Health Friday 10.24.2025 Open Thread: A Cautionary Tale

The free header stock image of a nursing home is courtesy of Vecteezy and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics.

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for AI-generated content. To the best of her knowledge and belief, there is none, except possibly that which is contained in URL links in today’s post. If readers wish to add AI-generated content to today’s discussion thread, they must cite their source. Thank you.

Please take a moment and remember our good GA/FL (Georgia Sibyl Swink Smith), who passed away on 8 October 2025. The time, energy, and ingenunity that GA/FL invested into decades of taking care of her late daughter, “Sally Q” Smith, after the latter’s diagnosis of Friedreich’s Ataxia at the age of 14, was amazing and inspiring. Sally Q passed away from the effects of this condition on 10 May 2025. Georgia was a devout Christian. May she and her daughter rest in eternal Peace. GA/FL will be sorely missed.

Today’s offering begins here: https://www.theburningplatform.com/2025/10/04/keeping-the-elderly-sheep-in-line/, by Donald Jefferies. The article is about nursing homes. Two screenshots from his article are below:

Yours Truly comes from a birth family that, on both sides, had a horror of having to go into “a home” (“a home” was “code” for a nursing home or care facility.) Grandparents, aunts, uncles — even one’s own father — vigorously preferred to remain at home, no matter what, and stay away from congregate living of any kind. Only as a last resort, did my maternal grandmother have to go to live at a nursing home. I think she had a premonition that she would not “come out alive” from the facility. She was correct. My own brother was discharged from the hospital to a nursing home, but that, too, was under “last resort” circumstances; he, also, did not “come out alive” from the facility. In both the cases of my maternal grandmother and of my brother, there were extremely serious medical conditions which excluded their ever living at their own homes again.

Nursing homes and care / rehabilitation facilities in the United States are inspected by the state health agencies where these are located. CMS (Medicare / Medicaid) will step in if a nursing home or care facility fails to meet state inspection standards, or if complaints are filed with either the state health department or CMS regarding a nursing home or care / rehabilitation facility. Please see: https://www.cms.gov/medicare/health-safety-standards/enforcement/nursing-home-enforcement, last updated 21 April 2025.

Nursing homes and care / rehabilitation facilities in the United States were especially negatively affected by the COVID-19 disaster. During the “lockdown” period, these places became off-limits to family and friends of the residents / patients. Untold numbers of these residents / patients died alone. Untold numbers of residents / patients were injected with the modRNA COVID-19 “vaccines”, whether they consented to this or not. According to data complied by the CDC, residents / patients of these facilities had increased risk of death if they were “vaccinated” against COVID-19: https://kirschsubstack.com/p/cdc-nursing-home-data-the-vaccine, “CDC Nursing Home Data: The vaccine increased the risk of the elderly dying from COVID”, Steve Kirsch, 5 September 2023. Please see the screenshots from this article, below:

The AMA (American Medical Association), on the other hand, made it clear, also in 2023, that deaths among the COVID-19 “vaccinated” simply underscored the “need” for persons to get a COVID-19 “vaccine booster shot”: https://www.ama-assn.org/public-health/infectious-diseases/why-covid-19-deaths-among-vaccinated-show-boosters-matter, Cynthia Cos, et al., 7 March 2023. Please see the screenshots from this article, below, in which Dr. Elaine Choi (a member of the AMA) is “explaining” why COVID-19 “vaccine booster shots” are a good thing, even though “vaccinated” persons were then dying from COVID:

Currently, the AMA, among other professional medical organizations, is speaking out regarding what they term the “new restrictions against COVID-19 vaccination” that were put into place by HHS Sec. Robert F. Kennedy, Jr., earlier this year. One example of such “speaking out” is here: https://www.chiefhealthexecutive.com/view/defending-vaccines-ama-nursing-leaders-speak-out, Ron Southwick, 22 September 2025. There is a video embedded in the article; two screenshots from the article’s text are below:

Note the old (and misinformation) canard about “if you’re young and healthy, get a COVID-19 vaccine so your grandparents won’t get COVID” from Mensik Kennedy.

Steve Kirsch posted an article this week on his Substack blog regarding the Japan CMRR data, which proves that the more COVID-19 “vaccine” injections a person takes, the more risk that person has of dying: https://kirschsubstack.com/p/japan-cmrr-data-website-shows-clear, “Japan CMRR data website shows clear mortality increase caused by COVID shot”, 20 October 2025. Please see the screenshot from his article, below. (Note: CMRR = Cumulative Mortality Risk Ratio.) The first screenshot is of the general summary chart:

The second screenshot is from the Kirsch KCOR analysis of the Japan data, along with text summary;

To access the KCOR analysis, please see: https://medicalfacts.info/kcor.rb.

Applying all of the above to persons who, for whatever reason, are residents / patients in nursing homes or care / rehabilitation facilities: How do these people, if they do NOT want to take a COVID-19 “vaccine” injection, make their decision clear to the staff, including to the medical staff? How are these people assured, that if they do NOT want to take a COVID-19 “vaccine” injection, and there is an outbreak of COVID at the facility, that they will have access to Ivermectin, Hydroxychloroquine, Vitamin D, Zinc, and other alternative treatments for prevention or treatment of a COVID infection? How are these people assured, if they do NOT want to take a COVID-19 “vaccine” injection, that they will NOT be moved into a “segregated area” of the facility; or, worse yet, be told (or, their family / guardian be told) that the resident / patient “has to find another facility?” The issue is compounded by the fact that almost all nursing homes and care / rehabilitation facilities receive CMS funding or payments of some kind. Also, there is the “Next Generation Gold Standard” of “evidence-based COVID-19 vaccination” guidelines that were announced and implemented by HHS / NIH / CDC / FDA earlier this year. These guidelines “recommend” that persons age 65 and older get a COVID-19 “booster shot” TWICE a year. What does this mean for the person living in a nursing home in, for example, Alabama, (a facility that receives CMS funding or payments) — a person who is competent to make their own decisions, and who decides to refuse to take a COVID-19 “vaccine” injection? What if that person refuses because of religious belief? What if the person refuses because the “vaccine” contains elements lab-recreated from aborted fetal blood cell lines (the HEK293 lines?) Does the facility then “have the right”, because of the “new guidelines” in the “Evidence-Based Approach to COVID-19 Vaccination” that have been implemented, to override the person’s decision and give the injection anyway? Does the facility now “have the right” to tell the person’s children / guardian that they need to “find another facility” to take the person? Please see: https://www.hhs.gov/press-room/hhs-nih-announce-generation-gold-standard.html; also, https://www.nejm.org/doi/full/10.1056/NEJMsb2506929, “An Evidence-Based Approach to COVID-19 Vaccination”, Martin Makary, MD, MPH, and Vinay Prasad, MD, MPH. Dr. Makary is the Commissioner of the FDA; Dr. Prasad is the Director of the CBER Division of the FDA. Please see the screenshot of Figure 3 from this NEJM paper, below:

