Health Friday Open Thread 5.16.2025: About That “Universal Vaccine” — There’s More Than Meets the Eye, Part Two

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

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

Health Friday is a series devoted to information 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 found here. NOTE: Yours Truly has checked today’s post for any AI-generated content. To the best of her knowledge and belief, there is none. If readers wish to post anything in the discussion thread for today that is AI-generated, they must cite their source. Thank you.

Today’s offering is Part Two (of two) regarding the HHS / NIH announcement regarding the establishment of the “Generation Gold Standard” for future development and testing of vaccines in the United States. “Generation Gold Standard” includes the development and testing of a “Universal Vaccine Platform”, which will incorporate elements from various viruses, including coronaviruses (such as the SARS-CoV-2 virus, aka the COVID-19 virus.) Part One can be found here: https://www.theqtree.com/2025/05/09/health-friday-5-9-2025-about-that-universal-vaccine-theres-more-than-meets-the-eye-part-one/. The HHS / NIH announcement is found here: https://www.hhs.gov/press-room/hhs-nih-announces-generation-gold-standard.html, 1 May 2025. Please refer to the screenshot below:

Yours Truly discussed several items in the above announcement in Part One, referred to above. Part Two is a further discussion of items related to the BPL-1357 intranasal “universal virus vaccine”, a “cornerstone” of the “Generation Gold Standard” program. The primary focus of Part Two will be on the “adjuvant” for BPL-1357, a compound called ALFQ. However, before the presentation, there is this short paper, from January 2025: https://doi.org/10.1093/ofid/ofae631.188, “593. Randomized, Double-Blinded, Placebo-Controlled, Phase 1 Study of the Safety of BPL-1357, A BPL-Inactivated, Whole-Virus, Universal Influenza Vaccine”, Jeffery Taubenberger, Matthew J. Memoli, et al., 29 January 2025. A screenshot of the Background section of the Abstract of this paper is below:

Note the description of BPL-1357: It is to cover several types of Avian Influenza viruses. Nothing about covering coronaviruses. Why was there a ‘challenge” with Influenza A type viruses, and nothing about “challenges” with Influenza virus types B or C (https://www.cdc.gov/flu/about/viruses-types.html.) How can BPL-1357 be considered a “Universal Vaccine” if it is only covers Avian Influenza viruses? How does this paper “stack up” vis-a-vis the HHS / NIH “Generation Gold Standard” announcement?

Then, there is the mysterious BPL-24910 (aka BPL-2491) vaccine, which is referred to in the HHS / NIH announcement, but of which there is no record at clinicaltrials.gov/, nor is much information available on the internet. Yours Truly was able to find a few items. The first one is here: https://www.ntd.com/health-officials-announce-new-effort-to-develop-universal-vaccines-targeting-multiple-virus-strains_1064264.html, by Zachary Stieber, 1 May 2025. Please see the screenshot from this article, below:

The NIAID awarded funds to a company called Lovelace Biomedical Research Institute for testing the toxicity of BPL-24910: https://www.usaspending.gov/award/CONT_AWD_75N93022F00001_7529_75N93021D00031_7529. Below are screenshots from this link:

Lovelace Biomedical Research Institute was founded in 1947 in Albuquerque, New Mexico. The institute joined Touro University in 2022. (https://www.lovelacebiomedical.org/, and Wikipedia.)

Now, on to the AFLQ “adjuvant” in BPL-1357:

ALFQ is a combination of two separate items: ALF plus QS21. ALF stands for monophosphoryl lipid A (aka 3D-PHAD.) It is also called “Army Liposome Formulation.” Please see the screenshot below, from https://www.cancer.gov/publications/dictionaries/cancer-drug/def/monophosphoryl-lipid-a:

What is an endotoxin? Please see: https://www.britannica.com/science/endotoxin. A screenshot from the Britannica entry is below:

It is unclear which version of ALF is actually used in BPL-1357: the “LPS” version, or the “MPLA” version.

Then, there is 3D-PHAD. Please see below, from https://www.sigmaaldritch.com/:

And, more on ALF (aka Army Liposome Formulation) is here: https://pmc.ncbi.nlm.nih.gov/articles/PMC7412170/, “Army Liposome Formulation (ALF) Family of Vaccine Adjuvants”, Carl R Alving, et al, 7 August 2020. Please see the screenshot from this paper, below:

Note the reference to HIV-1. More on this later in today’s post.

ALFQ contains a TLR4 agonist. What is TLR4? Also known as CD284, it is a “key activator of the innate immune response”, per https://en.wikipedia.org/wiki/Toll-like_receptor_4. An agonist is an agent that interacts with a particular cellular receptor, and produces an observable positive response.

The other component of ALFQ is QS21. What is QS21? It is a vaccine adjuvant derived from the soapbark tree (Quillaja saponaria.) QS21 is used in the Novavax COVID-19 “vaccine” as an adjuvant, as part of the company’s “Matrix-M” ingredient.

QS21 has been studied for some time. Here is an article, from the John Innes Centre, that describes the history of QS21: https://www.jic.ac.uk/advances/the-quest-for-qs-21/, Winter 2020-2021. Please see a screenshot from this article, below:

Yours Truly now presents some “interesting information.” One is not making any judgements or opinions; the reader may make their own. This has to do with the HIV-1 reference above in the post. The first item is this: https://doi.org/10.1016/S0264-410X(00)00415-1, “QS21 promotes an adjuvant effect allowing for reduced antigen dose during HIV-1 envelope subunit immunization in humans”, Thomas G. Evans, et al., 28 February 2001. A screenshot of the Abstract of this paper is below:

The second item is here: https://worldcouncilforhealth.substack.com/cp/162703289, “BOMBSHELL: HIV Contamination Found In Moderna’s Covid Shot”, 2 May 2025. There are actually two bombshells here: two separate molecules related to HIV-1 were found in the Moderna modRNA COVID-19 “vaccine” — gp145 and gp120. Please see the screenshots from the World Council for Health article, below:

The graphic created by Dr. McKernan, from the above article, showing where the gp145 HIV-1 molecule is in the Moderna modRNA COVID-19 “vaccine” sequence:

Regarding the gp120 HIV-1 molecule in the Moderna mRNA-1273 modRNA COVID-19 “vaccine”, it was the famous (or, infamous) “Pradhan, et al., paper” from January 2020 which showed that there were gp120 HIV-1 molecules in the SARS-CoV-2 (COVID-19) virus itself. The “Pradhan, et al., paper” was Withdrawn shortly after its publication, and is now difficult to find. Yours Truly was able to locate the paper here: https://academia.edu/79020098/Uncanny_similarity_of_unique_inserts_in_the_2019_nCoV_spike-protein_to_HIV_1_gp_120_and_Gag?f_ri-170, “Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag”, Prashant Pradhan, et al., 31 January 2020. A screenshot from the paper is below:

Recall that in January 2020, there were no COVID-19 “vaccines” in use anywhere. Note also that the gp120 HIV-1 molecule is present in the COVID-19 virus itself spike protein. Did the Pfizer-BioNTech developers of BNT162b2 remove any or all of the four HIV-1 related inserts in the COVID-19 spike protein (found by Pradhan, et al.) in the process of working on their “vaccine”? Why did Moderna leave the gp120 HIV-1 molecule (and also, it turns out, the gp145 HIV-1 molecule) in that company’s modRNA COVID-19 “vaccine”, mRNA-1273?

And, there is the involvement of the United States Army in HIV research (this is in addition to the Army’s developing the “adjuvant”, ALFQ): https://hivresearch.org/hiv-research/alf-adjuvants. This is the Military HIV Research Program.

