxic spike protein with devastating consequences.
From the outset, these injections should have never been authorized, let alone mandated. Clinical trials were rushed, safety signals ignored, and adverse effects brushed aside as "rare" while thousands suffered heart damage, neurological disorders, and immune dysfunction. Worse still, these shots failed at their only claimed purpose—providing immunity. Breakthrough infections exploded, proving these were never vaccines, but a dangerous, unstable genetic weapon system masquerading as medicine.
The damage is irreversible for countless victims. A mere withdrawal of these shots is not enough. We demand full judicial accountability—criminal prosecutions for those who pushed this atrocity, a new compensation system for the injured, and the complete dismantling of the corrupt regulatory bodies that allowed this.
The COVID vaccine scandal is one of the greatest medical crimes in history. Those responsible must pay. Medical freedom is non-negotiable—never again.
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“The shame of Minnesota”: Somali immigrants behind $250 million child nutrition fraud in largest COVID-era scam
In what federal prosecutors call "the largest COVID fraud case in U.S. history," a network of Somali immigrants allegedly siphoned $250 million from a federal program meant to feed hungry children. The scheme, centered around a sham nonprofit called Feeding Our Future, exploited pandemic-era funding waivers, submitting fabricated meal counts and rosters to the Minnesota Department of Education (MDE). Of the 70 individuals charged, nearly all are Somali refugees, with 37 pleading guilty and 7 convicted so far. The case exposes a staggering betrayal of public trust—one that raises troubling questions about immigrant assimilation, government oversight, and the vulnerabilities of welfare systems.
A perfect storm: how the fraud unfolded
Between March 2020 and January 2022, Aimee Bock, the executive director of Feeding Our Future, and her mostly Somali co-conspirators filed false claims for reimbursement, claiming to serve meals to thousands of children who didn’t exist. The MDE, operating under relaxed COVID-era rules, rubber-stamped the fraudulent submissions, even as red flags mounted.
• Fake meal counts: Some sites claimed to serve 5,000 children daily—more than entire school districts.
• Nonexistent board members: Feeding Our Future listed bartenders and a small-engine mechanic as board members, none of whom knew they were involved.
• Lavish spending: Defendants bought luxury cars, homes in multiple states, and properties in Kenya and Turkey with stolen funds.
A whistleblower from the MDE alerted the FBI in April 2021, leading to surveillance that revealed empty food sites where thousands of meals were supposedly served daily. By January 2022, federal agents raided locations across the Twin Cities in Minnesota’s largest-ever fraud bust.
Cultural & Political Context
• Minnesota has the largest Somali population in North America (100,000+), many arriving as refugees since the 1990s.
• Minnesota's liberal welfare policies and lax oversight enabled fraud.
• Some Somali immigrants have been linked to terrorism recruitment (ISIS, al-Shabab), though this case involves financial crime, not extremism.
• The Minnesota Department of Education (MDE) ignored red flags, allegedly due to fears of being accused of racism.
• Federal waivers during COVID made fraud easier.
• Governor Tim Walz and AG Keith Ellison (both Democrats) were criticized for not acting sooner.
• Abdihakim Osman Nur, a Somali immigrant, exposed corruption after witnessing $100,000 in gold gifts given to a Feeding Our Future employee at a wedding. His testimony helped prosecutors.
The fallout: Who pays the price?
While most defendants eagerly participated, one Somali immigrant, Abdihakim Osman Nur, publicly condemned the fraud. In a Facebook post, he described a Feeding Our Future staffer’s wedding, where vendors gifted the bride $10,000 in gold trays—paid for with stolen funds.
"We cannot close our eyes to such corruption... when we only have a few bad apples," Nur wrote.
Yet state officials remained silent. Governor Tim Walz claimed they "caught it very early" but refused to answer follow-up questions. Attorney General Keith Ellison, who once boasted "I know a scam when I see one," also declined to comment.
The case has left Minnesota reeling, with prosecutors calling it "the shame of Minnesota." Yet it also raises deeper questions:
• Why did oversight fail so spectacularly?
• Did political correctness prevent officials from acting sooner?
• Will this case change how refugee resettlement and welfare programs operate?
As Assistant U.S. Attorney Joe Thompson declared after the convictions: "This fraud is gross, disgusting, and despicable." But beyond the legal consequences, the scandal serves as a cautionary tale—one that forces us to ask: When generosity meets exploitation, who really suffers?
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Trump administration cuts $11 billion in COVID-era public health slush funds: Ending the era of waste and abuse
The Trump administration has taken decisive action to rein in government bloat by terminating $11 billion in unspent or misallocated COVID-era public health grants, signaling a long-overdue return to fiscal responsibility. The Department of Health and Human Services (HHS) confirmed this week that the Centers for Disease Control and Prevention (CDC) will recover billions in taxpayer dollars—money that had been sitting idle or funneled into questionable programs far removed from genuine public health needs.
A reckoning for pandemic excess
For years, conservative watchdogs warned that COVID relief funds were being mismanaged, propping up bloated bureaucracies and politically motivated initiatives rather than addressing urgent health crises. The Trump administration’s decision to claw back these funds is not merely a cost-cutting measure—it’s a necessary correction to years of unchecked spending.
"The COVID-19 pandemic is over, and HHS will no longer waste billions of taxpayer dollars responding to a crisis that Americans moved on from years ago," said HHS Director of Communications Andrew Nixon.
This isn’t the first time a Republican administration has had to clean up after Democratic fiscal irresponsibility. The Obama-era stimulus packages were notorious for funding pet projects like turtle tunnels and solar-powered sidewalks, while the Biden administration’s COVID spending spree—totaling trillions—fueled inflation and economic instability while lining the pockets of special interests.
State health departments resist accountability
Unsurprisingly, state health officials—accustomed to blank checks during the pandemic—are now protesting the cuts. Rhode Island’s Department of Health spokesperson Joseph Wendelken claimed the funding supported "critical work" beyond COVID, but details on how these funds were actually used remain scarce. Were they improving public health, or merely expanding bureaucracy?
