Tag: FDA

Health Friday 11.7.2025 Open Thread: What’s Going on at Pfizer-BioNTech?: Part One

The free image of vintage Pfizer vaccine vials for the header in today’s offering is courtesy of Dreamstime and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to 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 in their body. May they rest in eternal Peace.

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 perhaps for AI-generated images within linked URLS. If readers wish to post AI-generated content to the discussion thread for today’s offering, they must cite their source. Thank you.

This Part One trail begins here, with two news reports regarding the September 2025 agreement reached between the United States government and Pfizer (PfizerUSA, the United States co-partner of Pfizer-BioNTech; BioNTech, the other co-partner, is headquartered in Mainz, Germany.). First, from Virginia Business (https://virginiabusiness.com/pfizer-agrees-to-lower-drug-costs-70b-us-investment/), “Pfizer agrees to lower drug costs, $70B US investment”, 30 September 2025. A screenshot from this article is below:

And, second, the announcement from PfizerUSA (https://www.pfizer.com/news/press-release/press-release-detail/pfizer-reaches-landmark-agreement-us-government-lower-drug, “Pfizer Reaches Landmark Agreement with U.S. Government to Lower Drug Costs for American Patients”, 30 September 2025. A screenshot from this article is below:

Note that the specific details of this agreement, which will affect millions of Americans, “remain confidential.”

The company called Pfizer-BioNTech is a formal co-partnership between Pfizer, also known as PfizerUSA (CEO, Dr. Albert Bourla, DVM); and, BIoNTech of Mainz, Germany (CEO, Dr. Ugur Sahin, MD.) Both PfizerUSA and BioNTech were involved / still are involved, in the development and manufacture of the modRNA COVID-19 “vaccine” line, COMIRNATY (this “vaccine” was previously known as BNT162b2, or “Pfizer-BioNTech COVID-19 Vaccine.“) Both PfizerUSA and BioNTech have agreements regarding their sharing royalty payments for COMIRNATY “vaccines” purchased and used throughout the world. PfizerUSA and BioNTech are also involved in the development and manufacture of other drugs and vaccines, either separately or in coordination with each other.

The most recent (as of 5 August 2025) PfizerUSA (and Pfizer-BioNTech) product “pipeline” website is here: https://www.pfizer.com/science/drug-product-pipeline. Click on “Downloadable PDF” to view the entire pipeline. Screenshots of two pipeline areas, Internal Medicine and Vaccines, follow. The first screenshot, Internal Medicine, with discussion by Yours Truly, is below:

**** WHY is Paxlovid, a combo drug of nirmatrelvir (an antiviral) + ritonavir (an HIV/AIDS treatment drug that targets the immune system) going to be used on CHILDREN who become infected with COVID-19?

**** Ibuzatrelvir (PF-07817883), now in Phase 3 clinical trials, is an oral / enhanced “nirmatrelvir on steroids” treatment for COVID-19 infection that was granted “Fast Track” approval by the FDA The intended use of this drug appears to be as a “replacement” for Paxlovid.. Please see: https://pubs.acs.org/doi/10.1021/jacsau.4c00508, 30 July 2024. Pfizer has already patented this drug. Let’s take a look at the Overview of this Phase 3 clinical trial, as described here: https://clinicaltrials.gov/study/NCT06679140:

Does “Fast Track” approval by the FDA mean that the “Study Completion (Estimated)” of 6 May 2027 will be “bypassed”, and only the data from the “Primary Completion (Estimated)” of 12 December 2026 will be used to push this drug onto the market faster? In addition, WHY is the study subject pool so small (2330 persons) for a drug that would potentially be used on hundreds of thousands of persons?

And, from the Researcher View of this clinical trial, part of the Secondary Outcomes descriptions:

Note that the “viral load” measurement will be performed via EITHER a nasal sample, OR via a nasopharyngeal sample. If a nasopharyngeal sample swab is used, this is the extremely long swab that reaches all the way to the VERY BACK of the nasal cavity and can touch the COVERING OF THE BRAIN. By the way, the correct administration of the nasopharyngeal swab is also to ROTATE the swab a couple of times after insertion.

In addition, in the information about NCT06679140, the “placebo tablet” that will be used is NOT described at all. Is the “placebo tablet” going to be Paxlovid? Is the “placebo tablet” going to be a completely drug-free “empty” tablet?

And now, the second screenshot from the “pipeline” PDF, Vaccines, is below. Yours Truly will discuss an interesting new “vaccine” from this list, under development by PfizerUSA (in conjunction with BioNTech) — PF-07926307, a combination modRNA-based COVID-19 plus influenza “vaccine“:

The available-to-the-public information regarding PF-07926307 is both confusing and concerning. Pfizer-BioNTech insists that this “combo vaccine” is only for “prophylactic” use against COVID-19 plus influenza: https://investors.biontech.de/news-releases/news-release-details/pfizer-and-biontech-provide-update-mrna-based-combination, “Pfizer and BioNTech Provide Update on mRNA-based Combination Vaccine Program Against Influenza and COVID-19 in Individuals 18-64 Years of Age”, 16 August 2024. Only ONE of of the two outcomes measurements of the Phase 3 clinical trial for this “vaccine” were met (NCT06178991.) A screenshot from the company’s press release is below:

Note that this press release emanates from Germany, not the United States;, and that the “combination candidate” is not identified as PF-07926307.

**** In addition, it appears that PF-07926307 is actually a combination of TWO separate Pfizer-BioNTech modRNA “vaccines” formulations: BNT162b2 and BNT 161: https://investors.biontech.de/news-releases/news-release-details/biontech-outlines-2024-strategic-priorities-42nd-annual-jp, “BioNTech Outlines 2024 Strategic Priorities at the 42nd Annual J.P. Morgan Healthcare Conference”, 9 January 2024. Please see the screenshot from this article, below:

**** Note the clinical trial mentioned in the above screenshot: NCT05596734. The modRNA “combo vaccine” used in this clinical trial is none other than BNT162b2 (tozinameran, now marketed as COMIRNATY, but which was the ORIGINAL Pfizer-BioBNTech modRNA COVID-19 “vaccine” against the ORIGINAL Wuhan Hu1 SARS-CoV-2 [COVID-19] virus), plus BNT161 (famtozinameran, the ORIGINAL modRNA COVID-19 “vaccine” against the OMICRON variant BA.4/BA.5) Please see: https://covid-vaccine.canada.ca/comirnaty-original-omicron-ba4ba5/product-details, which also states, “Cancelled by sponsor May 3rd, 2024.”

**** However, at the same time, it appears that this Pfizer-BioNTech modRNA COVID-19 “combo vaccine” of BNT162b2 plus BNT161 — also known as PF-07926307 — IS being used — in Singapore: https://labeling.pfizer.com/ShowLabeling.aspx?id=20959, “Date of last revision: July 2024.” Please see the screenshot from the package information for this product administered in Singapore, below:

And, screenshots from Page 65 (of 65), from the package information for the above injectable:

BNT161, one of the component modRNA “vaccines” in PF-07926307, is an influenza “vaccine”, meaning that it can be used against EITHER influenza OR COVID-19 (Omicron BA.4/BA.5.) The German partner of PfizerUSA — BioNTech — has been working on this injectable since at least 2022: https://biontechse.gcs-web.com/news-releases/press-release-details/biontech-announces-third-quarter-2022-financial-results-and, “BioNTech Announces Third Quarter 2022 Financial Results and Corporate Update”, 7 November 2022. A screenshot from this article is below:

Note that the press release is from BioNTech Sweden.

A screenshot from the Adisinsight Drug Profile for BNT161 is below. Note that this modRNA “vaccine” is a quadrivalent influenza injectable (https://adisinsight.springer.com/drugs/800052769):

**** On the other hand, here is the article on PF-07926307 (BNT162b2 + BNT161) by the tech / AI / data collection and analysis platform, Patsnap: https://synapse.patsnap.com/article/what-is-pf-07926307-used-for?, 28 June 2024. A screenshot of the entire article is below; Yours Truly includes the entire article because it has a wealth of information and clues as to the possible real “agenda” behind this injectable:

**** Note that, per the article above, the “primary indication” for the use of PF-07926307 is for the treatment of cancers caused by overactive kinases responses, such as are found in lymphomas; with what may be called a “secondary indication” for treatment of chronic inflammatory diseases. Lymphomas or chronic inflammatory diseases induced by, say, modRNA COVID-19 “vaccine” injections, such as BNT162b2 (COMIRNATY?) Is it remotely possible that PF-07926307 (BNT162b2 + BNT161) is being redesigned as a “backdoor oncology and/or chronic inflammatory diseases treatment” injectable? How does this square with what Pfizer-BioNTech claims that this “vaccine” is to be used for — against COVID-19 + influenza infection? What is the truth here?

**** In any case, WHY is Pfizer-BioNTech apparently using BNT162b2, the company’s original modRNA COVID-19 “vaccine”, as a foundational component in the development of a “New Molecular Entity” called PF-07926307, which is to used as a “prophylactic” against COVID-19 plus influenza? What happened regarding all those other modRNA COVID-19 “vaccines” made by this company, to be used against the LATEST MUTATIONS of the SARS-CoV-2 virus, such as the “2025-2026 version” of COMIRNATY? Why is Pfizer-BioNTech going all the way back to the ORIGINAL Wuhan Hu1 SARS-CoV-2 virus contained in BNT162b2 (COMIRNATY) to formulate PF-07926307?

What is going on at Pfizer-BioNTech? Does the United States government know about PF-07926307 (BNT162b2 + BNT161)? Did the “Specific terms of the agreement remain confidential” regarding the deal between the United States government and PfizerUSA reached in September 2025 include provisions that our government “looks the other way” about the activities of PfizerUSA’s co-partner, BioNTech? Does the HHS / FDA / CDC / BARDA have the complete details of the “Specific terms of the agreement remain confidential” provisions? Are the “specific details” being shared with only the “top brass” of the FDA / CDC / BARDA — and that HHS Sec. Kennedy, Jr., is being kept in the dark?