Yours Truly will reiterate that one is not making judgements or opinions here; readers will make their own. However, the following needs to be said: the gp120 molecule in HIV-1 attacks the body’s CD4 cells. Please see this paper, from 2010: https://pubmed.ncbi.nlm.nih.gov/20088758/, “The GP120 molecule of HIV-1 and its interaction with T cells”, V Yoon, et al., 2010. A screenshot of the Abstract of this paper is below:

Also: the SARS-CoV-2 virus itself attacks the body’s CD4 cells: https://doi.org/10.7554/eLife.84790, “SARS-CoV-2 uses CD4 to infect T helper lymphocytes”, Natalia S Brunetti, et al., 31 July 2023. A screenshot of the Abstract of this paper is below:

And, there is this paper: https://doi.org/10.3389/fimmu.2020.596631, “Sharing CD4+ T cell Loss: When COVID-19 and HIV Collide on Immune System”, Jean-Pierre Routy, et al., 14 December 2020. Note that this paper was published just a few days after the initial EUAs were granted by the FDA for BNT162b2 and for mRNA-1273 in the United States (11 December 2020); therefore, the research into writing the Routy, et al., paper must have been accomplished at least a few months prior to December 2020. A screenshot of the opening statement of the paper is below:

Yours Truly will ask a question that perhaps is “inconvenient”, but needs to be asked: Is any potential connection between the presence of the gp120 HIV-1 molecule in the SARS-CoV-2 virus itself, AND its potential presence in the Pfizer-BioNTech modRNA COVID-19 “vaccines”, AND its potential presence in the Novavax COVID-19 “vaccine” (which uses the original SARS-CoV-2 virus itself spike protein as a foundation), AND the confirmed presence of BOTH the gp120 HIV-1 molecule and the gp145 HIV-1 molecule in the Moderna modRNA COVID-19 “vaccines” — with the multiple serious Adverse Events reports of autoimmune / immune-mediated, and related conditions, that are in the Appendix 1: List of Adverse Events of Special Interest section of this report: ttps://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf?

Another “inconvenient” question posed by Yours Truly: What, if anything, did Dr. Anthony Fauci, Dr. Francis Collins, Dr. Deborah Birx, Dr. Robert Redfield, and Dr. Janet Woodcock know about the presence of the gp120 HIV-1 molecule in the SARS-CoV-2 virus itself spike protein, AND in the Moderna modRNA COVID-19 “vaccine” mRNA-1273?

What will be done to make absolutely sure that there is NO molecule whatsoever related to HIV-1 present in the “Universal Vaccine” candidates BPL-1357 and BPL-24910, or in any other “Universal Vaccine” candidates? What will be done to hold accountable the people who allowed the gp120 HIV-1 molecule to be present in the original SARS-CoV-2 virus itself? What will be done to investigate the potential presence of the gp120 HIV-1 molecule in the Pfizer-BioNTech modRNA COVID-19 “vaccines”? What will be done to hold accountable the people who allowed HIV-1 molecules gp120 AND gp145 to be present in the Moderna modRNA COVID-19 “vaccines”?

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

To be continued in Part Two.

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

Health Friday 5.2.2025 Open Thread: The PREP Act Must be Repealed. Now.

The above vintage image of the United States Congress in session is courtesy of the Library of Congress and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. As today’s post speaks of the disaster of the lab-created bioweapons called COVID-19 — the COVID-19 virus itself; and, the COVID-19 “vaccines” — Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative effects of these bioweapons.

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

The PREP Act (also called PREPA) is a “License to Kill“, in the words of Sasha Latypova (https://sashalatypova.substack.com/.) The PREP Act removes accountability, liability, and transparency from the activities of the Health and Human Services Department of the United States Federal Government under the provisions of the Act. The PREP Act allows: unlimited research, development, and use of COVID-19 “countermeasures”, including, but not limited to, “vaccine” development and use; “respiratory devices” development and use (think ventilators); prescription drugs use (think Paxlovid and Remdesivir); “mandated” uses of masking, of “social distancing”, and even of “lockdowns”; the “mandated” administration of COVID-19 “vaccines”, including to newborn babies, to persons under the age of 18, to persons who wish to attend school or to work; and much more. The PREP Act allows the United States Federal government and its associated departments (including Health and Human Services and the United States Defense Department) to literally use American citizens as “human lab rats” in the administration and use of dangerous, deadly, COVID-19 “countermeasures” which are not “safe and effective”; but which, instead, damage and/or destroy the bodies and minds of the persons who take the COVID-19 “vaccines” and/or drugs such as Remdesivir. The PREP Act uses taxpayer monies, private research grants, collaboration with scientific labs all across the United States (think the Baric Lab at UNC, Chapel Hill), and with foreign labs (think the Wuhan Institute of Virology) to pursue the provisions of the PREP Act.

Yours Truly begins here: https://www.federalregister.gov/documents/2024/12/11/2024-29108/12th-amendment-to-declaration-under-the-public-readiness-and-emergency-preparedness-act-for-medical, “12th Amendment to Declaration Under the Public Readiness and Emergency Preparedness Act for Medical Countermeasures Against COVID-19”, signed by then-Health and Human Services Secretary Xavier Becerra, 11 December 2024. This 12th Amendment extends the PREP Act (also called PREPA) “emergency status” of COVID-19, along with all medical countermeasures used against COVID-19 (including development and use of “vaccines”, “respiratory devices”, and so on) — until 31 December 2029 (in other words, until after the 2028 General Election and into the Presidential administration that takes over on 20 January 2029.) It also means that, even though the “official” COVID-19 “state of emergency” ended in May 2023, the “virus emergency status” has not been ended. It also means that legal liability for any person, any medical professional, any drug manufacturer, any hospital / clinic / care facility, and supplier, and so on, that fall under the provisions of the 12th Amendment — are legally exempt from any and all liability. It also means that, while the current Health and Human Services Secretary can sign a document that rescinds and/or modifies the 12th Amendment, it must take an act of Congress to repeal the PREP Act.

Per Katherine Watt (paralegal and professional researcher), the two separate actions mentioned above are discussed here: https://bailiwicknews.substack.com/p/repealing-prep-act-and-terminating, “Repealing PREP Act and terminating HHS Secretary determinations and declarations issued under PREP Act are two different things.”, 4 April 2025. Please see the screenshots from her article, below:

For more information on the PREP Act (aka PREPA), please see: https://aspr.hhs.gov/legal/PREPact/pages/default.aspx. ASPR means the Administration for Strategic Preparedness & Response. The PREP Act was passed by Congress in 2005, under the administration of then-President George W. Bush. Please also see: https://aspr.hhs.gov/legal/PREPact/Pages/PREP-Act-Questions-and-Answers.aspx#COVID.

It appears that the various States of the United States have little room to challenge the provisions of the PREP Act. However, a recent case before the North Carolina Supreme Court, regarding a person under age 18 who was given a COVID-19 “vaccine” without consent, was decided in favor of the plaintiff: https://thefocalpoints.com/p/give-it-to-him-anyway-teen-given, “Give It to Him Anyway”: Teen Given COVID-19 mRNA Shot Without Consent — State Supreme Court Says Family Can Sue”, by Nicolas Hulscher, MPH, 24 March 2025. Please see the screenshot from the Hulscher article, below:

A lower court in North Carolina ruled that the family could not sue the school system, due to the “liability provisions” of the PREP Act. However, the North Carolina Supreme Court overruled the lower court, stating that the family can indeed sue:

Before turning to the final aspect of today’s offering, Yours Truly will expand the mention of Sasha Latypova above in the post. Ms. Latypova, a native of Ukraine, was trained in medical and pharmaceutical technology. She owned and ran several companies in this area. She worked with Pfizer-BioNTech and other drug manufacturers in medical technology. She is therefore a person with deep experience, in Yours Truly’s opinion, regarding the workings of these industries. After moving to the United States and subsequently retiring from these endeavors, Ms. Latypova began to research and write on how the medical technology and the pharmaceutical industries have now become entities that serve their shareholders and the government, not the patients they claim to serve. Regarding the PREP Act, here is one of her blog posts: https://sashalatypova.substack.com/p/prep-act-license-to-kill-must, “PREP Act Brief: “License to Kill” must be repealed.”, 21 April 2025. This article is densely-written and detailed. Below are a couple of screenshots from her post. Note: There are numerous hyperlinked information sources embedded in the article:

Please also see this post, an interview between Ms. Latypova and Ms. Watt (Bailiwick News) regarding the PREP Act: https://sashalatypova.substack.com/p/interview-with-the-former-feds-foundation, “Interview with the Former Feds Foundation: Katherine Watt and I discuss PREP Act as an act of treason.”, 25 April 2025.

Finally, there is this blog article from “Spartacus”: https://iceni.substack.com/cp/162062988, “Declaration of Sovereignty Pt. 1”, 24 April 2025 (this is a cross-post from the Mole substack website.) This post is long and intense; it traces the “Profane Myth of COVID-19.” A screenshot of part of this post is below:

It is the PREP Act which, in significant amounts, has placed the United States in the position where the country is today: just under 70% of the population has taken at least one injection of a dangerous, deadly COVID-19 “vaccine” (these injectables are NOT “safe and effective”, and mounting evidence proves this); the country is just beginning to emerge from the economic devastation and chaos of the “COVID lockdowns” period; and, the Medical Tsunami of COVID-19 “vaccine”-induced injuries, illnesses, disabilities, and deaths, which is starting to present among the “vaccinated.” There are many persons involved in the above who must now be held accountable; not the least of which are those who knew how dangerous and potentially deadly the COVID-19 “vaccines” are while working with “Operation Warp Speed”, and who withheld this information from then-President Donald Trump.

