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"Pharmacogenomics could save lives, but it exposes the fraud of one-size-fits-all vaccines," says Hulscher. Until then, parents are left to navigate a system that sacrifices children for profit.
The real solution is a complete restructuring of the CDC's childhood vaccine schedule, removing any recommendations for vaccines for babies under one year of age, and making it illegal for pediatricians, pharmacists, and family doctors to administer any of these high risk products in vulnerable, developing children.
The study’s authors urge immediate action:
• Ban toxic excipients like aluminum, polysorbate 80, and formaldehyde in vaccines.
• Halt preterm vaccinations until metabolic maturity is confirmed.
• Mandate autopsies for all SIDS cases, including brain stem analysis.
"Every ‘SIDS’ death should be treated as a potential vaccine homicide," says Jablonowski. "Parents deserve the truth—not another whitewashed lie."
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The tetanus “vaccine gap” – History repeats when science is silenced
From horse manure-choked streets to today’s billion-dollar vaccine markets, tetanus’s history mirrors a broader struggle over public health priorities. “We’re repeating 19th-century mistakes: blaming individuals instead of systemic factors like sanitation,” says Piper-Terry. As IV vitamin C trials languish and fertility-harming additives resurface, the urgent question remains: Who profits from fear, and who pays the cost?
For the modern parent or expecting mother, the choices are clear — but the answers, it seems, have been buried beneath layers of profit and silence.
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Nationally, COVID trends show a slight decline, with test positivity dropping from 2.9% to 2.7% in late May and emergency visits decreasing by 6.5%. However, in China, severe respiratory cases linked to COVID have nearly doubled, and Taiwan has reported a 78% weekly spike in ER admissions.
Symptoms of NB.1.8.1 mirror those of other variants, including fever, cough, fatigue, and loss of taste or smell. Standard COVID tests cannot distinguish between variants.
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DANGEROUS: New “Palantir Federal Advisory Board” of Pharma shills to oversee new PLANDEMICS AND SCAMDEMICS for USA fearmongering campaigns
There’s a new advisory board all prepped for a new plandemic that’s already begun in China again, most likely originating from some China folk eating infected bat soup and then taking a cruise ship to California. Yes, Palantir Technologies, Inc. has unveiled their new conglomeration of Pharma shills as leaders of the new scamdemic, ready to recommend lockdowns, face diapers, social distancing at 12 – 18 feet, and more deadly mRNA stabs to “flatten the curve,” which really means exterminate a couple billion people.
Palantir Technologies Inc., a leading data analytics firm known for its work with U.S. defense and intelligence agencies, has expanded its Federal Advisory Board (PFAB) with a roster of distinguished national security leaders. The move, announced on Oct. 19, 2022, underscores Palantir’s 'deepening commitment to addressing evolving threats through advanced technology'. The board includes former Pentagon officials, military commanders, and homeland security experts, positioning Palantir to better serve government clients amid rising geopolitical tensions.
The newly appointed PFAB members bring decades of Pharma shilling crisis response experience with them for the new scamdemic
• Christine H. Fox, former Acting Deputy Secretary of Defense
• Gen. Carter F. Ham (Ret.), ex-commander of U.S. Africa Command
• Deborah Lee James, former Secretary of the Air Force
• Adm. William H. McRaven (Ret.), former head of U.S. Special Operations Command
• Vice Adm. Peter V. Neffenger (Ret.), former TSA Administrator
Jeh Johnson, former Secretary of Homeland Security and current Palantir counselor, will also participate in PFAB meetings. Their collective expertise spans counterterrorism, cybersecurity, and large-scale logistics—critical areas where Palantir’s software is increasingly deployed.
Palantir, founded in 2003, has long been a key player in government data analysis, aiding missions from counterterrorism to pandemic response. The advisory board’s creation signals a strategic push to align private-sector innovation with national security priorities. As Alexander Karp, Palantir’s CEO, noted, “We invited these leaders … because of the exceptional contributions they have made to this country in their years of public service.”
The timing is significant. With global instability—from Russia’s war in Ukraine to supply chain disruptions—U.S. agencies face unprecedented demands for real-time data solutions. Admiral McRaven emphasized Palantir’s role, stating, “Having superior technology was instrumental in achieving success on the battlefield.”
The board’s input will shape Palantir’s offerings for federal clients, ensuring its platforms meet urgent operational needs. Aki Jain, President of Palantir USG, highlighted the group’s “230 years of first-hand experience” in tackling complex threats.
Deborah Lee James, reflecting on her tenure in the Air Force, added, “Leveraging our best engineers is vital for America’s defense.” Her remarks underscore a growing consensus: public-private partnerships are essential to maintaining U.S. technological superiority.
As Palantir integrates these “high-caliber” Pharma shills, the company solidifies its role as a bridge between Silicon Valley and Washington. In an era where data is as decisive as firepower, this collaboration could redefine how America confronts 21st-century challenges—from cyber warfare to global health crises. For now, all eyes are on how this elite board will steer Palantir’s next moves.
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Five years of restrictions and mass vaccinations have led to more disease
The NB.1.8.1 variant, now dominant in China, has already been detected in travelers abroad. Yet the World Health Organization (WHO), ever-compliant to Beijing, downplays the threat, calling it merely a "variant under monitoring."
Why the cover-up? Because admitting failure would shatter the CCP’s myth of infallibility. Instead, the regime quietly prepares for more lockdowns, building mobile hospitals while publicly insisting the outbreak is "under control."
Sadly, China's totalitarian lockdowns, unlawful mandates, and isolation procedures have become the standard globally. While other nations have slowly halted draconian policies, none are willing to hold China accountable for their continued human rights abuses. No nation has challenged China’s pandemic lies or its brutal lockdowns. No leader has demanded transparency or pointed out the flaws of global medical experimentation. Instead, global elites continue to parrot the same failed strategies — vaccine mandates, censorship, and bio-terror — proving they’ve learned nothing. To make matters worse, populations that once complied but have realized the damage of China's policies, have grown eerily quiet on these issues.
China’s COVID nightmare is a warning: Totalitarianism and medical tyranny doesn’t work. It only brings suffering. And until the world wakes up and actually does something about this pattern of abuse, the cycle will only continue.
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A legacy of harm and deception
The consequences of this betrayal are staggering. Myocarditis cases surged among young men, yet CDC officials buried the data. VAERS reports revealed thousands of deaths post-vaccination, yet agencies dismissed them as "pre-existing conditions." Even now, the FDA and CDC continue to obstruct FOIA requests, delaying accountability while pushing new mRNA-based vaccines for flu, RSV, and even food-borne applications.
"The lack of tools was not what endangered, injured, and killed Americans," Jablonowski said. "The lack of integrity did."
But this goes beyond a "lack of integrity."
Just a couple years ago, the FDA and CDC were weaponized to conceal the facts about mRNA vaccines, obviously to carry out some kind of domestic terror and mass murder operation that corresponds with a greater depopulation agenda around the world. The mRNA vaccines and the "pandemic" that was propagated into existence, pave the way for multiple new investments in vaccines, for investors and financial systems to reap profit from.
The mRNA COVID jabs were a Trojan horse to introduce vaccine passports and a medical police state, but even more importantly - to introduce a pipeline for hundreds of new vaccines and medical exploitation. These new vaccines are being delivered through the food, through the air, subcutaneously through patches and fine needles, and even through mass aerosol programs.
The mRNA medical fraud paves the way for the CDC and FDA to pose as false authorities, false fronts of authority and safety regulation for a behemoth of a vaccine industry that seeks to control and depopulate. Furthermore, this axis of evil seeks to access people as data sources, probing their physiology for surveillance, programming, and genetic control using vaccine and testing programs as the conduit. New pandemics are being planned and created, and pathogens are being manipulated and deployed for ultimate control over the human race, with vaccine and testing programs securing global, technological power over the gullible masses.
This axis of evil - CDC, FDA, and the vaccine industry must be confronted. There is no time to coddle, appease, and reform these government agencies. They must be dismantled and/or replaced - their inner nucleus prosecuted.
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CDC wants plane travel LOCKDOWN for all humans who haven’t received the toxic MEASLES PLANDEMIC VACCINE, even though vaccines don’t work
Look, up in the sky, it’s a bird, it’s a plane, no, it’s the measles flying around the world infecting anyone who travels anywhere by plane, supposedly. Yes, the CDC is at it once again, led by the Vaccine Industrial Complex, telling all Americans that measles is the biggest threat to your survival and if you don’t go get the toxic measles jab today, you will most likely die tomorrow from this rather benign infection that even the Brady Bunch show used to make light of getting.
