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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

What does this mean regarding the concept of FOCUS?

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

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

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

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

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

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

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

Peace, Good Energy, Respect: PAVACA

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

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

The vintage header image of “The Trial of the Lewis Deer Raiders at Edinburgh” for today’s offering is courtesy of iStock and Google Images.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

The following are the opinions of Yours Truly:

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

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

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

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

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

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

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

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

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

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

Peace, Good Energy, Respect: PAVACA

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

Health Friday 2.27.2026 Open Thread: Moderna’s mRNA-1010 and the End Run Around HHS Sec. Kennedy, Jr.: Part One

The header image for today’s offering of an end run is courtesy of Grammarist and Google Images.

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

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

Today’s offering is Part One regarding the current situation with Moderna’s latest entry into the mRNA-based “vaccine” platform: the company’s influenza “vaccine”, mRNA-1010.

On 11 February 2026, Dr. Vinay Prasad, director the CBER division of the FDA (Center for Biologics Evaluation and Research) sent an RTF letter (Refusal to File letter) to Moderna in response to that company’s BLA application (BIologics License Application) review request for mRNA-1010, a modRNA-based “vaccine” against several strains of influenza. Dr. Prasad cited the lack of a true placebo control group in a study by Moderna using this “vaccine candidate.” Please see the screenshots, below, from https://pharmacally.com/fda-issues-refusal-to-file-letter-for-modernas-mrna-1010-flu-vaccine/, 11 February 2026:

However, by a few days later, the situation had changed completely: the FDA “reversed course”, agreeing to review Moderna’s BLA (amended) application for mRNA-1010.

By 18 February 2026, a “Type A” meeting had been arranged between the FDA and Moderna regarding the RTF letter. Moderna agreed to submit an “amended” BLA application to the FDA for mRNA-1010. The FDA accepted the amended BLA application. The FDA will make a final decision on approving mRNA-1010 by 5 August 2026. Please see the screenshot, below, from https://www.biospace.com/fda/fda-reverses-course-on-modernas-mrna-flu-shot-application-promising-august-decision, Heather McKenzie, 18 February 2026:

Note: A Type A meeting at the FDA is a “high-priority” meeting; sometimes, Type A meetings are called “milestone meetings.” Per https://facetlifesciences.com/ and https://seed.nih.gov/ searches.

Please see the screenshots, below, on this “volte-face” from https://www.thefocalpoints.com/p/fda-reverses-course-will-now-review, “FDA Reverses Course, Will Now Review Moderna’s Controversial mRNA Flu Vaccine”, Peter A. McCullough, MD, MPH, 20 February 2026:

Then, from https://www.biopharmadive.com/news/fda-reverses-course-review-moderna-approval-application-influenza-812432/, “FDA reverses course on Moderna’s flu vaccine”, Delilah Alvardo, 19 February 2026 (the quotation in the screenshot is from Mani Foroohar):

Note that last sentence, by Mr. Faroohar. It clarifies three “behind-the-scenes” aspects of mRNA-1010:

**** One: That Moderna will do whatever it takes to get mRNA-1010 approved — including being “more assertive” with the FDA, and arranging it so that the FDA will “work with” Moderna.

**** Two: That Moderna will do a “post-marketing study” on mRNA-1010 AFTER it is FDA-approved — meaning that ANYONE who takes mRNA-1010 AFTER the FDA approves it is being treated as a “human lab rat” by Moderna. This is the same type of situation that occurred when the FDA approved Moderna’s modRNA COVID-19 bioweapon “vaccine”, mRNA-1273.

**** Three: That Moderna considers the FDA approval of mRNA-1010 as the “stepping-stone” to what the company appears to believe is the “Holy Grail” of modRNA-based “vaccines” — the company’s “combo” modRNA-based influenza + modRNA-based COVID-19 “vaccine”, mRNA-1083 (the clinical trials for which have been completed)

There are, in addition, two other aspects to the situation: What appears to be pressure on Dr. Martin Makary, MD (FDA Commissioner) to “knuckle under” to what Moderna wants; and, what appears to be a coordinated campaign to have Dr. Vinay Prasad removed from his position as CBER division director at the FDA. In Yours Truly’s opinion, these relate to the “sudden arrangement” of the FDA “Type A” meeting between Moderna representatives and the FDA almost immediately after the Refusal to File was issued by Dr. Prasad. Please see the screenshots, below, from https://www.biospace.com/fda/makary-prasad-under-fire-as-fda-turmoil-reaches-president-trump, Heather McKenzie, 20 February 2026:

Peter Pitts, by the way, was an FDA employee whose position was that of a “senior communications and policy adviser” of the agency (https://www.centerforbiosimilars.com/authos/peter-pitts.) It appears that Mr. Pitts and CMPI are involved in a campaign to have Dr. Prasad removed from the FDA.

In Yours Truly’s opinion: Dr. Martin Makary is compromised, due to his involvement with BIO.org/, the group that is implementing a campaign to have HHS Sec. Robert F. Kennedy, Jr., removed; and, Dr. Prasad is compromised, due to what appears to be lack of support within FDA, combined with innuendoes regarding his professional behavior at the agency.

In Yours Truly’s opinion, It appears that there is a combination of chaos, mistrust, internecine feuding, and active resistance going on within the FDA; plus, exterior pressure on the agency from companies and other entities to restore the FDA back to the “good old days”, when drugs and other biologics were authorized and approved in what may be called a kind of “rubber-stamp” process. It also appears that HHS Sec. Kennedy, Jr., is either being “kept out of the loop” regarding what is going on with the FDA; or, cannot, for whatever reason, root out personnel within the FDA who are fomenting trouble.

Yours Truly now turns to the Moderna-funded published paper on mRNA-1010, which was cited by Dr. Prasad as the reason for his issuing the Refusal to File letter to the company: https://doi.org/10.1038/s41541-025-01340-5. “mRNA-1010 influenza vaccine elicits distinct and enhanced humoral immunity compared to adjuvanted inactivated vaccines.” Paulina Kaplonek, et al. 15 December 2025. Moderna completely funded this study; all of the paper’s co-authors are either current or former Moderna employees; and, the current Moderna employees who are co-authors of the paper are also stockholders in the company. All of these in and of themselves, in Yours Truly’s opinion, represent massive conflicts of interest that should, under normal circumstances, disqualify the paper from any serious consideration by the FDA for a BLA application review. This is aside from the flaws in the clinical trial NCT05397223, on which the paper was based (more on this below in today’s offering.) Please see the screenshots from this paper, below:

Note the use of the word, “may.” This word is used in several areas of the paper, as in, “may elicit”; “may reflect”; and, “may induce.” In other words, Moderna does not KNOW if mRNA-1010 can actually be helpful against influenza. The company is guessing that it “may.” However, the company is still pursuing the BLA application with the FDA to get the “vaccine” approved — without having provided ANY proof that the “vaccine” actually does what it is “supposed” to do — which is, to prevent influenza infection better than the licensed influenza “vaccines” already on the market.

The following screenshots from the paper relate to how mRNA-1010 works, including: Figure 4B and Figure 4D, which show that the “vaccine” minimizes the crucial natural body’s activity of IgM cells (the “recognize an enemy and signal the other cells” immune cells); which show that there is an apparent increase of IgG4 cells (the “tolerate but never clear” cells); and, which appear to hint at mRNA-1010 being used as a kind of “universal influenza vaccine” candidate:

The blue image is the results of the “comparator influenza vaccine”, FLUAD; the red image is the results of mRNA-1010.

Then, from the section that discusses the results of Figure 4B and Figure 4D:

The Moderna paper co-authors did not prove that mRNA-1010 provides mucosal protection from influenza.

Following is a screenshot from the paper regarding the non-involvement of IgM cells induced by mRNA-1010:

Followed by the “hint” that mRNA-1010 may be used as a “universal influenza vaccine” candidate:

Finally, the Acknowledgements section, and the Ethics Declarations section, of the paper:

As shareholders in Moderna, the above employees (and co-authors of the paper on mRNA-1010) stand to make money off the sale and use of this “vaccine.”