———————————————————————————

All current COVID-19 “vaccines” — ALL of them — MUST be pulled off the market and from use. Now.

All research and development of “new” COVID-19 “vaccines” that are in ANY form — injectable; oral; nasal; micro-needle — MUST be stopped. Now.

There MUST be complete analysis of the ingredients and mechanisms of the current COVID-19 “vaccines”, performed by impartial testing entities, and with complete results made public. Now.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Notice: With the exception of links to published media reports and links to published scientific papers, the ideas and conclusions of today’s post are by PAVACA. Proper credit must be given to PAVACA if other blog writers, or persons on podcasts, social media, or print media, use the ideas and/or conclusions of today’s post. Thank you.)

Health Friday 10.31.2025 Open Thread: Echoes

My older brother, Sam, circa 1960 – 1961, dressed to perform in a school band concert:

My older brother, Sam, December 2021:

My older brother, Sam, early summer 2024, after his having taken at least five injections of a COVID-19 “vaccine”, beginning in early 2021:

Requiescat in Pace aeterna, frater mi. Lux perpetua tibi luceat.

My older brother, Sam: 24 November 1948 – 29 October 2024.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. Today’s offering is dedicated 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. May they rest in eternal Peace.

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 perhaps for AI-generated images within URL links. If readers wish to add AI-generated content to today’s discussion thread, they must cite their source. Thank you.

————————————————————

My older brother, Sam, passed away on 29 October 2024. He was only 75 years old. He had taken at least five (possibly, six) injections of COVID-19 “vaccines”, starting in early 2021. His last “vaccine” injection was taken around Thanksgiving of 2023, although he may have been given yet another shot while he was residing in a nursing home in the early fall of 2024. Yours Truly has written for this board regarding the health decline of Sam after he took the COVID-19 “vaccine” shot in November 2023: please see https://www.theqtree.com/2024/10/18/health-friday-10-18-2024-special-edition-neurological-effects-of-the-covid-19-vaccines-physical-and-psychological/; and, https://www.theqtree.com/2025/07/25/health-friday-7-25-2025-open-thread-more-on-the-covid-19-vaccines-and-what-they-do-to-the-brain/. Within the period of fewer than six months after his taking that COVID-19 “vaccine” shot in November 2023, my brother had lost interest in things he had once enjoyed, such as helping out with his grandchildren; had stopped going to church; had a “freak accident” in which he wrecked his car and then decided not to drive again; had lost interest in taking care of himself and eating properly; and so on. Then, there was the catastrophic fall he sustained in his home in early July 2023; then, to two weeks in the ICU; then, to be being discharged to a nursing home; then, to the diagnosis of “sudden-onset dementia” at that facility; then, to his losing the ability to walk and becoming bed-bound; then, to his contracting pneumonia in late October 2023 at this facility; then, to his death.

My brother had co-morbidities that complicated his health profile: among them, COPD from decades of smoking (he quit in 2010 after that diagnosis and was treated); and, prostate cancer (diagnosed and treated in 2019.) He had lost his wife in the October 2018, just shy of their 47th wedding anniversary; she passed away from an undiagnosed aneurysm that ruptured. He had spent several years after her death taking counseling and medications, which assisted in his processing of this tragedy.

What ultimately happened with my brother was despite the fact that he had “good longevity genes” in his makeup — there were multiple older members on both sides of our birth family who had lived well beyond their 80th, and even their 90th, birthdays. What happened with my brother was also despite the fact that he had made it a point of taking better care of his health since the diagnosis of COPD in 2010. While it is not possible for Yours Truly to state this definitively, I will say I firmly believe that it was the ingredients and mechanisms of the COVID-19 “vaccines” that Sam took which, over time and incrementally, compromised his brain — cognitively and emotionally — with terrible consequences. I firmly believe that it was the COVID-19 “vaccine” injection that my brother took at Thanksgiving 2023 which was the “straw that broke the camel’s back” for him.

However, even before my brother passed away, Yours Truly’s cousin Bill died in September 2023, a “died suddenly and unexpectedly” situation. Cousin Bill had also had taken COVID-19 “vaccines”, starting in 2021. By early 2022, this previously-healthy, active man had been diagnosed with cardiac problems and was undergoing treatment. According to what I understand of the issue, he was “doing well” in treatment. I am also more than fairly certain that my cousin Bill continued to take COVID-19 “booster vaccine” injections, likely based on the recommendations of his doctors. And then, September 2023 happened. Cousin Bill’s death was the first close-family death of the COVID-19 era for Yours Truly. To say that his death was hard for me is an understatement. I have good memories of cousin Bill. His father had passed away in 1993; his mother had passed away in 2017. They did not have to deal with the death of their son.

To say that the passing away of my own brother was devastating to Yours Truly is an understatement of Malthusian proportions. His death has shaken me down to my core. The last time I spoke to him (by phone) was twelve days before his death. It was heartbreaking and gut-wrenching to hear him fighting the “sudden-onset dementia” that had closed in on his brain. To know that he would never leave the nursing home, go back to his house and his nice old dog, go and be with his adult children and his grandchildren. To hear him tell me to send him books on the Civil War or World War II so he could “brush up” on his reading (the truth was, that by this time, he couldn’t read more than one or two sentences from anything.) To know that what had happened to him was so senseless, so incredibly senseless. It was (and still is) heartbreaking to go through the “what-if?” scenarios in my head — What if he had listened to me when I tried to warn him about the dangers of the COVID-19 “vaccines”, and refused to take any more of those injections? What if he had taken Ivermectin to try and clear out at least some of the COVID-19 “vaccine”-induced damage to his body and mind? What if the ingredients and mechanisms of the COVID-19 “vaccines” Sam took aggravated the lung damage from his COPD? What if the ingredients and mechanisms of the COVID-19 “vaccines” he took aggravated or re-established any emotional / psychological issues still lingering after the death of his beloved wife? What if? What if? Our mother had passed away in 1992; our father, in 2006. They did not have to deal with the death of Sam.

Yours Truly is not writing the above in order to solicit sympathy. I am writing the above to illustrate the kinds of things that went on — that are going on now — and, that will go on — in millions of families when the damage induced by the COVID-19 “vaccines” that were taken by family members starts to present (and the damaging effects that have started to present already.) It is all well and good to have a general “working knowledge” of the negative effects these “vaccines” (Bioweapon Toxin Injections) can, and do, induce in those who take them. It is quite another thing to lose close family members due to the negative effects of these “vaccines” that they took. It is quite another thing to have to deal with the knowledge that loved ones in the “here and now” who are COVID-19 “vaccinated” have had their bodies and brains damaged from these “vaccines.” It is quite another thing to listen to them tell those who try to warn them that they aren’t interested — that they “follow the science”; that they “trust their doctor”; among other responses.

Yours Truly will therefore say to those reading today’s offering who have taken COVID-19 “vaccines”:

**** The COVID-19 “vaccines” in your body have already damaged your natural immune system, perhaps even destroyed it: https://jessicar.substack.com/p/the-bnt162b2-mrna-vaccine-against, “‘The BNT162b2 mRNA vaccine against SARS-CoV-2 reprograms both adaptive and innate immune responses”, 16 December 2021. Please see the screenshot from her article, below, the Figure 3 from the cited paper in the article:

Figure 3 shows how the modRNA COVID-19 “vaccines” systematically damage and destroy the natural immune system cells of the “vaccinated” person’s body.

**** The COVID-19 “vaccines” in your body are damaging your heart and lungs: https://doctors4covidethics.org/wp-content/uploads/2022/08/causality-article.pdf, “Vascular and organ damage induced by mRNA vaccines: irrefutable proof of causality”, Michael Palmer, MD, and Sucharit Bhakdi, MD, 18 August 2022. Please see the screenshots of Slide 7 and its description from the above paper, which clearly shows myocarditis induced by modRNA COVID-19 “vaccines”:

Please see the screenshot of Slide 12 from the above paper, which clearly shows lung damage induced by modRNA COVID-19 “vaccines”:

Note: the slides in the above paper are from autopsies of persons who passed away after COVID-19 “vaccination.”

**** The COVID-19 “vaccines” in your body crossed the Blood-Brain Barrier and damaged the cells and functions of your brain: https://eurmedres.biomedcentral.com/articles/10.1186/s40001-023-00992-0, “A review of neurological side effects of COVID-19 vaccination”, Roya Hosseini and Nayere Askari, 25 February 2023. Please see the screenshot of Figure 1 from this paper, below:

**** The COVID-19 “vaccines” in your body can induce psychosis: https://nature.com/articles/s41380-024-02627-0, “Psychiatric adverse events following COVID-19 vaccination: A population-based cohort study in Seoul, South Korea”, Eun Mi Chun, et al., 4 June 2024. Please see the screenshot of Figure 2 from this paper, below:

It is a mistake to dismiss the above paper and its conclusions “because it’s from South Korea.” The modRNA COVID-19 “vaccines” used in South Korea that are examined for the above paper are the same as those used in the United States (COMIRNATY, by Pfizer-BioNTech; and, SPIKEVAX, by Moderna.)

