Archive for the ‘Activism’ Category

Bird Flu Outbreak in Wisconsin Cattle Just as Study is Published From H5N1 Outbreak Simulation & WHO Now Controls a Bioweapon Lab – What Could Go Wrong?

https://childrenshealthdefense.org/defender/exclusive-bird-flu-outbreak-40-miles-wisconsin-lab-sparks-concern-gain-of-function-experiments

Exclusive: Bird Flu Outbreak 40 Miles From Wisconsin Lab Sparks Concern About Gain-of-Function Experiments

A bird flu outbreak in a Wisconsin dairy cattle herd has fueled speculation that gain-of-function research at a nearby university lab — where scientists are working to develop a bird flu vaccine for cattle — may be behind the outbreak. The lab has a history of safety violations.

by Michael Nevradakis, Ph.D.
January 15, 2026
dairy cows and test tube with words "bird flu"

A bird flu outbreak in a Wisconsin dairy cattle herd has fueled speculation that gain-of-function research at a nearby university lab — where scientists are working to develop a bird flu vaccine for cattle — may have played a role in the outbreak.

Last month, the U.S. Department of Agriculture (USDA) identified what it said was the first known case of highly pathogenic bird flu in a Dodge County, Wisconsin, dairy cattle herd.

The USDA’s Animal and Plant Inspection Service (APHIS) characterized the outbreak as a new “spillover” event — from wildlife to cattle.

The two scientists who conducted the whole genome sequencing for APHIS and identified the virus responsible for the Dodge County outbreak work at the University of Wisconsin-Madison School of Veterinary Medicine, the university confirmed.

Those same scientists — Keith Poulsen, DVM, Ph.D., and Yoshihiro Kawaoka, DVM, Ph.D. — have also co-authored studies on gain-of-function research, including studies related to the H5N1 virus.

One of the scientists, Kawaoka, directs the university’s Influenza Research Institute, known to conduct gain-of-function research on H5N1. Kawaoka was director of the high-security lab in 2019, when it came under scrutiny for a safety breach.

The institute’s lab is about 40 miles from the bird flu outbreak in Dodge County.

Kawaoka is also the co-founder of flu vaccine manufacturer FluGen. And he is among a group of scientists working on the development of a bird flu vaccine for livestock.

Will Cushman, with the University of Wisconsin-Madison’s Office of Strategic Communication, confirmed that virologists Poulsen and Kawaoka are performing H5N1 research. However, he denied that it is gain-of-function research. (See link for article)

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H5N1 clade 2.3.4.4b genotype D1.1 is responsible for the Dodge County outbreak. The D1.1 genotype contains characteristics that may increase the transmissibility of the virus, including to humans.  The D1.1 strain is linked to a 3 year old’s death in Mexico, according to the WHO.

In 2023 lawmakers proposed Assembly Bill 413 to shut down gain-of-function research at Wisconsin universities, but UW lobbied against it and defeated it in April, 2024.

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Although the following Bird flu simulation was done in early 2025, the study wasn’t submitted until July, wasn’t accepted until December, with an online publish date if Jan. 8, 2026 – just in time as bird flu fear porn is intensifying.

https://jonfleetwood.substack.com/p/portugal-runs-h5n1-bird-flu-outbreak?

Portugal Runs H5N1 Bird Flu Outbreak Simulation—Echoing Pre-COVID Pandemic Exercises

Patients refusing to use personal protective equipment, like masks, defined as “threats.”

Jon Fleetwood
Jan 13, 2026

Portuguese health authorities conducted a formal avian influenza (H5N1) simulation exercise in early 2025 to test how primary health care units would respond to a bird flu outbreak, according to a study published last week in Acta Médica Portuguesa and indexed by the U.S. National Library of Medicine.

The exercise comes as bird flu is simultaneously being advanced through expanded PCR surveillance, laboratory-engineered H5N1 research, and revived mRNA vaccine programs, raising questions given the similar convergence of testing, research, and preparedness measures that preceded COVID-19.

The exercise took place on February 3, 2025, and was coordinated by the Infection Prevention and Control Programme responsible for primary health care units in Northern Lisbon, within the Santa Maria Local Health Unit.

According to the authors, the event was a tabletop exercise—a structured simulation used to rehearse decision-making during hypothetical outbreaks—designed to assess whether frontline clinics could identify, isolate, and manage patients during high-risk infectious disease scenarios.  (See link for article)

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Important to note: those refusing to use PPE were seen as threats, not as patients with autonomy.

It truly appears nothing whatsoever has been gleaned from COVID tyranny.

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https://drtesslawrie.substack.com/p/urgent-attention-the-swiss-government?