Some states, however, are adjusting pragmatically. Alabama’s Arrol Sheehan acknowledged that temporary emergency funds were never meant to last forever, stating, "ADPH has already made staffing and budget adjustments to accommodate changes in funding." Meanwhile, the National Association of County and City Health Officials (NACCHO) is reportedly preparing for layoffs—proof that many agencies became dependent on crisis funding rather than sustainable budgets.
Refocusing on long-term priorities
The Trump administration’s move aligns with a broader effort to shift federal health spending toward long-term priorities, such as chronic disease prevention, under the "Make America Healthy Again" initiative. This stands in stark contrast to the Biden administration’s approach, which extended emergency declarations long after the crisis had passed, effectively turning temporary measures into permanent entitlements.
HHS Secretary Robert F. Kennedy Jr. has already eliminated millions in dubious grants, including funding for politically charged initiatives like "vaccine hesitancy" studies and LGBTQ-focused health programs—many of which appeared more ideological than medically necessary. An internal CDC review confirmed that the $11 billion in cuts targeted wasteful or redundant spending, validating conservative criticisms that pandemic-era funding spiraled out of control.
Why this matters now
The COVID-19 pandemic was a crisis, but it also became an excuse for unprecedented government expansion. Emergency powers justified sweeping mandates, prolonged school closures and massive spending with minimal oversight. Now, as the nation moves forward, a critical question remains: How much of that spending was truly essential?
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Budesonide emerges as lifeline for measles patients amidst hospital system turmoil
In a heartening turn of events, a 4-year-old girl named Lyla from West Texas has made a remarkable recovery from secondary pneumonia following a measles infection, thanks to the timely administration of budesonide. This case highlights the urgent need for better-equipped hospital systems and more informed medical professionals in the face of infectious diseases. The story of Lyla's treatment, which took place at Covenant Children's Hospital in Lubbock, exposes the systemic failures and lack of preparedness that have plagued the medical community, particularly in the aftermath of the COVID-19 pandemic.
A mother's desperate plea for effective treatment
Lyla was admitted to the emergency room of Covenant Children's Hospital on February 28, suffering from severe breathing difficulties. Her condition was critical, and her parents, MaryAnn and Henry, were deeply concerned. Just two days earlier, another child, a 6-year-old girl, had died from pneumonia following a measles infection at the same hospital. The deceased child had not received any breathing treatments before her untimely death.
MaryAnn and Henry, who chose not to vaccinate their children due to concerns about vaccine injuries, had been using natural remedies to support their children's recovery from measles. However, when Lyla's respiratory issues worsened, they knew they needed more than natural remedies. "I started noticing she wasn’t breathing as well," MaryAnn recalled. "She was breathing very heavy on her chest and her fever was coming back."
Desperate for help, MaryAnn contacted her former doctor at Covenant Medical Center, who had saved her life 12 years earlier. "I trusted you with my life 12 years ago, and I trust you with my daughter’s life now," she pleaded. The doctor arranged for Lyla to be airlifted to Lubbock Covenant Children's Hospital, where she would receive the care she desperately needed.
Hospital System failures exposed
Upon arrival at the hospital, Lyla's parents faced a series of distressing encounters with hospital staff. Henry recounted an exchange with a head nurse who questioned his knowledge of his daughter's condition, asking, "Are you a doctor?" in a condescending tone. When Henry offered to show photos of his children with measles, the nurse demanded proof, revealing a troubling lack of trust and empathy.
Even more alarming, hospital staff denied Lyla food and water for nine hours, citing concerns that she might vomit if her condition worsened. This decision left Lyla hungry and thirsty, adding to her parents' distress. Henry questioned the decision, asking the ER doctor, "Is there any medical reason that this child shouldn’t eat or drink?" The doctor responded, "No. Why would we deny this child anything? She needs to eat and drink as much as she wants to get better."
Budesonide: A game-changer in respiratory treatment
Lyla's turnaround came when Dr. Richard Bartlett, a West Texas emergency room physician with extensive experience in treating respiratory inflammation, intervened. Bartlett, who had successfully used budesonide during the COVID-19 pandemic, persuaded Lyla's doctor to try the treatment. "I’ve never lost anyone with COVID," Bartlett told the doctor. "Can we try it on this patient?"
Budesonide, a generic, widely available inhaled corticosteroid, has a long history of safety and effectiveness in easing respiratory inflammation. After just three treatments, Lyla's condition improved dramatically. Her oxygen levels rose, and she was able to go home within 36 hours of her first budesonide treatment.
Lyla's story is a testament to the power of basic, effective treatments like budesonide, which can be used for any infectious disease affecting the respiratory tract. It also underscores the need for hospital systems to be better prepared and for medical professionals to be more informed about the full range of treatment options available.
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How the Vaccine Industry escaped accountability for nearly FOUR DECADES, endangering children’s lives for false hopes of protection
The National Childhood Vaccine Injury Act (NCVIA), enacted in the late 1980s, was designed to shield the vaccine industry from legal liability and financial ruin, rather than protecting children from harm caused by vaccines. Signed into law under the guise of ensuring vaccines remain accessible, the act established a unique federal compensation system that places blame solely on parents of vaccine-injured children. This system, criticized for its unfairness, redefines vaccine injuries in a way that makes it nearly impossible for families to receive justice. While the act claims to prioritize the well-being of children, critics argue it prioritizes corporate interests over public health and parental rights.
The origins of the NCVIA stem from a time when the vaccine industry faced mounting lawsuits over vaccine-related injuries and deaths. Instead of addressing the root causes of these harms, the act created a no-fault compensation program administered by the Department of Health and Human Services (HHS). Parents of vaccine-injured children are directed to a bureaucratic system, often referred to as a "kangaroo court," where the burden of proof is stacked against them. The strict definitions of vaccine injuries and convoluted criteria for compensation leave countless families denied the justice they deserve, burying their stories under a system designed to protect industry profits.