**** The COVID-19 “vaccines” in your body will alter your DNA and change your body’s genomic codes. These effects are permanent, and are involved in cancers that present after COVID-19 “vaccination”: https://www.thefocalpoints.com/p/breaking-first-peer-reviewed-study-715, “BREAKING: First Peer-Reviewed Study Finds Direct Molecular Evidence of mRNA “Vaccine” Genomic Integration”, Nicolas Hulscher, MPH, 14 October 2025. Please see the screenshot from this article, below (the image was AI-generated):

**** The COVID-19 “vaccines” in your body, if you are a female, have destroyed up to 60% of the lifetime supply of eggs in your ovaries: https://www.thefocalpoints.com/p/mrna-shots-are-crippling-humanitys, “mRNA Shots Are Crippling Humanity’s Ability to Reproduce—And No Government is Ending COVID-19 Vaccination”, Nicolas Hulscher, MPH, 15 May 2025. Please see the screenshot from this article, below (Yours Truly believes that the graphic image of how COVID-19 “vaccines” destroy primordial follicles is AI-generated):

**** Every injection of a COVID-19 “vaccine” WILL SHORTEN THE LIFE OF THE “VACCINE” RECIPIENT: Please see: https://slaynews.com/news/major-study-confirms-covid-vaccine-dose-shortens-lives-recipients/, “Major Study Confirms Every Covid ‘Vaccine’ Dose ‘Shortens the Lives of Recipients'”, by Frank Bergman, 14 October 2025. The published paper is here: https://ijvtpr.com/index.php/IJVTPR/article/view/123/423, “Were the COVID-19 Shots Good, Bad, or Just Ugly? Dispensing with the Only Reasonable Objection to the Empirical Fact that Each Dose of the COVID-19 Shots, on the Average, Shortened the Lives of the Recipients”, John W. Oller, Jr., PhD, and Daniel Santiago, PharmD, 7 October 2025. Screenshots from this paper are below; first, of the Figure 2 from the paper, the all-age mortality figures reported to Public Health England:

Followed by Table 3 from the paper, the Connecticut Medicare Records:

Next, of Figure 5 from the paper, also derived from the Connecticut Medicare Records:

Then, from the Conclusions section of the paper:

These are the COVID-19 “vaccines” that you allowed to be injected into your body.

These are the COVID-19 “vaccines” that you allowed to be injected into the bodies of your children.

And why did you allow these unproven-technology, not-completely tested, “vaccines” to be put into your body, and into the bodies of your children? Because you “trusted the science“; because you “trusted your doctor“; because you were told that “it was the right thing to do“; because you were told that the COVID-19 “vaccines” were “safe and effective“; because you were told that the “the known and potential benefits of the COVID-19 vaccines outweigh the known and potential risks”; because you were told to “get COVID-19 vaccinated in order to keep yourself, your children, and your parents, safe“; because were you told “get COVID-19 vaccinated in order to keep your job, in order to travel, in order to go to school.” You were lied to. Every step of the way. Lied to by the government — by the CDC and the FDA — by your doctors — by your employer — by your school. They are continuing to lie to you.

The above is courtesy of https://www.theburningplatform,com/2025/10/27/why-are-these-criminals-free/. The Five Times August tweet is here: https://x.com/FiveTimesAugust/status/1982469251098153444.

Yours Truly has questions for those reading today’s offering who are COVID-19 “vaccinated”:

**** What are you going to do to try and mitigate the damage that these injections have done to your body and brain? To the bodies and brains of your children?

**** What are you going to do to educate yourself regarding how dangerous and deadly these injections are?

**** Do you plan to challenge and question any “recommendation” or “mandate” to have yourself and/or your children injected with more COVID-19 “vaccine” shots?

**** Do you plan to at least think about refusing to take any more COVID-19 “vaccines”, and to think about refusing COVID-19 “vaccines” being injected into your children?

Interested persons may wish to investigate these websites:

The Wellness Company (Dr. Peter A. McCullough, MD): https://www.twc.health

Leading Edge Clinic (Dr. Pierre Kory, MD): https://drpierrekory.com/

Independent Medical Alliance (Dr. Joseph Varon, MD): https://imahealth.org/

For those medical professionals who are COVID-19 “vaccinated”, Yours Truly has extra questions, below. These are based on my 5 1/2+ years of being an independent COVID-19 researcher and writer:

**** With all due respect: Have you recognized that the modRNA COVID-19 “vaccines” induce multiple types of serious adverse events, medical conditions, and can also kill? Have you read this report?: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, 5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021, FDA time-stamped on 30 April 2021 09:26 (GMT).

**** With all due respect: Do you understand, that since you are COVID-19 “vaccinated”, there is a strong likelihood that you have also had negative effects induced from these “vaccines”?

**** With all due respect: Why are you still recommending and/or administering these “vaccines”, given the above evidence of damage and death induced by these injectables? Did you perform your own research into the COVID-19 “vaccines” to satisfy yourself that the CDC / FDA claims of “safe and effective” regarding these injectables were / are, true? And, with all due respect, before there are objections to what Yours Truly is writing, please see these websites, by medical doctors, who have actually investigated the COVID-19 “vaccines” and know how dangerous and deadly they are : https://www.thefocalpoints.com/ (Dr. Peter A. McCullough, MD, MPH); https://pierrekorymedicalmusings.com/ (Dr. Pierre Kory, MD, MPA, Certified Tribal Practitioner); https://doctors4covidethics.org/ (Dr. Michael Palmer, MD, Dr. Sucharit Bhakdi, MD); https://imahealth.org/ (Dr. Joseph Varon, MD, FCCM, FCCP).

**** With all due respect: Why are you not demanding that your employer; your State Medical Licensing Board; your medical professional organization; your Medical Specialty Credentialing organization; the CDC, FDA, AMA — impartially investigate the mounting evidence that the modRNA COVID-19 “vaccines” are dangerous and deadly? Do you, perhaps, have concerns about “retribution” from these entities by doing so?

————————————————–

Yours Truly will remember the echoes of my older brother, Sam, before he started taking COVID-19 “vaccines.” I will remember the echoes of my Cousin Bill before he “died suddenly and unexpectedly.” The pain and the sense of loss from their deaths will never completely go away, since the human mind stores everything in the subconscious and the memory. One can only integrate the pain and the sense of loss into their own being in the healthiest way possible while moving onward.

And, in memory of those who have passed away from the negative effects of the COVID-19 “vaccines” that they took, “The Lark Ascending”, by Ralph Vaughan Williams: https://www.youtube.com/watch?v=ZR2JIDnT218&list=RDZRJIDnT218&start_radio=1

The COVID-19 “vaccines” — ALL OF THEM — MUST be removed from the market and from use. NOW.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Disclaimer: With the exception of URL links to scientific papers and online articles listed above, the ideas and conclusions of today’s offering are by PAVACA. Proper credit must be given to PAVACA if other blog writers, social media, podcasters, or print media, use or refer to the ideas and conclusions of today’s offering.)

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 10.10.2025 Open Thread: A Letter to Dr. Martin Makary, FDA Commissioner

The free vintage header image of writing a letter for today’s offering is courtesy of Shutterstock and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for AI-generated content. To the best of her knowledge and belief, there is none. If readers wish to post AI-generated content in today’s discussion thread, they must cite their source. Thank you.

Today’s offering is dedicated to all persons, of whatever age or location, who have suffered negative consequences from an infection of the COVID-19 virus itself after recovering from the infection; to all persons, of whatever age or location, who have COVID-19 “vaccine”-induced injuries, illnesses, and/or disabilities; and, to all persons, of whatever age or location, who have passed away from either an infection of the COVID-19 virus itself, or from the negative effects of the COVID-19 “vaccines” they had in their body.

“Dr. Martin Makary, MD, MPH, Commissioner, United States Food and Drug Administration (FDA)

10903 New Hampshire Ave., Silver Spring, MD, 20993

Dear Dr. Martin Makary:

Greetings. This letter is in reference to certain questions that the writer poses regarding the FDA, under your leadership, still promoting the use of the COVID-19 “vaccines” (actually, mRNA gene therapies) in the United States. This includes the modRNA COVID-19 “vaccine” COMIRNATY, by Pfizer-BioNTech; the modRNA COVID-19 “vaccines” SPIKEVAX and NEXSPIKE, by Moderna; and, the “inactivated virus” COVID-19 “vaccine” NUVAXOVID, by Novavax. Thank you in advance for your attention. The questions follow:

Question One: Have you read through the report on BNT162b2 that Pfizer-BioNTech submitted to the FDA on 21 January 2021, regarding the Pharmacokinetics tests results for this modRNA COVID-19 “vaccine” (which was subsequently approved by the FDA in 2022 under the name COMIRNATY)?

Would you please answer, in detail, your reasoning behind the continued FDA approval of COMIRNATY based on the results of this report? The report is found here: https://phmpt.org/wp-content/uploads/2022/03/125742_S1_M2_26_phramkin-tabulated-summary.pdf, “BNT162b2 2.6.5 Pharmacokinetics Tabulated Summary”, time-stamped by the FDA on 21 January 2021 at 23:22 (GMT), and starting with FDA CBER document identification number FDA-CBER-2021-5683-0013907. For your convenience, images of Page 7 and Page 8 of this report are below; first, Page 7:

And, Page 8:

The writer of this letter assumes that you understand that the BNT162b2 formulation used in the Wistar lab rats experiments above is the same formulation that the FDA granted the initial EUA to for use in the United States on 11 December 2020.

Question Two: Have you read through the Post-marketing Experience report on BNT162b2 that Pfizer-BioNTech submitted to the FDA on 30 April 2021? In particular, have you read through the APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST section of this report, which begins on Page 30? The report is found here: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, “BNT162b2 5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports”, time-stamped by the FDA on 30 April 2021 at 09:26 (GMT), starting with FDA CBER document identification number FDA-CBER-2021-0000054. The APPENDIX 1. section covers only those serious adverse events reports to Pfizer-BioNTech that were submitted between 11 December 2020 (the date that the FDA granted the initial EUA for BNT162b2 to be used in the United States), and 28 February 2021 — a period of fewer than 12 weeks. There are over 1,200 different listings of serious adverse events reports in the APPENDIX 1. section of the document.

Would you please answer, in detail, your reasoning behind the continuing FDA approval of COMIRNATY, given this document? Would you please answer, in detail, your reasoning why the FDA would simply accept this document without demanding an investigation of why there are so many different serious adverse events reports for BNT162b2? For you convenience, an image of Page one of the APPENDIX 1. section (Page 30 of the report document) is below:

The APPENDIX 1. section of the report runs from Page 30 to Page 38.

