Our mission, as God-fearing and God-loving patriots, is to defend this Constitutional Republic and to increase its greatness, in all good things and ways, by using our voices in free but courteous speech, by discussing the happenings of the world and coming to a profound understanding of those things, and by sharing and promulgating these Truths on both this platform and others.
The vintage image of a doctor’s office sign for today’s offering header is courtesy of iStock and Google Images. Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: AI-generated items in today’s offering will be cited as such. If readers wish to post AI-generated items in today’s discussion thread, they must cite their source. Thank you. >>>>>>>>>>>>>>>>>>>> The AMA Wants Americans to Take More Poison “Vaccines” Note: AMA stands for the American Medical Association, a private organization founded in 1847. The AMA currently has approximately 270,000 members (https://www.ama-assn.org/.) The organization has a large and powerful lobbying presence on Capitol Hill. The subject of today’s offering is a JAMA Learning interview (Journal of the American Medical Association) by JAMA Deputy Editor, Preeti Malani, MD, MPH, with former Director of the CDC Rochelle Wolansky, MD, MPH. Please see: https://edhub.ama-assn.org/jn-learning/audio-player/19096301, “Influenza, RSV, and COVID-19 Vaccines: Effectiveness, Safety, and Trust in 2026.” Note that Dr. Wolansky, as Director of the CDC from 20 January 2021 until 30 June 2023, was one of the prime figures in the implementation of Operation Warp Speed; she resigned from the CDC after the COVID-19 pandemic was declared ended on 11 May 2023 (https://archive.cdc.gov/.) Dr. Wolansky is currently a professor at the Harvard University School of Medicine. The following are four items from the Transcript of Dr. Malani’s interview with Dr. Wolansky:
The copyrighted items above are from the American Medical Association, and are available on the Internet.
Dr. Wolansky is a co-author of the following report, produced by the AMA in conjunction with the Vaccine Integrity Project (https://vax.integrity.cidrap.umn.edu), itself a division of CIDRAP (Center for Infectious Disease Research and Policy, https://cidrap.umn.edu.) It appears, in Yours Truly’s opinion, that the Vaccine Integrity Project views itself as an “ACIP / CDC replacement vaccine recommendations organization”, since the actual ACIP group was disbanded by Federal Judge Brian E. Murphy earlier this year, and that there is no current ACIP roster past 24 July 2026 (https://www.cdc.gov/acip/membership/roster-archive.html.) The Vaccine Integrity Project, in conjunction with the AMA, released its’ “independent vaccine evidence” report on 2 September 2026: https://www.ama-assn.org/press-center/ama-press-releases/ama-vaccine-integrity-center-unveil-independent-vaccine-evidence. The summary of the “recommendations” of this “ACIP / CDC replacement vaccine recommendations organization” is here: https://www.ama-assn.org/system/files/vip-reviews-highlights.pdf; which “recommendations” are, of course, that all Americans continue to take: the RSV “vaccine” the COVID-19 bioweapon “vaccines” the influenza vaccines (see above regarding Dr. Wolanky’s enthusiastic endorsement of mRNA-1010 (mFLUSIVA). Translation: Establishment Medicine (the AMA; the Vaccine Integrity Project; the American Academy of Pediatrics; the American College of Obstetricians and Gynecologists — all prime examples) is continuing to “recommend” that Americans continue to “follow the science”, to “listen to the trusted messengers”, and have more of the above injectable poisons put into their bodies.
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Hulscher, et al., have just published a paper on Zenodo which proves that CHILDREN who take COVID-19 bioweapon “vaccines” are at higher risk for developing anxiety / autism / ADHD / needing Special Education services: https://www.thefocalpoints.com/p/breaking-study-covid-19-vaccination-9fd. “BREAKING STUDY: COVID-19 “Vaccination” of Children Linked to AUTISM, ADHD, ANXIETY, and SPECIAL-ED Use”, Nicholas Hulscher, MPH, 5 October 2026. Note: there is an AI-generated image in this article. Please see the screenshots, below, from the Hulscher piece:
The paper is found here: https://zenodo.org/records/23165256, “Neurodevelopmental Outcomes in COVID-19 Vaccinated Versus Unvaccinated U.S. Children: Analysis of the National Health Interview Survey 2022 – 2024”, Nicolas Hulscher, MPH, John Catanzano, NMD, PhD, et al.; 5 October 2026. Please see the screenshot of the Conclusions of this paper, below:
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Americans must educate themselves regarding the dangers of the injectables that they are “recommended” to take, or for injectables that are “recommended” for their children. Demand to see the healthcare provider Package Insert for the injectable, NOT the “dumbed-down” Information Sheet for Patients and Caregivers for the product. Read the healthcare provider Package Insert. Ask the healthcare provider to clarify or explain any questions. Ask WHY the injectable is being “recommended” for the patient. Yes, there are circumstances where an injectable drug may be indicated or necessary — however, the patient has the right to ask the reasoning behind the indication. In Yours Truly’s opinion, the “good old days” of blindly rolling up the sleeve and “taking the shot” are finished.
Peace, Good Energy, Respect: PAVACA1
(Intellectual Property Disclaimer and Notice: Except for the linked URLs and other items available on the Internet in today’s offering, the ideas and/or opinions above are by PAVACA1 (M.E. Forbes, aka M.E.C. Forbes.) Credit must be given to PAVACA1 if ideas and/or opinions in today’s offering are used by other blog writers; by podcasters; or in print or social media.)
The free image of the trumpets of the Battle of Jericho for today’s offering header is courtesy of Shutterstock and Google Images. Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: AI-generated items in today’s offering will be cited as such. If readers wish to post AI-generated items in today’s discussion thread, they must cite their source. Thank you.
Dismantle Them. Salt the Ground. Start All Over Again. Do It Right Next Time: Part Two
The focus of today’s offering regards the continuing issues and situations with respect to: One: non-modRNA-based “vaccines”; Two: the “revolving door” between the FDA and Big Pharma / Big Donors; and, Three: medical lobbyists and Establishment Medicine organizations keeping the “vaccine religion” going. What follows are what may be called “snapshots” of each area.
One: non-modRNA-based vaccines: Please see: https://kirschsubstack.com/p/a-list-of-evidence-consistent-with, “A list of evidence consistent with the hypothesis that “vaccines cause autism””, 12 September 2026. There are 30 items on the list. Two examples from the list: Number 17: “Aluminum concentration in the brains of autistic kids are among the highest measured (Exley 2017 study.) The title of the Exley, et al. paper: “Aluminum in brain tissue in autism”, Christopher Exley, et al.; Journal of Trace Elements in Medicine and Biology, Volume 46, March 2018, Pages 76 – 82; and, Number 31: “Vaccines cause autism in baby monkeys. What is different about people that it wouldn’t also cause autism in people?” Please see the screenshot from the Kirsch article regarding Number 31, below:
Granted, the study concerned the effects on infant macaque monkeys. However, the vaccines used were ones approved for human use. In Yours Truly’s opinion, even if thimerosal (mercury compound) were completely removed from all vaccines, there possibility still remains that negative effects could occur due to the other ingredients.
Two: the “revolving door” between NIH / NIAID: Here is a prime example of this “revolving door”: Mark Raza, the former chief counsel for the FDA, and who had just left that agency — was immediately hired by a very large Big Pharma-connected law firm. Please see: https://aaronsiri.substack.com/p/the-revolving-door-the-media-wont, “The Revolving Door the Media Won’t Expose”, 15 September 2026. Also, please see:
The now former chief counsel at FDA, which receives half its revenue from pharma, now gets a cushy job at a major law firm that directly represents pharma companies.
He’s not alone: the law firm also recently hired the former chief of staff at FDA and the former director of…
Note the mention of hiring numerous other FDA former employees, in addition to now having Mr. Raza on their roster.
But wait, there’s more! Please see: https://www.2ndsmartestguyintheworld.com/p/the-fda-is-a-criminal-cia-handled, “THE FDA IS A CRIMINAL CIA-HANDLED “HEALTH” AGENCY: Former FDA Chief Counsel Now Hired By Major BigPharma Law Firm”, 13 September 2026. In this article, there is a list of former FDA employees who now work for Big Pharma (or are connected with Big Pharma.) Examples from this list: Dr. Peter Marks, MD (former CBER director, FDA) —> now working for Big Pharma company, Eli Lilly; Mark McClellan (former FDA employee tasked with regulating Johnson & Johnson) —> now a board member of Johnson & Johnson; Dr. Scott Gottlieb, MD (former FDA commissioner in charge of regulating PfizerUSA) —> now on the board of directors for PfizerUSA; Dr. Stephen Hahn, MD (former FDA commissioner in charge of regulating Moderna) —> now Chief Medical Officer of Flagship Pioneering, the venture capital firm that bankrolls Moderna drug and “vaccine” development.
Three: medical lobbying and Establishment Medicine keeping the “vaccine religion” going: First, regarding medical lobbying: Pharmaceutical companies and Establishment Medicine (the American Medical Association [AMA]; the American Academy of Pediatrics {AAP]; and other similar medical professional organizations) have a “vested interest” in wielding influence in both chambers of the US federal government. Contributing to political campaigns for members of the House and the Senate can, so to speak, produce results that benefit these companies and professional medical organizations. For example, this 2023 article, from the AMA: https://www.ama-assn.org/about/leadership/how-does-ama-influence-public-policy, 22 August 2023. Which leads to this, from June 2026: https://www.ama-assn.org/system/files/ama-adocacy-impact-report.pdf. Please see the screenshots from this latter link, below. Note especially the claim in the first screenshot about how 73% of Americans “trust the AMA more than the CDC on vaccines”:
Followed by a screenshot, from the same link above, regarding the AMA’s political action committee, AMPAC:
Finally, regarding the ongoing, aggressive efforts by Establishment Medicine to “keep the “vaccine” train going”: Please see: https://www.thefocalpoints.com/p/why-do-pediatricians-blast-babies, “Why Do Pediatricians Blast Babies with Multiple Vaccines on Same Visit?”, Peter A. McCullough, MD, MPH, 12 September 2026. There is a video interview with Dr. McCullough, along with a text summary.
The “vaccines” that are currently “recommended” for children from age 0 (birth) to through age 4 years:
How can the still-forming and still-immature immune system of a child from birth until about age 7 years handle all of these antigens, especially if multiple injections of “vaccines” are administered in one healthcare visit?