Key points:
• The National Childhood Vaccine Injury Act (NCVIA) of 1986 granted vaccine manufacturers immunity from lawsuits, shielding them from accountability for injuries caused by vaccines.
• The act funnels vaccine-injured families into the National Vaccine Injury Compensation Program (VICP), a flawed system that rejects nearly half of claims and denies justice to countless children and families.
• This law prioritizes industry profits over child safety, allowing poor-quality vaccines to flood the market without rigorous safety standards.
• Robert F. Kennedy Jr. has emerged as a leading voice in the fight to reform this corrupt system, advocating for stricter safety measures and accountability for vaccine manufacturers.
The legislative shield that continues to harm children four decades later
The National Childhood Vaccine Injury Act of 1986 was not established to protect children but to protect vaccine manufacturers from legal accountability. This law, championed by Congress and the pharmaceutical industry, created a false narrative of public health triumph while quietly enabling Big Pharma to evade responsibility for vaccine-related injuries, deaths, and long-term health consequences. Since its inception, this corrupt system has left thousands of vaccine-injured children without justice, funneling their cases into a flawed compensation program that rejects the majority of claims. As the vaccine industry continues to profit from a liability-free environment, the call for systemic reform grows louder.
The National Childhood Vaccine Injury Act was born out of a series of lawsuits against vaccine manufacturers in the 1980s, particularly over the Diphtheria-Tetanus-Pertussis (DTP) vaccine. Parents of injured children began winning significant settlements, threatening the financial stability of pharmaceutical companies. Rather than addressing the root cause of the injuries, Congress sided with Big Pharma, passing the NCVIA to grant manufacturers unprecedented legal immunity.
Under this law, injured individuals are forced into the National Vaccine Injury Compensation Program (VICP), a bureaucratic nightmare that rejects more than half of claims. Families seeking justice are met with a labyrinth of red tape, arbitrary criteria, and a grossly insufficient compensation fund. Meanwhile, vaccine manufacturers operate with impunity, free from legal consequences regardless of the harm their products cause.
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The NIH reckoning: Battling censorship and restoring free speech in health research
Amid intensifying scrutiny over government involvement in influencing public discourse, the National Institutes of Health (NIH) has launched an internal inquiry that could reshape how it funds research with implications for free expression. This move comes as the agency braces for a free-speech reckoning under its new chief, Dr. Jay Bhattacharya.
An urgent call for transparency
According to STAT News, agency officials, in preparation for the swearing-in of incoming director Dr. Jay Bhattacharya, recently directed staff to identify any existing contracts potentially linked to "any form of censorship at all or directing people to believe one idea over another related to health outcomes." The request, which carried a deadline of noon Wednesday, signaled a sweeping reassessment of federally funded messaging campaigns.
Included in the NIH’s internal email were instructions to flag agreements tied to vaccine promotion or public health narratives emphasizing the “dangers of Covid or not wearing masks.” The directive also advised employees to search for terms such as “media literacy,” “social media,” “social distancing,” and “lockdowns” — all terms frequently associated with the suppression of dissenting viewpoints during the pandemic.
Canceling grants for "vaccine hesitancy"
This review comes on the heels of similar actions that preceded abrupt funding withdrawals. Earlier in the month, NIH notified researchers that at least 33 grants aimed at combating “vaccine hesitancy” would be canceled, with another nine slated for reduction or revision.
Hours after NIH director Bhattacharya was confirmed, the agency tackled one of his priorities — ending ‘censorship’ in science. The early morning email, marked “URGENT,” asked contracting officers at the NIH to respond by “noon today” with information on any contract that “may be related to any form of censorship at all or directing people to believe one idea over another related to health outcomes.”
Dr. Bhattacharya’s journey
President Donald Trump’s selection of Dr. Jay Bhattacharya to lead the National Institutes of Health signals a renewed commitment to transparency, scientific freedom and reform. A Stanford professor with dual training in medicine and economics, Bhattacharya has long emphasized data-driven decision-making and compassionate public health policy. During the COVID-19 pandemic, he became a national figure for challenging the dominant narrative on lockdowns and mandates, arguing they caused unintended harm.
Bhattacharya’s advocacy came at a cost. He was censored on major social media platforms and became a plaintiff in a landmark lawsuit alleging that the federal government colluded with Big Tech to suppress dissenting views on public health. Internal documents revealed that his views were intentionally downranked or hidden, despite being grounded in credible research and expertise. Rather than backing down, he fought back — defending not just his own speech, but the principle that science must remain open to challenge.
In October, Jay Bhattacharya posted on X: “If you favor government control of misinformation, you are an enemy of free speech.” This statement underscores his commitment to free expression and scientific integrity.
Why this matters today
The NIH’s internal inquiry and the cancellation of grants targeting "vaccine hesitancy" are significant steps in a larger battle for free speech and scientific openness. This issue gained prominence during the COVID-19 pandemic, when dissenting views on public health measures were often silenced or marginalized. Critics argue that such censorship not only stifles scientific debate but also erodes public trust in health institutions.
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European Court of Justice: Healthcare professionals who promoted or administered COVID-19 vaccines are CRIMINALLY LIABLE for any harm caused
In a groundbreaking decision that could reshape the medical landscape, the European Court of Justice (ECJ) has ruled that healthcare professionals who promoted or administered COVID-19 vaccines are civilly and criminally liable for any harm caused. This ruling, announced in early 2025, underscores the profound implications of medical professionals who participated in the mass vaccination campaign, a move that has long been a source of controversy and debate within the medical community.
A prophetic warning
Back in 2020, Dr. Vernon Coleman, a noted medical writer and health freedom advocate, issued a stark warning. He foretold that doctors who prescribed the then-experimental COVID-19 vaccines would face severe legal consequences, including lawsuits and potential imprisonment. Dr. Coleman's warning was grounded in his belief that the vaccines could cause significant harm, a stance that was met with skepticism and criticism from mainstream medical institutions.