Cancel all flights immediately! – Screams Big Media Fake News and the Centers for Disease Continuance. Would they do the same for chicken pox? Watch this clip of the Brady Bunch family all laughing about Peter catching the measles.
https://www.youtube.com/watch?v=5289k-dbOMY
CDC warns of measles spread on flights while urging everyone to get stabbed with a deadly concoction of neurotoxins and live viruses to help spread it
Health officials are fear-mongering again after confirming measles — one of the world’s most contagious diseases — is spreading on U.S. airplanes. Yes, measles has found the airplanes again and are living on those filthy tray tables the flight crews never clean.
The Centers for Disease Control and Prevention (CDC) upgraded its travel advisory Wednesday, urging unvaccinated Americans to postpone flights following multiple cases linked to air travel. Now remember, they did the same thing with the Covid campaign, even though all the vaccinated sheeple were the ones spreading the virus.
The CDC confirmed at least one instance of in-flight transmission after investigating 50 recent cases involving contagious passengers. A spokesperson told CBS News that 62 measles-infected travelers have been reported this year, with exposures occurring in airports, on planes, and at crowded events. On Friday, three passengers arriving at Denver International Airport on a Turkish Airlines flight tested positive — including one vaccinated adult. Run for your life!
"Travelers can catch measles in many travel settings, including airports, airplanes, and large events," the CDC stated in its latest advisory. The agency now recommends full measles vaccination before international travel and urges domestic travelers to Texas — where over 700 cases have been reported — to seek booster doses. Line up sheeple. Get your Covid jabs, your Swine flu shots, your Zika stabs, your Measles booster, and your fake flu shot all at once.
As measles continues to spread in travel hubs, health officials emphasize vaccination as the most effective safeguard, even though there’s absolutely ZERO science to back up this claim. The CDC’s updated guidance reflects growing concerns over gaps in immunity (from vaccinated people who are immunocompromised now) and the ease with which airborne diseases can move across borders. With cases rising, the agency’s message is clear: Get stabbed with known neurotoxins or feel the wrath of fake news daily.
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Mainstream AI hubs trained to SUPPORT VACCINATION, so was the entire pro-vaccine MAHA report written by pro-jab artificial intelligence?
Chat GPT and Microsoft Copilot are about as lame as Google when it comes to getting quality information spit out the other end. Most likely, some Deep State bureaucrats and Vaccine Industrial Complex shills used one of those AI platforms to write the allopathic MAHA report, that was rife with false research, fake sources, and fictional work cited. Why?
The VIC is too big, too powerful, and too entrenched in their depopulation agenda. Vaccines are the number one genocide tool and always have been, especially since the fake Polio jab was invented, and now that the mRNA clot shots are leading the charge with myocarditis, pericarditis, vascular clots, spontaneous abortions, SIDS, SADS (Sudden Adult Death Syndrome) and “all-cause mortality.”
1. AI-Generated Report Allegations: Experts claim the MAHA Commission Report was written using AI, citing "oaicite" markers (tags linking to OpenAI tools) in footnotes as evidence.
2.False Citations: The report includes references to non-existent authors and sources, raising concerns about its credibility.
3. Calls to Scrap the Report: Critics, including public health leaders like Georges C. Benjamin, argue the report is unreliable and should be discarded for policymaking due to its AI-generated inaccuracies.
4. AI "Hallucinations" Issue: The controversy highlights broader problems with AI-generated false content, prompting demands for stricter AI regulation.
5. White House Edits: The report has been updated multiple times to remove false references since its release.
The MAHA Report faces scrutiny over AI-generated content and fabricated sources, undermining its validity and sparking debates about AI's role in official documents
Trump is finding out that even with a mostly legitimate cabinet (non-Deep-State), he still can’t get much done, thanks to rogue Leftist judges, Deep State actors entrenched in the 3-letter agencies, and the powers that be that will always rule Big Pharma, Biotech, Big Food and the Vaccine Industrial Complex, most of all.
Too many sheeple believe whole-heartedly in getting jabbed up with known neurotoxins to quell their fear of infectious diseases, which has been catapulted by the fake news media and hucksters like Fauci and Bill Gates.
A controversial public health report commissioned by U.S. health authorities is under fire after experts alleged it was generated using artificial intelligence, raising concerns about fabricated citations and unreliable data. The MAHA Commission Report, intended to guide vaccine policy, has been criticized for including references to non-existent authors and sources, with critics pointing to footnote tags linked to OpenAI tools as evidence of AI involvement.
The report’s credibility has been further undermined by multiple revisions from the White House, which removed false references after its initial release. Public health leaders, including Georges C. Benjamin of the American Public Health Association, have called for the document to be scrapped, arguing that AI-generated inaccuracies render it unfit for policymaking.
This incident highlights a growing issue with AI "hallucinations" — instances where chatbots invent false information — prompting demands for stricter oversight of AI-generated content in official documents. Critics warn that reliance on unverified AI tools risks embedding misinformation in government reports, particularly in sensitive areas like public health.
The controversy echoes past debates over institutional trust, particularly following high-profile cases of flawed research influencing policy, such as the retracted Lancet study linking vaccines to autism. Skepticism toward pharmaceutical influence has also intensified since the COVID-19 pandemic, with critics alleging conflicts of interest among regulators and industry stakeholders.
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CDC STILL highly recommends deadly COVID JABS for “moderately immunocompromised” children who are MORE LIKELY to die from mRNA prions
So far, it’s not looking like Robert F. Kennedy, Jr. will be able to change the insidious methods and madness of the Vaccine Industrial Complex much at all. The MAHA movement may be able to get Big Food to filter a few choice chemicals from children’s cereals and cough syrup, but the toxic jab industry is just shifting and maneuvering around any efforts at curbing the genocidal mRNA plandemic. So, the vaccine violence continues exactly as the plandemic playbook plays out.
CDC shapeshifts Covid jab policy for kids to "Parent-Provider" co-decision making, meaning the physicians have been instructed to coerce and brainwash parents into getting the deadly jabs
In a significant policy shift, the Centers for Disease Control and Prevention (CDC) updated its childhood immunization schedule late Thursday, October 20, 2022, altering its COVID-19 vaccine recommendations for children. Instead of universally urging all and older and older and older to get vaccinated, the agency now advises "shared clinical decision-making" between parents and healthcare providers for children who are not moderately immunocompromised. The change follows criticism over the lack of transparency in the CDC’s initial unanimous endorsement of COVID-19 shots for kids and raises questions about the evidence behind such recommendations.
The CDC’s revised guidance means parents and pediatricians must weigh individual health risks before administering COVID-19 vaccines to children ages six months to 17 years. Attorney Rick Jaffe noted, “For the first time since the pandemic began, it’s no longer classified as a routine vaccine for children.” While some advocates celebrated the shift as a step toward medical autonomy, others criticized the CDC for not removing the shots entirely from the schedule.
Dr. Kat Lindley, a vocal opponent of mandating COVID-19 vaccines for children, called the change “a win” but added, “Do I like the recommendation? No, because in my opinion, no children should get the shot… But at least there is no longer an outright recommendation for it.”
Despite the policy adjustment, COVID-19 vaccines will remain covered by most health insurance plans and the federal Vaccines for Children Program, which provides free immunizations for low-income families. However, Jaffe suggested pediatricians may no longer face pressure to stock or administer the shots, though enforcement remains uncertain.
The CDC’s decision drew mixed reactions. Medical associations condemned the shift as out of step with public health norms, while vaccine skeptics argued the shots should be removed entirely. Substack writer Sasha Latypova highlighted the CDC’s broader stance on parental authority, stating, “According to the CDC, you DO NOT have any decision-making authority with regard to what they want to inject in your children for ~70 ‘routine’ injections.”
Meanwhile, confusion persists over the CDC’s pregnancy recommendations. Despite U.S. Health and Human Services Secretary Xavier Becerra’s announcement that COVID-19 vaccines would no longer be advised for healthy pregnant women, the CDC’s website still states the shots are “safe and effective” during pregnancy.
The CDC’s move follows months of internal debate. In April 2022, an advisory panel poll showed 76% of members supported shifting from a universal to a risk-based recommendation, but no formal vote occurred until October. Critics argue the agency has yet to clarify the scientific basis for its initial unanimous endorsement of childhood COVID-19 vaccines, particularly amid emerging concerns over efficacy and safety data.
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Lipid nanoparticles: The hidden danger in COVID vaccines fueling hyper-inflammation and faulty immune responses
The COVID vaccine rollout was sold as a miracle of modern science—a life-saving intervention backed by "safe and effective" technology. But beneath the glossy PR campaign lies a darker truth: lipid nanoparticles (LNPs), the delivery system for mRNA vaccines, may be triggering catastrophic immune responses, systemic toxicity, and long-term damage. Vaccine manufacturers like Pfizer and Moderna refuse to disclose critical safety data, leaving billions of people as unwitting test subjects in a global experiment. As adverse reactions mount, one question demands an answer: Were these LNPs ever truly safe, or are they a ticking time bomb for chronic illness?