Please see the latest CDC immunization schedule recommendations for persons age 19 years and older as of 1 October 2025, here: https://www.cdc.gov/vaccines/hcp/imz-schedules/adult-age.html#table-age. A screenshot of the schedule is below:

In addition, please see the age 65 and older immunization schedule recommendations for other injectables on the chart above — Influenza; RSV; pneumonia; Monkeypox; Herpes Zoster (“Shingles”); Hepatitis A and Hepatitis B; and more.

There is now supposed to be “Shared Clinical Decision-Making” between patient and healthcare provider regarding the COVID-19 “vaccines” for persons age 19 and above. Does that also apply across the board to persons living in nursing homes or care / rehabilitation facilities who are competent, but the facility they reside or stay in is also receiving CMS and/or Medicare-Medicaid payments?

There are multiple “Notes” sections regarding the administration of the other “vaccines” listed above in persons age 65 and older (and, in some cases, age 60 and older.) These “Notes” are found here: https://www.cdc.gov/vaccines/hcp/imz-schedules/adult-notes.html#note-covid-19; please scroll down this webpage and click on the topic to read about, such as, “Influenza vaccination.” There are multiple “vaccines” that are considered to be “routine”, such as the influenza “vaccine”, the RSV “vaccine”, and so on. What if a person living in a nursing home or care / rehabilitation facility decides to refuse all of these “routine” injectables, or decides to take only one or two? What happened to “Shared Clinical Decision-Making” in regards to this? Especially in light of new research that proves, for example, that the pneumonia “vaccines” actually increase the risk of contracting pneumonia and dying from said infection? Please see: https://www.thefocalpoints.com/p/breaking-223-million-person-study, “BREAKING: 2.23 Million Person Study Finds Pneumococcal Vaccines Increase Risk of Pneumonia and Death”, Nicolas Hulscher, 22 October 2025.

And, what about the COVID-19 “vaccinated” personnel (administration staff; doctors; nurses; CNAs / PCAs; facility maintenance staff; kitchen staff, etc.) who work at these nursing homes or care / rehab facilities? What about the “downstream Medical Tsunami” of negative effects on them of the “vaccines” that they took, which will present at some point, if not already? What about potential staff loss / turnover?

And, what about the vast majority of the adult children of these residents / patients, who are themselves also COVID-19 “vaccinated” — including the adult children who have already taken multiple injections of these “vaccines?” What about the “downstream Medical Tsunami” of negative effects on them of the COVID-19 “vaccines” that they took, which will present at some point, if not already?

And, what about the potential for another “pandemic emergency” being declared (including from some type of Avian Influenza outbreak) that “mandates” another round of “lockdowns”, which would effect nursing homes or care / rehab facilities?

In Yours Truly’s opinion, these are all things that need to be brought into the daylight and discussed. They represent another “ripple effect” aspect of the ongoing disaster of COVID-19.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Disclaimer: With the exception of links to published scientific papers, website articles, and other items in the public domain, the ideas and conclusions in this post are by PAVACA. Proper credit must be given if ideas or conclusions of this post are used by other blog writers, or on social media, or in print media. Thank you.)

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

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

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 7.11.2025 Open Thread: Establishment Medicine Declares War on HHS Secretary Robert F. Kennedy, Jr.

The above free image of physicians conferring is courtesy of LovePik 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 those persons, of whatever age or location, who have come down with “vaccine”-induced injuries, illnesses, or disabilities, as a result of the COVID-19 “vaccines” (Bioweapon Toxin Injections) that they had put into their bodies; and, also, to all those persons, of whatever age or location, who have passed away from the negative effects of the COVID-19 “vaccines” that they had put 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. If readers wish to post any AI-generated content in today’s discussion thread, they, must cite their source. Thank you.

Yours Truly has written extensively on this board regarding what she calls Establishment Medicine. Establishment Medicine can be found in multiple areas, among them: The teaching of “consensus-centered” medicine (otherwise known as “the science is settled” medicine) in medical schools (this appears to be the approach in medical education currently); the “suggestion” or “advice” that physicians who choose a specialty in which to practice (for example, Internal Medicine) “need” to become board-credentialed by a private medical credentialing board (for example, credentialing through ABIM (the American Board of Internal Medicine, https://www.abim.org/); physician membership in the American Medical Association https://www.ama-assn.org/; and, “adherence” to the “recommendations” of the “routine vaccination schedules” of the Centers for Disease Control (CDC, https://www.cdc.gov/); and, the “endorsed vaccination schedule” of the American Academy of Pediatrics (https://www.aap.org/); the “routine guidance” of the FDA (Food and Drug Administration, https://www.fda.gov/); and, the “rules” and “regulations” of the State Medical Licensing Board in the state in which the physician resides, and which physician’s License to Practice Medicine must be secured prior to starting medical practice, and which License must be renewed after a certain period of time). Yours Truly will make it clear at the outset that there are many caring, perceptive physicians — in hospitals, in medical clinics, in stand-alone private physicians’ offices, and so on — who likely do not blindly ascribe to the “diktats” of Establishment Medicine. Perhaps there are physicians among this number who understand that the COVID-19 “vaccines” are dangerous and deadly. Perhaps there are physicians among this number who observing that their COVID-19 “vaccinated” loved ones, patients, or colleagues are presenting with COVID-19 “vaccine”-induced injuries, etc. Perhaps there are physicians among this number who would prefer to speak the truth about the COVID-19 “vaccines”, but refrain, due to concerns that they could be “disciplined”, or lose their License to Practice Medicine, by their state Medical Licensing Board.