"Back in 2020, I warned that doctors who prescribed the then-new and experimental covid-19 vaccine would likely be sued (and also imprisoned) if it turned out, as I expected, that the vaccine caused harm to those who were injected," Dr. Coleman wrote in his new book, The End of Medicine. "I warned that doctors' insurers would not be able to cope and that thousands of doctors would go bankrupt."
The European Court of Justice ruling
The ECJ's recent ruling validates Dr. Coleman's predictions. The court determined that healthcare professionals had the autonomy to refuse the vaccines and, therefore, bear full responsibility for their actions. This decision has far-reaching consequences, not only for individual doctors but also for the broader healthcare system.
According to the ruling, doctors who urged people to be vaccinated or who administered the vaccines are both civilly and criminally liable. The court emphasized that physicians were not compelled to prescribe or administer the vaccines and thus must take responsibility for their choices. This ruling could exonerate those doctors who opposed the vaccines or criticized them and faced disciplinary actions.
"This ruling could result in those doctors who were subject to disciplinary proceedings because they opposed vaccinations, or because they criticized the vaccines, being exonerated," Dr. Coleman noted.
The financial implications
The financial ramifications of this ruling are staggering. If patients claim severe and permanent damage from the vaccines, the potential damages could run into millions of pounds, dollars, or euros per patient. Dr. Coleman estimates that the total financial burden could bankrupt the vast majority of doctors in countries such as the U.K., U.S., Canada, Australia and the EU.
"It seems likely that the sum per patient could run into millions of pounds/dollars/euros," Dr. Coleman stated. "I doubt if doctors' insurance companies would have enough money to satisfy millions of claims (with each patient demanding millions of pounds) and so the vast majority of doctors in the U.K., the U.S., Canada, Australia, the EU etc., etc., would go bankrupt."
Accountability and the Media
The ECJ's ruling also raises questions about the accountability of other entities that played a role in the vaccination campaign. Dr. Mike Yeadon @DrMikeYeadon, a former Pfizer executive, has been vocal about his belief that the COVID-19 vaccines were "deliberately designed intentionally to injure, kill and reduce fertility."
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Decentralize TV: Dr. Leonard Coldwell reveals shocking, heavily censored truths about CANCER, healing and the medical mafia complex
Renowned holistic health expert and cancer patient advocate Dr. Leonard Coldwell revealed shocking truths about the medical-industrial complex, the root causes of disease and the innate healing power within each individual during his appearance on "Decentralize TV."
His discussion with the Health Ranger Mike Adams and Todd Pitner, the program's hosts, exposed how the system profits from keeping people sick rather than curing them.
Coldwell, whose personal journey began when his mother was diagnosed with terminal liver cancer, shared how he defied medical predictions and healed her naturally – even extending her life by nearly five decades. His experience led him to develop the Instinct-Based Medicine System (IBMS), a revolutionary approach that identifies and eliminates the root causes of illness rather than merely suppressing symptoms.
"Cancer is not really an illness," Coldwell explained. "It's a condition. It's an accumulation of symptoms."
Coldwell, who holds the title of the most blocked healer from social media, continued that chemotherapy and radiation only mask symptoms while destroying the body. True healing, he added, comes from addressing the root cause – often chronic stress, emotional trauma or self-sabotage. Cancer and other autoimmune diseases stem from internal conflict, where the body attacks itself due to unresolved emotional or psychological distress.
The medical mafia's deadly agenda and the power of self-healing
Coldwell didn't hold back in condemning the pharmaceutical and medical industries. He cited Dr. Gary Null's seven-year study that concluded that modern medicine is the leading cause of death in the Western world.
"The main cause of illness is the pharmaceutical industry," he said. According to Coldwell, Big Pharma doesn't want cures for people – only repeat customers.
He also debunked the germ theory as "fraudulent," explaining that so-called viruses are actually exosomes – the body's natural detoxification process. When a cell becomes toxic, it expels waste in tiny sacs. Given this, sickness is just the body cleaning itself – but modern medicine calls these sacs "viruses" to sell fear and vaccines.
Ultimately, Coldwell asserted that only the individual can cure themselves. He explained to Adams and Pitner that the same person who made you sick – you yourself – is the same one who can heal you. Coldwell also stressed the importance of instinct, calling it "God talking to us" and urging people to trust their intuition rather than blindly following medical authorities.
Debunking the lies about nutrition and toxins
Coldwell also tackled dietary myths, explaining that processed foods, fluoride and artificial medications poison the body. Nicotine itself isn't addictive, but the chemicals in cigarettes create dependency.
He also noted that coffee is anti-aging and prevents dementia; Coldwell himself drinks eight to 12 cups daily. Sugar cane juice in its raw, organic form can reverse cancer in just 21 days.
Ultimately, Pitner raised a critical point: Fear is the real pandemic. Coldwell agreed, noting that the media, governments and Big Pharma use fear to control people. In turn, demons and evil entities feed on this fear and become stronger.
His solution? Reject fear, embrace self-confidence, and take control of your health. True healing comes from within – through instinct, self-love and natural remedies.
Watch the full interview between Dr. Leonard Coldwell, Todd Pitner and the Health Ranger Mike Adams on "Decentralize TV" below.
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COVID-19 scandal linked to CANCER SURGE: Billionaire researcher sounds alarm
The COVID-19 Scandal and its cancerous aftermath
In a recent interview with Tucker Carlson, Dr. Patrick Soon-Shiong, a transplant surgeon and biotech billionaire, issued a stark warning that has sent shockwaves through the medical community. He posits that the COVID-19 scandal, marked by medical tyranny and mass iatrogenic error, may be responsible for a surge in aggressive cancers, particularly among younger individuals. This alarming assertion has sparked a heated debate, with scientists and policymakers scramble to address the potential link between mRNA vaccines and an unprecedented rise in cancer cases.
