Tag: Big Pharma

Health Friday 8.22.2025 Open Thread: “Clean Sweep” Edition: An Opinion Piece

The header image of smallpox vaccination in Paris in 1905 used in today’s offering is courtesy of Alamy and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks of the disaster of COVID-19, Yours Truly dedicates it to all persons, of whatever age or location, who have suffered injuries, illnesses, or disabilities, either COVID-19 “vaccine”-induced, or as the result of a COVID-19 infection; and, to all persons, of whatever age or location, who have passed away either from the negative effects of the COVID-19 “vaccines” they had in their bodies, or as the result of a COVID-19 infection.

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 AI-generated images that may be included in links in today’s offering. If readers wish to add any AI-generated content to the discussion thread today, they must cite their source. Thank you.

“Clean Sweep.” This means completely dismantling the FDA (the Food and Drug Administration); the NIH (the National Institutes of Health); and, the NIAID (the National Institute of Allergy and Infectious Diseases), all of which are divisions of the United States Department of Health and Human Services (HHS) — and completely rebuilding them from the top down. Why “Clean Sweep” for these divisions? Because it is becoming more apparent by the week that they are more devoted to using “career” medical bureaucrats/officials, many of whom are “holdovers” from the “Collins / Fauci era” in the NIH and NIAID; they are more devoted to injecting American citizens with the proven-dangerous, proven-deadly COVID-19 “vaccines” than they are to approving readily-available, cheap drugs (such as, Ivermectin) and other therapeutics (such as, Zinc) to prevent or to treat COVID-19 infection; and, they are more devoted to pushing through injectables via “Fast Track” or “accelerated approval” methods, rather than taking the time to fully test and analyze test data. “Completely rebuilding them from the top down” means establishing entirely redesigned divisions that are fully devoted to the betterment of the public health.

Yours Truly presents a transcript of the op-ed published in the Washington Post on 12 August 2025 by Dr. Jay Bhattacharya, the current Director of the NIH (National Institutes of Health); the op-ed appears here: https://www.washingtonpost.com/opinons/2025/08/12/nih-mrna-vaccines-jay-bhattacharya/, “Jay Bhattacharya: Why the NIH is pivoting away from mRNA vaccines”, 12 August 2025. Yours Truly provides her personal commentary, which will appear in Bold and surrounded in brackets. (The Washington Post op-ed is behind a paywall; Yours Truly is indebted to Shannon Joy, whose X tweet has the entire article: https://xcancel.com/ShannonJoy/status/1956140133474034025.) Note: Yours Truly will make it clear that the commentary is done with all due respect to Dr. Jay Bhattacharya, MD.

The transcript:
“The U.S. Department of Health and Human Services’ decision to wind down its mRNA vaccine development activities marks a necessary pivot in how we steward public health innovation in vaccines. The right path requires us to consider the inherent strengths and weaknesses of a technology as well as any alternatives, along with public attitudes and experience with the technology. The mRNA platform is promising technology. I do not dispute its potential. In the future, it may yet deliver breakthroughs in treating diseases such as cancer, and HHS is continuing to invest in ongoing research in oncology and other complex diseases.”

[YT: First of all, if HHS is truly going to “wind down” mRNA vaccine development, why is Moderna being allowed to progress to Phase 3 clinical trials of its modRNA “vaccine” against CMV (Cytomegalovirus), mRNA-1647? This “vaccine” contains six different mRNA sequences, two different antigens, the dangerous lipid nanoparticle SM-102 (the same LNP that is in the Moderna modRNA COVID-19 “vaccine”, SPIKEVAX), and apparently targets both the IgG immune system cells and the CD4-CD8 cells of the body. Please see: https://doi.org/10.1128/jvi.01603-23, “Characterization of humoral and cellular immunologic responses to an mRNA-based human cytomegalovirus vaccine from a phase 1 trial of healthy adults”, Kai Wu, et al.; J Virol. 2024 Mar 25;18(4):e01603-23. Please refer to Fig. 2 and Fig.4. Secondly, the current modRNA (aka mRNA) COVID-19 “vaccines” have demonstrated that they do not have “inherent strengths”: in fact, they only have what may be called “inherent dangers.” These “inherent dangers” include: altering of the LINE1 Human Liver cell line; replacement of natural Uridine RNA with the lab-created N1-Methylpseudouridine; crossing the Blood-Brain Barrier to attack areas of the brain that are not protected by this barrier (for example, the Pituitary Gland); causing autoimmune attack on heart tissue via aggregation of lymphocytes induced by the COVID-19 “vaccines” in that organ; and, causing infiltration of lymphocytes in lung tissue. Regarding the DNA alteration, and heart and lung damage, caused by the COVID-19 “vaccines”, please see: https://doctors4covidethics.org/wp-content/uploads/2022/08/causality-article.pdf, “Vascular and organ damage induced by mRNA vaccines: irrefutable proof of causality”, Michael Palmer, MD, and Sucharit Bhakdi, MD, Slide 9 through Slide 14. Thirdly, why on Earth is oncology (cancer study, diagnosis, and treatment) included in the phrase “and other complex diseases?” Yours Truly calls this a writing mistake; however, one believes someone should have proofread the op-ed for “context or syntax” issues before publication.]

“But as a vaccine intended for broad public use, especially during a public health emergency, the platform has failed a crucial test: earning public trust. No matter how elegant the science, a platform that lacks credibility among the people it seeks to protect cannot fulfill its public health mission.”

[YT: The “public trust” for the COVID-19 “vaccines” was destroyed when it was proven that hundreds of persons who took these injectables passed away from immediate heart attacks induced by them just after being injected; when “vaccinated” persons began to present with myocarditis or pericarditis after being injected; when stillbirths and miscarriages began to be reported among pregnant women who had been injected; and much, much more. And, by the way, the initial modRNA COVID-19 “vaccine” rollout in December 2020 was intended for the elderly and for healthcare workers; it was when the “COVID-19 health emergency” was declared in March 2021 that the “vaccines” began to be “mandated” for all persons. “Elegant science?” Does “elegant science” include the kind of “science” that was rushed through the initial EUAs for the modRNA COVID-19 “vaccines” without proper testing and data analyses?]

“It is critical to understand the development of the mRNA coronavirus vaccines in the context of the very successful Operation Warp Speed launched during the first Trump administration.”

[YT: Does “the development of the mRNA coronavirus vaccines” include the fact that neither Pfizer-BioNTech, nor Moderna, had never previously brought a successful mRNA injectable to market prior to “Operation Warp Speed?” And that Dr. Albert Bourla, DVM, the CEO of PfizerUSA, admitted on video that he had been “convinced” by Pfizer scientists to use the then-new and unproven mRNA technology in a COVID-19 “vaccine?” (10 March 2022, “Albert Bourla on why mRNA technology was “counterintuitive” to producing an effective vaccine”, https://www.youtube.com/watch?v=t9_YRw7jBF4.)]

“Operation Warp Speed represented a paradigm shift in how the government should invest in new technologies and solutions and embrace strategic investments in public-private partnerships, innovation in trial design and removal of bureaucratic red tape to allow parallel rather than sequential vaccine development. It produced a new vaccine in record time and also helped develop a successful monoclonal antibody.”

[YT: Really? “Embrace strategic partnerships in public-private partnerships?” What about that “public-private partnership” document between the NIAID and Moderna, which includes development of RNA-based vaccines, and that was filed with the SEC in 2015, several years BEFORE the COVID-19 disaster? That “partnership” is still going on, with patent-ownership sharing, royalty payments sharing, “partnering” in developing new COVID-19 “vaccines”, and so on, until at least 2041. “Innovation in trial design?” — Meaning the “Next Gold Generation Standard”, announced in May 2025, in which lab testing with animals using humane, safe protocols, then progressing to better and safer human-subject testing, may well be replaced with “Petri-dish testing” only” for new “vaccines”? “Parallel vaccine development?” — Meaning that “Universal Vaccine” that’s touted in the “Next Gold Generation Standard?”]

“Unfortunately, the Biden administration did not manage public trust in the coronavirus vaccines, largely because it chose a strategy of mandates rather than a risk-based approach and did not properly acknowledge Americans’ growing concerns regarding safety and effectiveness.”

[YT: So, “risk-based approach?” Like the “risk populations chart” in the “opinion piece” that Dr.Martin Makary and Dr. Vinay Prasad published in the New England Journal of Medicine in May 2025 (https://doi.org/10.1056/NEJMsb2506929, “An Evidence-Based Approach to Covid-19 Vaccination”— a chart in which, for example, even healthy pregnant women are considered to be at “risk” for “severe complications from COVID-19” and should get COVID-19 “vaccinated?” And what about the statements about how the “known and potential benefits of the for COVID-19 vaccines outweigh the known and potential risks?” — like the one here: https://www.cdc.gov/vaccines/covid-19/planning/children/6-things-to-know.html, “6 Things to Know about COVID-19 Vaccination for Children.“]

“Consider the data: In a late 2024 Pew Research Center survey, 60 percent of American adults reported no intention of getting an updated coronavirus mRNA vaccine despite the Center for Disease Control and Prevention’s advice that nearly all adults receive yet another dose. As of late April 2025 (the latest data published reported by the CDC), only 13 percent of children between the ages of 6 months and 17 years had received an updated coronavirus vaccine, even though the Biden-era CDC had placed the vaccine on the childhood immunization schedule.”

[YT: It appears that the real reason behind why “only 13 percent of children between the ages of 6 months and 17 years had received an updated coronavirus vaccine” is that their parents or guardians have concluded that these “vaccines” are more dangerous than helpful. And how did these adults come to this conclusion? Because of the news spreading that these “vaccines” cause myocarditis / pericarditis in children; because of the news spreading that these “vaccines” do not prevent COVID-19 infection, but instead actually damage the “vaccinated” person’s immune system, making it vulnerable to COVID-19 infection; and so on. In Yours Truly’s opinion, the COVID-19 “vaccines” have no place in the CDC Childhood Immunization Schedule whatever — due to the foregoing and other reasons.]

“In 2021, the Biden administration’s HHS spent nearly a billion dollars on a campaign supporting the coronavirus vaccine, the most expensive pharmaceutical campaign in history. The government spent the money on a vast number of TV, radio and internet spots, which misinformed the American public that the vaccine would protect them from contracting and spreading covid. Nevertheless, just a few years later, less than half the U.S. adult population will heed the CDC’s guidance. Some outlets have blamed the poor coronavirus mRNA vaccine uptake on poor messaging or “anti-vax” counter-messaging. But the Biden administration made suppression of speech — and a mandate for all on the vaccines — into a priority.”