Until very recently, all was going well for Establishment Medicine — its control over the health of the American public was “unchallengeable” — then, two important things happened: One, that the American public in general began to realize the dangers and deadliness of the COVID-19 “vaccines”; and, Two, the confirmation of Robert F. Kennedy, Jr., as the Secretary of Health and Human Services (HHS) of the new administration under the forty-seventh President of the United States, Donald J. Trump, a few months ago.

On 9 June 2025, the seventeen then-current members of the CDC’s ACIP committee (Advisory Committee for Immunization Practices) were fired by Secretary Robert F. Kennedy, Jr. (https://www.hhs.gov/press-room/hhs-restores-public-trust-vaccines-acip.html, “HHS Takes Bold Step to Restore Public Trust in Vaccines by Reconstituting ACIP”, 9 June 2025.) Please see the screenshot from this announcement, below:

The reason? — Corruption of the ACIP committee members. The United States Congress reported on this corruption back in 2000: https://www.thefocalpoints.com/p/decades-of-corruption-congressional, “DECADES OF CORRUPTION: Congressional Report Confirms CDC’s ACIP Has Been Compromised Since the 1990s”, by Nicolas Hulscher, MPH, 10 June 2025. Please see the screenshot from this article, below:

One of the most-compromised (now former) members of the ACIP committee was Dr. Paul Offit.

And, of course, there was a large outcry from all over Establishment Medicine. One example: https://www.cbsnews.com/news/rfk-jr-removes-members-cdc-immunization-advisory-committee-acip/, “RFK Jr. removes every member of CDC vaccine advisory committee”, 10 June 2025. Please see the screenshot from this article, below, and keep it in mind for later on regarding today’s offering:

The ACIP Adult Immunization Schedule that was issued in May 2025 is found here (the actual CDC website no longer lists this schedule): https://www.dph.ncdhhs.gov/news/press-releases/2025/06/03/cdc-updates-covid-19-vaccine-schedule. The ACIP Adult Immunization Schedule that was issued in May 2025 has several changes; among them, the previous CDC “recommendation” that all pregnant women get COVID-19 “vaccinated.” The May 2025 schedule, instead, encourages “shared clinical decisions” between the physician and the pregnant patient. And this is where “the rest of the story” begins.

The outcry against the immunization schedule changes by Establishment Medicine was instant, loud, and immense. For example, this: https://www.pharmacist.com/APhA-Press-Releases/apha-withholds-enforsement-of-acip-adult-immunization-schedule. Please see a screenshot from this article, below:

Then, on 9 June 2025, when HHS Secretary Kennedy, Jr., fired the seventeen then-current ACIP members, he replaced them with eight new members: Dr. Joseph Hibbeln, MD, ABNP, CAPT USPHS (Ret.); Martin Kullorff, PhD; Retself Levi, PhD; Robert W. Malone, MD; Cody Meissner, MD; James Pagano, MD, FACEP; Vicky Pebsworth, PhD, RN; and, Michael Ross, MD. Their biographies are here: https://www.cdc.gov/acip/membership/roster.html. (Dr. Ross withdrew from the ACIP committee due to “financial holdings” reasons.) Establishment Medicine countered with hue and cry that none of these medical professionals were “experienced in vaccines”, and so on.

The June ACIP meeting was held on 25-27 June 2025, with the now-seven new members in attendance. Even while the meeting was going on, Establishment Medicine was “sounding the alarm” over the new committee and what they would do. Please see: https://www.cidrap.umn.edu/adult-non-flu-vaccines/vaccine-public-health-advocates-warn-fallout-acip-meeting, “Vaccine, public health advocates warn of fallout from ACIP meeting”, by Chris Dall, MA, 27 June 2025. Please see the screenshots from this article, below:

In fact, the American Academy of Pediatrics (AAP) issued this statement: https://publications.aap.org/aapnews/news/32529/AAP-will-continue-to-publish-its-own-vaccine, “AAP will continue to publish its own vaccine recommendations after CDC advisers sow distrust”, by Melissa Jenco, 26 June 2025. Please the screenshot from this article, below:

Keep the above statement from the AAP in mind, as it is pertinent what happened in early July 2025. It appears that, while Establishment Medicine was making statements about how they opposed the new ACIP members, the new ACIP vaccine schedules and the new CDC policies, they were also making behind-the-scenes preparations for suing HHS Secretary Kennedy, Jr. And, in fact, this is what occurred: on 2 July 2025, several Establishment Medicine groups filed suit against HHS Secretary Robert F. Kennedy, Jr., to force HHS to reinstate the former ACIP recommended vaccine schedules: https://www.thefocalpoints.com/p/breaking-medical-cartel-sues-rfk, “BREAKING: Medical Cartel Sues RFK Jr. for Pulling COVID Shot Recommendations for Kids and Pregnant Women”, by Nicolas Hulscher, MPH, 7 July 2025. Please see the screenshots from this article, below:

Note: The blue hyperlinks in the Hulscher article (one needs to go The Focal Points website for the Hulscher article link) lead to scientific articles about the dangers of the COVID-19 “vaccines”, and to the AAP, et al., lawsuit against Secretary Kennedy, Jr.

The AAP statement regarding the lawsuit, here, https://publications.aap.org/aapnews/news/32580, “AAP suing HHS over vaccine policy”, 7 July 2025, also has the link to the filed lawsuit against Secretary Kennedy, Jr. Please see the screenshot below from the AAP statement:

Screenshots of portions of the forty-two page lawsuit document are below:

Another link to the entire lawsuit document is here: https://www.documentcloud.org/documents/25992348-aap-et-al-v-rfk-et-al-filed-complaint/.