Dr. Soon-Shiong, a pioneer in cancer immunotherapy and the founder of ImmunityBio, has spent decades studying the human immune system's response to cancer. In the interview, he shared harrowing anecdotes of encountering metastatic cancers in children and young adults — cases he described as "terrifyingly aggressive." These observations, he argues, are unprecedented in his five-decade medical career.
"I never saw pancreatic cancer in children," Dr. Soon-Shiong recounted during the interview. "The greatest surprise to me was a 13-year-old with metastatic pancreatic cancer." He also cited instances of young children diagnosed with colon cancer and ovarian cancer in women in their 30s — phenomena he attributes to the COVID-19 scandal.
The science behind the scare: inflammation and immune suppression
Dr. Soon-Shiong's hypothesis hinges on the idea that both the SARS-CoV-2 virus and the mRNA COVID-19 vaccines could be driving an increase in cancer cases by triggering chronic inflammation and immune system exhaustion. The virus is known to cause a massive inflammatory response, which some cancers exploit to grow and metastasize.
Furthermore, he points to emerging research suggesting that the spike protein in the virus and vaccines might interfere with critical cellular processes, potentially suppressing tumor-suppressor proteins. While these findings are preliminary, they add a layer of biological plausibility to his concerns.
The broader health crisis: excess deaths and disabilities
Independent research firms, such as Phinance Technologies, have identified worrying trends in post-COVID health outcomes. Their data reveals a significant increase in excess deaths and disabilities among working-age populations, particularly those who received vaccines. Between 2021 and 2022, the U.S. saw a 23% rise in excess deaths among 25-64-year-olds and a 24.6% increase in disabilities in the workforce—statistics that raise eyebrows, especially since these groups are typically healthier than older populations.
Edward Dowd, co-founder of Phinance Technologies, notes a concerning correlation between the vaccine rollout and these adverse health outcomes. "The healthiest segment of the population… saw a greater relative increase in disabilities after Q1 2021," he observed, suggesting that the vaccines may have had unforeseen consequences.
While some oncologists, such as Dr. Angus Dalgleish from St. George’s, University of London, echo Dr. Soon-Shiong's fears, others remain skeptical. Infectious disease experts argue that there is insufficient evidence linking vaccines to cancer, though they acknowledge the need for further research into long-term health effects.
In a statement to FactCheck. org, one expert dismissed the claims, stating, "There isn't evidence to date that COVID-19 vaccines cause cancer or lead to worsening cancer." However, this dismissal overlooks the increasing anecdotal reports from clinicians who have observed cancer progression in patients post-vaccination.
Has medical tyranny become the New Normal?
Dr. Soon-Shiong's warnings raise profound ethical and moral questions. What are the limits of medical innovation, especially when it involves unprecedented interventions like mRNA vaccines? Can we afford to overlook potential long-term health consequences in our haste to combat a global crisis?
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As Attkisson noted in 2023: "You probably haven’t heard much about these incendiary findings." Why? Because admitting failure would collapse a $6 billion flu vaccine industry. How many more buried studies will it take before we stop trusting "experts" who refuse to follow the science?
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Watch Dan Hartman talking about his fight for answers about his son's untimely demise with Dr. Chris Shoemaker in this clip.
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Woman contracts WORLD’S DEADLIEST VIRUS after unknowingly being given the WRONG VACCINE
In yet another careless misstep of the Vaccine Industrial Complex, a woman was jabbed with the wrong dirty vaccine and ended up with a severe case of the world’s deadliest disease. She walked into a clinic to get an MMR jab, if that’s not toxic enough, but the medical practitioner shot her up with the dirty tuberculosis stab, and it took the woman SIX MONTHS to recover from the TB infection she got directly from the dirty jab.
The toxic TB jab is injected into babies right after they’re born, making horrific adverse events quite popular for the little ones. Many of these babies get life-threatening lesions in the lungs, spleen or liver, plus inflamed bones and widespread infection from the dirty TB jabs.
Dirty Vax recipient developed deadly abscess with oozing pus and deathly TB-causing bacteria spread throughout her body from the dirty TB jab
Walking into any hospital is a roll of the dice with your health and safety, even in America. Unless you have a severe wound, deadly infection, or are having a baby, you might want to weigh your other options. The BCG vaccine for TB contains bacteria and can easily be injected incorrectly or administered to the wrong patient. Healthcare professionals often misread the label on the vaccines, because they are careless. Sometimes surgeons will cut off the wrong arm or leg or operate on the wrong organ for this same reason.
The TB vaccine (BCG) contains weakened Mycobacterium bovis and is meant to be injected just below the skin to trigger a localized immune response without spreading. Unlike viral vaccines (e.g., MMR), the bacteria in BCG must be carefully controlled; injecting it into the muscle can allow uncontrolled spread, leading to severe complications.
This case involved a healthy 30-year-old woman who developed an arm abscess after a misplaced BCG injection into her deltoid muscle. Other similar errors have occurred, such as an eight-month-old girl who developed a thigh abscess after an incorrect intramuscular BCG injection. The slow-growing M. bovis infection formed a mass that required drainage. While localized abscesses are rarely fatal, untreated systemic infections can be deadly in up to 80% of cases.
Doctors emphasize that injection errors are the primary cause of severe reactions, which may include abscesses, lymph node inflammation, bone pain, or systemic infections. This case, published in the American Journal of Case Reports, highlights the importance of proper vaccine administration, even in healthy adults. Most complications occur in pediatric or immunocompromised patients, making this an unusual occurrence.
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RFK Jr. slashes HHS bureaucracy, saves taxpayers $1.8B while refocusing on chronic disease epidemic
Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. announced sweeping reforms that will eliminate 10,000 federal jobs, consolidate redundant divisions, and save taxpayers $1.8 billion annually in a bold move to streamline government inefficiency and refocus on America’s worsening health crisis.