Question Three: Have you read the paper, published in the journal Frontiers in Cellular and Infection Microbiology on 15 September 2021, in which the authors prove that both the modRNA COVID-19 “vaccines” of Pfizer-BioNTech and of Moderna, and the viral vector COVID-19 “vaccines” (for example, of Janssen), cross the placenta of a COVID-19 “vaccinated” pregnant woman and enter into the body and brain of the fetus she is carrying? And, that, similarly, these “vaccines” also cross into the breast milk of the nursing mother who was “vaccinated”, therefore also entering into her nursling’s body and brain? The paper is found here: https://doi.org/10.3389/fcimb.2021.735394, “COVID-19 Vaccination in Pregnancy and Lactation: Current Research and Gaps in Understanding”, Lydia L. Shook, Parisa N. Fallah, Jason N. Silberman, Andrea G. Edlow, 15 September 2021. For your convenience, a screenshot of Figure 1 from the paper is below:

Which means, according to the graphic above from the paper, that the fetus and the nursling will get COVID-19 “vaccinated” along with the mother, due to the ingredients and mechanisms that cross into the placenta and/or the breast milk from the “vaccinated” mother. The natural immune systems of a fetus or of a nursling child are not mature enough, or strong enough, to handle the antibody-manufacturing demands of the COVID-19 “vaccines” that involuntarily enter their body and brain via the “vaccinated” mother.

Would you please describe, in detail, your reasoning for the FDA continuing to recommend COVID-19 “vaccination” of pregnant women, and/or breastfeeding mothers, based on the Frontiers In paper report?

Question Four: Are you aware that the modRNA COVID-19 “vaccines” by Pfizer-BioNTech and by Moderna, contain N1-Methylpseudouridine, a lab-created compound, that replaces the natural RNA in the Uridine of the “vaccinated” person’s body with this compound? Are you aware that N1-Methylpseudouridine was specifically created and included in the modRNA COVID-19 “vaccines” because this lab-created compound facilitates the entry of the ingredients of these “vaccine” into every cell of the “vaccinated” person’s body? Are you aware that, by replacing the RNA of the natural Uridine in the “vaccinated” person’s body, the multiple beneficial functions of Uridine RNA are damaged or lost? Are you aware that, among the multiple beneficial functions of Uridine RNA include cognitive elements (learning, memory), and emotional/psychological elements (mood regulation?) Are you aware that N1-Methylpseudouridine is present in all COVID-19 “vaccines” by Pfizer-BioNTech? For your convenience, please see: https://www.theqtree.com/2024/11/08/health-friday-11-8-2024-open-thread-the-insidious-n1-methylpseudouridine-in-the-covid-19-vaccines/; and, https://www.theqtree.com/2025/03/21/health-friday-3-21-2025-open-thread-more-on-the-n1-methylpseudouridine-in-the-modrna-covid-19-vaccines/. The Patent Declaration by Pfizer-BioNTech for BNT162b2, which describes the inclusion of N1-Methylpseudouridine in this “vaccine”, and what it does, is found here: https://patents.google.com/patent/WO2021213945A1/en. For reference, the following screenshot is from this Patent Declaration:

Would you please explain, in detail, your reasoning behind why the FDA should continue to approve for use in the United States, an injectable (the Pfizer-BioNTech modRNA COVID-19 “vaccine”) that specifically includes a lab-created compound (N1-Methylpseudouridine) which replaces natural Uridine RNA — and that this replacement is performed without the advance knowledge and consent of the person receiving this “vaccine?”

Question Five: The writer of this letter assumes that you, Dr. Makary, are aware that the modRNA COVID-19 “vaccines” induce cardiovascular issues and conditions, such as, myocarditis and pericarditis. This would mean induction of these conditions by the Pfizer-BioNTech modRNA COVID-19 “vaccine” (COMIRMATY); or, by the Moderna modRNA COVID-19 “vaccine” (SPIKEVAX.) The writer of this letter will focus on the Moderna product. The Package Insert for the Moderna modRNA COVID-19 “vaccine”, SPIKEVAX, is found here: https://www.fda.gov/media/155675/download. For your convenience, screenshots of the the following portions of this document are below; first, the Warnings and Precautions section:

The writer of this letter notes that the Warnings and Precautions are not enclosed in a “Black Box Warning.” Why is this the case?

Then, from section 5.2 Myocarditis and Pericarditis:

And, from section 6.2 Postmarketing Experience:

There actually is information available regarding the potential for long-term sequelae of myocarditis or pericarditis after taking COVID-19 “vaccines.” It is here: https://doi.org/10.61577/ijcri.2025.100001, “Myocarditis after SARS-CoV-2 Infection and COVID-19 Vaccination: Epidemiology, outcomes, and new perspectives”, M. Nathaniel Mead, Jessica Rose, William Makis, Kirk Milhoan, Nicolas Hulscher, and Peter A. McCullough, 20 March 2025. For your convenience, a screenshot of the Abstract of this paper is below:

And, Figure 6 from the paper, VAERS reports of myocarditis after COVID-19 “vaccination”:

Would you please describe, in detail, your reasoning why the FDA needs to continue to promote the use of the modRNA COVID-19 “vaccines” in the United States, for any age group, based on the paper above?

Finally, Question Six: Would you please describe, in detail, what medical school and/or Residency classes you took in which you learned that it was acceptable for patients to be given injections of an mRNA gene therapy treatment platform (in this case, the modRNA COVID-19 “vaccines”) without that injectable first having gone through a rigorous testing and analysis protocol beforehand?

Sincerely,

An independent COVID-19 researcher for the past five and a half years.”

The COVID-19 “vaccines” — ALL of them — must be removed from the market and from use. Now.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 9.5.2025 Open Thread: Human LINE-1, Chromosomes, and the modRNA COVID-19 “Vaccines”: Part One

The header image for today’s offering is courtesy of https://genesdev.cshlp.org/content/37/21-24/948.full, “LINE-1 retrotransposition and its regulation in cancers: implications for therapeutic opportunities”, Carlos Mendez-Dorantes, and Kathleen H. Burns, 13 December 2023.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks of the disaster of COVID-19 (the COVID-19 virus itself, and the COVID-19 “vaccines”), Yours Truly dedicates it to all persons, of whatever age or location: who have contracted a COVID-19 infection and recovered from it, but who also have residual complications from the infection; who have suffered COVID-19 “vaccine”-induced injury, illness, disability, or “Long COVID”; or, who have passed away, either from complications from an infection of the COVID-19 virus itself, or from COVID-19 “vaccine”-induced issues caused by these “vaccines” they had in 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 none, except for perhaps some AI-generated images embedded in links cited in today’s offering. If readers wish to include any AI-generated content in today’s discussion thread, they must cite their source. Thank you.

Today’s offering is Part One of two. It is not a lesson on human anatomy or on human genetics: it is a presentation of some of the most-recent information regarding the dangers and deadliness of the COVID-19 “vaccines” (Bioweapon Toxin Injections.) Yours Truly will emphasize at the start that more and more information that exposes these dangers and deadliness is coming out by the week — the “information trickle” of previous years regarding this situation is becoming a torrent. There is also information that potentially links some of the deleterious effects of the COVID- 19 “vaccines” back to the original Wuhan Hu1 SARS-CoV-2 (COVID-19) virus itself. Please bear with me: what may look like “diffuse parts” are all important pieces of the whole.

There is some “background information” that is necessary to “lay the groundwork” for the rest of today’s offering. Yours Truly begins here, with a paper by Ralph Baric, PhD, of the University of North Carolina, Chapel Hill, from 2006. The paper is found here: https://www.jcvi.org/sites/default/assets/projects/synthetic-genomics-options-for-governance/Baric-Synthetic-Viral-Genomics.pdf, “Synthetic Viral Genomics: Risks and Benefits for Science and Society”, Ralph S. Baric, PhD. In Yours Truly’s opinion, this paper can be viewed as a “blueprint” for the future Gain-of-Function (GoF) lab-experimentation with, and the lab-creation of, viruses such as the Wuhan Hu1 SARS-CoV-2 (COVID-19) virus; and the more-recent GoF experiments with strains of the H5N1 (Avian Influenza) virus. Please see the screenshots from Dr. Baric’s 2006 paper, below:

YT: Note the mentions, right at the start in the paper, about “biological warfare” and “biodefense.”

YT: The above images are from the Baric 2206 paper. Figure 4b appears to “outline” how to lab-create (Gain-of-Function work) of “synthetic coronavirus” genome codes.

Yours Truly will specially point out the passage above, “…data will provide detailed predictions regarding easy approaches to humanize zoonotic strains by retargeting the attachment proteins to recognize human, not the animal receptors (43-45).” This, in my opinion, is a direct “tie-in” to the gene code pieces from the Pangolin MP789 coronavirus that were used in the lab-creation of the original Wuhan Hu1 SARS-CoV-2 virus (COVID-19 virus) itself — the same virus that is the foundation of all the modRNA COVID-19 “vaccines”, including the “booster shots” and the “latest formula vaccines.” The MP789 coronavirus gene code has multiple “areas” that the human body can be receptive to — including the PRRAR / PRRARSV “backdoor key” to nucleus of every cell. Please see the following for more information about MP789 and its connection to the PRRARSV “backdoor key” that both the modRNA COVID-19 “vaccines” by Pfizer-BioNTech and by Moderna contain: https://www.theqtree.com/2023/05/01/pfizer-and-moderna-vaccines-both-contain-the-prrarsv-key-to-the-cell-nucleus/; https://www.theqtree.com/2024/11/22/health-friday-11-22-2024-open-thread-lets-talk-about-prrarsv-the-backdoor-key/; and, https://www.theqtree.com/2024/11/27/placeholder-open-thread-11-27-2024-prrarsv-part-2-pangolin-edition/.