In other words, in Yours Truly’s opinion, the AAP and the other medical organizations listed in the screenshot above want to force Secretary Kennedy, Jr., to “go back to the good old days” of the “old ACIP and the old CDC” — the same entities that “recommended” the dangerous, deadly COVID-19 “vaccines” without first demanding complete, detailed, and analyzed data from “clinical trials” for these injectables. Back to the “good old days” when every state legislature, every pharmacy, every medical clinic, every hospital, and almost every licensed physician, blindly followed the CDC “recommendations” regarding vaccinations of children and of adults. Back to the “good old days” of “the science is settled” — and those physicians who boldly told the truth, and continue to tell the truth, about the dangers and deadliness of the COVID-19 “vaccines” (for example, Dr. Peter A. McCullough, MD; Dr. Ryan Cole, MD; Dr. Pierre Kory, MD; Dr. Charles Hoffe, MD; and, Dr. Robert Malone, MD) were belittled; were marginalized by their medical specialty organizations; were fired from their jobs; were prosecuted by their Medical Specialty licensing organizations; were prosecuted by their state Medical Licensing Boards — were “disciplined” by these Boards, or had their License to Practice Medicine “restricted”, or even revoked, by these Boards. Back to the “good old days” when Establishment Medicine was the sole arbiter of health in the United States.

In Yours Truly’s opinion, the lawsuit by Establishment Medicine against HHS Secretary Kennedy, Jr., is the culmination of months of negative reactions regarding his nomination as the new HHS Secretary; regarding his confirmation for the position; regarding what appear to be some ambiguous and/or conflicting statements he has made since his confirmation; and certainly regarding his actions as HHS Secretary to attempt to rein in the tyranny of Establishment Medicine in HHS decisions. In some ways, the AAP, et al., lawsuit against Sec. Kennedy, Jr., may be similar to liberal “Judicial Establishment” actions against President Donald Trump 47 regarding blocking his efforts to deport illegal aliens in the United States.

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 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

STOP PRESS EDITION: HHS Secretary Robert F. Kennedy, Jr., Needs to Get Control, or to Resign — Now.

The above image of a vintage vaccine vial and syringe is courtesy of Google Images.

This post is a STOP PRESS EDITION. It has to do with the FDA BLA (Biologics License Application) approval of the Moderna COVID-19 modRNA “vaccine” mRNA-1283. This “vaccine” was FDA-approved without any clinical trial in which there was a placebo control group. mRNA-1283 contains a “shorter portion” of the COVID-19 virus spike protein. This “vaccine” also contains elements of the H7N9 Avian Influenza strain that was used in Gain-of-Function experiments by Dr. Yoshihira Kawaoka, DVM, PhD, in 2013, along with other scientists, at the University of Wisconsin (Madison.)

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 this post 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 the discussion thread of today’s offering, they must cite their source. Thank you.

Today’s offering is short and to the point. Special Thanks to our good duchess01, to https://www.thefocalpoints.com/, and to http://mole.substack.com/. Please refer to the following posts by Yours Truly for relevant background information regarding today’s offering: https://www.theqtree.com/2025/05/30/health-friday-5030-2025-open-thread-what-is-going-on-at-hhs-the-fda-and-the-cdc/; and, https://www.theqtree.com/2025/05/16/health-friday-open-thread-5-16-2025-about-that-universal-vaccine-theres-more-than-meets-the-eye-part-two/.

Please see the following breaking news outlets pieces regarding the FDA granting the BLA for the Moderna “newest COVID-19 “vaccine”, mRNA-1283: First, this one: https://www.thefocalpoints.com/cp/164898171, “BREAKING: FDA Goes Rogue — Approves Moderna’s Next-Gen COVID-19 mRNA Injection Without a Placebo-Controlled Trial”, Nicolas Hulscher, May 2025. Please see the screenshots from this article, below:

HOWEVER, there is another aspect to the mRNA-1283 modRNA COVID-19 “vaccine” — this injectable appears to be a combination of BOTH the SARS-CoV-2 virus AND elements of the deadly H7N9 Avian Influenza virus. Please see: https://jonfleetwood.substack.com/cp/164803097, “FDA Approves Moderna COVID Jab Containing GOF Bird Flu Gene Segment That PCR Could Mistake for Infection”, 31 May 2025. The “bird flu gene segment” is from the Gain-of-Function experiments with the H7N9 Avian Influenza virus conducted by Dr. Yoshihiro Kawaoka, Ron Fouchier, and other scientists, under the aegis of the University of Wisconsin (Madison), where Dr. Kawaoka has his lab. These Gain-of-Function experiments were “outed” when serious lab accidents occurred; it appears that the experiments were then stopped. But not before Dr. Fouchier wrote this article: https://www.science.org/doi/10.1126/science.1243325, “Gain-of-Function Experiments on H7N9”, 9 August 2013, in which Dr. Fouchier attempted to justify further Gain-of-Function experimentation.

Please see the following screenshot, below, from the Wikipedia entry on H7N9 (https://en.wikipedia.org/wiki/Influenza_A_virus_subtype_H7N9):

The archived article regarding the H7N9 experiments at the University of Wisconsin (Madison), is found here: https://archive.ph/LX7MP, “Study: Lab-derived H5N1 virus component binds to human receptors”, Robert Roos, 13 April 2013.

In Yours Truly’s opinion, Robert F. Kennedy, Jr., the Secretary of Health and Human Services, is not doing his job. BOTH the FDA and the CDC have now “gone rogue” — first, with the “sleight-of-hand” regarding the CDC’s “new recommendations” about the COVID-19 “vaccines” (per Dr. Susan Monarez, PhD, the current Acting Director of the CDC, as of 30 May 2025); and, second, with the FDA (Dr. Martin Makary, Commissioner) granting approval of the Moderna modRNA COVID-19 + H7N9 gene pieces combination “vaccine”, mRNA-1283 (as of 31 May 2025.) It is time, in Yours Truly’s opinion, for Secretary Kennedy, Jr., to either get control of the FDA and CDC — after all, these agencies are part of HHS — or, to resign, and allow President Trump47 to find someone who will.