Key points:
• Lipid nanoparticles (LNPs) act as adjuvants, provoking hyper-inflammatory immune responses that can lead to severe reactions and even death.
• Moderna’s own trials revealed 100% of high-dose participants experienced adverse effects, yet regulators approved the shots without full transparency.
• LNPs contain polyethylene glycol (PEG) and cationic lipids—known toxins—yet manufacturers refuse to release safety data sheets or quantify LNP doses per vial.
• Oxidized lipids in LNPs disrupt cellular function, potentially triggering neurodegenerative and autoimmune disorders.
• Vaccine makers admit they don’t know how many LNPs are injected per dose, calling the question "irrelevant" despite mounting evidence of harm.
The silent assault on immune function
Lipid nanoparticles were marketed as a breakthrough—tiny fat bubbles protecting fragile mRNA strands until they could hijack human cells. But these LNPs are far from inert. They act like biological grenades, revving up the immune system through pathways like NF-?B, a master regulator of inflammation. A study by the World Council for Health found that even empty LNPs—without mRNA—triggered inflammatory responses comparable to known immune activators like LPS, a toxin found in bacterial infections.
Dr. Maria Gutschi, a researcher who filed FOIA requests for LNP data, was met with silence. Moderna dismissed her inquiry, claiming the number of LNPs per dose was "irrelevant." The UK’s MHRA never responded. This lack of transparency raises alarming questions: If these particles are harmless, why the secrecy?
Toxicity hiding in plain sight
The LNPs in Pfizer and Moderna’s vaccines contain SM-102 and ALC-0315—cationic lipids notorious for their toxicity. Oxidation studies reveal these lipids degrade into reactive aldehydes, which can crosslink cell membranes, disrupt calcium channels, and impair glucose metabolism. In simpler terms: They poison cells from the inside out.
Worse, oxidized lipids bind to inflammatory receptors (TLRs, PPARs), turning the body’s defense system against itself. This could explain the surge in autoimmune conditions post-vaccination, from lupus-like syndromes to sudden-onset diabetes. As one researcher noted, "Billions of people have been injected with a poorly characterized chemical delivery system—and now we’re just starting to see the fallout."
A legacy of long-term damage
LNPs don’t just vanish after injection. Traces of synthetic lipids linger in the bloodstream for days, potentially accumulating in organs like the liver, spleen, and brain. Animal studies show LNPs breaching the blood-brain barrier, raising the specter of neurodegenerative diseases like Alzheimer’s or Parkinson’s.
A new study has found that lipid nanoparticles (LNPs) used in Pfizer-BioNTech’s BNT162b2 mRNA COVID-19 vaccine stimulate critical pathways in immune cells, potentially aiding the vaccine’s perceived effectiveness. Researchers discovered that the LNPs not only deliver mRNA but also directly activate NF-kB signaling in innate immune cells like monocytes, a mechanism similar to certain pathogen-recognition receptors. This immune response is merely a reaction to a foreign substance, and does not establish learned immunity to the correct, targeted pathogen.
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The poll’s findings paint a clear picture. Americans, regardless of political affiliation, are fed up with opaque health policies, corporate favoritism and lax oversight. The Make America Healthy Again movement, once a fringe idea, has surged into the mainstream – uniting voters around transparency, accountability and individual choice.
Watch this Fox News report about President Donald Trump ordering the establishment of the MAHA Commission following the swearing-in of Robert F. Kennedy Jr. as health secretary.
https://www.brighteon.com/8e1629bd-67eb-4d0d-a34d-ee461e86781a
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CDC drops COVID-19 vaccine recommendation for healthy kids and pregnant women
In a significant reversal of federal health guidance, the Centers for Disease Control and Prevention (CDC) has removed the Wuhan coronavirus (COVID-19) vaccine from its recommended immunization schedule for healthy children and pregnant women.
Health Secretary Robert F. Kennedy Jr. announced the reversal Tuesday, May 27, in a video posted on X. He delivered the news while flanked by National Institutes of Health Director Dr. Jay Bhattacharya and Food and Drug Administration (FDA) Commissioner Dr. Marty Makary.
"Today, the COVID-19 vaccine for healthy children and healthy pregnant women has been removed from the CDC recommended immunization schedule," Kennedy said. He mentioned that the Biden administration urged healthy children to get injected with the COVID-19 vaccine "despite the lack of any clinical data to support the repeat booster strategy in children."
The health secretary's announcement marks a departure from the previous Democratic administration's aggressive promotion of widespread vaccination, including for low-risk groups. It also follows mounting scrutiny over vaccine safety, particularly concerning myocarditis in young males, and aligns with policies already adopted by several other nations.
Bhattacharya echoed the sentiment, calling the shift "common sense and good science." Meanwhile, Makary noted that most countries no longer recommend the vaccine for children due to insufficient evidence of benefit.
Move to drop COVID-19 injections for kids lines up with MAHA promise
The CDC under the Biden administration had previously urged repeated boosters for all age groups, initially claiming the shots prevented infection before revising guidance to acknowledge they only reduced symptoms.
Critics argue that mandating vaccines for healthy children – who face minimal risk of severe COVID-19 outcomes – was never justified. Data showing serious cases of myocarditis in adolescent males further fueled skepticism. The FDA has since pressured Pfizer and Moderna to expand warnings about potential heart inflammation, particularly for males aged 16 to 25.
Public health recommendations have evolved as new data emerges – from the retraction of thalidomide for pregnant women in the 1960s to hormone replacement therapy decades later. This latest shift underscores the importance of adapting policies to emerging evidence rather than rigid adherence to initial mandates.
Vianca N. Rodriguez Feliciano, press secretary for the Department of Health and Human Services (HHS), affirmed the commitments of the CDC and its parent agency to "gold standard science." She continued: "With the COVID-19 pandemic behind us, it is time to move forward."
The decision signals a broader reckoning with pandemic-era policies, balancing public trust with scientific transparency. For now, the CDC's updated guidance offers a clearer path for parents and physicians navigating a post-pandemic world. Kennedy concluded his Tuesday announcement by reiterating that the removal of the COVID-19 injection from the immunization schedule brings the HHS "closer to realizing President [Donald] Trump's promise to Make America Healthy Again."
Watch Jefferey Jaxen and Del Bigtree revealing that the CDC refused to publish data on the effectiveness of COVID-19 boosters in this clip.
https://www.brighteon.com/3619df15-1066-49c3-98d5-e8a9b5b871ff
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HHS axes $700M Moderna bird flu vaccine contract — is this a pivot to more dangerous, self-replicating mRNA jabs?
In a stunning reversal, the U.S. government has abruptly terminated a $700 million contract with Moderna to develop an mRNA-based bird flu vaccine — raising urgent questions about whether this signals an end to pandemic fearmongering or merely a shift toward even riskier genetic injection technologies. While the cancellation offers a temporary reprieve from Moderna’s predatory vaccine schemes, skeptics warn that the vaccine industry may still be pushing forward with experimental "self-amplifying mRNA" (sa-mRNA) shots, a technology that forces the body to mass-produce viral proteins indefinitely.
Key points:
• The U.S. government has canceled Moderna’s $700 million bird flu vaccine contract, halting late-stage development of its H5N1 mRNA injection.
• Despite the cancellation, federal agencies are still funding next-generation "universal flu vaccines," including self-replicating sa-mRNA platforms.
• Moderna’s CEO insists the company will pursue "alternative paths" for its bird flu jab, despite mounting evidence of mRNA vaccine injuries.
• The Biden autopen regime previously awarded Moderna $176 million for avian influenza vaccine development, raising concerns about ongoing pandemic profiteering.
• Health Freedom warriors warn that government-funded gain-of-function research on bird flu viruses is creating the very pandemics used to justify mass vaccination campaigns.
Moderna’s failed COVID empire and the push for bird flu jabs
Moderna’s financial survival has long depended on taxpayer-funded vaccine contracts, particularly after its COVID-19 shots — linked to heart damage, immune disorders and excess deaths — failed to secure long-term market demand. With plummeting stock prices and dwindling public trust, the company has aggressively lobbied governments to bankroll new pandemic threats, including avian influenza.
The now-canceled H5N1 contract was part of a broader push by the Biomedical Advanced Research and Development Authority (BARDA), an HHS agency notorious for funneling billions into Big Pharma’s experimental projects. Moderna had already received $176 million in 2023 to fast-track its mRNA bird flu shot, despite zero long-term safety data.