It is Yours Truly’s opinion that people must educate themselves regarding: the medicines that they take; the “vaccines” that are “recommended” for themselves and their children; the ongoing efforts to gaslight the general public by Big Pharma and Establishment Medicine; the lobbying of local, state, and federal elected officials by Big Pharma; and, the current state of affairs at the FDA / CDC.
Peace, Good Energy, Respect: PAVACA1
(Intellectual Property Disclaimer and Notice: Except for the linked URLs and other items available on the Internet in today’s offering, the ideas and/or opinions in today’s offering are by PAVACA1. Credit must be given to PAVACA1 if ideas and/or opinions in today’s offering are used by other blog writers; by podcasters; or in print or social media.)
This DePat Tuesday Open Thread honors the author of the original Tuesday open thread on this site, namely the late Susie Sampson, a.k.a. Deplorable Patriot, among her other handles, pen names, etc.
For more on the untimely passing of Dear DePat, please see these three posts.
At one time, DePat handled FOUR daily open threads here, in addition to taking care of her relatives, choir duties, and numerous other responsibilities. She was a powerhouse – a dynamo – a true force of nature.
DePat’s faith in Trump, Q, “The Plan”, the White Hats, and “the anons” in general, was legendary. Although I didn’t always agree with her quick acceptance of some sketchier evidence and fringier theories, I will gladly admit to “coming around” to numerous so-called “conspiracy theories” which she championed first. I was always careful to give her credit for being right, too, when I had been wrong.
It is impossible to overstate how much DePat did for not only this site, but for her country. I urge all to say a quick prayer of thanks, whenever you think of her, for the privilege of knowing, in life or after death, such an exemplary human being, and lover of God.
And thank you, Susie, for the firm foundation which you left us, when you were called to your true home!
The Alpha-Gal Switcheroo – Is Bill Gates Using “Boxes of Ticks” Misdirection to Protect Vaccines?
Let’s do an experiment. Answer this question.
If you realized that – because you were getting vaccines – there was an increasing and dose-related chance you would become allergic to beef, and would have to stop eating beef – would you keep getting vaccines?
THAT is the question of the century. And it is a question nobody in Big Harma wants you to ask.
Stop for a moment to think about your answer, because IMO this question is NOT merely rhetorical. IMO, it’s REAL.
Speaking for myself, I’m not taking one more vaccine until I am shown the BOX it comes in, and then given WEEKS to research what is in that vaccine. Most vaccines will fail my standards, for one reason or another, and there are many good reasons. The exception might be a non-mRNA rabies vaccine after just being bitten by a bat, but otherwise, yeah. I am going to be a VERY difficult sell on any vaccine. You see, I read a very interesting scientific paper. You need to read it, too.
But before I tell you about it, I want to teach you about how I believe misdirection prejudiced me into believing an inferior scientific theory FIRST.
How the Scam Works
Magic – scams – con artist games – dirty FIB political manipulations – they almost all work by misdirection.
So how does that play out here? This is hypothetical, but tell me this doesn’t make all kinds of sense.
Bill Gates is deep in the weeds, controlling vaccines world-wide, for some reason (let’s not get into that now)
people have to want to take vaccines, because if they don’t (“hesitancy”), vaccines have no power to do whatever it is that they’re capable of doing (which includes literally remaking humanity)
suppose that vaccines start causing a problem
suppose that ticks also cause the same problem
suppose that pockets within vaccine science become aware that injection itself is and always has been a problematic methodology, due to side effects, including unwanted immune responses, off-target antibodies, etc.
well, if ticks alone can be blamed by those scientists, then vaccination and other injections can get off scot-free
even better, a vaccine for the “tick disease” can be turned into a hero, and any problems with THAT vaccine can then be blamed on ticks
note how COVID vaccine problems were blamed on the virus and “super-spreaders” who allegedly spread the virus right after the vaccine was given in nursing homes – same principle – misdirection
In the PAST – when I believed in an INFERIOR scientific theory – it was the “ticks alone can be blamed” part.
NOW – I believe the SUPERIOR and MORE GENERAL theory that injection itself can be, and often is, problematic. I am now a WISE GUY, who knows the same stuff as the people who wanted to blame everything on ticks.
It’s an AWESOME SCAM. Absolutely brilliant. But, in the words of every AI slop video….. IT’S OVER.
How I got from the bad theory to the good theory is next.
The Idea That Changed Everything and Opened My Third Eye to the Scams
I had heard of this “alpha gal allergy” that was spread by ticks – and I believed it all. It sounded a bit strange, but many parasitic and parasite-borne diseases (or in this case, really a “disorder”) are strange.
The fact that we had never experienced this condition before, but now it was going like gangbusters – well, that’s suspicious, too, but not unprecedented. I was willing to accept it.
The fact that Bill Gates was involved with it – sad, maybe outrageous, but typical. The man has a nose for BAD THINGS. Malaria, mosquitoes, failing vaccines. Its like he has an injection fetish. Ticks fit right into it. Not unbelievable, either.
And then I got an email for a substack article. Shown here as a tweet.
BREAKING: FIRST-EVER STUDY LINKS VACCINES TO THE 10,000% RISE IN ALPHA-GAL SYNDROME
We found more than 90% of U.S. children are injected with ~54 mg of alpha-gal-bearing mammalian gelatin through routine childhood vaccines before school entry.
We found more than 90% of U.S. children are injected with ~54 mg of alpha-gal-bearing mammalian gelatin through routine childhood vaccines before school entry. The evidence points to two possible pathways: 1) DIRECT: Vaccines may DIRECTLY promote alpha-gal sensitization. 2) PRIME-BOOST: Vaccines may PRIME the immune system, so a later tick bite BOOSTS the response to clinically relevant alpha-gal IgE levels. Yet the most obvious experiment has NEVER BEEN DONE: Measure alpha-gal antibodies BEFORE AND AFTER vaccination. This could help explain why suspected Alpha-Gal Syndrome has exploded by nearly 10,000% since 2013, while only a fraction of people bitten by ticks ever develop the condition. Alpha-Gal Syndrome has been known for 18 YEARS, yet no scientific paper bothered to investigate whether alpha-gal containing vaccines could be contributing. With 104 references, our study is one of the most comprehensive papers on Alpha-Gal Syndrome to date, covering its explosive rise, tick biology, vaccine exposures, immune mechanisms, genetic susceptibility, prevention, and treatments. This major McCullough Foundation–The Wellness Company collaboration brings together researchers across epidemiology, medicine, immunology, and public health to confront one of the biggest unanswered questions in Alpha-Gal Syndrome.
Figure 1. Rising incidence of suspected alpha-gal syndrome in the United States, 2013-2024. Incidence of alpha-gal-specific IgE seropositivity among adults tested within the TriNetX US Collaborative Network, rising from 0.95 per 100 patient-years in 2013-2014 to 94.06 in 2023-2024. Redrawn from data reported by Rama et al.12 The event was defined by a positive alpha-gal IgE result without a requirement for documented symptoms; such patients meet the standard surveillance definition of a suspected rather than a confirmed case. Rates are calculated among persons who underwent testing and therefore reflect clinical recognition and testing practice as well as any true change in occurrence.Figure 3. Two proposed pathways by which vaccine-derived alpha-gal could contribute to alpha-gal sensitization. Neither pathway is demonstrated, and the two are not mutually exclusive. Pathway 1, direct induction. Historical aluminum-adjuvanted DTP and DTaP preparations delivered gelatin-borne alpha-gal parenterally. Dendritic cells take up the epitope in an aluminum-conditioned, Th2-biased environment, and alpha- gal-specific memory B cells undergo IL-4-dependent sequential class switching to IgE without tick involvement. The pathway is depicted for historical formulations because every gelatin-containing vaccine in current United States use is unadjuvanted. Pathway 2, priming followed by tick-bite boosting. Gelatin in live viral vaccines such as measles-mumps-rubella and varicella carries alpha-gal and expands the alpha-gal-specific memory pool, with or without detectable circulating IgE. A subsequent lone star tick bite delivers alpha-gal on a salivary glycoprotein carrier with intrinsic adjuvant activity, boosting a recall response to clinically relevant titers. Amblyomma americanum is depicted as the dominant vector, although other tick species have been implicated. Convergence. In both pathways, alpha-gal-specific IgE bound to mast cells and basophils through the high-affinity IgE receptor FcεRI mediates the delayed reaction occurring 3 to 6 hours after ingestion of mammalian meat that defines clinical alpha-gal syndrome. Because all humans carry non-allergic anti-gal IgG and IgM, neither pathway requires primary priming against a novel epitope; the required event is redirection of an existing response toward the IgE isoty
This new thinking makes incredible sense to me.
Tick bites are common, but they’re small, and neither leave much nor take much. The tiny payload makes sense for communicable diseases, which require only a tiny amount of biological material to cause a huge problem, but for allergies, the larger assault of vaccines just makes more sense than a tick bite.
The recent appearance of the disease – also neatly explained by vaccines. NOT well explained by ticks.
No – in my mind, vaccines need to share EQUAL HYPOTHETICAL LIABILITY with ticks – and IMO it’s actually more likely to be vaccines that are ultimately responsible.
Again, I urge you to look at the paper, and maybe download it.
That post mentions SIX other posts, all of which cover what appear to be various wicked machinations by Billy Ghoul Gates of Hell (as some call him).
But my big question is THIS.
Has Bill Gates gone too far this time? Has he actually entered FRAUD territory? Has he even done something comparable to the SPLC supporting Nazis with donor money, as a way to stir up useful trouble to make MORE donor money?
Think about it. What if vaccines, in general, have an “off-target immunity problem” that can stem from the immunogen, the adjuvant, or BOTH. If so, misdirecting the public – and science – away from this alpha-gal story THROUGH Gates’ own enemies, would be a very smart move. Actually a diabolical move, but still. Very smart.
But is it legal? I don’t know the answer to that. Maybe DOJ does. At the very least, it’s reprehensible, IMO.
Let me put it this way. I don’t think these “Bill Gates is shipping boxes of ticks” stories are real. I certainly don’t think they’re organic. They’re obviously phony – but I think they’re phony with a purpose. A purpose that seems to help GATES and not US.
Is Gates behind those stories? Is there a money trail, like with SPLC?
I think these tick stories are a psy-op that is designed to gets blamed on the “anti-vax” and “anti-Gates” crowd – to sap the credibility of Gates’ enemies. At the same time, I think this psy-op is designed to mislead people – AWAY from vaccines – which Bill Gates is defending with all his might – and TOWARDS ticks – which Gates really doesn’t care about.