There is also something else of interest to point out regarding one of the References in the 2006 Baric paper: Reference 45. The referenced paper is found here: https://www.embopress.org/doi/full/10.1038/sj.emboj.7600640, “Receptor and viral determinants of SARS- coronavirus adaptation to human ACE2.”, Li, W., et al., 24 March 2005. This paper discusses the GoF experiments performed to determine and then lab-create elements of various rat and palm civet coronaviruses to the ACE2 receptor cells of humans. Recall that rat and civet coronaviruses experiments were performed at the Wuhan Institute of Virology in the process of lab-creating the SARS-CoV-2 (COVID-19) virus itself. Please see the screenshots from the paper, below. The first is from the authors’ “summary” a the top of the paper; the second is the end of the Discussion section of the paper:

Ralph Baric, PhD, was also working on the “cross-species adaptation and transmission” aspects of SARS- coronaviruses. For example, this paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC2838128/, “Recombination, Reservoirs, and the Modular Spike: Mechanisms of Coronavirus Cross-Species Transmission”, Rachel L Graham, Ralph S Baric, 11 November 2009. The paper specifically discusses Spike 1 residues and ACE2 receptor cells in coronaviruses found in Himalayan palm civets; bats; and raccoon dogs — and the possibility that these coronaviruses can “leap” to humans.

And now, with the above as part of the context, Yours Truly presents LINE-1. First, via Wikipedia (https://en.wikipedia.org/wiki/LINE1):

And, Second, from ActiveMotif (https://www.activemotif.com/blog-line-1, “LINE-1 Elements: Walk the LINE-1”, Michelle Tetrault Carlson, PhD, 13 September 2022):

LINE-1 cells are found throughout the human body. LINE-1 aberrations are involved in the following conditions: Genetic disease; cancers (lung; ovarian; bladder; colon; breast; brain [glioma]; and, liver.) LINE-1 aberrations / changes are also involved in aging and “aging related diseases” (per the article above, in the “LINE-1 and Aging” section.)

LINE-1 (also called L1) cells have been studied for some time; in particular, the association between L1 “retrotransposition” and disease. This is important in the context of what will be discussed next.

L1 cells can be “retrotransposed.” This will create “genetic instability.” Such retrotransposition can occur as an aberration resulting from genetic predisposition in the body. Please see: https://doi.org/10.1016/S0092-8674(02)00839-5, “Human L1 Retrotransposition Is Associated with Genetic Instability”, David E. Symer, et al., 9 August 2002. The Abstract from this paper is below:

This paper also discusses the role of SV40 in L1 retrotransposition. In addition, there is a section entitled, “L1 Is an Engine for Genetic Change.”

“Transposed” L1 cells can be involved in the establishment of cancers: https://doi.org/10.1101/gad.351051.123, “LINE-1 retrotransposition and its deregulation in cancers: implications for therapeutic opportunities”, Carlos Mendez-Dorantes, Kathleen H. Burns, 13 December 2023. Please see the screenshot from this paper (a graphical “process image” of L1 being “retrotransposed”), below:

The alarm bells have been ringing regarding the dangers of LINE-1 (L1) retrotranposition (“reverse transcription”) effect of the modCOVID-19 “vaccines” for some time. Examples: the “Maurol, et al.” paper of March 2022: https://www.hilarispublisher.com/articles/intracellular-reverse-transcription-of-covid19-mrna-vaccine-eminvitroem-in-human-cell-87770.html, “Intracellular Reverse Transcription of COVID-19 mRNA Vaccine In-Vitro in Human Cell.”, Maurol, Luisette Mauro, Naseer Almukthar, Tarro Giulio, and Gamal abdul Hamid, et al., J Genet DNA Res6(2022):116. Please see the screenshot from this article, below:

YT: Note the mention of a timeframe of 5-10 years that is needed to study the effects of the “transcription activity.” Keep this in mind when reading the end of today’s offering.

Then, there is the “Alden, et al.” paper from April 2022: https://www.mdpi.com/1467-3045/44/3/73, “Intracellular Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line”, Markus Alden, Yang De Marinis, et al., 11 April 2022. Please see the screenshots from this paper, below. The first is from the paper itself; the second, an image of the Pfizer-BioNTech BNT162b2 reverse transcription of DNA, is Slide 14 from the Doctors for COVID Ethics article (https://doctors4covidethics.org/wp-content/uploads/2022/08/causality-article.pdf, “Vascular and organ damage induced by mRNA vaccines: irrefutable proof of causality”, Michael Palmer, MD, and Sucharit Bhakdi, MD, August 2022):

And, the “Acevedo-Whitehouse and Bruno” paper from February 2023: https://doi.org/10.1016/j.mehy.2023.111015, “Potential health risks of mRNA-based vaccine therapy: A hypothesis”, K. Acevedo-Whitehouse, R. Bruno, 6 February 2023. Please see the screenshots from this paper, below; the first is part of the Abstract; the second is the end of the Consequences and discussion section:

Which all lead to this, from Dr. Peter McCullough in May 2025: https://www.americaoutloud.news/genetic-bombshell-covid-19-vaccines-change-the-human-genome/, 24 May 2025. Please see the screenshots from this article, below. First, this one:

This harks back to the information that there are natural reasons for DNA alteration in a person’s body (for example, inherited genetic aberrations.) **** However, the issue here is the fact that the modRNA COVID-19 “vaccines” by Pfizer-BioNTech and by Moderna contain ingredients and mechanisms that deliberately and permanently alter the DNA of the human LINE-1 cell lines of any person who takes these “vaccines” — even one injection of them. This includes DNA alteration in the body of a fetus of an expectant mother who takes modCOVID-19 “vaccines”, due to the fact that these “vaccines” cross the placenta and into the body of the fetus. (And, by the way, those same ingredients and mechanisms are present in all “descendant clone” modRNA COVID-19 “vaccines” made by these companies, including the “booster shots” and the “latest version formula” injectables. This is because these are based on, and contain elements of, the original modRNA COVID-19 “vaccines” by these companies.)

Then, the second screenshot, below:

YT: **** Please read this phrase again, from Dr. McCullough, regarding the modRNA COVID-19 “vaccines” by Pfizer-BioNTech and by Moderna: “…sadly, both Pfizer and Moderna do permanently alter DNA via reverse transcription.” It is the “permanently alter DNA via reverse transcription” effects from these injectables that the COVID-19 “vaccinated” in the United States and all over the world are starting to present. It is impossible that the FDA did not know about the potential DNA-altering effects of the modRNA COVID-19 “vaccines” — especially after scientific papers were published which demonstrated that this indeed is the case.

Another piece of the situation has just been published: According to the CDC, 76.4% of all American adults have at least one chronic disease (2023 figures), compared to baseline 2013 figures. The CDC paper is here: https://cdc.gov/pcd/issues/2025/04_0539.htm#ContribAff, “Trends in Multiple Chronic Conditions Among US Adults, By Life Stage, Behavioral Risk Factor Surveillance System, 2013 – 2023”, Kathleen B. Watson, MD, et al., 17 April 2025. All of the authors of this paper are either employees of the CDC; or, of the United States Uniformed Health Services. While it is true that chronic diseases, such as arthritis, can develop for many reasons during adult years, there is NOT ONE WORD in this paper regarding COVID-19 “vaccination” in this age group (18 years – 65+ years) being involved in the increase of any of the chronic diseases that are listed. In other words — the CDC still has its “head firmly in the sand” regarding the dangers and deadliness of the modRNA COVID-19 “vaccines”, and the role of these “vaccines” in inducing and/or aggravating multiple types of chronic conditions.

**** What are “COVID-19 “vaccinated” Joe or Jane Average American” going to do when they find out and understand (which they will, eventually) that the most fundamental “building block” of their body — their DNA — was deliberately and permanently altered without their knowledge or consent, if they took any injection of a Pfizer-BioNTech or a Moderna modRNA COVID-19 “vaccine”? That it doesn’t matter when the “vaccine” injection was put into their body, or how many injections? That their modRNA COVID-19 “vaccinated” children ALSO had their DNA deliberately and permanently altered without their parents’ or guardian’s knowledge or consent? That the state and local governments who “mandated” or legislated that the modRNA COVID-19 “vaccines” be taken by their children in order for them to attend school were complicit in the DNA alteration in their children?

**** What will “COVID-19 “vaccinated” Joe or Jane Average American” do when they find out and understand (which they will, eventually) that the altered DNA in their “vaccinated” body will “lurk” in the body and brain, creating permanent dysfunction of multiple organs of said body, until a modRNA COVID-19 “vaccine”-induced injury, illness, or disability presents later on? That is very likely no “cure” or “turning the clock back” for this altered DNA in the “vaccinated” body?

**** What will “COVID-19 “vaccinated” Joe or Jane Average American” do when they find out and understand (which they will, eventually) that the medical professionals they trusted when they took the modRNA COVID-19 “vaccines” have betrayed them at the most basic level —“Do No Harm”— by not doing the investigation which would have alerted them to this danger — but, which medical professionals, instead, followed the CDC / FDA / AMA mantras of, “The COVID-19 vaccines are safe and effective”, and “The known and potential benefits of the COVID-19 vaccines outweigh the known and potential risks”?

The people who included the elements and mechanisms in the Pfizer-BioNTech and Moderna modRNA COVID-19 “vaccines” that guarantee the deliberate and permanent reverse-transcription of the LINE-1 DNA of every COVID-19 “vaccinated” person; the people who knew about these reverse-transcription elements and mechanisms, but still allowed EUAs and “FDA full approval” of these “vaccines” to proceed; the people who intentionally withheld vital information regarding the real dangers and deadliness of the modRNA COVID-19 “vaccines” from President Trump45 during “Operation Warp Speed”; the people who, even today, are still “recommending” COVID-19 “vaccination” for anyone of any age (paging Dr. Martin Makary, current FDA Commissioner) — all must answer for their actions. All modRNA COVID-19 “vaccines” must be removed from use and pulled off the market — now.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA


Health Friday 8.29.2025 Open Thread: Gain-of-Function Research Is Still Going On

The featured vintage image of a laboratory for today’s offering is courtesy of iStock and Google Images.