“These clinical data in pandemic influenza underscore the critical role mRNA technology has played as a countermeasure to emerging health threats,” Moderna CEO Stéphane Bancel claimed in a press release — a statement that ignores the thousands of injuries reported from COVID-19 mRNA shots.
The rise of self-replicating mRNA: A more dangerous alternative?
While the cancellation appears to be a setback for Moderna, the government has not abandoned its pandemic preparedness agenda. Instead, federal agencies are quietly shifting toward even more experimental platforms, including self-amplifying mRNA (sa-mRNA) vaccines. Unlike traditional mRNA shots, which degrade quickly, sa-mRNA injections hijack the body’s cells to continuously produce viral proteins — a process with unknown long-term consequences.
In November 2023, FDA approved its sa-mRNA bird flu vaccine, ARCT-2304, signaling a dangerous new frontier in genetic experimentation. Meanwhile, the U.S. Government Accountability Office (GAO) confirmed plans for a "universal flu vaccine" trial in 2026, raising fears that synthetic, multi-strain injections could trigger catastrophic immune responses.
Gain-of-function: Manufacturing pandemics to sell the "cure"
The abrupt cancellation of Moderna’s contract does little to address the root of the problem: government-funded gain-of-function research that artificially engineers pandemic threats. Since early 2024, the USDA has been conducting high-risk experiments on H5N1 viruses — potentially enhancing their transmissibility — while simultaneously developing mRNA "solutions" for the very pathogens they helped create.
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Biden administration targeted mask and vaccine opponents as “terrorists,” new docs reveal
Newly released documents, obtained by Public and Catherine Herridge Reports via a Freedom of Information Act (FOIA) request, reveal a coordinated effort by the Department of Homeland Security (DHS), the FBI and the National Counterterrorism Center to redefine constitutionally protected speech as extremism.
The December 2021 report listed views against vaccine and mask mandates as “prominent narratives” linked to violence, citing beliefs that the policies were part of a governmental or “global conspiracy.” These narratives could “resonate” with “violent” groups like QAnon adherents, the report claimed. Yet the document acknowledged such beliefs—and even quoting DVE-affiliated individuals—are protected under the First Amendment, unless the speaker is a “threat actor.” That critical term, however, remains undefined.
Former FBI Agent Steve Friend explained the policy’s far-reaching implications: “This created an articulable purpose to begin an FBI assessment against specific individuals.” Meaning: Dissenting voices could face federal scrutiny merely for questioning mandates, with no evidence of violent behavior required.
Catherine Herridge, titular co-founder of Public, noted the report “draws a straight line between mandate opposition and domestic terrorism,” a charge critics argue erodes liberties in the name of safety.
The censorship complex
The implications extended beyond surveillance. According to Friend, the DVE label became a cudgel to pressure Big Tech into censorship.
“You don’t want to propagate domestic terrorism? Take down these posts,” Friend summarized the administration’s leverage. Exchanges between agencies and platforms, revealed in the “Twitter Files,” confirm this collusion. In 2023, the House investigated FBI collusion with Twitter to suppress pandemic-critical content.
Dr. Mary Holland, CEO of Children’s Health Defense, branded the policy Orwellian. “The goal was never public health—it was obedience,” she said. “Labeling dissenters as terrorists monopolizes the narrative. You’re not allowed to question central authority.”
The February 2022 DOJ report added urgency, warning school vaccination mandates could “spur conspiracy theories” and “increase the potential for violence.” Meanwhile, parents in Maine, Vermont and North Carolina sued school districts after children were vaccinated without consent—a practice the report paradoxically claimed could incite attacks.
A two-tiered system of power
The duality here is stark. While the Biden administration framed mandate critics as dangerous plotters, federal agencies showed leniency toward violent crimes on their own side.
As noted in the House committee report on federal weaponization, school board protests—a staple of parent opposition to vaccine mandates— drew FBI scrutiny as “potential terrorist activity.” But when Capitol rioters overran Congress in January 2021, the Biden DOJ treated most defendants leniently, often dropping charges.
“This was political,” said Public’s Darren Samuelsohn, referencing the report. “The terror label only applied to those challenging Biden’s policies.”
Jeffrey Tucker of the Brownstone Institute called it “a roadmap to weaponize public health.” He noted mandates quickly mutated from pandemic measures into tools to purge dissent: requiring vaccination for medical insurance, jobs and education, thereby “ferreting out dissenters” via humiliation.
Sayer Ji of Stand for Health Freedom described a broader pattern: “Public health became the new religion. Dissent became heresy.” Government reports, he added, created a “sprawling, coordinated machine” with NGOs, tech giants and European allies targeting dissent.
The Orwellian clock is ticking
The implications expand beyond vaccines. If benign disagreement qualifies as “violent extremism,” the line between dissent and “national security threat” blurs entirely.
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China’s low death rates stir skepticism amid rising caseloads
China’s reported seven monthly deaths from the variant, despite widespread transmission, has drawn scrutiny. Dr. Liu questioned the data, noting Canada alone recorded 2,000 deaths during comparable months. “Their stats defy basic epidemiology,” he stated, alleging possible underreporting or unaccounted mortality misclassification.
Hong Kong health authorities acknowledged hospitalization spikes but echoed WHO findings — that NB.1.8.1 does not breach severity thresholds — while reinforcing mask mandates on public transit. “Prevention remains key,” said Dr. Li Tongzeng of Beijing You’an Hospital, expecting China’s peak in cases by late May.
Navigating the pandemic legacy
As NB.1.8.1 blurs the line between pandemic recovery and recurring waves, the U.S. faces a pivotal moment. The CDC’s cautious surveillance, paired with FDA’s restrictive policies, risk a fractured response to variants that disproportionately impact vulnerable populations. With trust in public health institutions already waning globally, clarity and equitable solutions will be critical.
For now, mitigation strategies — masks, updated shots for eligible groups and robust data-sharing — remain the foundation. “We’ve got the tools,” Gounder said. “The challenge is ensuring they reach everyone before the next variant arrives.”
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New research exposes how vaccines trigger SIDS — medical establishment covering up infant deaths with MISDIAGNOSIS
For decades, grieving parents have been told their infants died of "sudden infant death syndrome" (SIDS), a vague diagnosis that conveniently absolves vaccine manufacturers of blame. But groundbreaking research now reveals the chilling truth: Vaccines are killing babies — and the medical establishment has been hiding it. A new study published in the International Journal of Medical Sciences uncovers the biological mechanisms linking vaccines to SIDS, proving that toxic vaccine ingredients overwhelm infants’ underdeveloped detox pathways, leading to fatal inflammation, brainstem damage and respiratory failure.
Key points:
• Infants lack mature liver enzymes (CYP450) needed to process toxic vaccine ingredients like aluminum, formaldehyde, and polysorbate 80.
• Vaccines suppress CYP450 function, creating a deadly cycle where toxins accumulate, inflame the brainstem, and disrupt breathing.
• 75% of SIDS cases in VAERS occur within a week of vaccination, peaking 48 hours post-shot — proof of causation buried by regulators.
• Preterm babies are especially vulnerable, yet hospitals aggressively vaccinate them, ignoring their fragile metabolic limits.
• Autopsies often miss vaccine-induced brain damage, allowing SIDS to be weaponized as a cover-up for vaccine fatalities.
How vaccines silently suffocate babies
The study reveals that infants — especially preemies — are born with immature CYP450 enzymes, which normally detoxify drugs and poisons. But modern medicine bombards newborns with a chemical onslaught their physiology were never prepared to handle or adapt to on an evolutionary basis. "In the absence of modern medicine, the newborn baby consumes only mother’s milk," explains Karl Jablonowski, Ph.D., a senior scientist at Children’s Health Defense. "Now, babies are expected to process the hepatitis B vaccine at birth, followed by eight more toxic shots by two months old."
The consequences are catastrophic:
• Toxin overload: Aluminum adjuvants and formaldehyde can’t be broken down, flooding the bloodstream and crossing the blood-brain barrier.
• Brain stem inflammation: Toxins trigger cytokine storms that damage the medulla, crippling the brain’s ability to regulate breathing and heart rate.
• Serotonin system collapse: Studies show 70% of SIDS cases involve disrupted serotonin pathways, preventing babies from waking during apnea episodes.
• Metabolic sabotage: Vaccines further suppress CYP450 enzymes, trapping infants in a lethal feedback loop where each shot increases toxicity.
The smoking gun: VAERS data exposes the cover-up
Epidemiologist Nicolas Hulscher analyzed 2,605 infant deaths reported to VAERS from 1990–2019 and found a damning pattern: 75% of SIDS cases occurred within 7 days of vaccination, with deaths spiking on day two. "This is not random — it’s a biological signature," Hulscher warns. Yet coroners routinely ignore neuropathology evidence, dismissing vaccine deaths as "unexplained."