**** Regarding the clinical trial which was the foundation for the Moderna paper that was published on 15 December 2025, NCT05397223, details of which are found here: https://clinicaltrials.org/study/NCT05397223. This clinical trial did NOT have a true saline placebo Control Group. Per the Clinical Trials website, there are TWO separate parts to the study. In Part One, study subjects received injections of: of mRNA-1345 (a modRNA-based “vaccine” against RSV); or, of mRNA-1647 (a modRNA-based “vaccine” against Cytomegalovirus);, or, of mRNA-1273 (the modRNA COVID-19 “vaccine”), all by Moderna. In Part Two, study subjects received injections of either: FLUAD (the “comparator” licensed inactivated influenza vaccine by Seqirus); or, of mRNA-1010. Please see the screenshot, below, from the Clinical Trials website for NCT05397223, the Secondary Outcomes Measures section:

However, there is not a single word in the Moderna-funded paper cited above in which the outcomes for ANY of the “vaccines” used on the study subjects other than FLUAD or mRNA-1010, are found. Nothing for mRNA-1345, for mRNA-1647, or for mRNA-1273. It is unknown if any of these three “vaccines” induced any interactions with either FLUAD or with mRNA-1010. There are “No Results Posted” on the Clinical Trials website for NCT05397223.

Moderna has been in the process of developing and testing mRNA-1010 for the past several years. The company applied pressure, which apparently went all the way up to the Oval Office, in order to force the FDA to reverse course and agree to review the (amended) BLA application for mRNA-1010, despite the flaws of the clinical trial NCT053972723, and despite the Refusal to File letter sent by Dr. Vinay Prasad.

To be continued in Part Two.

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

Peace, Good Energy, Respect: PAVACA

(intellectual Property Disclaimer and Notice: With the exception of linked items that are found on the internet, the ideas and opinions of today’s offering are by PAVACA. Credit must be given to PAVACA if ideas or opinions in today’s offering are used by other blog writers; by podcasters; or in social or print media.)

Health Friday 2.20.2026 Open Thread: Pfizer-BioNTech COVID-19 modRNA “Vaccine” Negative Effects Proven Ongoing Over Three Years Post-Injection: Part Three

The header image of 1955 vintage Pfizer penicillin bottles is courtesy of Pond5 and Google Images.

Health Friday is a series devoted to information on Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to the negative effects and outcomes of the modRNA COVID-19 BIOWEAPON “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have suffered, and/or continue to suffer, injuries, illnesses, or disabilities induced by these “vaccines” that they took; and, to those who have passed away from the negative effects and outcomes induced by these “vaccines” that they took.

There are Important Notifications by our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: If there is AI-generated content in today’s offering, it will be labeled as such. If readers wish to post AI-generated content in today’s discussion thread, they must cite their source. Thank you.

Today’s offering is Part Three of three. The previous two parts of this series are here: https://www.theqtree.com/2026/02/06/health-friday-2-6-2026-open-thread-pfizer-biontech-covid-19-modrna-vaccine-negative-effects-proven-ongoing-over-three-years-post-injection-part-one/; and, https://www.theqtree.com/2026/02/13/health-friday-2-13-2026-open-thread-pfizer-biontech-covid-19-modrna-vaccine-negative-effects-proven-ongoing-over-three-years-post-injection-part-two/.

The Hulscher, McCullough, et al., paper that is the basis for this series is here: https://zenodo.org/records/18460099. “Unprecedented Persistence of Vaccine mRNA, Plasmid DNA, Spike Protein, and Genomic Dysregulation Over 3.5 Years Post-COVID-19 mRNA Vaccination.” Nicolas Hulscher, MPH, Peter A. McCullough, MD, MPH, et al. 2 February 2026.

Today’s offering will discuss the findings of ongoing heart / cardiovascular damage induced by the Pfizer-BioNTech COVID-19 modRNA “vaccine”, BNT162b2, in the patient described in the above-cited paper. Below, from the paper, are screenshots of sections that discuss the heart and cardiovascular damage that was found in the patient well after he took this “vaccine”:

The results of the patient’s home-administered cardiac readout tests:

As can be seen, the evidence of irregular heart rhythm are unmistakable. However, refer to the text above — the symptoms were apparently dismissed as “unlikely” for myocarditis / pericarditis, even though Emergency Room visit records when the patient presented there appear to show otherwise.

Continuing, from the paper:

Finally, a cardiac MRI was performed, which confirmed symptoms “consistent with COVID-19 vaccine-induced myocarditis…”; see below, a reduced image from the paper:

The following are several scientific papers and articles. The first one is the 1992 paper by Dr. Ralph Baric, PhD, of the results of his experiments to induce myocarditis and Congestive Heart Failure (CHF) in rabbits that he injected with a rabbit coronavirus (https://academic.oup.com/jid/article/165/1/134/986090. “An Experimental Model for Myocarditis and Congestive Heart Failure after Rabbit Coronavirus Infection.” Ralph S. Baric, et al. January 1992.) Please see the screenshots from this paper, below. First, the general summary:

Followed by two portions from the Discussion section. “RbCV” = rabbit coronavirus.

Following is a look at Reference paper number 17, cited several times in the Baric, et al., paper above. Reference paper number 17 is found here: https://pmc.ncbi.nlm.nih.gov/articles/PMC2042305/. “Rabbit cardiomyopathy associated with a virus antigenetically related to human coronavirus strain 229E.” Small, JD, Aurelian, L., Squire, R.A., et al. June 1979. The following screenshots are from this paper. First, the general summary:

Then, from the Discussion section:

Note the mention of human coronavirus 229E and its potential for “cross-reactivity” with other coronaviruses, including gastroenteritis in swine. Recall that Dr. Ralph Baric, PhD, invented the “No See-m’s” method for “seamless assembly” of chimeric (lab-created) virus code pieces using the TGEV virus (swine transmissible gastroenteritis virus) model back in 2000 (https://journals.asm.org/doi/10.1128/jvi.74.22.10600-10611.2000. “A strategy for the assembly of large RNA and DNA genomes: the transmissible gastroenteritis virus model.” Ralph Baric, et al. 2000.)

Dr. Joseph Sansone, PhD, a psychotherapist in Florida, speaks to the COVID-19 modRNA “vaccines” causing heart disease, immune system conditions, and more, here: https://usawatchdog.com/world-ignoring-disaster-of-cv19-bioweapon-vax-dr-joe-sansone/, 8 February 2026. Dr. Sansone links to the Hulscher, McCullough, et al., article cited above in today’s offering. Please see the screenshot below, from this article:

There is an earlier article discussing heart damage — at the mitochondrial level — that is induced by the COVID-19 “vaccines”, at The Focal Points, here: https://www.thefocalpoints.com/p/spike-protein-exhausts-cardiomyocyte, “Spike Protein Exhausts Cardiomyocyte Mitochondria”, 8 September 2024. The paper referred to in this article is here: https://doi.org/10.3390/cells12060877. “Spike Protein Impairs Mitochondrial Function in Human Cardiomyocytes: Mechanisms Underlying Cardiac Injury in COVID-19.” Tin Van Huynh, et al. 11 March 2023.

Yours Truly believes that the Hulscher, McCullough, et al., February 2026 paper cited in today’s offering is of incalculable importance. This paper proves that these negative effects and outcomes in “vaccinated” persons can be found more than three years post-“vaccine” injection. This paper proves that an individual “vaccinated” person can present with numerous negative effects and outcomes induced by these “vaccines.” Yours Truly expresses deep appreciation of Dr. McCullough and his colleagues in working with this patient in the long and laborious testing that had to be performed in order to come to the correct diagnoses for the patient; and, from there, coming up with a treatment plan.