FLASH UPDATES! MORE ON THE “DIRTY BACKSTORY” RELATED TO THE FDA’s APPROVAL OF mRNA-1283 ON 30 MAY 2025:

ONE: The FDA’s Approval Letter to Moderna on 30 May 2025, regarding mRNA-1283: https://www.fda.gov/media/186740/download. Please see the screenshot of page nine of this document, below:

This is the PHASE 4 clinical study that Moderna is requested to perform for mRNA-1283, but which has NOT begun yet, nor has it ENROLLED any subjects yet.

TWO. This is the slide presentation for the CDC’s ACIP committee meeting for April 2025 related to the “2025-2026 COVID-19 Vaccines Formula” selections. Notice that there is NO vote that ACIP planned to take regarding mRNA-1283. Please see: https://www.cdc.gov/acip/downloads/slides-2025-04-15-16/05-Panagiotakopoulos-COVID-508.pdf. Below is a screenshot of the pertinent image from the slide presentation:

WHAT IS GOING ON HERE?

Peace, Good Energy, Respect: PAVACA

Health Friday 5.30.2025 Open Thread: What is Going On at HHS, the FDA, and the CDC?

The above graphic is with thanks to https://www.thefocalpoints.com/p/fda-recommends-more-mrna-shots-despite, “FDA Recommends More mRNA Booster Shots Despite New Study Showing Booster Failure — and Major Public Outcry”, by Nicolas Hulscher, 26 May 2025.

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

There are Important Notifications from our host, Wolf Moon; the Rules of 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 use any AI-generated material in the discussion thread for today’s post, they must cite their source. Thank you.

Yours Truly has been researching, reading about, and writing about, the COVID-19 disaster since March 2020. She had a sense, early in 2020 when the speculation about the development and use of a COVID-19 “vaccine”, that something was “off” in the hype regarding “how this will stop the spread” of the virus, “how this will prevent COVID-19 infection”, and so on. As it turns out, that “Suspicious Dog” feeling was the correct one — the COVID-19 “vaccines” have been, are now, and will be, a disaster. These injectables do not prevent COVID-19 infection. These injectables have injured, sickened, disabled, and even killed, millions of “vaccinated” persons all over the world. These “vaccines” will continue to injure, sicken, disable, and even kill, those who have them put into their body — not only because of the ingredients and mechanisms of these injectables, but now also because of the “new and improved” (not) faulty foundation of “lab-created antibody titer levels tests” that will be used in the development of the “latest mutation version” of the “vaccines”, instead of doing actual clinical trials with lab animals and/or with human subjects. I will make it clear at the start that today’s offering is not meant to “stir the pot.” There are, in my opinion, legitimate questions that need to be asked regarding certain recent news items.

There are several central elements of the current situation regarding the “2025-2026 COVID-19 Vaccine Formula”, and the actions of certain people and entities. One such entity is the FDA. The current Commissioner of the FDA is Dr. Martin Makary, MD, MPH, who is also a proponent of COVID-19 “vaccination” (including in pregnant women), and is himself “vaccinated.”

On 22 May 2025, the FDA’s VRBPAC (Vaccines and Related Biological Advisory Committee) members met to “consider” and then to “recommend” the “2025-2026 COVID-19 Vaccine Formula.” The committee voted unanimously, after “presentations” by Pfizer-BioNTech, by Moderna, and by Novavax, to “recommend” the “formulas” for the modRNA (Pfizer-BioNTech and Moderna) and the “inactivated protein” (Novavax) COVID-19 “vaccines.” Please see: https://www.contagionlive.com/view/fda-makes-recommendations-for-2025-2026-formula-for-covid-19-vaccines, 23 May 2025. A screenshot from this article is below:

These “vaccines” will be lab-developed, then lab-tested regarding the amount of “antibody titers” that “might” be “effective” in the “2025-2026 Formula COVID-19 Vaccines.” There will be no clinical trial testing of these “vaccines.” This protocol, outlined in the “Option 4” method, was adopted by the FDA on 28 June 2022. Please see the Briefing Document for this meeting: https://www.fda.gov/media/159452/download. “Option 4” is located on page 19. Please see the screenshot below:

Therefore, it appears that any person who takes an injection of the “2025-2026 Formula COVID-19 Vaccine” by Pfizer-BioNTech, by Moderna, or by Novavax, will be, in essence, a “human lab rat”, since these “vaccines” will only have been tested under “Petri-dish conditions” in a lab to confirm whether the “antibody titer amounts” expressed by the “vaccine” ingredients “might” be “effective” in humans.

There were over 95,000 public comments that were submitted to the FDA regarding the VRBPAC meeting of 22 May 2025, indicating a “major public outcry” against the “recommending” of more COVID-19 “vaccines.” Nonetheless, the VRBPAC members voted to endorse the “2025-2026 COVID-19 Vaccine” formulas, as described above, using the “Option 4” method. Please see: https://www.thefocalpoints.com/p/fda-recommends-more-mrna-shots-despite, “FDA Recommends More mRNA Booster Shots Despite New Study Showing Booster Failure — and Major Public Outcry”, Nicolas Hulscher, MPH, 26 May 2025. Please see the screenshot from this article, below:

The phrase, “immunogenicity data” refers to the “Petri-dish lab experiments” as described above.

The image below is from the “opinion piece” written and published by Dr. Martin Makary and Dr. Vinay Prasad, MD, MPH. Dr. Prasad is another important person in the current situation regarding the HHS / FDA / CDC. As of 6 May 2025, Dr. Prasad is the new Director of the FDA’s CBER department (Center for Biologics Evaluation and Research.) The “opinion piece” was published on 20 May 2025, two days prior to the FDA’s VRBPAC meeting. Please see: https://www.nejm.org/doi/full/10.1056/NEJMsb2506929. A screenshot of the combined Figure 2 and Figure 3 from the “opinion piece” are below:

Dr. Prasad made it clear, in a podcast, that the FDA will implement the elements outlined in the “opinion piece” as the “new framework” for COVID-19 “vaccination.” Please keep this in mind for later on in today’s offering.