In one harrowing legal case (Boatmon v. HHS), autopsy reports proved brainstem abnormalities were missed — a deliberate oversight to protect vaccine programs. Similarly, Dr. Paul Thomas found unvaccinated children in his practice had zero SIDS cases, while the vaccinated rate mirrored national averages.
Instead of pausing the vaccine schedule to investigate, hospitals double down on poisoning preemies. "Cesarean sections deliver babies earlier, and doctors compensate by vaccinating them more aggressively," says Jablonowski. Even worse, pediatricians push Tylenol post-vaccination — a drug that clogs CYP450 pathways, ensuring toxins stay trapped longer.
Genetic testing could identify high-risk infants, but the medical-industrial complex refuses to consider the evidence and be proactive at avoiding vaccine injury and death. It's easier to pretend the issue doesn't exist and just blame parents for their child dying in their sleep.
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Are you due for a tetanus shot? First, learn about the TRUE history, risks and alternatives
The Centers for Disease Control and Prevention (CDC) recommends tetanus boosters every decade, but a growing body of evidence calls into question both the necessity and safety of these inoculations. Recent investigations reveal that tetanus’s historical decline was due largely to improved sanitation, not vaccines, while ingredients like aluminum and cow’s milk proteins raise alarms about severe reactions, including anaphylaxis. Further unsettling revelations — such as the lack of safety studies for pregnant women and claims of population control schemes — paint a troubling picture of financial and ethical overreach. For those weighing vaccination choices, the risks versus benefits demand urgent scrutiny.
The myth of vaccine-driven progress: Tetanus’s decline began long before shots
In 1870s America, tetanus infected farmers and laborers via exposure to horse manure-laden streets. By the 1940s, deaths had already plummeted — not because of vaccines, but due to the rise of automobiles, which reduced manure pollution, and advancements in sewers and clean water systems. According to Marcella Piper-Terry, author of Let’s Talk About Tetanus, “The reduction in tetanus cases had more to do with modernization than needles.”
Vaccines were introduced in the late 1940s, but by then, fatalities were minimal. A review of historical data from the 1970s shows that 40% of children were unvaccinated, yet infection rates remained low. The World Health Organization (WHO) now notes that tetanus boosters for adults are unnecessary, but the CDC continues recommending them every decade — a stance critics argue prioritizes profit over science.
Toxic ingredients, deadly reactions: What’s truly in “preventative” shots
Tetanus vaccines — DTaP (for children), Tdap (adults) and DT (adults) — contain alarming additives. Piper-Terry highlights aluminum (up to 530 micrograms per dose), formaldehyde and polysorbate 80. All formulations are cultured in cow’s milk protein, warns the FDA, a component linked to severe allergic reactions.
VAERS data reveals over 3,200 reported deaths post-tetanus vaccination, though researchers estimate only 1% of adverse events are reported. Piper-Terry recounts her own daughter’s near-fatal anaphylactic shock from Tdap, despite a known milk allergy undetected by her pediatrician. A 2011 study confirmed milk proteins in DTaP vaccines cause anaphylaxis in susceptible individuals — a risk never adequately addressed.
Pregnant women left in the dark: Safety studies driven by dollars, not science
The CDC recommends Tdap during every pregnancy to “protect” infants from pertussis. Yet, Piper-Terry’s analysis of vaccine trials exposes shocking omissions. A pivotal 2020 study excluded 189,768 miscarriages or stillbirths linked to Tdap administration, citing “resource limitations.” With annual sales of $190 million for pregnancy Tdap injections, the conflict of interest becomes stark — the same pharmaceutical firms fund the research.
Dr. Carrie Madej and others connect tetanus vaccines to population control, citing a 2014 UNICEF campaign in Kenya where tetanus shots tested positive for human chorionic gonadotropin (hCG), a chemical linked to miscarriage and infertility. “Why is the U.S. pushing Tdap in pregnancy without proof of safety?” asks Piper-Terry. “The numbers suggest profit trumps people.”
A natural cure in plain sight: Vitamin C as a tetanus treatment alternative
Despite the CDC’s claim that tetanus has “no cure,” a 1996 Bangladesh study found IV vitamin C reduced mortality by 100% in children and 45% in adults. Piper-Terry argues doses were “likely too low” for efficacy in older patients. Though the Cochrane Review deems the study “poorly reported,” it raises questions about mainstream medicine’s dismissal of affordable, non-toxic alternatives.
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WUHAN CAVE VIRUS 2025: Covid face diapers highly recommended by health officials as new NB.1.8.1 variant from China spreads around USA
Some Chinamen must have eaten some infected bat soup again because the Wuhan Cave Virus is creeping around the globe gaining new “function” and supposedly claiming new lives. Quick, get home, lock yourself down for a year or two, mask up inside the house, lather up with antibacterial lotion (even though it’s a virus), and self-vaccinate with some wormwood parasitic cleanse. It’s your only chance at surviving Wuhan Flu 2025.
New Wuhan Cave Virus Variant NB.1.8.1 Detected in California, Sparks Concerns Over New Plandemic Mandates
1. New COVID Variant (NB.1.8.1): Health officials in California and other states are warning about a new variant first detected in China, now accounting for 19% of cases in California. It has also been found in travelers arriving in Washington, Virginia, Hawaii, Rhode Island, and New York.
2. Transmissibility Concerns: Lab tests suggest NB.1.8.1 may be more infectious than currently dominant strains (like LP.8.1, which makes up 73% of U.S. cases). However, it is not yet classified as a CDC-tracked variant.
3. Vaccine Efficacy Claims: Current vaccines (targeting JN.1) are expected to remain effective (at causing myocarditis and strange rubbery clots), though some officials, like Robert F. Kennedy Jr., oppose their inclusion in CDC recommendations for healthy children and pregnant women.
4. Global Trends:
◦ U.S. cases show a slight decline, but China reports a near-doubling of severe respiratory cases, and Taiwan has seen a 78% spike in ER admissions.
◦ Symptoms remain similar (fever, cough, fatigue, loss of taste/smell), and standard tests cannot distinguish variants.
5. Public Health Response: Some physicians advocate for renewed mask mandates, citing rising cases in regions like Hong Kong. Officials warn of seasonal surges but emphasize individual risk assessment over broad restrictions.
6.Alternative Sources: We encourage reliance on independent platforms (e.g., Plague. info, Natural News) for "truthful reporting" outside mainstream narratives, alleging corruption by traditional institutions.
Yes, they’re at it again. Disease “experts” around the globe are sounding the alarms about the new Covidian nightmare. Health officials in California are warning of a new COVID-19 variant, NB.1.8.1, which has been detected in the state and five others, raising concerns about increased transmissibility and potential surges in infections. First identified in China in January, the variant has supposedly grown from 2% of cases in California in April to 19% as of recent data, according to the California Department of Public Health (CDPH).
The Wuhan Cave Virus variant has also been found in international travelers arriving in Washington state, Virginia, Hawaii, Rhode Island, and New York City since March. While not yet prevalent enough to be tracked separately by the Centers for Disease Control and Prevention (CDC), lab tests suggest NB.1.8.1 may be more infectious than currently dominant strains, such as LP.8.1, which accounts for 73% of U.S. cases.
The CDPH stated, "COVID-19 continues to circulate in California, and future seasonal increases in disease levels are likely." Some physicians have called for renewed mask mandates, citing rising cases in regions like Hong Kong, where hospitalizations have reached a 12-month high.
Current vaccines, designed to target the JN.1 variant — a predecessor of LP.8.1 — are expected to remain effective against NB.1.8.1, according to health officials. However, Health Secretary Robert F. Kennedy Jr. has pushed to remove COVID-19 vaccines from the CDC’s recommended schedule for healthy children and pregnant women, though they remain listed for now.
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Federal authorities bust $25M COVID-19 relief fraud scheme, arrest 14 conspirators
Federal authorities have arrested 14 individuals in Southern California for allegedly orchestrating a sprawling fraud scheme that siphoned more than $25 million from Wuhan coronavirus (COVID-19) relief programs meant to aid struggling small businesses.
The defendants, including residents of the San Fernando Valley and Glendale, are accused of exploiting federal loan initiatives such as the Paycheck Protection Program and Economic Injury Disaster Loans. The conspirators defrauded the government by submitting fabricated tax returns, falsifying business records and laundering funds overseas.
Four additional suspects believed to be in Armenia remain at large, according to the Department of Justice (DOJ). The arrests made on Wednesday, May 28, followed a multi-agency investigation that uncovered a sophisticated criminal network operating since at least 2018.
Among those charged is 42-year-old Vahe Margaryan of Tujunga. He allegedly directed the creation of sham companies, falsified financial statements and purchased fraudulent tax returns to secure loans. Prosecutors claim Margaryan's operation laundered millions through shell accounts before his alleged activities were halted in January 2025.
