Archive for the ‘Activism’ Category

Revolving Door Strikes Again

https://www.midwesterndoctor.com/p/the-revolving-door-strikes-again?

The Revolving Door Strikes Again

Why did the FDA relentlessly suppress all evidence of vaccine injuries?

Many individuals I’ve spoken to believe Peter Marks is the government official most directly responsible for the entire COVID catastrophe, and those I know who directly interacted with him despise him. For that reason, six months ago, I published a detailed exposé of his conduct throughout the pandemic, both to highlight the systemic issues within our healthcare bureaucracy that must be fixed and to disincentivize other health officials from following in his footsteps. Since that time:

•Despite immense industry pushback, he was replaced with MAHA appointee Vinay Prasad

•Marks has made statements on the national media which display either a profound degree of ignorance of vaccines or a cult-like devotion to them, such as telling CBS the MMR vaccine absolutely does not cause encephalitis—despite this specific injury being one of the only vaccine injuries the Federal Government acknowledged as real and eligible for compensation when it created the the National Childhood Vaccine Injury Act of 1986.

Note: the primary reason DMSO (a safe and affordable substance with remarkable therapeutic applications against a wide range of “incurable” ailments) never entered mainstream medical practice was because the FDA, feeling DMSO’s broad therapeutic potential threatened their control of American medicine, waged a multi-decade war against it despite widespread opposition from the public, Congressmen, scientists and physicians across the country. One journalist who interviewed the successive FDA commissioners throughout this saga was struck by how “lacking [they were] in solid information about the most spectacular and controversial drug of our time” and how often they simply quoted nonsensical misinformation the FDA had previously put out about the drug without a basic understanding of it—something I would argue also applies to Peter Marks.

•Yesterday, it was announced that Peter Marks had started working with Eli Lilly, where he will oversee molecule discovery and infectious diseases at Lilly. While his salary has not been publicly announced, the AI systems I queried said given the existing precedent, he would likely get 2-6 million this year (a big upgrade from his roughly $200,000.00 FDA salary)—and possibly much more (e.g. 10-15 million).

This understandably enraged the vaccine injured parties who directly interacted with Marks over the last four years, so I felt it was important to revisit exactly what Marks did and discuss the broader revolving door in regulatory medicine.

Note: last year, the FDA approved Eli Lilly’s anti-amyloid monoclonal antibody for the treatment of Alzheimer’s disease (granting the application Fast Track, Priority Review, and Breakthrough Therapy designations). I showed in last weekend’s article, that these costly drugs do close to nothing (they may slightly slow the progression of Alzheimer’s disease) while simultaneously creating a variety of severe symptoms including giving over a quarter of recipients brain bleeds and brain swelling—yet remarkably, safer and much more effective Alzhemier’s therapies have languished in obscurity. (See link for article)

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**Comment**

I’m with Rodney Dangerfield on TOBAL,

“There Oughta be a law!”

For more:

Top Studies Caught Twisting Data To Make Clot Shots Appear ‘Safe & Effective’

https://slaynews.com/news/top-studies-twisted-data-covid-vaccines-appear-safe-effective/

Top Studies Caught Twisting Data to Make Covid ‘Vaccines’ Appear ‘Safe and Effective’

An explosive investigation has confirmed that leading medical journals published several early studies in 2020 that twisted safety data to deceitfully declare Covid mRNA “vaccines” to be “safe and effective.”

The scientists behind the investigation warn that the studies were so obviously manipulated to favor “vaccine” makers that they were “biased by design.”

Alarmingly, these highly cited studies helped to hide the dangers linked to the “vaccines” before they were rolled out for public use in early 2021.

The bombshell new analysis found that the studies deliberately downplayed deadly heart risks tied to both Pfizer’s mRNA shot and AstraZeneca’s viral-vector injection.

The new study of the old data was conducted by scientists from Children’s Health Defense  (CHD) and the Brownstone Institute.

The researchers reanalyzed U.K. government data that underpinned some of the most influential Covid “vaccine” safety studies in the world.

Their findings confirm what critics have long warned.

Instead of protecting the public, top scientific institutions twisted the data to reassure the world of “vaccine” safety while ignoring and even hiding alarming red flags.

The reanalysis found clear safety signals that were evident in the original data.

However, these safety signals were deliberately ignored in published studies.

(See link for article and studies)

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**Comment**

It’s actually much worse….

  • A new study concludes that ALL COVID shots & boosters increase cancer risk.
  • A FOIA reveals that the CDC scrambled to control the public’s perception of the experimental gene therapy shot by crafting public messaging that downplayed any and all concerns.
  • The CDC thwarted efforts to track COVID shot adverse reactions and admits it never monitored for ‘safety signals.’
  • The CDC also hid injuries people received after the shot.
  • The White House and the CDC knew the shots were causing myocarditis in 2021 but lied about it.
  • The FDA refused to release autopsy results on people who died after the shots.
  • When the CDC finally released the VAERS analysis due to a FOIA, there were clear safety signals for death and a range of highly concerning thrombo-embolic, cardiac, neurological, hemorrhagic, hematological, immune-system and menstrual adverse events (AEs) among U.S. adults.
  • The CDC manipulated VAERS data by arbitrarily excluding thousands of reports and by comparing deaths after ‘vaccination’ to deaths during a pandemic – a meaningless distortion.  They should have compared vaxxed to unvaxxed.
  • Steve Kirsch showed that by having a policy of COVID testing where it is mandatory to test the unvaccinated 2x/week but the vaccinated can totally skip testing, massively skewed all studies based on that data making an ineffective ‘vaccine’ look perfect.  The honest way to see if a ‘vaccine’ is working is to compare whole period all-cause mortality between those who got the shots and those who did not.
  • Due to another brave whistleblower, we learn that OSHA confirmed an internal directive telling healthcare employers NOT to report or track COVID shot injuries.
  • Adding insult to injury, the Ohio Supreme Court rejected a public records request seeking data on COVID-19 deaths and vaccinations. This allows critical information to remain buried.

So not only did the FDA and CDC bury alarming safety risks linked to the clot shots, with states now following suit, they underestimated risks through flawed statistical methods, suppression of safety alerts, and outright data gaps.

Never trust these agencies again and buyer beware!

ACTION: Stop Hemp Ban!

https://anh-usa.org/stop-the-hemp-ban-now/

Stop the Hemp Ban Now!

Stop the Hemp Ban Now!

A dangerous provision has been included in a Congressional spending bill that could spell the end of your access to full-spectrum hemp products. Action Alert!

Listen to the audio version of this article:


THE TOPLINE

  • A provision in the House Agriculture Appropriations Subcommittee’s FY 2026 spending bill would ban all ingestible hemp products containing “quantifiable amounts” of THC or THC-like cannabinoids—effectively outlawing many CBD and full-spectrum hemp oils that contain small, non-psychoactive amounts of THC.
  • While the measure is framed as targeting unregulated, intoxicating products like delta-8, it goes far beyond that by threatening the entire hemp industry and cutting off consumer access to safe, beneficial full-spectrum hemp products.
  • The provision still faces hurdles, including reconciliation with the Senate version of the bill and ongoing political uncertainty, but urgent grassroots opposition is needed to prevent it from becoming law.

If you rely on hemp, CBD, or full-spectrum hemp oil to support your health, listen up!

A dangerous provision buried in a House spending bill threatens to ban most of the hemp products currently available on the market. Just as research continues to confirm the remarkable healing potential of hemp and CBD—showing their impact on the body’s endocannabinoid system, which influences everything from mood to immunity—some in Congress are moving to strip away our access. We must raise strong grassroots opposition to stop this misguided policy.

The House Agriculture Appropriations Subcommittee’s spending bill for FY 2026 contains a deeply troubling provision that effectively bans the production and sale of all hemp-derived products that contain “quantifiable amounts” of THC (one of the psychoactive components of hemp that provides the “high”) or cannabinoids with similar, THC-like effects. What “quantifiable amounts” means specifically is to be determined later by regulators.

Put in plain terms, this would ban all ingestible hemp products with any level of THC in them. This means that many CBD oil and full-spectrum hemp oil products would suddenly become illegal.

The goal of the amendment is to close a loophole created by the previous Farm Bill that has allowed unregulated, intoxicating hemp products on the market. Recall that the 2018 Farm Bill legalized hemp at the federal level, defining it as a cannabis plant with less than 0.3 percent THC. In the six years since that bill became law, some companies found a way to stay within the guardrails put in place by the new law but still be able to chemically synthesize psychoactive or intoxicating products from legal hemp plants. These products include members of the THC family like delta-8 and delta-10. Delta-8 occurs naturally in the hemp plant at miniscule levels, but higher levels of delta-8 THC are produced artificially in the laboratory by chemically converting CBD through a process called isomerization.

While the merits of cracking down on delta-8 and other products can be debated, what’s crystal clear is that this amendment goes far beyond banning delta-8 and similar products and takes a huge swipe at the hemp industry as a whole without any justification.

Some of the best and healthiest products are full-spectrum hemp oils that contain all of the nearly 500 known compounds known to be present in hemp, including cannabinoids (>60), terpenes (>140), and fatty acids that occur naturally in the plant. Among this morass of compounds are tiny, non-psychoactive amounts of THC. The real benefits of hemp come from the “entourage effect” of all these different chemicals acting together. For example, a 2015 study found that highly purified CBD was somewhat effective in treating inflammation and anxiety in mice, but was substantially more effective when the CBD was present in a full spectrum extract because it benefits from the synergy from the full entourage of typically associated compounds.

Banning, in one fell swoop, all hemp products with “quantifiable amounts” of THC is the very definition of throwing the baby out with the bath water and will take vital products out of our medicine cabinets.

Remember, too, that is not the only threat to CBD access. Because CBD has been approved as a drug, the FDA maintains that it cannot be a supplement, though the agency appears only to be going after CBD companies making illegal disease claims. The agency has said that it believes a new regulatory pathway is needed to deal with CBD. Whatever that pathway is, you can bet the agency will do its best to protect drug industry profits by making it next to impossible to have affordable CBD supplements.

There are still a number of hurdles before this can ever become law. Similar language was added to the Senate version of this bill, but Senator Rand Paul (R-KY) was able to remove it. House and Senate versions of the bill would need to be further negotiated and reconciled before being sent to the President for approval. The possibility of a government shutdown in the coming weeks further complicates matters.

There is no time to lose. We must oppose this terrible policy and kill it before the bill moves any further.

Action Alert!

(Go to top link for sign petition)

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**Comment**

CBD oil has been a game changer for me and my husband.  It helps us sleep much more soundly.

It has come under attack before, with the FDA misleading the public on its safety.  CBD is one of the most well researched non-psychoactive cannabinoids and it has an incredible array of health benefits, with evidence showing that has profound anti-inflammatory and immune modulating effects and can help with painanxietydepressioncertain cancers, and even heart health.

Funny how the ‘the powers that be’ always seem mostly concerned with safe, inexpensive, effective products, but are completely blind, deaf, and dumb to unsafe, expensive, and ineffective ‘vaccines’ and drugs.

I’m sure the goal is to ban this so we are all forced to use something Big Pharma greatly profits from.

As My Daughter Got Sicker and Sicker, Our Quest For Answers Dragged On. How Did We All Miss Lyme Disease?

https://www.theguardian.com/world/2025/sep/28/as-my-daughter-got-sicker-and-sicker-our-quest-for-answers-dragged-on-how-did-we-all-miss-the-bacteria-taking-over-her-body

As my daughter got sicker and sicker, our quest for answers dragged on. How did we all miss the bacteria taking over her body?

I write about nature, but when Milly got sick with a mystery illness, it never occurred to me that a long-forgotten tick bite could be the cause

There are many reasons to feel guilty. I’m a nature writer who preaches about the importance of wild childhoods, and my daughter has been made chronically ill by one trip to the countryside. I’m a journalist whose job it is to interrogate information and yet I didn’t demand better answers for her from NHS doctors. But the guilt is most painful when I remember a freezing wet day in October 2021.

Milly’s U10s football club were playing the league’s top team. Milly, player of the year the previous season, a whirl of blond energy across the pitch, had lost her enthusiasm for the beautiful game. That morning, she really didn’t want to play: she was tearful and exhausted. There was nothing obviously wrong: no cough, sickness, temperature. Her twin, Esme, was playing but without Milly the team were a player short. I told Milly they needed her. Stoic, she staggered off but couldn’t step on to the pitch. Instead, she curled into a ball of misery and fatigue beside her coach. The rain fell. Her team lost 15-1.

I cringe when I flick through the notebook where I recorded my daughters’ football matches (I was tragically keen). Below most results from the 21/22 season, I’ve written “Milly ill” or, worse, “Milly played ¼” or “Milly played ½”. All the time, cajoled or compelled to lead her “normal” life, Milly was getting sicker and sicker. We had no idea what was wrong. Every morning she looked terrible, dark circles beneath her eyes. She complained of perpetual tiredness, talked of being “disconcentrated” – she later learned to call this “brain fog” – and mentioned strange stabbing pains, mostly in her feet when she walked. Soon, she was too ill to go to school. Lockdown was over but it had become a permanent state for Milly, my wife, Lisa, and me.

What we didn’t know then, and wouldn’t discover until this spring, was that Milly’s body was being invaded by an insidious bacterium, Borrelia burgdorferi, which hides in connective tissue, confounding immune systems, wreaking havoc. Milly had Lyme disease, which takes its name from Old Lyme, a coastal town in Connecticut. This bacterial infection is not contagious but is transmitted by a tick, a tiny, blood-sucking arachnid that hops on to human skin in the countryside, where it is transported by other mammals, particularly deer. There are 476,000, and rising, annual cases in North America alone. Global heating is making ticks, their bacteria – and human illnesses – much more prevalent. (See link for article)

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**Comment**

Another beautiful life side-lined by a bacteria we still know very little about that is infecting people by the millions and chronically affecting the lives untold numbers.

If I had a quarter for every misdiagnosis that was Lyme/MSIDS, I’d be a millionaire.