The Hulscher, McCullough, et al., February 2026 paper proves that there is risk of multiple types of negative effects and outcomes from having this “vaccine” in the body — damage that can be found years after the “vaccine” is injected into the body, and that can extend to the brain. This risk pool includes those who take the “latest version COMIRNATY COVID-19 vaccine”.

Yours Truly will make it clear that the patient in the Hulscher, McCullough, et al., February 2026 paper took three injections of BNT162b2: two in March 2021 (3 March and 24 March); and, the “booster” injection on 20 February 2022 — then did not take any further injections. The damage to his body and the accompanying associated emotional/psychological effects on him were traced back to these three injections over 3.5 years later. What about the millions upon millions of persons who took the BNT162b2 “primary series” of two injections back in 2021, then the original BNT162b2 “booster” injection in 2022, and then have taken injections of the BNT162b2 “descendant clone COVID-19 vaccines” (under the brand name, COMIRNATY), since the year 2022? What about the persons who have taken six injections so far of this Pfizer-BioNTech injectable — the “primary series” of two injections in 2021 + the “original booster injection” in 2022 + the 2023 “COMIRNATY booster” + the 2024 “COMIRNATY booster” + the 2025 “COMIRNATY booster”? If one person who took only three of the Pfizer-BioNTech COVID-19 “vaccine” injectables (the patient in the Hulscher, McCullough, et al., paper) and presents with multiple negative effects and outcomes over 3.5 years after stopping taking the injections — what about the millions of persons who have a total of at least six Pfizer-BioNTech (COMIRNATY) injections in their bodies as of now? If the potential for multiple negative effects and outcomes from the Pfizer-BioNTech COVID-19 injectables can be found in a “vaccinated” person over three years post-final injection, what is the potential for “rolling accumulated negative effects and outcomes” from these injectables in a person who has taken these injections every year since early 2021?

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The following is not medical advice. They are opinions:

Any person who has ever taken a COVID-19 “vaccine” injection — even if only one injection — of any type (modRNA, DNA viral vector, “protein subunit”, etc.) may be at risk for developing negative effects and/or outcomes induced by these “vaccines.” COVID-19 “vaccinated” persons may wish to consider having the following tests performed:

A lung scan, to investigate whether or not there are issues that can have been induced from these “vaccines”; such as, compromised alveoli or lung tissue inflammation.

A heart / cardiac scan, to investigate whether or not there are issues that can have been induced by these “vaccines”; such as, scarring of heart tissue or symptoms of preclinical myocarditis.

A D-dimer test performed, to investigate whether or not there are elevated levels of microclots in the blood, which can have been induced by these “vaccines.”

An IgG3 panel test and an IgG4 panel test performed, to investigate whether or not there are reduced levels of IgG3 cells (the “fight the enemy cells off” immune system cells), and/or elevated levels of IgG4 cells (the “tolerate but don’t fight off” immune system cells), both of which can have been induced by these “vaccines.”

Note: The above tests usually need to be ordered by a physician; or, by another licensed healthcare professional who is approved to order these types of tests.

Interested persons may wish to consider following a post-“vaccination” recovery treatment protocol, such as the one outlined here, from the Independent Medical Alliance: https://imahealth.org/protocol/i-recover-post-vaccine-treatment.

For those who are not COVID-19 “vaccinated”, there is the now-proven phenomenon of “vaccine shedding” from “vaccinated” persons onto other persons, including onto non-“vaccinated” persons. Please see: https://pierrekorymedicalmusings.com/p/newly-published-study-shows-shedding, “Newly Published Study Shows Shedding Of Covid mRNA Vaccine Products”, 9 December 2024.

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

THERE MUST BE ACCOUNTABILITY, JUSTICE, AND TRUTH.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Disclaimer and Notice: The ideas and opinions in today’s offering are by PAVACA. Credit must be given to PAVACA if ideas or opinions in today’s offering are used by other blog writers, by podcasters, or in social or print media.)

Health Friday 2.13.2026 Open Thread: Pfizer-BioNTech COVID-19 modRNA “Vaccine” Negative Effects Proven Ongoing Over Three Years Post-Injection: Part Two

The header image of vintage 1955 Pfizer penicillin vaccine bottles is courtesy of Pond5 and Google Images.

Health Friday is a series devoted to information regarding Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to the negative effects and outcomes of the modRNA COVID-19 BIOWEAPON “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have suffered, and/or continue to suffer, injuries, illnesses, or disabilities induced by these “vaccines” that they took; and, to those who have passed away from the negative effects and outcomes induced by these “vaccines” that they took.

There are Important Notifications by our host, Wolf Moon; the Rules of our late, good Wheatie;, and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: If there is AI-generated content in today’s offering, it will be labeled as such. If readers wish to post AI-generated content in today’s discussion thread, they must cite their source. Thank you.

Part One of this series on the ongoing negative effects of the Pfizer-BioNTech COVID-19 modRNA BIOWEAPON “vaccine”, BNT162b2, is here: https://www.theqtree.com/2026/02/06/health-friday-2-6-2026-open-thread-pfizer-biontech-covid-19-modrna-bioweapon-vaccine-negative-effects-proven-ongoing-over-three-years-post-injection-part-one/. Part One discusses one of the ongoing negative effects that this “vaccine” induces: a permanent skin condition called Grover’s Disease.

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Today’s offering, Part Two, discusses the ongoing damage that BNT162b2 induces in the mitochondria of the “vaccinated” person’s body.

What are the mitochondria of the human body? These tiny organelles are present in every area and organ of the body. Mitochondria are the “power plants” of the body’s cells: they create energy to fuel the functions and lifecycle of each cell. The National Institutes of Health (NIH) describes what mitochondria are, and what they do, here: https://www.nih.gov/news-events/nih-research-matters/mitochondria-health, ” Mitochondria and health”, 22 July 2025. Please see the screenshots from this article, below:

Below is an image of mitochondria in the heart muscle of a rat. The mitochondria cells are brown. They have multiple “folded areas” within them, which increase the area for energy production.

Urbano, et al., has a very good article that explains how the mitochondria function, their importance to human health, and more, here: https://doi.org/10.1016/j.bbadis.2025.167803, “Mitochondria: An overview of their origin, genome, architecture, and dynamics”. Ana M. Urbano, et al. 25 March 2025. Please see the screenshot, below, from this paper:

Walter Chesnut has several blog research articles on mitochondria and how they are adversely affected by the spike protein of the SARS-CoV-2 (COVID-19) virus itself. One such article is here: https://wmcresearch.substack.com/p/mitochondrial-carpet-bombing-the, “Mitochondrial Carpet Bombing: The Endothelium is the Gateway through which the Spike Protein Devastates the Mitochondrial Landscape”, 9 October 2023. Please see the image from this article, below:

The above image is from the paper by Luca Perico, et al., regarding the spike protein and the endothelium: https://doi.org/j.tim.2023.06.004, “SARS-CoV-2 and the spike protein in endotheliopathy.” Luca Perico, et al. 12 June 2023.

Another article by Mr. Chesnut on the damage that the COVID-19 virus spike protein does to the mitochondria of the body: https://wmcresearch.substack.com/p/the-spike-protein-causes-to-the-exact, “THE SPIKE PROTEIN CAUSES TO THE EXACT SAME DAMAGE TO THE ENDOTHELIUM AS IF IT HAD BEEN IRRADIATED”, 7 March 2022. Please see the screenshot from this article, below:

The Salk Institute article referred to above is here: https://www.salk.edu/news-release/the-novel-coronavirus-spike-protein-plays-additional-key-role-in-illness/, 30 April 2021. The paper is found here: https://doi.org/10.1161/CIRCRESAHA.121.318902. “SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE2.” John Y-J. Shyy, et al. 31 March 2021. Note: Endothelial cells are tiny cells that line the inner surface of blood vessels. The mitochondria of endothelial cells work in “signalling” cellular responses among these cells.