Felix Parker of North Hollywood was also among those arrested on Wednesday. The 77-year-old Parker allegedly obtained over $2 million by submitting fake tax returns for a nonexistent promotional products company.
The scheme extended beyond domestic borders. Forty-seven-year-old Axsel Markaryan of Pacoima, reportedly secured $5 million in Small Business Administration loans before transferring at least $100,000 to an accomplice in Armenia. Meanwhile, 37-year-old Sarkis Sarkisyan of Glendale allegedly fabricated an entire business to fraudulently claim more than $700,000 in Paycheck Protection Program funds.
DOJ cracks down, threatens decades in prison for pandemic fraudsters
Law enforcement seized $20,000 in cash, firearms and money-counting equipment – highlighting the operation's scale. According to the DOJ, each defendant would be facing decades behind bars if convicted.
The case highlights vulnerabilities in pandemic-era relief programs, which disbursed billions with limited oversight in the early stages of the crisis. Special Agent Tyler Hatcher of the Internal Revenue Service - Criminal Investigation's Los Angeles Field Office emphasized that the defendants "pilfered" funds intended for legitimate businesses in distress.
The DOJ's COVID-19 Fraud Enforcement Task Force, established in 2021, has since intensified efforts to recover stolen funds. Bill Essayli, interim U.S. Attorney for the Central District of California, vowed to pursue those who "cheat the system." He said the May 28 raid and subsequent arrests seek to "send a message to all criminals who take advantage of government programs designed to help those who need them most."
Historical parallels exist in past disaster relief fraud cases, such as after Hurricane Katrina, when lax oversight led to an estimated $1 billion in fraudulent payouts. Decades on, the current crackdown reflects a broader push to hold perpetrators accountable.
As the cases proceed, the DOJ urges the public to report suspected fraud through its National Center for Disaster Fraud hotline. For now, the arrests underscore a stark reality. While emergency funds serve as a lifeline for many, they also attract criminal networks eager to exploit crises.
Watch this clip from "Snyder Reports" on how unemployment benefits fraud cost Americans billions in tax dollars.
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China’s COVID nightmare returns: Students isolated, deaths hidden as regime doubles down on totalitarian policies
As the world moves on from the pandemic era, China remains trapped in a cycle of fear, control, and deception. A new wave of COVID-19 infections, driven by the XBB sub-lineage of the omicron strain, has swept through mainland China, prompting schools to isolate students and hospitals to quietly bury the truth. Despite years of draconian lockdowns, forced vaccinations, and relentless propaganda, the Chinese Communist Party (CCP) has failed to contain the virus — yet it continues to enforce the same failed policies, hiding the true toll of infections and deaths from its own people and the world.
Key points:
• Schools in multiple provinces are suspending classes and forcing students into quarantine, sparking fears of renewed lockdowns.
• Doctors and residents report severe symptoms and deaths far exceeding official CCP statistics, which have long been unreliable.
• The regime is quietly constructing mobile cabin hospitals while publicly downplaying the outbreak to avoid economic disruption.
• The XBB sub-lineage, including strains XBB.1.9, XBB.1.5, and Arcturus XBB.1.16, dominates infections, yet authorities refuse transparency.
• Neighboring countries detect the same variants in travelers, raising concerns about unchecked global spread due to China’s secrecy.
The return of medical tyranny: Students locked down, families silenced
Reports from Guangzhou, Shaanxi, and Jiangsu reveal a disturbing trend: Schools are once again isolating children under the guise of pandemic control. A leaked quarantine notice from a Guangzhou primary school, circulated on Douyin before being censored, showed a third-grade student forced into a seven-day isolation after testing positive. Similar measures have been imposed in other regions, with feverish students sent home—echoing the darkest days of China’s "zero-COVID" madness.
But this is not 2020. The world now knows that lockdowns do not stop viruses — they only destroy lives. Yet the CCP, addicted to control, refuses to admit failure. Instead, it suppresses dissent, censors social media, and manipulates data to maintain the illusion of competence.
Dr. Kang Hong, a Guangzhou clinic physician speaking under a pseudonym, told The Epoch Times that symptoms in this wave are "far more severe than the common cold," including white lung syndrome — a hallmark of COVID-19 damage. Hospitals use testing programs that fuel the pandemonium, leading government officials to take totalitarian actions to isolate people and further the social panic as protocols and mandates further the damage.
A regime of lies: Deaths hidden, doctors silenced
The CCP’s COVID deception is nothing new. Since 2020, it has systematically under-counted infections and deaths during Wuhan's initial wave, while concealing excess deaths after the population was mass vaccinated. Residents across China report sudden deaths, prolonged illnesses, and hospitals overwhelmed — yet official figures remain suspiciously low, as medical atrocities and mass immune system destruction of the population becomes a topic too contentious, the issue must be censored from discussion.
Mr. Xu, a Liaoning Province resident, described friends and relatives suffering relentless symptoms that "cannot be cured by medicine at all." He noted a spike in sudden deaths among middle-aged adults — a pattern ignored by state media. Meanwhile, in Inner Mongolia, clinic owner Liu Kun warned of an "explosive growth" of cases in June and July, with patients battling coughs, vomiting, and diarrhea for months. This is a population that has been heavily vaccinated, multiple times, subject to masking and isolation procedures for years.
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Axis of Evil: CDC and FDA concealed COVID vaccine dangers as injuries soared, new study reveals
The U.S. public was sold a lie—a carefully crafted deception that turned millions into unwitting test subjects for an experimental medical intervention. While government health agencies swore under oath that COVID-19 vaccines were "safe and effective," internal documents now expose a chilling reality: the FDA and CDC deliberately ignored alarming safety signals, suppressed data, and stonewalled transparency efforts. A bombshell peer-reviewed paper published by Children’s Health Defense (CHD) confirms what independent researchers have warned for years—the agencies tasked with protecting Americans instead betrayed them, prioritizing pharmaceutical profits over human lives. But it's more than just pharmaceutical profits these people are trying to acquire. The CDC and FDA's inner nucleus are defrauding the public, acting as a front group for an industry that is abusing, harming, and killing Americans. The mRNA COVID vaccine fraud opens the gateway for hundreds of new vaccine experiments, unleashing mass vaccination platforms and technologies of genetic control and data collection that will make COVID jabs look like a simple test run ten years down the road.
Key points:
• A new peer-reviewed study accuses the FDA and CDC of a "monumental betrayal" by failing to monitor and report COVID-19 vaccine injuries.
• Agencies ignored safety signals from VAERS and VSD databases, where COVID shots accounted for 78% of all reported vaccine deaths.
• Internal records show the FDA detected almost no safety signals for Pfizer and Moderna mRNA vaccines—despite widespread myocarditis cases.
• CDC withheld critical myocarditis data and dodged FOIA requests, delaying accountability for years.
• Experts warn that without transparent pharmacovigilance, the public remains defenseless against future vaccine injuries.
• The CDC and FDA must be replaced; their inner nucleus prosecuted for these crimes mentioned herein.
A system rigged from the start
Pharmacovigilance—the practice of monitoring drug and vaccine safety—was supposed to be the last line of defense for public health. Instead, it became a bureaucratic smokescreen. The CHD study, published in Medical Research Archives, reveals that the FDA and CDC abandoned their legal obligations, using flawed statistical methods to downplay injuries while fast-tracking mRNA injections onto the market.
VAERS, the government’s primary adverse event reporting system, has long been criticized for capturing only a fraction of injuries—Harvard researchers estimated in 2011 that less than 1% of vaccine harms are reported. Yet even this incomplete system logged 1.6 million COVID-19 vaccine injury reports by 2023, dwarfing all other vaccines combined over three decades.
"The clinical trial never ends," the CHD paper warns. "It’s just that our children become the subjects of the uncontrolled experiment."
The cover-up: How agencies hid the truth
Emails and internal documents obtained through litigation expose a pattern of negligence and deceit. While the CDC was legally required to use Proportional Reporting Ratios (PRR)—a straightforward method for detecting safety signals—it instead relied on Empirical Bayesian data mining, a complex statistical model that obscured risks.
During the brief period the CDC used PRR in 2022, it identified 743 safety signals, including myocarditis, stroke, and death. Yet the FDA—tasked with independently verifying these findings—claimed only three minor signals (a rash, breast milk exposure, and "drug ineffectiveness") for mRNA shots.
"The FDA and CDC didn’t fail to protect us—they just never tried," said Karl Jablonowski, Ph.D., CHD’s senior research scientist. "That they never tried is a dereliction."