[YT: Perhaps Dr. Bhattacharya should look at the FDA Package Insert for the modRNA COVID-19 “vaccine”, COMIRNATY (Pfizer-BioNTech), section 1 INDICATIONS AND USAGE. The Package Insert is here: https://www.fda.gov/media/151707/download. Notice that the FDA officially states that COMIRNATY is “to prevent coronavirus disease 2019 (COVID-19.)” Is the FDA “spreading misinformation?”

“The failure was thus not a communications problem. It is a trust problem due to the Biden administration’s scientific overreach, public pressure and, frankly, arrogance.”

[YT: Does this mean that “the new FDA”, and the “Next Generation Gold Standard”, and the “accelerated approval” of “vaccines” that may be lab-created in Petri-dishes will somehow magically restore public trust?]

“In addition to the trust problem, the mRNA technology has special biological features that make it different from other vaccines in that it (ideally) instructs our cells to produce proteins that subsequently invoke an immune response. To do so with complete confidence about vaccine safety and efficacy requires an exact understanding of dosage, biodistribution and off-target effects. Unfortunately, we fall short in all three. We lack clarity on how much antigen each mRNA molecule produces, where in the body the mRNA product winds up, how long it stays in the body, and whether unintended proteins are created.”

[YT: Unfortunately, this paragraph, in Yours Truly’s opinion, “has more holes than a Swiss cheese.” First: the mRNA “vaccines” do instruct the cells of the “vaccinated” person to “invoke an immune response”: that “response”, among other things, causes multiple types of autoimmune attack within the COVID-19 “vaccinated” person’s body — for example, in the heart (please refer above to the article by Doctors For COVID Ethics.) Second: Perhaps Dr. Bhattacharya would like to read this report, which Pfizer-BioNTech gave to the FDA in January 2021, regarding the biodistribution of BNT162b2 (FDA-approved in 2022 as COMIRNATY.) The report is here: https://phmpt.org/wp-content/uploads/2022/03/125742_S1_M2_pharmkin-tabulated-summary.pdf, “MODULE 2.6.5. PHARMACOKINETICS TABULATED SUMMARY.” Yours Truly has included images of Page 7 and Page 8 of this report, which are the Biodistribution Tables for BNT162b2. (The BNT162b2 used in this experiment is the same one that was granted the initial FDA for use in the United States in December 2020.) Third: Stephanie Seneff, PhD, and Greg Nigh, wrote back in 2021 about the unintended consequences of the mRNA COVID-19 “vaccines” creating “unintended proteins.” Their paper is here: https://www.semanticscholar.org/paper/Worse-Than-the-Disease-Reviewing-Some-Possible-of-Seneff-Nigh/, “Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19”, 16 June 2021, International Journal of Vaccine Theory, Practice and Research 2(1), May 10,2021 Page 389 – 430. The point is: there is an “exact understanding” of multiple aspects regarding the mRNA COVID-19 “vaccines” already.]

“From a regulatory perspective, getting approval for a vaccine with such inherent uncertainties should be difficult.”

[YT: Agreed— except that the “new FDA” is doing exactly that already (such as the recent FDA “approval” without any human trials testing of the “2025-2026 Formula COVID-19 Vaccines” by Pfizer-BioNTech, by Moderna, and by Novavax.)]

“Still, I do not believe the mRNA vaccines caused either mass harm on the one hand or saved 14 million lives on the other. Those estimates swing wildly based on speculative modeling, not concrete evidence. A recent modeling study conluded that the global coronavirus vaccination campaign saved 2.5 million lives from 2020 to 2024, mainly among the elderly.”

[YT: “Still I do not believe the mRNA vaccines caused either mass harm…” Really, Dr. Bhattacharya? Did you read through the OpenVAERS website? (https://openvaers.com/) Have you read through the thousands of actual reports of persons who took a COVID-19 “vaccine” and then either died from the injection, or had serious medical issues afterwards from the injection? Are you saying that these reports are “wildly based on speculative modeling?” Are you saying that these reports are not “concrete evidence?” Are you dismissing the extensive work of Ed Dowd, who analyzes statistical reports of claims from insurance companies, claims that have skyrocketed since the COVID-19 “vaccine” rollout in 2021? https://phinancetechnologies.com/, then click on the “Our Projects” PDF brochure on the webpage to find the “Current Projects” section, then click on any of the green arrows.]

“The scientific controversy over the vaccine’s effect on mortality rages on. Science isn’t propaganda agenda. It’s humility.”

[YT: Real science is truth. There isn’t a “controversy” about the “vaccine’s effect on mortality” — the COVID-19 “vaccines” have increased mortality across the board and across the world. Have you read Steve Kirsch’s Substack, Dr. Bhattacharya? (https://kirschsubstack.com/). Mr. Kirsch’s Substack has many articles that quote studies which show that the COVID-19 “vaccines” increase mortality across the board. However, since Mr. Kirsch is not a medical professional, that removes him from “credibility” in the medical professional world, as far as the NIH is concerned? It doesn’t matter that Mr. Kirsch makes his living from collecting and analyzing data (financial and medical)?]

“And when public health officials stopped communicating with humility, we lost much of the public, an absolute necessity for any vaccine platform.”

[YT: Actually: It’s when public health officials withheld the truth about the dangers and the deadliness of the COVID-19 “vaccines” (which the FDA knew about back in early 2021 — please see here: https://phmpt.org/wp-content/uploads/2022/11/5.3.6-postmarketing-experience.pdf, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021.” Please go to the APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST section.) — and the public had to find out the truth themselves — that public health officials “lost much of the public.”]

“I am not here to litigate the past. I am here to chart a better path forward. That is why the NIH, under the leadership of HHS Secretary Robert F. Kennedy, Jr., is investing in new vaccine technologies based on whole-virus inactivated vaccines, which offer a broader immune response and have a longer track record of safety and public acceptance.”

[YT: So, here, apparently, is the “kernel” of the op-ed. Dr. Bhattacharya is not interested in anything related to how dangerous and deadly the current types of COVID-19 “vaccines” have been, and still are. “Let bygones be bygones and just move on” seems to the situation. Not so fast, Doctor. And that “whole-virus inactivated vaccine” scheme that is central to the “Next Generation Gold Standard?” The “Universal Vaccine?” Which, according to the “Next Generation Gold Standard” ethos, may be developed in Petri-dishes in federal government-based facilities only? And the PATENT for which “Universal Vaccine” is owned by the current Acting Director of NIAID, Dr. Jeffery Taubenberger? (https://www.techtransfer.nih.gov/tech/tab-3388)]

“We are continuing the Operation Warp Speed model of investing in technology with the most potential to help Americans.”

[YT: And, will this “continued” Operation Warp Speed model again be done in such a way that important information is deliberately withheld from President Trump47, as was the case with the original Operation Warp Speed in President Trump’s first term?]

“We will move forward with scientific rigor, transparency, and humility. At the NIH, we will fund promising research based not on hype, but on evidence. And I will continue to use my platform to communicate candidly in public conversations where debate and disagreement are welcomed.”

[YT: “Humility” is always a good thing. So is TRUTH.]

“We are entering a new era of public health, grounded not in wishful thinking or performative consensus, but in open inquiry and respect for the American people’s intelligence. The only to rebuild trust is to earn it — one honest conversation at a time.”

[YT: The “one honest conversation at a time” must include the honest admission by the NIH / NIAID / FDA / CDC, that the entire COVID-19 “vaccine” disaster could have been prevented through FDA approval of using re-purposed items to prevent or to treat COVID-19 infection: Ivermectin, Hydroxycholorquine, Doxycycline, Zinc and Vitamin D supplementation. There are plenty of peer-reviewed, published scientific papers which prove that these work. Instead, the FDA, TO THIS DAY, still refuses to approve the use of these items to prevent or to treat COVID-19. Can you explain why this is still the case, Dr. Bhattacharya?]

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 8.15.2025 Open Thread: Special Report Edition

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:

There is another study from Japan, which also confirms that repeated COVID-19 “vaccine boosters” cause increases in mortality. Please see: https://slaynews.com/news/official-japanese-data-confirms-covid-vaccines-caused-worsening-excess-death-surge/, by Frank Bergman, 1 August 2025 (the article title is the same as the URL.) Please see the screenshots from this 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.

There is a Commentary to this paper, to be seen here: https://jxiv.jst.go.jp/index.php/jxiv/preprint/view/1398/, “Commentary: Immune imprinting and spike protein toxicity — rethinking COVID-19 vaccinesty: rethinking COVID-19 vaccines”, Yasuhiko Kamikubo; Takahashi, Atsushi, 2025. This Commentary is in a mixture of English and Japanese. The English translation (no figures included) is here: https://jxiv.jst.go.jp/index.php/jxiv/preprint/view/1398/3679.

The above items confirm this article, written in July 2025: https://justthenews.com/politics-policy/coronavirus/covid-boosters-correlate-worse-survival-rates-cancer-third-most-deaths, “COVID boosters correlate with worse survival rates for cancer with third-most deaths: study”, by Greg Piper, 9 July 2025. Please see the screenshots from this article, which relates to a study in Japan regarding survival rates among COVID-19 “vaccine boosted” pancreatic cancer patients, below:

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.

Further information regarding the “class switch” between IgG3 cells and IgG4 cells resulting from COVID-19 “vaccination” is here: https://jessicar.substack.com/p/the-immunological-mechanism-of-action, “The immunological mechanism of action for lost immunity, a shift to tolerance (and autoimmunity?) from the shots”, by Jessica Rose, PhD, 22 December 2022. Please also see: https://www.theqtree.com/2025/04/04/health-friday-4-4-2025-open-thread-the-covid-19-vaccines-decimate-the-igg-immune-system-cells/; and, https://www.theqtree.com/2024/12/06/health-friday-open-thread-12-6-2024-the-immune-system-after-covid-19-vaccination-and-a-note-on-the-virus-itself/.

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:

Another source of information regarding Chikungunya is here: https://www.who.int/news-room/fact-sheets/detail/chikungunya; please see the 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:

Let’s look at Dr. Zhiyong Xi. https://archive.md/b5xWD:

He is still a professor at Michigan State University in the United States: https://directory.natsci.msu.edu/Directory/Profiles/Person/101715, “Zhiyong Xi”:

And here is a portion of the work that Dr. Zhiyong Xi is doing at Michigan State University, via https://scholars.msu.edu/scholar/8639/ZHIYONG_XI:

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):

And, from the Package Insert for VIMKUNYA (https://bavariannordic.io/uploads/Vimkunya-pi.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.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 8.8.2025 Open Thread: Dr. Martin Makary Edition

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?