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

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

Today’s offering is about the “under-the-table” work, the “being performed but under another name” work, the “grandfathered-in” work, of Gain-of-Function (GoF) experiments that are onoing. These GoF experiments involve experiments with mRNA-based platforms; with “inactivated virus” platforms; and, with “novel delivery” platforms. These GoF experiments are being funded by “private Big Money”; and, by the United States government (in other words, with taxpayer money.) This post is long; please bear with me.

It is now well-known that the COVID-19 disaster was a product of GoF experiments, of two types: One, the GoF work that was performed in various labs (the Baric Lab at UNC, Chapel Hill; the Wuhan Institute of Virology, Wuhan, Communist China; the United States Army biological weapons labs at Ft. Detrick, Maryland, among others.) And, Two, the GoF work that was performed using the lab-created Wuhan Hu1 SARS-CoV-2 virus itself as the foundation for the modRNA (aka mRNA) COVID-19 “vaccines” that were developed by numerous companies, among them: PfizerUSA (at the company’s Pearl River, New York, facility; and, at other facilities); and, BioNTech (Mainz, Germany); Moderna (with the NIAID in Bethesda, Maryland, and at other facilities) — for use in the United States and also world-wide. (Note: PfizerUSA and BioNTech are separate companies that operate as a “joint venture” called Pfizer-BioNTech. PfizerUSA and BioNTech each have a separate CEO [Chief Executive Officer].)

Three articles by Jon Fleetwood start today’s offering. The first is here: https://jonfleetwood.substack.com/p/260-children-infected-with-tubersulosis, “260 Children Infected With Tuberculosis in Gates-Funded Study Injecting Children with Live Mycobacterium bovis Bacteria: “New England Journal of Medicine'”, 8 May 2025. The second is here: https://jonfleetwood.substack.com/p/new-bill-gates-funded-chimeric-polio, “New Bill Gates-Funded Chimeric Polio Vaccine Sheds 100% in Recipients, Spread Documented: ‘The Lancet’ Journal”, 18 August 2025. The third is here: https://jonfleetwood.substack.com/p/bill-gates-funds-slim-microneedle, “Bill Gates Funds ‘SLIM’ Microneedle Tech That Self-Assembles Inside the Body”, 24 April 2025.

Regarding the first Jon Fleetwood article: The 260 study subject children were living in South Africa, and were between the ages of 10 and 18 years. They were confirmed by to be HIV-negative at the time they were added to the study subject pool. They were injected with the Danish tuberculosis vaccine BCG1331 strain (Bacille Calmette-Guerin). The Package Insert for this vaccine is here: https://nibsc.org/documents/ifu/07-270.pdf. The BCG1331 strain is the Mycobacterium bovis strain, which causes tuberculosis in cattle and can also cause the disease in humans, especially in HIV-compromised persons. Please see the screenshot from the Fleetwood article, below:

The paper that resulted from the study is here: https://doi.org/10.1056/NEJMoa2412381, “BCG Revaccination for the Prevention of Mycobacterium tuberculosis Infection”, Alexander C Schmidt, et al., 8 May 2025. Please see the screenshot from this paper, below:

In other words, 260 children now have tuberculosis because of the BCG1331 strain vaccine that they were injected with. And that Bill Gates funded this “human guinea-pig experiment.” But there’s more — the Fleetwood article also describes the Bill Gates-funded Mycobacterium bovis experiments at the University of Texas, performed in 2012, that resulted in a what may be called a “turbo-charged Gain-of-Function” version of this tuberculosis bacterium. The paper that was published from the 2012 study is here: https://doi.org/10.1016/S1472-9792(13)70007-6, “Mycobacterium tuberculosis MtrAY102C is a gain-of-function mutant that potentially acts as a constitutively active protein”, Akash T Satsangi, et al., published December 2013.

Regarding the second Fleetwood article: Another Bill Gates-funded effort, this time about a lab-created chimeric polio oral “vaccine” that was tested on human subjects in the United States. The study results are nothing short of terrifying. Please the screenshot from the Fleetwood article, below:

There was a 100% incidence of “shedding” of this lab-created chimeric oral polio “vaccine.” Six human subjects were released from the study when it was found that testing of their stool showed they had possibly contracted the oral vaccine virus from other study subjects. Several human subjects had severe adverse reactions to this lab-created chimeric oral polio “vaccine.” This lab-created chimeric oral polio “vaccine” caused “unexpected” interactions with the type 2 poliovirus.

The team that lab-created this chimeric oral polio “vaccine” were from medical centers across the United States, including: University of North Carolina, Chapel Hill; University of Vermont; and, Dartmouth. The paper that was published from the study is here: https://www.thelancet.com/journals/laninf/article/PIIS1473-3099(25)00285-3/fulltext, “Safety and immunogenicity of novel live attenuated type 1 and type 3 oral poliomyelitis vaccines in healthy adults in the USA: a first-in-human, observer-masked, multicentre, phase 1 randomized controlled trial”, Laina D Mercer, PhD, et al., 13 August 2025. The clinical trial for this lab-created chimeric polio virus “vaccine” is listed here: https://clinicaltrials.gov/study/NCT04529538. Again, from the Fleetwood article:

Regarding the third Fleetwood article: Bill Gates has funded the creation of a new technology, called “SLIM microneedle”, which injects “microcrystals” of a contraceptive drug (levonorgestrel) into the body of a female; and, which microcrystals then”self-assemble” into an “implant” inside her body. Please see the screenshot from the Fleetwood article on this situation, below:

This type of “self-injected, self-assembly inside the body” approach has profound implications. Please see below, again from the Fleetwood article:

The paper that was published on this issue is here: https://www.nature.com/articles/s44286-025-00194-x, “Self-aggregating long-lasting injectable microcrystals”, Vivian K. Feig, et al., 24 March 2025. Note how “self-assembling” has magically become “self-aggregating” — in some attempt to hide the fact that the microcrystals really do “self-assemble?”

The SLIM “delivery system” for the contraceptive levonorgestrel (called “LNG” in the paper above) uses a solvent called Benzyl Benzoate (called “BB” in the paper above.) The paper describes the experiments performed to find the “right combination” of levonorgestrel + Benzyl Benzoate to create the SLIM delivery system — the “winning delivery system candidate” was named “LNG-BB.” Benzyl Benzoate is clearly dangerous. Part of Section 4 FIRST AID MEASURES from the MSDS Safety Sheet on Benzyl Benzoate from Spectrum Chemical (https://www.spectrumchemical.com/) is below:

And this is the “long-lasting solvent” that is used in the SLIM microneedle “self-aggregating” delivery system for levonorgestrel. Which means that this solvent will be acting in the body of the female who uses this delivery system for this drug for an (undetermined) amount of time.

Now, on to a recent GoF experiment, this one funded by NIH / NIAID, at the University of Pittsburgh. This GoF experiment resulted in the lab-creation of a chimeric H5N1 Avian Influenza virus strain that could infect dairy cattle. Jon Fleetwood wrote about this situation, here: https://jonfleetwood.substack.com/p/nih-funded-pennsylvania-researchers, “NIH-Funded Pennsylvania Researchers Build New Frankenstein Bird Flu Virus: ‘Journal of Virology'”, 26 August 2025. Vesicular stomatitis virus (VSV) is a virus that infects horses and cattle. In humans, Stomatitis infection can result in HSV-1 (the “cold sore” virus: per https://my.clevelandclinic.org/health/diseases/stomatitis-oral-mucositis.) However, the researchers at the University of Pittsburgh concentrated on “splicing” an element of VSV with H5N1. The paper that was published from this experiment is here: https://doi.org/10.1128/jvi.00621-25, “Dairy cattle herds mount a characteristic antibody response to highly pathogenic H5N1 avian influenza viruses”, Kevin R. McCarthy, et al., 25 August 2025. Please see the screenshots from the Fleetwood article on this issue, below:

Isn’t it “convenient timing” that this “new, chimeric VSV + H5N1 virus” comes on the heels of the announcement by the White House on 5 May 2025, that Gain-of-Function research would be stopped — but it appears that “certain contracts” would be permitted to “finish out”? And, that one of those “certain contracts” is with Arcturus Therapeutics for its self-amplifying RNA (saRNA) Avian Influenza “vaccine”, ARCT-2304? The White House announcement is here: https://www.whitehouse.gov/presidential-actions/2025/05/improving-the-safety-and-security-of-biological-research/. The news release related to the second quarter 2025 financial update and “pipeline progress” for Arcturus Therapeutics in which ARCT-2304 is mentioned, is here: https://www.biospace.com/press-releases/arcturus-therapeutics-announces-second-quarter-2025-financial-update-and-pipeline-progress, 12 August 2025. The clinical trial for ARCT-2304 is registered here: https://clinicaltrials.gov/study/NCT06602531; which, by the way, has NO saline-only Placebo control group; the only “control groups” in the study will be injected with a “control vaccine” or a “placebo vaccine” (which last, in and of itself, is not a true Placebo.)

And now, regarding something else: the GoF experiments that resulted in the lab-creation of an Avian Influenza “vaccine” which is a “Cocktail of Inactivated Avian Influenza Viruses”, a patent owned by Dr. Jeffery Taubenberger, a “career medical employee” of HHS and the federal government, and who is also the current Acting Director of the NIAID (National Institute of Allergy and Infectious Diseases, previously headed by Dr. Anthony Fauci), and who now is in control of the $500 Million dollars that was pulled from mRNA research activities in May 2025. This “bird flu vaccine cocktail” contains BPL (Beta-propiolactone), a known carcinogen.