The paper regarding the failure of COVID-19 “booster shots”, already online-published but will appear in a medical journal in June 2025, is found here: https://doi.org/10.1016/j.vaccine.2025.127257, “Effect of the 2022 COVID-19 booster vaccination campaign in people aged 50 years in England: Regression discontinuity analysis in OpenSAFELY-TPP”, Andrea L. Schaffer, et al., journal Vaccine, Volume 59, 20 June 2025, 127257. The salient image from this paper is below:

Regarding the impact of COVID-19 “vaccination” on the lifetime supply of eggs in a female’s ovaries, it is now known that BOTH the modRNA AND the “inactivated” COVID-19 “vaccines” have a devastating impact on this egg supply. Please see: https://doi.org/10.3390/vaccines/13040345, “Impact of mRNA and Inactivated COVID-19 Vaccines on Ovarian Reserve”, Enes Karaman, et al., 30 January 2025. This paper demonstrates that there is a 30% conception failure rate, and an overall loss of up to 60% of the lifetime egg supply in the female ovaries, both induced by COVID-19 “vaccination” in a female of child-bearing age.

Then, there is Dr. Jay Bhattacharya, MD, PhD, the new Director of the NIH (National Institutes of Health.) It appears that Dr. Bhattacharya may be “betting on both sides of the game” regarding COVID-19 and the COVID-19 “vaccines.” While it is true that Dr. Bhattacharya has stated that lockdowns, “mandated masking”, “social distancing”, and so on, are not real methods to deal with the virus, he also said this, in 2021, regarding the COVID-19 “vaccines”:

Link to the above: https://www.newsweek.com/stanford-doc-jay-bhattacharya-calls-vaccine-mandates-unethical-says-patients-can-choose-1611938. The above statement from Dr. Bhattacharya raises some questions: One, if COVID-19 is “basically a cold”, how can a “vaccine” protect against it? Two, if COVID-19 is “basically a cold”, why are there so many persons who have had a COVID-19 infection (either from the mechanisms of the COVID-19 “vaccines” themselves, or from the virus itself) and have since presented with symptoms of “Long COVID”? Three, if indeed a person who had a COVID-19 infection and recovered, is “protected against new disease”, why are people (COVID-19 “vaccinated” or not) still coming down with COVID-19 virus mutation infections?

Next is Susan Monarez PhD, the current Acting Director of the CDC. Previously, she had worked in the Department of Homeland Security with BARDA and with other HHS departments. Dr. Monarez is a “biosecurity expert” who has also endorsed the COVID-19 “vaccines.” Please see: https://www.nytimes.com/2025/03/24/health/cdc-director-monarez.html, “Trump Nominates Susan Monarez to Lead C.D.C.”, 24 March 2025. The pullquote from the article: “Monarez is a biosecurity expert who endorsed the Covid vaccines, and her selection may signal a growing impatience with anti-vaccine sentiment.”

And, finally, there is current HHS Secretary Robert F. Kennedy, Jr., an attorney who founded the Children’s Health Defense organization (https://childrenshealthdefense.org/), and who has been an outspoken opponent of the COVID-19 “vaccines.”

And here begins Yours Truly’s presentation of the Kabuki theater going on at HHS / FDA / CDC:

On Tuesday 27 May 2025, HHS Secretary Kennedy, Jr., appeared in a video with Dr. Markary and Dr. Bhattacharya to announce that the COVID-19 “vaccines” that are “recommended” (in actual practice, they are called “routine”) by the CDC for healthy children under age 18, and for healthy pregnant women, would be removed from the CDC Immunization Schedules. Please see: https://x.com/bennyjohnson/status/1927374665745342535, a screenshot of which is below:

Where was Dr. Monarez, the Acting Director of the CDC? Why wasn’t she included in the video? An “announcement” of this importance would surely have required her to be included. To the best of Yours Truly’s knowledge and belief, neither Dr. Makary (FDA), nor Dr. Bhattacharya (FDA CBER), have the direct authority to remove vaccines from the CDC Immunization Schedules. The CDC is a separate departmental entity of HHS.

However: In reality, nothing has changed regarding the CDC Immunization Schedules. The CDC is still using the same 2025 Immunization Schedules that were issued on 21 November 2024. Please see: https://www.cdc.gov/vaccines/hcp/imz-schedules/index.html. The CDC is still “recommending” that pregnant women get COVID-19 “vaccinated”. Please see: https://www.cdc.gov/vaccines-pregnancy/about/index.html. This “recommendation” was issued by the CDC on 17 June 2024.

The “elaborate costumes and dance of Kabuki theater” approach were on display during this video with Secretary Kennedy, Jr., Dr. Makary, and Dr. Bhattacharya. But it was a “performance.” And the audience suspended reality for the “performance.”

Yours Truly now turns to the blog article by Sasha Latypova, a former medical technology and pharmaceutical technology professional, about this “Kabuki theater performance” of 27 May: https://sashalatypova.substack.com/p/eugenics-for-dummies-aka-hhss-evidence, “Eugenics for Dummies, aka HHS’s “Evidence-Based Approach” to covid shots.”, 29 May 2025. Please see the screenshots from her article, below:

It appears that, in reality, what has happened is that the current CDC Immunization Schedules have been neatly “absorbed into” the “new evidence-based approach to the COVID-19 vaccines” so-called “opinion piece” of Dr. Makary and Dr. Prasad (see the links to their “opinion piece”, above; and, also, the statement by Dr. Prasad that this “new approach” will be implemented at the FDA / CDC (so, it seems, they aren’t “opinions” at all.)

Further confirmation of the “Kabuki theater” element regarding the 27 May “announcement” by Secretary Kennedy, Jr., Dr. Makary, and Dr. Bhattacharya, comes from The Kingston Report: https://karenkingston.substack.com/cp/164733998, “Who’s Calling the Shots at HHS?”, 29 May 2025.

