Tag: HHS

Health Friday 4.17.2026 Open Thread: The Sleight-of-Hand at HHS Must Stop. Now.

The vintage image of mass vaccination for today’s offering is courtesy of Google Images.

Health Friday is a series on 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 from Yours Truly, of which readers should be aware. They are linked here. Note: AI-generated items in today’s offering, if any, will be cited as such. If readers wish to post AI-generated items in today’s discussion thread, they must cite their source. Thank you.

The United States Department of Health and Human Services (HHS) is still funding Gain-of-Function research. This is despite the 5 May 2025 directive from the White House regarding pausing all Gain-of-Function research by HHS (https://www.whitehouse.gov/presidential-actions/2025/05/improving-the-safety-and-security-of-biological-research/.) Examples: Arcturus Therapeutics is still under a “Fast Track” status granted to the company in April 2025 by the FDA — a Fast Track status granted for the development and testing of the company’s self-amplifying RNA (saRNA) “influenza vaccine”, ARCT-2304 (also known as, LUNAR-FLU or as LUNAR-H5N1 (https://ir.acrturus.com/news-releases/news-release-details/acturus-therapeutics-receives-us-fda-fast-track-designation-0, 10 April 2025.)

Yours Truly begins here: https://jonfleetwood.substack.com/p/hhs-funds-gain-of-function-influenzacovid, “HHS Funds Gain-of-Function Influenza — COVID ‘Frankenvirus’ Combining Influenza Entry With SARS-CoV-2 Human Cell – Binding Domain”, 10 April 2026. Two screenshots regarding this are below: the first, from the Fleetwood article; the second, from the paper itself (published December 2025). Thanks to Mr. Fleetwood for this information:

By the way, NIH grant P01-AI165075 (going to Rockefeller University, New York) has multiple “permutations” in the https://reporter.nih.gov/ listing. **** The “permutation” that helped to fund the paper below (cited in the Fleetwood article) is 3P01AI165075 – 01S1, Sub-Project ID: 6568, awarding entity NIAID, total funding: $983,100. (And this is only ONE “permutation” of P01-AI165075.)

**** What this lab-created “combo virus”, called X31 H3 S-RBD in the paper, contains:

The RBD (Receptor Binding Domain) from the Wuhan Hu1 SARS-CoV-2 virus (the original COVID-19 virus); plus

Seven other viral RNAs (vRNAs) from the H1N1 (Influenza A) Puerto Rico/1/1934 strain (PR8)

The Abstract of this paper is below. It is a clear statement that Gain-of-Function was used to lab-create this “combo virus” (lines 28 – 35):

Let’s take a look at the involvement with the Chinese Academy of Medical Sciences (CAMS) in the study that produced this paper. The paper states that Tiong Kit Tan, of the Chinese Academy of Sciences – Oxford Institute, Nuffield Department of Medicine, University of Oxford, is one of the researchers/co-authors. CAMS is a collaborator with the Chinese Communist People’s Liberation Army (PLA.) CAMS is one of the “Top 5” domestic (Chinese-based) collaborators with the PLA. Please see: https://www.nature.com/nature-index/institution-outputs/china/people-s-liberation-army-pla/555c2052140ba014648b456b; scroll down the page to the list of “Domestic Collaborators.”

Further down the page, there is the list of “International Collaborators” with the PLA. It is interesting to note that NUS (National University of Singapore) is ranked as Number One here. It is also interesting to note that NUS has a large medical school that is a “satellite” of Duke University (Chapel Hill, North Carolina; https://www.duke-nus.edu.sg.)

CAMS also has ties to Yale University via the CMB Foundation Global Health Research Fellowship in Communist China (https://medicine.yale.edu/education/othereducation/cmb/foundation-global-health-research-fellowship-in-china/cams-pumc/; PUMC is Peking Union Medical College); to Harvard Medical School; and, to the NIH (https://www.science.org/cms/asset/ecaa3321-8b14-45e9-b549-1631422a83ea/cams_booklet_2016_11_18.pdf, pages 44-45.)

The question arises: How much research data, analyses, lab samples, and more, from these “international collaborators” with the Chinese Academy of Medical Sciences, wind up in laboratories run by the People’s Liberation Army in hospitals and universities throughout Communist China?

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Let’s look at a recent example of “Gain-of-Function Experiments Gone Wrong”: https://childrenshealthdefense.org/defender/exclusive-bird-flu-outbreak-40-miles-wisconsin-lab-sparks-concern-gain-of-function-experiments/, “Exclusive: Bird Flu Outbreak 40 Miles From Wisconsin Lab Sparks Concern About Gain-of-Function Experiments”, Michael Devradakis, PhD, 15 January 2026. A screenshot from this article is below:

Yoshihiro Kawaoka, DVM, PhD, is also the scientist who is heavily involved with Gain-of-Function experiments at the University of Wisconsin-Madison. And, that there is a record of prior accidents and leaks from his lab there: https://www.cidrap.umn.edu/biosecurity-issues/wisconsin-lab-broke-ebola-rules-watchdog-group-says, 25 September 2007; and, https://www.wispolitics.com/2023/wisconsin-congressional-republicans-demand-answers-on-biosafety-incident-at-uw-madison/, 23 April 2023.

The NIH grant that helped to fund Dr. Kawaoka’s work for the above cited paper is 75N93021C00014. The grant contract information is found here: https://www.highergov.com/contract/759321C00014/. An image of the Government Description of this grant, from the website, is below:

Note that sentence about, “Includes international and domestic basic and clinical influenza research…” — in other words, covering “collaborators” like CAMS. Note that “studies of viral evolution, transmission, and immune responses in animal models and humans” covers Gain-of-Function work.