Now, on to recent developments in the FDA under Dr. Makary: https://jonfleetwood.substack.com/p/fda-opens-drug-fast-track-with-approvals, “FDA Opens Drug Fast Track With Approvals in as Little as 30 Days – Safety Oversight Under Fire, 26 July 2025. Please see the screenshots from this article, below:

Below is a screenshot from the FDA’ announcement of the new CNPV scheme as it relates to the drug industry (Big Pharma). The FDA press release is found here: https://www.fda.gov/industry/commissioners-priority-voucher-cnpv-pilot-program, 22 July 2025:

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:

On 30 July 2025, Dr. Makary went on CNBC for an interview, in which he stated that the FDA “could hit a record number of approvals this year.” Please see: https://www.cnbc.com/video/2025/07/30/fda-commissioner-dr-marty-makary-the-agency-could-hit-a-record-number-of-approvals-this-year.html. This begs the question: is this FDA “record number of approvals this year” somehow tied into the new CNPV scheme?

While, at the same time, Dr. Makary is”making no plans” to remove mifepristone, the “abortion pill”. from the market. Please see: https://www.semafor.com/article/04/24/2025/fdas-marty-makary-no-plans-to-pull-abortion-pill-mifepristone, 24 April 2025. A screenshot from this article is below:

Yours Truly has written extensively on the board here regarding an organization called BIO (https://www.bio.org/.) Please see: https://www.theqtree.com/2025/07/04/health-friday-open-thread-7-4-2025-independence-day-edition-the-250th-birthday-of-the-united-states-of-america/. BIO is the organization that is actively working behind the scenes to have HHS Secretary Robert F. Kennedy, Jr., removed. This is the organization that “partners closely” with the United States Defense Department in the development of vaccines and other technologies. This organization held a conference for its “partners” and investors in March 2025. Dr. Martin Makary was a headliner speaker at this conference. Please see: https://convention.bio.org/program-1/fireside-chat-martin-makary-md-mph-commissioner-food-drugs-us-food-drug-administration. (Yours Truly was unable to find a copy of the video of this “fireside chat”, nor to find a transcript. It appears that this presentation was available only to attendees of the BIO convention.) Also see: https://convention.bio.org/speaker/martin-makary. Jon Fleetwood discusses this situation on his Substack, here: https://jonfleetwood.substack.com/p/trump-fda-chief-headlines-gates-tied, “Trump FDA Chief Headlines Gates-Tied ‘BIO 2025″ Biotech Convention as Pandemic Infrastructure Expands”, 17 June 2025. Please see the screenshot from the Fleetwood article, below:

In addition, there is another part of this “tapestry”: the statements by Dr. Makary himself as recorded in https://bgrdc.com/, a “Premier Bipartisan Public Affairs Firm” (per their website) based in Washington, DC. The following screenshots are from https://bgrdc.com/wp-content/uploads/2025/01/Dr-Makary-Policy-Positions.pdf:

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.

Yours Truly also wrote about the self-amplifying RNA “vaccine”, ARCT-2304, on this board. Please see: https://www.theqtree.com/2025/06/20/health-friday-6-20-2025-the-new-fda-did-hhs-secretary-robert-f-kennedy-jr-approve-of-all-this/.

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.

Peace, Good Energy, Respect: PAVACA

Health Friday 8.1.2025 Open Thread: The FDA and the CDC — Rebuild Them From Top To Bottom

The free vintage public health poster from World War II about washing the hands is courtesy of Open Culture and Google Images.

Health Friday is a series of information 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 by 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. Other than AI-generated images that may be embedded in URL links, to the best of her knowledge and belief, there is none. If readers wish to post any AI-generated content in today’s discussion thread, they must cite their source. Note Two: Nothing in today’s offering is intended to be, nor shall it be construed as, what might be termed “character assassination” regarding HHS Sec. Kennedy, Jr., or any employee (current or former) of the FDA or of the CDC. Thank you.

Today’s offering is about one topic: It is past time to: first, to shut down the Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) divisions of the United States Department of Health and Human Services (HHS); then, second, to rebuild these agencies from top to bottom so that they truly serve the public health of Americans.

Yours Truly begins here: https://sashalatypova.substack.com/p/another-day-another-episode-of-the, “Another day, another episode of the new FDA lying just like the old FDA…plus self dealing by MAHA Action”, by Sasha Latypova, 28 July 2025. This article regards certain statements by Dr. Martin Makary, the current Commissioner of the FDA. Ms. Latypova worked in Big Pharma for her professional career, designing and helping to implement clinical studies for drugs. She retired from her career when she realized that, in Yours Truly’s opinion, she concluded that it was all part of a “shell game” that was played by Big Pharma. Since retiring, Ms. Latypova has begun a new endeavor: to expose this “shell game.” There are those who may differ with certain of Ms. Latypova’s opinions; however, Yours Truly believes that she is right on the mark on multiple issues. Please see the screenshot from her article, below:

The Latypova 28 July article discusses several aspects of what appears to Yours Truly to be two things: first, an internecine war going on within the FDA; and, second, deep and potentially catastrophic conflicts of interest within certain key employees of the FDA regarding their personal prejudices versus the line of their duties within the FDA. The transcript portion above is from an interview with Dr. Martin Makary (current FDA Commissioner) by Jan Jekielek of American Thought Leaders (ATL) of 16 July 2025; the second screenshot is Ms. Latypova’s considered opinion as to what is going on “behind the scenes.” The Jekielek tweet about this interview, with an embed of the interview itself, is here: https://x.com/JanJekielek/status/1945560472909906288.

Yours Truly now turns to the case of Dr. Vinay Prasad, the now-former head of the CBER division of the FDA (Center for Biologics Evaluation and Research.) The CBER division of the FDA is responsible, among other duties, to make sure that “biological products” (drugs, vaccines, and so on) are “safe and effective” and are available “to those who need them” (https://www.fda.gov/about-fda/fda-organization/center-biologics-evaluation-and-research-cber). Dr. Prasad joined CBER as the new Director in May 2025, and he resigned abruptly on 29 July 2025. Sasha Latypova wrote the following article about the situation: https://sashalatypova.substack.com/p/breaking-vinay-prasad-is-out-from, “Breaking: Vinay Prasad is out from the FDA!”, 29 July 2025. Please see the screenshot from this article, below:

About the Sarepta decision: please see https://sashalatypova.substack.com/p/sarepta-plot-thickens, 25 July 2025, and the screenshot from this article, below:

Dr. Prasad was an opponent of the FDA re-instating the use of Elevidys for young people with Duchenne Muscular Dystrophy who can still walk (as opposed to the 18 July 2025 FDA request that the drug be stopped for all Duchenne Muscular Dystrophy patients.) He was overruled by Dr. Martin Makary.

The Latypova article above presents an argument that the FDA re-instatement of Elevidys is profound on several levels — among them, funding for the drug’s manufacturing company, Sarepta. And there are other “ripple effects” from this re-instatement: please see the screenshot of the stock value of Sarepta related to the FDA withdrawal of the drug; then, to the FDA re-instatement:

Yahoo Finance has this article regarding Sarepa, funding, and the Elevidys situation: https://finance.yahoo.com/news/fda-ask-sarepta-halt-elevidys-193245811.html. Please see the screenshot from this article, below:

Elevidys, by the way, has a list of adverse effects and other complications; among them is acute liver injury (this is what killed the patients who passed away after being treated with Elevidys.) Please see the Package Insert for this drug, available here: https://www.drugs.com/pro/elevidys.html, “Sarepta Refused FDA’s Request to Halt Elevidys Shipments”, 18 July 2025.

Regarding the departure of Dr. Prasad from the FDA’s CBER division, there are several “pieces to the puzzle” (and some of these “pieces” are still unknown.) However, Yours Truly has been able to trace the following:

ONE: Please see the items above in today’s offering related to the Sarepta / Elevidys situation and the involvement of Dr. Prasad.

TWO: It was Dr. Vinay Prasad who signed off on the Moderna modRNA COVID-19 “vaccine” SPIKEVAX being used on babies and young children ages 6 months to 11 years old. This “FDA full approval” was signed on 9 July 2025. Dr. Prasad did this signing off on his own authority as Director of the FDA’s CBER division, and without informing HHS Sec. Kennedy, Jr., who was on vacation. However, there is another aspect of the issue: Did Dr. Prasad confer with, and/or communicate with, Dr. Martin Makary, either in advance of, or after, this signing off? Please see: https://www.thegatewaypundit.com/2025/07/now-we-know-who-approved-spikevax-vaccine-children/, “Now We Know the Official Who Approved the Spikevax Vaccine for Children While Robert Kennedy Jr. Was Allegedly on Vacation”, by Jim Hoft, 31 July 2025. Please see a screenshot from this article, below:

THREE: The investigative reporter, Laura Loomer, posted multiple items regarding Dr. Prasad that, in his own words, paint him as a believer in left-wing political positions; as a person who actually despises President Donald Trump 47; and more. The 2nd Smartest Guy in the World Substack article on the Laura Loomer investigation is here: https://www.2ndsmartestguyintheworld.com/p/breaking-vinay-prasad-is-out-at-the, “BREAKING: Vinay Prasad is Out at the FDA”, 30 July 2025. Please see the screenshots from this article, portions of Ms. Loomer’s X posts of her investigation, below:

Laura Loomer’s X post is here: https://x.com/LauraLoomer/status/1947103566239289523.

Last, but not least, is the situation now at the CDC (Centers for Disease Control and Prevention.) The United States Senate, on a strictly “party-line vote”, just confirmed Susan Monarez, PhD, who had been serving as Acting Director of the agency, to be Director of the CDC. Dr. Monarez is a well-known proponent of “vaccines save lives.” Please see: https://apnews.com/article/susan-monarez-cdc-director-senate-hearing-rfk-c7c883f604711238643a9ffd1681bcc0, “CDC nominee Susan Monarez sidesteps questions about disagreements with RFK in Senate hearing”, by Jonel Aleccia, 25 June 2025. Please see the screenshots from this article, below:

Note Dr. Monarez’s emphasis on the role of “public health interventions, including immunizations…”.

Yours Truly’s opinion on all the above in today’s offering is that there are real and divisive issues with the FDA and the CDC, who both appear to be in opposition to HHS Secretary Robert F. Kennedy, Jr. In her opinion, it is time to shut down both agencies and to rebuild them from top to bottom, so that the new entities truly reflect their duty to serve the public health of Americans.

FLASH! JUST ON THE WIRES NOW: https://www.politico.com/newsletters/politico-pulse/2025/07/31/why-trump-ordered-ouster-of-fda-official-00485966, 31 July 2025. It appears that it was President Trump 47 himself who ordered the firing of Dr. Vinay Prasad, overruling both HHS Sec. Robert F. Kennedy, Jr., and Dr. Martin Makary, who opposed Dr. Prasad’s ouster. (Since it’s POLITICO, perhaps a “measure of salt” should be in order… it’s that “people with knowledge of the decision” stuff in the POLITICO article.)

