https://popularrationalism.substack.com/p/avian-flu-pandemic-or-pandemonium?

AVIAN FLU PANDEMIC OR PANDEMONIUM?

I Tried to Warn You All About the False Positives from Non‑Quantitative RT‑PCR on SARS‑CoV‑2

No One Acted.
Now AIV H5 RT‑qPCR Is Set to Repeat the Same Catastrophe.

The Pandemaniacs Are Everywhere. Proper standards for nucleic acid testing will keep them at bay. The time to act is NOW. Tomorrow, it could be too late. I urge you to read and act.

President, IPAK | Founder IPAK-EDU.org | Founder, NAATEC
Dec 01, 2025

The settings for a COVID 2.0 Pandemic of False Positives are all in place. “We must catch every case” is no excuse to misdiagnose individuals and let them cook and potentially die at home quarantined w/untreated, misdiagnosed bacterial pneumonia or other less virulent respiratory illnesses.

We could have saved millions and millions of lives if people had understood and acted in April 2020: False positives in PCR tests drove the COVID-19. We must not allow a repeat with avian flu.

In 2020, I warned—publicly, repeatedly, in articles, podcasts, and tweets, and with evidence, fighting censorship all the way—that using non‑quantitative RT‑PCR as the primary driver of pandemic policy would guarantee a tidal wave of false positives, distort epidemiology, and weaponize diagnostic noise as public fear. Those warnings were not vague or speculative; they were precise, technically grounded, peer‑reviewed, and absolutely correct.

I explained that without internal negative controls for Ct‑stratification, nested PCR confirmation, or sequencing, PCR tests would be repurposed into fear‑amplifiers rather than disease‑detectors. I warned that once governments built policy on raw PCR counts and arbitrary Ct values, no one would be able to distinguish real outbreaks from diagnostic artifacts. I said we would lose the ability to tell signal from noise, disease from contamination, and epidemiology from hysteria. I knew I was right. But too few could understand how central the diagnostic grift was the COVID-19 fear mongering.

People in high places heard the warnings. They understood them. I know, because I warned Peter Marks at US F.D.A. And others.

And he and the others who knew did nothing. Millions died after developing severe, untreated, misdiagnosed bacterial pneumonia.

That inaction helped create a world where some actors benefited from chaos—whether through political leverage, pharmaceutical opportunism, or supranational control frameworks. Call them what they are: enemies of stability who thrive when populations panic.

I warned too early. Nothing happened.

But then they came after all of our jobs. All of them. That got our attention. But cataclysmic damage was already done, including millions of deaths due to misdiagnosed and untreated bacterial pneumonia and sepsis.

We Must Call them “PANDEMANIACS”

Now, those same forces stand ready to exploit the next diagnostic mirage. Pandemaniacs are all over Twitter, Bluesky, everywhere posting one-off references to H5N1 as an inevitable next pandemic.

We must hold the line: NO PROOF OF SEQUENCE? NO DIAGNOSIS. NO CASE Count. NO NESTED CONFIRMATION. NO CURVE. NO PANDEMIC.

This is the line.
This is the standard.
This is the bright red boundary that must not be crossed again.

If sequencing is not performed, then PCR positives are NOT clinical cases, NOT epidemiological evidence, and NOT a valid basis for public‑health actions.

(See link for article)

______________

**Comment**

Spread the word and stand your ground.  

Refuse to be moved by fear tactics and those spouting a ‘follow the science’ mantra who are merely spreading and following a narrative.

Weiler rightly demands the following:

  • 100% nested RT‑PCR + Sanger sequencing of all early outbreak samples until ≥300 true positives are confirmed.
  • 2 to 20% ongoing sequencing confirmation, stratified across Ct bands (<25, 25–30, 30–35, >35), laboratories, and sample types to provide N>1000 empirical votes on SN, SP, FPR, and FDR.
  • Full disclosure of Ct distributions, LoD, assay design, primer/probe sequences, and sequencing confirmation rates.
  • Immediate audits of any laboratory with a confirmation rate <80% in any sample category.
  • Mandatory sequence deposition in open databases.
If a lab cannot meet these standards, it should not be generating case counts. Period.

Weiler points out:

A recent re‑analysis of a nationwide dataset (the German “ALM” consortium, which handled ~90% of the country’s SARS‑CoV‑2 PCR testing) found that when cumulative RT‑PCR positives were compared against later IgG seroconversion data, the scaling factor that best fit the observed antibody curves was 0.14 — meaning only ~14% of PCR-positive individuals ever developed detectable antibodies, consistent with actual infection.

Fourteen percent stopped the world, quarantined people, separated family members, foisted an unproven medical device on the populace which caused people lose their jobs for refusing it, and abandoned truly sick people.

For more:

https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-memo-links-10-child-deaths-covid-vaccines-nyt-reports-2025-11-29/

US FDA memo links 10 child deaths to COVID vaccines

By Reuters

WASHINGTON, Nov 29 (Reuters) – COVID-19 vaccinations probably contributed to the deaths of at least 10 children who died of heart inflammation, U.S. Food and Drug Administration chief medical and scientific officer Vinay Prasad told agency staffers.
“These deaths are related to vaccination (likely/probable/possible attribution made by staff),” Prasad wrote in a Friday memo seen by Reuters. “This is a profound revelation. For the first time, the U.S. FDA will acknowledge that COVID-19 vaccines have killed American children.”
Health Secretary Robert F. Kennedy Jr. has sharply changed government policy on COVID vaccines, limiting access to them to people 65 and older, as well as those with underlying conditions. Kennedy, a longtime anti-vaccine crusader before taking on the nation’s top health post under President Donald Trump, has also linked vaccines to autism and sought to rewrite the country’s immunization policies.
During Trump’s first term, when the pandemic erupted, and subsequently under his successor Joe Biden, U.S. health officials strongly endorsed the vaccines as lifesaving. The COVID-19 vaccines were released in 2020.
The memo did not disclose the health conditions of the children, or the vaccine manufacturers involved. The findings were based on an initial analysis of 96 deaths between 2021 and 2024, which Prasad said “concludes that no fewer than 10 are related” to COVID-19 vaccinations.
“It is difficult to read cases where kids aged 7 to 16 may be dead as a result of COVID vaccines,” Prasad wrote in the memo.
He announced plans to tighten vaccine oversight.  (See link for article)
__________________
**Comment**
Please remember that after THREE deaths from the Swine Flu vaccine, it was halted in nine states.  The entire program ended with only 20% of the population vaccinated due to reports of GBS.
How many more deaths will it take before they pull an ineffective but dangerous experimental gene therapy shot?
A twice-censored paper has shown that 74% of deaths were independently adjudicated as directly due to or significantly contributed to by COVID-19 vaccination.  Another paper has shown the gene therapy injections caused nursing home deaths to soar.
For more:

https://childrenshealthdefense.org/defender/chd-tells-fcc-protect-people-or-get-out-of-the-way-radiation-exposure

‘New Phase of Attack’: Children’s Health Defense Tells FCC to Protect People, or ‘Get Out of the Way’

In a motion filed today with the Federal Communications Commission (FCC), CHD urged the agency to comply with a 2021 court order to review evidence that radiation at levels currently allowed by the agency harms people, especially children, and the environment. If the agency ignores the motion, CHD is prepared to take the matter back to court.

Children’s Health Defense (CHD) is prepared to take the FCC back to court if the agency doesn’t comply with a 2021 court order directing it to review 11,000 pages of evidence supporting claims that wireless radiation at levels currently allowed by the FCC harms people — especially kids — and the environment.

In a motion filed today with the Federal Communications Commission (FCC), CHD urged the agency to collaborate with the U.S. Department of Health and Human Services (HHS) to set wireless radiation exposure limits that protect public health.

Miriam Eckenfels, director of CHD’s Electromagnetic Radiation (EMR) & Wireless Program, said the motion represents a “new phase of attack” against the FCC for its failure to comply with the 2021 court order.

“The document essentially tells the FCC to either protect people, or get out of the way and let other federal agencies, like HHS, set health and safety limits for wireless radiation exposure,” Eckenfels said.

The filing is important “because before we can go back to the D.C. Court and complain that the FCC hasn’t complied, we have to show that we’ve tried telling the FCC that they need to do what the court asked,” she added.

If the agency still doesn’t comply soon, CHD will be in a position to take the FCC back to court, she said.  (See link for article)

For more:

https://jonfleetwood.substack.com/p/fda-chief-says-lyme-disease-came

FDA Chief Says Lyme Disease Came from U.S. Military Lab 257, Suggests HIV Came from African Lab (Video)

“It came from Lab 257 on Plum Island.”

In a stunning exchange on the PBD Podcast (Episode 690), U.S. Commissioner of Food and Drugs (FDA) Dr. Marty Makary, a Johns Hopkins surgeon, dropped two bombshell admissions about pathogen origins—one about HIV, the other about Lyme disease.

Dr. Makary openly entertained the possibility that HIV “may very well have come from a lab in Africa,” saying the film Thank You, Dr. Fauci “explore[s] a non-traditional narrative, which has not gotten the attention it deserves.”

HIV (Human Immunodeficiency Virus) is said to be a retrovirus that targets and destroys CD4 T cells in the immune system, weakening the body’s ability to fight infections and potentially leading to AIDS if untreated.

When asked where Lyme disease originated, Makary answered directly: “I can tell you with a high degree of probability. It came from Lab 257 on Plum Island.”

Lyme disease is a bacterial infection caused by Borrelia burgdorferi, transmitted through bites from infected blacklegged ticks, often marked by an expanding “bull’s-eye” rash, fever, fatigue, and joint pain.

The head of the FDA has admitted that two major diseases originated not in nature, but in government laboratories, raising questions about other disease origins.  (See link for article)

________________

**Comment**

Here’s the brief 5 minute portion of the interview pertaining to HIV and LymeScroll to 2:44 hear the bit on Lyme disease.  Go here for entire interview.

For years, Lyme advocates have been gaslit for stating the exact same words Makary said.

In fact, after waiting an entire year for Representative Chris Smith‘s (R-NJ) proposed amendment passed by the House of Representatives directing the government’s ‘watchdog’ agency to investigate the DOD’s possible weaponization of ticks and other insects with Lyme disease, the inspector general at the Pentagon didn’t have the bandwidth to launch an investigation. (Translation – I don’t have any balls and I’m passing the football to someone else), so then it headed to the Government Accountability Office (GAO).  Ultimately, the Senate rejected the amendment for the GAO to investigate whether Lyme came from a Pentagon research laboratory

And despite an investigation into five NJ school districts revealing devastating effects of Lyme disease on the children there, cries have fallen on deaf ears.  The CDC refused to publish the school study despite telling the advocate that they would.

So while Makary affirms what we all know, the following problems remain:

https://mailchi.mp/ilads.org/upcoming-webinar-with-dr-tom-moorcroft-

ILADS WEBINAR

Wednesday, December 17, 7 PM ET/4 PM PT

At the Frontlines of Chronic Illness:
Conversations with ILADS Experts

Join us on Wednesday, December 17 at 7 PM ET for a public webinar, bringing together leading voices in the field of Lyme disease to answer your most pressing questions and provide clarity on some of the most misunderstood illnesses of our time.

This dynamic conversation will feature an expert panel of ILADS member clinicians and specialists: Eboni Cornish, MD, Chris Winfrey, MD, Melanie Stein, ND, Nicole Bell and Tania Dempsey, MD. Whether you’re a patient, caregiver, or simply curious about Lyme disease and other infection associated chronic conditions and their impact, this webinar is designed to empower you with knowledge, guidance, and hope.

This is a unique opportunity to hear directly from experts at the forefront of integrative and personalized Lyme care. This webinar is a part of supporting ILADS and ILADEF this holiday season. If you are able, please consider making a donation to ILADEF this holiday season. Your gift opens the door to knowledge that heals.

REGISTER NOW