CEIRR stands for Centers of Excellence for Influenza Research and Response. The website description of this research division of NIAID is here: https://www.niaid.nih.gov/research/centers-excellence-influenza-research-response. Scroll down the page to “Main Areas of Focus” to this statement: “To support projects to determine how influenza viruses evolve, adapt and transmit between humans and at interspecies interfaces”. This is “code” for supporting Gain-of-Function research on influenza viruses. There are multiple “permutations” of NIH grant 75N93021C00014 listed at https://reporter.nih.gov/search/6vlkhZH5302zeKPiGnsO5g/projects, most of which were awarded to the Icahn School of Medicine at Mount Sinai, New York (one of the CEIRR main hubs of research.)

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Yours Truly turns to what might be, in her opinion, called a “permutation” of Gain-of-Function research: experiments on human beings to further a Patent invention.

The Patent in question is: US11369675B2, “Broadly protective inactivated influenza virus vaccine”, held by Dr. Jeffery Taubenberger, MD, Acting Director of NIAID. The Patent declaration is found here: https://patents.google.com/patent/US11369675B2/en. The application for the Patent was filed on 12 October 2020; the Patent was granted on 28 June 2022; the “Adjusted expiration” date of the Patent is 24 January 2039; and, the Patent was assigned to the Department of Health and Human Services (HHS.) Dr. Taubenberger, during this timeline, was an employee of HHS, before he became Acting Director of NIAID. He, in fact, is a career HHS (NIH) employee.

Dr. Taubenberger’s Patent describes a “universal influenza vaccine.” Yours Truly has written on this situation; for example: 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/.

It appears that Dr. Taubenberger is working to further the Patent regarding the development of an intranasal “universal influenza vaccine.” His most recent published paper in this regard is here: https://pmc.ncbi.nlm.nih.gov/articles/PMC12375958/S#23, “Nasal and systemic immune responses correlate with viral shedding after influenza challenge in people with complex preexisting immunity”, Jeffery Taubenberger, et al., 6 August 2025. This paper describes a very small study of 74 persons (originally 80 persons) that was conducted in 2019 per the cited paper above (NCT01971255.) However, the ACTUAL study dates of NCT01971255, per https://clinicaltrials.gov/study/NCT01971255, indicate a timeframe between September 2013 and September 2015. In addition, the referenced paper number 11 in the cited paper above describes the same experimental study, but via a paper published about it in 2024 (https://pmc.ncbi.nlm.nih.gov/article/PMC10865821/, “Mucosal correlates of protection after influenza viral challenge of vaccinated and unvaccinated healthy volunteers”, Jeffery Taubenberger, et al., 9 January 2024.) This, to Yours Truly, raises questions regarding the timing of the publishing of these papers, since the actual study was conducted over 10 years ago. What goes on here?

The bottom lines of NCT10971255: there were 80 enrolled study subjects; half were vaccinated with a licensed influenza “vaccine”; half were unvaccinated; ALL subjects were then given an intranasal LIVE VIRUS H1N1 (swine flu), called Ca/04/2009/H1N1r Challenge Virus; ALL subjects were then tested numerous times via a middle turbinate nasal swab (this means that the swab samples were taken from well inside the upper nasal cavity each time); apparently, ALL subjects became ill with flu symptoms, some of which were severe; 6 study subjects withdrew for various reasons; all testing using the “intranasal challenge virus” was performed at the NIH Clinical Center in Bethesda, Maryland; the study subjects were brought there for the “challenge” (and likely had to stay there or in the immediate area, as they were assessed daily for a minimum of 9 days.)

Yours Truly will point out that Patent holders at HHS (NIH; NIAID) can earn significant royalty payments for the use of the their registered inventions. Please see: https://www.lankford.senate.gov/news/press-releases/lankford-hsgac/republicans-request-information-from-nih-on-the-disclosure-of-royalty-payments-to-nih-employees/, 1 June 2022.

Dr. Taubenberger is the recipient of NIAID research funding related to Avian Influenza viruses, his “universal influenza vaccine”, and to the SARS-CoV-2 virus — in the 2025 fiscal year, among other years. However, 2025 is the year in which Dr. Taubenberger became the Acting Director of NIAID. The “umbrella grant” prefix number is either 1ZIAAI00 or 1ZIAAI000, each followed with the suffix number: for example, 1ZIAAI001372-03, “Universal Influenza Vaccine Development”, for $2,153,677. This grant, as at least one other per https://reporter.nih.gov/ (search: Jeffery Taubenberger), lists NO contact data; NO Project Start Date; NO DUNS number; NO Budget End Date; among other lack of public information. What goes on here? Is Dr. Taubenberger perhaps granting NIAID research funds to himself?

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Finally, is appears that HHS Sec. Robert F. Kennedy, Jr., is going to start a podcast:

Sec. Kennedy, Jr., states that he will “…ask the questions and lift the taboos and expose the hypocrisy and the conflicts and the corruption…We’re going to follow the evidence wherever it leads, and we’re going to name the names of the forces that obstruct the paths to public health.”

All well and good. However — will Sec. Kennedy, Jr., “name the names”, such as: the person who invented the SARS-CoV-2 virus itself — Dr. Ralph Baric of the University of North Carolina, Chapel Hill? Such as, the person who could have stopped the entire COVID-19 “vaccine” disaster in the United States in December 2020, but who instead signed off on the CDC’s “recommendation” for the use of Pfizer-BioNTech’s modRNA COVID-19 bioweapon “vaccine”, BNT162b2, without any further investigation — Dr. Robert Redfield, then-Director of the CDC? Such as, the person who was responsible for the NIAID funding that produced the SARS-CoV-2 virus itself — Dr. Anthony Fauci, former NIAID Director? Such as, the USAMRIID personnel responsible for working with PfizerUSA (Pfizer-BioNTech) in the development of BNT162b2? Will Sec. Kennedy, Jr., “name the names” of the products that, by far, have obstructed, and continue to obstruct, “the paths to public health” — the COVID-19 bioweapon “vaccines”?

