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EPA Approves 2nd ‘Forever Chemical’ Pesticide in Two Weeks & Cloned Meat Reportedly Circulating Without Labels

https://organicconsumers.org/trump-epa-approves-its-second-forever-chemical-pesticide-in-two-weeks/

Trump EPA Approves Its Second ‘Forever Chemical’ Pesticide in Two Weeks

November 20, 2025 | Source: Center for Biological Diversity

WASHINGTON— The Environmental Protection Agency today approved the highly persistent pesticide isocycloseram for golf courses, lawns and food crops such as oranges, tomatoes, almonds, peas, and oats. The pesticide is a “forever chemical” — one of a group called PFAS, or perfluoroalkyl and polyfluoroalkyl substances.

Today’s announcement marks the second approval of a PFAS pesticide since Trump took office, with the first approval coming just two weeks before. The administration plans to approve three more PFAS pesticides in the coming year.

“To approve more PFAS pesticides amid the growing awareness of the serious, long-term dangers from these forever chemicals is absurdly shortsighted,” said Nathan Donley, environmental health science director at the Center for Biological Diversity. “The undeniable reality is that the Trump administration is knowingly putting the nation’s children at greater risk of developing serious reproductive and liver harms for generations to come.”

Isocycloseram is classified as moderately persistent to persistent and is known to transform into 40 smaller PFAS chemicals, some of which are much more highly persistent.  (See link for article)

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Cloned Meat Reportedly Circulating in U.S. Food Supply Without Labels

November 24, 2025

By the National Health Federation
According to a report from Slay News, unlabeled cloned “beef” and “pork” are already being sold in American supermarkets and restaurants, raising serious transparency and safety concerns. Slay News

Under existing FDA rules, meat from cloned animals and their offspring is considered “safe and nutritious,” while the agency does not require any special labeling. Slay News+2CBS News+2  Unlike the FDA, Health Canada recently paused a plan to greenlight cloned meat without safety reviews or labeling after public backlash. The situation in Canada has amplified public scrutiny.

Critics, such as the National Health Federation (NHF), have long contended that these policies deprive consumers not only of the basic right to know what they’re eating but of healthy food as well. Moreover, the NHF and others raise a range of concerns, from ethical and animal-welfare issues to long-term health risks and lack of genetic stability.

As manufactured “demand” for synthetic or biotechnologically derived foods is pushed upon consumers, they increasingly reject this “fake” food and are calling at least for clearer labeling rules and a reexamination of the FDA’s earlier approval of cloned meat from as far back as 2008, so that informed consumers can avoid this unhealthy food, which is also reportedly found in soup.

It has been reported on X that Campbell’s Soup is using bioengineered meat (printed from a 3D printer) in its soup, as per Campbell’s Soup Vice President Bally in a supposed “rant” that he made at a meeting about the poor quality of the company’s products. Campbell’s Soup denies the poor-quality claim but has not, to NHF’s knowledge, addressed the real issue of whether or not it is indeed using 3D-printed meat in its soups.

The Florida State Attorney General, James Ulthmeier, was concerned enough to announce on X that the State’s Consumer Protection Division is launching an investigation into the quality of Campbell’s products. He said, “Florida law bans lab-grown meat. Our Consumer Protection division is launching an investigation and will demand answers from Campbell’s.”

As NHF President Scott Tips says, “Instead of aiming for healthier and more nutrition-dense foods for consumers, food companies are taking the low road of developing highly processed foods with very low nutritional value that can also actually pose a health risk. We see this at Codex Alimentarius meetings of late, where the INGO front groups representing food manufacturers are pushing for the global adoption of standards that would allow them to sell this lab-grown ‘Franken-meat’ worldwide. And there are not even adequate label warnings that would allow consumers to differentiate between the ultra-processed meat and the traditional. If consumers were informed, then they could exercise their free-market power to drive the fake meat out of the marketplace by refusing to buy it.”

For more:

Measles Confusion: Vaccine or Virus?

You won’t hear this on the evening news…..

https://jonfleetwood.substack.com/p/95-of-infants-develop-fever-after?

95% of Infants Develop Fever After Measles Vaccination, 16% Develop More Serious Measles-Like Symptoms: Journal ‘BMC Infectious Diseases’

In 7 out of 10 vaccinated children with measles-like illness, health officials could not tell if the vaccine pathogen or a wild measles virus caused it.

A 2025 Shandong province CDC-authored study confirms that vaccinated infants, not unvaccinated, frequently develop clinically measles-like illness caused by live attenuated vaccine virus, and that these post-vaccination illnesses are often indistinguishable from wild measles in surveillance systems, contaminating official measles case data.