WHO IS IN CHARGE OF HHS? If Secretary Kennedy, Jr., can take the time to write letters to ask that ostriches in Canada are not “culled” due to a “possible” infection from Avian Influenza; if he can issue a directive to have titanium dioxide removed from candy (Skittles) — why did he participate in a “Kabuki theater performance” on 27 May regarding something incredibly important to the health of every American — the dangerous, deadly COVID-19 “vaccines”? Did he, or anyone else, at HHS, inform Dr. Monarez about the “change” in the CDC Immunization Schedules? If so, did she agree?

In Yours Truly’s opinion, there appears to be some sort of “issues” going on at HHS, the FDA, and the CDC. HHS Secretary Kennedy, Jr., needs to get to the bottom of all of them.

FLASH! AS OF TODAY, 30 MAY 2025: THE CDC HAS JUST ISSUED THE “NEW CHILDHOOD VACCINE IMMUNIZATION SCHEDULE” RELATED TO THE COVID-19 “VACCINES”:

It appears that Dr. Susan Monarez, PhD, has finally weighed in regarding the 27 May “announcement” (aka “Kabuki theater performance”) by HHS Secretary Kennedy, Jr., Dr. Makary, and Dr. Bhattacharya COVID-19 “vaccines” and the CDC Childhood Immunization Schedule. Please see Sasha Latypova’s presentation here: https://sashalatypova.substack.com/p/cdc-issued-the-anticipated-updates, “CDC issued the anticipated updates to the children’s schedule for covid shots”, 30 May 2025.

HOWEVER, there’s some “catches” in the “updates.” Huge “catches.” These have to do with the CDC “definition” of what a “healthy child” means. In short summary: It will be the CDC who decides if a child meets their “criteria” for being a “healthy child” (meaning, the COVID-19 “vaccines” aren’t “necessary” or “recommended”); it will be the CDC’s “guidance” on this that will be in control of any discussion between a child’s parent(s)/guardians, and the clinician who can administer COVID-19 “vaccines”; there are no provisions that Yours Truly can see in the CDC “guidance” for exemptions on religious or other grounds; and, that ANY clinician who is cleared to administer COVID-19 “vaccines” will ultimately make the decision on whether or not to COVID-19 “vaccinate” a child who does not fit the CDC “criteria” for a “healthy child.” This includes clinicians who have never treated the child (in other words, a CVS pharmacist, for example.) Please see the screenshots below, from the Latypova article of today:

Peace, Good Energy, Respect: PAVACA

Dear KMAG: 20250512 Trump Won Three Times ❀ Open Topic

Joe Biden never won. This is our Real President – 45, 46, 47.

AND our beautiful REALFLOTUS.

This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).

And yes, it’s Monday…again.

But we WILL get through it!

We will always remember Wheatie,

Pray for Trump,

Yet have fun,

and HOLD ON when things get crazy!

We will follow the RULES of civility that Wheatie left for us:

Wheatie’s Rules:

No food fights.
No running with scissors.
If you bring snacks, bring enough for everyone.

And while we engage in vigorous free speech, we will remember Wheatie’s advice on civility, non-violence, and site unity:

“We’re on the same side here so let’s not engage in friendly fire.”

“Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”

If this site gets shut down, please remember various ways to get back in touch with the rest of the gang:

Our backup site, The Q Tree 579486807, https://theqtree579486807.wordpress.com/
Our old alternative site, The U Tree, where civility is not a requirement
Our Gab Group, which is located at https://gab.com/groups/4178
Our various sister sites, listed in the Blogroll in the sidebar

Our beloved country is under Occupation by hostile forces.

Daily outrage and epic phuckery abound.

We can give in to despair…or we can be defiant and fight back in any way that we can.

Joe Biden didn’t win.

And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.

Wolfie’s Wheatie’s Word of the Week:

placeholder

noun

a dummy post on The Q Tree
other definitions we don’t care about
still more definitions we don’t care about

Used in a sentence

A placeholder is not the same as the command to place Holder under arrest.

Shown in a picture

Shown in a video

MUSIC!

Placeholder!

THE STUFF

Well, it looks like we have a placeholder for a nuclear clock!

Thorium. Useful stuff.

Just sayin’!

And remember…….

Until victory, have faith!

And trust the big plan, too!

And as always….

ENJOY THE SHOW

W

NOTE:

What you see above is essentially the “Monday Placeholder”. If you see nothing more, and no different, then you are seeing the placeholder.

If I have time and the inclination, I may swap in a new Word of the Week, some new videos, and possibly even an added topic.

Today, I will leave the placeholder alone, for reference, but I will add a topic. Thanks!

W

The Strategy I See Behind the New “Universal Vaccine Platform”

Some of you have to be asking yourselves why Robert F. Kennedy Jr. seems to have gone from being an opponent of vaccines, to being a proponent of them. I will try to explain.

To begin with, it helps to read the following document (H/T to PAVACA for producing these images). You can use this link, or the images below it.

HHS, NIH Launch Next-Generation Universal Vaccine Platform for Pandemic-Prone Viruses

LINK: https://www.hhs.gov/press-room/hhs-nih-announces-generation-gold-standard.html

It is hard for me to put into words, how much of a change this really is. But let me give you a quick “TL;DR” list of the big-ticket items.

Big Pharma is completely cut out of this platform – it’s US government owned and driven.
The vaccines are designed to be resistant to evolution of the pathogens they protect against. The vaxxes themselves are immune to “scariants”.
The vaccines completely abandon mRNA, cDNA, recombinant antigen, spike protein, lipid nanoparticle, and all genetic and related technologies.
The vaccines abandon Fauci’s always-failing strategy of targeting current variants, and instead seek to handle both current and future variants.
The result is fewer and less frequent shots. The better the shot, the more this is true.
The vaccines must pass rigorous safety standards, or otherwise fail to be approved.
The vaccines change direction and focus, from smaller subunits to whole-virus immunity.
The vaccines are potentially capable of inhibiting transmission.

IMO this is not just about changing the vaccines – it’s about changing minds in government science.

Most scientists, sadly, are sheep. They have neither the courage nor the inclination to challenge anything in the current scientific narrative – particularly as reported by our toxic media. If the media says “most scientists believe X”, then most scientists think this is true, and won’t bother to check, much less actively disagree.

The evil media has trained us all to believe certain myths.