The restructuring, which was unveiled this week, will reduce HHS’s 28 divisions to 15 and shift the agency’s priority toward combating chronic diseases by emphasizing clean food, water, and environmental toxin elimination. This marks a notable departure from the bloated administrative structures that have long plagued the department, especially under the Biden administration.
While critics in the mainstream media are predictably claiming that the cuts could jeopardize public health, Kennedy and supporters argue that this important overhaul will enhance efficiency, root out waste, and ultimately deliver better health outcomes for Americans.
Streamlining a bloated bureaucracy
Kennedy’s plan targets redundant offices, merging overlapping functions into a newly created Administration for a Healthy America (AHA), which will centralize key health initiatives. Regional offices will be halved from 10 to 5, and core operations—including human resources, IT, and procurement — will be unified to reduce waste.
“We aren’t just reducing bureaucratic sprawl. We are realigning the organization with its core mission and our new priorities in reversing the chronic disease epidemic,” Kennedy stated. “This Department will do more — a lot more — at a lower cost to the taxpayer.”
Specific cuts include 3,500 jobs at the FDA (19% of workforce), 2,400 at the CDC (18%), 1,200 at the NIH (6%), and 300 at Medicare/Medicaid Services (4%). The reductions follow 10,000 voluntary departures since the start of the Trump administration, which brings HHS’s total workforce down to 62,000 in a 25% reduction.
Shifting the focus to America’s health crisis
Rather than maintaining a sprawling bureaucracy, Kennedy’s reforms prioritize tackling chronic illnesses linked to environmental toxins, processed foods, and contaminated water. The AHA will absorb agencies like the Substance Abuse and Mental Health Services Administration and the Agency for Toxic Substances and Disease Registry, ensuring a coordinated approach to prevention.
Pediatrician Dr. Michelle Perro praised the move, calling it “a more streamlined and effective approach to addressing the tsunami of chronic diseases now affecting most Americans.”
Meanwhile, Sayer Ji, co-founder of Stand for Health Freedom, argued HHS had long been “a key architect of policies that have harmed countless individuals” and that restructuring was “long overdue.”
Media backlash vs. taxpayer wins
Despite the clear cost savings and mission refocus, outlets like NBC News warned the cuts risk “jeopardizing public health” — a claim Kennedy’s team dismisses as fearmongering. Karl Jablonowski, a senior research scientist at Children’s Health Defense, countered: “None of [the job numbers] are a metric of success. Secretary Kennedy’s tenure will be judged by the improvement of America’s health.”
The reforms also introduce an Assistant Secretary for Enforcement to combat fraud in federal health programs and an Office of Strategy to improve research coordination.
A leaner, more effective HHS
Kennedy’s overhaul marks a decisive break from business-as-usual in Washington. By cutting waste and refocusing on preventable health crises, HHS is poised to deliver tangible results rather than perpetuate bureaucratic bloat. As Kennedy declared: “Our goal is to Make America Healthy Again.”
For taxpayers and health advocates alike, that mission is long overdue.
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The cancer fear industry: How big pharma profits from panic—and what natural alternatives offer
In a revealing interview, health advocate Mike Adams and researcher Sylvie Beljanski expose the "cancer fear psyop" used to push aggressive treatments while suppressing natural alternatives. Beljanski highlights plant extracts like Pau Pereira and Rauvolfia vomitoria, which selectively target cancer cells without toxicity—contrasting sharply with chemotherapy’s collateral damage. Adams critiques the financial conflicts in oncology, citing cases like Dr. Farid Fata, who falsely diagnosed patients to profit from chemo. Both urge a shift toward prevention, detoxification, and non-toxic lifestyle choices to combat rising cancer rates.
The Suppression of Natural Cancer Solutions
Sylvie Beljanski’s journey into integrative cancer research was born from tragedy. Her father, Dr. Mirko Beljanski, a molecular biologist at Paris’ Pasteur Institute, pioneered research on plant extracts that selectively target cancerous DNA without harming healthy cells. His work showed promise—until it threatened the pharmaceutical industry’s profits. After treating French President François Mitterrand’s advanced prostate cancer (extending his life against medical predictions), Beljanski’s lab was raided, his research destroyed, and he was poisoned, dying of leukemia without access to his own remedies.
“This wasn’t about justice,” Sylvie explains. “It was about erasing evidence.” She later won a landmark case at the European Court of Human Rights, but the victory couldn’t undo the systemic suppression of non-toxic alternatives.
Plant Extracts vs. Chemo: A Stark Contrast
Beljanski’s research focuses on two potent botanicals: Pau Pereira (an Amazonian plant with antiviral properties) and Rauvolfia vomitoria (an African plant that regulates hormones). Unlike chemotherapy, which indiscriminately attacks cells, these extracts selectively inhibit cancer DNA replication. Under microscopy, healthy cells remain untouched while malignant ones are destroyed.
Recent studies at Kansas University Medical Center revealed even more startling results: mice injected with aggressive breast cancer stem cells showed zero metastasis when treated with Beljanski’s extracts. “Chemo shrinks tumors, but leaves behind resistant stem cells that cause relapse,” Sylvie notes. “Our approach targets the root.”
Mike Adams, a longtime advocate of natural therapies, emphasizes the hypocrisy of oncology’s financial incentives. He cites Dr. Farid Fata, a Michigan oncologist who falsely diagnosed patients to bill for chemo. “The system profits from panic,” Adams says. “Patients aren’t told their doctor earns $20,000 per prescription.”
Detox, Not Fear: A Path Forward
Both experts agree: cancer prevention begins with lifestyle, not luck. Adams avoids processed foods, synthetic chemicals, and wireless radiation; Beljanski advocates for clean skincare (her organic line uses cancer-fighting ginkgo and green tea extracts). “Your skin absorbs toxins in 26 seconds,” she warns. “Why slather on carcinogens?”