It’s not ticks. It’s vaccines. I’m convinced – at least right now – that they’re a better answer than ticks, on the question of alpha-gal syndrome. And it could even be that Bill Gates is defrauding all of us by blaming a vaccine problem on something else, and making his enemies be the mouthpiece for the phony alibi.
Bill Gates is innocent until proven guilty – just like SPLC. But I think somebody needs to look at this whole thing, and see if Gates has gone beyond just propping up bad science hit pieces like Lancetgate for corporate profits, which is perfectly legal, and has actually done any other things to defraud government, investors, and others – which are not legal. “Boxes of ticks” stories may be legal – but who knows? Maybe the people prosecuting SPLC would know.
As I said, things may get rough around here. Stay frosty. We’re up against the BIG-TIME trouble now.
The free vintage image for today’s offering header of Scène de la pestede 1720 by Michel Serre, of the Great Plague of Marseille, is courtesy of Google Images. For more information about the Great Plague of Marseille, please see: https://www.sciendirect.com/science/article/pii/S0755498222000318, “History of the plague of 1720 – 1722, in Marseille”, Michel Signoli, et al.; September 2022. For more information about the Black Death (Black Plague) in Europe, 1347 – 1351, please see: https://www.britannica.com/event/Black-Death. Note that the article on the Britannica website mentions the fact that the strain of Yersinia pestis (Y. pestis) that caused the Black Death plague in Europe is the ancestral strain of all other plague events since then.
The word “plague” generate images of the Black Death (Black Plague, the Bubonic Plague) that swept through Europe in the mid-1300s. Of thousands of dead people on the streets. Of entire families wiped out in a few days. Of the cries of “Bring out your dead.” And the Black Death is only one example of how devastating the plague can be. There have been numerous other incidents of plague attack, such as the 1720 – 1722 event that struck Marseille, France. Today’s offering discusses a “new aspect” of the plague — of a certain element of it being used as a “vaccine” ingredient. For purposes of today’s offering, Yersinia pestis and Y. pestis are used interchangeably.
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Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They linked here. Note: AI-generated items in today’s offering will be cited as such. If readers wish to post AI-generated items in today’s discussion thread, they must cite their source. Thank you.
However, there are other types of adjuvants that are either now in use, or are being studied for use, in injectable drugs. One such use being studied is the subject of today’s offering: an Avian Influenza “vaccine” adjuvant derived from the Yersinia pestis bacterium (the Black Death, the Black Plague, and also known as the Bubonic Plague.) To repeat: an Avian Influenza “vaccine” adjuvant derived from the Yersinia pestis bacterium (the Black Death, the Black Plague, and also known as the the Bubonic Plague.) Yours Truly begins here, with an article by Jon Fleetwood: https://jonfleetwood.substack.com/p/hhs-funds-chimeric-bird-flu-pandemic, “HHS Funds Chimeric Pandemic Bird Flu Vaccine Made With Engineered Plague Derivative BECC470s: Journal ‘mSphere'”, 13 August 2026. Please see the screenshots from this article, below:
The paper referred to in the Fleetwood article is here: https://journals.asm.org/doi/10.1126/msphere.00171-26, “Optimizing an avian influenza vaccine using a novel Bacterial Enzymatic Combinatorial Chemistry (BECC) TLR4 adjuvant”, Robert K. Ernst, et al.; 10 July 2026. The research was funded primarily via HHS-NIH-NIAID-BAA2017/HHSN272201800043C; via other HHS-NIH-NIAID grants; and, the Center for Vaccine Development and Global Health (University of Maryland School of Medicine.) The work of one co-author, Devon Riley, was funded via the United States Army Long-Term Health and Education Training Program.
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What is BECC470? Please see: https://www.fromtiersin.org/journals/immunology/articles/10.3389/fimmu.2026.187218/full, “Licensed and investigational TLR4 agonists as vaccine adjuvants: Structural basis, clinical progress, and future directions”; Jiasheng Zhou, et al.; 16 July 2026. Note that, except for one co-author of this paper (who is associated with the Communist Chinese version of the CDC), all other co-authors are associated with research institutes in Wuhan, Communist China. A screenshot of section 3.2 of this paper, which describes BECC (Bacterial Enzymatic Combinatorial Chemistry) is below. There are two versions of BECC470: BECC470b (the biological form of the Y. pestis element in the adjuvant); and, BECC470s (the lab-created synthetic form of the Y. pestis element in the adjuvant):
BECC438, BECC470b, and BECC470s are all derived from the lipid A in Y. pestis.
It appears that there are three separate publications of the Robert K. Ernst, et al., paper: the 10 July 2026 paper in the ASM Journals, cited above; another publication, a day later in July 2026, in journal Vaccines (https://www.sciencedirect.com/science/article/pii/S02644-10X26005839), “BECC-adjuvanted hemagglutinin influenza vaccine promotes enhanced immunogenicity and protective efficacy”, Robert K. Ernst, et al.; 11 July 2026; and, a Biorxiv preprint version, published in March 2026 (https://www.biorxiv.org/content/early/2026/03/05/2026.03.03.709477.full.pdf, “Optimizing an avian influenza vaccine using a novel Bacterial Enzymatic Combinatorial Chemistry (BECC) TLR4 adjuvant”, Robert K. Ernst, et al.; 5 March 2026. All three of these publications appear to have same parameters: One, that Gain-of-Function experiments were performed with multiple strains of Avian Influenza and then injected into the lab mice; Two, there is no direct mention that BECC438, or BECC470b, or BECC470s, are derived from the lipid A of Y. pestis; and, Three, that BECC adjuvants are “superior” to the other types of adjuvants currently in influenza “vaccines.”
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Back to the article by Jon Fleetwood. Something caught Yours Truly’s eye: It appears that the lipid A portion of a certain strain of Y. pestis, called KIM6+, is the one that was chosen to lab-create BECC470b, which was then chemically engineered to create BECC470s. Please see below:
Yours Truly did some digging into KIM6+. The 2023 paper, which also has Robert K. Ernst as co-author, is here: https://www.cell.com/action/showPdf?pii=S2405-8440(23)05327-6, “Physiochemical characterization of biological and synthetic forms of two lipid A-based TLR4 agonists”, Robert K. Ernst, et al.; available online 8 July 2023. Another paper, from 2021, by Bland, et al., discusses the KIM6+ strain of Y. pestis and its infectivity: https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1009995, “Acquisition of Yersinia murine toxin enabled Yersinia pestis to expand the range of mammalian hosts that sustain flea-borne plague”, David M. Bland, et al.; 14 Octocer 2021. Please see below, from the Results section of this paper:
It appears that the KIM6+ strain of Y. pestis is one that has about 50% more capability to infect. And it is the KIM6+ strain that was chosen to lab-create BECC470b; and then to have that chemically engineered to lab-synthesize BECC470s — both of which can be used as vaccine adjuvants.
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Robert K. Ernst holds at least two US Patents related to the use of KIM6+-derived Y. pestis lipid A constructs that can be used as adjuvants in vaccines: US10358667B2, 7 January 2016, “Adjusted expiration” of 19 March 2034: and, US11124815B2, 21 September 2021, “Adjusted expiration” of 7 March 2034. Both Patents have the same Title (“Immunotherapeutic Potential of Modified Lipooligosacchardies/Lipid A”); the same Inventors (Robert K. Ernst, et al.); and the same Licenses and Options (Licensed to TollereBio Corporation [Robert K. Ernst], Optioned to Virtici, LLC.)
Reading through US10358667B2, one finds, for example, that a BSL-2 biosafety laboratory level is, apparently, sufficient to work with the KIM6+ lipid A of Y. pestis, and to lab-create BECC470 adjuvants from this bacterium; that BOTH the “biological version” of BECC470 (BECC470b) and the “synthetic version” of BECC470 (BECC470s) can be used as vaccine adjuvants; and, that the BECC470 vaccine adjuvants, per the Patent, section VIII. Use of ExemplaryLipooligosaccharide/Lipid A-based Mimetic Compositions: “…is [sic] useful for…” the following vaccines, among others, listed in the Patent:
measles, mumps, rubella (think MMR);
polio;
plague;
chickenpox;
HPV;
Hepatitis B (think newborn “vaccination” with this one);
pertussis;
tetanus;
and, shigella (Shingles)
And, in fact, Dr. Ernst is at work creating a shigella “vaccine” that includes BECC-engineered adjuvants: https://www.sciencedirect.com/science/pii/S0264410X25000763, “BECC-engineered live-attenuated Shigella vaccine candidates display reduced endotoxicity with robust immunogenicity in mice”, Robert K. Ernst, et al.; 19 March 2025. This paper appears, in Yours Truly’s opinion, to “dance around” actually mentioning the apparent use of Y. pestis-derived elements in the Gain-of-Function shigella “vaccine” that was administered to lab mice (administered using various methods, including intramuscular injection and gastric injection.) The paper does list various Patents that are “related” to the paper, including both US10358667B2 and US11124815B2 (discussed above in today’s offering.) The paper also lists the 2018 Ernst, et al., paper regarding the use of Y. pestis-derived BECC438 in a vaccine administered to mice: https://www.sciencedirect.com/science/article/abs/pii/S0264410X18307680, “A lipid A-based TLR4 mimetic effectively adjuvants a Yersinia pestis rF-V1 subunit vaccine in a murine challenge model”, Robert K. Ernst, et al.; 27 June 2018.
In Yours Truly’s opinion, this entire situation raises important questions, among them: One: Why is the United States government (via HHS / NIH / NIAID), and the United States Army, funding research into using any element of the plague bacterium in a drug of any type, let alone a drug that can be injected? Two: How is it possible that a BSL-2 level laboratory can be considered to have sufficient biosafety to work with any element of the plague bacterium? Three: Why was KIM6+, apparently one of the most deadly and infective lipid A elements of Y. pestis, used to lab-create BECC470b and BECC470s? And, Four: Is it possible to completely “de-nature” the deadly effects of any element of Y. pestis sufficiently for such element to be used as an adjuvant in vaccines?
Peace, Good Energy, Respect: PAVACA1
(Intellectual Property Disclaimer and Notice: Except for the linked URLs and other items available on the Internet, the ideas and/or opinions in today’s offering are by PAVACA1 (M.E. Forbes, aka M.E.C. Forbes.) Credit must be given to PAVACA1 if ideas and/or opinions in today’s offering are used by other blog writers; by podcasters; or in print or social media.)