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 7.25.2025 Open Thread: More on the COVID-19 “Vaccines” and What They Do to the Human Brain

The header image of the pituitary gland and the influence it has on the human body is courtesy of https://www.123rf.com/ and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to the disaster of the COVID-19 “vaccines” (Bioweapon Toxin Injections), Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative, toxic effects of the the COVID-19 “vaccines” that they had injected into their body.

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 post for any AI-generated content. To the best of her knowledge and belief, the only AI-generated content are images that may be embedded in certain of the linked items in today’s post. If readers wish to post any AI-generated content in today’s discussion thread, they must cite their source. Note Two: the format of today’s offering will be a combination of “in-text” links, with other items having numerical identifiers such as would be used in a scientific research article or paper. Citations related to the numerical identifiers will be listed at the end of the post. Thank you.

Today’s offering regards more information on the negative effects that the COVID-19 “vaccines” have on the human brain. The trail begins here:

Recall that Dr. Sucharit Bhakdi, MD, a medical microbiologist who is involved with the Doctors for COVID Ethics organization (https://doctors4covidethics.org/), and who is a dual citizen of Thailand and of Germany, was put on trial in Germany for his anti-COVID-19 “vaccine” stance. The court returned a verdict of Not Guilty in May 2023. The prosecutor’s appeal of Dr. Bhakdi’s Not Guilty verdict, an appeal that was to go to court in February 2025, was postponed [1]. More on the story related to the tweet by Dr. Bhakdi is here: https://slaynews.com/news/renowned-microbiologist-mrna-vaccines-destroyed-brains-billions-people/, “Renowned Microbiologist: mRNA ‘Vaccines’ ‘Destroyed the Brains’ of ‘Billions of People'”, by Frank Bergman, 14 July 2025.

Yours Truly has written extensively on this board about some of the negative effects of the COVID-19 “vaccines” on the brain of the “vaccinated” person. These articles are found here: https://www.theqtree.com/2024/10/18/health-friday-10-18-2024-special-edition-effects-of-the-covid-19-vaccines-physical-and-neurological/; https://www.theqtree.com/2024/11/08/health-friday-11-0-2024-open-thread-the-insidious-n1-methylpseudouridine-in-the-modrna-covid-19-vaccines/; and, https://www.theqtree.com/2025/03/21/health-friday-3-21-2025-open-thread-more-on-the-n1-methylpseudouridine-in-the-modrna-covid-19-vaccines/.

Today’s offering speaks to the negative effects of the COVID-19 “vaccines” on the human brain having to do with two small, but very important, glands located in the brain: the pituitary gland and the pineal gland.

The pituitary gland, a small, pea-shaped gland,is found in the human brain near the hypothalamus. The pituitary gland secretes several hormones that are important to various body functions. The pineal gland, another small gland, is found in the center area of the human brain. The pineal gland, among other functions, secretes melatonin, a hormone that is important for the body’s circadian rhythm and for proper sleep. The pituitary gland, the pineal gland, and the hypothalamus are components of the endocrine system of the human body. Please see the screenshots below: the first is about the pituitary gland [2]; the second is about the pineal gland [3]; and the third is from an article on the pineal gland that includes a discussion about the endocrine system [4]:

The ingredients (and, therefore, the mechanisms) of the COVID-19 “vaccines”, once injected into the body, quickly spread, via the dangerous lipid nanoparticles “rapid delivery system” compounds that are contained in these injectables, to every area of the human body, including to the brain. Yours Truly has written and posted about these lab-created compounds. They are: ALC-0159 and ALC-0315 in the Pfizer-BioNTech modRNA COVID-19 “vaccines” (all of them); and, SM-102 in the Moderna modRNA COVID-19 “vaccines” (all of them.) It is now known that the COVID-19 “vaccines” cross the Blood-Brain Barrier of the human body and do damage to the brain. Once inside the brain, these “vaccines” can, and do, induce multiple problems ranging from Central Nervous System damage, to stroke, to cognitive impairment, to Alzheimer’s disease, and more. The Ota, et al., 2025 paper demonstrates that the COVID-19 spike protein (the foundation ingredient of the modRNA COVID-19 “vaccines”) enters the cerebral arteries [5]. Please see a screenshot from this paper, below:

The Roh, et al. paper, from 2024, demonstrates that the modRNA COVID-19 “vaccines” can induce Alzheimer’s disease [6]. Please see a screenshot from the Abstract of this paper, below:

A compilation of articles regarding how the COVID-19 “vaccines” enter the human brain and induce damage is here: https://www.2ndsmartestguyintheworld.com/p/vaids-bombshell-the-covid-vaccine, “VAIDS BOMBSHELL: “The ‘Covid Vaccine’ is a CHEMICAL LOBOTOMY. A recent study of 558,017 Koreans found that the mRNA shots Increase the Risk of Cognitive Impairment +137.7% & Alzheimer’s disease +22.5”, 23 July 2025. There are numerous links in this article to previous posts in this Substack which discuss brain issues after COVID-19 “vaccination.” The Ota, et al., paper is also mentioned.

There is another aspect of the issue regarding how the modRNA COVID-19 “vaccines” enter into every area (and, therefore, into the cells of these areas) of the “vaccinated” human body. This is the fact that the PRRARSV gene code piece from the Pangolin MP789 coronavirus is present in BOTH the Pfizer-BioNTech and the Moderna modRNA COVID-19 “vaccines” (all of them.) This particular gene code piece has a 90%+ compatibility to the human genome code. In the Pfizer-BioNTech modRNA COVID-19 “vaccines”, PRRARSV functions as a “backdoor key” to facilitate entry into every cell in the “vaccinated” person’s body. Both our host, Wolf Moon, and Yours Truly has written about this situation here, for examples: https://www.theqtree.com/2023/05/01/pfizer-and-moderna-vaccines-both-contain-prrarsv-key-to-the-cell-nucleus/; and, https://www.theqtree.com/2024/11/27/placeholder-open-thread-11-27-2024-prrarsv-part-2-pangolin-edition/.

Back to the pituitary gland and the pineal gland of the human brain. Dr. Michele Ross, PhD, discusses the four areas of the brain that are not specifically protected by the Blood-Brain Barrier. Please see a screenshot from her article [7], below:

The modRNA COVID-19 “vaccines” enter and damage the pituitary gland, one of the glands that is not specifically protected by the human Blood-Brain Barrier. The Taieb and Mounira paper from 2024 discusses this issue [8]. Two screenshots from their paper are below; the first is from the Abstract; the second is the Figure 2:

Another paper, by Verrienti, et al., from 2024, is a review of effects on the pituitary gland after COVID-19 “vaccination”[9]. Please see the screenshots from this paper, below. The first is the Conclusions section; the second is the Figure 1.

************ And now, to what may appear to be a minor point, but actually is, in Yours Truly’s opinion, an important aspect of the types of damage that the modRNA COVID-19 “vaccines” do to the pineal gland of the human brain: these injectables interfere with the ADAMTS3 enzyme (a protein), part of the adamalysin family of enzymes. The influences of the ADAMTS enzymes in the human body range from functions in the brain, to correct growth of the lymphatic vessels, and more. Please see the screenshot from the Wikipedia entry on ADAMTS [10], below:

One member of the ADAMTS family is ADAMTS3. This enzyme (protein) is involved with, among other functions, the proper regulating of the brain’s cortex (the cerebral cortex, the outer “covering” of the brain.) Please see the screenshot from the Wikipedia entry on ADAMTS3 [11], below:

Pay special attention to the mention of Reelin. This protein is essential to the lamination of the cerebral cortex (lamination of the cerebral cortex appears like “multiple folds.”) When Reelin is decreased during the human aging process, brain function is negatively affected. When Reelin is decreased at other times in the human lifespan, the result can be Schizophrenia and other neurological conditions. Please see the screenshot from the Sighild Lemarchant article of 2017 [12], below:

The Cleveland Clinic article on the cerebral cortex starts with the following [13]:

************ And here is the “tie-in” to the COVID-19 spike protein and the brain: the spike protein of this virus interferes with the functioning of ADAMTS3. The Seabra Rodrigues Dias, et al., 2022 paper discusses what COVID-19 does to disrupt the work of the ADAMTS enzymes in the body [14]. Please see the screenshots from this paper, below. The first is a portion of section 2.5 Adamalysin expression in COVID-19 patients; the second is the Table 2. of body areas and functions that ADAMTS3 influences:

************ It is Yours Truly’s considered opinion that, since the modRNA COVID-19 “vaccines” (and the COVID-19 virus itself) contain elements that accelerate the aging of the entire body, down to the mitochondrial level, they also accelerate aging of the Reelin function in the brain related to ADAMTS3. This accelerated aging of the Reelin function can “leave the door open” for the development of cognitive impairment, of dementia, of Alzheimer’s disease, and other neurological / psychological conditions. Please see: https://www.theqtree.com/2023/10/28/the-covid-19-virus-and-the-modrna-covid-19-vaccines-induce-accelerated-aging/.

Yours Truly will point out that, while the COVID-19 virus itself does not contain the lab-created compound N1-Methylpseudouridine, nor the dangerous lipid nanoparticles ALC-0159, ALC-0315, or SM-102 — the COVID-19 virus itself does contain the PRRARSV “backdoor key”, and it also appears to contain elements that interfere with ADAMTS enzymes (proteins) in the body, including ADAMTS3 and the function of the Reelin protein in the brain. In my opinion, these facts may contribute to the incidence of “Long COVID” in non-COVID-19 “vaccinated” persons who contract an infection of the COVID-19 virus itself, recover from it, but then can present with symptoms of “Long COVID.” This is aside from COVID-19 “vaccinated” persons who can also present with symptoms of “Long COVID.” These “Long COVID” symptoms may present as neurological and/or psychological issues (either new-onset, or aggravation of previously-diagnosed conditions.)