ALL GAIN-OF-FUNCTION WORK IN THE UNITED STATES, OF ANY TYPE, MUST BE STOPPED. NOW.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Disclosure and Notice: Except for the linked URLs and other items that can be found in the Internet, the ideas and/or opinions of today’s offering are by PAVACA. Credit must be given to PAVACA if the ideas and/or opinions of today’s offering are used by other blog writers, podcasters, or in social or print media.)

Health Friday 4.3.2026 Open Thread: Where the Focus Needs to Be Now: An Opinion Piece

The header image of FOCUS used for today’s offering is courtesy of Rio Salado College and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines. general health, and associated topics. There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: AI-generated items in today’s offering will be cited as such. If readers wish to post AI-generated items in today’s discussion thread, they must cite their source. Thank you.

To those who commemorate Passover; or, Holy Week, Good Friday and Easter Sunday: May the blessings of these observances be granted to you.

Yours Truly has posted dozens of articles on this board related to the COVID-19 bioweapon virus itself; and, to the COVID-19 bioweapon POISON “vaccines.” These articles have traced the origins of the virus itself; the development of the “vaccines”; the gaslighting and psyops techniques that have been used (and, are still being used) to frighten / suborn / coerce / “mandate”, billions of human beings into having these “vaccines” put into their body; the myriad of “vaccine”-induced or “vaccine”-aggravated illnesses, injuries, and disabilities that are presenting in “vaccinated” persons; the deaths caused by these “vaccines”; and more. https://www.theqtree.com/author/pavaca/.

To date, those who lab-created the COVID-19 virus itself; who lab-created the COVID-19 “vaccines”; who deliberately withheld important information about the virus itself, and about the “vaccines”, from then-President Donald Trump 45; who used the government (on all levels) to lock down millions of Americans for months to “stop the spread”, and to enforce “vaccination” on millions of Americans; who still inject thousands of Americans every day with these bioweapon POISON “vaccines” — have not been held to account. They have not been held account when they lied in sworn testimony before Congress (as did Dr. Anthony Fauci, when he stated in congressional testimony that he never knew or met Dr. Ralph Baric.) Please see: https://usrtk.org/covid-19-origins/fauci-discussed-gain-of-function-work-with-wuhan-collaborator-in-pandemics-earliest-days-emails-suggest/, by Emily Kopp, 21 February 2023.

It appears that the Department of Health and Human Services, along with its CDC and FDA divisions, are in the control of Big Pharma, Establishment Medicine organizations, and the Federal Judiciary. It appears that HHS Secretary Robert F. Kennedy, Jr., is focused on “side bar” issues, such as revamping the “official government food pyramid chart”, and removing artificial colorings from foods, among other items. While these are good and worthy efforts in and of themselves, they detract from the absolute importance of immediately stopping all COVID-19 bioweapon “vaccines” use in the United States, and taking these “vaccines” off the market. The damage, illnesses, injuries, and deaths induced by these products are increasing; dozens of peer-reviewed scientific papers have proven that these serious and deadly effects, induced by these products, are real. Disability claims have been skyrocketing since the rollout of these products in 2021 — please see the charts compiled by Ed Dowd at https://phinancetechnologies.com/.

It appears that there is a “latest new variant” of the COVID-19 bioweapon virus itself, called BA.3.2, nicknamed “Cicada“, after the insect that stays underground for years before hatching and emerging into the atmosphere. This variant is a mutation of the earlier B.3 mutant of the SARS-CoV-2 bioweapon virus that “went out of circulation” in early 2022. However, it then “re-appeared” as BA.3.2 in a sample taken from a patient in South Africa in November 2024: https://www.cdc.gov/mmwr/volumes/75/wr/mm7510a1.htm, “Early Detection and Surveillance of the SARS-CoV-2 Variant BA.3.2”, 19 March 2026. The BA.3.2 variant has now spread to multiple countries, including to the United States; it was found in wastewater samples from 25 states: https://news.northeastern.edu/2026/03/27/new-covid-19-cicada-variant/, “What you should know about the new COVID-19 ‘Cicada’ Variant”, Tanner Stening, 27 March 2026. A screenshot from the Stening article is below:

And, as if dutifully, the “mainstream media” is running with the “it’s a new variant outbreak” aspect: https://www.newsweek.com/map-shows-new-covid-variant-ba-3-2-spread-across-us-11745474, Giulia Carbonaro, 27 March 2026. A screenshot of the “outbreak map” in the article, courtesy of the CDC, is below:

Per Wikipedia (https://en.wikipedia.org/wiki/BA.3.2), the general summary list of SARS-CoV-2 virus variants:

Note where BA.3.2 is on this list. It is “descended” from a BA.3 Omicron variant (BA.1.1.529.3.) This places BA.3.2 (the “Cicada” variant that is the “new, latest variant”) closer up the list to the original Omicron variant (B.1.1.529) — hence, the “Cicada” nickname. Like the insect that hatches years after its eggs have been in the soil.