There will be more and more exotic diseases coming at us from nature
There will need to be more and more vaccines, and more and more injections of them
Vaccines get better by using newer technology, not by working better for people
Vaccine hesitancy is a bad thing, and must be prevented at all costs
Vaccines are all safe, and rumors that any are bad, are dangerous

Apparently, despite the iron fist of Faucism, somebody in NIAID was thinking in ways that lead in the opposite direction from where Pfizer was taking us. I suspect that these forces sat tight, waited for “reinforcements to arrive” (Trump, RFKJ, and Dr. Jay), and had their proposal working up the chain of command as soon as Trump won.

Will this vaccine approach work? IMO it will work better than mRNA. Whether it works well enough to pass Kennedy’s new standard, based on comparison to placebos and true controls, is another question.

For the sake of those who still want vaccines, I hope so.

I suspect that these vaccines will be safer than mRNA, but not completely safe – particularly with a pathogen like COVID. As long as these vaccines are not mandated, I’m OK with their existence. In any case, the vaccines will have to prove themselves safe and effective.

Will I trust that determination?

Maybe. Or maybe not.

W

Health Friday Open Thread 5.9.2025: About That “Universal Vaccine”–There’s More Than Meets the Eye, Part One

Antique London’s photographs: Goldsmith Hall, The Assay Office

The above free vintage image of a laboratory is courtesy of iStock and Google Images.

Health Friday is a series devoted to information regarding Big Pharma, vaccines, general health, and associated topics.

There are Important Notifications by 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 anything in the discussion thread for today’s post that is AI-generated, they must cite their source. Thank you.

Due to the nature of today’s topic, there will be two separate posts. Part One, today’s offering, starts here: https://www.hhs.gov/press-room/hhs-nih-announces-generation-gold-standard.html, “HHS, NIH Launch Next-Generation Universal Vaccine Platform for Pandemic-Prone Viruses”, 1 May 2025. Please see the following screenshots from the announcement:

To unpack the announcement, Yours Truly will begin with a 2016 document from the EPA regarding beta-propiolactone, aka BPL (as in BPL-1357): https://www.epa.gov/sites/default/files/2016-09/documents/beta-propiolactone.pdf. Please see the following screenshots from this document:

Notice the risks associated with inhalation of beta-propiolactone (which is being used in the development and testing of the “new Gold Standard” intranasal version of the “new Universal Pandemic Vaccine”, BPL-1357.)

Note the language regarding irritations of various types; of damage to the corneas; convulsions; and “extreme acute toxicity.”

Note the language about cancer being induced in lab rats and mice by the use of beta-propiolactone, but no information being available regarding the inducement of cancer in humans by the use of beta-propiolactone.

The funds for Generation Gold Standard, in the amount of $500 million dollars, will come from reallocation of monies within BARDA (Biomedical Advanced Research and Development Authority: https://www.fiercebiotech.com/biotech/hhs-unveils-500m-universal-vaccine-initiative-calls-biden-era-covid-vax-accelerator, “HHS unveils $500M universal vaccine initiative, calls Biden-era COVID vax accelerator ‘wasteful'”, 1 May 2025. Please see the screenshots from this article, below:

Both Dr. Memoli and Dr. Taubenberger have been with the NIH / NIAID for years. Also, note the tiny subject pool of 45 adult subjects in the Phase 1 study of BPL-1357.

On a “tangential point”, there is this FDA announcement of 10 April 2025: https://www.fda.gov.media/186092/download, “Roadmap to Reducing Animal Testing in Preclinical Safety Studies”, by new FDA Director Dr. Marty Makary. Sasha Latypova analyzed the announcement here: https://sashalatypova.substack.com/p/you-didnt-want-that-mrna-vax-tested, “You didn’t want that mRNA vax tested only on 8 mice? Marty Makary, FDA, has a solution — no more mice!”, 28 April 2025.

That’s right. Dr. Makary wants to reduce, then end, animal testing for vaccines in the preclinical stage, and to substitute testing them instead by using in silico models; then, to move to human subject testing; and, even to NOT have ANY human subject clinical trials at all in “certain circumstances.” Please see the screenshots below from the Latypova article:

Yours Truly understands that the use of animals in lab experiments must be done in the most humane manner possible — no more of the “Fauci tortured Beagles” situations. However, one is of the opinion that there is a place for using animals in lab experiments — to study physical reactions and/or reproductive issues related to the drug or injectable under investigation before human tests begin: something that an in silico model or an AI model cannot do. And, the part about no clinical trials at all in “certain circumstances”:

Note: the red text in the screenshots above link to other articles and information from the Latypova article. Also, recall that Ms. Latypova worked in medical and pharmaceutical techology for years before retiring from the field.

This is the same Dr. Marty Makary who recommended that pregnant women get COVID-19 “vaccinated”:

To finish today’s Part One offering, Yours Truly presents the involvement of United States Defense Department in the use of the “AFLQ adjuvant” that is going to be tested in clinical trials for BPL-1357: https://hivresearch.org/hiv-research/alf-adjuvants. This is the United States military research program into “Military HIV.” This article had a link that led to the following press release by the United States Army, from 2021: https://wrair.health.mil/News-Media/Press-Releases/Article/3166852/phase-1-clinical-trial-of-wrair-developed-covid-19-vaccine-begins/, 5 April 2021. The clinical trial is NCT04784767, that began with 29 subject enrollees on 5 April 2021, and had an “Estimated Study Completion Date” of 30 October 2023 (https://clinicaltrials.gov/study/NCT04784767.) The title of the clinical trial: “SARS-CoV-2 Spike Ferritin Nanoparticle Vaccine with ALFQ Adjuvant for Prevention of COVID-19 in Healthy Adults.” Below is a screenshot of the WRAIR article (WRAIR stands for Walter Reed Army Institute of Research):

Note the statement by Dr. Modjarrad that this “US Army COVID-19 Vaccine” would “pave the way for a universal vaccine to protect against not only the current virus, but also counter future variants…” — “universal vaccine” — sound familiar? “Who is driving this bus?” comes to mind.

To be continued in Part Two.

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA