Tag: COVID-19 “vaccines”

Health Friday 4.24.2026 Open Thread: The COVID-19 Bioweapon “Vaccines”: Why Are They Still In Use?, Part One: Pfizer-BioNTech (COMIRNATY)

The vintage image of a vaccination record from 1867 for today’s offering header is courtesy of iStock and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. There are Important Notifications from our host, Wolf Moon; theRules 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 content in today’s discussion thread, they must cite their source. Thank you.

Today’s offering begins here: https://icandecide.org/wp-content/uploads/2022/03/125742_S1_M2_26_pharmkin-tabulated-summary.pdf, “MODULE 2.6.5 PHARMACOKINETICS TABULATED SUMMARY“, FDA Approved on 21 January 2021 at 23:22 GMT (Greenwich Mean Time.) This is the report regarding biodistribution data of the Pfizer-BioNTech modRNA COVID-19 bioweapon “vaccine”, BNT162b2, for which the FDA had granted the initial EUA (Emergency Use Authorization) for use in the United States on 11 December 2020. The experiments performed by Pfizer-BioNTech to produce the report, using BNT162b2 injections, were conducted on Wistar Han lab rats, Sprague Dawley lab rats, Cynomologus monkeys, and human liver microsomes and liver fractions. Data were extracted from in vivo and from in vitro results. The formulation of BNT162b2 used in the experiments was the same as that which was granted the FDA Emergency Use Authorization of 11 December 2020 for use on human beings in the United States.

Yours Truly presents images of page 7 and page 8 of this report:

Note: the above data are the results from the injections given to the Wistar Han lab rats. Note also the accumulations of the lipid nanoparticles (LNPs), ALC-0159 and ALC-0315, used in the BNT162b2 formulation. Again, this is the same formulation that was granted the initial FDA Emergency Use Authorization on 11 December 2020, for BNT162b2 to be used on human beings in the United States. LNPs are the tiny fat molecules-based, lab-created “delivery system” that encases the “vaccine” ingredients to protect them from being detected and eliminated by the natural immune system of the body. Instead, the LNPs facilitate the entry of the “vaccine” into every cell of the body. Look at the highest accumulation amounts:

Adrenal Glands: 18.2. The adrenal glands release hormones, such as, adrenaline, directly into the bloodstream. These glands are crucial in the proper function of blood pressure and the body’s stress response. https://my.clevelandclinic.org/health/body/23005-adrenal-glands

Injection Site: 165. The injection of COMIRNATY into the arm of a human being results in the following: The body immediately sends “alarm signals” that there is an “enemy invader”, and starts the natural immune system process of fighting it / eliminating it. This is manifested in several ways, including: pain at the injection site, and/or a “rash” at the injection site. However, these immediate reactions can also indicate early-warning signals of anaphylactic shock — and must be closely monitored. Establishment Medicine explains this away by, first, stating that this reaction is “rare”, then proceeding to minimize the situation: https://ubiehealth.com/doctors-note/rash-after-covid-vaccine-causes-serious-warning-49121exp1, “Why do some people get a rash after the COVID vaccine and when is it serious?”, Yoshinori Abe, MD, 17 December 2025. This situation is called “COVID Arm.” In fact, Establishment Medicine minimizes “COVID Arm” reaction even if it occurs DAYS or a WEEK after “vaccination”: https://medlineplus.gov/ency/imagepages/19970.htm. “Arm Rash After COVID-19 Vaccination”, updated by Linda J. Vorvick MD, 1 January 2025.)

Liver: 24.3. This incredibly important organ performs five hundred different functions in the body to maintain health. https://www.michiganmedicine.org/health-lab/what-does-the-liver-do-and-how-do-i-keep-mine-healthy

Ovaries: 12.3. The female ovaries make and release eggs for fertilization. They also produce hormones. At birth, a female has all the eggs that she will ever have. The ovaries constantly “communicate” with the brain. https://axiawh.com/resources/5-things-you-didnt-know-about-your-ovaries/

Spleen: 23.4. The spleen creates white blood cells and stores red blood cells. It helps to regulate blood platelets (which assists in proper blood clotting.) It filters out old or damaged blood cells. https://www.healthline.com/health/what-does-the-spleen-do

The above report, in Yours Truly’s opinion, needs to be required reading for any healthcare professional who is still “recommending”, let alone administering, COMIRNATY. And, in case a healthcare professional raises objections, such as, “The new COMIRNATY formula is different”, the facts that ALC-0159, ALC-0315, N1-Methylpseudouridine (all which were in the original BNT162b2 formulation), and the S1 spike protein (that can be traced back to the original Wuhan Hu1 SARS-CoV-2 strain) are ingredients in the “2025-2026 COMIRMATY” version of the injectable.

There is a reason behind why the accumulations of ALC-0159 and ALC-0315 are so high for the above body areas and organs: these lipid nanoparticles ensure that the ingredients and mechanisms of COMIRNATY enter these areas and organs: with the result that said areas and organs are interfered with, and/or damaged, and/or that the body’s ability to properly use them is destroyed. Example: over 60% of the lifetime supply of a female lab rat’s eggs are either damaged or destroyed due to it being “vaccinated” with COMIRNATY: https://www.thefocalpoints.com/p/breaking-covid-19-mrna-shots-destroy, “BREAKING: COVID-19 mRNA Shots Destroy Over 60% of Female Non-Renewable Egg Supply”, Nicolas Hulscher, 9 May 2025. If this is what happens with female Wistar lab rats being injected with these “vaccines”, the potential for damage to human female eggs is ALSO THERE: and, in fact, the Manniche, et al., study demonstrates this: https://www.preprints.org/manuscript/202504.2487/v1, “Rates of Successful Conceptions According to COVID-19 Vaccination Status: Data from the Czech Republic”, Vibeke Manniche, et al., 29 April 2025. Note: this paper is a preprint — therefore, it can be Removed, Retracted, or Withdrawn at any time. Yours Truly urges interested readers to download or otherwise archive this paper.

Before leaving the discussion of ALC-0159 and ALC-0315, please see the following images from the MSDS Safety Sheets for these lipid nanoparticles, below. First, from https://cdn.caymanchemical.com/cdn/msds/34336m.pdf, for ALC-0159:

And, from https://cdn.caymanchemical.com/cdn/msds/34337m.pdf, for ALC-0315:

Note that both compounds are for research only. In fact, both compounds rate as a carcinogen (ethanol content.) In particular, the Cayman Chemcial MSDS for ALC-0315 reads like a textbook example of a very dangerous compound.

**** Note from the images of Page 7 and Page 8 above, that BNT162b2 crosses the Blood-Brain Barrier, as seen in the accumulation data images above: the “vaccine” accumulates in the Brain and in the Pituitary Gland. In addition, there is BNT162b2 accumulation in the Skin and in the Kidneys — this indicates that the “vaccine” ingredients can be “shed” from the skin and/or excreted via the kidneys into urine.

The Appendix 1: List of Adverse Events of Special Interest section of this report about BNT162b2, also given to the FDA by Pfizer-BioNTech (April 2021) has the reports listings of over 1,200 serious / fatal side effects induced by this “vaccine.” The report is found here: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021“, FDA date-stamped 30 April 2021 at 09:26 GMT. This, in Yours Truly’s opinion, also needs to be required reading for any healthcare professional who is still “recommending”, let alone administering, COMIRNATY.

The COVID-19 bioweapon “vaccines” are actually gene-altering injectable therapies: they are not, strictly speaking, vaccines. Please see: https://academic,oup.com/intimm/article/33/10/521/6194108, “Development of COVID-19 vaccines utilizing gene therapy technology”, Hironori Nakagami, 27 March 2021. Every single person who has ever taken an injection of COMIRNATY has had a gene-altering therapy “cocktail” (under the guise of “it’s a vaccine”) injected into their body: something that “vaccinated” persons were never told about, nor for which they never explicitly granted permission to have put into their body.

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HHS Secretary Robert F. Kennedy, Jr., is not being allowed to do his job — and, in fact, to quote another blog writer, he is being “muzzled.” The COVID-19 bioweapon “vaccines” have been, via the American Academy of Pediatrics lawsuit and subsequent “ruling” by Federal Judge Brian E. Murphy, are now fully back into the CDC Childhood Immunization Schedule. The new nominee to head the CDC, Dr. Erica Schwartz, is an Establishment Medicine “vaccine” proponent: https://aaronsiri.substack.com/p/the-queen-of-mandating-vaccines, 18 April 2026. A screenshot from this article is below:

Please also see: https://www.2ndsmartestguyintheworld.com/p/iatrocide-by-design-rfk-jr-bombshell, “Iatrocide by Design: RFK Jr. Bombshell: “They had to DESTROY Ivermectin and Hydroxychoroquine…” “, 23 April 2026. A screenshot from the latter article is below:

The linked tweet from the above article:

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

THERE MUST BE MUCH MORE RESEARCH INTO THESE DELIVERY PLATFORMS, WITH EXTENSIVE TESTING AND DATA ANALYSES, AND WITH THE RESULTS BEING MADE PUBLIC.

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

Peace, Good Energy, Respect: PAVACA

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

Health Friday 4.10.2026 Open Thread: Some Interesting Links

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

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

Some Interesting Links:

Regarding the November 2025 exposure of an employee at the Rocky Mountain Lab (part of the NIH) to the Crimean-Congo Hemorrhagic Fever virus. The virus is being experimented on at this facility. Our good Aubergine posted a comment on this situation, which began a discussion: https://theqtree.com/2026/04/03/health-friday-4-3-2026-open-thread-where-the-focus-needs-to-be-now-an-opinion-piece/#comment-1595800. It has been proven that this virus does indeed shed; the shedding can be present in the body secretions and blood of the exposed / infected person. The published paper regarding shedding of Crimean-Congo Hemorrhagic Fever virus is here: https://pmc.ncbi.nlm.nih.gov/articles/PMC7078823/, “Monitoring Crimean-Congo haemorrhagic fever virus RNA shedding in a body secretions and serological status in hospitalized patients, Turkey, 2015.” Dilek Yagci-Caglayik, et al. 12 March 2020. (Yours Truly: While the paper is about the shedding of this virus in hospitalized patients, it, in my opinion, opens up the possibility that the virus can shed from non-hospitalized exposed or infected persons.)

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In Maryland, if a newly-proposed law there comes into effect, pharmacists will be able to order certain “vaccines” for patients; while, at the same time, placing the names of those persons into the Maryland state database for immunization tracking: https://jonfleetwood.substack.com/p/maryland-bill-lets-pharmacists-order, “Maryland Bill Lets Pharmacists Order Vaccines for You — Logging Your Name in State Tracking System Without Any Patient-Request Requirement”, 3 April 2026. A screenshot from this article is below:

Note that this bill regards pharmacists being granted permission to order vaccines — and to do so without the patient’s knowledge, consent, or request. The name of the patient is put into a state tracking database. The vaccines are paid for by private insurance (if the patient’s private insurance information is on file at the pharmacy), or are covered by Medicare/Medicaid. This opens up the potential for both the pharmacy and the state to “keep tabs” on the patient in order to get “vaccine compliance” from the patient.

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Why hasn’t James Lloyd Austin, III, Secretary of Defense under former “President” Joe Biden, been held to account for his “mandating” over 90% of United States military personnel being “vaccinated” with modRNA COVID-19 bioweapon “vaccines”? https://www.thefocalpoints.com/p/breaking-study-half-of-covid-19-vaccinated, “BREAKING STUDY: Half of COVID-19 Vaccinated Military Personnel Suffered Subclinical Heart Stress”, Nicolas Hulscher, MPH, 31 March 2026. The paper cited in the article is here: https://doi.org/10.1016/j.vaccine.2026.128535, “Transient elevation of NT-proBNP after mRNA COVID-19 vaccinations in healthy adults: A longitudinal biomarker analysis.” Pavel Dlouhy, et al. 30 April 2026.

Note that this paper studies heart issues that appeared in 50% of 83 healthy, adult military personnel after their being “vaccinated” with either BNT162b2 (Pfizer-BioNTech) or with mRNA-1273 (Moderna.) The military personnel were stationed at the Air Transportation Base Facility in Prague, Czech Republic. The troponin levels of their hearts were found to have gone up. Elevated troponin levels in the heart indicate stress on the heart muscle. Elevated troponin levels can indicate heart problems even if there are no overt symptoms. If that is what occurred in half of the “vaccinated” personnel tested at an air transportation base in the Czech Republic, how many thousands of United States military personnel potentially had the same effect after they were “mandated” to be “vaccinated” by former Defense Secretary Austin? (Austin was the former Secretary of what is now called the Department of War.)

Note also that the military personnel at the air transportation base in Prague were well over the age of 17 — in fact, the mean age of the 83 tested personnel was 39 years. This blows clean out of the water ALL of the claims of Big Pharma, Establishment Medicine, the CDC, the FDA, the AMA, and many other entities, that heart problems associated with COVID-19 “vaccination” are “rare” —and, are “confined mostly to persons between the age of 12 and 17 years.”

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Another example of how a physician who stood up against Big Pharma, the CDC / FDA, the AMA, and the AAP (American Academy of Pediatrics), was persecuted: his License to Practice Medicine in his home state (Oregon) was suspended in 2020; then, his License to Practice Medicine was revoked in the state where he had been credentialed (Washington State); then, his board credentials in the AAP were revoked; then, he had to surrender his License to Practice Medicine in Oregon in 2022 (https://omb.oregon.gov/Clients/ORMB/Public/VerificationDetails.aspx, effective 5 December 2022.) This was the journey of Dr. Paul Thomas, a highly-respected pediatrician: https://www.2ndsmartestguyintheworld.com/p/doctor-published-study-showing-vaccinated, “Doctor Published Study Showing Vaccinated Children Have 500% Increase In Chronic Diseases Only To Have License Suspended & Get Cancelled By BigPharma”, 8 April 2026. The study was Retracted by MDPI, the preprint publisher. It is available here: https://www.researchgate.net/publications/346088816_Relative_Incidence_of_Office_Visits_and_Cuulative_Rates_of_Billed_Diagnoses_Along_the_Axis_of_Vaccination. James Lyons-Weiler, Paul Thomas. 22 November 2020. (Yours Truly: Note that this paper was accepted and peer-reviewed before it was published.)

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Dr. Peter A. McCullough addresses the nexus among cancer patients who then get COVID-19 “vaccinated” and thereupon afterwards present with symptoms of Long COVID: https://www.thefocalpoints.com/p/the-hollow-promise-of-protection, 7 April 2026. A screenshot from this article is below (access to the entire particle is for subscribers only):

The paper cited in the above article is here: https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2847136. “Postacute Sequelae Following Omicron COVID-19 in Patients With Cancer.” Ling En Wee, MPH, et al. 31 March 2026.

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A related topic to the heart issues situation found in the military personnel at the air transportation base in Prague who had been COVID-19 “vaccinated”: This one regards subclinical myocarditis/pericarditis in COVID-19 “vaccinated” persons: https://www.thefocalpoints.com/p/breaking-peer-reviewed-paper-finds, “BREAKING: Peer-Reviewed Paper Finds mRNA “Vaccines” Convey Silent Heart Damage—Presents Approach to Diagnosis and Management”, Nicolas Hulscher, MPH, 31 December 2025. A screenshot from this paper is below:

The paper is found here: https://doi.org/10.1810/mra.v13i11.7078, “COVID-19 Vaccine-Induced Subclinical Myopericarditis: Pathophysiology, Diagnosis, and Clinical Management.” Peter A. McCullough, MD, MPH, M. Nathaniel Mead, MSc, PhD, Nicolas Hulscher, MPH. 30 November 2025.

Yours Truly: The above paper speaks to subclinical myocarditis/pericarditis in COVID-19 “vaccinated” persons — and makes it clear that, although many of the reported cases were found in “vaccinated” males under age 21, there were cases found in other “vaccinated” persons (male and female), and in other age groups. On the other hand, there is also the real phenomenon of “vaccine” shedding from “vaccinated” persons onto others, including onto non-COVID-19 “vaccinated” persons. Who knows how many non-COVID-19 “vaccinated” persons (including children) have been exposed to the ingredients and mechanisms of these “vaccines” that induce heart problems? At the same time, there are other factors that need to be considered when talking about what engenders or aggravates heart issues. Examples of other factors can include, but are not limited to: chronic stress; hypertension; family history of / predisposition to, heart disease; and, COPD (https://www.ummhealth.org/health-library/copd-and-heart-disease.)

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.

ALL GAIN-OF-FUNCTION ACTIVITIES IN THE UNITED STATES MUST BE STOPPED, NOW.

ALL COVID-19 BIOWEAPON “VACCINES” MUST BE PULLED OFF THE MARKET AND REMOVED FROM USE IN THE UNITED STATES, NOW.

Peace, Good Energy, Respect: PAVACA

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 3.13.2026 Open Thread: Meet Moderna’s mRNA-1283, mNEXSPIKE, the Other Component of mRNA-1083, mCOMBRIAX: Part One

The colorized vintage image of vaccination for today’s header is courtesy of MedPage Today and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: 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.

The Moderna “combination modRNA influenza + modRNA COVID-19 vaccine”, mRNA-1083, also called mCOMBRIAX, has just been approved for use in Europe. mRNA-1083 (mCOMBRIAX) is a combination of the Moderna modRNA multi-strain influenza “vaccine”, mRNA-1010, plus the company’s “other” modRNA COVID-19 bioweapon “vaccine”, mRNA-1283 (mNEXSPIKE.) Yours Truly has written about the mRNA-1010 component of this “combo vaccine” here: https://www.theqtree.com/2026/02/27/health-friday-2-27-2026-open-thread-modernas-mrna-1010-and-the-end-run-around-hhs-sec-kennedy-jr-part-one/; and, here: https://www.theqtree.com/2026/03/06/health-friday-3-6-2026-open-thread-modernas-mrna-1010-and-the-end-run-around-hhs-sec-kennedy-jr-part-two/.

And now, on to the mRNA-1283 (mNEXSPIKE) component of mRNA-1083. Today’s offering is Part One of two:

Moderna’s “other” modRNA COVID-19 bioweapon “vaccine”, mRNA-1283 (mNEXSPIKE), was approved for use in the United States on 30 May 2025. The FDA Approval Letter to Moderna is here: https://www.fda.gov/media/186740/download. The Approval Letter for mNEXSPIKE was signed by David C. Kaslow, MD, Director of the Office of Vaccines Research and Review (a subdivision of FDA’s CBER department [Center for Biologics Evaluation and Research]). Dr. Kaslow is a Biden-era “holdover” at the FDA; he has been with CBER since 11 October 2022.

It appears that Dr. Kaslow relied solely on the “data” that was given to the FDA by Moderna regarding the “safety and efficacy” of mRNA-1283, prior to that agency’s granting approval of the BLA (Biologics License Application) that Moderna submitted for the product. In addition, it appears that Dr. Kaslow believed that the “data” that Moderna supplied to the FDA was sufficient enough to warrant a bypass of the review process by the VRBPAC group of the FDA (Vaccines and Related Biological Products Committee.) Please see the screenshot from Dr. Kaslow’s Approval Letter to Moderna for mRNA-1283 (mNEXSPIKE), below:

By the way, on 20 May 2025, Dr. Martin Makary (FDA Commissioner) and Dr. Vinay Prasad (Director of the FDA’s CBER division) published an “opinion piece” in the New England Journal of Medicine that purported to be their “opinions” regarding a “new approach” to COVID-19 “vaccination” in the United States. However, this was not really an “opinion piece” — it was implemented as FDA policy. This article by Dr. Prasad and Dr. Makary was published just 10 days before Dr. Kaslow sent the Approval Letter to Moderna for mRNA-1283 (mNEXSPIKE.) Did Dr. Prasad and Dr. Makary know in advance that Dr. Kaslow was going to issue this Approval Letter? Did HHS Secretary Kennedy, Jr., know? The “opinion piece” is here: https://doi.org/10.1056/NEJMsb2506929. “An Evidence-Based Approach to COVID-19 Vaccination.” Vinay Prasad, MD, MPH, and Martin Makary, MD, MPH. 20 May 2025. Below are two screenshots from this article: from the text; and, the Figure 2, which lists the “groups at severe risk from COVID-19.” The persons who would fall under one or more of the categories listed in Figure 2, even if these persons are under age 65, would “qualify” for “vaccination” with mNEXSPIKE:

The Package Insert for healthcare professionals for mRNA-1283 (mNEXSPIKE) is here: https://www.fda.gov/media/186738/download. Please see the screenshots of the following sections of this Package Insert, below: first, section 11 Description; then, section 12 Clinical Pharmacology, and section 13 Nonclinical Toxicology:

It would appear that Dr. Kaslow was comfortable in approving an injectable by Moderna (mRNA-1283, also called mNEXSPIKE) that contains the dangerous lipid nanoparticle SM-102; that contains at least PEG-related element (polyethylene glycol); and, that was not tested for carcinogenicity (the potential to cause cancer), for genotoxicity (the potential to damage genes, or to cause changes to genes, either of which can also cause cancer), or for impairment of male fertility.

It would also appear that Dr. Kaslow was comfortable with approving this modRNA COVID-19 bioweapon “vaccine” (mRNA-1283, also called mNEXSPIKE), which is purported to “prevent infection of COVID-19” — but, which claim has been proven to be wrong. From the FDA Package Insert for mNEXSPIKE:

The “prevent coronavirus disease 2019 (COVID-19)” statement is still being used by the FDA on COVID-19 bioweapon “vaccines” Package Inserts, despite the fact that Shrestha, et al., demonstrated in 2023 that “fully up-to-date vaccinated” Cleveland Clinic employees were more likely to become COVID-19 infected than those who were not “fully up-to-date” with COVID-19 “vaccination” (https://doi.org/10.1101/2023.06.09.23290893. “Risk of Coronavirus Disease (COVID-19) Among Those Up-to-Date and Not Up-to-Date on COVID-19 Vaccination.” Nabin K. Shrestha, et al. 13 June 2023.) Please the screenshot from this paper, below:

Why aren’t the Moderna “original” modRNA COVID-19 bioweapon “vaccine”, mRNA-1273 (SPIKEVAX), and the Moderna modRNA COVID-19 bioweapon “vaccine”, mRNA-1283 (mNEXSPIKE), the same? Please see the screenshot, below, from this article (https://www.drugs.com/medical-answers/what-difference-between-spikevax-mnexspike-3580787/, “What is the difference between SPIKEVAX and mNEXSPIKE?”, 2 September 2025:

However, regarding mNEXSPIKE, there apparently is a “blurred line” as to the use of it in persons under age 65 who do not have an “underlying medical condition.” Please see the screenshot below, from this article: https://health.mountsinai.org/blog/heres-what-you-need-to-know-about-the-new-covid-19-vaccines/, 23 September 2025; the advice is from Dr. Bernard Camins, MD, MSc, of Mount Sinai Hospital, in the “FAQ” section:

Note the language above, from Dr. Camins, regarding the ability of pharmacists to “prescribe vaccines off-label.”

Why is the N-terminal domain of the SARS-CoV-2 virus so important to Moderna that the company crafted a modRNA COVID-19 bioweapon “vaccine”, mNEXSPIKE, to utilize it? The N-terminal domain area is the “closest” (in terms of placement) to the receptor-binding domain (RCB) on the SARS-CoV-2 virus code. The N-terminal domain is also close to the S1/S2 cleavage site on the virus code. The receptor-binding domain is the part of the virus code that “makes sure” that the “payload” of the “vaccine” binds itself (enters into) the cells of the “vaccinated” person. These, in this writer’s opinion, make the N-terminal domain a “prime target” for the development of modRNA COVID-19 bioweapon “vaccines” that do not need to include the entire virus code, but still can “deliver the payload” through the receptor-binding domain mechanism. Please see: https://doi.org/10.3389/fcimb.2020.587269. “SARS-CoV-2: Structure, Biology, and Structure-Based Therapeutics Development.” Mei-Yue Wang, et al. 24 November 2020. Figure 1.) This is in contrast to the other modRNA COVID-19 bioweapon “vaccines” (by Moderna and by Pfizer-BioNTech) that contain the entire spike protein sequence (S1 and S2 areas.)

The issue regarding developing a modRNA COVID-19 bioweapon “vaccine” that only utilizes the N-terminal domain and the receptor-binding domain appears to have been determining exactly what “binding pocket” of the N-terminal domain would work. Scientists had been experimenting with the N-terminal domain to find such a “binding pocket”: for example, as described in this paper, from 2022: https://doi.org/10.1016/j.csbj.2022.11.004. “Structural and energetic analyses of SARS-CoV-2 N-terminal domain characterise sugar binding pockets and suggest putative impacts of variants on COVID-19 transmission.” Jonathan Lees, et al. 17 November 2022. Please see the screenshots from this paper, below; first, the Abstract; followed by the Graphical Abstract:

It appears that Moderna did find such an N-terminal “binding pocket” to use for the development of mNEXSPIKE. And, it appears that the company’s decision to “harness” the mechanism to the S1 area of the SARS-CoV-2 spike protein, as opposed to using the entire S1/S2 sequence, is due to the fact that the S1 area is that which appears to be the most “effective” in regards to the Delta and Omicron variants of the virus. Please refer to: https://pubmed.ncbi.nlm.nih.gov/38034565. “SARS-CoV-2 spike protein S1 subunit induces potent neutralizing responses in mice and is effective against Delta and Omicron variants.” Tarlan Mamedov, et al. 14 November 2023. Please see the screenshot, below, of the Conclusion from this paper:

Note that Mamedov, et al., used a tobacco plant to produce the S1 protein from SARS-CoV-2, which they then tested against Delta and Omicron virus variants.

In this writer’s opinion, mRNA-1283 (mNEXSPIKE) cannot be thought of as “mRNA-1273 (SPIKEVAX) Lite.” mNEXSPIKE contains the S1 spike protein of an Omicron variant of SARS-CoV-2. mNEXSPIKE contains the dangerous lipid nanoparticle, SM-102, that mRNA-1273 (SPIKEVAX) also contains. mNEXSPIKE contains N1-Methylpseudouridine (which will destroy the RNA of the “vaccinated” body’s natural Uridine, replacing it with a lab-created chemical compound that has no natural, beneficial mechanism for the body), which mRNA-1273 (SPIKEVAX) also contains. In this writer’s opinion, the only difference between mRNA-1273 (SPIKEVAX) and mNEXSPIKE is that the latter “vaccine” does not contain the S2 area of the spike protein.

To be continued in Part Two.

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 INTO THESE GENE-ALTERING THERAPY PLATFORMS AND PRODUCTS. THERE MUST, SECOND, BE IRREFUTABLE PROOF THAT THESE GENE-ALTERING THERAPY PLATFORMS AND PRODUCTS ARE TRULY “SAFE AND EFFECTIVE.”

Peace, Good Energy, Respect: PAVACA

(Intellectual Disclaimer and Notice: Other than URLs and related items available on the Internet, the ideas and opinions of today’s offering are by PAVACA. Credit must be given to PAVACA if the ideas and opinions of 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 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.

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

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.

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

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 11.14.2025 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.)

Health Friday 10.31.2025 Open Thread: Echoes

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

My older brother, Sam, December 2021:

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

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

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

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. Today’s offering is dedicated to all persons, of whatever age or location, who have passed away from the negative effects of the COVID-19 “vaccines” that they had injected into their body. May they rest in eternal Peace.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Then, from the Conclusions section of the paper:

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

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

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

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

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

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

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

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

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

Interested persons may wish to investigate these websites:

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

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

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

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

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

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

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

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

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

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

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

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

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

Health Friday 10.24.2025 Open Thread: A Cautionary Tale

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

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