Note also the combination of both the BA.2 AND the BA.3 variants in BA.3.2. Both the BA.2 and the BA.3 variant lines are “heavily mutated.” And, in fact, the BA.3.2. “new, latest variant” has 70 to 75 mutations within it (per the Stening article, above.) In addition, per the CDC’s testing of samples of BA.3.2, this “new, latest variant” evades antibodies. The Scientific American article on BA.3.2, which mentions this, is here: https://www.scientificamerican.com/article/new-cicada-covid-variant-is-spreading-in-the-u-s-heres-what-to-know/, Tanya Lewis, 30 March 2026. A screenshot from this article is below:

It appears that both the BA.3 and the BA.3.2 SARS-CoV-2 virus variants were first detected in South Africa (regarding the emergence of BA.3: https://en.wikipedia.org/wiki/SARS-CoV-2_Omicron_variant#BA.3.) Let’s examine this situation.

First: GAVI (Global Alliance for Vaccines and Immunization, https://www.gavi.org/, was founded in Davos, and is funded by the Gates Foundation, among other entities / persons.) In 2021, GAVI announced an “investment opportunity” regarding launching a COVID-19 bioweapon “vaccine” program in South Africa: https://https://www.gavi.org/news/media-room/united-states-host-launch-event-gavi-covax-amc-2021-investment-opportunity. A screenshot from this press release is below:

The United States Secretary of State in April 2021 was Antony Blinken. The USAID Administrator in April 2021 was Gloria Steele (Acting Administrator; Samantha Power was sworn in as the Administrator on 3 May 2021.)

GAVI, the Gates Foundation, and COVAX went right to work on getting South Africa COVID-19 “vaccinated.” Per the Wikipedia entry regarding this situation (https://en.wikipedia.org/wiki/COVID-19_vaccination_in_South_Africa), the “vaccine” distribution pie chart, as of 2021:

The COVAX program in South Africa was ended on 31 December 2023: https://www.unicef.org/supply/covax-ensuring-global-equitable-access-covid-19-vaccines. COVAX was a coalition involving GAVI, WHO, and CEPI. CEPI (Coalition for Pandemic Preparedness Innovations, https://cepi.net/.) Among the funders of (investors in) CEPI are the Bill and Melinda Gates Foundation and the World Economic Forum (https://cepi.net/investors.) Below is a screenshot from the UNICEF article:

Does the reader see how the game is played? GAVI organizes an “investment opportunity” virtual meeting regarding funding for COVID-19 bioweapon “vaccine” programs in Africa, including in South Africa. The United States is heavily involved, via the Secretary of State and the USAID Administrator. Further involvement is orchestrated by GAVI to include UNICEF, CEPI, WHO, and (by extension) the WEF. Massive amounts of the COVID-19 modRNA bioweapon “vaccine” BNT162b2 are furnished by Pfizer-BioNTech for the “vaccination” program. Almost 80% of the eligible population in South Africa is “vaccinated” with BNT162b2, starting in early summer 2021. The BA.3 variant of SARS-CoV-2 emerges in South Africa, then it “doesn’t take off” and disappears — until it “re-emerges” (like the cicadas after years of dormancy) as BA.3.2 in November 2024 — in South Africa, from whence it is now detected in at least 23 countries, including in the United States. The CDC begins to “raise alarm” over this situation, especially since BA.3.2 has an “uncanny ability” to evade the antibodies supposedly “created” via the current COVID-19 modRNA bioweapon “vaccines”, or via prior COVID-19 infection and recovery.

Do not forget that the modRNA COVID-19 bioweapon “vaccines” do the following: One, to “trick” the “vaccinated” person’s body into thinking it is infected with the SARS-CoV-2 virus; which then forces the body to produce large amounts of immune system cells to “fight off” the “fake infection”, and which “vaccines” are at work in the body for at least 700 days post-injection (per the Yale LISTEN study); and, Two, to destroy the crucial RNA of the body’s natural Uridine, which under normal circumstances, would “alert” the body that there is an “enemy” (infection.) The RNA destruction is done by the N1-Methylpseudouridine in these “vaccines.” One of the principal scientific researchers who worked on One and Two above is Dr. Drew Weissman. Please see: https://www.brandeis.edu/now/2020/september/weissman-vaccine-mrna.html, Lawrence Goodman, 29 September 2020; and, https://www.brandeis.edu/magazine/2024/winter/the-brief/weissman-nobel.html. Two screenshots from these articles are below: the first, from the 2020 article; the second, from the 2024 article. Dr. Weissman, along with Dr. Katalin Kariko, received the Nobel Prize for their work with mRNA “vaccine” development:

Which illuminates the “why” behind the emergence of the BA.3 and the BA.3.2 variants in South Africa after the COVID-19 “vaccination” programs began in 2021; which illuminates the “why” behind the emergence of all the other SARS-CoV-2 variants; which illuminates the “why” behind the “breakthrough infections” and the “becoming infected with COVID despite being vaccinated” incidences since the rollout of these “vaccines” in December 2020; which illuminates the “why” behind the steady damage to / destruction of, the immune system of the “vaccinated” body.

And where is the “new ACIP roster” which was stated was coming, after Federal Judge Brian E. Murphy disbanded the group and reinstated the former CDC Childhood Immunization Schedule in his “ruling” of 16 March 2025? NOWHERE. There IS NO “new ACIP members roster.” There IS NO announcement of a meeting scheduled by this group.

What does this mean regarding the concept of FOCUS?

It means: Focus on the truth that the CDC (and, by extension, HHS and the FDA) are now controlled by outside interests: https://www.theqtree.com/2026/03/27/health-friday-3-27-2026-open-thread-hhs-is-controlled-by-big-pharma-the-american-academy-of-pediatrics-and-the-federal-judiciary/.