URGENT ATTENTION: The Swiss Government Handed Control of a Bioweapons Lab to the WHO—What Could Possibly Go Wrong?

PLEASE SHARE WITH GRASSROOTS AND POLITICAL LEADERS ALIKE

Tess Lawrie, MBBCh, PhD​
Jan 15, 2026

Have you been wondering where the WHO will collect, store, amplify and share pathogens for its Pathogen Access and Benefit System outlined in the WHO Pandemic Treaty for future WHO-declared pandemics? Well, now we know…

Concerns about a WHO-controlled Swiss bioweapons laboratory, the Spiez laboratory, in the heart of “neutral” Switzerland led representatives of a Swiss citizens group called Swiss Association WIR to send a letter to President Trump this week requesting support.

Today I had a conversation with Christian Oesch, President of Swiss Association WIR, about the letter and more. You can listen below in link above.

“Bioweapons are never defensive – they can only ever be offensive.”~ Christian Oesch, president of the Swiss Association WIR.

For more:

Category:

Activism, Viruses

U.S. Military Uses AI to Accelerate Viral Outbreak Modeling & Funds Intranasal Spray Self-Replicating sa-mRNA H5N1 Bird Flu Vax

https://jonfleetwood.substack.com/p/darpa-uses-ai-to-push-viral-pandemic?p

DARPA Uses AI to Push Viral Pandemic Outbreak Modeling From Weeks to Days

Speed is being prioritized over scrutiny, with AI-generated models designed to justify interventions before they can be meaningfully challenged.

Jon Fleetwood
Jan 09, 2026

The U.S. military is funding artificial intelligence (AI) systems designed to drastically accelerate viral outbreak modeling—compressing a process that typically takes weeks into something that can be produced in days, then used to steer real-world interventions.

In other words, the faster the model, the less time there is to question whether the response is justified at all.

This acceleration follows DARPA’s already-documented pre-COVID pandemic infrastructure  designed to turn digital genetic sequences into synthesized viruses and mass-produced mRNA countermeasures on a fixed timeline. (See link for article)

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https://jonfleetwood.substack.com/p/us-military-funds-intranasal-spray?

U.S. Military Funds Intranasal Spray Self-Replicating sa-mRNA H5N1 Bird Flu Vaccine Built From Chimeric Viral Constructs: Journal ‘Nature Communications’

U.S. government is not slowing its push toward intranasal self-replicating RNA vaccine technology.

Jon Fleetwood
Jan 15, 2026

A U.S. military–funded research program has developed an intranasal, self-replicating RNA (sa-mRNA) vaccine targeting H5N1 avian influenza, built using chimeric viral constructs assembled through reverse genetics.

The work was disclosed in a 2026 Nature Communications paper and explicitly funded through a U.S. Army–administered biodefense contracting mechanism.

The vaccine is said to force cells to produce H5N1 bird flu antigen while simultaneously producing viral replication enzymes that copy the self-amplifying RNA inside the cell.

The U.S. government is funding the creation of next-generation bird flu vaccines while funding the creation of purported chimeric “Frankenstein” bird flu viruses.

Congress, the White House, the Department of Energy, the FBI, the CIA, and Germany’s Federal Intelligence Service (BND) have confirmed that the COVID-19 pandemic was likely the result of lab-engineered pathogen manipulation.

Why is the government making the bird flu pandemic problem and solution at the same time, just like it was doing with coronaviruses before the COVID-19 outbreak?  (See link for article)

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What could possibly go wrong?

Category:

Activism, vaccines, Viruses

The War Over Your Medical Rights: AAP Sues RFK While IMA Seeks to End Medical Mandates

The war is on…..

https://thevaccinereaction.org/2026/01/aap-and-other-medical-groups-sue-secretary-of-health-and-human-services/

AAP and Other Medical Groups Sue Secretary of Health and Human Services

by Carolyn Hendler, JD

Published 

Large medical groups including the American Academy of Pediatrics (AAP) have sued U.S. Secretary of Health and Human Services Robert F. Kennedy, Jr. in response to recent changes to federal vaccine policy, including removal of the COVID shot from the federally recommended childhood vaccine schedule for healthy children  The AAP, American College of Physicians, Infectious Disease Society of America (IDSA), American Public Health Association, Society for Maternal-Fetal Medicine, Massachusetts Public Health Alliance, and a pregnant woman filed a lawsuit in July 2025 against HHS Secretary Kennedy in the U.S. District Court for the District of Massachusetts.1

Plaintiffs alleged that changes to federal vaccine policy were made without scientific review and without following regulatory norms. They argued that the replacement of 17 members of the Advisory Committee on Immunization Practices (ACIP) and the cancellation of certain advisory meetings not only violated federal law, but also serves to erode public confidence in the public health infrastructure and the federal government’s mass vaccination program.

Plaintiffs aim to stop the vaccine policy changes implemented by Kennedy and restore the previous vaccine schedule.2 Plaintiffs further allege that the replacement of previous ACIP members created a new panel of biased members in order to support Kennedy’s views on vaccination and the harm associated with mRNA biologics such as the COVID shot.3

Federal Judge Allows Case to Continue

The government moved to have the case dismissed for lack of standing, but on Jan. 6, 2026, a Massachusetts federal judge decided that the lawsuit can continue.

In order to bring a lawsuit, a party needs standing which means they have shown they suffered actual and direct harm from the challenged action.4 Judge Brian Murphy of the U.S. District Court for the District of Massachusetts ruled that the plaintiffs have legal standing to sue the Secretary.

The government argued that the plaintiffs lacked standing to sue because they failed to show that they suffered direct harm from the new vaccine schedule and the changes that took place as a result of ACIP recommendations. However, Judge Murphy concluded that the changes at ACIP violates the requirements of the Federal Advisory Committee Act, which sets forth that membership on government advisory panels be “fairly balanced.”5  (See link for article)

Important quote:

While I am somewhat surprised that the court found that plaintiffs have standing to sue here, [the ruling] reflects misperceptions about vaccines and children’s health generally [and the decision] does not reflect the reality that the American Academy of Pediatrics and other organizations are in many respects trade organizations for their professions — primarily protecting the interests of their members, not children.7 ~ Kim Mack Rosenbert, Attorney for CHD

https://imahealth.substack.com/p/breaking-imas-national-network-of?

Breaking: IMA’s National Network of Independent Doctors Anchors New Coalition to End Medical Mandates in all 50 States

“This is the next step in bringing patient-centered reform to American healthcare. We’re mobilizing thousands of independent doctors to dismantle medical mandates state by state” – Dr. Joseph Varon

 
Independent Medical Alliance
Jan 15, 2026
 
new coalition

“This is the next step in bringing patient-centered reform to American healthcare. We’re mobilizing thousands of independent doctors to dismantle medical mandates state by state, restoring true patient-informed choice and freedom.” – Dr. Joseph Varon

The Independent Medical Alliance (IMA), a powerhouse network of independent physicians, providers, and researchers, today announced its role as a founding member of the Medical Freedom Act Coalition. Launched alongside Stand for Health Freedom (SHF) and Health Freedom Defense Fund (HFDF), this alliance unites over a dozen organizations to prohibit medical mandates in all 50 states and safeguard informed consent, parental rights, and doctor-patient autonomy.

“America’s patchwork of coercive mandates is eroding patient rights,” said IMA President and Chief Medical Officer Dr. Joseph Varon. “We’re mobilizing thousands of independent doctors to dismantle them state by state and restore true freedom of choice in healthcare decisions.”

Building on Idaho’s groundbreaking 2025 Medical Freedom Act, the coalition targets the coercive regulations eroding personal health freedoms. IMA mobilizes its tens of thousands of doctors to drive state-level reforms, ensuring no American faces discrimination over medical decisions.

“No American should fear that their medical choices will impact their right to live a normal life,” said HFDF Founder Leslie Manookian in an announcement news release.

See the full Health Freedom Defense Fund news release here. For more information, contact Lynne@IMAHealth.org.

 

Category:

Activism, vaccines

U.S. Intelligence Classified & Redacted COVID PCR Test Findings & The Replacement for PCR Has Arrived

https://jonfleetwood.substack.com/p/us-intelligence-classified-and-redacted?

U.S. Intelligence Classified and Redacted Findings on COVID-19 PCR Tests: New FOIA Documents

New records show top U.S. nuclear, national security laboratories scrutinized primers used to define the pandemic—but hid the results.

Jon Fleetwood
Jan 14, 2026

Newly released Department of Energy (DOE) records obtained by U.S. Right to Know through a Freedom of Information Act (FOIA) request show that U.S. federal intelligence agencies classified and redacted the results of an internal review of COVID-19 PCR test primers, even as those tests were used to define “cases,” drive emergency policy, and justify unprecedented social and economic controls.

The documents reveal that during the pandemic, the U.S. government quietly subjected PCR test primer sets—the molecular components that determine what PCR tests detect—to classified scrutiny by top national security laboratories, while withholding the findings from the public under national-security and intelligence exemptions.

At the center of the release is a classified internal communication titled “DRAFT memo on Primer Sets,” circulated through the DOE’s Office of Intelligence and Counterintelligence and reviewed by assay experts at Lawrence Livermore National Laboratory, Los Alamos National Laboratory, and Pacific Northwest National Laboratory.

The memo itself remains classified.

Its conclusions were redacted.

No public explanation was ever provided.

PCR Testing Was Treated as a Classified Intelligence Issue

PCR tests do not detect an intact virus and do not prove infection.

They work by using short genetic sequences—primers—to bind to matching genetic material and amplify it until a signal is detected.

What a PCR test detects depends entirely on what its primers bind to. (See link for article)

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**Comment**

What this means is while the public was repeatedly told COVID testing was reliable, specific, and settled science, the test was never handled in a public scientific manner but as a classified intelligence issue.

This should tell you everything you need to know, but it’s actually far worse.

In 2020 we were warned about the CDC’s monopolized COVID testing – something those in Lymeland have had to live with for over 40 years.

Experts have now shown repeatedly that the genetic sequences used in PCRs to detect suspected SARS-CoV-2 as well as the flu, and to diagnose cases of illness and death attributed to Covid-19 are present in dozens of sequences of the human genome itself and in those of about a hundred microbes. And that includes the initiators or primers, the most extensive fragments taken at random from their supposed “genome” and even the so-called “target genes” allegedly specific to the “new coronavirus”.

The test is worthless and all “positive” results obtained so far should be scientifically invalidated and communicated to those affected; and if they are deceased, to their relatives. Stephen Bustin, one of the world’s leading experts on PCR, in fact says that under certain conditions anyone can test positive.

https://www.thefocalpoints.com/p/the-replacement-for-pcr-tests-has?  Go here for article & video interview

The Replacement for PCR Tests Has Arrived

Dr. Roger Hodkinson breaks down how MultiSeq could replace PCR and fix infectious disease testing with multi-target panels and confirmatory Sanger sequencing.
Nicolas Hulscher, MPH
Jan 13, 2026

The COVID era exposed a diagnostic failure that can no longer be ignored: PCR-based testing is not a true “gold standard” for clinical infection diagnosis. PCR is widely treated as definitive, but mechanistically it is not an identification method—it is an amplification step that simply makes more copies of genetic material. The real weakness comes from what many systems use after amplification: probe-based fluorescence detection, which generates a “signal” without actually confirming what is present. That is how medicine ends up with false positives, misclassification, and policy decisions built on unstable data.

In my interview with Dr. Roger Hodkinson—a highly respected pathologist and Chairman of MultiSeq—he explains why the PCR problem is structural: probe-based testing functions like a “lock-and-key,” where partial matches can still trigger a positive signal. Even worse, infectious syndromes (cough/cold, diarrhea, suspected STI) are rarely caused by only one organism—yet most PCR workflows are narrow, slow, and often treated as confirmatory when they’re not. In practice, clinicians are forced into an “educated guess” model because results frequently come back days later and only cover a limited scope.

MultiSeq is attempting to replace this entire model with something fundamentally different: sequence-confirmed diagnosis. Instead of relying on probe fluorescence to “suggest” identity, it uses modified Sanger sequencing to directly read the nucleotide sequence and confirm which pathogen is actually present.  (See link for article & video)

Category:

Activism, Testing, Viruses

Treating Lyme & TBDs on a Budget With Herbs

Webinar: Treating Lyme and Tick-Borne Diseases on a Budget

Date: Wednesday, March 18

Time: 6:00-7:00 PM ET

Presenter: Teresa Holler, MS, PA-C, FMAPS

Free to ILADS members/$49 for non-members

Register Here

Description:

Teresa will discuss a simple, effective, and well researched approach to utilizing herbals in the management of Lyme disease, bartonella, and babesia. Participants will leave the presentation with treatment options that are easy to implement.

Upon completion of Teresa’s presentation, participants will be aware of the following:

• Unique signs and symptoms to help differentiate between borrelia, bartonella, and babesia by history and physical exam
• What causes microbial persistence and how to address these difficulties
• Awareness of clinical studies comparing several antibiotic protocols to herbal products
• Review the properties of the most efficacious herbs for the treatment of Lyme disease, bartonella and babesia.

This webinar will be recorded and sent to all registered attendees.

Available through ILADS

To access the FREE 1.5 hour ILADS December webinar titled “At the Frontlines of Chronic Illness: A Conversation with ILADS Experts”, go here.

It features ILADS panelists:

  • Chris Winfrey, MD
  • Melanie Stein, ND
  • Nicole Bell (Galaxy Diagnostics)
  • Tania Dempsey, MD responding to patient questions

Category:

Activism, Babesia, Bartonella, Herbs, Lyme, Treatment