It is obvious how important the mitochondria are to the proper functioning and life cycle of every cell in the human body.

Yours Truly turns again to the just-published paper by Hulscher, McCullough, et al., which was presented in Part One of this series. The paper is here: https://zenodo.org/records/18460099, “Unprecedented Persistence of Vaccine mRNA, Plasmid DNA, Spike Protein, and Genomic Dysregulation Over 3.5 Years Post-COVID-19 mRNA Vaccination.” Nicolas Hulscher, MPH, Peter A. McCullough, MD, MPH, Wei Zhang, PhD, et al. 2 February 2026. Please see the screenshots from this paper, below, regarding damage to the “vaccinated” patient’s body in the discussion of genomic dysregulation symptoms that were found: this genomic dysregulation indicates that multiple areas of mitochondrial-level damage had been induced. First, the summary paragraph:

Then, the “persistent plasmid DNA fragments“: text from the paper; then, Fig. 5c-d from the paper:

Followed by, the “exosomal vaccine mRNA“: first, the text from the paper; then, Fig. 5b from the paper:

Note: “exosomal” refers to the exosomes, tiny cells in the body that serve as “carry it from one place to another” cells. Exosomes are found in many areas of the body, including in sweat, saliva, tears, in other types of body fluids; in cells on the surface of the skin; and so on.

And, the “long-lived spike protein“: first, the text from the paper; then, the Fig. 5a from the paper:

The descriptions and abbreviations key of the Fig. 5 from the paper:

Finally, Fig. 7 from the paper, an AI-generated image of the types of bodywide damage that was induced in the patient after he took the three injections of the Pfizer-BioNTech COVID-19 modRNA BIOWEAPON, BNT162b2. Please see the box “Genomic Dysregulation“:

Yours Truly wrote about the potential for the SARS-CoV-2 (COVID-19) virus itself, and the potential for the COVID-19 modRNA BIOWEAPON “vaccines”, to damage and/or cause dysfunction of the mitochondrial cells of the “vaccinated” person’s body, here: https://www.theqtree.com/2023/10/28/the-covid-19-virus-and-the-modRNA-covid-19-vaccines-induce-accelerated-aging/. Note: some of the linked URLs in this post may not work any more; for example, the paper by Peter S Rabinovitch, “Mitochondrial oxidative stress in aging and health span”, May 2014, is now found here: https://pubmed.ncbi.nlm.nih.gov/24860467/.

Yours Truly will again emphasize that the Hulscher, McCullough, et al., paper, quantifies and proves that multiple negative effects and outcomes of the COVID-19 modRNA BIOWEAPON “vaccines” can be detected in a “vaccinated” person’s body for over 3.5 years post-injection SO FAR. One firmly believes that the negative effects and outcomes of these “vaccines” can, and likely will, continue to manifest for many years, if not the entire lifetime, in the “vaccinated” person. It is likely that, as in the case of the Grover’s Disease that the patient in the cited paper was diagnosed with, there can be negative effects and outcomes that are permanent, with therapeutic approaches that include symptoms control and/or lifestyle-dietary changes as the only options for treatment. The presence of “Long COVID” may also be a permanent aspect in “vaccinated” persons; also controllable, but never completely eradicated from the body.

Those who lab-created the SARS-CoV-2 (COVID-19) BIOWEAPON virus itself worked for years to produce this virus. In a very real way, the word “virus” does not fully describe to this creation. Instead, it is a man-made, lab-created splicing together of bits and pieces of various animal coronaviruses, inventing something that would never have occurred naturally in the animal world.

Those who lab-created (and still are lab-creating) the COVID-19 BIOWEAPON “vaccines” — the modRNA versions, the DNA viral vector versions, and the “subunit protein” / “Inactivated” versions — use at least part of the Wuhan Hu1 SARS-CoV-2 (COVID-19) BIOWEAPON virus as the foundation for their injectables. This includes the “vaccine booster shots”, which use one or more Wuhan Hu1 “variants” as the foundation (Delta, Omicron, etc., all the way down through the “latest variant”, XFG.)

A chart of the “lineage” of the COVID-19 BIOWEAPON virus is here: https://www.cdc.gov/covid/php/variants/variants-and-genomic-surveillance.html. The source virus is the “Original Strain” at the far left of the chart image in this article. “Original Strain” = the Wuhan Hu1 original SARS-CoV-2 (COVID-19) virus. Below is a screenshot of this chart:

To date, over 70% of the population of the United States has taken at least one COVID-19 BIOWEAPON “vaccine” injection. Millions of people in the United States have taken multiple injections of these “vaccines.” The Medical Tsunami of negative effects and outcomes induced by these “vaccines” is ongoing. Unless there are complete, detailed, and sophisticated testing performed, as was done for the patient in the Hulscher, McCullough, et al., paper cited in today’s offering — the “fingerprints” of the damage induced by these “vaccines” are very difficult to trace.

Will every person who ever took an injection of BNT162b2 (or any of its “descendant clone vaccines” — the “latest COVID-19 booster vaccine” injection) — suffer the bodywide negative effects and outcomes that the patient in the Hulscher, McCullough, et al., paper, suffer? This is impossible to foretell. However, the potential for multiple negative effects and outcomes in the body (and brain) of a “vaccinated” person has now been proven to exist.

To be continued in Part Three.

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

THERE MUST BE ACCOUNTABILITY, JUSTICE, AND TRUTH.

Peace, Good Energy, Respect: PAVACA

Health Friday 2.6.2026 Open Thread: Pfizer-BioNTech COVID-19 modRNA “Vaccine” Negative Effects Proven Ongoing Over Three Years Post-Injection: Part One

The vintage image of 1955 Pfizer penicillin vaccine bottles is courtesy of Pond5 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 negative effects of the modRNA COVID-19 BIOWEAPON “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have suffered, and/or continue to suffer, injuries, illnesses, or disabilities induced by these “vaccines” that they took; and, to those who have passed away from the negative effects induced by these “vaccines” that they took.

Today’s offering is a further discussion of what Yours Truly brought to the board earlier this week, regarding the just-published paper by Nicolas Hulscher, MPH, Dr. Peter A. McCullough, MD, MPH, Wei Zhang, PhD, et al., which proves that the negative effects of the modRNA COVID-19 BIOWEAPON “vaccine” by Pfizer-BioNTech, BNT162b2, are detectable in the body of the “vaccinated” person over 3.5 years post-injection. It is impossible to overstate the profound importance of this paper.

The Focal Points story on the paper is here: https://www.thefocalpoints.com/p/breaking-vaccine-mrna-plasmid-dna, “BREAKING: Vaccine mRNA, Plasmid DNA, and Spike Protein Can Persist in Humans More Than 3.5 Years After COVID-19 Vaccination”, Nicolas Hulscher, MPH, 2 February 2026. Mr. Hulscher is one of the co-authors of this paper. Please see the screenshots from this article, below, from the summary of the paper; from the Case Presentation; from the discussion section; and, from the Conclusion:

The paper, published on the Zenodo preprint server, is here: https://zenodo.org/records/18460099, “Unprecedented Persistence of Vaccine mRNA, Plasmid DNA, Spike Protein, and Genomic Dysregulation Over 3.5 Years Post-COVID-19 mRNA Vaccination”. Nicolas Hulscher, MPH, Vanessa Schmidt, PhD, Michael Morz, MD, Claire Rogers, PA-C, Natalia von Ranke, PhD, Wei Zhang, PhD, John A. Catanzano ND, PhD, Peter A. McCullough, MD, MPH. 2 February 2026. Yours Truly urges interested readers to download or otherwise archive this paper — it is a prime target to be Retracted / Removed / Withdrawn, due to pressure on the publisher by Pfizer-BioNTech (PfizerUSA) and/or other Big Pharma or Big Government entities.