It means: Focus on the truth that HHS Secretary Robert F. Kennedy, Jr., is effectively negated in his ability to direct the department (and, by extension, the CDC and the FDA) — in other words, to do his job.

It means: Focus on the fact that it is “open season” on the people of the United States — from BEFORE birth and up until death — to be “vaccinated” with products that do NOT prevent disease; that do NOT prevent hospitalization from disease; that INDUCE a myriad of negative side effects, including death; that AGGRAVATE or RE-ESTABLISH pre-existing medical conditions that were under control / in remission, including cancer; to be injected with products that are NOT fully tested, the data NOT fully analyzed, and instead to be used as “human lab rats” for the Big Pharma companies that lab-develop / lab-create these products.

**** It means: Focus on the fact that people MUST do their own research — MUST do their own thinking — MUST make their OWN decisions, related to taking ANY “vaccine.” To allowing ANY “vaccine” to be put into their children. To question ANY healthcare provider who “recommends” ANY “vaccine.” To DEMAND to see the Package Insert for ANY “vaccine” that is “recommended” and to READ IT. To REFUSE ANY “vaccine” that raises ANY questions regarding “safety and efficacy” in the mind of the patient / parent(s) / guardian. To READ the reports in VAERS related to COVID-19 bioweapon “vaccine” serious adverse reactions / serious events. To stop blindly rolling up the sleeve for a “vaccine” injection because “Follow the science.”

THERE IS NO PLACE IN THE HUMAN BODY FOR AN mRNA, A modRNA, AN saRNA, OR A taRNA PRODUCT OF ANY KIND, IN ANY FORM.

THERE MUST BE, FIRST, MUCH MORE RESEARCH INTO THESE PLATFORMS, WITH COMPLETE AND PROPER TESTING, DATA ANALYSES, AND SAFETY AND EFFICACY REPORTING.

THERE MUST BE, SECOND, A TOTAL STOP TO ALL GAIN-OF-FUNCTION RESEARCH IN THE UNITED STATES.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Disclaimer and Notice: Except for linked URLs and other items available on the Internet in today’s offering, the ideas and opinions above are by PAVACA. Credit must be given to PAVACA if ideas and opinions in today’s offering are used by other blog writers, by podcasters, or in print or social media.)

Health Friday 3.27.2026 Open Thread: HHS is Controlled by Big Pharma, the American Academy of Pediatrics, and the Federal Judiciary

The vintage header image of “The Trial of the Lewis Deer Raiders at Edinburgh” for today’s offering is courtesy of iStock 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: AI-generated items in today’s offering will be cited as such. If readers wish to post AI-generated items in today’s discussion thread, they must cite their source. Thank you.

Today’s offering discusses the recent court ruling by Federal Judge Brian E. Murphy, which as effectively gelded the Centers for Disease Control and Prevention (CDC) division of the United States Department of Health and Human Services (HHS.)

On 16 March 2026, Federal Judge Brian E. Murphy, of Boston, ruled for the plaintiffs in a lawsuit against the CDC, the ACIP group of the CDC (Advisory Committee on Immunization Practices), HHS Secretary Robert F. Kennedy, and other defendants. The lawsuit was brought by a coalition of health organizations, headed by the AAP (American Academy of Pediatrics.) The Murphy ruling, among other items, enjoined the ACIP group from undertaking its scheduled meeting in March, 2026; it stayed any proposed changes to the CDC Childhood Immunization Schedule, changes that were to have been approved at this meeting; and, nullified all recommendations, directives, and other actions, made by the ACIP group since July 2025. Fierce Pharma covered the ruling here: https://www.fiercepharma.com/pharma/judge-pumps-brakes-rfk-jr-vaccine-overhaul-targering-acip-and-cdc-schedule-revamp, Eric Sagonowsky and Fraiser Kansteiner, 16 March 2026.

The ruling by Judge Murphy is here: https://fingfx.thomsonreuters.com/gfx/legaldocs/gdpzawegkvw/03162026vaccine.pdf. The list of plaintiffs, and more coverage of the Murphy ruling, are here: https://www.apha.org/news-and-media/news-releases/apha-news-releases/federal-judge-blocks-immunization-schedule-changes, “Federal Judge Blocks Immunization Schedule Changes, Stays ACIP Member Appointments”, 16 March 2026. Please see the screenshot, below, from this article:

Dr. Jessica Rose, PhD, discussed the ruling here: https://jessicar.substack.com/p/more-on-the-judgy-mcjudgefaceacip-situation, “More on Judge Brian E Murphy/ACIP situation”, 21 March 2026. Please see the screenshots, below, from this article:

Yours Truly went to the article (referred to in the post by Dr. Rose), written by an experienced practicing attorney, regarding the Murphy “ruling.” The attorney is Bobbie Anne Flower Cox, Esq. Her article is here: https://brownstone.org/articles/when-judges-go-rogue/, 23 March 2026. Please see the screenshots from this article, below:

But wait, there’s more! Judge Murphy, in his “ruling”, also “critiqued” each (then)-member of the ACIP group, finding every one of them “lacking” in what he deemed to be the “amount of expertise” to be making any decisions regarding the CDC vaccination schedule. Please see the screenshots from his “ruling”, below: Page 29 and Page 30:

And then, with even more breathtaking condescension, the following, from Page 31 of the Murphy “ruling”:

It appears that the (then)-members of the ACIP group were supposed to “present evidence” to him that they ARE qualified to sit on the committee? And, if the JUDGE deems their “level of expertise” is “lacking”, that the JUDGE can dismiss such members from the committee? Were the credentials of, for example, (then)-ACIP member Dr. Robert Malone not “good enough” for Judge Murphy? — After all, Dr. Malone discovered how mRNA can be “packaged” into a lipid nanoparticle. And why does it appear that Judge Murphy has a “particular axe to grind” regarding (then)-ACIP member Dr. Retsef Levi?

Back to the Bobbie Anne Cox article. It appears the Judge Murphy was doing all he could to find ways to “legislate from the bench.” Please see below, from Ms. Cox’s article:

Regarding the last point, about the American Academy of Pediatrics (AAP) having no standing: Guess what? The AAP gets large donations from Big Pharma entities, such as, Pfizer, Moderna, and, Seqirus. The AAP is completely compromised and should never have been a party to this (bogus) lawsuit in the first place. Please see: https://www.aap.org/en/ways-to-give/current-corporate-and-organizational-supporters/, from 10 October 2025:

The AAP is a direct beneficiary of Big Pharma. AAP pediatrician members make significant amounts of income from “vaccinating” children with products manufactured by the Big Pharma entities that give large amounts of money to the AAP. See how the cycle works?

If, as Attorney Cox states, the Murphy “ruling” can be overturned in court, why did HHS apparently choose NOT to fight the “ruling”, opting instead to “reconstitute” the ACIP group? Please see: https://imahealth.substack.com/cp/191534018, “Breaking News: Chairman Milhoan Confirms that ACIP Disbanded in Response to Federal Court Ruling: Sources Indicate Administration Opts to Reconstitute ACIP Rather Than Appeal”, 16 March 2026. A screenshot from this article is below:

In addition, pediatricians receive “financial incentives” from Big Pharma companies and from insurance companies via programs to ensure that children are “vaccinated.” This, despite the denials and “fact-checking” by media and by organizations such as the AAP about such “incentive payments.” In fact, Texas Attorney General Ken Paxton has initiated an investigation into these payments given to pediatricians in his state. Please see: https://www.texasattorneygeneral.gov/news/releases/attorney-general-ken-paxton-launches-wide-sweeping-investigation-unlawful-financial-incentives, “Attorney General Ken Paxton Launches Wide-Sweeping Investigation into Unlawful Financial Incentives Related to Childhood Vaccine Recommendations”, 21 January 2026. Please see the screenshot, below, from this article:

There is yet another aspect to the Murphy “ruling” situation: A combination of conflicting statements, apparent miscommunications, and what appears to be personnel from the Oval Office “taking a more active role” in HHS activities. Please see: https://www.fiercepharma.com/pharma/acip-members-miscommunication-vaccine-panels-future-adds-confusion-after-earlier-upset-court, “ACIP member’s miscommunication on vaccine panel’s future adds to confusion about ruling”, 20 March 2026, Fraiser Kansteiner. Please see the screenshots from this article, below:

Note that Yours Truly used the phrase, “appears to be personnel from the Oval Office” related to the HHS situation — the Wall Street Journal cites “unnamed sources.” However, what can be said, with a fair amount of accuracy, is that the HHS (and its CDC and FDA and NIH and NIAID divisions) have been roiling due to the attempts of HHS Sec. Kennedy, Jr., to curtail / stop, the “good old days” in the department. The “good old days” when drugs and “vaccines” were granted EUAs or Full Approval without proper full testing and data analysis; when the CDC “recommended” more and more “vaccines” for children from birth to age 18; when the FDA granted EUAs and Full Approvals for drugs and biologics that were clearly dangerous to patients (VIOXX [pain reliever]; and, Aduhelm [Alzheimer’s disease drug] are cases in point.) What can be said, with a fair amount of accuracy, is that Gain-of-Function experiments in the United States are still being funded by NIH, even though a “ban” on such experiments and funding was declared in 2025 — and, in addition, such experiments are also being conducted by other agencies within the federal government; as, for example, the H5N1 Avian Influenza experiments being conducted at the USDA Southeast Poultry Division facility in Georgia (https://jonfleetwood.substack.com/p/trump-admin-keeps-ties-to-who-influenza, “Trump Admin Keeps Ties to WHO Influenza System as U.S. Funds Bird Flu Gain-of-Function and Mass Vaccine Programs”, 24 January 2026.)

The following are the opinions of Yours Truly:

What the situation is today: Big Pharma, the American Academy of Pediatrics, and the Federal Judiciary, are in control of the Department of Health and Human Services. What the situation is today: HHS has opted to “reconstitute” the ACIP group, instead of fighting the Murphy “ruling” in court — in effect, acquiescing to the “ruling.” This acquiescing “kicks the door off the hinges” for any Federal Judge to stop / stay / delay, any directive, recommendation, committee, or activity of that committee, of the HHS, CDC, or FDA.

What the situation is today: Millions of children, from birth to age 18, are at risk for complications of all kinds induced by the multitude of “vaccines” that they are “recommended” to get according to the old CDC Childhood Immunizations Schedules.

What the situation is today: By HHS Sec. Kennedy, Jr., focusing on creating a new “food pyramid chart”, along with other “side-bar” programs — which, of themselves, are worthy — but not as important as focusing on completely rooting out any influence of Big Pharma and Establishment Medicine at HHS, he has allowed these entities to manipulate the Federal Judiciary into neutering the entire agency. By HHS Sec. Kennedy, Jr., focusing on other programs, he is NOT doing anything substantive regarding completely STOPPING the use of COVID-19 “vaccines” in the United States — arguably, the most dangerous, deadly, and poisonous products ever designed. By HHS Sec. Kennedy, Jr., focusing on other programs, he is NOT doing anything substantive regarding bringing those to account for their roles in creating the COVID-19 virus itself, or the COVID-19 “vaccines.”