They also debunk the “genetic doom” myth. Only 5% of cancers are purely hereditary; the rest are triggered by environmental toxins and poor diet. “Genes load the gun, but lifestyle pulls the trigger,” Adams says.
The solution? Education and empowerment. Beljanski’s upcoming Integrative Cancer Conference (April 25–27, Austin) will spotlight natural therapies suppressed by mainstream medicine. “Fear is the industry’s tool,” she says. “But we have alternatives—if we dare to look.”
Final Thought: As Adams puts it, “We’ve been lied to for decades. Cancer isn’t inevitable—it’s an industry.” The question remains: Will we keep funding its fear machine, or choose the science they tried to bury?
Watch the full episode of the "Health Ranger Report" with Mike Adams, the Health Ranger, and Sylvie Beljanski as they discuss cancer therapy breakthroughs that are suppressed by world governments.
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Dr. Suzanne Humphries makes bombshell appearance on Joe Rogan podcast, exposing vaccine industry deception back to POLIOMYELITIS
In a bombshell interview on The Joe Rogan Experience, Dr. Suzanne Humphries—former nephrologist and co-author of Dissolving Illusions: Disease, Vaccines, and the Forgotten History—ripped open the vaccine industry’s darkest secret: legal immunity birthed reckless science.
Before 1986, vaccine makers faced lawsuits for injuries like Guillain-Barré syndrome from the 1976 swine flu shot. "They couldn’t even get insurance," Humphries explained. Their solution? Bully the government into a bailout. The result was the National Childhood Vaccine Injury Act, sold as "compensation for families" but designed as a kangaroo court that denies 70% of injury claims.
With zero liability, companies like Wyeth (now Pfizer) unleashed untested adjuvants, skipped saline placebo trials, and expanded the childhood schedule—all while profits soared. "Vaccines are tested against other vaccines, not placebos," Humphries noted. "The few saline studies show vaccines often increase susceptibility to the diseases they claim to prevent."
More key points on vaccine deception:
• Polio was never eradicated—diagnostic criteria were changed post-vaccine rollout, masking ongoing cases as Guillain-Barré, lead poisoning, or viral infections.
• Vaccine manufacturers admitted their products were "unavoidably unsafe" yet gained legal immunity in 1986, leading to lax safety testing and rampant use of toxic adjuvants like aluminum and mercury.
• Environmental toxins like DDT and arsenic—not vaccines—mirrored polio’s rise and fall; paralysis declined as pesticide use dropped.
• SV40, a cancer-linked monkey virus, contaminated polio vaccines and remains transmissible between humans today.
• Natural immunity and public health improvements (clean water, nutrition) drove disease decline—not vaccines.
• Modern vaccines are tested against other vaccines, not inert placebos, masking their true risks.
Polio’s vanishing act: a shell game of definitions
The sacred myth of polio’s eradication, Humphries revealed, is a semantic trick. "Polio is still here. It’s just called different names now," she said. Pre-vaccine, diagnoses required paralysis + viral detection. Post-vaccine, cases were reclassified as:
•Guillain-Barré syndrome
•Coxsackievirus
•Lead/mercury/arsenic poisoning
Other compounding issues with polio include:
•DDT poisoning: The real culprit behind polio’s decline? The phase-out of neurotoxic pesticides like DDT and arsenic. "The tonnage of DDT production exactly mirrored polio diagnoses," Humphries said. Countries still using DDT, like India, still report "polio." Meanwhile, the poliovirus itself is harmless in 95–99% of infections, as shown by studies of the Javante Indians, who carried immunity without paralysis.
•Then there’s the Rockefeller lab disaster: In 1916, researchers injected monkey brains and human spinal fluid into monkeys to create a hyper-virulent polio strain. An accidental leak triggered the deadliest polio epidemic in history—with a 25% mortality rate.
•And there’s bulbar polio, which was commonplace after children’s tonsils were removed.
•Studies of the Javante Indians showed 99% had polio antibodies without a single case of paralysis. This is because the polio virus is a commensal microbe, and the condition of poliomyelitis only shows up when the individual's terrain is compromised and their immune system is suppressed.
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Scientists demand FDA withdraw mRNA COVID vaccines amid contamination and gene therapy concerns
A global reckoning: FDA complicity in a public health disaster
In a damning indictment of the U.S. Food and Drug Administration (FDA), a coalition of scientists, immunologists, and legal experts has filed a formal petition demanding the immediate suspension or withdrawal of Pfizer and Moderna’s mRNA COVID-19 vaccines. The petition, now open for public comment, exposes shocking evidence of synthetic DNA contamination, regulatory fraud, and the deliberate misclassification of these experimental gene therapies as "vaccines"—a deception that has placed millions at risk of irreversible harm.
The petition, spearheaded by Australian law firm PJ O’Brien & Associates, accuses the FDA of enabling one of the greatest medical frauds in modern history. By greenlighting Pfizer and Moderna’s mRNA injections without proper environmental assessments—a legal requirement for gene therapies—the agency allowed these dangerous products to flood the market under the false pretense of "emergency use."
"This misclassification denied Americans transparency and informed consent, violating federal law and rendering approvals void from the start," the petition states.
Among the petition’s signatories are prominent figures such as attorney Julian J. Gillespie, immunologist Dr. Jessica Rose, and virologist Dr. David J. Speicher. Kevin McKernan, chief scientific officer of Medicinal Genomics and the first to uncover DNA contamination in the shots, warns that the FDA’s silence is indefensible.
"How do they ever expect to regain the public’s trust?" McKernan asked. "They recently recalled some protein bars for a threat of peanut allergies, yet every American knows multiple people with COVID-19 vaccine injuries, yet the FDA is head-in-the-sand silent."
DNA contamination: a ticking time bomb in every dose
Independent studies cited in the petition reveal that Pfizer and Moderna’s mRNA injections contain synthetic DNA at levels 6 to 470 times above safety thresholds, including SV40 promoter sequences—a known cancer risk. These contaminants, shielded by lipid nanoparticles (LNPs), can integrate into human DNA, triggering genomic instability, immune dysfunction, and malignancies.
• A September 2023 study by McKernan found DNA contamination 18 to 70 times above regulatory limits.
• An FDA-supervised study in December 2024 confirmed contamination up to 470 times over safety limits.
• German and French researchers have replicated these findings, proving this is not an isolated issue but a systemic failure.
"This is not just an American crisis—it’s a global reckoning," Gillespie declared. "Governments must act now to halt further harm and support those already affected."
FDA’s unlawful approval: rewriting the rules to protect Big Pharma
The petition exposes how Pfizer and Moderna exploited regulatory loopholes by falsely labeling their mRNA products as "vaccines" instead of gene therapies. Under U.S. law, gene therapies require rigorous environmental assessments—a step the FDA illegally bypassed.
"Had the FDA properly demanded Environmental Assessments, the American public would have been informed of the gene therapy nature of these shots," the petition states. Instead, the agency colluded with manufacturers to fast-track untested, hazardous technology into the arms of billions.
Dr. Jessica Rose minced no words: "The petition evidences potent facts that should lead to the suspension of use of these experimental nucleoside-modified RNA gene-based products."
As the petition lands on the desk of HHS Secretary Robert F. Kennedy Jr., the world watches to see if the U.S. government will finally hold the FDA and Big Pharma accountable? With mounting evidence of genetic contamination, regulatory fraud, and catastrophic health consequences, one question remains: How many more lives must be destroyed before the FDA admits its crimes?
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The Trump administration’s decision sets a crucial precedent. Government should not operate in a perpetual state of emergency, nor should taxpayer dollars fund indefinite bureaucratic bloat. By reclaiming these funds, the administration is restoring accountability and ensuring that federal health spending serves the public—not political agendas.
A return to fiscal sanity
The reckoning is here—and it’s about time. The Trump administration’s $11 billion cut sends a clear message: Emergency spending must be temporary, transparent and tied to measurable outcomes. Future administrations must follow this example, ensuring that taxpayer dollars are spent wisely rather than wasted on bureaucratic excess.
This move isn’t just about balancing the books—it’s about restoring trust in government and reaffirming that fiscal responsibility matters. The era of blank-check pandemic spending is over. Now, the real work of efficient, effective governance begins.
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Despite surge in MMR vaccination in Texas, measles outbreaks continue: Is VACCINE SHEDDING fueling the spread?
Vaccine-induced shedding: a hidden driver of outbreaks?
As measles cases surge across Texas in early 2025, public health officials face an unsettling paradox: despite a statewide push to administer more measles-mumps-rubella (MMR) vaccines, the outbreak has already eclipsed the total number of U.S. cases reported in all of 2024. With 309 confirmed infections—up from just 285 nationwide last year—the spike follows a 15,000-dose increase in measles vaccinations. But buried in decades of scientific literature is a rarely discussed phenomenon: the measles vaccine itself can spread the virus.
A 1995 CDC study published in the Journal of Clinical Microbiology detected measles virus RNA in the urine of 83% of vaccinated children for up to two weeks after receiving the MMR shot. The researchers, led by Paul A. Rota, noted that viral shedding began as early as one day post-vaccination and persisted in some cases for 14 days. Similar findings were replicated in a 2024 Journal of Clinical Virology study, which identified shedding for 29 days in recently immunized individuals. This raises a critical question: Could aggressive vaccination campaigns inadvertently amplify community transmission?
"The vaccine virus is alive, replicating, and excreted," explains Dr. Suzanne Humphries, a nephrologist and vaccine researcher. "When you inject a live virus into a person, especially someone immunocompromised, that virus can escape into the environment."
Gain-of-function engineering: a more invasive measles strain
Compounding the issue is the MMR vaccine’s design. A 2016 study in The Journal of Infectious Diseases revealed that the vaccine’s Edmonston strain was engineered through gain-of-function (GOF) techniques to bind CD46—a receptor found on nearly all human nucleated cells. Wild measles primarily targets CD150, a marker on immune cells.
Original (Wild-Type) Measles Virus (Montefiore 89 Strain):
The naturally occurring measles virus primarily infects immune cells by binding to the CD150 receptor.
Lab-Modified (Vaccine) Strain (Edmonston Strain):
In contrast, the vaccine strain has been altered in the lab to gain the ability to bind CD46—a receptor found on nearly all nucleated human cells and present in much higher abundance than CD150. Because of this engineered adaptation, the vaccine strain of measles virus has the potential to enter a broader range of cells compared to the wild-type virus, due to its expanded receptor usage.
This manipulation means the vaccine virus can infect a broader range of tissues than its natural counterpart. Combined with prolonged shedding, the risk of vaccine-derived transmission escalates—particularly among the unvaccinated or those with weakened immunity.
Texas: a case study in failed containment
Gaines County, Texas, saw a 242% spike in measles cases after a health district distributed free MMR vaccines in early 2024. Now, with statewide cases soaring, health officials admit the outbreak is likely under-counted and expected to worsen.
Historical context sharpens the concern:
1966: Measles antigen was detected in vaccinated individuals’ urine for 16 days post-injection.
1995: CDC confirmed viral RNA shedding in children.
2024: Peer-reviewed studies extended the shedding window to 29 days.
However, with vaccine shedding well known for decades, public health messaging continues to blame the unvaccinated, ignoring the vaccine’s own role in viral spread. With measles dominating headlines in 2025, the Texas outbreak forces a uncomfortable debate: Are we trading short-term "herd immunity" for long-term viral persistence? As vaccine-derived cases mount, the medical establishment faces a dilemma—one that echoes the early days of polio, where the vaccine itself seeded outbreaks.
"When you vaccinate millions," warns biologist Dr. Stephanie Seneff, "you’re conducting an uncontrolled experiment on the whole population."
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