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

Health Friday 4.25.2026: The AMA is Still Pushing “Strategies” for Physicians to “Combat Vaccine Hesitancy”

The free vintage image above of children being vaccinated is courtesy of iStock and Getty Images, via Google Images.

Health Friday is a series devoted to information regarding Big Pharma, vaccines, general health, and associated topics. As today’s post speaks to the disaster of the COVID-19 “vaccines” (Bioweapon Toxin Injections), Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative effects of these lab-created bioweapons.

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

Yours Truly has written about the American Medical Association (the AMA) on previous occasions. The AMA is one of the most powerful professional organizations for physicians in the United States. The organization, which does not provide a list of its members to the general public, is also one of the most powerful lobbying agents in Congress. In addition, the AMA owns the rights to use the CPT codes, which are the codes for medical procedures, examinations, tests, for ordering medical equipment, and much more. The CPT codes are used to bill CMS (Medicare / Medicaid), and to bill private insurers. Please see below for screenshots from, first, https://www.opensecrets.org/orgs/american-medical-association-summary; and, second, https://www.influencewatch.org/non-profit/american-medical-association/, regarding AMA spending on lobbying:

And, not surprisingly, the CPT code royalties paid to the AMA for use of these codes appear to generate the bulk of income for the organization — no wonder the AMA can spend over $21 million on lobbying efforts. Please see: https://paddockpost.com/2024/12/16/how-revenue-is-spent-at-the-ama-2022/.

The AMA has multiple “sub-units” within the organization. These “sub-units” range from DEI (Diversity, Equity, and Inclusion), to “health equity”, and to LGBTQ++ “health inclusion”, among others. The organization offers numerous CME (Continuing Medical Education) online courses and webinars for AMA members, to assist them in accumulating the yearly CME credits they must earn in order to maintain their License to Practice Medicine. It also publishes numerous medical papers, articles, and other media; among them, JAMA (the Journal of the American Medical Association.) Please see: https://www.theqtree.com/2024/04/24/the-ama-edhub-window-to-establishment-medicine/.

An example of an AMA-published article regarding “physician strategies to combat vaccine hesitancy among patients” is here: https://www.ama-assn.org/delivering-care/public-health/covid-19-vaccine-hesitancy-10-tips-talking-patients#, “COVID-19 vaccine hesitancy: 10 tips for talking with patients”, by Tanya Albert Henry, 15 December 2023. Here are the “10 tips”: “Know you are the most trusted information source”; “Tell patients they need to get the vaccine”; Understand your patients’ concerns”; “Ask why a patient is hesitant”; Counter any misinformation”; “Tailor your message”; “Address patients’ fear about side effects”; “Prepare our staff to answer questions”; “Show your vaccination pride”; “Tell stories to make impact”.

But, what are physicians supposed to say to the patient in order to “convince” them to take a COVID-19 “vaccine”? Again, the AMA has answers: for example, the “templates” in this published study: https://www.sciencedirect.com/science/article/pii/S0264410X24004377, “Patient concerns and physician strategies for addressing COVID-19 vaccine hesitancy”, Joy Melnikow, et al., 22 May 2024. Below are three screenshots from this paper: section 2.1 Study sample; followed by Table 2, then Table 3:

All of above is to get a patient to agree to having a COVID-19 Bioweapon Toxin Injection (aka a COVID-19 “vaccine”) injected into their body. In Yours Truly’ opinion, if a physician follows the above “templates”, they are functioning not as physicians who swore to “Do No Harm”; in fact, they may be considered as “government representatives” under the current “extension” of the PREP Act for COVID-19 Countermeasures” that was signed by then-HHS Secretary Xavier Becerra in December 2024. Notice also the use of various aspects of direct psychological manipulation and of gaslighting in the “templates” for the physicians to follow. One wonders: What would these physicians say in response to a “vaccine-hesitant” patient who gives them a hard copy of a published study that clearly shows what the COVID-19 “vaccines” actually do to damage a “vaccinated” person’s body?

And now, to the most recent AMA “strategies for physicians to use on patients with vaccine hesitancy” effort, from the AMA EdHub series: https://doi.org/10.1001/jama.2025.4882, “Strategies for Communicating with Parents About Vaccines”, Sean T. O’Leary, MD, MPH, 9 April 2025. This article is full-access for AMA members; through an institution; or, via renting it through DeepDyve. Yours Truly went to DeepDyve and was able to get the following screenshot from the first page of Dr. O’Leary’s article, below:

Note the “strategies” that are to be used by the physician, listed in the Table above. Again, it appears to be yet another mixture of “your physician is the most trusted source of information”; plus, “It’s the responsible thing to do for your child”; plus, something new, “Prebunking“, which appears to be a type of psychological manipulation of / gaslighting of, the parent regarding any information they may find online from other physicians (say, Dr. Peter A. McCullough) regarding the dangers of taking the COVID-19 “vaccines”; or, other researchers (say, Steve Kirsch, about how childhood vaccination can induce autism [via the aluminum in the vaccines], and who cites medical statistics to support his contention.) Please see: https://kirschsubstack.com/p/two-pieces-of-evidence-that-together, “Two pieces of evidence that together show that vaccines cause autism”, 21 April 2025. Please also see: https://jessicar.substack.com/p/aluminum-exposure-and-autism-prevalence, 19 April 2025. Dr. Rose cites the following image, from data collected by the CDC:

The following article describes various adjuvants to vaccines, including Aluminum: https://www.chop.edu/vaccine-education-center/vaccine-safety/vaccine-ingredients/aluminum, Children’s Hospital of Philadelphia, 15 December 2022, reviewed by Dr. Paul A. Offit, MD.

Why is the AMA still pushing psychological manipulation / gaslighting “strategies” for physicians to use to “convince” patients to take a COVID-19 “vaccine”, or to allow their child (children) to be COVID-19 “vaccinated”, or to allow their child (children) to be “vaccinated” with injectables that contain substances such as Aluminum? Why does the CDC have dozens of “vaccines” listed on the agency’s Child and Adolescent Immunization Schedule (https://www.cdc.gov/vaccines/hcp/imz-schedules/downloads/child/0-18yrs-child-combined-schedule.pdf)? With “vaccines” that are to be administered to newborns immediately after birth? Why do almost all public school systems “require” certain “vaccines” to be given to a child in order to attend public school? Why do state legislatures give the force of law to the CDC Child and Adolescent Immunization Schedule through legislative fiat for public school attendance — given that the CDC states on the schedule that the injectables are “Recommended”, not “Required”? Why do the AMA, the CDC, and the FDA refuse to acknowledge that the COVID-19 “vaccines” are dangerous and deadly, given the mountain of evidence currently in print which proves this to be the case?

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

Health Friday 4.18.2025 Open Thread: Cellphone Radiation — Blood Cell Clustering and Damage to the Immune System

The above free image of a cellphone in use is courtesy of iStock and Google Images. There may some AI-generated aspects to this image: therefore, Yours Truly is citing the sources (iStock and Google Images.)

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. Today’s offering, part of a “mini-series”, speaks to the emerging dangers of 5G radiation effects as they relate to cellphone use.

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. NOTE: Yours Truly has checked today’s offering for any AI-generated content. To the best of her knowledge and belief, there is only the possible AI-generated “details” in the header image; and has cited this as such. If readers wish to post anything in today’s discussion thread that is AI-generated, they must cite their source. Thank you.

Today is Good Friday. It is also the sixth day of Passover.

(A side note: Today’s offering may sound, in some ways, like “another conspiracy theory” to some readers. However, given that many things that were called “conspiracy theories” about the COVID-19 “vaccines”, things which now are proving to be true, what is presented today may ultimately fit into the “down the road, toldjah” category.)

Just about everyone has a cellphone. Most of these cellphones are versions of a “smart phone” that have either Apple-based, or Andoid-based, technology built into them. Many people carry their smartphones in a pocket of their clothing. Other people carry their smartphones in a holder device connected to a lanyard that is worn around the neck. Many people hold their smartphones up to their ears when speaking or listening. Most smartphones are now connected to a 5G technology signal transfer system. These 5G signals are carried by cellphone “towers”; they are also carried by “mini-system stations” that are being added to existing telephone lines; they are also carried by other “mini-system devices” that are being attached to existing street lights, or are already built into new street lights. It is now possible to see 5G “mini-system stations” or “mini-system devices” on entire stretches of street lights.

5G technology is supposed to be the “new standard” for technology transfer (until it is likely eclipsed by higher transmission rates, such the “up and coming” 7G); for telecommunications; and for ease and speed of information transfer. However, there is another side to this situation: the radiation signals from 5G smartphones can interfere with red blood cell function in the person with the 5G smartphone, causing these cells to form clusters (also called aggregations) that resemble stacked coins.

Yours Truly begins here: https://www.thefocalpoints.com/p/study-direct-smartphone-exposure, “STUDY — Direct Smartphone Exposure Triggers Rapid Red Blood Cell Aggregation”, by Nicolas Hulscher, MPH, 1 April 2025. The paper referred to in the article is found here: https://doi.org/10.3389/fcvm.2025.1499499, “Hypothesis: ultrasonography can document dynamic in vivo rouleaux formation due to mobile phone exposure”, Robert R. Brown, Barbara Biebrich, 11 February 2025. A screenshot from this paper is below:

Rouleaux formation is the “coin stacking” appearance of red blood cells. Another screenshot from the paper is below, which includes an image of red blood cells in rouleaux formation:

The scientific community has apparently given 5G technology a “go-ahead”, despite numerous concerns that have been expressed regarding the safety and the possible negative effects from 5G radiation. Two articles that have discussed these concerns are: One: https://expose-news.com/2022/11/19/an-international-appeal-halt-rollout-of-5g/; and, Two: https://expose-news-com/2024/04/14/ten-new-studies-detail-health-risks-of-5g-analysis-by-dr-joseph-mercola/.

A third article, by Mr. Hulscher, on the same subject, is here: https://www.thefocalpoints.com/p/the-5g-safety-myth-assumed-safe-not, “The 5G Safety Myth: Assumed Safe, Not Proven Safe”, 15 March 2024. The paper cited in this article is here: https://doi.org/10.3389/fpubh.2023.1058454, “The Assumption of safety is being used to justify the rollout of 5G technologies”, Victor Leach, et al., 26 January 2023. Two screenshots from this paper follow; first, the Figure 1:

And, from the Conclusions section of the paper:

As to the potential for 5G radiation negatively affecting the immune system of humans, please see: https://www.vigilantfox.com/p/emfs-wrecking-immune-system, “EMFs are Quietly Wrecking Your Immune System, Scientists Warn”, via the GMI Research Group, 2 April 2025.

There is now a collective name for the various types of illnesses that can be induced by 5G radiation: EMR Syndrome. Dr. Joseph Mercola writes about it here: https://www.theburningplatform.com/2025/04/10/wireless-radiation-sickness-gets-a-new-name-emr-syndrome/#more-364767. Dr. Mercola discusses EMR Syndrome and offers suggestions on how to avoid it and/or mitigate it. Please see the screenshots below:

Finally, Yours Truly again emphasizes the fact that COVID-19 “vaccination” weakens and/or destroys the natural immune system of the “vaccinated” person; in addition to potentially inducing and/or aggravating cancers, cardiovascular conditions, neurological conditions, and much more. This situation opens the door to what, in Yours Truly’s opinion, may be called “Interactive Conditions” potential, between the damage done by the COVID-19 “vaccines” that a person has in their body, and the possibility of 5G radiation-induced illnesses among the “vaccinated.”

Be aware — Please protect and keep good health.

Peace, Good Energy, Respect: PAVACA

STOP PRESS Edition: The FDA Just Granted “Fast Track” Approval for the ARCT-2304 saRNA Avian Flu “Vaccine”

The image of a “Suspicious Dog” is from Yours Truly’s files. The source is unknown, but to the best of Yours Truly’s knowledge and belief, it is not AI-generated.

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. If readers wish to post anything that is AI-generated on the discussion thread for today’s special edition post, they must cite their source. Thank you.

Today’s STOP PRESS Edition post is devoted to one topic: the “Fast Track” approval that the FDA just granted to CSL / Arcturus Therapeutics for the company’s self-amplifying RNA (saRNA, aka sa-mRNA) Avian Influenza “vaccine”, ARCT-2304. Another version of this type of “vaccine” by the same company, called ARCT-154 or KOSTAIVE, for COVID-19 infection “prevention”, is already “fully approved” and in use in Japan and in the European Union / Scandinavia. Both of these “vaccines” are discussed in this article: https://finance.yahoo.com/news/arcturus-gets-fdas-fast-track-154900033.html, “Arcturus Gets FDA’s Fast Track Tag for Influenza Vaccine Candidate”, 11 April 2025. Two screenshots from this article are below:

Take note of the last sentence in the screenshot above: “A biologics license application for Kostaive in the United States is expected to be filed later in 2025.”

Now, the press release from Arcturus Therapeutics in January 2025, regarding ARCT-2304, found here: https://ir.arcturusrx.com/news-releases/news-release-details/acturus-therapeutics-announces-initiation-phase-1-h5n1-flu, “Arcturus Therapeutics Announces Initiation of Phase 1 H5N1 Flu Vaccine Trial”, 10 January 2025. The clinical trial for ARCT-2304 is registered here: https://clinicaltrials.gov/study/NCT06602531. Note that this is a PHASE 1 human clinical trial. Some of the details are below:

NCT06602531: Study Start Date: 12-12-2024

Primary Completion Date: 7-21-2025 (This means ONLY SEVEN MONTHS of a PHASE 1 human clinical trial before the Primary Completion Date. This is also a RED FLAG indication that Arcturus Therapeutics may likely apply for either a EUA or for a BLA (Biologics License Application, otherwise known as “full FDA approval”) BY THE LATE SUMMER / EARLY FALL OF 2025. In Yours Truly’s opinion, it is SCIENTIFICALLY IMPOSSIBLE to know in FEWER THAN AT LEAST TWO YEARS OF TESTING, WHETHER OR NOT A “VACCINE” ACTUALLY WORKS, LET ALONE BE “SAFE AND EFFECTIVE.”) In Yours Truly’s opinion, any claim by a “vaccine” manufacturer that a DNA-viral vector-based /RNA-based / “protein subunit”-based / “cell-based” / mRNA-based / saRNA-based / sa-mRNA-based “vaccine” — can be SAFELY developed, “tested” and granted either an EUA or “full approval” by the FDA, in fewer than at least two years, must be considered to be not only suspect — but as outright fabrication or wishful thinking.

Estimated Study Completion Date: 12-19-2025 (This would mean that the Phase 1 human clinical trial would be “completed” IN ONE YEAR PLUS ONE WEEK.)

Recruitment Information: Not Yet Recruiting

Contacts and Locations: NO locations are listed; there is only an 888 area code number to call the “Clinical Trials Disclosure Manager” for further information (which, by the way, said information would only be released to “researchers.” One assumes this means “degree-holding scientific researchers”, not to non-scientific-degree-holding researchers, let alone to the general public.)

Clicking on the Researcher View tab on the main study registration page yields some ** interesting ** information. Some examples: There will be a total of 200 persons used in the clinical trial; the ages will range from 18 years old to 80 years old; there is a “control group” that will receive injections of what appears to be a “standard influenza vaccine” plus, and/or, a saline placebo; and, there will be THREE levels of injectable used on the study subjects, at a “low” dose, a “medium” dose, and a “high” dose — of which, NO amounts of “vaccine candidate” are delineated; among other information.

A short summary of how saRNA (aka sa-mRNA) “vaccines” work is here: https://www.promegaconnections.com/how-do-self-amplifying-rna-vaccines-work/, by Jordan Nutting, 6 February 2024. Please see the screenshots from this article, below:

Note the language above regarding what saRNA does in the body: “...it’s like having a built-in printing press that produces additional vaccine in cells.” (Yours Truly: This “printing press” is at work in the body of the person who takes an saRNA “vaccine” for an unknown time — perhaps indefinitely.)

Note the language about the very long length of the mRNA sequences that must be used in saRNA (aka sa-mRNA) “vaccines.”

WHY IS THERE THIS UNHOLY RUSH TO GET ARCT-2304 THROUGH THE CLINICAL TRIAL PROCESS AND INTO EITHER EUA OR BLA STATUS WITH THE FDA, AND THEREFORE GET INTO USE IN THE UNITED STATES? In Yours Truly’s opinion, the answer may involve: Peter Marks, MD, PhD.

When it relates to a new drug or biologic product (including vaccines and other injectables), BOTH the FDA’s CBER (Center for Biologics Evaluation and Research) AND CDER (Center for Drug Evaluation and Research) departments are involved. Peter Marks, MD, PhD, was the director of CBER from 1 January 2016 (this made him an Obama administration holdover at the FDA) until his resignation from CBER on 29 March 2025 (his resignation became effective on 5 April 2025.) It appears that unless Dr. Marks resigned, he was going to be fired by now-HHS Secretary Robert F. Kennedy, Jr. Please see the screenshots below from this article on the situation (https://www.thefocalpoints.com/p/breaking-peter-marks-issues-veiled, “BREAKING – Peter Marks Issues Veiled Threat to America About Man-Made Biological Threats”, by Nicolas Hulscher, MPH, 5 April 2025.) The first is from Dr. Marks’ resignation letter; the other is from the article by Mr. Hulscher:

The screenshot below is from the interview transcript with Dr. Marks on CNN on 4 April 2025:

During this CNN interview, Dr. Marks made the “oblique threat” above.

On 2 April 2025, the FDA chose Scott Steele, PhD, as the Acting Director of CBER. Dr. Steele has been a full-time CBER advisor in late 2022 (this makes him a “Biden administration” holdover; and, Dr. Steele started with the FDA in June 2020 as an advisor in that agency’s Office of Medical Policy Initiatives.) Please see: https://www.fiercepharma.com/pharma/fda-taps-scott-steele-lead-cber-acting-basis-after-marks-departure, 2 April 2025. On 10 April 2025, the FDA granted “Fast Track” process approval for ARCT-2304. Who chose Dr. Steele to be the Acting Director of CBER on 2 April 2025?

In Yours Truly’s opinion, it is inconceivable that Dr. Steele and his colleagues at the related department of CDER, Dr. Jacqueline Corrigan-Curay, MD, and Peter P. Stein, MD — do not know what saRNA (aka sa-mRNA) does and how dangerous it can be to the human body; and, do not know that a “vaccine” product needs at least two to as long as five years to be properly developed, tested, results analyzed, and applications submitted to the FDA for EUA or for “full approval” of the injectable.

In Yours Truly’s opinion, what may be going on at the FDA regarding ARCT-2304 is a combination of an “end-run” around what Secretary Robert F. Kennedy, Jr., is trying to do to bring the agency into account for what is it supposed to do — to work in the best interests of the public health of the American people; plus, what appears to be personal bias against Mr. Kennedy, Jr., himself; plus, what appears to be a “H3ll-bent mindset” in the FDA to force the use of self-amplifying RNA products on the American people without going through the proper (lengthy) processes of testing, analysis, and proof of “safety and efficacy.”

Yours Truly presents the situation and her opinions. Readers can do their own due diligence and make their own conclusions.

FLASH! UPDATES, MONDAY 15 APRIL 2025:

First, this: https://twitter.com/RenzTom/status/1910780397899964560

Then, these: https://www.vigilantfox.com/p/fda-fast-tracks-vaccine-nightmare, 14 April 2025. Please scroll down the page to find the interview with Attorney Tom Renz; also: https://sayerji.substack.com/p/the-self-amplifying-rna-vaccine-threat, “The Self-Amplifying RNA Vaccine Threat and the Rise of BIo-Digital Warfare”, 11 April 2025. A screenshot from this article is below:

And, finally, from 2024: https://www.theqtree.com/2024/10/04/health-friday-open-thread-10-04-2024-self-amplifying-fda-sarna-a-primer-on-how-to-amplify-a-disaster/.

Peace, Good Energy, Respect: PAVACA

Health Friday 4.11.2025 Open Thread: The New Paper Detailing the Cardiovascular Dangers of the COVID-19 “Vaccines”

The above free vintage image of a hand-drawn heart is courtesy of VectorStock and Google Images.

Health Friday is a series devoted to information regarding Big Pharma, vaccines, general health, and associated topics. As today’s post speaks to the disaster of the COVID-19 “vaccines”, Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative effects of these lab-created bioweapons.

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. NOTE: Yours Truly has checked today’s offering for any AI-generated content. To the best of my knowledge and belief, there is none. Also: Readers who wish to post anything in the discussion thread of today’s post that is AI-generated, must cite their source. Thank you.

Today’s offering is part of a “mini-series” devoted to a single topic and/or scientific paper. Yours Truly presents a new paper confirming the increased risk for stroke, heart attack, and other cardiovascular serious events, after COVID-19 “vaccination.”

One begins here: https://www.thefocalpoints.com/p/breaking-85-million-person-study, “BREAKING: 85-Million-Person Study Finds Increased Risks of Stroke, Heart Attack, Coronary Artery Disease, and Arrhythmia Following COVID-19 Vaccination”, by Nicolas Hulscher, MPH, 7 April 2025. The new paper cited in his article is found here: https://doi.org/10.4103/ijpvm.ijpvm_260_24, “COVID-19 Vaccination and Cardiovascular Events: A Systematic Review and Bayesian Multivariate Meta-Analysis of Preventive Benefits and Risks”, Raheleh Karimi, et al., 14 March 2025. (A discussion on how Bayesian Multivariate Meta-Analysis models work is here: https://bookdown.org/MathiasHarrer/Doing_Meta_Analysis_in_R/bayesian-ma.html.) Two screenshots from the Hulscher article follow: One is from the paper; the other is his statistical analysis:

Note: The AstraZeneca viral vector DNA COVID-19 “vaccine” uses a “delivery platform” similar to that of the Johnson & Johnson (Janssen) viral vector DNA COVID-19 “vaccine” that was used in the United States from 2021 until it was discontinued in 2023 (https://www.yalemedicine.org/news/coronavirus-vaccine-blood-clots, 17 May 2023.) However, the this “vaccine” (under the brand name, Janssen) is still in use in many other countries around the world (https://en.wikipedia.org/wiki/List_of_COVID-19_vaccines_authorizations#Janssen; scroll down the page to “Janssen.”)

The Karimi, et al., paper, in Yours Truly’s opinion, if one is reading it correctly, while being detailed and using sophisticated models for its conclusions, appears to endorse COVID-19 “vaccination” as a way to reduce the incidence of stroke: and, also, the authors appear to state that multiple injections of a COVID-19 “vaccine” reduce the potential for cardiovascular damage. Yours Truly believes that the paper’s authors have ignored a couple of important items: First, the fact that cardiovascular damage induced from COVID-19 “vaccination” can be incremental and cumulative over time. Please see: 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; refer to Slide 8 through Slide 11 of this article. And, Second, there is the paper published this year, based on the Yale LISTEN Study. Please see: https://doi.org/10.1101/2025.02.18.25322379, “Immunological and Antigenic Signature Associated with Chronic Illnesses after COVID-19 Vaccination”, Akiko Iwasaki, et al. This paper clearly demonstrates that the spike protein in the COVID-19 modRNA “vaccines” (and, therefore, the potential for “vaccine”-induced damage) is present in the “vaccinated” person’s body for as long as, if not longer than, 709 days post-injection.

The following is the Conclusions section of the Karimi, et al., paper. It is astonishing to read that the authors appear to believe that the COVID-19 “vaccines” are “safe and effective” — just that persons with known (or suspected) cardiovascular issues should be tested before they are offered the opportunity to take one of these “vaccines”:

Why on Earth would a person (with cardiovascular issues or not) agree to have a COVID-19 “vaccine” that can cause (or aggravate) cardiovascular issues injected into their body? Why are cardiologists recommending that patients with heart conditions take COVID-19 “vaccines”? Please see: https://www.rush.edu/news/cardiologists-recommend-covid-19-vaccine-heart-patients, “Cardiologists Recommend COVID-19 Vaccine for Heart Patients Doctors say the vaccine can help prevent further heart and health complications”, copyright 2025 Rush University Medical Center (Chicago, Illinois.) Are these cardiologists not aware of the Palmer and Sucharit article cited above? Are they not aware that the FDA knew back in April 2021, that the COVID-19 “vaccines” can, and do, cause numerous types of heart and cardiovascular serious adverse effects in COVID-19 “vaccinated” persons? Please see the Appendix 1. List of Adverse Events of Special Interest section of this report, which Pfizer-BioNTech gave to the FDA in April 2021 regarding the company’s “flagship” modRNA COVID-19 “vaccine”, BNT162b2: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf. Scroll through the pages of the Appendix 1. to see the various types of heart and cardiovascular serious adverse events that were reported in persons who took this “vaccine.” For example, here is Page 2 of the Appendix 1. Note the multiple serious adverse events that were reported regarding cardiovascular conditions.

And there are many more types of cardiovascular serious adverse events reported in the Appendix 1. There are listings under “Coronary”; under “Thrombo”- (for example, Thrombocytopenia; and, under “Vascular” — among others.

The information regarding how dangerous and deadly the COVID-19 “vaccines” are is increasing from a “trickle” to a “torrent.” Why are physicians still recommending these injections? Why are these injections still listed on the CDC Child and Adolescent Immunization Schedule?

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

Health Friday 4.4.2025 Open Thread: the COVID-19 “Vaccines” Decimate the IgG Immune System Cells

The above free image of an 1867 vaccination certificate is courtesy of iStock and Google Images.

Health Friday is a series devoted to information regarding Big Pharma, vaccines, general health, and associated topics. As today’s post speaks to the disaster of the COVID-19 “vaccines”, Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative effects of these lab-created bioweapon toxin injections.

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 post for any AI-generated content. To the best of her knowledge and belief, there is none. If readers wish to post any AI-generated content in the discussion thread for today’s post, they must cite their source. Thank you.

Today’s Health Friday offering is one of a “mini-series” devoted to one topic and to one important news item related to that topic (although there may be other items related to the topic presented as supporting and/or clarifying information. The topic for today is what the COVID-19 “vaccines” do to damage and/or destroy the crucial IgG3 immune system cells in the “vaccinated” person’s body.

Yours Truly begins here, with the news item, and the paper cited in the article: https://www.theburningplatform.com/2025/03/27/immune-changes-from-repeated-mrna-jabs-are-linked-to-a-higher-risk-of-covid/, by Alex Berenson. Below is a screenshot from the article:

This 80% higher risk was found in persons who had had multiple injections of COVID-19 “vaccines.”

The COVID-19 “vaccines”, especially via repeated injections, damage and destroy the crucial IgG3 (“fight it off”) immune system cells in the “vaccinated” person’s body; while, at the same time, fostering the increase of the IgG4 (the “tolerate but never clear”) immune system cells. Another screenshot from the Berenson article is below:

Among the many other online media outlets that have reported on the Monocunill, et al., paper are these: https://www.thefocalpoints.com/p/breaking-study-covid-19-mrna-injections, “BREAKING Study — COVID-19 mRNA Injections Dangerously Reprogram the Immune System, Increasing Infection Risk”, by Nicolas Hulscher, MPH, 27 March 2025; and, https://justthenews.com/politics-policy/coronavirus/spanish-fluke-repeat-covid-jabs-provoke-two-kinds-inferior-antibodies. “Repeat COVID vaccines provoke two kinds of inferior antibodies, study finds”, by Greg Piper, 30 March 2025.

The paper referred to in the Berenson article is here: https://doi.org/10.1016/j.jinf.2025.106473, “Post-Vaccination IgG4 and IgG2 class switch associates with increased risk of SARS-CoV-2 infections”, Gemma Monocunill, et al., 18 March 2025. Below is a screenshot from this paper:

An important paper regarding descriptions and functions of the IgG immune system cell class in the human body is here: https://journals.aai.org/jimmunol/aticle/205/12/3400/107683/IgG-Subclasses-Shape-Cytokine-Responses-by-Human, “IgG Subclasses Shape Cytokine Responses by Human Myeloid Immune Cells through Differential Metabolic Reprogramming”, Willianne Hoepel, et al., 15 December 2020. A screenshot of the Abstract of this paper is below:

Note that this paper was published after the modRNA COVID-19 “vaccines” by Pfizer-BioNTech and by Moderna were granted their initial EUAs in the United States by the FDA (this occurred on 11 December 2020), but before these bioweapon toxin injections entered widespread use.

Yours Truly has written about the IgG immune system cells subclasses, and what the modRNA COVID-19 “vaccines” do to damage the IgG3 cells, here: https://www.theqtree.com/2024/12/06/health-friday-open-thread-12-6-2024-the-immune-system-after-covid-19-vaccination-and-a-note-on-the-virus-itself/.

Back to the Monocunill, et al., paper. There is mention in the paper regarding the involvement of the T17 cells in the “vaccinated” person’s body in the IgG subclass switching. Yours Truly wrote about the importance of the T17 cells (also called Th17 cells or T17 Helper Cells), and the role of the N1-Methylpseudouridine in the modRNA COVID-19 “vaccines” in “turning off” these cells in the “vaccinated” person’s body (thus paving the way for continuous inflammation of many types) here: https://www.theqtree.com/2025/03/21/health-friday-3-21-2025-open-thread-more-on-the-n1-methylpseudouridine-in-the-modrna-covid-19-vaccines/.

However, there is another aspect of the situation discussed in the Monocunill, et al., paper that is of huge importance: The similarities between malaria, COVID-19 infection, and the class switch to IgG4 that the COVID-19 “vaccines” induce. Below is a screenshot from the Discussion section of the paper regarding this:

Yours Truly will now blow something out of the water regarding the FDA’s and the CDC’s official opposition to, and prohibition of, using Ivermectin or Hydroxychloroquine to prevent or to treat COVID-19 infection.

Malaria and COVID-19 infect the lungs in similar ways. Ivermectin can be used to treat malaria. Please see: https://www.isglobal.com/en/-/nueva-evidencia-respalda-el-uso-de-ivermectina-como-una-herramiente-en-la-eliminacion-de-la-malaria, “New Evidence Supports the Use of Ivermectin as a Tool for Malaria Elimination” (article in English translation regarding malaria treatment in Africa), 28 March 2018.

And, Hydroxycholoquine (and also Chloroquine) can be used to treat malaria AND COVID-19. Please see this paper from September 2020: https://pmc.ncbi.nlm.nih.gov/articles/PMC7476892/, “Chloroquine and hydroxychloroquine in the treatment of malaria and repurposing in treating COVID-19”, Zi-Ning Lei, et al. (USA and CCP), 8 September 2020.

In Yours Truly’s opinion, it is inconceivable that the NIH / NIAID / FDA / CDC did not know about the existence of these papers. Instead, by September 2020, these entities were hell-bent in pushing through the unproven modRNA “technology” for the Pfizer-BioNTech and the Moderna modRNA COVID-19 “vaccines” then in development. This meant that the FDA / CDC accepted the manipulated / incorrect “data” that were given to them from the truncated “clinical trials” for these “vaccines” by Pfizer-BioNTech and by Moderna. This meant that the FDA / CDC did not question the sudden “vaccine”-manufacturing switch from the original “Process 1” method to the “Process 2 method” that occurred in August 2020, that is still in use by both companies in the production of their respective “new formula” COVID-19 “vaccine booster shots”, and is based on “culturing” the modRNA of the said “vaccines” in a “bath” of E. coli.

Further confirmation that malaria and COVID-19 infect the lungs in similar ways is here: https://pmc.ncbi.nlm.nih.gov/articles/PMC9445119/, “The striking mimics between COVID-19 and malaria: A review”, Emadeldin Hassan E Konozy, et al. A screenshot from this paper is below:

Note the mention of the ACE2 receptors as regards malaria infection. These cells are also attacked by the COVID-19 virus itself (and, therefore, since they are based on the virus, so do the COVID-19 “vaccines” attack the ACE2 receptors of the “vaccinated” person’s body.)

In short: the FDA / CDC pushed, and continue to push, COVID-19 “vaccines” to “prevent” COVID-19 infections, while knowing that Ivermectin and Hydroxychloroquine also prevent — and treat — COVID-19 infections. Why is this still going on? How about ASKING BILL GATES. UNDER OATH.

This is aside from the fact that those who lab-created the bioweapon of the COVID-19 virus itself, and those who lab-created-and-enhanced the bioweapons of the COVID-19 “vaccines” — knew that malaria and COVID-19 would attack the lungs in similar ways. They knew what would “turn off” the T17 cells that are so important for the immune system and for Uridine in the human body. They knew what would damage or destroy the crucial IgG3 cells of the natural immune system of the human body, while fostering the increase of the IgG4 cells that allow illness and medical conditions to take hold and thrive. These things they incorporated into the creation of the COVID-19 virus itself, and into the creation of the COVID-19 “vaccines.”

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

Health Friday 3.28.2025 Open Thread: COVID-19 Memoirs—An Ongoing Story

The above free image of memoir writing is courtesy of iStock and Google Images.

Health Friday is a series devoted to information regarding Big Pharma, vaccines, general health, and associated topics. As today’s post speaks about the disaster of COVID-19 (the COVID-1 p9 virus itself, and the COVID-19 “vaccines”), Yours Truly dedicates it to the memory of all persons, of whatever age or location, who have passed away from the negative effects of these lab-created bioweapons.

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 found here. NOTE: Yours Truly has checked today’s offering for any AI-generated content. To the best of my knowledge and belief, there is none. Also: If readers wish to post anything in the discussion thread for today’s offering that is AI-generated, they must cite their source.

Today’s post is a COVID-19 Memoir, with this post as the inspiration: https://www.theburningplatform.com/2025/03/17/a-covid-contrarian-speaks-out-about-all-she-has-lost/, a guest post by Alex Berenson. This post describes the memoir statement of Jennifer Sey, who lost her job, her friends, family ties, and more, because she refused to bow to the demands of the organized psy-op that was the “command and control method” used over literally billions of human beings during the COVID-19 pandemic — and which organized psy-op is still being used today. Readers are welcome to post their own COVID-19 memoirs on today’s discussion thread, leaving out or referring to in an “oblique” manner, those details they wish to keep private.

Others on the board here have shared their COVID-19 Memoirs. Some of these postings have detailed dealing with an infection of the COVID-19 virus itself. Other postings have described the experiences of watching “vaccinated” family or friends becoming ill from the negative effects of the “vaccines” that they had taken. Still others have described their own issues after being “shed upon” by COVID-19 “vaccinated” persons. Sadly, our own Deplorable Patriot (Susie Sampson) passed away from the combined effects of the COVID-19 infection she very likely caught in November 2024 from a recently COVID-19-“boosted” choir member.

Yours Truly now adds her own COVID-19 Memoir. It began in December 2019, with the first media reports of a “mystery illness” that was infecting and killing people in Communist China, which “mystery illness” then making its way to the United States. This “illness” was variously called “Wuhan coronavirus”, “coronavirus”, or “novel coronavirus” (among other names), finally settling on the name “COVID-19” or “SARS-CoV-2” in early 2020. The issue became more “personal” in mid-February 2020, when Yours Truly contracted an illness that had all the hallmarks of an infection by the COVID-19 virus itself, most likely via exposure either at a restaurant in Chapel Hill, or at a local discount store in Durham. One was very sick for almost a month, subsisting on hot tea with honey and lemon, vitamins, scrambled eggs and toast, Tylenol^(R), DayQuil^(R), and guaifenesin cough syrup; after that, it was another month before the fatigue began to lift, the coughing to lessen and stop, and taste and smell to fully return. I was literally sequestered to my house for over six weeks. At the same time that I was sick, I was also taking care of my little Yorkie, Sona, who was entering the end stage of the kidney disease that resulted in his being put to sleep in my arms in mid-August of 2020.

It was during this period that I began to research about, read about, think about, and to eventually write about, this virus. My first decision was that I would never permit the deep-nasal probe PCR “test” to be administered to me. I began to order in groceries; to wear disposable gloves whenever I had to leave the house to do absolutely necessary things like getting gasoline for the car; to change clothes and bathe after I returned from being out of the house; and so on. Amazon became my source for many items. The United States went into “lockdown” on almost all aspects of the economy, and of life in general, by mid-March of 2020. The fear was palpable.

By the summer of 2020, there was speculation regarding the development and use of COVID-19 “vaccines.” There was speculation regarding the development and use of monoclonal antibody therapy for COVID-19 virus infected persons. Persons hospitalized for COVID-19 infection were being put on Remdesivir and ventilators, killing many. Antigen tests to determine whether or not a person had been infected with the COVID-19 virus were being used by September 2020. Then, the Pfizer-BioNTech and the Moderna modRNA COVID-19 “vaccines” were granted their initial Emergency Use Authorizations for use in the United States on 11 December 2020. Starting in January 2021, all of the members of my family, with the exception of Yours Truly, were getting COVID-19 “vaccinated”; in many cases, this was “mandated” or “required” in order for them to keep their jobs, for travel, and so on. In the spring of 2021, I began to shift much of my focus to researching about the COVID-19 “vaccines” — and came to the conclusion that a “vaccine” that had been developed and put on the market as quickly as these products were, was likely not a good thing. I made a decision to never allow myself to be COVID-19 “vaccinated.” This was the beginning of strained relationships with “vaccinated” family and friends, once Yours Truly informed them that these “vaccines” were not for her. I contacted a physician through AFLDS (America’s Frontline Doctors), and started taking prescribed Hydroxychloroquine and Zinc. Afterwards, I contacted the then-FLCCC Alliance (now the Independent Medical Alliance) and began taking prescribed Ivermectin. Yours Truly is still not COVID-19 “vaccinated.”

It is now, in March 2025, five years from the first COVID-19 “lockdowns.” Yours Truly lost a cousin in September 2023 due to the negative effects of the COVID-19 “vaccines” he had taken. Yours Truly lost her brother in October 2024 due to the negative effects of the COVID-19 “vaccines” he had taken. Yours Truly is now concerned about the other “vaccinated” members of her family. She had tried to warn some of them, based on my research, of the dangers and uncertainties of these bioweapon toxin injections, but was met with “We follow the science” or “I trust my doctor.” I hope the ongoing strained relationships between certain “vaccinated” family members and Yours Truly will heal. I have made certain decisions regarding how I interact with people and situations outside the family circle when encountering them in public places.

Life as it was before November 2019 will never be the same. COVID-19 is the perfect example of an “equal-opportunity” bioweapon. The COVID-19 virus itself, if a person is infected with it, can have lingering, or even permanent, issues that remain after the person recovers. The COVID-19 “vaccines”, since they contain the virus, plus “enhancements” such as N1-Methylpseudouridine, permanently and negatively affect “vaccinated” persons throughout the body, including the brain. “Long COVID”, resulting either from an infection of the COVID-19 virus itself, or from being COVID-19 “vaccinated”, is now recognized medical condition. There is also the emerging issue of COVID-19 “vaccine shedding” from “vaccinated” persons onto other persons, including onto the non-“vaccinated.”

Those adults who are not COVID-19 “vaccinated” (the percentage of people in this category is anywhere between 15% – 25% of the entire population of the Earth) have, in a sense, “defeated COVID-19” — even if they contracted an infection of the virus and recovered. This has nothing to do with the “Joe X is not COVID-19 “vaccinated”, so he is a pureblood” depiction; or with the “Joe X is not COVID-19 “vaccinated”, so he is somehow morally superior to those who are “vaccinated”” allegation — this has everything to do with personal decision making. Those adults who are not COVID-19 “vaccinated” have resisted the gaslighting, the “mandates” and the “recommendations” to get COVID-19 “vaccinated”; the urging from “vaccinated” family and friends; the loss of employment, of schooling, of opportunities, of relationships. They have grieved and mourned for “vaccinated” family members and/or friends who have passed away from the negative effects of the COVID-19 “vaccines” that they had taken. They have, in many instances, done their own research into the “vaccines” and vowed never to take them. They have, in many instances, decided to never allow their children to be COVID-19 “vaccinated.” They have learned that “safe and effective”, as applied to these bioweapon toxin injections, was — and is — a lie. They are stronger than they knew. They are stronger than they know. They will need this strength in the future.