What the situation is today: Is is more important then ever for all persons (including parents of children from birth up to age 18) to take charge of their health. To question the “why” behind a “recommendation” by a healthcare professional regarding taking any “vaccine”, let alone any drug. To refuse to take any “vaccine”, or to have any “vaccine” put into their children, that the patient (or patient’s parents) do not approve. To fight to have “vaccine liberty” from school boards, employers, and insurance companies that request “compliance” with “recommendations” or “mandates” for “vaccination.”

What the situation is today: Since Big Pharma, the American Academy of Pediatrics, and the Federal Judiciary are now in control of the Department of Health and Human Services — it is now the responsibility of HHS Sec. Kennedy, Jr., to stop this situation; or, for the current Administration to find someone who will.

What the situation is today: An example of the new “power base” that is in control of HHS / CDC / FDA: Pfizer-BioNTech wants the FDA to approve the company’s new Lyme disease “vaccine” (which appears to be mRNA-based) that it is developing with a French company, Valneva. The “vaccine candidate” is called VLA15. This, despite the fact that the Phase 3 clinical trial for VLA15 did NOT meet its primary outcome goal — which goal was to demonstrate effectiveness. This, despite the fact that the CDC has NOT YET “reconstituted” the ACIP group, which group is SUPPOSED TO RECOMMEND new “vaccines” for authorization or for approval by the FDA. If the FDA does not bow to Pfizer-BioNTech’s request to approve VLA15, what is to stop the company from suing the FDA and, via a Federal Judge (for example, Judge Brian E. Murphy), forcing the agency to approve the “vaccine?” Please see: https://tdefender.substack.com/cp/1921132650, “Pfizer Wants FDA to Approve Its Vaccine for Lyme Disease — But Does It Have a Shot?”, Brenda Baletti, PhD, 25 March 2026.

THERE IS NO PLACE IN THE HUMAN BODY FOR AN mRNA, A modRNA, AN saRNA, OR A taRNA PRODUCT OF ANY KIND, IN ANY FORM.

THERE MUST, FIRST, BE MUCH MORE RESEARCH PERFORMED ON THESE TECHNOLOGIES AND PLATFORMS.

THERE MUST BE, SECOND, EXTENSIVE TESTING OF PRODUCTS USING THESE TECHNOLOGIES AND PLATFORMS, WITH COMPLETE ANALYSES OF SAFETY AND EFFICACY DATA.

ALL GAIN-OF-FUNCTION EXPERIMENTS IN THE UNITED STATES, OF ANY KIND, PERFORMED BY ANY DEPARTMENT OF THE UNITED STATES GOVERNMENT, MUST BE STOPPED.

Peace, Good Energy, Respect: PAVACA

(Intellectual Disclaimer and Notice: Except for linked URLs and other items available on the Internet, the ideas and opinions of today’s offering are by PAVACA. Credit to PAVACA must be given if the ideas and opinions of today’s offering are used by other blog writers, by podcasters, in social or in print media.)

Health Friday 12.26.2025 Open Thread: Year-End Wrap-Up Edition

The header image for today’s offering is courtesy of The Productive Woman and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks of the COVID-19 disaster, Yours Truly dedicates it to all persons, of whatever age or location, who have suffered further illness, or injuries, or disabilities, from an infection of the COVID-19 virus itself, or from the COVID-19 “vaccines” they have in their bodies; or, who have passed away from complications related to an infection of the COVID-19 virus itself, or from issues induced from the COVID-19 “vaccines” they have in 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 AI-generated content. There may be AI-generated content (images, text, etc.) in certain linked URLs in today’s offering. If readers wish to add AI-generated content to today’s discussion thread, they must identify it as such. Thank you.

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Today’s offering is the Year-End Wrap-Up Edition. It has been a year of implementation of some of the Make America Healthy Again agenda of President Donald Trump 47 and of HHS Secretary Robert F. Kennedy, Jr.

It has also, sadly, been a year of health issues and of losses among the denizens of The Q Tree. Susan Sampson (DePat / Deplorable Patriot) and Georgia Swink Smith (GL/FL) have departed this world and are badly missed. There are those at The Q Tree who have lost family members, dear friends, and other loved ones, who are badly missed. May all of the deceased rest in eternal Peace under the Wings of the Almighty God. There are also those at The Q Tree who are still dealing with health issues. SteveInCO decided to leave the blog; our good Kalbokalbs has taken over the Saturday article spot. If Yours Truly has left anyone out, apologies: it is not intentional. The Q Tree soldiers on.

Links to The COVID-19 Information Files: Part One: https://www.theqtree.com/2024/11/01/health-friday-open-thread-11-1-2024-the-covid-19-vaccines-information-file-part-one/; Part Two: https://www.theqtree.com/2025/03/07/health-friday-3-7-2925-open-thread-the-covid-19-informaiton-file-part-two-the-virus-itself-and-the-vaccines/; Part Three: https://www.theqtree.com/health-friday-11-21-2025-open-thread-the-covid-19-information-file-part-three-compendium/.

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It appears that HHS Secretary Robert F. Kennedy, Jr., is taking steps to rein in the decades-long “strangle-hold” that Big Pharma has on that department. Two examples: One: cutting $500 million in development grants under BARDA for further research and development of mRNA-based “vaccines.” Please see: https://www.hhs.gov/press-room/hhs-winds-down-mrna-development-under-barda.html, 5 August 2025. BARDA is the Biomedical Advanced Research and Development Authority, a division of ASPR (Administration for Strategic Preparedness and Response, itself a division of the United States Public Health Service.) BARDA, ASPR, and the United States Public Health Service are all under the purview of the Department of Health and Human Services. And, Two: terminating millions of dollars in grants to the American Academy of Pediatrics, after that organization sued HHS over changes that HHS Sec. Kennedy and others made to the “recommended vaccination schedules” of the CDC. Please see: https://www.nbcnews.com/health/health-news/hhs-cuts-millions-grants-american-academy-pediatrics-rcna249769, “HHS cuts millions in grants to the American Academy of Pediatrics,” 17 December 2025.