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The MAHA report’s alleged AI origins add fuel to these concerns, as opponents argue that automated systems could amplify bias or manipulation in policymaking. While proponents view AI as a tool for efficiency, this case underscores the need for transparency and verification in its use — especially when public health decisions are at stake.
The debate extends beyond vaccines, touching on fears that AI could be weaponized to control narratives, particularly in news and public discourse. Quotes like, “It’s our job to tell you what to think” — have resurfaced in discussions about AI’s potential to curate or censor information.
As lawmakers grapple with AI regulation, the MAHA report serves as a cautionary tale: without safeguards, automated systems risk eroding trust in institutions already under scrutiny.
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The CDC’s updated guidance marks a pivotal moment in pandemic policy, granting parents more agency in their children’s healthcare decisions. Yet the lack of transparency surrounding the agency’s decision-making process — and its conflicting messaging on pregnancy — underscores ongoing tensions between public health mandates and individual choice. As the debate continues, the revised recommendations may signal a broader reassessment of how vaccines are integrated into routine healthcare for children.
Bottom line: The Dirty Jab Complex will still be injecting depopulation prion “technology” into pregnant women, newborn babies, kids, teens, healthy adults, and everybody who’s already suffering from cancer, heart disease, diabetes and dementia, so expect the wave of “all-cause-mortality” to continue skyrocketing.
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The study evaluated the immune response triggered by empty LNPs (without mRNA) in THP-1 monocyte cells. Results showed that LNPs dose-dependently activated the NF-kB pathway, comparable to low doses of TLR agonists like R848 (activating TLR7/8) and LPS (activating TLR4). However, LNPs did not activate the interferon regulatory factor (IRF) pathway, which is central to antiviral responses.
This can cause serious long term issues:
Endosomal escape compromised
While LNPs aim to exit endosomes for mRNA delivery, oxidized or modified lipids in these particles may accumulate in lysosomes. This interference could impair normal lysosomal function, potentially disrupting the body’s cellular waste management pathways.
Receptor-mediated immune and metabolic effects
Oxidized lipid components of LNPs could interact aberrantly with receptors such as PPARs, TLRs, and CD14. Such interactions might dysregulate signaling pathways involved in immune response (e.g., TLR-induced inflammation) and lipid metabolism (e.g., PPARs and CD14 pathways), contributing to metabolic disturbances or inflammatory states.
Sustained membrane vulnerabilities
Long-term exposure to lipid oxidation products—or structural modifications caused by hydrolysis and crosslinking—might gradually compromise membrane integrity. Over time, these changes could disrupt cell membrane function and communication, potentially linking to chronic conditions such as neurodegenerative disorders or autoimmune phenomena, where cellular dysfunction plays a role.
Despite these risks, regulators fast-tracked the shots without long-term safety studies. Now, as cases of myocarditis, blood clots, and mysterious deaths pile up, the medical establishment remains eerily silent.
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Lethal injection: Twin babies DIE days after routine vaccinations
A heartbroken Idaho family is demanding answers after their 18-month-old twins died mysteriously in their sleep just one week after receiving routine vaccinations.
Dallas and Tyson Shaw, described by their parents as "perfect, happy little babies," were found dead on May 1 by their mother Andrea. The twins' demise followed a wellness visit where they were given the Hepatitis A, flu and DTP (diphtheria, tetanus and pertussis) vaccines.
Despite Andrea's warning that her husband's family had a history of severe reactions to the flu shot, the pediatrician dismissed concerns and administered the vaccines anyway. Now, as police investigate the deaths as a possible homicide, the grieving parents face accusations while waiting for toxicology reports that may finally reveal the truth.
Andrea took her twins to their pediatrician on April 23 for a standard checkup. Aware of her husband Nathaniel's family history of adverse reactions, she expressed hesitation about the shot.
But the pediatrician assured her the babies would be fine. Along with the flu vaccine, the twins received the Hepatitis A and DTP immunizations – three shots in one visit. Within hours, their health deteriorated rapidly.
The next morning, the twins were lethargic; their lips blue and their eyes sunken. "Tyson walked just about to the entrance of my living room and just lay down and wouldn't get up," Andrea recalled. "Dallas, the best she could, ran to me."
Alarmed, Andrea called her mother-in-law, who urged her to take the children to the emergency room. A doctor there acknowledged the symptoms could be a vaccine reaction, but sent them home after administering Tylenol and popsicles.
For days, the twins suffered vomiting, diarrhea and extreme fatigue. By April 30, their condition seemed to stabilize – until the next morning, when Andrea found them lifeless in their shared bed.
Police suspect foul play, treat parents as suspects
Instead of receiving sympathy, the twins' parents were immediately treated as suspects. Police confiscated Andrea's phone, preventing her from calling Nathaniel. The distraught father only learned of his children's deaths when an officer coldly told him, "Hey, I hate to inform you, but your kids are dead."
Detectives interrogated the couple for hours, suggesting Andrea had a "postpartum blackout" and smothered the twins – a theory she vehemently denies. "It made me feel crazy," she said. "I was telling them my truth, and they were getting into my head that I had done it."
The circumstances of the deaths have raised significant questions for investigators, and reignites the fierce debate over vaccine safety and medical consent. Critics argue that dismissive attitudes toward parental concerns – like Andrea's warning about family allergies – can have tragic consequences.
"The doctor didn't even ask why we were worried," Andrea said. "She just said, 'They'll be fine.'"
Police have not ruled out foul play, but no arrests have been made as of writing. Toxicology reports and autopsy results are pending. Meanwhile, the Shaws have filed a report with the Vaccine Adverse Effect Reporting System, hoping their tragedy will prompt closer scrutiny of vaccine protocols.
Watch Del Bigtree explaining that avoiding vaccines could prevent 200,000 cardiovascular deaths and six million cancer cases in the U.S. annually in this video.
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Poll: Overwhelming majority of Americans demand Big Pharma ACCOUNTABILITY for vaccine injuries
Americans across the political spectrum are demanding greater accountability from pharmaceutical companies, stricter vaccine safety oversight and more transparency in government health policies, according to a new poll.
The survey, conducted this month by the Center for Excellence in Polling (CEP) and commissioned by the Foundation for Government Accountability, reveals that 88 percent of respondents believe drug manufacturers should be held financially responsible if their vaccines cause harm. Its most striking revelation is the near-unanimous agreement among both Republicans and Democrats on this issue.
The CEP poll's findings reflect deep-seated distrust in public health institutions and Big Pharma, fueled by years of contentious debates over vaccine mandates, emergency-use authorizations and corporate liability protections. It also aligns with growing frustration over the 1986 National Childhood Vaccine Injury Act, which shields vaccine manufacturers from most lawsuits. Critics argue this legal immunity has allowed companies to profit without sufficient accountability, even as reports of adverse effects persist.
Similarly, 88 percent of respondents insisted that new Wuhan coronavirus (COVID-19) boosters must demonstrate clear health benefits before receiving Food and Drug Administration (FDA) approval. The demand for rigorous clinical testing signals a public wary of rushed authorizations, particularly after the controversial emergency rollout of mRNA vaccines during the pandemic.
Half of those surveyed supported allowing parents to opt their children out of school vaccine requirements without penalty – a stance that sharply divides along party lines. Republicans (68 percent) overwhelmingly backed the measure, while only 37 percent of Democrats agreed. The debate over mandates has intensified in recent years, with some states rolling back exemptions while others expand them.
The results mirror a November 2024 John Zogby Strategies poll, which found 57 percent of Americans believe vaccine-injured individuals should be able to sue manufacturers. Additionally, 51 percent opposed vaccine mandates outright, with 72 percent rejecting experimental vaccines like those authorized under emergency use.
Poll also reflects growing distrust in public health agencies
The CEP poll underscores a broader erosion of trust in federal health institutions. Ninety-five percent of respondents demanded full public access to government-funded health studies, including unfavorable findings. Ninety-three percent called for mandatory disclosure of financial ties between regulators and drug companies, while 87 percent said health officials should be barred from owning stock in companies they oversee.
Beyond pharmaceuticals, respondents overwhelmingly supported stricter food regulations. Ninety-six percent backed warning labels for foods with harmful chemicals, while 91 percent wanted additives clearly listed on packaging. Eighty-four percent supported banning synthetic dyes already prohibited abroad, and 77 percent believed states should have the power to enact stricter food bans than federal standards.
Recent moves by the FDA, such as phasing out petroleum-based dyes, suggest regulators are responding to public pressure. But critics argue these changes are long overdue given Europe's more aggressive stance on food additives.
The survey also revealed strong bipartisan support for healthier school meals. Ninety-five percent wanted fresh fruits and vegetables served daily, while 88 percent demanded full ingredient transparency. Eighty-one percent supported letting states set stricter nutrition standards than federal guidelines.