The free header image of the Andes Mountains for today’s offering is courtesy of Shutterstock and Google Images.
Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: AI-generated items in today’s offering will be cited as such. If readers wish to post AI-generated items to today’s discussion thread, they must cite their source. Thank you.
Today’s offering is not an elegant, “gardens of Versailles”-type layout. There are many items to consider. This is an evolving situation: details, news items, and so on, multiply by the day. There are a few relevant screenshots / images below. Yours Truly’s opinion is:
Those who **planned** for the COVID-19 bioweapon virus itself, followed by the COVID-19 bioweapon “vaccines”, to perform the task of immediately/within a short amount of time, culling the population of the Earth down to a “manageable” number of approximately 500 million persons (per the late Ted Turner) — and, finding that this task was not performed “properly” — have resorted to a “Plan B”: using an outbreak of the Andes Hantavirus (ANDV) on the MV Hondius as the excuse to generate a new “plandemic”, complete with gaslighting/fear operations, calls for “masking”, “lockdowns”, “vaccination”, and more. There may be other new”plandemic” measures in the wings. This new “plandemic” takes advantage of the weakened / destroyed immune systems in persons who are “vaccinated” with COVID-19 bioweapon “vaccines.” Many of the same actors in the COVID-19 disaster are involved with this Andes Hantavirus (ANDV) new “plandemic” rollout: the WHO; the CDC; USAMRIID; Fort Detrick; Big Pharma; Big Donors (Gates Foundation) — among others.
If readers suspect that the above sounds like a “rerun” of the COVID-19 virus PPE (Personal Protection Equipment) CDC recommendations — that is correct.
WHY, if it is the case that the Hantavirus outbreak on the MV Hondius is so concerning, did the WHO (World Health Organization) facilitate the IMMEDIATE RELEASE of the passengers from the ship to be “assessed” when the vessel docked at the Canary Islands?https://armageddonprose.substack.com/p/who-inexplicably-immediately-releases, “WHO Inexplicably, Immediately Releases All Passengers on Hantavirus Cruise Ship Without Quarantine”, 8 May 2026. The video announcement about this situation by Dr. Tedros Ghebreyesus, Director General of the WHO, is below:
WHO announces plan to fly #hantavirus cruise passengers all around the globe in order to milk the terror for all its worth pic.twitter.com/TnDh6XCq6W
Especially since it can take as long as 42 days post-exposure to the Andes Hantavirus (ANDV)for symptoms to appear? If readers are “starting to smell a rat”, that would be correct. If readers’ “interior antennae” are starting to register, “This feels like the start of the COVID lockdowns and “mandates” again, but now it’s Hantavirus”, that also would be correct.
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There is, currently, one vaccine against Hantavirus, an “inactivated” injectable called Hantavax (per Wikipedia.) It is only available for use in South Korea. Hantavax is not approved for use in other countries. There are, however, numerous “vaccines” against Hantavirus that are in development. Nicolas Hulscher, MPH, of The McCullough Foundation, notes that thirteen Hantavirus “vaccines” are currently under investigation: https://www.thefocalpoints.com/p/why-ivermectin-and-hydroxychloroquine, “Why Ivermectin and Hydroxychloroquine Could Work for Hantavirus”, 8 May 2026. Per Mr. Hulscher’s 6 May 2026 article on this situation, there are: 6 DNA-based “vaccines” (USAMRIID); 3 mRNA-based “vaccines” (Moderna; Communist China; Canada); 2 “viral vector vaccines” (UK; Canada); 1 “inactivated vaccine” (the Hantavax injectable, South Korea, in use there only); 1 “protein subunit vaccine” (Canada.) Note that the majority of the Hantavirus “vaccines” in development are under the aegis of the US Army (USAMRIID) — which indicates that the Department of War is involved. (https://www.thefocalpoints.com/p/the-vaccine-cartel-and-us-army-are, Nicolas Hulscher, MPH, 6 May 2026.)
The “situational briefing” from neodrop.ai on the current Hantavirus situation is here: https://neodrop.ai/feed/10x3geiL3Sz, “Hantavirus Global Situational Briefing — May 9, 2026.” Below, from the article, is the graphic regarding the “pipeline” of Hantavirus “vaccines” and antivirals in development:
Yours Truly found the USAMRIID Hantavirus “vaccine” clinical trial: https://clinicaltrials.gov/study/NCT04333459, “Safety and Immunogenicity of a Hantaan Virus DNA Vaccine and a Puumala Virus DNA Vaccine, For the Prevention of Hemorrhagic Fever With Renal Syndrome.” Per the Clinical Trials website, NCT04333459 is “Unknown status. Last known status: Recruiting.” The Study Start was 23 August 2021; the Study Completion (Estimated) was to be 31 December 2023. The Puumala virus (PUUV) is another form of Hantavirus; it infects persons in Scandinavia, Russia, and other countries.
BUT — the clinical study NCT03443459, which led this THIS paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC11570633/, “Phase 1 clinical trial of Hantaan and Puumala virus DNA vaccines delivered by needle-free injection”, Jay W Hooper, et al.; 17 November 2024: which study and paper were funded by USAMRIID, and conducted by USAMRIID personnel (Hooper, et al., above): is ACTUALLY a paper about an EARLIER study, NCT02776761 (https://clinicaltrials.gov/study/NCT02776761, “A Single-blind Study to Evaluate the Safety, Tolerability, and Immunogenicity of a Hantaan Puumala Virus DNA Vaccine”), which ended on 27 September 2017. Digging into the details for NCT02776761, it appears that Jay W Hooper owns two Patents for Hantavirus and for Puumala “vaccines”: US8183358B2 and US7217812B2, both of which were assigned to USAMRIID. However, it appears that the Patent for US7217812B2 is “Status: Expired – Lifetime” as of 2 October 2021. If this is the case, why does it appear that this Patent “vaccine” formulation for the Puumala virus used in the clinical trial NCT04333459? This, however, did not stop Mr. Hooper from publishing yet another paper on the same topic: https://academic.oup.com/jid/article/229/1/30/7209758, “Safety and Immunogenicity of an Andes Virus DNA Vaccine by Needle-Free Injection: A Randomized, Controlled Phase I Study”; Jay W Hooper, et al. 28 June 2023. Except that, for this paper, there was also funding via HHS / NIH: Grant number HHS 272201300016I. Which indicates involvement with HHS grants funding and US military funding for biolab work at Fort Detrick.
HOWEVER — and this is a big HOWEVER — there IS a modRNA-based “Hantavirus vaccine” that has gone beyond “development”: a lab-created “vaccine” was PATENTED in 2025 by researchers at the University of Texas, Austin. A “vaccine” that’s ready to be “tested” and either granted an EUA from the FDA, or be “approved” by the FDA. The team of researchers at the University of Texas, Austin, was led by Dr. Jason McLellan, PhD (who may, in Yours Truly’s opinion, be considered as “The Successor to Ralph Baric” in terms of using Gain-of-Function experiments to lab-create viruses and “vaccine” templates.) Dr. McLellan’s Gain-of-Function based research on the COVID-19 virus spike protein was used by Pfizer-BioNTech, by Moderna, and by Novavax, in the development of these companies’ COVID-19 bioweapon “vaccines.” https://en.wikipedia.org/wiki/Jason_McLellan
Yours Truly dug into Dr. McLellan’s modRNA-based Hantavirus “vaccine” Patent. The Patent document is here: https://patents.google.com/patent/US20250127870A1/en, “mRNA Vaccines Against Hantavirus”, published 24 April 2025. The first application for this Patent was filed on 15 September 2022. Current status is “Pending.” The Patent may be summarized as the “invention” of a Gain-of-Function produced, modRNA-platform based “vaccine” that has an artificial “cleavage area” between the Gn and Gc proteins, which proteins are used as the “antigens” for the “vaccine.”
But it goes much deeper than just the above. The “meat” of the descriptions of the multiple ingredients and combinations for this “Hantavirus vaccine” are found along the left side of the Patent Description list (not the “Claims” list, which is on the right side of the document.) The Description list is numbered. Without going too far “into the weeds”, some of the more striking Description items on the list follow. If readers think that the Patent for BNT162b2 describes a “witches’ brew”, this “Hantavirus Vaccine” Patent, in Yours Truly’s’ opinion, goes far beyond (Bolding is mine):
#0019: Adenosine is replaced with N6-methyladenosine (also known as “m6a”) “to evade the host innate immunity and improve the translation.” [of the other ingredients of the “vaccine.”] Adenosine is one of the four “building blocks” of RNA. Please see: https://www.alidabio.com/blog-post/m6a_minor_modification_major_impact/, by Zachary Miles.)
#0033: Confirms the use of the Andes Hantavirus (ANDV) as the basis for the “vaccine.”
#0041: Formulation list of adjuvants: this list includes dozens of types of adjuvants that can be used in the “Hantavirus vaccine.” One such adjuvant, JVRS-100, is a cationic lipid DNA compound; another adjuvant is Cholera toxin. A screenshot of part of the adjuvants list is below:
#0046 and #0049: The “Hantavirus vaccine” can be used as a “primary” and as a “booster” injectable.
#0047: Routes of administration: can used as an injectable, an intranasal, etc.
#0048: The “Hantavirus vaccine” can contain AZT (zidovudine), used in treating HIV/AIDS.
#0057: This section of the Description is the “justification” for using Gain-of-Function.
#0092: IRES Sequences. This is important. IRES = internal ribosome entry site. Ribosomes are combinations of RNA and proteins. Ribosomes are where protein synthesis occurs in a cell. https://www.genome.gov/genetics-glossary/Ribosome. One of the main goals of the “Hantavirus vaccine” is to “hijack” and change / replace RNA in the body of the person who takes this “vaccine.” In this “Hantavirus vaccine”, some of the IRES Sequences that can be used come from: the Coxsackie virus (CVB3); the Polio virus (PV); Foot and Mouth Disease virus (FMDVD); Simian Immune Deficiency viruses (SIV.)
#00128: from the Pharmaceutical Compositions section: This “Hantavirus vaccine” can be administered to humans / non-human primates / mammals / birds and poultry.
#0143 – 0144: List of lipid nanoparticles (LNPs) that be used in the “vaccine.” Examples of the LNPs that can be used in this “Hantavirus vaccine” include: DODMA (https://www.medchemexpress.com/dodma.html); the description clearly states, “For research use only); and, DOXIL (a form of the anticancer drug, doxorubicin: https://www.cancer.gov/publications/dictionaries/cancer-terms/def/doxil.) There are MULTIPLE other types of LNPs that are listed in sections #0143 – 0144. This also proves that this “Hantavirus vaccine” can contain at least ONE cancer treatment drug.
#0159: This “Hantavirus vaccine” can be used in “Multi-Dose & Repeat Dose Administration.”
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Yours Truly turns to the “lockstep, orchestrated gaslighting and fear COVID-19 virus campaign redone as Hantavirus” situation that is unfolding. Please see: https://maninamerica.substack.com/p/cp/197274890, “Hantavirus, Plandemics & Pre-Made Vaccines…Do You See It?”, 11 May 2026. The writer describes the various methods and actors being used to create a new “plandemic” of Hantavirus. Please also see: https://www.thefocalpoints.com/p/virus-in-the-dust-exposing-the-fabricated, “Virus in the Dust: Exposing the Fabricated Contagion of Andes Hantavirus”, Peter A. McCullough, MD, MPH, 10 May 2026.
HOWEVER — and this is another BIG HOWEVER — there is something ELSE in play here: the COVID-19 modRNA bioweapon “vaccines”, the damage / destruction these do to the immune system of the “vaccinated” person, and the documented THOUSANDS of serious adverse side effects and events (including death) from these “vaccines.”
Look at Page 33 (Page 4 of the Appendix 1. List of Adverse Events of Special Interest section) of https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, “BNT162b2 5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports“, given by Pfizer-BioNTech to the FDA on 30 April 2021. Please see the screenshot below, part of Page 33:
Does this mean that some BNT162b2 (approved by the FDA under the name COMIRNATY) “vaccinated” person(s) traveled to a place where the Andes Hantavirus (ANDV) is found, stayed there, had close / prolonged contact with infected rat droppings/saliva, or with a person there who was already infected with the Andes Hantavirus, THEN got positive test results for this virus?
OR — does it mean that BNT162b2 has elements of the Andes Hantavirus (ANDV) INCLUDED in the formulation?
OR — does it mean that the husband and wife who were bird-watching in Argentina, in a place where infected rats are prone to be, THEN the husband boards the MV Hondius, shows symptoms of ANDV infection and dies onboard, AND whose wife (who was NOT on board) ALSO becomes ill with ANDV infection and dies onshore, AND who were both COVID-19 “vaccinated” (therefore, their immune systems were badly damaged by said “vaccinations”) — had some kind of “activation” of ANDV infectious elements that were present in their COVID-19 “vaccinated” bodies: an “activation” which occurred while they were bird watching?
This is a non-transmissible organism. 98% synonymous mutations. 1 amino acid is not going to make it transmissible and cross species. The whole story is theatre.
Jikkyleaks thinks that USAMRIID “seeded” the virus on board the MV Hondius. A further discussion of the entire situation, including what Jikkyleaks tweeted, is on Dr. Jessica Rose’s blog: https://jessicar.substack.com/p/is-andv-hanta-natural-spillover-or, “Is ANDV hanta natural spillover or lab design?”, 13 May 2026.
And, WHY did the captain of the MV Hondius permit the body of the husband who DIED of an ANDV infection ON BOARD the vessel to REMAIN on board for TWO WEEKS, until it was offloaded, instead of performing a respectful, but IMMEDIATE, burial at sea? Why did the captain of the MV Hondius permit the body of the German woman who DIED of an ANDV infection CAUGHT ON BOARD to REMAIN on board for EIGHT DAYS? Again, WHY was there no respectful, but IMMEDIATE, burial at sea of this deceased woman’s body? No matter what “morgue-like” conditions these bodies were held in on board the MV Hondius, the corpses potentially exposing MULTIPLE persons on the ship to ANDV infection (think enclosed air-circulation system).
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The following articles are, in Yours Truly’s opinion, must-read items. The information in these articles point in the same general direction: there may be a new “plandemic” on the horizon (Andes Hantavirus [ANDV]); combined with “the usual suspects” rushing to, at the same time, implement some combination of COVID-19 disaster-style “lockdowns”, “masking”, “vaccines” development (and potential “mandated vaccination” schemes), plus control of information and coordination with compliant media to gaslight/frighten the general public:
From Dr. Peter A. McCullough, MD, MPH: https://www.thefocalpoints.com/p/source-of-contagion-hantavirus-andv, “Source of Contagion, Hantavirus ANDV, on MV Hondius: Rodent Excreta, Possibly Infected Corpses on Board for 22 Days”, 14 May 2026. There is a video interview with Dr. McCullough in the article.
USAMRIID is involved in the Andes Hantavirus / ANDV situation up to the eyeballs and beyond: https://jonfleetwood.substack.com/p/hantavirus-genome-was-built-from, “Hantavirus Genome Was Built From Human Blood at U.S. Military Biolab Fort Detrick Using Incomplete Computer Assembly and Reference Genome ‘Fill-Ins'”, 13 May 2026.
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Which brings Yours Truly to one final item: the nomination of Dr. Erica Schwartz, MD, MPH, JD, as the next Director of the CDC. Dr. Schwartz, while serving in the U.S. Coast Guard as a physician, was also instrumental in the enforcement of the “military mandate” for all U.S. military personnel to be COVID-19 “vaccinated.” She is also called “the queen of vaccines.” If confirmed, Dr. Schwartz would be in a position to sign off on a CDC “recommendation” for an Andes Hantavirus (ANDV) and/or Puumala virus (PUUV) “vaccine” to be used on the general public in the United States. (https://www.theqtree.com/2026/05/08/health-friday-5-8-2026-open-thread-two-establishment-medicine-nominees-an-opinion-piece/)
Individual awareness and self-education, in Yours Truly’s opinion, are important aspects to the totality of the Andes Hantavirus (ANDV) / MV Hondius situation.
Peace, Good Energy, Respect: PAVACA
(Intellectual Disclaimer and Notice: With the exception of linked URLs and other items available on the Internet, the ideas and/or opinions in today’s offering are by PAVACA. Credit must be given to PAVACA if ideas and/or opinions in today’s offering are used by other blog writers, podcasters, or in print or social media.)
The free header image of a “swirl clock” for today’s offering is courtesy of 123RF and Google Images.
Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics.
There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for AI-generated content. To the best of her knowledge and belief, there is none. If readers wish to post AI-generated content in today’s discussion thread, they must cite their source. Thank you.
Charlie Kirk, conservative activist, commentator, husband and father, was assassinated on Wednesday of this week (10 September 2025) as he was speaking at a “Prove Me Wrong” debate and rally at Utah Valley University in Orem, Utah. He was shot on the left side of his neck by a sniper who fired from approximately 200 yards away. It appears that the sniper’s single shot fired hit Mr. Kirk’s carotid artery. Mr. Kirk was pronounced dead at the hospital to which he was rushed after the hit. He leaves behind his wife, their two very young children, his parents, other relatives, and many friends. He leaves behind his work with Turning Point USA (TPUSA, of which he was the founder and chairman), and his other endeavors (his Salem Media Group talk show, his social media activities, and so on.) May Charlie Kirk rest in eternal Peace; and may the Almighty God sustain his widow and young children. May the assassin be found, along with those who recruited him. May Justice be meted out to them.
The cold-blooded, planned assassination of Charlie Kirk was Evil In Our Time. Make no mistake about this.
Today’s offering is not about the COVID-19 disaster: it is about the potential for a “new pandemic on the horizon”: H5N1 (Avian Influenza), another Evil In Our Time. Yours Truly has written about this situation in other Health Friday posts. Today’s post regards the latest Evil In Our Time news related to this issue: the lab-creation of TWO new chimeric types of H5N1 virus by the Chinese Communist government-owned company, Sinopharm. The first of these new, lab-created chimeric H5N1 viruses “attaches” to host cells at a rate 64 times higher than other strains of H5N1 viruses; the second of these new, lab-created chimeric H5N1 viruses has a “kill rate” of 100% in lab animals.
The story is here: https://jonfleetwood.substack.com/p/china-lab-engineers-two-new-bird, “China Lab Engineers Two New Bird Flu Constructs: One Binds to Host Cells 64x Stronger, the Other is 100% Lethal in Mammals”, Jon Fleetwood, 8 September 2025. Please see the screenshots from this article, below:
The paper published by the Sinopharm scientists who performed the work is here: https://doi.org/10.1016/j.virol.2025.110672, “H5N1 influenza virus-like particles based on BEVS induce robust functional antibodies and immune responses”, Yongbo Qiao, et al., 29 August 2025.
The Sinopharm scientists actually did two things: First, they lab-created two new, chimeric types of H5N1 virus that would guarantee either “attachment” to host cells at a rate 64 times higher than current H5N1 strains; or, would be lethal 100% of the time. Then, Second, they lab-created a “VLP-based vaccine” that would “induce robust functional antibodies and immune responses” to the said two new, chimeric H5N1 viruses. Please see the screenshots of the Abstract from this paper, and the Graphical Image from this paper, below:
Note that “Antigen presentation in lymph node” is the attack by these lab-created new, chimeric H5N1 viruses on the CD4 – CD8 T cells in the lymph nodes— the same things that the SARS-Cov-2 (COVID-19) virus itself, and the COVID-19 ‘vaccines”, do. Proper function of the CD4 – CD8 T cells is crucial to proper function of the human immune system in general.
This type of state-sponsored and state-funded Gain-of-Function work is Evil In Our Time. It’s not so much “the advancement of science.”
By the way, the Sinopharm lab where the work was performed is a BSL-3 lab — like the ones in many other bioweapons labs, and in university labs (like the Baric Lab at UNC, Chapel Hill.) http://en.sinopharm.com/2023-02/c_18829.html, 24 February 2023 (Sinopharm R&D webpage — be aware, it’s not secure.)
ALL GAIN-OF-FUNCTION WORK, NO MATTER WHERE IT IS PERFORMED, AND NO MATTER ON WHAT, MUST BE STOPPED. NOW. ALL EFFORTS TO MOUNT A “NEW PANDEMIC” OF H5N1, NO MATTER OF WHAT STRAIN, MUST BE STOPPED. NOW.
The free header image for today’s offering is courtesy of Shutterstock and Google Images.
Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. As today’s offering is related, in part, to the disaster of the COVID-19 “vaccines”, Yours Truly dedicates it to all persons who have contracted injures, illnesses, or disabilities, induced or aggravated by the COVID-19 “vaccines” that were injected into their bodies; and, to the memory of all persons who have passed away from the negative effects of the COVID-19 “vaccines” that were injected into their bodies.
There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for any AI-generated content. To the best of her knowledge and belief, there is none, except for perhaps AI-generated images in any of the linked URLs below. If readers wish to post any AI-generated content in today’s discussion thread, they must cite their source. Thank you.
There are two sections to today’s Special Report offering: the first section, regarding the now-proven linkage of COVID-19 “vaccine boosters” to increases in cancer and in general mortality; the second section, regarding what appears to be the potential emergence of the “next plandemic” in Communist China. Please bear with Yours Truly: one does not want to “weary by recitals”, as the Duc de Saint-Simon once wrote — but there is a lot of information, multiple screenshots, and so on. The evolving knowledge regarding the disaster called COVID-19 (the virus itself, and the “vaccines”) is gaining speed with each passing day. This evolving knowledge base is important to understand in light of the developments regarding the new information about the “Chikungunya outbreak” currently in China, and which is apparently spreading to other countries (shades of the original COVID-19 virus itself outbreak in China.)
First section, the linkage between COVID-19 “booster vaccines” with increases in cancer and in general mortality. COVID-19 “vaccine boosters” means any injection of a “latest version” of a COVID-19 “vaccine.” This includes the FDA- approved 2025-2026 “new formula COVID-19 vaccine versions” of the Pfizer-BioNTech modRNA COVID-19 “vaccine”, COMIRNATY; of the Moderna modRNA COVID-19 “vaccine”, SPIKEVAX; and, of the Novavax COVID-19 “vaccine”, NUVAXOVID.
Yours Truly begins here: https://slaynews.com/news/renowned-oncologist-sounds-alarm-cancer-deaths-now-surging-among-covid-boosted/, “Renowned Oncologist Sounds Alarm: Cancer Deaths Are Now Surging Among Covid-Boosted”, by Frank Bergman, 6 August 2025. There is an embedded video statement by Prof. Dr. Angus Dalgleish (St. George’s, University of London.) Dr. Dalgleish warns, in no uncertain terms, that it is the suppression of T-cell immune cells in the body of the COVID-19 “vaccine boosted” that is causing the surge of cancer among these persons. Please see the screenshot from the Slay News article, below:
The paper referenced above is here: https://www.researchsquare.com/article/rs-6899448/v2, “Factors contributing to the sharp rise in excess mortality in Japan since 2021”, Atsushi Takahashi, 17 July 2025. This paper is a pre-print. Please see the screenshots from this paper, below. They are: portions of the Results section; Figure 4; and, Figure 9:
The identifier names are those of the Prefectures in Japan that were studied. Even with taking other factors into consideration (examples: the size and population of the various Prefectures; the number of adults in age brackets in the Prefectures; whether or not a Prefecture was “rural” in character and location, as compared to “urban”), it is clear that the increase in mortality is tied to an increased amount of COVID-19 “vaccine boosters” that were administered.
The peer-reviewed paper on the Japan study is here: https://doi.org/10.3390/cancers17122006, “Repeated COVID-19 Vaccination as a Poor Prognostic Factor in Pancreatic Cancer: A Retrospective, Single-Center Cohort Study”, Makoto Abue, et al., 16 June 2025.
Yours Truly has written extensively for the board here regarding the damage / destruction of the natural immune system of the person who takes COVID-19 “vaccines.” These injectables were designed to attack, damage / destroy the CD4 – CD8 immune system cells. These injectables were designed to attack, damage / destroy the IgG3 immune system “fighter” cells, while at the same time, fostering the increase of IgG4 immune system “tolerate and never clear” cells. This damage / destruction increases with each injection of a modRNA COVID-19 “vaccine”, including injections of the “latest formula version” of said “vaccines”, which includes the “2025-2026 Formula versions” of said “vaccines” (COMIRNATY [Pfizer-BioNTech]; SPIKEVAX [Moderna]; and, NUVAXOVID[Novavax.])
The “Seneff and Nigh” paper of 10 May 2021 discusses how “immune system imprinting” in the the body of persons who take the COVID-19 “vaccines” have the potential to result in what the authors call “unintended consequences.” The paper is available here: https://dpbh.nv.gov/uploadedFiles/dpbhnvgov/content/Boards/BOH/Meetings/2021/SENEFF-1.PDF, “Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19”, Stephanie Seneff and Greg Nigh; International Journal of Vaccine Theory, Practice, and Research 2(1), May 10, 2021, Page 38-79. Please see the screenshots from this article, below. They are: the Abstract; the “Unprecedented” box; and, Figure 2.
Second section, regarding the potential for the “next plandemic” to come from Communist China. This has to do with the current emergence of mosquito-borne Chikungunya infections in several areas of China, which has resulted in various government-enforced measures. There is also an ** interesting connection ** to the United States involved in this situation.
What is Chikungunya? It is a virus transmitted by the bite of an infected female mosquito of (usually) the Aedes aegypti or the Aedes albopictus species. (As an aside: female mosquitos of these species can also transmit Dengue fever via bites.) The virus that is transmitted causes joint pain and fever; these can progress to severe. Most people infected with Chikungunya, however, make a full recovery. The virus is an RNA alphavirus. Please see: https://my.clevelandclinic.org/health/diseases/25083-chikungunya; there is a screenshot from this article, below:
Two recent articles regarding the Chikungunya outbreak in China: the first, here: https://jessicar.substack.com/p/the-new-pending-plandemic-is-it-scheduled, “The new pending “plandemic” — is it scheduled for November?”, by Jessica Rose, PhD, 12 August 2025. Dr. Rose makes it clear that the “alphavirus + saRNA-LNP platform” (self-amplifying RNA + lipid nanoparticles “vaccine” platform) is based on the VEEV alphavirus (Venezuelan Equine Encephalitis Virus.) Please see the screenshots from her article, below:
**** Note the mention of immune system issues that are induced in persons who are COVID-19 “vaccinated”, and how this can potentially severely complicate any infection by Chikungunya.
The second article is here: https://www.2ndsmartestguyintheworld.com/psyop-25-scamdemic-update-chinese, “PSYOP-25 SCAMDEMIC UPDATE: Chinese Authorities Mandating Blood Tests, Releasing Lab Mosquitoes to Fight Chikungunya Outbreak”, 13 August 2025. Please see the screenshots from this article, below:
The founder of the “mosquito lab” in Guangzhou is Dr. Zhiyong Xi. Please see the screenshot below from the above link:
Which work, at least in part, is being funded by NIAID (division of NIH — both divisions part of HHS.)
Which begs the following questions: WHY is Dr. Zhiyong XI still doing mosquito research in the United States if he founded a mosquito study lab in Communist China? WHY is Dr. Zhiyong Xi’s research at Michigan State University being funded, at least in part, by the NIH / NIAID?
There are two “FDA-approved vaccines” against Chikungunya: IXCHIQ, and VIMKUNYA. BOTH of these “vaccines” were FDA-approved under “accelerated approval” methods. Please see the screenshots, below, from the Package Inserts for these injectables. First, from the Package Insert for IXCHIQ (https://ixchiqhcp.com/PI-new.pdf):
Note the presence of Aluminum Hydroxide as an adjuvant in VIMKUNYA.
NOTE THAT THE “EXACT MECHANISM OF PROTECTION’ HAS NOT BEEN DETERMINED FOR EITHER IXCHIQ OR FOR VIMKUNYA. In other words, the United States government (via the FDA) is fine with injecting people with these “vaccines” WITHOUT THE FDA KNOWING THE EXACT MECHANISMS OF PROTECTION FOR EITHER OF THEM. What are the “CHIKV-specific immune responses” that these injectables supposedly elicit?
And, by the way, both IXCHIQ and VIMKUNYA can be “shed” onto newborn children if the expectant mother is sick with a virus (this is called viremia) at the time of delivery. A pregnant female who takes either one of the above “vaccines” runs the risk of contracting “viral viremia.” Neither IXCHIQ, nor VIMKUNYA have had proper testing for potential effects on pregnant females, their fetuses, or their newborns (section 8.1 Pregnancy in either Package Insert.)
All of the above begs the following questions: Does HHS Sec. Robert F. Kennedy, Jr., know about these Chikujgunya “vaccines”? Does he know that the FDA approved them under “accelerated approval” methods? Does he understand that the FDA does NOT know the “exact mechanism of protection” for either IXCHIQ or VIMKUNYA? Does Dr. Martin Makary (FDA Commissioner) know about this situation? Do either Sec. Kennedy, Jr., or Dr. Makary know that “career FDA types” in the CBER division signed the FDA Approval Letters for IXCHIQ (signed by R. Douglas Pratt, MD, 6 August 2025) and for VIMKUNYA (signed by David C. Kaslow, MD, 14 February 2025)?
Yours Truly will again emphasize that it is critically important for all persons, whether COVID-19 “vaccinated” or not, to follow some type of COVID-19 spike protein mitigation / prophylaxis protocol. It is also critically important that all persons, whether COVID-19 “vaccinated” or not, to do all they can to build and maintain their general health, and the health of their immune system, so as to be in the best shape possible.
The header image of a vintage doctor’s office sign for today’s offering is courtesy of iStock and Google Images.
Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics.
There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note One: Yours Truly has checked today’s offering for any AI-generated content. To the best of her knowledge and belief, there is none, except for some possible AI-generated images embedded in certain of the links below in the post. If readers wish to post any AI-generated content in today’s discussion thread, they must cite their source. Note Two: Today’s offering is not intended to be, nor is it to be construed as, defamation or “character assassination” of the person who is the subject of the post. Thank you.
Today’s offering is about Dr. Martin Makary, MD, MPH, the current Commissioner of the Food and Drug Administration (FDA) of the United States Department of Health and Human Services (HHS.) Dr. Makary serves under HHS Secretary Robert F. Kennedy, Jr. There is some “interesting information”, along with multiple screenshots, in today’s post. All information is searchable on the internet. Yours Truly will highlight opinions of her own in Italics.
The official FDA biography of Dr. Martin Makary, MD, MPH, is here: https://www.fda.gov/about-fda/fda-organization/martin-makary. Yours Truly cannot find a biographical entry on Dr. Makary that states when he was born. What is known is that Dr. Makary was born in Liverpool, England, and came with his birth family to the United States when he was a child. What is known is that Dr. Makary graduated with a B.S. degree from Bucknell University (likely about 1994), and graduated with his MD degree from the medical school of Thomas Jefferson University in 1998. This would, likely, place his year of birth in about 1970. Dr. Makary held a position at The Johns Hopkins University Hospital System as a Surgical Oncologist. He has also served as a professor in the Business School of The Johns Hopkins University. He also served as a consultant for the World Health Organization (WHO) in 2009 in that organization’s “Patient Safety Initiative”, in which Dr Makary assisted in creating the “Surgery Checklist” for surgeons (https://iris.who.int/bitstream/handle/10665/44185/9789241598552_eng.pdf, page 121.) Dr. Makary was confirmed as the current Commissioner of the Food and Drug Administration (FDA) division of the United States Department of Health and Human Services (HHS) in March 2025.