The 55-year-old male patient subject of the paper had taken the “primary series” of two injections (spaced out) of BNT162b2 in March 2021. By May 2021, he was starting to present with bodywide “vaccine”-induced symptoms; in October 2021, he presented at the Emergency Room with more serious symptoms. Per the paper, “Testing was limited”, and the symptoms were dismissed as due to “anxiety.” The next month, November 2021, the patient was back in the ER with much more serious cardiovascular symptoms, which required hospitalization.

The patient then took the BNT162b2 COVID-19 “original booster shot” in February 2022. It was shortly after this that his symptoms increased and became “widespread.” The patient had also developed severe anxiety. However, his symptoms were again attributed to the anxiety. It was not until April 2024, after a cardiac MRI was performed, that the patient was diagnosed with COVID-19 “vaccine”-compatible-induced myocarditis.

Yours Truly includes below a screenshot of the discussion in the cited paper of the severe anxiety that was induced by the negative effects of the BNT162b2 injections that the patient took. In Yours Truly’s opinion, this confirms what she has been writing on the board here for some time: that the modRNA COVID-19 BIOWEAPON “vaccines”, in addition to inducing bodywide negative physical outcomes, ALSO induce negative emotional/psychological outcomes. This is because the “vaccines” cross the Blood-Brain Barrier and attack the areas of the brain that regulate mood and emotional response (the pineal gland and the pituitary gland.) This is IN ADDITION to the fact that the modRNA COVID-19 BIOWEAPON “vaccines” DESTROY the natural RNA of the Uridine produced in the body (which assists in mood and emotions regulation, learning, and memory), replacing the natural RNA with the lab-created compound N1-Methylpseudouridine. Please see the screenshot, below:

Further information regarding how the modRNA COVID-19 BIOWEAPON “vaccines” negatively affect cognitive and emotional / psychological health is here: https://www.theqtree.com/2024/10/18/health-friday-10-18-2024-special-edition-neurological-effects-of-the-covid-19vaccines-physical-and-psychological/.

Yours Truly will focus on three BNT162b2-induced conditions that the patient was diagnosed with: Grover’s disease; mitochondrial damage; and, blood and cardiovascular damage. Today’s offering, Part One, will discuss Grover’s disease.

Grover’s disease (also called Grover’s Disease, Grover disease, or GD):

Please see the screenshot, below, from https://www.pcds.org.uk/clinical-guidance/grovers-disease-syn-transient-acantholytic-dermatosis1, “Grover’s disease (syn. transient acantholytic dermatosis”, The Primary Care Dermatology Society (UK; copyright 1994-2026):

Grover’s disease is a permanent condition. The symptoms can be controlled or managed; however, the eruptions will continue and can increase. Zabewski, Jr., et al., have described this situation, here: https://emedicine.medscape.com/article/1124347-treatment, “Transient Acantholytic Dermatosis (Grover Disease) Treatment & Management”. Edward J. Zabewski, Jr., DO, MBA, et al. Updated 25 November 2024. Please see the screenshot of this article, below:

What causes Grover’s Disease? Yale Medicine (https://www.yalemedicine.org/conditions/grovers-disease) has this to say:

**** However, there is another viewpoint regarding what may cause, or at least be involved in, Grover’s Disease: dysfunction of the IgA and IgG immune system cells of the patient’s body. Phillips, et al. describes this issue, here: https://doi.org/10.1111/exd.12266, “Is Grover’s disease an autoimmune dermatosis?”, Courtney Phillips, et al. 22 December 2013. Please the screenshots of the Abstract and of the Figure 1. from this paper, below:

Yours Truly has written extensively regarding the damage that the COVID-19 BIOWEAPON “vaccines” do to the IgG3 immune cells of the body (and to other types of Ig immune system cells of the body) on this board. Another source of information on this issue is here, from Dr. Jessica Rose, PhD: https://jessicar.substack.com/p/igg4-antibodies-induced-by-repeated, ” “IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein” “, 30 May 2023.

In Yours Truly’s opinion, at least part of the situation regarding Grover’s disease as a negative outcome from modRNA COVID-19 “vaccination” is that these injectables “imprint” on the body’s natural immune system — and, in multiple negative ways. Please see: https://www.thefocalpoints.com/p/immense-covid-19-vaccine-antigenic, “Immense COVID-19 ‘Vaccine’ Antigenic Sin Research Library Published”, Nicolas Hulscher, MPH, 13 January 2025. The paper referred to in the Hulscher article is here: https://zenodo.org/records/14632346 “COVID “vaccines” immune imprinting library.” Erik Sass, et al. 11 January 2025. Please see the screenshot from the opening statement of this paper, below:

Recall that the “original Wuhan strain” of the SARS-CoV-2 (COVID-19) virus itself is based on the SARS-CoV-2 virus “template” that was created by Dr. Ralph Baric, PhD, in his laboratory at the University of North Carolina, Chapel Hill. It was Dr. Baric who invented the concept of Synthetic Genomics — the lab-creation of chimeric viruses spliced together from pieces of gene codes from other viruses (https://www.jcvi.org/sites/default/files/assets/projects/synthetic-genomics-options-for-governance/Baric-Synthetic-Viral-Genomics.pdf. 2006.) It was Dr. Baric who invented the “seamless assembly” process of these virus code pieces — a process that he named, “No See-‘ms” (https://journals.asm.org/doi/epub/10.1128/jvi.74.22.10600-10611.2000, “Strategy for Systemic Assembly of Large RNA and DNA Genomes: Transmissible Gastroenteritis Virus Model.” Ralph Baric, et al. 15 November 2000. It was Dr. Baric who obtained a Patent for this process of lab-creating viruses (https://patents.google.com/patent/US7279327B2/ru, “Methods for producing recombinant coronavirus.” Ralph Baric, et al. Published 9 October 2007.) Please see https://theqtree.com/2026/01/09/health-friday-1-9-2026-open-thread-the-baric-files-part-four-ecohealth-alliance-wuhan-institute-of-virology-dr-zheng-li-shi-the-template-patent/ for further information.

**** Grover’s disease can be caused by COVID-19 virus infection. Grover’s disease can ALSO be caused by an autoimmune reaction induced by the modRNA COVID-19 BIOWEAPON “vaccines.” The paper which describes this is here: https://doi.org/10.1007/s00292-022-01126-9, “Dermapathology of COVID-19 infection and vaccination”, Fernandez-Figueras, MT. Journal Die Pathologie. 5 October 2022. (The article is partly in German, and partly in English.) Please see the screenshots (in English) from this paper, below: the Abstract; part of the section Cutaneous Side Effects; and, from the section Practical Conclusion:

Yours Truly will be “plain-spoken” regarding the following:

Look at the “layers” of illness, treatment pathways, and lifelong consequences of just ONE of the multitude of negative effects of the Pfizer-BioNTech COVID-19 BIOWEAPON “vaccine”, BNT162b2 — Grover’s disease. Look at the multitude of negative side effects that this injectable induced in ONE person — the patient described in the Hulscher, McCullough, et al., paper discussed above in today’s offering. Multiply this potential for numerous negative side effects in ONE person by the billions of persons who took BNT162b2 (or any of its “booster shots.”) What results is incalculable potential damage to billions of human bodies and brains.

**** It also needs to be emphasized that the Hulscher, McCullough, et al., paper discussed above in today’s offering describes the numerous negative side effects and other issues induced by BNT162b2 in ONE patient that cover ONLY the approximately 3.5 years after the patient took three doses of this “vaccine.” To this date, no one knows EXACTLY how long the modRNA COVID-19 BIOWEAPON “vaccines” will induce serious/negative side effects in the body and/or the brain of the “vaccinated” person; the Hulscher, McCullough, et al., paper proves that these negative side effects are detectable for as long as 3.5 years post-injection SO FAR.