The study showed 95.24% of vaccinated infants developed fever, 16.40% developed measles-defining symptoms, ~70% of cases could not be genetically classified, and when classification succeeded, 90.91% matched the vaccine strainestablishing vaccine-derived illness as a measurable contributor to reported measles cases.

That means many measles cases routinely cited by the mainstream media could be caused by the measles vaccine itself, not a “wild” virus.

The study, “Molecular and epidemiological analysis of measles vaccine-associated rash illnesses in Shandong province, China, 2014–2021,” was published last week in BMC Infectious Diseases. (See link for article)

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**Comment**

It’s important to note that the CDC obfuscates vaccine data is by classifying 95% of measles cases as ‘unvaccinated or unknown’two fundamentally different categories.

The agency purposely merges unknown cases with unvaccinated ones maximizing the association between measles cases and non-vaccination while obscuring uncertainty in the data.  It purposely does not apply the same logic in reverse – merging ‘unknown cases with vaccinated cases maximizing the association between measles cases and vaccination, which very well could be true.

This allows them to smugly reinforce a predetermined narrative.

The MMR vaccine contains a live measles virus that was created through a laboratory process U.S. military biodefense experts state “could be considered, by current definitions, gain-of-function research.”  Peer-reviewed studies further document vaccine-strain replication and shedding, measles-like illness following vaccination, and frequent inability to distinguish vaccine-strain illness from wild measles in symptomatic cases.

For more:

Download the Measles Fact Sheet

Gates Pours $3.3M into mRNA Purification Tech- Admitting COVID Vax Impurity Problem as Platform Becomes Permanent

https://jonfleetwood.substack.com/p/gates-pours-33m-into-mrna-purification?

Gates Pours $3.3M Into mRNA Purification Tech—Admitting COVID Vaccine Impurity Problem as Platform Becomes Permanent

Press release admits current mRNA-based vaccine are not effective enough and contain too many impurities.

Despite mainstream attempts to downplay the alarming contamination problem plaguing COVID-19 vaccines, the Gates Foundation has awarded $3.3 million to a team of scientists at New York’s Rensselaer Polytechnic Institute (RPI) to develop “breakthrough purification technologies” for producing mRNA-based vaccines.

A September Autoimmunity study confirms that both Pfizer-BioNTech and Moderna’s mRNA COVID-19 injections contain many hundreds of times more contamination than the FDA and WHO limit.

The grant is an implicit admission that contamination is in fact a problem posed by mRNA vaccines, as well as a sign that the platform is here to stay.  (See link for article)

Important excerpt:

Despite the disease, hospitalizations, and deaths linked to mRNA jabs, the technology isn’t going anywhere.

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The following contaminants have been found by researchers in the vials:

    1. At least 55 undeclared chemical elements
    2. Green Monkey DNA
    3. metals, including graphene
    4. parasites and eggs
    5. moving “self aware” organisms
    6. hexagonal crystalline structures with 4-sided rectangular structures with regularly spaced dots in the form of a grid
    7. particulate foreign matter
    8. PEG
    9. nanotechnology
    10. lipid nanoparticle
    11. gene sequence that forces your body to make a foreign spike protein
    12. black particles
    13. white floating matter
    14. impurities from human fetal cell lines

Federal Roundtable Lyme Disease Reflections

By Project Lyme

Federal Roundtable Reflections

On December 15, 2025, the U.S. Department of Health and Human Services (HHS) convened a public roundtable, “Invisible Illness: Leading the Way with Lyme Disease,” bringing renewed federal attention to Lyme disease and related tick-borne illnesses. The discussion was moderated by HHS Secretary Robert F. Kennedy Jr., who shared personal family experiences with Lyme disease—including his own uncomplicated recovery, a son who experienced Lyme-induced Bell’s palsy, and another who continues to live with chronic Lyme disease.

Secretary Kennedy’s statement that the “gaslighting of Lyme patients is over” marked a notable shift in tone and approach, signaling a federal commitment to patient-centered care, scientific rigor, and collaboration across government, medicine, and advocacy. For a community that has long struggled to be seen and believed, this visibility matters.

Participants included senior HHS leadership such as CMS Administrator Dr. Mehmet Oz and NIH Director Dr. Jay Bhattacharya; Members of Congress, including Senator Susan Collins (ME), Congressman Morgan Griffith (VA), and Congressman Chris Smith (NJ); as well as patients, advocates, clinicians, researchers, and innovators. Project Lyme was represented by Executive Director Michelle Cuevas and Board Chair Ali Moresco.

The conversation emphasized Lyme disease as an often-overlooked invisible illness, highlighting persistent challenges related to diagnosis, access to care, and the validation of patient experiences. Key announcements included the renewal of the LymeX Innovation Accelerator—a major public-private partnership with the Steven & Alexandra Cohen Foundation focused on advancing diagnostic tools—and clarification that Medicare coverage includes Lyme-related care, including guidance on chronic care management.

HHS reaffirmed four core priorities closely aligned with Project Lyme’s mission: strengthening medical education, investing in innovation, expanding prevention and public awareness, and improving insurance coverage. There was explicit recognition of the complexity and persistence of Lyme disease, including infection-associated chronic conditions, alongside a call to address stigma and misinformation.

HHS also unveiled an updated centralized federal Lyme disease website, signaling increased national coordination. As we look ahead, this moment presents an opportunity to align priorities, partnerships, and resources to advance focused, actionable solutions that drive meaningful and lasting change.

http://

Lyme Disease Roundtable

Dec. 15, 2025

Secretary Kennedy Convenes Lyme Disease Patients and Providers to Announce New Diagnostic Efforts

 

CDC Flu PCR Primers Match Human DNA Across the Genome

UPDATE:

BLAST analysis shows that the CDC’s measles RT-PCR forward primer, reverse primer, and fluorescent probe all have near-perfect contiguous matches to the human genome, which means the positive test is based on human genetic material rather than measles virus itself.

https://jonfleetwood.substack.com/p/cdc-flu-pcr-primers-match-human-dna?

CDC Flu PCR Primers Match Human DNA Across the Genome: New BLAST Data

Are we detecting viruses or ourselves?

The CDC’s ‘Influenza SARS-CoV-2 (Flu SC2) Multiplex Assay’ is a real-time reverse-transcription polymerase chain reaction (rRT-PCR) laboratory test used to detect influenza A, influenza B, and SARS-CoV-2 in upper or lower respiratory samples.

Mainstream health authorities use PCR tests to quantify how many infection cases there are.

Case numbers are used to declare pandemics and justify pandemic response measures like lockdowns, masking, social distancing, and vaccination campaigns.

But what if these tests aren’t detecting viruses?

What if they’re detecting human DNA?

That would mean the primary justification for pandemic declarations is built on signals that may not represent viral infection at all, but amplified fragments of the human genome—calling into question the scientific basis for case counts, emergency powers, and every downstream policy decision tied to them.

Scrutiny of the PCR test is warranted, given the high likelihood of an incoming bird flu pandemic and the international coordination documented on this website.

A new BLAST analysis of the CDC’s Influenza SARS-CoV-2 (Flu SC2) Multiplex Assay reveals that every variant of the influenza A forward primer, reverse primer (across all ambiguity resolutions), and probe independently produces dozens to over 100 significant partial matches—often perfect over 15–18 bp core segments—scattered across nearly every human chromosome, establishing widespread human genomic homology.  (See link for article)

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**Comment**

This is not the first person to notice this troubling issue.

The genetic sequences used in PCRs to detect suspected SARS-CoV-2 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!

In this report we are going to add the results of a particular research we have done from the data published on the alleged SARS-CoV-2 and on the protocols endorsed by the WHO for the use of RT-PCR as well as the data corresponding to the rest of the “human coronaviruses”. And the conclusions are extremely serious: none of the seven “human coronaviruses” have actually been isolated and all the sequences of the primers of their respective PCRs as well as those of a large number of fragments of their supposed genomes are found in different areas of the human genome and in genomes of bacteria and archaea, such as these: Shwanella marina JCM, Dialister succinatiphilus, Lactobacillus porcine, Lactobacillus manihotivorans, Leptospira sarikeiensis, Bizionia echini, Sanguibacteroides justesenil, Bacteroides massiliensis, Lacinutrix venerupis, Moraxella bovis, Leptospira saintgironsiae, Winogradskyella undariae, Acetobacterium puteale, Chryseobacterium hispanicum, Paenibacillius koleovorans, Tamiana fuccidanivorans, Fontibacillua panacisegetis, Ru bacter ruber , Skemania piniformis, Chryseobacterium shigense, Caloramator peoteoclasticus, Cellulosilyticum ruminicola, Nitrosopumilius evryensis and a long list of others.  Go here for research showing that those claiming to have isolated coronaviruses relied on ‘isolates’ of previous ‘human coronaviruses,’ as well a the sequences of covid are found in both humans and numerous microbes.

Read this informative article by Dr. Mullis, the creator of the PCR on how it was never intended to be used to diagnose people.

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