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Some recent COVID-19 news:

First, a new paper by Dr. Peter A. McCullough, et al., proving that the modRNA COVID-19 “vaccines” do indeed induce cancer and other types of serious adverse medical conditions among the “vaccinated” [1], [2]. Please see the screenshot of the Abstract of this paper, below:

The above paper takes the place of the earlier one by McCullough, et al., on the same subject; an earlier paper which was published, then had thousands of views online, before it was abruptly Removed by the publisher. This earlier paper has vanished; only the Removal notice is available to see.

Second, a recently-published paper by Dasa He., et al., which demonstrates that chemotherapy can “awaken” dormant cancer cells [3]. Please see the Abstract and the Graphical Summary from this paper, below. Note: the entire article is available only via institutional access; or, via subscription access; or, via article purchase.

Third, this, from https://www.2ndsmartestguyintheworld.com/p/80-lawsuits-against-hospitals-to, “80 Lawsuits Against Hospitals To Administer IVERMECTIN To Sick COVID Patients”, 24 December 2025. Please see the screenshot from the article, below:

There is an embedded video interview with Dr. Bret Weinstein, PhD, on this situation. The information regarding the lawsuits is taken from the book by Dr. Pierre Kory, MD, The War on Ivermectin: The Medicine that Saved Millions and Could Have Ended the Pandemic (available on https://www.amazon.com/.)

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The “freight train-like approach” of the next “Plandemic”, this one of Avian Influenza (and, likely, an Avian Influenza that will be “cobbled together” from elements of multiple strains of this virus AND lab-tested to make sure that the strain that is created is deadly to birds, animals, and humans alike), is steadily gathering steam. Two of the most recent developments in this situation are below:

First: https://jonfleetwood.substack.com/p/bill-gates-cepi-revives-moderna-mrna, “Bill Gates’ CEPI Revives Moderna mRNA Bird Flu Vaccine Development With $54M Investment After HHS Terminated Funding”, 19 December 2025. HHS Secretary Kennedy, Jr., had terminated grants totaling over $700 Million dollars to Moderna in May of 2025 related to research and development of mRNA-1018, the company’s modRNA-based Avian Influenza “vaccine.”

Second: https://jonfleetwood.substack.com/p/usdas-bird-flu-test-matches-bird, “USDA’s Bird Flu Test Matches Bird and Cow DNA, Not Just Viral DNA: BLAST Data”, 20 December 2025. Mr. Fleetwood put the the USDA’s current Avian Influenza PCR test through the BLAST software (Basic Local Alignment Search Tool, provided by the United States government), and discovered that the test results data reveal exact matches for multiple DNA genome codes in both birds and cows. In other words, the USDA’s current Avian Influenza PCR test is not only NOT accurate — it can result in multiple “false positives” for Avian Influenza infection. Please see the screenshot from the article, below:

Yours Truly firmly believes that the groundwork for a “worldwide Avian Influenza pandemic” is in the final stage of development. This is something to “be on the lookout” about.

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Finally, Katherine Watt closed her Bailiwick News Substack this month. Ms. Watt did enormous and detailed research into the legal documents between the United States Army, the Department of Health and Human Services, and Pfizer-BioNTech and Moderna, related to the development of the COVID-19 virus itself, and the development of the modRNA COVID-19 “vaccines.” A selection of her research has been archived here: https://bailiwicknewsarchives.wordpress.com/. Yours Truly wishes her well.

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THE COVID-19 “VACCINES” — ALL OF THEM — MUST BE REMOVED FROM THE MARKET AND FROM USE IN THE UNITED STATES. NOW. PERIOD.

ALL GAIN-OF-FUNCTION RESEARCH, NO MATTER ON WHAT DRUG OR “VACCINE”, MUST STOP. NOW. PERIOD.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Notice and Disclaimer: With the exception of published papers and websites listed in today’s post, the ideas and conclusions in this post are by PAVACA. Proper credit must be given to PAVACA if ideas and conclusions from today’s post are used by other blog writers, by podcasters, on social media, or in print media.)

References:

[1]: “Synthetic messenger RNA vaccines and transcriptomic dysregulation: Evidence from new-onset adverse events and cancers post-vaccination.” Von Ranke NL, Zhang W, Anokhin P, Hulscher N, McKernan K, McCullough P, Catanzano J. World J Exp Med 2025; 15(4):11386. https://doi.org/10.5493/wjem.v15.i4.113869. 20 December 2025.

[2]: “BREAKING: Our CENSORED Study Showing mRNA Injections Induce Severe Genetic Disruption Linked to Cancer and Chronic Disease Is Now Peer-Reviewed and Published.” https://www.thefocalpoints.com/p/breaking-our-censored-study-showing. 19 December 2025.

[3]: “Chemotherapy awakens dormant cancer cells in lung by inducing neutrophil extracurricular traps.” Dasa He, et al. https://doi.org/10.1016/j.cell.2025.06.007. Cancer cell. 2025 Sep8; 43(9):1622-1636.e7. Epublished 3 July 2025.

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.

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

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for any AI-generated content. To the best of her knowledge and belief, there is one AI-generated image in The Focal Points article, cited below. If readers wish to add any AI-generated content to the discussion thread for today’s offering, they must cite their source. Thank you.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 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