What IS known is that these “vaccines” WILL change the DNA of the LINE1 human liver cell line; what IS known is that “vaccines” WILL destroy the RNA of the natural Uridine of the “vaccinated” person’s body, replacing it with a lab-created compound that has NO benefit (N1-Methylpseudouridine); what IS known is that these “vaccines” cross the Blood-Brain Barrier and attack cognitive and emotional centers of the brain; what IS known is that these “vaccines” contain the SV40 African Green Monkey cancer promoter-enhancer gene code piece. What IS known is that the Moderna modRNA COVID-19 BIOWEAPON “vaccine” also contains N1-Methylpseudouridine and the SV40 cancer promoter-enhancer gene code piece.

In Yours Truly’s opinion, based on her now-six years of combined researching and writing about the COVID-19 disaster — that ANY person or entity who is still “recommending”, let alone “mandating”, that people take ANY of the COVID-19 BIOWEAPON “vaccines” is complicit in the damage to humankind that these injectables induce. THERE IS NO BENEFIT FROM TAKING THE COVID-19 “VACCINES” — ANY OF THEM— THERE IS ONLY INCALCULABLE AND LIFELONG RISK, IN ADDITION TO THE POTENTIAL FOR INCALCULABLE SUFFERING OF THE HUMAN BODY, MIND, AND SPIRIT THAT THE NEGATIVE EFFECTS OF THESE “VACCINES” INDUCE.

To be continued in Part Two.

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

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

Intellectual Notice and Disclaimer: With the exception of published scientific papers and/or articles, and other sources found on the internet, the ideas and conclusions of today’s offering are by PAVACA. Proper credit must be given to PAVACA if ideas and/or conclusions in today’s offering are used by other blog writers; by podcasters; in social media; or, in print media.

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

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

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks of the COVID-19 disaster, Yours Truly dedicates it to all persons, of whatever age or location, who have suffered further illness, or injuries, or disabilities, from an infection of the COVID-19 virus itself, or from the COVID-19 “vaccines” they have in their bodies; or, who have passed away from complications related to an infection of the COVID-19 virus itself, or from issues induced from the COVID-19 “vaccines” they have in their bodies.

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for AI-generated content. There may be AI-generated content (images, text, etc.) in certain linked URLs in today’s offering. If readers wish to add AI-generated content to today’s discussion thread, they must identify it as such. Thank you.

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

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

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

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

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Some recent COVID-19 news:

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

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

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

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

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

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

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

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

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

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

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

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

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

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

References:

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

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

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

Health Friday 11.28.2025 Open Thread: Thanksgiving Season

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

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

Yours Truly is thankful that our gracious host, Wolf Moon, has established this blog to be a haven for truth; to be a place for honest discussion (and honest disagreement, too); to be a place for the sharing of life’s joys, and of life’s difficulties and sorrows; as a place for those who come to this Tree to encourage and support one another. One is grateful to be an author on this blog; grateful for all the other authors on this blog, including our gracious host; grateful for all who comment.

Yours Truly is grateful to those Pilgrims who came to Plymouth Rock, and to those earlier colonists who came to what is now the Commonwealth of Virginia (courtesy of our good Aubergine providing this latter knowledge), to establish a country based on freedom and on the Divine Providence of the Supreme Being: the country which became the United States of America. Yours Truly is grateful for her grandparents and great-grandparents who left their homes in England, Ireland, and Scotland, to come to the United States to make new lives for themselves, to marry, and to raise their children in this country.

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And, on the concept of gratefulness: Yours Truly is also grateful for one particular thing: the successful completion of the difficult, time-consuming (seven months long), physician-supervised process of “tapering-down the dose, then weaning off, leading to discontinuation” of the SSRI prescription drug that she had been taking, on and off, for six years. (SSRI = Selective Serotonin Reuptake Inhibitor.)

Yours Truly was put on this SSRI in February 2019, after being diagnosed with PTSD (Post-Traumatic [or, Posttraumatic] Stress Disorder) following the death of my late husband. Please see the screenshot below, from Psychiatry.org/, “What is Posttraumatic Stress Disoder (PTSD)?”, reviewed by Donald Egan, M.D., March 2025 [1]:

In Yours Truly’s case, the PTSD was one of “delayed onset”, meaning that the symptoms began to appear months after my husband’s death.

Anti-depressant drugs are routinely prescribed by healthcare professionals for persons who are diagnosed with PTSD. Below is a screenshot from the Cleveland Clinic regarding SSRIs [2]:

Note the phrase above regarding SSRIs – that “they tend to cause fewer and milder side effects compared to other options.” Let’s look at the side effects lists for the SSRI that Yours Truly had been taking, paroxetine (Paxil), from Drugs.com/ [3]. Paroxetine is available in several different formulations — tablet; oral suspension; extended-release tablet; and, capsule. The Mayo Clinic list of paroxetine‘s brand names is: Brisdelle; Paxil; Paxil CR;, and, Pexeva [4].

How can any of the side effects listed above be called “fewer and milder”? Let’s take a look at only one of the side effects lists of paroxetine from Drugs.com/, from the For healthcare professionals section [5]:

The For healthcare professionals section lists of paroxetine side effects includes eighteen different areas, from General to Endocrine, that have adverse reactions and/or side effects from the use of this drug. Literally every organ or function of the human body is interfered with, and/or could be damaged by, paroxetine use. How can any of this be described as “fewer and milder” side effects?

Dr. Robert Malone, MD, penned a recent blog article, “Well Being: Selective Serotonin ReUptake Inhibitors (SSRI)”, regarding the routine prescribing of SSRIs by physicians [6]. Please see the screenshots, below, from his article:

A Midwestern Doctor, in their blog, has written extensively regarding the dangers of SSRIs; the multiple marketing and other ploys used to acclimate physicians to prescribing them, and patients to take them; and how difficult it is to follow the process of taper down the dose, wean off the drug, and have it finally discontinued. The following screenshots are from these articles: first, “The Dark Side of Antidepressants”, of 24 January 2025 [7]. Note: Some of the articles from A Midwestern Doctor are accessible in the entirety only if the reader subscribes (for free); and/or becomes a paying subscriber.

Then, from their article, “The Hidden Dangers of Antidepressants and Why They’re So Hard To Stop Taking”, [8] 9 February 2025:

And, from their article, “”Why Are Antidepressants So Harmful?”, [9] 26 November 2023:

Yours Truly was fortunate so have been able to get the taper down – wean off – discontinue process successfully completed (as regards stopping the taking of paroxetine) in about six months. However, the “wiring” of one’s brain to accept this SSRI and allow it to operate within the brain began in early 2019, when I was put on the drug by the PCP after diagnosis of PTSD. Thus, even with the discontinuation of the physical process of taking the drug, the “rewiring” of the brain back to pre-use of the drug is ongoing. One already feels much better since the “endemic physical effects” of the drug have ceased. One has also made a decision to never take another psychotropic drug.

What has helped Yours Truly to make real progress in “rewiring” the brain after the paroxetine discontinuation process was completed? A daily program that includes:

Probiotics (this includes yogurt)

Vitamin D, 2500IU

Vitamin C, 3000mg

Walking and free-weights exercise

Exposure to sunshine

Being well-hydrated

Cutting sugar, cutting simple carbohydrates, replacing them with complex carbohydrates, and using very little honey as a sweetener

Eating meat, eggs, and fish, rotating these during the week

Eating more green vegetables

Journaling — meditating — connecting with the Divine

Getting out and doing things — being with family; walking the dog; working in the yard

Reducing / eliminating stressors to the extent possible

Attitude — one is absolutely determined to “rewire” the brain back to pre-SSRI

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Let’s take a look at serotonin, the crucially important element that the human gut makes — and which is the “target” of SSRIs. Below are screenshots from the 2022 Cleveland Clinic article, “What is serotonin?” [10]:

And, regarding the “gut-brain axis”, an article, “That gut feeling”, Dr. Siri Carpenter, [11] 1 September 2012, a screenshot from which is below:

Yours Truly does not fault the physician who started one on paroxetine in early 2019, nor the physician-therapist who continued the drug until I had had enough of the side effects by September 2024 and requested to go through the process to taper down — wean off — discontinue the drug. They were following conventional medical “recommendations.” However, Yours Truly, by the late summer of 2024, had also done enough research to understand that SSRIs are dangerous and addictive, that the decision to request going through the process was what had to be done. How many people taking SSRIs do the research necessary to understand what these drugs are doing to their bodies and their brains? Why don’t physicians who prescribe SSRIs (or, indeed, any psychotropic drug) caution the patient that there are multiple and potentially serious side effects and/or adverse reactions to these drugs? Why don’t physicians make it their business to ensure that, unless there is clear indication that the patient needs a higher dose, to start the patient on the lowest possible dose of an SSRI, and at the the first indication that the patient is having real trouble with side effects and/or adverse reactions, to begin the process of taper down — wean off — discontinue the drug; while, at the same time, ensuring that the patient starts or continues therapeutic counseling and healthy lifestyle changes? Similarly, why don’t physicians make it their business to ensure that, there is clear indication that the patient needs a higher dose of an SSRI drug, to start and keep the patient on the lowest possible dose?

The human gut is where over 90% of the body’s serotonin is produced. The human brain produces 10% or less of the body’s serotonin. Because of the “gut-brain axis” system in the body, serotonin produced in the gut “travels” to the brain via the bloodstream. Why aren’t physicians trained in the nutritional knowledge necessary to counsel patients with emotional/psychological issues to eat foods that would assist in proper and healthy serotonin production — foods such as, salmon, eggs, cheese, nuts, and turkey? Why don’t physicians realize that taking SSRI drugs actually block the normal “gut-brain axis travel” of serotonin to the brain — leaving the brain with only a small amount of serotonin; and which low level of serotonin is targeted by SSRI drugs? [12]

Yes, there are circumstances in which a physician makes the decision that the emotional/psychological issues of the patient warrant the need for that patient to take an SSRI. However, Yours Truly believes that, in addition to the SSRI, the patient needs to be counseled to eat foods that will help the gut produce healthy serotonin in proper amounts, to get out into the sunshine, to move their body, to get restful sleep, to have therapeutic psychological counseling if necessary; and, to understand that what they’re experiencing isn’t just “all in their head” — it’s also “that gut feeling.”

Peace, Good Energy, Respect: PAVACA

References:

[1]: “What is PTSD?”. https://www.psychiatry.org/patients-families/ptsd/what-is-ptsd. Reviewed by Donald Egan, M.D. March 2025.

[2]: “SSRIs (Selective Serotonin Reuptake Inhibitors.” https://.my.clevelandclinic.org/health-treatments/24795-ssri. Last reviewed on 09/26/2025 by Cleveland Clinic.

[3]: “Paroxetine side effects.” https://www.drugs.com/paroxetine.html#side-effects.

[4]: “Paroxetine – oral route.” https://www.mayoclinic.org/drugs-supplements/paroxetine-oral-route/description/drg-20067632.

[5]: “Paroxetine – side effects. For healthcare professionals.” https://www.drugs.com/sfx/paroexetine-side-effects.html.

[6]: “Well Being: Selective Serotonin ReUptake Inhibitors (SSR).” https://www.malone.news/cp/179662213. 12 November 2025.

[7]: “The Dark Side of Antidepressants.” https://www.midwesterndoctor.com/p/the-dark-side-of-antidepressants. 24 January 2025.

[8[: “The Hidden Dangers of Antidepressants and Why They’re So Hard To Stop Taking.” https://www.midwesterndoctor.com/p/the-hidden-dangers-of-antidepressants. 9 February 2025.

[9]: “Why Antidepressants Are So Harmful?” https://www.midwesterndoctor.com/p/why-are-antidepressants-so-harmful. 26 November 2023.

[10]: “What is serotonin?” https://my.clevelandclinic.org/health/articles/22572-serotonin. Last reviewed on 03/18/2022.

[11]: “That gut feeling.” https://www.apa-org/monitor/2012/09/gut-feeling. Dr. Siri Carpenter, PhD. 1 September 2012.

[12]: “Chronic SSRI Treatment Exacerbates Serotonin Deficiency in Humanized Tph2 Mutant Mice.” William B. Siessner, et al. https://doi.org/10.1021/cn300127h. 1 October 2012.

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

Health Friday 11.14.2025 Open Thread: What’s Going on at Pfizer-BioNTech?: Part Two

The header image of vintage Pfizer vaccine vials for 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 modRNA COVID-19 “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have passed away from the negative effects of these “vaccines” that they had in the 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 items that are linked in the post. If readers wish to post AI-generated content to today’s discussion thread, they must cite their source. Thank you.

Please refer to Part One of this two-part set, found here: https://www.theqtree.com/2025/11/07/health-friday-11-7-2025-open-thread-whats-going-on-at-pfizer-biontech-part-one/, regarding recent activities of PfizerUSA (also known as Pfizer), the United States-based co-partner of Pfizer-BioNTech. Today’s presentation will discuss some of the activities of the other co-partner, Germany-based BioNTech. Of necessity, some of today’s presentation will include items related to Pfizer (PfizerUSA.)

The current “pipeline” for the BioNTech product line is found here: https://www.biontech.com/int/en/home/pipeline-and-products/pipeline.html. The full PDF of the “pipeline” is found here: https://www.biontech.com/content/dam/biontech-corporate/global/pdf/home/pipeline-and-products/pipeline/assets/BioNTech-Clinical-Pipeline-EN-Q3.pdf, “Status: November 3, 2025.” A screenshot of the Infectious Diseases section of this pipeline is below:

Note the Collaborator / Partner listings on the far right of the image. There are two entities involving Bill Gates: the Gates Foundation; and, CEPI. There are two mentions of Pfizer (also known as PfizerUSA.) There is one mention of the University of Pennsylvania. Note also the BioNTech rights listings: the company fully owns the mRNA (modRNA) “vaccines” under development for Tuberculosis, for Malaria, and for Monkeypox (Mpox.) More on the Fosun Pharma collaboration / partnership will be presented further below in today’s post.

It appears that the modRNA-based “combo vaccine” for COVID-19 + influenza, also known as either BNT162b2 + BNT161, or as tozinameran + famtozinameran, is actually being developed and tested by BioNTech, with PfizerUSA (Pfizer) as a kind of “stand-by” or “silent” co-partner. Please see the screenshots below, from registered clinical trials information, per https://clinicaltrials.gov/:

**** NONE of these clinical trials have a true Control Group (study subjects injected with a plain saline solution “placebo vaccine.”)

BioNTech is ALSO working on a “new” version of of the modRNA COVID-19 “vaccine”, BNT162b2. However, the only BioNTech listing is this: https://clinicaltrials.biontech.com/trials/C4591076, which “translates” to the NCT07069309 clinical trial referenced above. “C459” is the prefix for Pfizer-BioNTech clinical trials for their modRNA COVID-19 “vaccines” — for example, the huge C4591001 original clinical trial for BNT162b1 / BNT162b2 / BNT162b3, from which BNT162b2 was the “vaccine candidate” chosen by the company in the late summer/early fall of 2020 to proceed through the Emergency Use Authorization applications in the United States and in the EU / Scandinavia.

The question Yours Truly has regarding the “new COVID-19 “vaccine candidate” being used in NCT07069309: Is this “new COVID-19 vaccine candidate” ALSO being used in the clinical trial NCT06821061, also listed above? The modRNA COVID-19 “vaccine” called Investigational COVID-19 Vaccine per the Researcher View of NCT06821061?

Gentle reader, does one see how this aspect of the modRNA “vaccine” game works? BioNTech (the co-partner of PfizerUSA/Pfizer) comes up with a “new vaccine candidate” for COVID-19 — a “new vaccine candidate” which, in reality, is for the current circulating virus variant, LP.8.1. — and appears to use it it as an Investigational COVID-19 Vaccine in one clinical trial (NCT068210161): while, at the same, time, also using this same injectable in another clinical trial (NCT07069309)? How many study subjects in either clinical trial were told of this?

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And now, a dive into the “collaborators”, and what may be termed “the other partners”, the “investments partners”, and other entities that are involved with Pfizer-BioNTech, either with PfizerUSA(Pfizer), or with BioNTech. Yours Truly begins with the “active partners” list of PfizerUSA (Pfizer): https://www.pfizer.com/partners/venture-investments/our-portfolio. Below is a screenshot from this article regarding one of these “venture investments partners” — Saama:

What the above article does not mention is the fact that PfizerUSA (Pfizer), along with a group of other healthcare entities, acquired a majority stake in Saama back in October, 2021: https://carlyle.com/media-room/news-release-archive/carlyle-and-leading-healthcare-focused-venture-funds-announce-investment-saama, 20 October 2021. A screenshot from this article is below:

On the other hand, PfizerUSA (Pfizer), wanting to enter more fully into the weight-loss drug marketplace, began acquisition talks with a company called Metsera in August 2025. Metsera is developing a GLP-1 based weight-loss drug, MET-097i, a GLP-1 drug. GLP-1 drugs (Glucagon-like Peptide 1) drugs are designed to lower blood sugar in people taking them, thus (theoretically) leading to weight loss. However, another company, Novo Nordisk, also wanted to acquire Metsera, and, at one point, was working on an “agreement in principle” with the company. This led to a “battle of offers” for Metsera between Pfizer and Novo Nordisk, leading to a lawsuit filed by Pfizer on 1 November 2025 against Metsera and against Novo Nordisk’s offers to Metsera (https://sbj.net/stories/pfizer-sues-metsera-novo-nordisk,101765, Springfield Business Journal, 3 November 2025.) It also appears that Pfizer possibly contacted the United States Federal Trade Commission about the situation — with the result that Novo Nordisk backed away due to a letter sent to the company by the FEC; and, Pfizer, then having the “green light”, could move forward with the acquisition deal for Metsera (https://www.fiercebiotech.com/biotech/pfizer-beats-out-novo-10b-agreement-buy-metsera, Eric Sagonowsky, 8 November 2025.)

Gentle reader, does one see how this aspect of the game is played? It appears that PfizerUSA (Pfizer) gets the United States Federal Trade Commission involved in blocking a deal that a rival company (Novo Nordisk) is working on, in order for Pfizer to acquire the target company?

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Meanwhile, what of the “collaborators” and “partners” with BioNTech, other than their co-partner, PfizerUSA (Pfizer)? Following is a “snapshot” of this situation:

BioNTech and CEPI (Gates Foundation) are “partnered” in expanding mRNA “vaccine” research, development, and manufacturing, in Kigali, Rwanda: https://cepi.net/biontech-and-cepi-expand-partnership-strengthen-africas-mrna-vaccine-ecosystem, 28 May 2024. A screenshot of the summary from this article is below:

This article emanated from Mainz, Germany, and Oslo, Norway.

**** Note also the use of a new term: “mRNA vaccine ecosystem.” Gentle reader, does one see how this aspect of the game is played? First, create the “problem” (the COVID-19 virus); Second, create the “solution” (modRNA COVID-19 “vaccines”); Third, convince / coerce / frighten / gaslight, billions of people into taking this unproven gene-therapy technology; Fourth, create an “mRNA vaccine ecosystem” in which endless types of mRNA-based / modRNA-based “vaccines” are created and administered to the convinced / coerced / frightened / gaslighted, billions of people as part of the “mRNA vaccine ecosystem”, with the underlying “passive-aggressive threat” of “people must take these “vaccines”, otherwise they would likely get very sick and/or die”.

Yours Truly now turns to the “partnership” between BioNTech and the Communist China-based pharmaceutical company, Fosun Pharma.

Fosun Pharma, also known as Shanghai Fosun Pharmaceutical (Group) Co., Ltd., was founded in 1994. The company has since “spun off” into other related entities, such as Fosun International, and https://fosunpharmausa.com/. Lest there is any doubt that the Chinese Communist Party holds a significant stake in Fosun Pharma, please see this: https://en.fosun.com/Upload/File/202104021739947_5055.pdf, “Corporate Social Responsibility Report – Fosun”, for the year 2012. A graphic from Page 11 of this report is below:

The Wikipedia entry on Fosun Pharma is here: https://en.wikipedia.org/wiki/Fosun_Pharma.

However, it also appears that Guo Guangchang, founder and chairman of Fosun International, has run afoul of the Chinese government at least twice. He “disappeared” in 2015 and in 2017, only to “resurface” after what appears to have been detention and interrogation (for the 2015 “disappearance”, at least) by Chinese authorities: https://variety.com/2015/biz/asia/missing-chinese-executive-released-1201660214/, Patrick Frater, 13 December 2015.

Fosun Pharma and BioNTech went into partnership regarding the development and distribution of BNT162b2 in Communist China. Please the screenshot from the Wikipedia entry regarding this, below:

Please refer also to the BioNTech “pipeline” graphics further above in today’s offering. Fosun Pharma is listed in the Infectious Diseases section as Collaborator / Partner with BioNTech regarding the development and distribution of the modRNA COVID-19 “vaccine” BNT162b2 (now known as COMIRNATY.)

The Fierce Pharma story regarding the Fosun Pharma – BioNTech “partnership” and BNT162b2 is here: https://www.fiercepharma.com/manufacturing/biontech-fosun-pharma-eye-1b-doses-covid-19-vaccine-capacity-new-china-jv, Angus Liu, 10 May 2021. A screenshot from this article is below:

In addition, Fosun Pharma is also “partnering” with PfizerUSA (Pfizer) in the manufacture of a generic form of Paxlovid (owned by Pfizer) for international use: https://medicinepatientpool.org/story-post/fosun-pharmas-global-impact-expanding-access-to-covid-19-treatments-and-beyond-through-voluntary-licensing-with-mpp, 22 November 2024. This sublicense agreement with Medicine Patient Pool (MPP) was signed in March 2022. MPP is, in turn, a division of Unitaid (https://unitaid.org/.) More information regarding MPP is here: https://medicinepatientpool.org/who-we-are/about-us.

Gentle reader, does one see how this aspect of the game is played? The Big Pharma company “creates partnerships” or “sublicensing agreements” with other companies around the world to push the drugs and / or “vaccines” that the Big Pharma company creates and manufactures. Smaller pharmaceutical companies; alternative treatment entities and their products; other avenues of treatment opportunities — are left out / choked off / minimized.

The 2024 salary of Dr. Ugur Sahin, MD, CEO of BioNTech: $287 million dollars.

The 2024 salary of Dr. Albert Bourla, DVM, CEO of PfizerUSA (Pfizer): $24.6 million dollars.

Per: https://www.fiercepharma.com/special-reports/big-pharmas-10-highest-paid-ceos-2024, 16 June 2025.

Meanwhile, the Medical Tsunami of documented modRNA COVID-19 “vaccine”-induced or aggravated illnesses, injuries, or disabilities, among those who took / take these “vaccines”, rolls on. Meanwhile, the Medical Tsunami of documented modRNA COVID-19 “vaccine”-induced or related deaths among those who took these “vaccines” rolls on.

All persons — COVID-19 “vaccinated” or not — need to be following some type of SARS-CoV-2 spike protein detox / mitigation protocol. All persons — COVID-19 “vaccinated” or not — need to keep their immune system in the best shape possible.

All modRNA COVID-19 “vaccines” 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 Notice: With the exception of linked articles and/or scientific papers that are available online, the ideas and conclusions in today’s offering are by PAVACA. Proper credit must be given to PAVACA for any other blog writer, podcaster, or social media outlet, in using the ideas or conclusions in today’s offering.)

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?

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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.)