Welfare reforms also garnered broad approval. Sixty-nine percent backed restrictions on junk food purchases with food stamps, while 72 percent supporting work requirements for Medicaid recipients.
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This corrupt cycle mirrors the COVID, where taxpayer-funded research at the Wuhan Institute of Virology preceded a global pandemic and unprecedented vaccine windfalls for companies like Moderna.
Will Moderna face accountability?
Despite the contract termination, Moderna shows no signs of retreating. The company recently opened a 290,000-square-foot U.K. facility capable of churning out 250 million vaccines annually, suggesting it still expects lucrative government contracts.
For those who have witnessed the devastation of COVID-19 mandates, the cancellation is a small victory—but the war is far from over. Until gain-of-function research is banned and vaccine manufacturers are held legally accountable for injuries, the medical police state will continue exploiting public health crises for profit.
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Dr. Meryl Nass @DrMerylNass of Door to Freedom cited a February 2022 DHS bulletin declaring the U.S. in a “heightened threat environment” due to “false narratives”—without evidence these narratives caused harm. “They target specific ideologies,” she said, “not violence.”
Nebraska chiropractor Ben Tapper, another “Disinformation Dozen” listee, echoed her skepticism: “Labeling opponents ‘terrorists’ was a smear to silence dissent. Our courts won’t fix it—the system’s rigged.”
Gabbard, the lone Democrat to declassify the findings, vowed to root out federal weaponization. Yet Tapper doubts reform. “When the establishment can label critics as terrorists, there’s little recourse,” he said.
The slippery slope of “public safety”
The documents reveal a chilling fusion of power. By redefining questioning of authority as extremism, the Biden administration institutionalized a precedent: dissent = threat.
Historically, this mirrors COINTELPRO surveillance against civil rights groups, where dissent was conflated with disloyalty. Now, it’s medical mandates—a far more relatable trigger to the masses.
As Jeffrey Tucker warns: “If a democratic society requires obedience to stay safe… what’s left of democracy?”
The Biden-era papers are more than a pandemic relic. They’re a blueprint for how governments can—and will—hijack crisis response to punish dissenters. The real test may come next time—and this time, the mask might be figurative.
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POST-PANDEMIC DEATH SPIRAL: Over 1.5 million avoidable deaths occurred in USA AFTER Covid-19 mostly disappeared – must be the deadly mRNA JABS
Oh, the carnage of the clot shots. The world can see it now. How many people who got the deadly mRNA spike prion blood-clotting jabs for Covid would NEVER get another one now? Millions, if not billions, of people around the globe are suffering nightmarish health outcomes from the turbo-cancer injections and the ones who are still alive have lost faith in the Vaccine Industrial Complex’s lies and deception about “safe and effective,” as they follow the science and their own health detriment to cast judgment.
The facts are in folks. Over 1.5 million excess deaths of people UNDER 65 have occurred since the “novel virus” has waned and basically disappeared from ill-effects, and now JAMA Health Forum has published the analysis suggesting these deaths were preventable. What’s the story then? Why did this happen. Let’s take an inside look.
U.S. Excess Deaths Hit Record Highs Post-Pandemic, Shocking Study Reveals
A new study has found that the United States recorded 1.5 million excess deaths in 2022 and 2023—far surpassing pre-pandemic levels—despite the waning of COVID-19. Researchers from Boston University and the University of Minnesota published their findings in JAMA Health Forum, revealing that nearly half of all deaths among Americans under 65 last year could have been prevented if the U.S. matched the health outcomes of peer nations. The study raises urgent questions about systemic failures in American public health.
The analysis compared U.S. mortality data with that of 21 other high-income countries, including Canada, the U.K., and Japan, examining over 337 million deaths from 1980 to 2023. The results were staggering: 820,000 excess deaths in 2022 and 705,000 in 2023—marking the highest non-pandemic excess death totals since World War II. In 2023 alone, 23% of U.S. deaths were classified as "excess," meaning they likely would not have occurred if the nation had maintained average mortality rates of its economic peers.
“The U.S. has been in a protracted health crisis for decades, with health outcomes far worse than other high-income countries,” said Jacob Bor, associate professor at Boston University’s School of Public Health. “One out of every two U.S. deaths under 65 is likely avoidable. Our failure to address this is a national scandal.”
Historical context underscores the severity of the trend. In 1980, the U.S. had 42,000 fewer deaths than expected compared to peer nations. But by 2000, excess deaths surged to 355,000, climbing to 409,000 by 2010. The pandemic exacerbated the crisis, with 1 million excess deaths in 2020 and 1.1 million in 2021. Yet even after COVID-19 receded, mortality rates remained alarmingly high—suggesting deeper, unresolved issues.
Elizabeth Wrigley-Field, a University of Minnesota sociologist and co-author, noted that the 2023 figures align with pre-pandemic trends. “The 700,000 excess American deaths in 2023 is exactly what you’d predict based on prior rising trends, even if there had never been a pandemic,” she said. Contributing factors include drug overdoses, gun violence, traffic fatalities, and preventable chronic diseases like diabetes and heart disease.
The study concludes that achieving health parity with peer nations could have saved 1.5 million lives in the last two years—and 15 million since 1980. As policymakers grapple with these findings, the data presents a sobering challenge: without systemic reforms, the U.S. may continue to lag behind its peers in one of the most fundamental measures of societal well-being—life itself.
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CDC pushes emergence of China-linked COVID-19 variant in U.S. amid global surge
A newly identified variant, NB.1.8.1 — linked to a surge in China — has surfaced in the United States, prompting increased public health monitoring, though confirmed cases remain below official tracking thresholds. Meanwhile, the FDA’s controversial decision to restrict broader booster access has ignited debates over pandemic strategy, while discrepancies in China’s reported mortality data raise concerns about transparency.
Tracking NB.1.8.1: Transcontinental spread and CDC’s surveillance
The Centers for Disease Control and Prevention confirmed to the Epoch Times on May 25 that fewer than 20 cases of NB.1.8.1, a sub-lineage of the XDV strain of SARS-CoV-2 (an Omicron descendant), have been identified in U.S. surveillance data. The agency highlighted the variant’s “growing transmissibility” but noted that current case numbers remain below the threshold for inclusion in its weekly pandemic tracking dashboards. “Should its prevalence increase, it will automatically appear on the tracker,” a spokesperson said.
In China, NB.1.8.1 is now dominant, with experts citing a distinctive burning sore throat as a key symptom. Hong Kong officials observed a spike in hospitalizations, though they stressed there is no evidence of heightened severity compared to earlier variants. The World Health Organization labeled NB.1.8.1 a “variant under monitoring,” citing rapid spread but no new risks beyond comparable lineages.
The variant’s arrival in the U.S. mirrors past pandemic patterns. “History repeats itself — new variants always find a way across borders,” said Dr. Jonathan Liu of the Canadian College of Traditional Chinese Medicine, noting parallels to the B.1.1.7 strain detected in 2020.
Transmissibility trumps severity: Expert insights and public guidance
While NB.1.8.1 appears highly contagious, health researchers stress it does not portend an abrupt return to severe illness or death rates seen earlier in the pandemic. “Symptoms align with prior variants — fever, cough, fatigue — but the burning throat may set it apart,” said microbiologist Subhash Verma of the University of Nevada’s School of Medicine, referencing data from Chinese medical journals.
Dr. Amy Edwards of Case Western Reserve University added that lab studies show the variant’s “tighter binding to human cells” likely fuels transmissibility, not pathogenicity. “Hospitalizations in China suggest a surge in cases due to its reach, not threat. Think seasonal flu-like dynamics,” she said.
The CDC’s current guidance mirrors global advice: masking in high-transmission settings, staying home when symptomatic and updating vaccines for at-risk groups. In Delhi, Health Minister Pankaj Singh emphasized preparedness without panic: “Mild symptoms dominate. Keep hospitals stocked, but no need to reimpose lockdowns.”
FDA’s vaccination policy sparks frustration and uncertainty
The pandemic’s next chapter faces a stark challenge: access to updated vaccines. The FDA announced stricter safeguards last week, restricting NB.1.8.1-targeted boosters to seniors and those with underlying conditions — approximately 100 million Americans — while mandating new clinical trials for broader distribution. “This creates two Americas: one protected, one left guessing,” said Céline Gounder, KFF Health News editor, on "CBS Mornings Plus."
Critics warn the rules could delay or deter immunization as the variant spreads. Verma noted the policy could erode public trust: “If people don’t qualify, why bother seeking a vaccine at all? This undermines community immunity.”
Secretary Robert F. Kennedy Jr., who chairs the FDA under the current administration, has openly criticized vaccine mandates — a stance experts argue clashes with scientific consensus. Dr. Verma pressed for “clearer language on eligibility” and urged transparency on the new booster formula.
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