TO CONCLUDE: It is Yours Truly’s considered opinion that the modRNA COVID-19 “vaccines” were designed to damage, to injure, and/or to destroy, the human body. This damage, injury, and/or destruction includes every organ and area of the body of a person who has taken any injection of modRNA COVID-19 “vaccines.” This damage, injury, and/or destruction begins the moment that the modRNA COVID-19 “vaccine” is injected into the body. The modRNA COVID-19 “vaccines” contain a lab-created compound, N1-Methylpseudouridine, that replaces the natural Uridine in the “vaccinated” person’s body with a “fake” Uridine combined with a type of methane. Natural Uridine plays crucial roles in multiple types of brain function, in mood regulation, and in the regulation of the “gut-brain axis” functions of the body. N1-Methylpseudouridine has no role in the body beyond replacing natural Uridine, thus weakening the “vaccinated” person’s body natural immune system against the other ingredients and mechanisms of the “vaccines.” The modRNA COVID-19 “vaccines” contain dangerous lab-created lipid nanoparticles, which quickly spread the ingredients (and, therefore, the mechanisms) of the modRNA COVID-19 “vaccines” throughout the body of the “vaccinated” person, including crossing the Blood-Brain Barrier and entering the brain. The modRNA COVID-19 “vaccines” induce multiple types of damage and injury to the brain, including to the areas of the brain that are not specifically protected by the Blood-Brain Barrier, such as the pituitary gland and the pineal gland. The modRNA COVID-19 “vaccines” contain elements that interfere with the important ADAMTS3 enzyme (protein) of the body; a protein that plays critical roles in multiple areas, including the proper regulation of the cerebral cortex covering of the brain. The spike protein in the modRNA COVID-19 “vaccines” interfere with the proper function of the Reelin protein in the brain as it relates to ADAMTS3. The modRNA COVID-19 “vaccines” also contain the PRRARSV gene code piece from the Pangolin MP789 coronavirus; PRRARSV acts as a “backdoor key” that facilities the entry of the COVID-19 spike protein in the modRNA “vaccines” to enter the nucleus of every cell in the “vaccinated” person’s body. [The above are aside from the fact that the modRNA COVID-19 “vaccines” also contain a SV40 cancer promoter gene code piece from the African Green Monkey.] The COVID-19 virus itself contains the PRRARSV gene code piece; and, it also appears to contain elements that interfere with the important ADAMTS3 enzyme of the body. In addition, there is the now-known phenomenon of COVID-19 “vaccine” spike protein “shedding” from “vaccinated” persons onto other persons, including onto non-COVID-19 “vaccinated” persons. It is Yours Truly’s considered opinion that this “shedding” can also potentially result in negative neurological effects, among other negative effects, in non-COVID-19 “vaccinated” persons. Yours Truly is NOT advocating that non-COVID-19 “vaccinated” persons avoid all contact with persons who may be COVID-19 “vaccinated”: but, instead, to be following a prophylatic COVID-19 spike protein protocol. In addition, ALL persons who have ever taken a COVID-19 “vaccine”, and ALL non-COVID-19 “vaccinated” persons who have been infected with COVID-19 and recovered, ALSO need to be following a COVID-19 spike protein mitigation / reduction protocol.

************ Yours Truly will state the following: It is past time for all COVID-19 “vaccines” to be taken off the market, and to be completely removed from use; to have all COVID-19 “vaccines” completely removed from any and all “recommendation lists” issued by any government agency, any private or non-governmental agency or organization, any hospital, clinic, pharmacy, nursing home or care facility, and any school board or educational facility; to have all COVID-19 “vaccine” inventories that are used on human beings reduced to zero; to retain only those COVID-19 “vaccine” vials that will be used for complete analysis and data compilation regarding the exact ingredients in these injectables and the sources of these ingredients, with the resulting information and data analyses made public; and, to hold to full account those who created the COVID-19 virus itself and the COVID-19 “vaccines.”

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Citations:

[1] “Timeline: Prof. Sucharit Bhakdi Case”. https://doctors4covidethics.org/timeline-of-the-events/

[2] “Pituitary Gland: What It Is, Function & Anatomy”. Last reviewed on 04/04/2022/ https://my.clevelandclinic.org/health/body/21459-pituitary-gland.

[3] “5 Functions of the Pineal Gland”. Neel Duggal, medically reviewed by Avi Varna, MD, MPH, AAHIVS, FAAFP. Updated December 20, 2022. https://www.healthline.com/health/pineal-gland-function.

[4] “Pineal gland”. Last reviewed on 06/22/2022. https://my.clevelandclinic.org/health/body/23334-pineal-gland.

[5] Ota N., Itani M., Aoki T., Sakurai A., Fujisawa T., Okada Y., Noda K., Arakawa Y., Tokuda S., Tanikawa R. Expression of SARS-CoV-2 spike protein in cerebral Arteries: Implications for hemhorrhagic stroke Post-mRNA vaccination. J Clinical Neuroscience. Volume 136, June 2025 111223.

[6] Jae Hoon Roh, Inha Jung, Yunsun Suh, Min-Ho Kim, A potential asssociation between COVID-19 vaccination and development of Alzheimer’s disease, QJM: An International Journal of Medicine, Volume 117, Issue 10, October 2024, Pages 709-716, https://doi.org/10.1093/qjmed/hcae103.

[7] “4 Parts of the Brain Not Protected by the Blood-Brain Barrier”, Michele Ross, Phd. n.d. https://drmicheleross.com/brain-not-protected-blood-barrier/.

[8] Taieb A, Mounira EE. Pilot Findings on SARS-CoV-2 Vaccine-Induced Pituitary Diseases: A Mini Review from Diagnosis to Pathophysiology. Vaccines (Basel). 2022 Nov 24; 10(12):2004. doi.10.3390/vaccines10122004. PMID: 36560413; PMCID: PMC9786744.

[9] Verrienti, M., Picciola, V., Ambrosio, M.R. et al. Pituitary and COVID-19 vaccination: a systematic review. Pituitary 27, 970-985 (2024). https://doi.org/10.1007/S11102-024-01402-2.

[10] “ADAMTS”. https://en.wikipedia.org/wiki/ADAMTS.

[11] “ADAMTS3”. https://en.wikipedia.org/wiki/ADAMTS3.

[12] Relevance of the Proteolytic Processing of Reelin by ADAMTS-3 in Brain Functions. Sighild Lemarchant. Journal of Neuroscience 19 July 2017, 37 (29) 6814-6815; DOI: 10.1523/JNEUROSCI.1077-17.2017.

[13] “Cerebral Cortex”. https://my.clevelandclinic.org/health/articles/23073-cerebral-cortex. Last reviewed on 05/23/2022.

[14] “Adamalysins in COVID-19 — Potential mechanisms behind exacerbating the disease” Ivo Ricardo de Seabra Rodrigues Dias, Zhijian Cao, Hang Fai Kwok. J Biomedicine & Pharmacotherapy. Vol. 150, June 2022, 112970.

Peace, Good Energy, Respect: PAVACA

Health Friday 7.18.2025 Open Thread: Moderna, the FDA, and the NIH/NIAID

The header image for today’s post is courtesy of iStock and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to the disaster of the COVID-19 “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have passed away from the negative effects of the COVID-19 “vaccines” that they had injected into their body.

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 one AI-generated image in The Focal Points article, cited below. If readers wish to add any AI-generated content to the discussion thread for today’s offering, they must cite their source. Thank you.

The phrase to keep in mind when reading today’s post is: Follow the money.

Today’s post begins here: https://www.thefocalpoints.com/p/fda-commits-grave-betrayal-fully, “FDA Commits Grave Betrayal: Fully Approves Deadly Genetic Injections for Infants”, by Nicolas Hulscher, MPH, 11 July 2025. There is an embedded video interview with Mr. Hulscher in this article. This article and interview regard the FDA “full approval” on 10 July 2025 of the Moderna modRNA COVID-19 “vaccine”, SPIKEVAX, to be used on infants and young children from age 6 months to 11 years old. A screenshot of a portion of the Table 2. from this article is below, showing the amounts of “loose” DNA in this “vaccine”:

The published scientific paper that is linked in the above Hulscher article is here: https://publichealthpolicyjournal.com/review-of-calls-for-market-removal-of-covid-19-vaccines-intensify-risks-far-outweigh-theoretical-benefits/, “Review: Calls for Market Removal of COVID-19 Vaccines Intensify as Risks Far Outweigh Theoretical Benefits”, Nicolas Hulscher, Mary Bowden, Peter A. MCullough, 28 January 2025.

Yours Truly now turns to a crucial component of the Moderna modRNA COVID-19 “vaccine” situation: the “tied to the hip” relationship that this company has with the NIAID (National Institute of Allergy and Infectious Diseases), part of the NIH (National Institutes of Health.) Both the NIAID and the NIH are institutes of the federal government Department of Health and Human Services (HHS.) Katherine Watt, of Bailiwick News, has studied and written about the “coziness” between Big Pharma entities such as Pfizer-BioNTech and Moderna with federal government agencies, such as the FDA. Please see: https://bailiwicknews.substack.com/p/why-pfizer-and-moderna-and-fda-are, “Why Pfizer and Moderna and FDA are working toward government authorization to inject babies and small children”, 23 March 2022. Ms. Watt includes a statement made by Robert F. Kennedy, Jr. in 2021, on this situation. Please see: https://wsau.com/2021/12/31/robert-f-kennedy-jr-explains-why-fauci-is-going-after-children/, by Meg Ellefson, 31 December 2021. A screenshot from the Bailiwick News article on this is below:

There are SEC filings and “Confidential Agreements” between Moderna, the FDA. and the NIAID, regarding the funding and development of mRNA “vaccines.” There are patent co-ownership and revenue-sharing agreements between Moderna and the NIAID. There is a Moderna – NIH Confidential Agreement that goes back to 2015.

The trail begins here: https://www.reuters.com/business/healthcare-pharmaceuticals/moderna-make-milestone-payments-nih-covid-vaccine-2023-02-24/,”Moderna to make milestone payments to NIH for COVID vaccine”, 24 February 2023. Please see the screenshot from this article, below:

By the way, milestone payments would include payments for items such as, developing the “latest version” of a COVID-19 modRNA “vaccine” — for examples: the Moderna (SPIKEVAX) “2025-2026 COVID-19 Formula Vaccine” that was just “recommended” by the ACIP committee of the CDC; and, the FDA “full approval” of SPIKEVAX being used on infants and young children age 6 months to 11 years old, which “full approval” was granted on 10 July 2025. It appears that Moderna had attempted to “modify” or “avoid” certain types of sharing agreements stipulations, royalty payments to the HHS (via the NIAID), and HHS – Moderna co-owned patents agreements; and, for which, the company was taken to court by the HHS. The decision was rendered against Moderna, with an order to make a multi-million dollar “catch-up payment” to HHS -NIAID.