Peter A. MCullough, MD, with his co-authors, published a paper in October 2024 regarding the COVID-19 infodemic and censorship. The paper is found here: https://researchandappliedmedicine.com/revistas/vol2/revista3/a-narrative-review-of-the-covid-19-infodemic-and-censorship-in-healthcare-doi-8.pdf. It is also found here: https://doi.org/10.55634/2.3.8, “A Narrative Review of the COVID-19 Infodemic and Censorship in Healthcare.” Below are screenshots of the Abstract from this paper; followed by Table 2 from the paper:

Yours Truly believes that, in order for society to heal from the COVID-19 disaster, to have trust in the medical profession, to have trust in the government, the perpetrators of the COVID-19 disaster must be brought to justice; and that the unsafe, ineffective, dangerous and deadly COVID-19 “vaccines” must be withdrawn from the market worldwide. The “establishment medicine” entities (the American Medical Association; the American Academy of Pediatrics; the American College of Obstetricians and Gynecologists; and many more); the government agencies (the CDC; the FDA; the Department of Health and Human Services; and many more) — who are still “recommending” these injectables, who still have them on the Immunization Schedules — must stop these activities. All mRNA-based “vaccine” funding and development must be stopped until the entire issue of the safety and efficiency of these injectables is thoroughly investigated and analyzed. Medical freedom of choice must be returned to the general public — for example, Ivermectin and Hydroxychloroquine must be made readily available at a low cost. Physicians must be permitted to prescribe these safe and effective prophylactic / treatment drugs for COVID-19 infection without fear of being “disciplined” or “restricted” by the their state medical licensing board; let along having their License to Practice Medicine revoked. Hospitalized COVID-19 patients must be allowed freedom of choice to be treated inpatient with Ivermectin or Hydroxychloroquine, Vitamin D, and other effective treatments that are, even now, being denied because the FDA does not “authorize” or “approve” them.

There are many persons who must be held accountable for their actions during the entire COVID-19 disaster. Among them: The first person, in Yours Truly’s opinion, who must be held accountable for his actions during the entire COVID-19 disaster is Dr. Anthony Fauci. Now in “retirement”, he commands $100,000 per “motivational talk”, like the one he is scheduled to give on 14 April in Sarasota, Florida. Please see: https://rescue.substack.com/p/serious-questions-for-fauci, by Matt Walsh, 23 March 2025.

The next two persons, in Yours Truly’s opinion, who must be held accountable for their actions during the entire COVID-19 disaster are: Dr. Francis Collins (Dr. Fauci’s superior at the NIH; now retired); and, Peter Daszak, PhD, of EcoHealth Alliance (funneling Gain-of-Function funds to the Wuhan Institute of Virology, among other research facilities, for the lab-creation of the COVID-19 virus, and coordinating the “official” government communications to the media; Dr. Daszak has recently been fired from EcoHealth Alliance. )

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

Health Friday 3.21.2025 Open Thread: More on the N1-Methylpseudouridine in the modRNA COVID-19 “Vaccines”

The above image of the chemical structure of Uridine is courtesy of SOMA Analytics and Google Images.

Health Friday is a series devoted to information regarding Big Pharma, vaccines, general health, and associated topics. As today’s post speaks of the disaster of COVID-19 (the COVID-19 virus itself, and the COVID-19 “vaccines”), Yours Truly dedicates it to the memory of all persons, or whatever age of locations, who have passed away from the negative effects of these lab-created bioweapons.

There are Important Wolf Moon Notifications; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. The are linked here. NOTE: Yours Truly has checked today’s offering for any AI-generated content. To the best of my knowledge and belief, there is none. Also: If readers wish to post anything in the discussion thread for today’s post that is AI-generated, they must cite their source.

Today’s post is one of a Health Friday “mini-series” devoted to discussion of a single topic. The topic for this offering is the chemical compound N1-Methylpseudouridine in the modRNA COVID-19 “vaccines.”

Yours Truly has written in broader form about this compound. Please see: https://www.theqtree.com/2024/11/08/health-friday-11-8-2024-open-thread-the-insidious-n1-methylpseudouridine-in-the-covid-19-vaccines/. Today’s offering is some further information regarding this compound and how it can affect COVID-19 “vaccinated” persons.

The purpose for putting N1-Methylpseudouridine into the modRNA COVID-19 “vaccines” was for this compound to replace the RNA of the natural Uridine in the “vaccinated” person’s body with a synthetic form of Pseudouridine, plus a form of methane.

Uridine (U or Urd) is an RNA synthesis component of the human body. It is present in blood plasma and in the cerebrospinal fluid. It is synthesized by the mitochondrial cells of the body. Two sources of information are: One: https://www.sciencedirect.com/topics/neuroscience/uridine, 14 May 2010. A screenshot of part of Chapter Four of one reference book from this source is below:

The Chapter Four is found here: https://doi.org/10.1016/8978-0-12-374927-7.00004-2, “Chapter 4 – Substances Involved in Neurotransmission”, George M. Kapalka. Note the mention of food sources for Uridine in the screenshot above.

And, Two: https://nootropicsexpert.com/uridine-monophosphate/, David Tomen, 3 April 2024. A screenshot from this article is below:

Both of the above make it clear that Uridine is an important RNA synthesis component of the human body. It is also very clear that Uridine is an important element in both parts of the “gut-brain connection.”

What is Pseudouridine, and what does it do? Please see: https://pmc.ncbi.mln.nih.gov/articles/PMC8007080/, “Regulation and Function of RNA Pseudouridylation in Human Cells”, Erin K. Borchardt, et al., 23 November 2021. A screenshot from the Introduction of this paper is below:

Note that Pseudouridine interacts “with protein and other RNAs.”

Now, to the lab-created compound N1-Methylpseudouridine: and here, in Yours Truly’s opinion, is where the topic gets “very interesting.” A detailed and meticulous paper on how this compound works is here: https://doi.org/10.1093/narlgkad, “Nanopore sequencing for N1-methylpseudouridine in RNA reveals sequence-dependent discrimination of the modified nucleotide triphosphate during transcription”, Aaron M. Fleming, Cynthia J. Burrows, 16 January 2023. (Note: the monophosphate in Uridine is “transformed” into a triphosphate in N1-Methylpseudouridine.) Several screenshots from this paper are below; first, the Abstract:

Note the mention of T17. Yours Truly will return to this later.

Followed by Figure 1 from the paper:

Followed by Figure 7C, the new “base pairs” created by N1-Methylpseudouridine in RNA:

And, followed by one more item from the paper, regarding T cells, from the Results section:

Now, to T17 cells. These T helper cells are also called Th17 cells orT_H17 cells. They belong to the CD4 helper lymphocyte cell subset. T17 helper cells are found in Uridine: https://pmc.ncbi.nlm.nih.gov/articles/PMC4137509/, “Th17 Cells in Autoimmune and Infectious Diseases”, J.F. Zambrano-Zaragoza, et al., 3 August 2024. This paper discusses multiple roles for T17 cells. These cells produce a protein called interleuken 17 (IL-17.) Below is a screenshot from the section 1. Introduction of the above paper:

Yours Truly concludes: The N1-Methylpseudouridine in the modRNA COVID-19 “vaccines” replaces the natural Uridine (along with the T17 helper cells present) with Pseudouridine plus a form of methane. Neither of these “replacement elements” can perform the functions of the natural T17 helper cells in Uridine. In fact, the effect of N1-Methylpseudouridine in the modRNA COVID-19 “vaccines” is to “kick the door open” for the onset of multiple types of inflammation, both in the body and in the brain of the “vaccinated” person. In the brain, this can, and does, include: onset of mood changes (that can signal the onset of psychosis); onset of cognitive impairment; pave the way for the onset of dementia and/or of Alzheimer’s disease; and more. In the body, this can, and does, include the onset of abdominal / bowel disorders; general inflammation; and more. The addition of of N1-Methylpseudouridine to the modRNA COVID-19 “vaccines”, in Yours Truly’s opinion, is one of the major “can’t find the fingerprints down the road” elements related to persons presenting with serious adverse effects after COVID-19 “vaccination.” The perpetrators who lab-created the modRNA COVID-19 “vaccines” drew on accumulated knowledge regarding the role of the T17 helper cells in the Uridine RNA—and inserted N1-Methylpseudouridine into these “vaccines” to negate the beneficial effects of the T17 helper cells in the Uridine RNA. The “scientific rationale” for the inclusion of N1-Methylpseudouridine was that this compound “increased the effectiveness of the vaccine.” One of the plethora of papers that “heralded” this “discovery” is here: https://doi.org/10.1021/acscentsci.1c00197, “Modifications in an Emergency: The Role of N1-Methylpseudouridine in COVID-19 Vaccines”, Kellie D. Nance, Jordan L. Meier, 6 April 2021. While it is a correct statement that N1-Methylpseudouridine does indeed “increase the efficiency” of the modRNA COVID-19 “vaccines” — it was “conveniently” left out of the “scientific rationale” explanation that this compound would also serve as a sort of “master switch” to “turn off” the beneficial T17 helper cells in the “vaccinated” person’s body (with no option to go back to the “on” setting) — and what would be the consequences.

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA