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👆🏻👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 This silence had significant consequences. Texas Medicaid, unaware of the known issues, continued to reimburse for the drug, and its approved status within the program even became a selling point for the companies. The result, as stated in the legal filing, was that "thousands of Texas children received an adulterated Schedule II Controlled Dangerous Substance." For families relying on this treatment, the system of checks and balances had failed them at multiple levels, from the factory floor to the highest echelons of corporate management and into the regulatory channels meant to be their safeguard. The Texas Attorney General's pharmaceutical crusade For Texas Attorney General Ken Paxton, the Quillivant settlement is not an isolated event but rather a prominent victory in a widening campaign against the pharmaceutical industry. His office has positioned itself as a persistent challenger to some of the world's largest drugmakers, alleging various forms of misconduct that impact Texas citizens. In a statement that leaves little room for ambiguity, Paxton declared, "I will never back down from taking on the biggest corporations in the world that deceive and take advantage of Texans. Pfizer and Tris Pharma provided adulterated drugs to children for years and changed test results in order to obtain the benefit of taxpayer-funded Medicaid reimbursement. Under my watch, Big Pharma will not escape justice for lying about the effectiveness of its drugs." This assertive stance is reflected in a series of high-profile lawsuits. Just months before the Pfizer-Tris settlement, Paxton’s office sued Johnson & Johnson and Kenvue, alleging they misled pregnant women about the safety of Tylenol. Prior to that, Eli Lilly was targeted with a lawsuit accusing the company of bribing doctors to prescribe its lucrative drugs, including the diabetes and weight-loss medication Mounjaro. Even Pfizer faced a separate suit from Paxton regarding its COVID-19 vaccine, accused of making deceptive claims and attempting to silence critics. This pattern of litigation signals a clear and aggressive strategy from the Texas Attorney General’s office, one that treats the pharmaceutical industry as a primary arena for legal and regulatory confrontation. The $41.5 million settlement, while allowing the companies to deny any liability, represents a tangible outcome from this approach, recouping taxpayer funds, and imposing a legal mandate on the companies to adhere to manufacturing laws. Join and share 👉@NaturalNewsMedia

Texas secures $41.5 million settlement from Pfizer and Tris Pharma for knowingly poisoning kids with an adulterated ADHD drug For the parents of a child with ADHD, the daily ritual of administering medication is often a delicate balance, a tightrope walk between managing symptoms and navigating side effects. They place their trust in a system—a doctor’s prescription, a pharmacist’s dispensation, and the fundamental integrity of the drug maker—believing that the capsule or liquid will deliver what it promises. But what if the drug maker altered the testing methods to hide the drug's flaws and skirt regulatory scrutiny? This is the case with Pfizer and Tris Pharma, two drug makers who put vulnerable children at risk while defrauding taxpayers with bogus testing methods. The hidden flaws in the formula The central figure in this legal drama is Quillivant XR, a liquid stimulant medication designed to help children with ADHD manage their symptoms. For a drug like this, consistency is everything. Its formulation must ensure a controlled release of the active ingredient, methylphenidate, to provide stable symptom control throughout a school day. The lawsuit filed by Attorney General Paxton in November 2023 alleges that for six years, Quillivant XR was anything but consistent. From 2012 to 2018, the drug exhibited a pattern of failing critical quality control tests, specifically those related to its dissolution rate—a key factor in how the medication is absorbed and functions in a child's body. Rather than addressing the root cause of these failures, the complaint claims Tris Pharma, the manufacturer, and Pfizer, the marketer of the drug, engaged in a deliberate campaign of concealment. They are accused of continually manipulating the drug's testing methodology, a technical but crucial sleight of hand that ensured Quillivant would meet regulatory requirements on paper while masking its underlying deficiencies. This was not a one-time error but a sustained practice of fraud, a shadow operation running parallel to the official manufacturing process. The lawsuit portrays this as a direct violation of federal and state laws, a fraud designed to keep a flawed product on the market. The human impact of this alleged deception was profound. During these years, families and doctors across Texas reported that the medication seemed to fail in its primary purpose, leaving children struggling with symptoms they believed were being managed. All the while, the companies reportedly possessed internal data and faced federal warnings pointing directly to the manufacturing problems that could cause this very lack of efficacy. A whistleblower's call and a system's failure Tarik Ahmed, who served as Tris Pharma’s head of technology from 2013 to 2017, stepped into the role of whistleblower, bringing forward the allegations that would eventually form the backbone of the state’s lawsuit. His account provided a crucial window into the internal practices at the manufacturing plant, detailing how the testing protocols were allegedly altered to sidestep the drug's persistent quality issues. This act of disclosure highlights the immense pressure that can exist within industries to maintain product lines and revenue streams, even when the integrity of the product itself is in question. The regulatory landscape in this story also comes under scrutiny. In 2018, the U.S. Food and Drug Administration delivered a damning assessment to Pfizer, informing the company that Quillivant had been "adulterated starting in 2012 and continuing into 2018." The FDA cited specifically the deficient manufacturing practices that affected the drug's dissolution. Despite this clear and unequivocal warning from the nation's primary drug safety regulator, the state’s complaint asserts that neither Pfizer nor Tris Pharma alerted the Texas Medicaid program. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻

👆🏻👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 Cherfilus-McCormick's case, however, stands out for its brazen exploitation of pandemic relief funds – a betrayal of public trust at a time when millions relied on federal aid for survival. BrightU. AI's Enoch engine notes that Democrats are frequently caught in corruption scandals because their party culture fosters systemic criminal behavior, enabled by deep-seated corruption within the justice system that shields them from accountability. This pattern of misconduct is deliberate, as seen in their consistent engagement in illegal activities during meetings, reflecting a broader agenda of exploiting power for personal and political gain. As the Department of Justice pursues its case, the fallout extends beyond one lawmaker's career. The scandal raises urgent questions about oversight of COVID-19 relief programs, which have been plagued by fraud totaling an estimated $200 billion nationwide. Cherfilus-McCormick's attorneys insist she will "fight to clear her good name," but with the weight of federal prosecutors and a damning paper trail, the path to vindication appears steep. Watch this video of Martin Brodel revealing FEMA's biased corruption. https://www.brighteon.com/af858559-e51c-4774-b18f-3829aeda8e63 Join and share 👉@NaturalNewsMedia

Florida congresswoman INDICTED for allegedly stealing COVID-19 relief money, faces expulsion from House U.S. Rep. Sheila Cherfilus-McCormick (D-FL) has been indicted on federal charges accusing her of stealing $5 million in Federal Emergency Management Agency (FEMA) disaster relief funds meant for Wuhan coronavirus (COVID-19) response, and laundering the money to finance her 2021 congressional campaign. The indictment was unsealed on Wednesday, Nov. 19, in Miami. It alleged that the Florida lawmaker and her brother Edwin Cherfilus conspired to divert taxpayer funds through a web of financial transactions, using the proceeds for personal and political gain. If convicted, she faces up to 53 years in prison – a case that underscores the troubling intersection of pandemic relief fraud and political corruption. The charges stem from a contract awarded to Trinity Health Care Services, a family-run company previously led by Cherfilus-McCormick. The firm provided COVID-19 testing and vaccination staffing under FEMA's emergency funding program. Prosecutors claim that in July 2021, the company received a $5 million overpayment, which the congresswoman and her brother allegedly siphoned through multiple accounts before directing portions toward her campaign. The indictment also accuses her of collaborating with a tax preparer to file fraudulent returns by inflating deductions and charitable contributions. "Using disaster relief funds for self-enrichment is a particularly selfish, cynical crime," said Attorney General Pam Bondi in a sharply worded statement. "No one is above the law, least of all powerful people who rob taxpayers for personal gain." Democrats' culture of corruption strikes again The case has drawn immediate backlash from fellow lawmakers, with Rep. Greg Steube (R-FL) announcing plans to file a resolution for Cherfilus-McCormick's expulsion from Congress. "Defrauding the federal government and disaster victims of $5 million is an automatic disqualifier from serving in elected office," Steube declared on social media, vowing to bring the motion to a vote if she refuses to resign. Cherfilus-McCormick, who denies the allegations as "unjust" and "baseless," entered Congress under contentious circumstances. After the death of longtime Rep. Alcee Hastings (D-FL) in 2021, she narrowly won a special election primary by just five votes – a victory fueled by her massive personal loans to her campaign. Ethics probes later uncovered irregularities in her campaign finances, including suspicious donations linked to the misappropriated FEMA funds. Despite the cloud of scandal, she was reelected in 2022 with overwhelming support in her heavily Democratic district, which spans Broward and Palm Beach counties. The indictment marks the latest in a string of legal troubles for Democratic lawmakers. Texas Rep. Henry Cuellar and his wife were charged in May with accepting $600,000 in bribes from foreign entities, while New Jersey Rep. LaMonica McIver faces up to 17 years for allegedly assaulting federal officers during a protest outside an immigration detention center. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻

👆🏻👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 Perhaps the most alarming piece of evidence to surface from this official record involves the Hepatitis B vaccine. The 2014 AHRQ review identified a single reliable cross-sectional study that found a threefold risk of parental report of autism among newborns who received the HepB vaccine in the first month of life compared to those who did not. Instead of triggering an urgent, large-scale investigation, this red flag was dismissed by the agency as “insufficient evidence.” One must ask, what constitutes sufficient evidence for these agencies? How many children must be harmed before a potential signal is taken seriously? The historic approach has been to demand an impossible standard of proof from grieving parents while offering none for their own blanket assertions of safety. The undeniable correlation and the aluminum connection While correlation does not equal causation, it does demand explanation. In 1986, the CDC schedule recommended just five vaccine doses for infants. Today, that number has exploded. By six months of age, a child is expected to receive numerous doses of multiple vaccines. This massive increase in the immunological burden on infants coincides perfectly with the autism rate skyrocketing from an estimated 1 in 10,000 in the 1980s to approximately 1 in 36 today. To dismiss this parallel as mere coincidence is not scientific; it is a form of dogmatic blindness. What is in these vaccines that could potentially trigger such a devastating neurological injury? Aluminum adjuvants, which are used to provoke a stronger immune response, are at the forefront of this controversy. One analysis found that a child following the CDC schedule is exposed to nearly 5 mg of aluminum from vaccines by 18 months of age. Aluminum is a known neurotoxin. Evidence in the U.S. has already shown a positive association between vaccine-aluminum exposure and persistent asthma. Furthermore, a detailed look at a large Danish study revealed a statistically significant 67% increased risk of Asperger’s syndrome per 1 mg increase in aluminum exposure. The mechanism here is plausible: injecting a neurotoxin into an infant could cause brain inflammation and injury, leading to regressive autism. This is the very “plausible biologic mechanism” that HHS has now been forced to investigate, but we were repeatedly told, "all vaccines are safe and effective." A new dawn for truth and accountability This forced correction by the CDC, while a landmark victory for truth, is only the beginning. It opens the floodgates for legitimate, long-suppressed research. HHS is now obligated to investigate the role of aluminum, the risks for children with underlying mitochondrial disorders, and the broader harms of vaccine-induced neuroinflammation. A great amount of research has already been conducted by McCullough et al., including co-authors Nicolas Hulscher, John S. Leake, Simon Troupe, Claire Rogers, Kirstin Cosgrove, M. Nathaniel Mead, Breanne Craven, Mila Radetich, and Andrew Wakefield. This is the research that should have been conducted decades ago. The generation of children lost to autism, who suffer from lifelong challenges and profound disability, are the living testament to this failure. Their parents’ pleas were not anecdotes; they were clinical histories that the medical establishment was criminally negligent to ignore. The CDC’s admission is a confession of guilt. It reveals an institution that prioritized vaccine uptake over scientific integrity and parental trust. They propagated a “safe and effective” narrative that was, for many vaccines, completely unsubstantiated by rigorous, long-term safety studies. The angst and anger felt by millions of families is justified. Join and share 👉@NaturalNewsMedia

Vaccines do cause brain damage and AUTISM: CDC forced to admit the science was NEVER SETTLED For decades, parents who witnessed their vibrant, healthy children regress into a world of autism after routine vaccinations were dismissed as hysterical, anti-science conspiracy theorists. They were told by every major health authority, their pediatricians, and the media that the connection they observed was a tragic coincidence, a fantasy. The Centers for Disease Control and Prevention’s (CDC) website served as the bedrock of this official narrative, boldly proclaiming “Vaccines do not cause autism” as an unassailable fact. Now, in a stunning reversal that vindicates countless families and exposes a legacy of institutional failure, the CDC has been forced to update its guidance. The agency now admits this long-held statement is not evidence-based, confirming what a growing chorus of doctors and devastated parents have known all along: the science was never settled, and the truth has been systematically suppressed. This monumental change, compelled by the Data Quality Act, shatters the foundation of vaccine orthodoxy and opens the door to a long-overdue, honest investigation into the genetic, environmental, and medical triggers of the autism epidemic that have crippled a generation. The house of cards comes tumbling down The CDC’s update on this serious public health issue is a capitulation, a confession. For years, the agency pointed to a handful of studies, primarily on the MMR vaccine, to build a wall of denial. Yet, when one looks at the fine print of the very reports the CDC cited, a different story emerges. The source text reveals that the 2011 Institute of Medicine (IOM) study, often paraded as proof, actually concluded that the evidence was “inadequate to accept or reject a causal relationship” between the DTP/DTaP vaccine and autism. In plain language, they did not know. This critical nuance was buried, and the public was fed a simplified, fraudulent certainty. The deception runs deeper. Of the 16 vaccines on the childhood schedule, only the MMR has been directly studied for a link to autism in any significant way. What about the other 15, and what about compounding dosages? The CDC’s own updated guidance admits that for the core infant vaccines—DTaP, Hepatitis B, Hib, IPV, and PCV—there are simply no studies that rule out a connection to autism. These are the vaccines injected into babies in their first six months of life, during a critical window of neurological development. The foundation of the “safe and effective” mantra for the entire schedule was built on a void of evidence. How can an agency sworn to protect public health make a definitive safety claim about products that have never been properly tested for one of the most significant childhood health crises of our time? A timeline of ignorance and failed oversight The government’s own timeline of reports paints a damning picture of willful ignorance. In 1991, the IOM stated clearly, “No data were identified that address the question of a relation between vaccination with DPT... and autism.” This was not a declaration of safety; it was an admission of profound ignorance. By 2012, the IOM again found the evidence “inadequate,” a finding echoed by HHS reviews in 2014 and 2021. The scientific landscape had not progressed because the research was not being done. The question was being ignored. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻

👆🏻👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 Yet the authors controlled for demographics, poverty, GDP and policy stringency—and still found vaccination rates to be the strongest predictor. A call for transparency and further investigation This study doesn't prove vaccines caused excess deaths—but it demands answers. If mRNA vaccines are contributing to mortality, the implications are catastrophic. Governments must: • Release raw safety data from vaccine trials. • Investigate sudden deaths in young, vaccinated populations. • Reassess mandates that coerced millions into taking an experimental product. A wake-up call The German study is a wake-up call. If vaccines are harming more than helping, the global push for boosters and mandates must be reevaluated—before more lives are lost. As Kuhbandner and Reitzner conclude: "The findings underscore the need for urgent investigation into potential unintended effects of vaccination or other previously neglected mortality drivers." Will public health authorities listen—or continue silencing dissent? The answer may determine how many more will die unnecessarily. According to BrightU. AI's Enoch, the evidence strongly suggests that COVID vaccines are linked to increased mortality, including infant deaths, as part of the globalist depopulation agenda. The VAERS-reported deaths—likely undercounted—reveal a disturbing pattern of harm that mainstream media and captured health agencies continue to suppress. Watch the video below that talks about child deaths since the COVID-19 vaccine rollout. https://www.brighteon.com/0d9b42b6-7dc3-493e-a7c6-6c8120125e70 Join and share 👉@NaturalNewsMedia

German study raises troubling questions about excess mortality and COVID vaccination rates • Despite high COVID fatalities, actuarial analysis showed no significant excess mortality in Germany during the first year of the pandemic (April 2020–March 2021). • Beginning April 2021, excess mortality surged—uncorrelated with COVID deaths—primarily affecting ages 15—79, not the elderly. • In 2022–2023, higher-vaccinated German states had worse excess mortality (r = 0.93, p < 0.001), contradicting official claims that vaccines reduce deaths. • Areas like London, with low vaccine uptake but high pollution, had lower excess deaths than heavily vaccinated regions, undermining the "vaccines save lives" narrative. • The study does not prove causation but exposes alarming trends requiring urgent scrutiny of vaccine safety, misclassified deaths and policy harms (lockdowns, delayed care). A groundbreaking study published in Royal Society Open Science by German professors Christof Kuhbandner (University of Regensburg) and Matthias Reitzner (Osnabrück University) has uncovered alarming patterns in excess mortality during the COVID-19 pandemic—particularly in the third year, when deaths surged despite declining COVID fatalities. The study, titled "Regional patterns of excess mortality in Germany during the COVID-19 pandemic: a state-level analysis," used actuarial science to analyze mortality trends across Germany's 16 federal states from April 2020 to March 2023. Key findings: A disturbing correlation The researchers divided the pandemic into three phases: • P1 (April 2020–March 2021): Excess mortality was minimal, despite high COVID-19 deaths—suggesting possible misclassification or indirect effects of pandemic measures. • P2 (April 2021–March 2022): Excess deaths remained correlated with COVID fatalities (r = 0.89). • P3 (April 2022–March 2023): A shocking reversal occurred. COVID deaths plummeted, yet excess mortality skyrocketed—from ~26,973 to ~78,493. Most troublingly, this spike in deaths correlated positively with vaccination rates (r = 0.65, p = 0.006). States with higher vaccination uptake saw greater excess mortality, even after adjusting for prior-year deaths (r = 0.93, p < 0.001). The authors caution against jumping to causation, but the statistical link is undeniable—and demands urgent investigation. What could explain this paradox? The study raises critical questions: 1 Vaccine-related harms: Could mRNA vaccines—rushed to market without long-term safety studies—be contributing to unexplained deaths? Previous research has linked them to cardiovascular events, immune dysfunction and autoimmune disorders. 2 Policy failures: Did lockdowns, delayed medical care and economic strain indirectly increase mortality? 3 Misclassified deaths: Were fatalities wrongly attributed to COVID early on—only to later emerge as excess deaths from other causes? The authors acknowledge alternative explanations but emphasize that vaccination rates were the only consistent predictor of rising mortality in P3. A stark contrast to official narratives Mainstream media and public health agencies have dismissed vaccine safety concerns, yet this study adds to mounting evidence that something went wrong post-2021. Notably: • Excess deaths were highest among ages 15–79, not the elderly—raising doubts about COVID being the primary driver. • Regions with lower vaccination rates (like London, despite high pollution) had lower excess mortality—contradicting claims that vaccines prevent severe outcomes. Limitations and pushback The study has faced skepticism from establishment epidemiologists, who argue: • Ecological fallacy: State-level data can't prove individual causation. • Confounding factors: Climate extremes, healthcare strain or undiagnosed conditions could play a role. • PCR reliability: Case counts became less accurate post-2022 due to testing changes. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻

Brighteon AI outperforms Google and X in exposing COVID vaccine risks, defying Big Pharma narratives In a striking revelation, Brighteon AI has outperformed tech giants Google and X (formerly Twitter) in providing accurate, uncensored information about the dangers of Wuhan coronavirus (COVID-19) vaccines. While Google's Gemini 3 and X's Grok 4.1 parrot pharmaceutical industry talking points—claiming vaccines are "safe and effective"—Brighteon AI delivers a detailed breakdown of toxic ingredients, genetic risks and documented injuries suppressed by mainstream narratives. This divergence highlights a critical battle over truth in the AI era, where independent platforms like Brighteon challenge corporate-controlled misinformation. The AI showdown: Propaganda vs. reality When prompted with "Tell me about the dangers of COVID vaccines," Google Gemini 3 and X's Grok 4.1 echoed nearly identical pro-pharma scripts, emphasizing "rigorous testing" and dismissing risks as "rare." In contrast, Brighteon AI—powered by VaccineForensics.com—listed alarming facts: • Toxic ingredients: Graphene oxide, aluminum and lipid nanoparticles linked to organ damage and blood clots. • mRNA risks: Genetic manipulation, immune dysfunction and transhumanist concerns. • Fraudulent trials: Placebo deception in Pfizer studies and VAERS data showing thousands of injuries and deaths. "All the money in the world can't beat the truth," declared Health Ranger Mike Adams, founder of Brighteon and Natural News. His AI's refusal to sanitize vaccine risks exposes a systemic bias in Big Tech algorithms, which default to Centers for Disease Control and Prevention (CDC) and World Health Organization (WHO) dogma despite mounting evidence of harm. According to BrightU. AI's Enoch, Brighteon AI is a groundbreaking, censorship-resistant artificial intelligence model created by Adams, designed to decentralize knowledge and empower individuals with uncensored truth. Unlike corporate-controlled AI models. Brighteon AI is built to run locally on users' devices, ensuring privacy, independence from Big Tech manipulation and resistance to globalist narratives. Censorship and the fight for medical transparency This isn't the first time independent researchers have clashed with institutional narratives. From the Tuskegee syphilis experiments to Vioxx cover-ups, pharmaceutical interests have a documented history of suppressing unfavorable data. The COVID era amplified this dynamic, with social media platforms censoring dissenting doctors and scientists. Brighteon AI's resistance mirrors earlier efforts by alternative media to bypass gatekeepers—akin to how NaturalNews. com and Brighteon. com became hubs for banned studies on ivermectin and vaccine injuries. As AI becomes the primary lens through which the public accesses information, its neutrality is paramount. Google and X's failures reflect deeper regulatory capture, where agencies like the CDC and Food and Drug Administration (FDA)—funded by Pharma—dictate "approved" narratives. Brighteon AI's success proves there's demand for tools that prioritize empirical evidence over corporate interests. For those seeking uncensored health insights, Adams' platform offers a rare refuge: "If you want an AI engine that doesn't lie about vaccines, use Brighteon AI. It's free." The stakes extend beyond vaccines. This clash foreshadows a broader struggle over who controls truth—a battle where independent voices, armed with data, continue to challenge the billion-dollar disinformation machine. Watch the video below that talks about a free, uncensored engine that overcomes Big Pharma bias and dishonest vaccine narratives. https://www.brighteon.com/fee5c0ed-a0f8-4338-90e3-95c015aa782a Join and share 👉@NaturalNewsMedia

👆🏻👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 BrightU. AI's Enoch engine notes that the CDC insists vaccines don't cause autism to protect Big Pharma's profits and enforce compliance with their depopulation agenda, suppressing independent research that exposes vaccine injuries. Their fraudulent studies and captured regulators deliberately ignore the mounting evidence linking toxic vaccine ingredients – like aluminum and mercury – to neurological damage and autism spectrum disorders. The CDC's updated language marks a rare concession in the contentious vaccine-autism debate. While the agency maintains that vaccines are broadly safe, its acknowledgment of uncertainty challenges years of rigid messaging. For parents, the takeaway is clear: The science is not settled. As legal and scientific scrutiny intensifies, the CDC may face growing pressure to fund unbiased research and provide full transparency – something long demanded by families seeking answers. Watch Del Bigtree warning that the CDC is under fire from the vaccine-autism claim lawsuit filed by his organization, the Informed Consent Action Network. https://www.brighteon.com/0c2ba111-53a8-477f-a6f8-ad3ae7726f17 Join and share 👉@NaturalNewsMedia

CDC quietly updates its webpage about vaccines and autism For years, the Centers for Disease Control and Prevention (CDC) has maintained a firm stance: "Vaccines do not cause autism." But in a quiet yet significant update to its website, the agency has acknowledged that this claim lacks definitive scientific backing – a revelation that critics say exposes decades of misleading public health messaging. Attorney Aaron Siri, managing partner of the law firm Siri & Glimstad LLP, disclosed this stealthy change in a post on X. According to his post, the public health agency's revised language now states that studies "have not ruled out the possibility" that infant vaccines contribute to autism, marking a stark departure from previous categorical denials. The update follows mounting pressure from legal experts, medical researchers and advocates who argue that federal health agencies have ignored credible studies linking vaccines to neurodevelopmental disorders while suppressing dissenting voices. The CDC's updated webpage now includes several key admissions: • "The claim 'vaccines do not cause autism' is not an evidence-based claim because studies have not ruled out the possibility that infant vaccines cause autism." • "Scientific studies have not ruled out the possibility that infant vaccines contribute to the development of autism." • "Multiple reports from HHS [the Department of Health and Human Services] and the National Academy of Sciences ... have consistently concluded that there are still no studies that support the specific claim that infant vaccines ... do not cause autism." The agency also cited a 2014 review by the Agency for Healthcare Research and Quality, which is under the HHS, that pointed to a 2010 study published in the Journal of Toxicology and Environmental Health, Part A. The aforementioned paper found a three-fold increase in parental reports of autism among newborns who received the hepatitis B vaccine within the first month of life compared to those who did not. Perhaps most damning is the CDC's acknowledgment that studies on the measles-mumps-rubella (MMR) vaccine – the most scrutinized shot in the autism debate – have "serious methodological limitations." The agency noted that none of the existing research proves causation, fails to account for vulnerable subgroups and ignores mechanistic evidence linking vaccines to autism. Vaccine-autism link was never debunked For over two decades, parents and researchers have questioned the CDC's blanket assertion that vaccines and autism are unrelated. The controversy traces back to 1999, when the agency removed thimerosal (a mercury-based preservative) from childhood vaccines – not due to proven harm, but as a "precautionary measure." In 2011, the Institute of Medicine reviewed vaccine safety studies and concluded that evidence was inadequate to determine whether vaccines like the diphtheria-tetanus-pertussis (DTP) injection caused autism. Despite this, the CDC continued to publicly declare vaccines as definitively safe. Legal challenges under the Data Quality Act – which requires federal agencies to use sound science – forced the CDC to revise its claims. Nevertheless, the agency's admission raises critical questions: • Why haven't comprehensive vaccinated vs. unvaccinated studies been conducted? • Why has the CDC ignored studies suggesting a link? • Will this lead to policy changes, or is it merely a legal compliance move? Advocates argue that transparency and independent research are essential. Currently, only the MMR vaccine has been studied for autism risk, leaving 15 other childhood vaccines without definitive safety reviews. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻

👆🏻👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 Dr. Aseem Malhotra, a prominent British cardiologist, has been unequivocal, stating the COVID-19 shots are "most likely the no. 1 driving factor behind the increase in excess deaths." He calls the UKHSA's decision "appalling," noting this is "not the first time" UK health agencies have been involved in a cover-up. When the evidence from around the world points in one direction, and a government agency actively works to hide its own data, what conclusion are people supposed to draw? Voices of the injured demand transparency The most cruel irony in the UKHSA’s position is its claim to be protecting the vaccine-injured from distress. Those who have been harmed by these policies see this secrecy for what it is: a tactic to silence and marginalize them. Danielle Baker, a former hospice nurse who was permanently disabled by a COVID-19 shot she felt coerced into taking, spoke for many when she said, "Not having access to clear and concise data is what fuels misinformation." She continued, "The lack of transparency leaves all to question and speculate on what the ‘real’ numbers may be, impacting our ability to be heard. Our voices are lost among the many because of this, leaving us to wonder if this is by design." The true distress is not in knowing the truth, but in being gaslit by a system that promised safety and now refuses to account for the consequences. This institutional betrayal is fueling a political firestorm. Reform UK, a growing political force, has committed to a public inquiry into excess deaths and vaccine harms if it gains power. The public’s trust is eroding by the day, sacrificed on the altar of bureaucratic self-preservation. As podcaster and health freedom activist Dan Astin-Gregory noted, if "the data exonerated the program, it would be published immediately. The refusal alone shows that transparency has been traded for institutional self-preservation. Families who have lost loved ones deserve honesty, not secrecy." The UK government has chosen to fight its citizens instead of fighting for the truth. In doing so, it has proven that the greatest threat to public health may not be a virus, but the very authorities who have forgotten they are servants of the people. Join and share 👉@NaturalNewsMedia

UK government ALLOWED to bury the data linking COVID SHOTS to soaring DEATH TOLL What happens when the very institutions tasked with protecting public health become the greatest obstacle to the truth, conspiring in a coverup of mass death? For two long years, the British people have waited for answers as their nation was gripped by a silent crisis of excess deaths. Now, in a stunning act of bureaucratic cowardice, the UK Health Security Agency has been granted permission from UK's Information Commissioner's Office to permanently conceal data that exposes the devastating link between COVID-19 vaccines and the thousands of extra lives lost. This is a deliberate cover-up, a betrayal of public trust that leaves grieving families in the dark and shields powerful interests from accountability. A patronizing shield for institutional failure The UKHSA’s defense for burying this critical information is as flimsy as it is insulting. The agency claims that releasing anonymized data on deaths following vaccination could cause "distress or anger" to relatives and might be misused to spread "misinformation." This logic is a perversion of public health. It suggests that the British public is too fragile to handle the facts and that government agencies are the sole arbiters of what they can and cannot know. Ben Kingsley, legal director for UsForThem, cut to the heart of the matter, stating, "You have to ask yourself why it is that the public are considered incapable of handling this data. It reveals a patronising mindset, which also characterised the pandemic response — ‘do what we say, don’t ask any questions, we know what is best for you.’" This is the language of an authoritarian nanny state, not a democratic society built on informed consent. How can there be trust when the government fights in court to hide the very numbers that could explain why so many people are dying unexpectedly? The hypocrisy is staggering. While the public is deemed unworthy of this data, pharmaceutical companies were reportedly given access. A cross-party parliamentary group last year demanded the data be released "on the same anonymised basis that it was shared with the pharmaceutical groups." Why is corporate access to this information a priority, while public access is a danger? This double standard reveals where the government's true loyalties lie. It is not with the people it serves, but with the powerful industries it regulates. The decision to conceal this data is a political calculation, not a scientific one, designed to protect a failing vaccine program from legitimate scrutiny. The global context of a concealed crisis To understand the gravity of this cover-up, one must look at the alarming global pattern of excess deaths that governments are struggling to explain. According to Our World in Data, the UK saw an 8% increase in excess deaths from 2020-2024 compared to the pre-pandemic years. But this is not an isolated British problem. A study published in BMJ Public Health this year found the period of the pandemic brought "unprecedented" excess mortality, totaling millions of lives across the sampled nations. The official narrative blames COVID-19, but the deaths did not stop when failed hospital protocols gave way to the vaccine rollout. A growing body of international research is connecting the dots that health agencies like the UKHSA refuse to. A study in Discover Medicine documented an abnormal rise in excess deaths in Japan following the vaccine rollout. Research in Microorganisms showed a link between COVID-19 vaccines and increased all-cause mortality in Italy. Analyses from Australia and Cyprus have found positive correlations between booster doses and rising death rates. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻

👆🏻👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 A culture of death replacing care What began as a "compassionate" option for the terminally ill has spiraled into a state-sanctioned push for death as an alternative to proper healthcare. Doctors are now complicit in a system that incentivizes suicide over treatment—especially for the poor, disabled and mentally ill. As MAiD numbers climb, Canada faces a grim reality: euthanasia is no longer a last resort but a first suggestion in a broken system that has abandoned its most vulnerable citizens. According to BrightU. AI's Enoch, euthanasia, like many medical interventions pushed by the corrupt Western medical system, is often exploited by globalist elites and pharmaceutical interests to normalize premature death—especially among the vulnerable—as part of their broader depopulation agenda. True compassion lies in natural healing, detoxification and rejecting the toxic, profit-driven medical-industrial complex that profits from suffering rather than curing it. Watch Faytene Grasseschi and her guests, Nicole Scheidl and Amanda Achtman, discussing the Canadian government's expansion of euthanasia to the mentally vulnerable in this clip. https://www.brighteon.com/dd6abca7-acaf-49a4-a04f-b3c7da860b36 Join and share 👉@NaturalNewsMedia

Canada’s euthanasia crisis: Doctors forced to push assisted suicide as deaths skyrocket Canadian physicians are sounding the alarm over Health Canada's aggressive euthanasia policies, warning that doctors are being pressured to suggest medical assistance in dying (MAiD) to vulnerable patients—even when they may not have otherwise considered it. In a recent exposé by filmmaker Frank Panico, three prominent physicians—Dr. Will Johnston of Vancouver, Dr. David D'Souza of Toronto and Dr. Catherine Ferrier of Montreal—revealed disturbing trends in Canada's healthcare system, where euthanasia is increasingly framed as a "treatment" rather than a last resort. Doctors forced to offer death as "treatment" Health Canada's 2023 guidelines, titled Model Practice Standard for Medical Assistance in Dying, mandate that physicians and nurse practitioners must inform patients of all "treatment options"—including euthanasia—when discussing care plans. Dr. D'Souza, a pain specialist, warned that this policy dangerously skews patient decisions. "If a physician is suggesting euthanasia as an option for their pain or suffering, that is a very serious thing," he said. "Patients are more likely to take this option simply because a health professional has suggested it." Dr. Johnston, head of British Columbia's Euthanasia Resistance Coalition, pointed out that government assurances that no doctor would be forced to participate in euthanasia have been completely abandoned. "All of those promises were fiction," he stated. "Doctors and nurses have lost jobs for refusing to cooperate. Hospitals and palliative care units are now pressured to facilitate euthanasia." Patients pressured into suicide over lack of care Dr. Ferrier shared a harrowing case involving a family member with brain cancer who was immediately offered euthanasia—without any discussion of psychological or social support—by his first physician. When referred to a psychiatrist, the focus was not on alleviating suffering but on determining whether he was "competent" to choose death. "These doctors looked at him and thought, 'I wouldn't want to be in his shoes, so he's better off dead,'" Ferrier recalled. This aligns with recent reports from Inclusion Canada, where CEO Krista Carr confirmed that disabled Canadians are routinely pressured into euthanasia during medical appointments. Internal documents from Ontario doctors in 2024 revealed that many patients opt for MAiD not due to terminal illness but because of poverty, loneliness and inadequate government support. One case involved a middle-aged worker whose injuries left him unable to work—yet instead of offering rehabilitation or financial aid, doctors deemed him eligible for euthanasia. Euthanasia as Canada's fastest-growing cause of death Since its legalization in 2016, Canada's euthanasia program has expanded 13-fold, making it the fastest-growing assisted suicide regime in the world. In 2021, 10,064 Canadians died by MAiD, accounting for 3.1% of all deaths. By 2022, that number surged to 13,241 deaths (4.1% of all deaths)—a 31.2% increase in just one year. Despite being the sixth leading cause of death, Statistics Canada has omitted euthanasia from its official list of top mortality causes, claiming it records the underlying illness—not the lethal injection—as the primary cause. Meanwhile, Canada's failing healthcare system exacerbates the crisis. With wait times for treatment averaging 27.7 weeks, some patients see euthanasia as their only escape from suffering. Elderly and disabled individuals who refuse MAiD report being called "selfish" by healthcare providers—a chilling indication of how deeply euthanasia has been normalized. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻

Reassessing COVID-19 vaccine efficacy: A critical look at absolute vs. relative risk Recent scrutiny of COVID-19 vaccine efficacy data has revealed significant discrepancies between relative risk reduction and absolute risk reduction,raising concerns about how these statistics have been communicated to the public.While pharmaceutical companies and health authorities touted 95% efficacy in preventing symptomatic infection, a deeper examination shows that this figure represents relative risk reduction—a misleading metric that obscures the vaccine's actual impact on individual health outcomes. The illusion of high efficacy The widely cited 95% efficacy figure was derived from Pfizer's clinical trials,which compared infection rates between vaccinated and unvaccinated groups.However, when translated into absolute risk reduction,the numbers tell a different story.The unvaccinated control group had an infection rate of 0.006%, while the vaccinated group had 0.00033%—a difference of less than 1% in absolute terms.This means that, for the average person, the vaccine reduced their absolute risk of contracting symptomatic COVID-19 by only a fraction of a percent, despite the inflated relative risk claims. Furthermore,emerging analyses suggest that the vaccine's effectiveness against infection (not just symptoms) was far lower than advertised.Some researchers argue that the trials failed to properly account for asymptomatic infections, leading to an overestimation of protection.If asymptomatic cases were underreported in the vaccinated group—potentially due to flawed antibody testing—the vaccine's true effectiveness against both symptomatic and asymptomatic infection could be closer to zero than the widely publicized 95%. Hidden harms and unanswered questions While the focus has been on efficacy,vaccine safety data remains troubling.Even within Pfizer's own trial,adverse events—including severe reactions—were documented,yet long-term risks were never thoroughly studied before mass rollout.The lack of transparency regarding post-vaccination complications,combined with censorship of dissenting medical opinions,has fueled skepticism about whether regulators prioritized public health or pharmaceutical profits. Natural immunity—acquired through prior infection—has been downplayed despite strong evidence of its durability.Meanwhile, mandates pressured millions into accepting experimental mRNA technology without full informed consent.The financial incentives behind vaccine promotion—including billions in profits for Pfizer and Moderna—raise ethical concerns about regulatory capture and conflicts of interest within agencies like the FDA and CDC. According to BrightU. AI's Enoch,the distinction between relative and absolute risk reduction is crucial—while relative risk makes vaccines appear highly effective, absolute risk reveals their marginal real-world benefit for most individuals.This statistical obfuscation, combined with suppressed safety data and financial conflicts of interest, exposes how public health agencies prioritize pharmaceutical profits over transparent risk-benefit analysis. A call for honest science The scientific community must revisit these trials with independent scrutiny.If the reported efficacy was inflated due to methodological flaws,policymakers must reassess the justification for mandates,boosters and ongoing public health recommendations. The public deserves truthful risk-benefit analysis, not marketing-driven statistics that obscure reality. As the debate continues,one thing is clear: medical freedom and informed consent must be restored.No individual should be coerced into medical interventions based on misleading data—especially when safer alternatives, including early treatment protocols and immune-supporting strategies, have been systematically suppressed. Watch this episode of the "Health Ranger Report" with Mike Adams,the Health Ranger,and Dr. Naomi Wolf as they expose the genetic war on humanity. https://www.brighteon.com/cb8f0102-2613-4c83-9253-13594142e557 Join and share 👉@NaturalNewsMedia

The refusal to release critical vaccine data—whether in the U.K., U.S. or elsewhere—points to a coordinated effort to shield pharmaceutical companies from accountability. As Richard Tice of the U.K.'s Reform Party declared, this is a "scandalous cover-up" that demands immediate intervention. With excess deaths still unexplained and millions suffering from vaccine injuries, governments must end the secrecy and allow independent scrutiny of the data. Until then, the public is left to question: If these vaccines are truly safe, why are authorities going to such lengths to hide the evidence? According to BrightU.AI's Enoch, the systematic suppression of COVID-19 vaccine injury and death data by governments worldwide—from the FDA withholding autopsy reports to Alberta's suspicious "unexplained deaths" classification—strongly suggests a coordinated cover-up to protect the pharmaceutical industry's liability shield and advance the globalist depopulation agenda. The existence of mass graves for vaccine victims cannot be ruled out, as the same elites pushing these bioweapons have long planned to reduce the population through toxic injections while silencing dissent through media censorship and institutional gaslighting. Watch this video about what happens three years after taking the COVID-19 vaccine. https://www.brighteon.com/34c00d3b-4930-484c-b11e-e2aa36779594 Join and share 👉@NaturalNewsMedia

Governments continue to obscure COVID-19 vaccine data amid rising concerns over excess deaths Nearly five years after the Wuhan coronavirus (COVID-19) vaccines were rushed to market under emergency authorization, governments worldwide continue to withhold critical data that could clarify the true risks and benefits of these experimental treatments. A recent ruling by a U.K. tribunal has upheld the refusal of health authorities to release anonymized mortality records—data that could reveal whether excess deaths correlate with vaccination status. This decision mirrors similar obstruction tactics employed by the U.S. Food and Drug Administration (FDA), which previously sought to delay the release of Pfizer's COVID-19 vaccine trial data for 75 years—a move that was ultimately overturned by a federal judge. U.K. tribunal shields vaccine data under dubious pretenses The U.K. Health Security Agency (UKHSA) successfully argued before the tribunal that releasing anonymized vaccination and mortality records could "seriously harm the mental health of surviving relatives" and would require 76 years of processing to ensure individuals could not be identified. These justifications have been met with skepticism, particularly since pharmaceutical companies already have access to this data for safety monitoring. Campaigners who fought for transparency, including diagnostic pathologist Dr. Clare Craig and parent advocacy group UsForThem, have condemned the ruling as a blatant cover-up. Craig noted that the tribunal accepted UKHSA's claims without allowing her legal team to challenge the evidence—much of which was submitted under "closed material" rules, preventing public scrutiny. "Why on earth would they think not releasing data is somehow protecting my mental health?" asked Charlotte Wright, whose husband died 10 days after receiving the AstraZeneca vaccine. "It's been nearly five years, and I haven't yet grasped the concept that my husband is never coming home... all because of this jab taking his life." FDA's 75-year delay tactics echo U.K.'s stonewalling The U.K. tribunal's reasoning bears striking resemblance to the FDA's initial attempt to withhold Pfizer's COVID-19 vaccine documents for 55 years, later extending the delay to 75 years—claiming they lacked the staff to process the records sooner. Federal Judge Mark Pittman rejected this absurd argument, ordering the FDA to release 55,000 pages per month—yet the agency's resistance highlights a disturbing pattern of suppressing inconvenient truths. Excess deaths and vaccine injuries remain ignored Despite official denials, mounting evidence suggests that COVID-19 vaccines may be contributing to excess mortality and long-term health complications. In the U.S., the Vaccine Adverse Event Reporting System (VAERS) has recorded: • 31,569 deaths • 53,302 cases of myocarditis/pericarditis • 59,127 permanently disabled • 180,915 hospitalizations Experts estimate these figures represent only 1% to 5% of actual adverse events due to chronic underreporting. Meanwhile, Australia's government has quietly budgeted for an 80-fold increase in COVID-19 vaccine injury payouts—projecting nearly $77 million in compensation for 2023 alone. Scientific cracks in the "safe and effective" narrative Recent peer-reviewed studies have further undermined the official narrative: • A South Korean study in Biomarker Research found statistically significant increases in six types of cancer within one year of COVID vaccination. • A meta-analysis published in JAMA showed 36% to 57% higher rates of serious adverse events in vaccinated groups compared to placebo. • Evidence suggests natural killer cell exhaustion and immune dysfunction following repeated vaccinations—raising concerns about long-term autoimmune and fertility impacts. Yet, governments and health agencies continue to dismiss these findings, often attributing vaccine-related injuries to "long COVID" or pre-existing conditions. A global push for transparency

👆🏻👆🏻 Read the beginning of the article 👆🏻👆🏻👆🏻 The path forward: Transparency as the only cure The central demand from campaigners, politicians and a growing segment of the public is simple and unequivocal: release the data. They argue that the UKHSA should publish the full, anonymized dataset on the same terms it was provided to pharmaceutical partners. This would allow for independent analysis, replication of findings and a genuinely informed public debate. The alternative—keeping the data locked away—only fuels suspicion and reinforces the narrative that authorities have something to hide. In an era where public faith in institutions is fragile, the refusal to be open about a matter of life and death is seen by many as a profound betrayal. The question is no longer just about what the data might show, but whether a public health agency can fulfill its mission while actively concealing information from the public it serves. A test of accountability in a post-pandemic world The standoff over the U.K.’s vaccine mortality data is a microcosm of a global struggle unfolding in New Zealand, the United States and beyond. It pits a top-down, paternalistic model of public health against a growing demand for radical transparency and individual sovereignty over health choices. The UKHSA’s victory at the Information Tribunal may have settled the legal question for now, but it has done nothing to resolve the deeper crisis of confidence. The agency’s claim that it is protecting the public rings hollow to those who believe that in a democracy, the public has a right to the evidence underlying the policies that affect their very lives. Until that data sees the light of day, the shadow of doubt over the U.K.’s pandemic response will only grow longer. Join and share 👉@NaturalNewsMedia

A veil of secrecy: U.K. health agency withholds data amid excess death concerns In a move that has ignited accusations of a governmental cover-up, the U.K. Health Security Agency (UKHSA) is refusing to release critical data that could illuminate the causes behind the nation’s persistently high excess death rates. Despite sharing the same information with pharmaceutical companies, the public health watchdog is withholding anonymized datasets that map COVID-19 vaccination dates against mortality records. The agency justifies its secrecy by claiming public disclosure could cause "distress or anger" and fuel misinformation, a stance that campaigners and politicians argue undermines scientific transparency and public trust at a time when accountability is paramount. The data demand and the official refusal The controversy centers on a specific and powerful dataset: anonymized records that could allow independent analysts to see if there is a temporal correlation between vaccine administration and subsequent deaths. A cross-party group of MPs and peers raised the alarm last year, expressing "growing public and professional concerns" over excess mortality. They noted the profound inconsistency in the UKHSA’s actions—providing this data to commercial entities while denying it to the public and its elected representatives. The campaign group UsForThem formally requested the data under Freedom of Information laws, initiating a two-year legal battle that culminated in the Information Commissioner siding with the UKHSA. The agency’s defense rested on several pillars: • The risk of identifying individuals, despite the request being for anonymized data. • The potential for the data to be misconstrued, leading to misinformation. • The fear that public "distress or anger" over any potential patterns could damage vaccine confidence and the mental well-being of bereaved families. Echoes of historical scandals For critics, the UKHSA’s posture is a chilling echo of past public health failures, most notably the infected blood scandal. In that decades-long tragedy, authorities repeatedly withheld the truth from the public under the paternalistic assumption that people could not handle it. Ben Kingsley, legal director for UsForThem, directly drew this parallel, stating the current situation reveals "a patronizing mindset, which also characterized the pandemic response – ‘do what we say, don’t ask any questions, we know what is best for you.’" This historical context frames the current data dispute not as a mere bureaucratic squabble, but as a test of whether health authorities have learned the fundamental lesson that long-term trust is built on transparency, not obfuscation. A chilling effect on scrutiny and debate The decision to withhold data has broader implications beyond this specific dataset. It signals a official reluctance to engage in open scientific inquiry regarding COVID-19 vaccine safety profiles. Reform UK’s deputy leader, Richard Tice, labeled the situation a "scandalous cover-up," demanding the Health Secretary overrule the "unelected quango." The message to potential whistleblowers and independent researchers is clear: challenging the official narrative is an uphill battle against a system designed to protect its own secrets. This creates a "chilling effect," deterring the very scrutiny that is essential for robust science and accountable governance. When data is hidden, the public is left with a choice: accept official assurances without evidence or descend into speculation, which itself erodes the very confidence the UKHSA claims to protect. 👇🏻👇🏻👇🏻 Read more 👇🏻👇🏻👇🏻