Another aspect of the trail is here: https://thehill.com/opinion/congress-blog/4533574-how-the-national-institutes-of-health-became-a-den-of-cronyism/, by Sen. Rand Paul, MD (R-KY), 15 March 2024. Please see the screenshot from this article, below:

Now, to the 2015 “Confidential Agreements” between Moderna and the NIH. The document is found here: https://www.documentcloud.org/documents/6935195-NIH-Moderna-Confidential-Agreements/, November 2015. This document has numerous “amendments” and “additions” that go through the year 2018 — and, the last of which appears to “cover” all items related to COVID-19 “vaccines”. On page 16 of the document, with special attention to page 19, start the CRADA stipulations (Cooperative Research and Development Agreement stipulations between Moderna and the NIH.) The language here has numerous Proprietary Information redactions; however, it appears to be broad enough to cover the later co-ownership by Moderna and the NIH of the SPIKEVAX patents and their Expiry Dates (more on these below.)

Here are page 19 and a portion of page 20 of the NIH/NIAID and Moderna CRADA agreement, below:

Recall that the director of the NIAID in 2015 was Dr. Anthony Fauci; and, the director of the NIH in 2015 was Dr. Francis Collins.

The third part of the trail is here, the SEC filing that details the NIH – Moderna agreements to share COVID-19 “vaccine” development, patents, and royalty payments for use of said “vaccines”, is found here: https://www.sec.gov/ix?=docs/Archives/edgar/data/1682852/000168285223000011/mrna-20221231.html, filed 31 December 2022.

Page 41 of this document names the “partners” that will be included in the agreements: DARPA; BARDA; and, the Bill and Melinda Gates Foundation.

Page 43 of this document details the SPIKEVAX patents and Expiry Dates that will be co-owned by Moderna and the NIH. A screenshot of this page is below:

There is also a “vaccine mechanisms” series of sections in this agreement. A screenshot of one of these sections is below:

And, there is a section regarding the “Drug Design Studio” section of the SEC document. Please see the screenshot from this section, below:

On 7 July 2025, HHS Secretary Robert F. Kennedy, Jr., cancelled the 10 July meeting that was scheduled for the USPSTF committee of the HHS (United States Preventive Services Task Force committee.) If Sec. Kennedy, Jr., can do this, why can’t he do something to modify / rescind / cancel the NIH / NIAID – Moderna “Confidential Agreements”, the related royalty-sharing payments agreements, and the 31 December 2022 SEC filing? Is it because of the “SPIKEVAX Patents and Expiry Dates” agreement, the screenshot of which from the SEC filing is above, and which runs, in total, until 22 October 2041? Are his hands tied? “Inquiring minds want to know.”

FLASH ADDENDUM: Our good Gail Combs asked to have the following added to today’s offering, regarding the development of a new BLACK PLAGUE strain variation that was just done by scientist in Israel. Yours Truly is also adding another item related to other work developing BLACK PLAGUE strain variations.

ISRAELI scientists have just developed an mRNA-based BLACK PLAGUE (Yersinia Pestis, or Y. Pestis) vaccine, using a lab-modified gene and adding N1-Methylpseudouridine as the lipid nanoparticle “delivery system.” Please see: https://jonfleetwood.substack.com/cp/168494356, “Israel Engineers Mutant Plague — Puts Its Genes in mRNA Shot That Makes Human Cells Produce Virulence and Immune-Evasion ‘Black Death’ Proteins: Journal ‘Advanced Science'”, 16 July 2025. This is the “BLACK PLAGUE version” of the modRNA + N1-Methylpseudouridine COVID-19 “vaccines” — except that the “payload” is a lab-created genetically altered and more virulent version of the BLACK PLAGUE.

Recall that Yours Truly has written extensively about the mechanism of the N1-Methylpseudouridine used in the Pfizer-BioNTech and in the Moderna modRNA COVID-19 “vaccines” (there’s the connection to Moderna.) This lab-created compound ingredient replaces the natural Uridine in the COVID-19 “vaccinated” person’s body, kicking the door wide open for catastrophic immune system evasion by said “vaccine”: evasion that will occur throughout the body and also the brain. The connection to both Moderna and to Pfizer-BioNTech in regards the use of N1-Methylpseudouridine is that BOTH companies specifically included this lab-created chemical compound in their modRNA COVID-19 “vaccines”, the description of which inclusion IS IN THE PATENT DOCUMENTS THAT WERE FILED BY EACH COMPANY. This begs the question: Did the Israeli scientists pay either Pfizer-BioNTech or Moderna for the “rights” to use this compound IN THEIR BLACK PLAGUE VARIATION “VACCINE” EXPERIMENTS?

The peer-reviewed paper that is referred to in the Jon Fleetwood article is here: https://doi.org/10.1002/advs.202501286, “Novel Bivalent mRNA-LNP Vaccine for Highly Effective Protection Against Pneumonic Plague”, Dan Peer, et al., 25 April 2025. A screenshot from the Fleetwood article is below:

But wait, there’s more! The Fleetwood article links to a paper published in 2024 regarding research by the United States Army Combat Capabilities Development Command Chemical Biological Center in Gunpowder, Maryland, ALSO on lab-creating a variation of the BLACK PLAGUE. This variation was “cultured” in a “bath” of Escherichia coli (E. coli, the same type of “culturing material” that is used by both Pfizer-BioNTech and by Moderna to produce their respective modRNA COVID-19 “vaccines.” The paper is here: https://doi.org/10.1099/acmi.0.000723.v3, “Towards a Yersinia Pestis lipid A recreated in an Escherichia coli scaffold genome”, Nathan D. McDonald, Erin E. Antoshak, 17 July 2024. A screenshot of the Abstract of this paper is below:

In Yours Truly’s opinion: The entire “let’s make a lab-created RNA + lipid nanoparticle vaccine” situation is out of control. The entire “let’s alter a gene or two from a deadly infectious disease and make a variation of this disease” situation is out of control.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday Open Thread 7.4.2025: Independence Day Edition: The 249th Birthday of the United States of America

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.

Peace, Good Energy, Respect: PAVACA

Health Friday Open Thread 6.20.2025: The “New FDA” — Did HHS Secretary Robert F. Kennedy, Jr., Approve All of This?

The above free image of an approval stamp is courtesy of Depositphotos and Google Images.

Health Friday is a series regarding Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to the disaster of the COVID-19 “vaccines” (in reality, dangerous and deadly Bioweapon Toxin Injections), Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative effects of the COVID-19 “vaccines” that they had permitted be 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. There appears to be an AI-generated image in the Children’s Health Defense article by Dr. Brenda Baletti, PhD, that is cited below in today’s offering, just below the header title. If readers wish to add any AI-generated content to today’s discussion thread, they must cite their source. Thank you.

Note 2: Yours Truly is aware that there are other very important news stories and events that are unfolding that are not health-related. However, the following needs to be presented.

Robert F. Kennedy, Jr., an attorney, an outspoken critic of Big Pharma and other entities that, up to now, had an undue influence on government health agencies, and who is the founder of Children’s Health Defense (https://childrenshealthdefense.org/), has been confirmed as the Secretary of the Department of Health and Human Services (HHS) under the new administration of the 47th President of the United States, Donald Trump. Secretary Kennedy, Jr., has already done several things to re-focus the mission and activities of HHS in the direction of being more responsive to the public health of all Americans. Among these moves was his rescinding a previously-awarded HHS grant of $590 million dollars to Moderna to develop Avian Influenza and “pandemic vaccines.” This grant was awarded to Moderna by outgoing HHS Secretary Xavier Becerra in the final days of the previous administration of former President Joe Biden. Please see: https://www.cidrap.umn.edu/avian-influenza-bird-flu/hhs-cancels-funding-moderna-s-candidate-h5-avian-flu-and-pandemic-vaccines, by Lisa Schnirring, 29 May 2025.

On the other hand, HHS has, under Secretary Kennedy, Jr., also made some decisions that have raised eyebrows: for example, in April 2025, the Food and Drug Administration (FDA, a division of HHS) granted “Fast Track” approval for the self-amplifying modRNA H5N1 “pandemic vaccine”, ARCT-2304, to be tested in the United States. Please see: https://www.contagionlive.com/view/fda-grants-fast-track-status-to-arct-2304-for-h5n1-influenza-protection, by Sophia Abene, 10 April 2025. ARCT-2304 is expected to submit the BLA (Biologics License Application) documents and data for ARCT-2304 by early fall 2025. However, there’s something else that’s eyebrow-raising about this situation: The clinical trial for ARCT-2304, the data from which is going to be used in the BLA submission, has no true Placebo Control Group (a Placebo that uses Saline solution) — instead, the “Placebo Control Group” in the clinical trial is being injected with a “Placebo Vaccine.” How does this fit in with the “new FDA” that requires Placebo testing? Does the “new FDA” concept of “Placebo” now mean anything that is not the actual “candidate” drug or injectable when used in a clinical trial? Please see: https://sashalatypova.substack.com/p/arcturus-self-amplifying-rna-shots, “Arcturus self-amplifying RNA: US approval expected this year”, 11 June 2025. A screenshot from this article is below:

Also, the FDA granted “full approval” for Moderna’s “next-generation” COVID-19 “vaccine”, mNEXSPIKE, on 31 May 2025, despite a clinical trial in which there was no placebo Control Group. Please see: https://www.fda.gov/vaccines-blood-biologics/mnexspike, 31 May 2025. Please also see: https://www.theqtree.com/2026/06/06/health-friday-6-6-2025-open-thread-tlr4-s1-and-mrna-1283-mnexspike-a-scientific-gourmanderie/.

It is now well known that the modRNA COVID-19 “vaccines” can, and do, cause multiple types of serious adverse events reactions, medical conditions of both body and mind, and death, among the COVID-19 “vaccinated.” Thousands of these reports are found in the VAERS database, and can also been searched here: https://openvaers.com/. But the FDA still has not removed these dangerous, deadly injections from the market. However, one new drug, for certain types of Multiple Sclerosis (MS) — ELEVIDYS — was just removed by the FDA after ONLY TWO DEATHS in the “post-marketing trials” group. Please see: https://www.pharmaceutical-technology.com/news/sarepta-and-roche-halt-dmd-gene-therapy-use-after-second-death/?cf-view&cf-closed, 16 June 2025. ELEVIDYS was FDA-approved on 20 June 2024. As with the modRNA COVID-19 “vaccines”, the FDA required Sarepta / Roche to perform “post-marketing trials” of the injectable (in effect, using the persons who would take ELEVIDYS as “human lab rats” to see if the injectable really worked, and to see if there would be serious adverse events in the persons who took the injectable.) Please see the FDA-issued Package Insert for ELEVIDYS, here: https://www.fda.gov/media/184855/download. Screenshots of section Warnings and Precautions; of section 11 Description; and, of section 13 Nonclinical Toxicology are below:

And, by the way, ELEVIDYS apparently “sheds” into areas around inside the body of the person who takes this injectable. Please see section 12.3 Pharmacokinetics Vector Distribution and Vector Shedding of the ELEVIDYS Package Insert linked above.

Then, there is the recent FDA approval of the use of the meningococcal “vaccine”, MenQuadfi, in infants between two months and two years of age (although it appears that this injectable may be used in infants as young as six weeks of age.) MenQuadfi is already FDA-approved for use in persons age two years and older. Attorney Aaron Siri believes this FDA “extension of use” approval is based on the “Pyramid Scheme of Vaccine Safety.” Please see: https://www.2ndsmartestguyintheworld.com/p/all-vaccines-will-kill-you-menquadfi, “ALL VACCINES WILL KILL YOU: MenQuadfi Approval and the Pyramid Scheme of Vaccine Safety”, 15 June 2025. A screenshot of Attorney Siri’s statement from the article is below:

Which reminds Yours Truly of FDA approvals of “the latest version modRNA COVID-19 vaccine”, approvals based solely on “safety and efficacy data” from earlier “latest version modRNA COVID-19 vaccines.”

Before Yours Truly turns to yet another eyebrow-raiser FDA approval, a new article by Dr. Martin Makary, MD, MPH (FDA Commissioner) and Dr. Vinay Prasad, MD, MPH (director of the CBER division of the FDA) in the Journal of the American Medical Association: https://jamanetwork.com/journals/fullarticle/2835314, “Priorities for a New FDA”, 10 June 2025. This article is discussed by Dr. Meryl Nass, MD, on her Substack: https://merylnass.substack.com/p/another-makary-prasad-article-lists, “Another Makary-Prasad article lists the changes they are making at FDA: but again, it comes with flaws”, 10 June 2025. Screenshots from Dr. Nass’ article are below. The passages with the orange line are from the Dr. Makary – Dr. Prasad article; the rest of the language is from Dr. Nass:

This new article follows on the heels of the first one published by Dr. Makary and Dr. Prasad in the New England Journal of Medicine in May 2025: https://www.nejm.org/doi/full/10.1056/NEJMsb2506929, “An Evidence-Based Approach to COVID-19 Vaccination”, in which Dr. Makary and Dr. Prasad made it clear that the FDA would follow “new guidelines” in the approval process and implementation of “new versions” of the COVID-19 “vaccines”, including in numerous “high risk” populations. Among the populations now considered by the FDA to be at “high risk” of severe complications from COVID-19 infection (and, therefore, “in need” of being COVID-19 “vaccinated”) is that of healthy pregnant women.

Yours Truly now turns to the most recent eyebrow-raising move by the FDA: the agency’s approval of lab-grown salmon, an approval based only on the manufacturing company’s “safety claims.” Please see: https://childrenshealthdefense.org/defender/fda-approves-first-lab-grown-salmon-based-solely-manufacturers-safety-claims/, “FDA Approves First Lab-Grown Salmon Based Solely on Manufacturer’s Safety Claims”, by Brenda Baletti, PhD, 10 June 2025. The manufacturer is a company in San Francisco called Wildtype Foods. Please see the screenshot from this article, below:

The FDA Letter of Approval for the lab-grown salmon is found here: https://www.fda.gov/media/186752/download. Below are screenshots from the FDA Letter of Approval:

Mark A. Hartman is a holdover appointee from the Biden Administration. His job at the FDA began on 29 December 2024. Previous to this, Mr. Hartman worked for the EPA. Please see: https://www.lawbc.com/oppt-deputy-director-mark-hartman-will-become-will-become-director-of-fdas-office-of-food-chemical-safety-dietary-supplements-and-innovation/, 13 December 2024. From what Yours Truly can find, Mr. Hartman has no background in chemistry, in health, or in science. His Master’s degrees are in Environmental Studies and in Public Administration. To Yours Truly, this begs the following questions, among many more: Did HHS Secretary Kennedy, Jr., know about this man? Did he know in advance about the FDA’s approval of lab-grown (“cell-cultured”) salmon to be sold and used for consumption in the United States? Exactly what “testing” was performed on this “cell-cultured” salmon to make quite sure that is not carcinogenic? What exact “ingredients” are “fed” to the “cell-cultured salmon cells” in the “steel tanks” at Wild Type Foods (aka Wildtype, Inc.) during the “culturing” process? How many unsuspecting people will be eating this “cell-cultured” salmon in restaurants and other places? What exactly was the “Cell Culture Consultation CCC ooooo5” listed in the FDA’s Approval Letter about? What data were presented?

What on Earth is really going on at the “new FDA”?

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 6.13.2025 Open Thread: Chemtrails? Yes, Virginia, They’re Real

The above image of chemtrails over Taiwan in May 2025 is courtesy of https://chemtrailsexposed.com/.

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 found here.

Today’s offering follows a different path from the posts on the COVID-19 disaster. Yours Truly will make it clear that she is not a climatologist, nor a meteorologist. However, the topic warrants discussion.

Assume, for argument’s sake, that one wakes up in the morning and sees a nice, clear sky from the window looking out to the southeast. Assume, for argument’s sake, that a couple of hours later, one sees a few (or, perhaps, more) “streaks” in the sky, that resemble thin lines; these “thin lines” do not look like real clouds forming. Assume, for argument’s sake, that one hears what sounds like a small plane (or, perhaps, a couple of small planes) in the sky. Assume for argument’s sake, that one sees more of these “thin lines” that have “spread out” into what may appear to be “low-level clouds” — except, that these “clouds” follow a strange pattern of horizontal, vertical, diagonal, and/or oblique directions. Assume, for argument’s sake, that these “clouds” are seen in the southeast sky, which then “spread out” towards the northwest, and appear not to “generate” on the opposite direction on the compass (in other words, in the northwest direction.) Assume, for argument’s sake, that on days when there are multiples of these “not-real-clouds” in the air, there is also “something” that makes the sinuses hurt, that make one feel as if a bad allergy day is occurring, that makes the eyes sting, and that the usual remedies for allergy symptoms (antihistamine, saline nasal spray) have minor or no effect.

Yours Truly has seen and felt all of these things, both in the Spring of last year and also this Spring. Photos of examples of what was seen are below:

View of the sky to the SE, early morning, April 2025.

View of the sky to the SE, around Noon, April 2025.

View of the sky to the NW, morning, April 2025.

Then, there is ** something ** that was different about the Central North Carolina pollen that was in the air, on the car, covering the front porch floor, on the window sills, and just about everywhere else — including getting into one’s lungs. In the Spring, starting in about mid-March, the Central North Carolina pollen starts to show up. It is a slightly “greasy”-feeling and looks like a yellow and green mixture. Not so this year. What one observed this Spring was a dry, yellow-colored powder that coated everything. It had a slightly acrid smell. Photos of what Yours Truly observed of this yellow-colored powder are below, taken in April. The first photo is from what I scraped onto a clean index card; the second photo is this stuff on the front porch floor:

Yours Truly began to research about “chemtrails”, one of those “conspiracy theories” that has been around for some years. What she found out is quite interesting. And, Yes, they are real.

In the first place, there is a difference between “chemtrails” and “contrails.” Please see: https://welovetrump.com/2023/02/05/the-difference-between-contrails-and-chemtrails/. A screenshot from this article is below:

Another explanation of the difference is found here, in a video clip by Pennsylvania Senator Doug Mastriano: https://www.theburningplatform.com/2025/04/30/pa-senator-doug-mastriano-explains-the-obvious-difference-between-contrails-chemtrails/, 30 April 2025.

Two other websites for information regarding chemtrails is here: https://chemtrailsnews.com/; and, https://stateofthenation.co/?p=185241, “CHEMTRAILS: The Planetary Catastrophe Caused by Chemical Geo-engineering”, 8 September 2023.

One understands that “seeding” of the sky has been going on for years. However, the old-style “cloud seeding to induce rain” approach has changed — into “seeding” the sky with other types of chemicals. Please see: https://www.naturalnews.com/2024-09-10-chemtrails-no-longer-conspiracy-globalists-battle-climate-change.html, “Chemtrails no longer a conspiracy theory as globalists call it an essential part of their battle against “Climate Change””, S.D. Wells, 9 October 2024.

Another item regarding the chemicals being sprayed into the air that Americans breathe is here: https://www.theburningplatform.com/2024/07/02/pilots-testify-bill-gates-is-carpet-bombing-cities-with-chemtrails/, via Forbidden Knowledge, 2 July 2024. This article has portions of statements from former pilots who have observed chemtrails. A screenshot from this article is below:

The state senate of Florida recently approved a bill that bans geo-engineering and “weather modification.” Please see: https://floridaphoenix.com/2025/04/03/florida-senate-approves-ban-on-geoengineering-and-weather-modification/, by Mitch Perry, 3 April 2025. Also see: https://www.flgov.org/eog/news/press/2025/governor-ron-desantis-celebrates-action-protect-floridians-chemical-and, “Governor Ron DeSantis Celebrates Action to Protect Floridians From Chemical and Technological Interference”, 6 May 2025. A screenshot from this article is below:

And, HHS Secretary Robert F. Kennedy, Jr., has weighed in on the issue. Please see: https://uk.news.yahoo.com/trump-administration-claims-us-behind-143951527.html, “Trump administration claims US is behind sinister ‘chemtrails’ programme once thought to be conspiracy theory”, by Joshua Nair, 2 May 2025. Please a screenshot from this article, below:

DARPA = Defense Advanced Research Projects Agency, a unit of the United States Defense Department.

In Yours Truly’s opinion, if “there’s something in the air” that is being sprayed without the knowledge and consent of the American public, that is wrong and must be stopped.

Peace, Good Energy, Respect: PAVACA

Health Friday 6.6.2025 Open Thread: TLR4, S1, and mRNA-1283 (mNEXSPIKE): A Scientific Gourmanderie

The above image of TLR Signalling Pathways is courtesy of BioFinder and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering is related to the disaster of the COVID-19 virus itself, and of the COVID-19 “vaccines”, Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative effects of these lab-created Biological Toxin Weapons.

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 in today’s discussion thread, they must cite their source. Thank you.

And now, to the reader’s Edification Smorgasbord, a “feast of information” regarding just how dangerous and potentially deadly mRNA-1283 (mNEXSPIKE) is, Yours Truly offers the following Menu:

APPETIZER: WHAT IS TLR4?

TLR4 (aka Toll-like receptor 4) is a transmembrane protein that exists across a cell membrane. TLR4 functions as a kind of “sensing device” within the body. It detects foreign bacteria and viruses. When a foreign element is detected by TLR4, it begins to send messages to the natural immune system to activate the immune response. TLR4 is crucial to the correct functioning of the natural immune system. Please see the screenshots below for more information:

Citation: https://en.wikipedia.org/wiki/Toll-like_receptor_4

Citation: https://doi.org/10.1016/j.intimp.2007.05.016, “Toll-like receptors in inflammation, infection and cancer”, Keqiang Chen, et al., October 2007. Found via: https://www.sciencedirect.com/topics/immunology-and-microbiology/tlr4.

FIRST COURSE: THE FDA APPROVES “mNEXSPIKE” IN MAY 2025:

The “newest version” COVID-19 “vaccine”, mRNA-1283 (aka mNEXSPIKE), was “fully approved” by the FDA on 30 May 2025. Yours Truly wrote about this situation here: https://www.theqtree.com/2025/06/01/stop-press-edition-hhs-secretary-robert-f-kennedy-needs-to-resign-now/. This “vaccine” claims to be “more effective” in “preventing” an infection of COVID-19. The claim is based on the fact that mRNA-1283 (aka mNEXSPIKE) uses “only” the S1 protein and the N sector of said S1 protein of the COVID-19 virus spike protein, as opposed to using the entire spike protein (as in mRNA-1273, the original “flagship” modRNA COVID-19 “vaccine” by Moderna.) Please see: https://doi.org/10.1093/infdis/jiaf022, “Safety and Immunogenicity of SARS-CoV-2 Spike Receptor-Binding Domain and N-Terminal Domain mRNA Vaccine”, Spyros Chalkias, et al., 15 April 2025 (most of the authors of this “informational paper” are either affiliated with Moderna, or are employees of Moderna.) A screenshot of the Background section of the Abstract of this paper is below:

At first glance, this “new development” by Moderna may appear to be a “positive” achievement. However, there are other issues that arise:

First, there is the fact that the S1 protein of the SARS-CoV-2 virus contains both the RCB (Receptor-Binding Domain) AND the N-terminal domain of the virus. It is the RCB that allows the virus to “attach” itself , or to “dock” itself, to cells in the body — for example, to the ACE2 cell receptors; and, to TLR4 cells. The N-terminal domain is the “end part” of the S1 protein; it is a “free” group at the end of the protein, while, at the same time, it “initiates” a polypeptide chain.

Second, there is the fact that the S1 protein of the SARS-CoV-2 virus interacts with TLR4 cells. Yours Truly begins with this: https://news-medical.net/news/20210510/Research-suggests-Pfizer-BioNTech-COVID-19-vaccine-reprograms-innate-innate-immune-responses.aspx, Sally Robertson, B.Sc., 10 May 2021. Please see the following screenshots from this article:

While the above article refers to the Pfizer-BioNTech modRNA COVID-19 “vaccine” BNT162b2, the modRNA COVID-19 “vaccine” from Moderna, mRNA-1273, also targets the RBD, which interacts with TLR4 cells in the “vaccinated” person’s body. In addition, all of the modRNA “descendant clone” COVID-19 “vaccines” by both companies also use the RBD, there interacting with TLR4 cells in the “vaccinated / boosted” person’s body.

TLR4 cells are also present in multiple areas and organs of the body. The modRNA COVID-19 “vaccines” will interact with these cells. This is due to the fact that the S1 protein of the SARS-CoV-2 virus contains certain amino acids residues (numbers 1-1208) that interact with TLR4 cells. Please see: https://doi.org/10.1016/j.heliyon.2021.306187, “SARS-CoV-2 spike protein S1 subunit induces pro-inflammatory responses via toll-like receptor 4 signaling in murine and human macrophages”, Ken Shirato, Takako Kizaki, February 2021. A screenshot of the Abstract of this paper follows:

Regarding the S1 amino acids residues 1-1208 and TLR4, please see this paper, from 2020: https://europepmc.org/article/ppr/ppr170060, ” Structural characterization of a nanobody derived from a naive library that neutralizaes SARS-CoV-2″, M Dumoux, et al., 1 June 2020. Below are screenshots from the Methods section and from a portion of the Supplementary Table section of this paper (the Supplementary Table portion shows some of the gene code for the S1 1-1208 residues):

Further information regarding SARS-CoV-2 spike protein and its interaction with TLR4 is found here: https://doi.org/10.3389/fimmu.2024.1368946, “TLR2/4 are novel activating receptors for SARS-CoV-2 spike protein on NK cells”. Nadine Landolina, et al., 30 May 2024. “NK” stands for “Natural Killer” cells in the body. A screenshot from this paper is below:

Then, there is the issue of clinical trial used by the FDA to “justify” the “full approval” of mRNA-1283 (aka mNEXSPIKE), NCT05137236 (https://clinicaltrials.gov/study/NCT05137236.) There was NO Placebo Control Group in this study. The study participants (study subjects) were injected with the following Moderna modRNA COVID-19 “vaccines”: mRNA-1273; OR, mRNA-1283; OR, mRNA-1283.211; OR, mRNA-1283.529. Why was there no Placebo Control Group? Assuming that the study subjects knew, in advance, they would be injected with any one of FOUR different variations of a modRNA COVID-19 “vaccine”, were they fine with that?

And, there is the “opinion piece” by Dr. Martin Makary (FDA Commissioner) and Dr. Vinay Prasad (new head of the FDA’s CBER division), regarding the “new approach” that the FDA will use for COVID-19 “vaccines.” Please see:

SECOND COURSE: WHAT DOES THE modRNA COVID-19 “VACCINE”, mNEXSPIKE, CONTAIN?

Please see the FDA-issued Fact Sheet for Healthcare Providers (aka the Package Insert) for mRNA-1283, mNEXSPIKE: https://www.fda.gov/media/186738/download. Below is a screenshot of section 11 Description, section 12 Clinical Pharmacology, and section 13 Nonclinical Toxicology of this document:

Which plainly states that mNEXSPIKE contains the same types of dangerous, deadly lipid nanoparticle and excipient that all the other modRNA COVID-19 “vaccines” by Moderna contain: SM-102, and PEG2000-DMG. This means that mNEXSPIKE will be rapidly spread into every cell in the “vaccinated” person’s body. It is also clear that mNEXSPIKE has NOT been tested for mutation potential, cancer-inducement potential, or reproductive impairment potential.

Yours Truly then performed a search to ascertain whether or not mNEXSPIKE contains N1-methylpseudouridine. She has written extensively on this board about this lab-created “fake Uridine plus a form of methane”, which completely replaces the natural RNA in the Uridine in the body. Recall that natural Uridine is crucial to multiple body functions and mechanisms: regulation of mood, of learning and memory, and of “gut-brain connection” functions. Lo and behold, the US Patent for mRNA-1283 (aka mNEXSPIKE) does have language describing “various types” of pseudouridine, including N1-methylpseudouridine, are used in all of Moderna’s modRNA COVID-19 “vaccines” — which would also include mNEXSPIKE. The US Patent for mRNA-1283 is found here (US 20240382581A1): https://patents.google.com/patent/US20240382581A1/en?q=(mRNA-1283)&oq=mRNA-1283, “Pan-human coronavirus vaccines”, ModernaTX, published 21 November 2024. Please see sections 0120, 0121, 0122, and 0123 of this document for descriptions of the “various types” of pseudouridine.

Lastly, there is the question as to whether mNEXSPIKE contains any saRNA (self-amplifying RNA) component. Yours Truly searched for information regarding this, since the IM dose (intramuscular injection dose) of this COVID-19 “vaccine” is a very small amount — 0.2mL. She found this, which appears to be a “dancing all around the truth” description of this “vaccine.” Please see: https://synapse.patsnap.com/article/what-is-mrna-1283-used-for?, 28 June 2024. A screenshot from this article is below:

Read the last sentence in the second paragraph above, especially “…a robust and durable immune response, potentially requiring fewer doses and offering longer-lasting immunity compares to other vaccines.” Sounds like a description of the saRNA H5N1 “vaccine”, KOSTAIVE, currently approved for use in the EU / Scandinavia, and in Japan; and, a version of which “vaccine” is to begin clinical trials in the United States (NCT06602531), under the name ARCT-2304.

DESSERT AND BEVERAGES: REACTIONS AND QUESTIONS:

First, this: https://www.thefocalpoints.com/p/maha-movement-flabbergasted-covid, “MAHA Movement Flabbergasted COVID-19 Vaccines Remain on Market”, Peter A. McCullough, MD, MPH, 2 June 2025. There is an embedded interview with Dr. McCullough in this article, along with a linked copy of the “Kabuki Theater performance” regarding “stopping” the COVID-19 “vaccines” in the United States by Dr. Martin Makary (FDA), Dr. Jay Bhattacharya (NIH DIrector), and HHS Secretary Robert F. Kennedy, Jr., on 27 May 2025. A screenshot from the McCullough article is below, giving his views on the current situation:

Second, this tweet, from Dr. William Makis: https://x.com/MakisMD/status/1930296443434348771, 4 June 2024. Two screenshots from his tweet are below: first, a statement from HHS Secretary Kennedy, Jr.; and, second, from Dr. Makis:

Questions, posed by Yours Truly: Why did the FDA “fully approve” a “new”, modRNA COVID-19 “vaccine” that specifically targets person over age 65, and persons who “fit” a detailed list of “persons at risk of severe COVID-19 infection”, as complied by Dr. Martin Makary and Dr. Vinay Prasad? Why was there a “Kabuki Theater performance” on 27 May 2025 by Drs. Makary and Bhattacharya, along with HHS Secretary Kennedy, Jr., when it was obvious by that date that the FDA “full approval” of mNEXSPIKE was “a done deal”? Why did the FDA issue an Approval Letter to Moderna for mNEXSPIKE that has so many “caveats”, “requests for more information”, and an “order” for the company to perform a Phase 4 clinical study on the “vaccine” — a “vaccine” that the FDA had just “fully approved”? Please see: https://www.fda.gov/media/186740/download; and, the screenshot of Page 9 of this document, regarding the “order” for the Phase 4 study, below:

More questions, posed by Yours Truly: How many elderly persons are going to be pressured / cajoled / “mandated” (by the nursing home or care facility where they live), to take mNEXSPIKE? Will they be told that this injectable is “safer” than mRNA-1273, “because the dose is smaller”? What about persons who “fit” into the multiple categories of “persons at high risk for severe COVID-19 infection” according to Drs. Makary and Prasad? What pressure will these persons be subjected to in order to get them to agree to take mNEXSPIKE? Finally, will people be told the truth that mNEXSPIKE, just because it does not contain the S2 portion of the SARS-CoV-2 spike protein, is NOT “mRNA-1273 Lite” — but, rather, it is another version of a dangerous, potentially deadly modRNA COVID-19 ‘”vaccine”?

Peace, Good Energy, Respect: PAVACA