The NIH TechTransfer information on this “cocktail” invention by Dr. Taubenberger is here: https://www.techtransfer.nih.gov/tech/tab-3388, “Broadly Protective Influenza Vaccine Compromising a Cocktail of Inactivated Avian Influenza Viruses”. Sounds “benign,” yes? Until one starts reading the actual Patent document itself, found here: https://image-ppubs.uspto.gov/dirsearch-public/print/downloadPdf/11369675, filed 21 July 2020. The following are screenshots from the Patent document:

Note it appears that Dr. Taubenberger was experimenting with as many as sixteen different strains of Avian Influenza to lab-create his “cocktail vaccine.”

Note it appears that Dr. Taubenberger is perfectly all right with “vaginal” and “rectal” administration of his “cocktail vaccine.”

Note that the Patent was registered in July 2020 — which can only mean that work on the experiments to lab-create this “Avian Influenza cocktail vaccine” must have begun at least nine months earlier. This would place the commencement of the experiments around October 2019 — just before the COVID-19 original virus was unleashed on on the world.

Here are two screenshots from the MSDS Safety Sheet for Beta-propiolactone from Sigma Aldritch (https://www.sigmaaldritch.com/US/en/sds/sigma/p5648):

And THIS ingredient is part of the “Avian Influenza Cocktail Vaccine” of Dr. Jeffery Taubenberger, two possible methods of administration of which are INTRANASAL or INHALED, per the Patent document images above?

It is not enough that HHS Secretary Robert F. Kennedy, Jr., terminated 22 contracts for mRNA research in May of this year, but allowed “certain contracts” for mRNA (and saRNA) research to “finish out.” It is not enough that the White House announced a ban on Gain-of-Function research, since this type of research is still going on — funded by “private Big Money”, and/or by the NIH / NIAID (in other words, the United States government). The entire Gain-of-Function situation must be stopped, from all funding sources and on all levels of research and experimentation — until there are clear, firm, and enforceable regulations and restrictions on who can perform this type of research; that such research can only be permitted under strict circumstances; that such research must be under tight supervision; and, that such research can only be performed where there is a clear need in the area of public health — not what amounts to a “chimeric fishing expedition” to lab-create viruses. It is time for any and all “go-along-to-get-along” activities to stop — such as, bowing to the “demand” by Sen. Dr. Bill Cassidy for his “cooperation” in “working with” HHS as regards hiring, or anything else. By the way — Sen. Dr. Cassidy has received donations from multiple pharmaceutical entities (United Health, AstraZeneca, Pediatrix Medical Group, and so on: per Open Secrets (https://opensecrets.org/.) And — that the further development of the above-discussed “Avian Influenza Cocktail Vaccine” must be stopped.

HHS Secretary Kennedy, Jr.: Please understand that the “career medical bureaucrats” in the CDC, the FDA, and the other divisions of the HHS, are not inclined to your views. They want “the good old days” of these divisions brought back. They are working “behind the scenes” in some instances, and in other instances, out in the open, to obstruct, delay, and thwart your efforts to clean up HHS and “re-tool” the department to reflect Make American Healthy Again. There is even what may be called “soft interference” by persons not employed by HHS such as, Sen. Dr. Cassidy.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 8.15.2025 Open Thread: Special Report Edition

The free header image for today’s offering is courtesy of Shutterstock and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. As today’s offering is related, in part, to the disaster of the COVID-19 “vaccines”, Yours Truly dedicates it to all persons who have contracted injures, illnesses, or disabilities, induced or aggravated by the COVID-19 “vaccines” that were injected into their bodies; and, to the memory of all persons who have passed away from the negative effects of the COVID-19 “vaccines” that were injected into their bodies.

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

There are two sections to today’s Special Report offering: the first section, regarding the now-proven linkage of COVID-19 “vaccine boosters” to increases in cancer and in general mortality; the second section, regarding what appears to be the potential emergence of the “next plandemic” in Communist China. Please bear with Yours Truly: one does not want to “weary by recitals”, as the Duc de Saint-Simon once wrote — but there is a lot of information, multiple screenshots, and so on. The evolving knowledge regarding the disaster called COVID-19 (the virus itself, and the “vaccines”) is gaining speed with each passing day. This evolving knowledge base is important to understand in light of the developments regarding the new information about the “Chikungunya outbreak” currently in China, and which is apparently spreading to other countries (shades of the original COVID-19 virus itself outbreak in China.)

First section, the linkage between COVID-19 “booster vaccines” with increases in cancer and in general mortality. COVID-19 “vaccine boosters” means any injection of a “latest version” of a COVID-19 “vaccine.” This includes the FDA- approved 2025-2026 “new formula COVID-19 vaccine versions” of the Pfizer-BioNTech modRNA COVID-19 “vaccine”, COMIRNATY; of the Moderna modRNA COVID-19 “vaccine”, SPIKEVAX; and, of the Novavax COVID-19 “vaccine”, NUVAXOVID.

Yours Truly begins here: https://slaynews.com/news/renowned-oncologist-sounds-alarm-cancer-deaths-now-surging-among-covid-boosted/, “Renowned Oncologist Sounds Alarm: Cancer Deaths Are Now Surging Among Covid-Boosted”, by Frank Bergman, 6 August 2025. There is an embedded video statement by Prof. Dr. Angus Dalgleish (St. George’s, University of London.) Dr. Dalgleish warns, in no uncertain terms, that it is the suppression of T-cell immune cells in the body of the COVID-19 “vaccine boosted” that is causing the surge of cancer among these persons. Please see the screenshot from the Slay News article, below:

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

The paper referenced above is here: https://www.researchsquare.com/article/rs-6899448/v2, “Factors contributing to the sharp rise in excess mortality in Japan since 2021”, Atsushi Takahashi, 17 July 2025. This paper is a pre-print. Please see the screenshots from this paper, below. They are: portions of the Results section; Figure 4; and, Figure 9:

The identifier names are those of the Prefectures in Japan that were studied. Even with taking other factors into consideration (examples: the size and population of the various Prefectures; the number of adults in age brackets in the Prefectures; whether or not a Prefecture was “rural” in character and location, as compared to “urban”), it is clear that the increase in mortality is tied to an increased amount of COVID-19 “vaccine boosters” that were administered.

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

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

The peer-reviewed paper on the Japan study is here: https://doi.org/10.3390/cancers17122006, “Repeated COVID-19 Vaccination as a Poor Prognostic Factor in Pancreatic Cancer: A Retrospective, Single-Center Cohort Study”, Makoto Abue, et al., 16 June 2025.

Yours Truly has written extensively for the board here regarding the damage / destruction of the natural immune system of the person who takes COVID-19 “vaccines.” These injectables were designed to attack, damage / destroy the CD4 – CD8 immune system cells. These injectables were designed to attack, damage / destroy the IgG3 immune system “fighter” cells, while at the same time, fostering the increase of IgG4 immune system “tolerate and never clear” cells. This damage / destruction increases with each injection of a modRNA COVID-19 “vaccine”, including injections of the “latest formula version” of said “vaccines”, which includes the “2025-2026 Formula versions” of said “vaccines” (COMIRNATY [Pfizer-BioNTech]; SPIKEVAX [Moderna]; and, NUVAXOVID [Novavax.])

The “Seneff and Nigh” paper of 10 May 2021 discusses how “immune system imprinting” in the the body of persons who take the COVID-19 “vaccines” have the potential to result in what the authors call “unintended consequences.” The paper is available here: https://dpbh.nv.gov/uploadedFiles/dpbhnvgov/content/Boards/BOH/Meetings/2021/SENEFF-1.PDF, “Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19”, Stephanie Seneff and Greg Nigh; International Journal of Vaccine Theory, Practice, and Research 2(1), May 10, 2021, Page 38-79. Please see the screenshots from this article, below. They are: the Abstract; the “Unprecedented” box; and, Figure 2.

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

Second section, regarding the potential for the “next plandemic” to come from Communist China. This has to do with the current emergence of mosquito-borne Chikungunya infections in several areas of China, which has resulted in various government-enforced measures. There is also an ** interesting connection ** to the United States involved in this situation.

What is Chikungunya? It is a virus transmitted by the bite of an infected female mosquito of (usually) the Aedes aegypti or the Aedes albopictus species. (As an aside: female mosquitos of these species can also transmit Dengue fever via bites.) The virus that is transmitted causes joint pain and fever; these can progress to severe. Most people infected with Chikungunya, however, make a full recovery. The virus is an RNA alphavirus. Please see: https://my.clevelandclinic.org/health/diseases/25083-chikungunya; there is a screenshot from this article, below:

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

Two recent articles regarding the Chikungunya outbreak in China: the first, here: https://jessicar.substack.com/p/the-new-pending-plandemic-is-it-scheduled, “The new pending “plandemic” — is it scheduled for November?”, by Jessica Rose, PhD, 12 August 2025. Dr. Rose makes it clear that the “alphavirus + saRNA-LNP platform” (self-amplifying RNA + lipid nanoparticles “vaccine” platform) is based on the VEEV alphavirus (Venezuelan Equine Encephalitis Virus.) Please see the screenshots from her article, below:

**** Note the mention of immune system issues that are induced in persons who are COVID-19 “vaccinated”, and how this can potentially severely complicate any infection by Chikungunya.

The second article is here: https://www.2ndsmartestguyintheworld.com/psyop-25-scamdemic-update-chinese, “PSYOP-25 SCAMDEMIC UPDATE: Chinese Authorities Mandating Blood Tests, Releasing Lab Mosquitoes to Fight Chikungunya Outbreak”, 13 August 2025. Please see the screenshots from this article, below:

The founder of the “mosquito lab” in Guangzhou is Dr. Zhiyong Xi. Please see the screenshot below from the above link:

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

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

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

Which work, at least in part, is being funded by NIAID (division of NIH — both divisions part of HHS.)

Which begs the following questions: WHY is Dr. Zhiyong XI still doing mosquito research in the United States if he founded a mosquito study lab in Communist China? WHY is Dr. Zhiyong Xi’s research at Michigan State University being funded, at least in part, by the NIH / NIAID?

There are two “FDA-approved vaccines” against Chikungunya: IXCHIQ, and VIMKUNYA. BOTH of these “vaccines” were FDA-approved under “accelerated approval” methods. Please see the screenshots, below, from the Package Inserts for these injectables. First, from the Package Insert for IXCHIQ (https://ixchiqhcp.com/PI-new.pdf):

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

Note the presence of Aluminum Hydroxide as an adjuvant in VIMKUNYA.

NOTE THAT THE “EXACT MECHANISM OF PROTECTION’ HAS NOT BEEN DETERMINED FOR EITHER IXCHIQ OR FOR VIMKUNYA. In other words, the United States government (via the FDA) is fine with injecting people with these “vaccines” WITHOUT THE FDA KNOWING THE EXACT MECHANISMS OF PROTECTION FOR EITHER OF THEM. What are the “CHIKV-specific immune responses” that these injectables supposedly elicit?

And, by the way, both IXCHIQ and VIMKUNYA can be “shed” onto newborn children if the expectant mother is sick with a virus (this is called viremia) at the time of delivery. A pregnant female who takes either one of the above “vaccines” runs the risk of contracting “viral viremia.” Neither IXCHIQ, nor VIMKUNYA have had proper testing for potential effects on pregnant females, their fetuses, or their newborns (section 8.1 Pregnancy in either Package Insert.)

All of the above begs the following questions: Does HHS Sec. Robert F. Kennedy, Jr., know about these Chikujgunya “vaccines”? Does he know that the FDA approved them under “accelerated approval” methods? Does he understand that the FDA does NOT know the “exact mechanism of protection” for either IXCHIQ or VIMKUNYA? Does Dr. Martin Makary (FDA Commissioner) know about this situation? Do either Sec. Kennedy, Jr., or Dr. Makary know that “career FDA types” in the CBER division signed the FDA Approval Letters for IXCHIQ (signed by R. Douglas Pratt, MD, 6 August 2025) and for VIMKUNYA (signed by David C. Kaslow, MD, 14 February 2025)?

Yours Truly will again emphasize that it is critically important for all persons, whether COVID-19 “vaccinated” or not, to follow some type of COVID-19 spike protein mitigation / prophylaxis protocol. It is also critically important that all persons, whether COVID-19 “vaccinated” or not, to do all they can to build and maintain their general health, and the health of their immune system, so as to be in the best shape possible.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 8.8.2025 Open Thread: Dr. Martin Makary Edition

The header image of a vintage doctor’s office sign for today’s offering is courtesy of iStock and Google Images.

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

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note One: Yours Truly has checked today’s offering for any AI-generated content. To the best of her knowledge and belief, there is none, except for some possible AI-generated images embedded in certain of the links below in the post. If readers wish to post any AI-generated content in today’s discussion thread, they must cite their source. Note Two: Today’s offering is not intended to be, nor is it to be construed as, defamation or “character assassination” of the person who is the subject of the post. Thank you.

Today’s offering is about Dr. Martin Makary, MD, MPH, the current Commissioner of the Food and Drug Administration (FDA) of the United States Department of Health and Human Services (HHS.) Dr. Makary serves under HHS Secretary Robert F. Kennedy, Jr. There is some “interesting information”, along with multiple screenshots, in today’s post. All information is searchable on the internet. Yours Truly will highlight opinions of her own in Italics.

The official FDA biography of Dr. Martin Makary, MD, MPH, is here: https://www.fda.gov/about-fda/fda-organization/martin-makary. Yours Truly cannot find a biographical entry on Dr. Makary that states when he was born. What is known is that Dr. Makary was born in Liverpool, England, and came with his birth family to the United States when he was a child. What is known is that Dr. Makary graduated with a B.S. degree from Bucknell University (likely about 1994), and graduated with his MD degree from the medical school of Thomas Jefferson University in 1998. This would, likely, place his year of birth in about 1970. Dr. Makary held a position at The Johns Hopkins University Hospital System as a Surgical Oncologist. He has also served as a professor in the Business School of The Johns Hopkins University. He also served as a consultant for the World Health Organization (WHO) in 2009 in that organization’s “Patient Safety Initiative”, in which Dr Makary assisted in creating the “Surgery Checklist” for surgeons (https://iris.who.int/bitstream/handle/10665/44185/9789241598552_eng.pdf, page 121.) Dr. Makary was confirmed as the current Commissioner of the Food and Drug Administration (FDA) division of the United States Department of Health and Human Services (HHS) in March 2025.

It is also known that Dr. Makary has apparently refused to take COVID-19 “vaccines” himself. Please see the screenshot, below, from this article: https://www.arabnews.com/node/2580559/amp. “Trumps names two Arab Americans for his Cabinet”, 25 November 2024:

Which, if the above is true, begs the question: If Dr. Makary did not take COVID-19 “vaccines” himself, why is he “recommending” these injectables for anyone else — for example, for people now deemed “at risk of severe complications from COVID-19 infection”, which includes pregnant women and women who have just given birth?

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

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

There are sections of the FDA website (URL above) regarding “Background and Program Priorities”, “Eligibility Criteria” for drug companies, “Solicitation of Statements of Interest”, and “Submission and Selection” for the program, underneath the FDA announcement.

This FDA announcement comes on the heels of another “opinion piece” by Dr. Martin Makary and Dr. Vinay Prasad, “Priorities for a New FDA”, published on JAMA Network on 10 June 2025. Their article is found here: http://jamanetwork.com/journals/jama/fullarticle/2835314. Please see the screenshots from this “opinion piece”, below:

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

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

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

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

Dr. Makary is involved with drug and/or other companies:

Which begs the question: Does this indicate that Dr. Makary may have conflicts of interest in certain areas?

Dr. Makary: Herd immunity from COVID-19 is via infection AND COVID-19 “vaccination”:

Dr. Makary: The non-COVID-19 “vaccinated” should avoid “vaccination” until new COVID-19 “vaccines” are authorized:

Dr. Makary: The need for “universal masking” against COVID-19:

Dr. Makary: On the other hand, “universal masking” harms children:

Dr.Makary: COVID-19 “lockdowns” are acceptable:

PRIOR to his being confirmed as Commissioner of the FDA, Dr. Makary questioned the concept of FDA authorization of COVID-19 “vaccines” without proper testing:

And, last but not least, Dr. Makary urges people to not “dissect” what now-HHS Secretary Kennedy, Jr., said years ago:

Which last screenshot begs the question: Has Dr. Makary apparently applied the “don’t dissect what someone said years ago” standard to himself as regards “the new FDA” that he and Dr. Prasad have created and that Dr. Makary is now implementing at the FDA?

There is a final piece to the “tapestry”, regarding the announcement by HHS Secretary Robert F. Kennedy, Jr., on 5 August 2025, that HHS was cancelling 22 contracts for “vaccine development under BARDA.” Please see: https://www.hhs.gov/press-room/hhs-winds-down-mrna-development-under-barda.html. However, BARDA is going to be “allowed” (how did this happen?) to complete contracts already begun for the ARCT-2304 self-amplifying RNA (saRNA) Avian Influenza “vaccine”, AND for the development of the “latest RNA technology platform”, called trans-amplifying RNA (taRNA.) And it was the FDA, under Dr. Martin Makary, who granted Arcturus Therapeutics (the developer of ARCT-2304) “Fast Track” status on 10 April 2025 — just after he was confirmed as the new Commissioner of the FDA. Fierce Biotech has an article on the BARDA continuation of these two contracts. Please see: https://www.fiercebiotech.com/biotech/hhs-cancels-all-mrna-vaccine-development-funded-barda, “HHS winds down mRNA vaccine development funded by BARDA”, by Darren Incorvaia, 5 August 2025. A screenshot from this article is below:

Jon Fleetwood discusses this situation on this Substack, here: https://jonfleetwood.substack.com/p/hhs-terminated-22-mrna-projectsbut, “HHS Just Terminated 22 mRNA Projects — But Quietly Preserved the Bill Gates-Funded Bird Flu Shot”, 6 August 2025. Please see a screenshot from this article, below:

There is also an embedded video of an interview with Mr. Fleetwood in his article above.

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

So, it would appear that, at the very least, FDA Commissioner Dr. Martin Makary “went along”, for whatever reason(s), with the cancelling of mRNA “vaccine” contracts, while at the same time, allowing BARDA to continue with the development of two very dangerous and unproven “vaccine platform technologies”: self-amplifying RNA and trans-amplifying RNA.

Refer above in today’s offering regarding the presence of Dr. Makary as a “headliner” at the BIO.org/ convention in March of this year. Representatives of both CSL Behring and Seqirus were at this convention. Arcturus Therapeutics IS A PARTNER WITH CSL / SEQIRUS in the development of ARCT-2304. Please see: https://arcturusrx.com/mrna-medicines-business-development/, under “Partnered RNA Medicines.”

Trans-amplifying RNA (taRNA), by the way, is a COMBINATION of two, “shorter” RNA fragments: one fragment encodes the antigen; the other fragment encodes the “replicase” (a replicase is an enzyme that facilitates the synthesis of another RNA molecule.)

Summary: In Yours Truly’s opinion, Dr. Martin Makary, the current Commissioner of the FDA, is a person of many convictions and viewpoints, some of which may be conflict with each other. It is up to individual readers to do their own research and form their own opinions.

Peace, Good Energy, Respect: PAVACA

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

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

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

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats by Yours Truly, of which readers should be aware. They are linked here. Note One: Yours Truly has checked today’s offering for any AI-generated content. Other than AI-generated images that may be embedded in URL links, to the best of her knowledge and belief, there is none. If readers wish to post any AI-generated content in today’s discussion thread, they must cite their source. Note Two: Nothing in today’s offering is intended to be, nor shall it be construed as, what might be termed “character assassination” regarding HHS Sec. Kennedy, Jr., or any employee (current or former) of the FDA or of the CDC. Thank you.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 7.18.2025 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