It is also known that Dr. Makary has apparently refused to take COVID-19 “vaccines” himself. Please see the screenshot, below, from this article: https://www.arabnews.com/node/2580559/amp. “Trumps names two Arab Americans for his Cabinet”, 25 November 2024:
Which, if the above is true, begs the question: If Dr. Makary did not take COVID-19 “vaccines” himself, why is he “recommending” these injectables for anyone else — for example, for people now deemed “at risk of severe complications from COVID-19 infection”, which includes pregnant women and women who have just given birth?
There are sections of the FDA website (URL above) regarding “Background and Program Priorities”, “Eligibility Criteria” for drug companies, “Solicitation of Statements of Interest”, and “Submission and Selection” for the program, underneath the FDA announcement.
This FDA announcement comes on the heels of another “opinion piece” by Dr. Martin Makary and Dr. Vinay Prasad, “Priorities for a New FDA”, published on JAMA Network on 10 June 2025. Their article is found here: http://jamanetwork.com/journals/jama/fullarticle/2835314. Please see the screenshots from this “opinion piece”, below:
Dr. Makary is involved with drug and/or other companies:
Which begs the question: Does this indicate that Dr. Makary may have conflicts of interest in certain areas?
Dr. Makary: Herd immunity from COVID-19 is via infection AND COVID-19 “vaccination”:
Dr. Makary: The non-COVID-19 “vaccinated” should avoid “vaccination” until new COVID-19 “vaccines” are authorized:
Dr. Makary: The need for “universal masking” against COVID-19:
Dr. Makary: On the other hand, “universal masking” harms children:
Dr.Makary: COVID-19 “lockdowns” are acceptable:
PRIOR to his being confirmed as Commissioner of the FDA, Dr. Makary questioned the concept of FDA authorization of COVID-19 “vaccines” without proper testing:
And, last but not least, Dr. Makary urges people to not “dissect” what now-HHS Secretary Kennedy, Jr., said years ago:
Which last screenshot begs the question: Has Dr. Makary apparently applied the “don’t dissect what someone said years ago” standard to himself as regards “the new FDA” that he and Dr. Prasad have created and that Dr. Makary is now implementing at the FDA?
There is a final piece to the “tapestry”, regarding the announcement by HHS Secretary Robert F. Kennedy, Jr., on 5 August 2025, that HHS was cancelling 22 contracts for “vaccine development under BARDA.” Please see: https://www.hhs.gov/press-room/hhs-winds-down-mrna-development-under-barda.html. However, BARDA is going to be “allowed” (how did this happen?) to complete contracts already begun for the ARCT-2304 self-amplifying RNA (saRNA) Avian Influenza “vaccine”, AND for the development of the “latest RNA technology platform”, called trans-amplifying RNA (taRNA.)And it was the FDA, under Dr. Martin Makary, who granted Arcturus Therapeutics (the developer of ARCT-2304) “Fast Track” status on 10 April 2025 — just after he was confirmed as the new Commissioner of the FDA. Fierce Biotech has an article on the BARDA continuation of these two contracts. Please see: https://www.fiercebiotech.com/biotech/hhs-cancels-all-mrna-vaccine-development-funded-barda, “HHS winds down mRNA vaccine development funded by BARDA”, by Darren Incorvaia, 5 August 2025. A screenshot from this article is below:
Jon Fleetwood discusses this situation on this Substack, here: https://jonfleetwood.substack.com/p/hhs-terminated-22-mrna-projectsbut, “HHS Just Terminated 22 mRNA Projects — But Quietly Preserved the Bill Gates-Funded Bird Flu Shot”, 6 August 2025. Please see a screenshot from this article, below:
There is also an embedded video of an interview with Mr. Fleetwood in his article above.
So, it would appear that, at the very least, FDA Commissioner Dr. Martin Makary “went along”, for whatever reason(s), with the cancelling of mRNA “vaccine” contracts, while at the same time, allowing BARDA to continue with the development of two very dangerous and unproven “vaccine platform technologies”: self-amplifying RNA and trans-amplifying RNA.
Refer above in today’s offering regarding the presence of Dr. Makary as a “headliner” at the BIO.org/ convention in March of this year. Representatives of both CSL Behring and Seqirus were at this convention. Arcturus Therapeutics IS A PARTNER WITH CSL / SEQIRUS in the development of ARCT-2304. Please see: https://arcturusrx.com/mrna-medicines-business-development/, under “Partnered RNA Medicines.”
Trans-amplifying RNA (taRNA), by the way, is a COMBINATION of two, “shorter” RNA fragments: one fragment encodes the antigen; the other fragment encodes the “replicase” (a replicase is an enzyme that facilitates the synthesis of another RNA molecule.)
Summary: In Yours Truly’s opinion, Dr. Martin Makary, the current Commissioner of the FDA, is a person of many convictions and viewpoints, some of which may be conflict with each other. It is up to individual readers to do their own research and form their own opinions.
Joe Biden never won. This is our Real President – 45, 46, 47.
AND our beautiful REALFLOTUS.
This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).
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Our beloved country is under Occupation by hostile forces.
Daily outrage and epic phuckery abound.
We can give in to despair…or we can be defiant and fight back in any way that we can.
Joe Biden didn’t win.
And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.
Well, it looks like we did. GOOD!!!
Wolfie’s Wheatie’s Word of the Week:
yird
noun, verb
earth, sod, soil, topsoil, loam, etc.
ground
to bury
to inter
Used in a sentence
The yird in the yard ain’t no place to yird your momma, but it will work for the old squirrel killed by pesticides.
Used in the title of a homemade horror movie
Used in a poem
MUSIC!
The Yirdbards! Whoops, I mean the Yardbirds!
THE STUFF
TL;DR- Bug sprays are the new vax, and you are the bugs they want to control.
It’s time to start talking about pesticides and depopulation. I will explain why in a few minutes.
Begin with this old video.
Robert Malone just re-blogged a really excellent article on MAHA and pesticides, and it is very helpful background for what I want to talk about. Please check it out.
TL;DR- The first step in going full vax, is getting vax-level legal protection.
Will Congress give the pesticide industry a de facto liability shield?
Guest essay by Dr. Meryl Nass, exclusive to Malone.News
The “public” bottom line is that the pesticide industry has seen how the vaccine industry protected itself from consequences – and they want some of that “protected monopoly” action, too!
The “hidden” bottom line, driven by the depoppers hiding behind plausible deniability and their industrial puppets, is that depop by vaccine is SO busted, but “Depop Plan B” using pesticides on both humans and animals is quite doable, and is now getting the big green light.
If we are not careful, a NEW form of depopulation will be granted a “free pass” to begin culling where vaccines left off, when we refused to take them.
I will share what I am learning in that regard.
Pesticides Tag in as Vaccines are on the Ropes
Did you know that CHINA wants to spray your yard, your house, your deck, your basement, your garden plants – with a chemical that goes right into those plants INTENTIONALLY – and will depopulate the hives of the bees that visit those flowers? Oh, yeah – and the squirrels and birds in your yard? Maybe even the vultures that eat the carcasses? That will cause measurable changes to your cardiovascular system? And for which they will charge you something approaching a grand per year – and that they will make you sign an almost unbreakable contract, which you can’t break – EVEN FOR HEALTH REASONS – without losing most of your money?
You had better wise up fast, because China figured out that Americans aren’t going to take those vaccines, and they have a NEW PLAN.
And I’m here to tell you all about it.
I have an organic yard and house. Yeah, I have to use some herbicides and some pesticides, but I generally avoid them almost entirely. If I absolutely must, I use weak, natural insecticides like natural pyrethrins VERY occasionally. I use borax traps for ants. I use pheromone traps for Japanese beetles. I use SPIDERS for most insects, and HOUSE CENTIPEDES to keep the spiders under control. The rule is that my little natural friends have to stay hidden, and they learn fast, just like little AI robots. Scare them good, and you won’t see them again.
I use natural oil repellents for rabbits, squirrels, and deer in the gardens. This natural system works like crazy. Good dehumidification also helps in a big way, to keep bugs out of the house. I pass those tips along to all my friends, too, just like they were passed on to me. A natural and dry house is a surprisingly clean and bug-free house.
We have birds, squirrels, rabbits, deer, coyotes, skunks, racoons, groundhogs, bats, woodpeckers, hawks, owls, chipmunks, field mice, and every other critter you can imagine. We treat the animals well, and they entertain us all year long. The insects can’t come in the house, however, and our pampered little predators take care of the few that do.
However, not all of my friends and neighbors have stood up to the blatant, merciless, and sometimes literally illegal solicitations by the pestilence of “green” pesticide companies, trying to sell their services to the unwary.
I am going to warn you about them.
What follows is a combination of my experiences with those of my friends, my neighbors, and their friends and neighbors. Most of this is first-hand information given directly to me by the people involved. Some is second-hand. Some is my own experience. I’m going to wrap it all up in one ball – a single “friend” – to keep all these people anonymous, and bury my connections to them.
My “friend” has some serious warnings for you. Pay attention – and LIVE.
My friend actually thinks the home pesticide racket is built for depop. I knew this person was wise to depop with vaccines, but not pesticides, so when they told me the current pressure by green pesticide companies was all about depopulation, I was stunned. I wasn’t even fully there yet. But when you hear my friend’s story, it makes sense.
Yes – depopulation by nasty elites and progs is almost a mainstream belief now.
The high-pressure sales by these “green pesticide” companies has gone up by a full quantum level. We used to get the top two or three companies coming to our door, once every few years, but lately they’re all everywhere, all the time. The competition is FIERCE. I’ve seen them coming to most of my friends’ houses, too. The companies send both college kids and seasoned pros on these calls, and it seems like most of these salespeople will just ignore “NO SOLICITORS” signs.
My friend is an avid gardener and a DIY type, and had avoided using a pesticide company for years. However, because they were in the middle of a very wet summer with a lot of insects getting into the house, AND because the salesman made it sound like their people were just applying organic plant extracts to the exterior, and promised it would solve the problem, my friend made the mistake of trusting the sales pitch, and signed a 1-year contract to try it out. HUGE mistake.
“Plant-based” doesn’t mean “plant extracts”. Nor does it mean organic. Nor does it mean natural. It means “there exist natural substances with the same mode of bug-killing action, but this newer, stronger, and more persistent synthetic poison is not one of them.”
It’s the difference between “pyrethrins” (moderately toxic natural substances in chrysanthemum flowers) and “pyrethroids” (synthetic molecules that kinda look like the natural ones, but are many times more potent and toxic).
Ditto for “neonicotinoids“, which function at the same insect (or mammal) receptors as nicotine, but have molecules which increasingly look almost nothing like nicotine.
Neonicotinoids, a.k.a. “neonics“, are contentious because (IMO) they are both over-accused in some ways, and under-accused in others. Let’s just say that they are not without controversy.
That is what is being called “plant-based”, “organic”, etc. Technically, it’s true, or almost true, but realistically, it’s so close to a lie, you need a spark-plug gapper to find the space. IMO, the term “plant-based” is a bridge between SCAMMERS and MARKS – nothing more. It is designed to get people who are very reluctant to spray synthetic poisons around their houses, to spray synthetic poisons around their houses.
Caveat emptor.
What it meant in practice for my friend, was a mixture of AGRICULTURAL INSECTICIDES sprayed all over the exterior of the house, sprayed on the ground all around the house and on the decks, sprayed all over the garden, and then delayed-release pellets of still more insecticides being scattered all over the lawn.
The very first casualty was one of my friend’s favorite squirrels – a big old thing – dead on the ground where the company had sprayed, two days later. They weren’t sure if it walked through the sprayed areas or munched on one of the timed-release pellets, but based on the maggot and ant activity, the squirrel likely died within hours of the first application.
It definitely took care of the insects (it took a few days) – they were GONE from the garden – including all the pollinators. There were definitely fewer insects coming into the house. The stuff works.
HOWEVER, my friend felt ILL within hours of spraying, and within 2-3 days knew that something was very wrong. They almost went to the doctor, and only held off from doing so, because they felt better after about a week to 10 days.
Now – here is the kicker. A few weeks later, my friend was told by their FitBit (health wrist watch) that there had been an improvement in exercising heart rate – that their pulse had gone down significantly. My friend found that surprising, and looked at a graph of the health data. Yes, it had gone down – from an unexpected increase earlier. What was very obvious was full recovery from a HUGE increase in heart rate starting the very day that the pesticides had been applied, topping out in 3-4 days, then going back to normal in a week to 10 days. After that, a flat line of normalcy.
My friend even remembered ignoring an earlier notification about heart rate – probably when it increased.
The truth was all in the data.
Good thing my friend only has mild cardiac issues. What if this would have happened to somebody with serious cardiac problems?
I repeat. My friend has medical evidence of health effects due to the applied pesticides. My guess is that they suffered from both of the chemicals sprayed on the house – one is a powerful pyrethroid, which can cause nerve problems like the symptoms they described – the other is a neonicotinoid, meaning it’s biologically like nicotine, and that is the one that IMO likely raised their heart rate.
My friend canceled the service a.s.a.p. and told the company why. One might think that a person would get their money back for a health-related exit, but no – the contract required almost complete payment of the full contract for discontinuing for ANY reason. My friend did NOT give a damn – they were OUT.
Lesson learned.
Now, that squirrel wasn’t the only casualty. A different company came to my friend’s house later, and mentioned (as a selling point) that they had secured contracts with two families just down the road. Well, what do you know – a few days later, there was a HUGE vulture pecking at what looked like a small dead mammal in the first mentioned neighbor’s yard. And if that’s not enough, there was ANOTHER dead mammal – some kind of squirrel or chipmunk – found later next door to the second property mentioned by the happy salesman.
I repeat – these are were mammals.
Between my neighbor’s symptoms preserved in data, and 3 dead mammals in or near 3 treated yards, I know that I for one sure don’t want to have anything to do with these “green” pesticides. My suspicions of them have been confirmed.
If you want to read more about the health effects of pesticides, this is a really good slideshow:
Go back to Malone’s hosted article by Dr. Nass. You will find that a certain big pesticide company merged with ChemChina. ChemChina is STATE-OWNED – meaning it’s the CCP.
Well, that company which is under CCP control, happens to be the one that produced the mixture of chemicals which likely sickened my friend and killed the squirrel. So if you wouldn’t trust China to “safely” put poisons in your yard and on your house, then strongly consider hiring some spiders to take care of the insects, and some house centipedes to take care of the spiders. Let the birds take care of the insects. Let the bees take care of the flowers. And let the hawks take care of the squirrels.
The above image is courtesy of Lincolnton, NC, and Google Images.
Health Friday is a series regarding Big Pharma, vaccines, general health, and associated topics.
There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for any AI-generated content. To the best of her knowledge and belief, there is none. If readers wish to post any AI-generated content to today’s discussion thread, they must cite their source. Thank you.
Today’s offering is slightly different from others in this series. It is an honor and a privilege for Yours Truly to present today’s post on this day, 4 July 2025, the 249th birthday of the representative republic known as the United States of America.
Facsimile of the United States Declaration of Independence made by William Stone in 1823.
The above image of Declaration of Independence is courtesy of iStock and Google Images.
Our good TradeBait2 has posted many articles on the board regarding the signers of the Declaration of Independence. These amazing men understood what it meant to sign a document in which they stated, “And for the support of this Declaration, with a firm reliance on the protection of divine Providence, we mutually pledge to each other our Lives, our Fortunes, and our sacred Honor.” They were not perfect individuals, but they understood how high the stakes were. They were ready to deal with whatever would happen to them. Many of them lost their own lives, the lives of family members, their land, their homes, and much more, because of the document that they signed. We, the citizens of the United States of America today, honor and remember them for their courage and for their sacrifices in laying the foundation for breaking the tyrannical stranglehold of British Monarchy in order to create a new and free country. It is the responsibility of American citizens to fight enemies, “both foreign and domestic.”
Regarding health, the United States of America is beginning to recover from the disaster of the lab-created bioweapons called COVID-19 virus itself and the COVID-19 “vaccines”: a disaster that was unleashed on the globe in the fall of 2019, and in the development of which both the United States Defense Department and the United States National Institutes of Health were involved. Millions of Americans became infected with the virus; thousands died from the complications and from “hospital protocols” (the use of Remdesivir, ventilators, Paxlovid, molnupiravir, and so on.) Thousands more have died from the dangerous, deadly effects of the COVID-19 “vaccines” that were injected into their bodies. Millions of Americans have COVID-19 “vaccine”-induced injuries, illnesses, or disabilities (https://openvaers.com/.) People are seeing their COVID-19 “vaccinated” loved ones, friends, and colleagues succumb to the dangerous, deadly effects of these injectables. Thankfully, more information and confirmation regarding the dangers and deadliness of these “vaccines” are coming into public view by the day. The American people are indebted to many courageous medical professionals who have labored, and continue to labor, to expose the truth about both the COVID-19 virus itself and the COVID-19 “vaccines” — Dr. Robert Malone, MD; Dr. Ryan Cole, MD; Dr. Peter A. McCullough, MD; Dr. Pierre Kory, MD; Dr. Stephanie Seneff, PhD; Dr. Jessica Rose, PhD; among others. The United States Department of Health and Human Services, under the current Secretary, Robert F. Kennedy, Jr., is taking steps to curtail the imposition of these “vaccines.” The cheap and effective preventative and treatment for COVID-19, Ivermectin, is finally being made available to the public — now, it needs FDA approval, which it still does not have. Many persons involved in the lab-creation of the COVID-19 disaster must be held to account.
There is one COVID-19 “vaccine”-related news item that Yours Truly will present in today’s offering: the coordinated plot by https://www.bio.org/ to remove current HHS Secretary Robert F. Kennedy, Jr.; and, to “redesign” the FDA into the vassal of Big Pharma that it was for many years previous to January 2025, the start of the second administration of President Donald Trump47. BIO.org partners closely with the United States Defense Department in the development of vaccines and other technologies. Please see the screenshots below from the company’s website.
The Partnering with the Department of Defense webpage also has three embedded videos, related to “rapid development of vaccines” and “how to work with the DoD.”
Regarding the coordinated effort by BIO.org to remove Secretary Kennedy, Jr., and related items, please see the screenshots below. The first one is from Yours Truly on The Q Tree. The rest of the screenshots are from the PDF of the BIO.org Vaccine Policy Steering Committee meeting that occurred on 3 April 2025. The link to the Substack article by Dr. Rose is: https://jessicar.substack.com/p/the-plot-to-remove-rfk-by-big-pharma.
The BIO.org meeting was held on 3 April 2025. Yours Truly corrects a date mistake in The Q Tree comment screenshot, above.
It appears that BIO.org is making it clear that they want “the good old HHS and good old FDA back”, and will do all they can to have this happen. It also appears that BIO.org believes that Dr. Martin Makary (current Commissioner of the FDA) is “manageable.” This may be a result of Dr. Makary’s recommendation for pregnant women to get COVID-19 “vaccinated.”
This is the same Dr. Martin Makary and his FDA that granted “Fast Track” approval in April 2025 for the H5N1 Avian Influenza “vaccine”, ARCT-2304, a self-amplifying RNA (saRNA) “vaccine.” Please see: https://www.contagionlive.com/view/fda-grants-fast-track-status-to-arct-2304-for-h5n1-influenza-protection, 10 April 2025. Surely Dr. Makary understands that saRNA, once injected into the body, turns that “vaccinated” body into a “literal interior Xerox machine” for manufacturing the modRNA of an injected saRNA “vaccine”, and that this “literal interior Xerox machine” effect can be permanent?
It appears that BIO.org is planning to foment distrust and disagreement between President Trump47 and Secretary Kennedy, Jr.
It also appears that BIO.org is planning to “work with” the United States Senate in coordinating the removal of Secretary Kennedy, Jr.
It is Yours Truly’ opinion that every United States Senator needs to see the BIO.org meeting document from April 2025; either the document itself; or, the link to the Dr. Jessica Rose article, above.
It is up to We, the People of the United States, to stop the efforts of BIO.org, of Big Pharma, of the World Health Organization, of the United Nations, of the American Medical Association, and other entities and persons, in hobbling, let alone taking away, health freedom in America.