Will things ever change?

For more:

ACTION: Repeal Real ID & Exit the UN

This website recently posted how tariffs are being used to propel UN sustainable development goals.  Information on Digital ID is also included.

The action here is for Real ID, a physical ID card that meets federal standards primarily for air travel and federal access while Digital ID is a digital version stored in a Smartphone that can be used for similar purposes.  Both serve to verify identity but can and will be used for so much more.

The problem with both is the fact it centralizes all of your data into one easy place which can and will be used against you.  We already have driver’s licenses, passports, passport cards and many other forms if identification.

Didn’t get your latest ‘vaccine,’ suddenly you can’t purchase food at the store.  It’s that easy.

In short, an ultimate diabolical plan is in place which would tokenize everything, trapping us in a digital prison where getting help for Lyme/MSIDS will become harder if not impossible. Real ID is the first step toward the plan.

It’s hard enough as it is for Lyme/MSIDS patients who are required to go out of mainstream medicine to find experienced and knowledgable Lyme literate doctors who typically don’t take insurance.  These independent doctors could save your life but are already being persecuted for defying an accepted narrative.

https://standforhealthfreedom.com/actions/repeal-realid/  Go here to sign petition

Repeal Real ID

Our Stand: At-A-Glance

  • The Safeguarding Personal Information Act of 2025 (S.2769), which was filed by Senator Rand Paul, would fully repeal Title II of the REAL ID Act of 2005.
  • That section of law forces states to turn driver’s licenses into a single, federally controlled ID system. After nearly twenty years of delays, the government started enforcing it nationwide by May 7, 2025.
  • The bill, introduced September 11, 2025, is simple and powerful: “Title II of the REAL ID Act of 2005 is repealed.”
  • No loopholes. No half-measures. Just a return of identification standards to the states and the people.

Why Repeal Matters

  • Privacy: REAL ID centralizes personal data, creating a ready-made national citizen database vulnerable to misuse.
  • Civil Liberties: Conditioning the right to travel on federal approval sneaks around the Fourth Amendment and state sovereignty.
  • Mission Creep: The REAL ID law allows the Department of Homeland Security to expand ID requirements “for any other purposes,” inviting future surveillance and digital tracking.
  • Federal Control: The plan for REAL ID is to move from physical to digital identification to be used for “verification” of a person when they want to do things like open a bank account.
  • Digital Surveillance: REAL ID could be integrated into a digital wallet, along with banking and personal health information.

What You Can Do Right Now

  1. Contact your U.S. Senators. Urge them to co-sponsor and vote for the Safeguarding Personal Information Act of 2025.
  2. Spread the word. Share this message with neighbors, faith communities, and privacy advocates so Congress hears a united voice.

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https://standforhealthfreedom.com/actions/exitun/  Go here to sign petition

Freedom First: Exit the UN!

Push Congress to Pass HR 1498 & S 669
Published: Sep 30, 2025

Our Stand: At-A-Glance

  • Last week, Secretary Kennedy publicly declined to sign the United Nations political declaration on noncommunicable diseases and mental health, citing its failure to address the chronic disease epidemic and what he described as the World Health Organization’s inability to produce meaningful reform. His statement underscored a larger problem: an international body seeking authority over the health policies of sovereign nations.
  • Secretary Kennedy’s rejection makes this the most opportune time to support and pass HR 1498 and S 669, the Disengaging Entirely From the United Nations Debacle (DEFUND) Act of 2025. These companion bills would end U.S. membership in the United Nations and every one of its agencies, including the World Health Organization, and permanently halt American funding for those institutions.
  • What the DEFUND Act Would Do
    • Terminate U.N. membership and funding: Repeals the 1945 United Nations Participation Act, directs the President to withdraw from the UN and all its specialized agencies, and stops all U.S. contributions, assessed or voluntary.
    • Close U.N. operations on U.S. soil: Orders the closure of the U.S. Mission to the U.N., repeals the 1947 Headquarters Agreement that allows the U.N. to operate in New York, and revokes related diplomatic privileges.
    • End participation in the World Health Organization: Repeals the 1948 resolution authorizing U.S. involvement in the WHO and blocks any future U.S. funding or staffing.
    • Prevent future re-entry without Senate approval: Requires explicit Senate consent for any future attempt to rejoin the U.N. or its agencies, with a guaranteed right of withdrawal.

The global “one-size-fits-all” policies, whether on public health, taxation, or digital surveillance, undermine the ability of American communities to shape their own decisions. Secretary Kennedy’s rejection of the U.N. health declaration highlights concerns that international authorities are seeking to expand control at the expense of national and local governance.

Take Action: Tell Congress to cosponsor and vote YES on HR 1498 and S.669. Contact your Representatives and Senators today, now is the time to apply pressure.