Health Friday 6.6.2025 Open Thread: TLR4, S1, and mRNA-1283 (mNEXSPIKE): A Scientific Gourmanderie

The above image of TLR Signalling Pathways is courtesy of BioFinder and Google Images.

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

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

And now, to the reader’s Edification Smorgasbord, a “feast of information” regarding just how dangerous and potentially deadly mRNA-1283 (mNEXSPIKE) is, Yours Truly offers the following Menu:

APPETIZER: WHAT IS TLR4?

TLR4 (aka Toll-like receptor 4) is a transmembrane protein that exists across a cell membrane. TLR4 functions as a kind of “sensing device” within the body. It detects foreign bacteria and viruses. When a foreign element is detected by TLR4, it begins to send messages to the natural immune system to activate the immune response. TLR4 is crucial to the correct functioning of the natural immune system. Please see the screenshots below for more information:

Citation: https://en.wikipedia.org/wiki/Toll-like_receptor_4

Citation: https://doi.org/10.1016/j.intimp.2007.05.016, “Toll-like receptors in inflammation, infection and cancer”, Keqiang Chen, et al., October 2007. Found via: https://www.sciencedirect.com/topics/immunology-and-microbiology/tlr4.

FIRST COURSE: THE FDA APPROVES “mNEXSPIKE” IN MAY 2025:

The “newest version” COVID-19 “vaccine”, mRNA-1283 (aka mNEXSPIKE), was “fully approved” by the FDA on 30 May 2025. Yours Truly wrote about this situation here: https://www.theqtree.com/2025/06/01/stop-press-edition-hhs-secretary-robert-f-kennedy-needs-to-resign-now/. This “vaccine” claims to be “more effective” in “preventing” an infection of COVID-19. The claim is based on the fact that mRNA-1283 (aka mNEXSPIKE) uses “only” the S1 protein and the N sector of said S1 protein of the COVID-19 virus spike protein, as opposed to using the entire spike protein (as in mRNA-1273, the original “flagship” modRNA COVID-19 “vaccine” by Moderna.) Please see: https://doi.org/10.1093/infdis/jiaf022, “Safety and Immunogenicity of SARS-CoV-2 Spike Receptor-Binding Domain and N-Terminal Domain mRNA Vaccine”, Spyros Chalkias, et al., 15 April 2025 (most of the authors of this “informational paper” are either affiliated with Moderna, or are employees of Moderna.) A screenshot of the Background section of the Abstract of this paper is below:

At first glance, this “new development” by Moderna may appear to be a “positive” achievement. However, there are other issues that arise:

First, there is the fact that the S1 protein of the SARS-CoV-2 virus contains both the RCB (Receptor-Binding Domain) AND the N-terminal domain of the virus. It is the RCB that allows the virus to “attach” itself , or to “dock” itself, to cells in the body — for example, to the ACE2 cell receptors; and, to TLR4 cells. The N-terminal domain is the “end part” of the S1 protein; it is a “free” group at the end of the protein, while, at the same time, it “initiates” a polypeptide chain.

Second, there is the fact that the S1 protein of the SARS-CoV-2 virus interacts with TLR4 cells. Yours Truly begins with this: https://news-medical.net/news/20210510/Research-suggests-Pfizer-BioNTech-COVID-19-vaccine-reprograms-innate-innate-immune-responses.aspx, Sally Robertson, B.Sc., 10 May 2021. Please see the following screenshots from this article:

While the above article refers to the Pfizer-BioNTech modRNA COVID-19 “vaccine” BNT162b2, the modRNA COVID-19 “vaccine” from Moderna, mRNA-1273, also targets the RBD, which interacts with TLR4 cells in the “vaccinated” person’s body. In addition, all of the modRNA “descendant clone” COVID-19 “vaccines” by both companies also use the RBD, there interacting with TLR4 cells in the “vaccinated / boosted” person’s body.

TLR4 cells are also present in multiple areas and organs of the body. The modRNA COVID-19 “vaccines” will interact with these cells. This is due to the fact that the S1 protein of the SARS-CoV-2 virus contains certain amino acids residues (numbers 1-1208) that interact with TLR4 cells. Please see: https://doi.org/10.1016/j.heliyon.2021.306187, “SARS-CoV-2 spike protein S1 subunit induces pro-inflammatory responses via toll-like receptor 4 signaling in murine and human macrophages”, Ken Shirato, Takako Kizaki, February 2021. A screenshot of the Abstract of this paper follows:

Regarding the S1 amino acids residues 1-1208 and TLR4, please see this paper, from 2020: https://europepmc.org/article/ppr/ppr170060, ” Structural characterization of a nanobody derived from a naive library that neutralizaes SARS-CoV-2″, M Dumoux, et al., 1 June 2020. Below are screenshots from the Methods section and from a portion of the Supplementary Table section of this paper (the Supplementary Table portion shows some of the gene code for the S1 1-1208 residues):

Further information regarding SARS-CoV-2 spike protein and its interaction with TLR4 is found here: https://doi.org/10.3389/fimmu.2024.1368946, “TLR2/4 are novel activating receptors for SARS-CoV-2 spike protein on NK cells”. Nadine Landolina, et al., 30 May 2024. “NK” stands for “Natural Killer” cells in the body. A screenshot from this paper is below:

Then, there is the issue of clinical trial used by the FDA to “justify” the “full approval” of mRNA-1283 (aka mNEXSPIKE), NCT05137236 (https://clinicaltrials.gov/study/NCT05137236.) There was NO Placebo Control Group in this study. The study participants (study subjects) were injected with the following Moderna modRNA COVID-19 “vaccines”: mRNA-1273; OR, mRNA-1283; OR, mRNA-1283.211; OR, mRNA-1283.529. Why was there no Placebo Control Group? Assuming that the study subjects knew, in advance, they would be injected with any one of FOUR different variations of a modRNA COVID-19 “vaccine”, were they fine with that?

And, there is the “opinion piece” by Dr. Martin Makary (FDA Commissioner) and Dr. Vinay Prasad (new head of the FDA’s CBER division), regarding the “new approach” that the FDA will use for COVID-19 “vaccines.” Please see:

SECOND COURSE: WHAT DOES THE modRNA COVID-19 “VACCINE”, mNEXSPIKE, CONTAIN?

Please see the FDA-issued Fact Sheet for Healthcare Providers (aka the Package Insert) for mRNA-1283, mNEXSPIKE: https://www.fda.gov/media/186738/download. Below is a screenshot of section 11 Description, section 12 Clinical Pharmacology, and section 13 Nonclinical Toxicology of this document:

Which plainly states that mNEXSPIKE contains the same types of dangerous, deadly lipid nanoparticle and excipient that all the other modRNA COVID-19 “vaccines” by Moderna contain: SM-102, and PEG2000-DMG. This means that mNEXSPIKE will be rapidly spread into every cell in the “vaccinated” person’s body. It is also clear that mNEXSPIKE has NOT been tested for mutation potential, cancer-inducement potential, or reproductive impairment potential.

Yours Truly then performed a search to ascertain whether or not mNEXSPIKE contains N1-methylpseudouridine. She has written extensively on this board about this lab-created “fake Uridine plus a form of methane”, which completely replaces the natural RNA in the Uridine in the body. Recall that natural Uridine is crucial to multiple body functions and mechanisms: regulation of mood, of learning and memory, and of “gut-brain connection” functions. Lo and behold, the US Patent for mRNA-1283 (aka mNEXSPIKE) does have language describing “various types” of pseudouridine, including N1-methylpseudouridine, are used in all of Moderna’s modRNA COVID-19 “vaccines” — which would also include mNEXSPIKE. The US Patent for mRNA-1283 is found here (US 20240382581A1): https://patents.google.com/patent/US20240382581A1/en?q=(mRNA-1283)&oq=mRNA-1283, “Pan-human coronavirus vaccines”, ModernaTX, published 21 November 2024. Please see sections 0120, 0121, 0122, and 0123 of this document for descriptions of the “various types” of pseudouridine.

Lastly, there is the question as to whether mNEXSPIKE contains any saRNA (self-amplifying RNA) component. Yours Truly searched for information regarding this, since the IM dose (intramuscular injection dose) of this COVID-19 “vaccine” is a very small amount — 0.2mL. She found this, which appears to be a “dancing all around the truth” description of this “vaccine.” Please see: https://synapse.patsnap.com/article/what-is-mrna-1283-used-for?, 28 June 2024. A screenshot from this article is below:

Read the last sentence in the second paragraph above, especially “…a robust and durable immune response, potentially requiring fewer doses and offering longer-lasting immunity compares to other vaccines.” Sounds like a description of the saRNA H5N1 “vaccine”, KOSTAIVE, currently approved for use in the EU / Scandinavia, and in Japan; and, a version of which “vaccine” is to begin clinical trials in the United States (NCT06602531), under the name ARCT-2304.

DESSERT AND BEVERAGES: REACTIONS AND QUESTIONS:

First, this: https://www.thefocalpoints.com/p/maha-movement-flabbergasted-covid, “MAHA Movement Flabbergasted COVID-19 Vaccines Remain on Market”, Peter A. McCullough, MD, MPH, 2 June 2025. There is an embedded interview with Dr. McCullough in this article, along with a linked copy of the “Kabuki Theater performance” regarding “stopping” the COVID-19 “vaccines” in the United States by Dr. Martin Makary (FDA), Dr. Jay Bhattacharya (NIH DIrector), and HHS Secretary Robert F. Kennedy, Jr., on 27 May 2025. A screenshot from the McCullough article is below, giving his views on the current situation:

Second, this tweet, from Dr. William Makis: https://x.com/MakisMD/status/1930296443434348771, 4 June 2024. Two screenshots from his tweet are below: first, a statement from HHS Secretary Kennedy, Jr.; and, second, from Dr. Makis:

Questions, posed by Yours Truly: Why did the FDA “fully approve” a “new”, modRNA COVID-19 “vaccine” that specifically targets person over age 65, and persons who “fit” a detailed list of “persons at risk of severe COVID-19 infection”, as complied by Dr. Martin Makary and Dr. Vinay Prasad? Why was there a “Kabuki Theater performance” on 27 May 2025 by Drs. Makary and Bhattacharya, along with HHS Secretary Kennedy, Jr., when it was obvious by that date that the FDA “full approval” of mNEXSPIKE was “a done deal”? Why did the FDA issue an Approval Letter to Moderna for mNEXSPIKE that has so many “caveats”, “requests for more information”, and an “order” for the company to perform a Phase 4 clinical study on the “vaccine” — a “vaccine” that the FDA had just “fully approved”? Please see: https://www.fda.gov/media/186740/download; and, the screenshot of Page 9 of this document, regarding the “order” for the Phase 4 study, below:

More questions, posed by Yours Truly: How many elderly persons are going to be pressured / cajoled / “mandated” (by the nursing home or care facility where they live), to take mNEXSPIKE? Will they be told that this injectable is “safer” than mRNA-1273, “because the dose is smaller”? What about persons who “fit” into the multiple categories of “persons at high risk for severe COVID-19 infection” according to Drs. Makary and Prasad? What pressure will these persons be subjected to in order to get them to agree to take mNEXSPIKE? Finally, will people be told the truth that mNEXSPIKE, just because it does not contain the S2 portion of the SARS-CoV-2 spike protein, is NOT “mRNA-1273 Lite” — but, rather, it is another version of a dangerous, potentially deadly modRNA COVID-19 ‘”vaccine”?

Peace, Good Energy, Respect: PAVACA

STOP PRESS EDITION: HHS Secretary Robert F. Kennedy, Jr., Needs to Get Control, or to Resign — Now.

The above image of a vintage vaccine vial and syringe is courtesy of Google Images.

This post is a STOP PRESS EDITION. It has to do with the FDA BLA (Biologics License Application) approval of the Moderna COVID-19 modRNA “vaccine” mRNA-1283. This “vaccine” was FDA-approved without any clinical trial in which there was a placebo control group. mRNA-1283 contains a “shorter portion” of the COVID-19 virus spike protein. This “vaccine” also contains elements of the H7N9 Avian Influenza strain that was used in Gain-of-Function experiments by Dr. Yoshihira Kawaoka, DVM, PhD, in 2013, along with other scientists, at the University of Wisconsin (Madison.)

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 this 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 of today’s offering, they must cite their source. Thank you.

Today’s offering is short and to the point. Special Thanks to our good duchess01, to https://www.thefocalpoints.com/, and to http://mole.substack.com/. Please refer to the following posts by Yours Truly for relevant background information regarding today’s offering: https://www.theqtree.com/2025/05/30/health-friday-5030-2025-open-thread-what-is-going-on-at-hhs-the-fda-and-the-cdc/; and, https://www.theqtree.com/2025/05/16/health-friday-open-thread-5-16-2025-about-that-universal-vaccine-theres-more-than-meets-the-eye-part-two/.

Please see the following breaking news outlets pieces regarding the FDA granting the BLA for the Moderna “newest COVID-19 “vaccine”, mRNA-1283: First, this one: https://www.thefocalpoints.com/cp/164898171, “BREAKING: FDA Goes Rogue — Approves Moderna’s Next-Gen COVID-19 mRNA Injection Without a Placebo-Controlled Trial”, Nicolas Hulscher, May 2025. Please see the screenshots from this article, below:

HOWEVER, there is another aspect to the mRNA-1283 modRNA COVID-19 “vaccine” — this injectable appears to be a combination of BOTH the SARS-CoV-2 virus AND elements of the deadly H7N9 Avian Influenza virus. Please see: https://jonfleetwood.substack.com/cp/164803097, “FDA Approves Moderna COVID Jab Containing GOF Bird Flu Gene Segment That PCR Could Mistake for Infection”, 31 May 2025. The “bird flu gene segment” is from the Gain-of-Function experiments with the H7N9 Avian Influenza virus conducted by Dr. Yoshihiro Kawaoka, Ron Fouchier, and other scientists, under the aegis of the University of Wisconsin (Madison), where Dr. Kawaoka has his lab. These Gain-of-Function experiments were “outed” when serious lab accidents occurred; it appears that the experiments were then stopped. But not before Dr. Fouchier wrote this article: https://www.science.org/doi/10.1126/science.1243325, “Gain-of-Function Experiments on H7N9”, 9 August 2013, in which Dr. Fouchier attempted to justify further Gain-of-Function experimentation.

Please see the following screenshot, below, from the Wikipedia entry on H7N9 (https://en.wikipedia.org/wiki/Influenza_A_virus_subtype_H7N9):

The archived article regarding the H7N9 experiments at the University of Wisconsin (Madison), is found here: https://archive.ph/LX7MP, “Study: Lab-derived H5N1 virus component binds to human receptors”, Robert Roos, 13 April 2013.

In Yours Truly’s opinion, Robert F. Kennedy, Jr., the Secretary of Health and Human Services, is not doing his job. BOTH the FDA and the CDC have now “gone rogue” — first, with the “sleight-of-hand” regarding the CDC’s “new recommendations” about the COVID-19 “vaccines” (per Dr. Susan Monarez, PhD, the current Acting Director of the CDC, as of 30 May 2025); and, second, with the FDA (Dr. Martin Makary, Commissioner) granting approval of the Moderna modRNA COVID-19 + H7N9 gene pieces combination “vaccine”, mRNA-1283 (as of 31 May 2025.) It is time, in Yours Truly’s opinion, for Secretary Kennedy, Jr., to either get control of the FDA and CDC — after all, these agencies are part of HHS — or, to resign, and allow President Trump47 to find someone who will.

FLASH UPDATES! MORE ON THE “DIRTY BACKSTORY” RELATED TO THE FDA’s APPROVAL OF mRNA-1283 ON 30 MAY 2025:

ONE: The FDA’s Approval Letter to Moderna on 30 May 2025, regarding mRNA-1283: https://www.fda.gov/media/186740/download. Please see the screenshot of page nine of this document, below:

This is the PHASE 4 clinical study that Moderna is requested to perform for mRNA-1283, but which has NOT begun yet, nor has it ENROLLED any subjects yet.

TWO. This is the slide presentation for the CDC’s ACIP committee meeting for April 2025 related to the “2025-2026 COVID-19 Vaccines Formula” selections. Notice that there is NO vote that ACIP planned to take regarding mRNA-1283. Please see: https://www.cdc.gov/acip/downloads/slides-2025-04-15-16/05-Panagiotakopoulos-COVID-508.pdf. Below is a screenshot of the pertinent image from the slide presentation:

WHAT IS GOING ON HERE?

Peace, Good Energy, Respect: PAVACA

Health Friday 5.30.2025 Open Thread: What is Going On at HHS, the FDA, and the CDC?

The above graphic is with thanks to https://www.thefocalpoints.com/p/fda-recommends-more-mrna-shots-despite, “FDA Recommends More mRNA Booster Shots Despite New Study Showing Booster Failure — and Major Public Outcry”, by Nicolas Hulscher, 26 May 2025.

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

There are Important Notifications from our host, Wolf Moon; the Rules of 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 use any AI-generated material in the discussion thread for today’s post, they must cite their source. Thank you.

Yours Truly has been researching, reading about, and writing about, the COVID-19 disaster since March 2020. She had a sense, early in 2020 when the speculation about the development and use of a COVID-19 “vaccine”, that something was “off” in the hype regarding “how this will stop the spread” of the virus, “how this will prevent COVID-19 infection”, and so on. As it turns out, that “Suspicious Dog” feeling was the correct one — the COVID-19 “vaccines” have been, are now, and will be, a disaster. These injectables do not prevent COVID-19 infection. These injectables have injured, sickened, disabled, and even killed, millions of “vaccinated” persons all over the world. These “vaccines” will continue to injure, sicken, disable, and even kill, those who have them put into their body — not only because of the ingredients and mechanisms of these injectables, but now also because of the “new and improved” (not) faulty foundation of “lab-created antibody titer levels tests” that will be used in the development of the “latest mutation version” of the “vaccines”, instead of doing actual clinical trials with lab animals and/or with human subjects. I will make it clear at the start that today’s offering is not meant to “stir the pot.” There are, in my opinion, legitimate questions that need to be asked regarding certain recent news items.

There are several central elements of the current situation regarding the “2025-2026 COVID-19 Vaccine Formula”, and the actions of certain people and entities. One such entity is the FDA. The current Commissioner of the FDA is Dr. Martin Makary, MD, MPH, who is also a proponent of COVID-19 “vaccination” (including in pregnant women), and is himself “vaccinated.”

On 22 May 2025, the FDA’s VRBPAC (Vaccines and Related Biological Advisory Committee) members met to “consider” and then to “recommend” the “2025-2026 COVID-19 Vaccine Formula.” The committee voted unanimously, after “presentations” by Pfizer-BioNTech, by Moderna, and by Novavax, to “recommend” the “formulas” for the modRNA (Pfizer-BioNTech and Moderna) and the “inactivated protein” (Novavax) COVID-19 “vaccines.” Please see: https://www.contagionlive.com/view/fda-makes-recommendations-for-2025-2026-formula-for-covid-19-vaccines, 23 May 2025. A screenshot from this article is below:

These “vaccines” will be lab-developed, then lab-tested regarding the amount of “antibody titers” that “might” be “effective” in the “2025-2026 Formula COVID-19 Vaccines.” There will be no clinical trial testing of these “vaccines.” This protocol, outlined in the “Option 4” method, was adopted by the FDA on 28 June 2022. Please see the Briefing Document for this meeting: https://www.fda.gov/media/159452/download. “Option 4” is located on page 19. Please see the screenshot below:

Therefore, it appears that any person who takes an injection of the “2025-2026 Formula COVID-19 Vaccine” by Pfizer-BioNTech, by Moderna, or by Novavax, will be, in essence, a “human lab rat”, since these “vaccines” will only have been tested under “Petri-dish conditions” in a lab to confirm whether the “antibody titer amounts” expressed by the “vaccine” ingredients “might” be “effective” in humans.

There were over 95,000 public comments that were submitted to the FDA regarding the VRBPAC meeting of 22 May 2025, indicating a “major public outcry” against the “recommending” of more COVID-19 “vaccines.” Nonetheless, the VRBPAC members voted to endorse the “2025-2026 COVID-19 Vaccine” formulas, as described above, using the “Option 4” method. Please see: https://www.thefocalpoints.com/p/fda-recommends-more-mrna-shots-despite, “FDA Recommends More mRNA Booster Shots Despite New Study Showing Booster Failure — and Major Public Outcry”, Nicolas Hulscher, MPH, 26 May 2025. Please see the screenshot from this article, below:

The phrase, “immunogenicity data” refers to the “Petri-dish lab experiments” as described above.

The image below is from the “opinion piece” written and published by Dr. Martin Makary and Dr. Vinay Prasad, MD, MPH. Dr. Prasad is another important person in the current situation regarding the HHS / FDA / CDC. As of 6 May 2025, Dr. Prasad is the new Director of the FDA’s CBER department (Center for Biologics Evaluation and Research.) The “opinion piece” was published on 20 May 2025, two days prior to the FDA’s VRBPAC meeting. Please see: https://www.nejm.org/doi/full/10.1056/NEJMsb2506929. A screenshot of the combined Figure 2 and Figure 3 from the “opinion piece” are below:

Dr. Prasad made it clear, in a podcast, that the FDA will implement the elements outlined in the “opinion piece” as the “new framework” for COVID-19 “vaccination.” Please keep this in mind for later on in today’s offering.

The paper regarding the failure of COVID-19 “booster shots”, already online-published but will appear in a medical journal in June 2025, is found here: https://doi.org/10.1016/j.vaccine.2025.127257, “Effect of the 2022 COVID-19 booster vaccination campaign in people aged 50 years in England: Regression discontinuity analysis in OpenSAFELY-TPP”, Andrea L. Schaffer, et al., journal Vaccine, Volume 59, 20 June 2025, 127257. The salient image from this paper is below:

Regarding the impact of COVID-19 “vaccination” on the lifetime supply of eggs in a female’s ovaries, it is now known that BOTH the modRNA AND the “inactivated” COVID-19 “vaccines” have a devastating impact on this egg supply. Please see: https://doi.org/10.3390/vaccines/13040345, “Impact of mRNA and Inactivated COVID-19 Vaccines on Ovarian Reserve”, Enes Karaman, et al., 30 January 2025. This paper demonstrates that there is a 30% conception failure rate, and an overall loss of up to 60% of the lifetime egg supply in the female ovaries, both induced by COVID-19 “vaccination” in a female of child-bearing age.

Then, there is Dr. Jay Bhattacharya, MD, PhD, the new Director of the NIH (National Institutes of Health.) It appears that Dr. Bhattacharya may be “betting on both sides of the game” regarding COVID-19 and the COVID-19 “vaccines.” While it is true that Dr. Bhattacharya has stated that lockdowns, “mandated masking”, “social distancing”, and so on, are not real methods to deal with the virus, he also said this, in 2021, regarding the COVID-19 “vaccines”:

Link to the above: https://www.newsweek.com/stanford-doc-jay-bhattacharya-calls-vaccine-mandates-unethical-says-patients-can-choose-1611938. The above statement from Dr. Bhattacharya raises some questions: One, if COVID-19 is “basically a cold”, how can a “vaccine” protect against it? Two, if COVID-19 is “basically a cold”, why are there so many persons who have had a COVID-19 infection (either from the mechanisms of the COVID-19 “vaccines” themselves, or from the virus itself) and have since presented with symptoms of “Long COVID”? Three, if indeed a person who had a COVID-19 infection and recovered, is “protected against new disease”, why are people (COVID-19 “vaccinated” or not) still coming down with COVID-19 virus mutation infections?

Next is Susan Monarez PhD, the current Acting Director of the CDC. Previously, she had worked in the Department of Homeland Security with BARDA and with other HHS departments. Dr. Monarez is a “biosecurity expert” who has also endorsed the COVID-19 “vaccines.” Please see: https://www.nytimes.com/2025/03/24/health/cdc-director-monarez.html, “Trump Nominates Susan Monarez to Lead C.D.C.”, 24 March 2025. The pullquote from the article: “Monarez is a biosecurity expert who endorsed the Covid vaccines, and her selection may signal a growing impatience with anti-vaccine sentiment.”

And, finally, there is current HHS Secretary Robert F. Kennedy, Jr., an attorney who founded the Children’s Health Defense organization (https://childrenshealthdefense.org/), and who has been an outspoken opponent of the COVID-19 “vaccines.”

And here begins Yours Truly’s presentation of the Kabuki theater going on at HHS / FDA / CDC:

On Tuesday 27 May 2025, HHS Secretary Kennedy, Jr., appeared in a video with Dr. Markary and Dr. Bhattacharya to announce that the COVID-19 “vaccines” that are “recommended” (in actual practice, they are called “routine”) by the CDC for healthy children under age 18, and for healthy pregnant women, would be removed from the CDC Immunization Schedules. Please see: https://x.com/bennyjohnson/status/1927374665745342535, a screenshot of which is below:

Where was Dr. Monarez, the Acting Director of the CDC? Why wasn’t she included in the video? An “announcement” of this importance would surely have required her to be included. To the best of Yours Truly’s knowledge and belief, neither Dr. Makary (FDA), nor Dr. Bhattacharya (FDA CBER), have the direct authority to remove vaccines from the CDC Immunization Schedules. The CDC is a separate departmental entity of HHS.

However: In reality, nothing has changed regarding the CDC Immunization Schedules. The CDC is still using the same 2025 Immunization Schedules that were issued on 21 November 2024. Please see: https://www.cdc.gov/vaccines/hcp/imz-schedules/index.html. The CDC is still “recommending” that pregnant women get COVID-19 “vaccinated”. Please see: https://www.cdc.gov/vaccines-pregnancy/about/index.html. This “recommendation” was issued by the CDC on 17 June 2024.

The “elaborate costumes and dance of Kabuki theater” approach were on display during this video with Secretary Kennedy, Jr., Dr. Makary, and Dr. Bhattacharya. But it was a “performance.” And the audience suspended reality for the “performance.”

Yours Truly now turns to the blog article by Sasha Latypova, a former medical technology and pharmaceutical technology professional, about this “Kabuki theater performance” of 27 May: https://sashalatypova.substack.com/p/eugenics-for-dummies-aka-hhss-evidence, “Eugenics for Dummies, aka HHS’s “Evidence-Based Approach” to covid shots.”, 29 May 2025. Please see the screenshots from her article, below:

It appears that, in reality, what has happened is that the current CDC Immunization Schedules have been neatly “absorbed into” the “new evidence-based approach to the COVID-19 vaccines” so-called “opinion piece” of Dr. Makary and Dr. Prasad (see the links to their “opinion piece”, above; and, also, the statement by Dr. Prasad that this “new approach” will be implemented at the FDA / CDC (so, it seems, they aren’t “opinions” at all.)

Further confirmation of the “Kabuki theater” element regarding the 27 May “announcement” by Secretary Kennedy, Jr., Dr. Makary, and Dr. Bhattacharya, comes from The Kingston Report: https://karenkingston.substack.com/cp/164733998, “Who’s Calling the Shots at HHS?”, 29 May 2025.

WHO IS IN CHARGE OF HHS? If Secretary Kennedy, Jr., can take the time to write letters to ask that ostriches in Canada are not “culled” due to a “possible” infection from Avian Influenza; if he can issue a directive to have titanium dioxide removed from candy (Skittles) — why did he participate in a “Kabuki theater performance” on 27 May regarding something incredibly important to the health of every American — the dangerous, deadly COVID-19 “vaccines”? Did he, or anyone else, at HHS, inform Dr. Monarez about the “change” in the CDC Immunization Schedules? If so, did she agree?

In Yours Truly’s opinion, there appears to be some sort of “issues” going on at HHS, the FDA, and the CDC. HHS Secretary Kennedy, Jr., needs to get to the bottom of all of them.

FLASH! AS OF TODAY, 30 MAY 2025: THE CDC HAS JUST ISSUED THE “NEW CHILDHOOD VACCINE IMMUNIZATION SCHEDULE” RELATED TO THE COVID-19 “VACCINES”:

It appears that Dr. Susan Monarez, PhD, has finally weighed in regarding the 27 May “announcement” (aka “Kabuki theater performance”) by HHS Secretary Kennedy, Jr., Dr. Makary, and Dr. Bhattacharya COVID-19 “vaccines” and the CDC Childhood Immunization Schedule. Please see Sasha Latypova’s presentation here: https://sashalatypova.substack.com/p/cdc-issued-the-anticipated-updates, “CDC issued the anticipated updates to the children’s schedule for covid shots”, 30 May 2025.

HOWEVER, there’s some “catches” in the “updates.” Huge “catches.” These have to do with the CDC “definition” of what a “healthy child” means. In short summary: It will be the CDC who decides if a child meets their “criteria” for being a “healthy child” (meaning, the COVID-19 “vaccines” aren’t “necessary” or “recommended”); it will be the CDC’s “guidance” on this that will be in control of any discussion between a child’s parent(s)/guardians, and the clinician who can administer COVID-19 “vaccines”; there are no provisions that Yours Truly can see in the CDC “guidance” for exemptions on religious or other grounds; and, that ANY clinician who is cleared to administer COVID-19 “vaccines” will ultimately make the decision on whether or not to COVID-19 “vaccinate” a child who does not fit the CDC “criteria” for a “healthy child.” This includes clinicians who have never treated the child (in other words, a CVS pharmacist, for example.) Please see the screenshots below, from the Latypova article of today:

Peace, Good Energy, Respect: PAVACA

Health Friday Open Thread 5.23.2025: The FDA’s EUA to Pfizer-BioNTech for BNT162b2 on 11 December 2020 Is Invalid

The above free vintage image of a vaccine vial and syringe is courtesy of iStock and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering is related to the COVID-19 biological toxin injections, aka the COVID-19 “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have been injured, made ill, become disabled, or have passed away, from the negative effects of these “vaccines” that they had in their body.

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They can be 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 any AI-generated content in today’s discussion thread, they must cite their source. Thank you.

Yours Truly began writing about the results of the huge C4591001 clinical trial of the Pfizer-BioNTech modRNA COVID-19 “vaccine”, BNT162b2, on the board here back in 2023. I was reading through document after document that the company generated related to this clinical trial, documents that were released to the general public only after Pfizer-BioNTech, in partnership with the FDA, lost their case in federal court to keep all of the data about C4591001 sealed for 75 years, and they were then sued by Attorney Aaron Siri’s group, Public Health and Medical Professionals for Transparency (PHMPT.) Please see: https://www.biospace.com/non-profit-group-wins-transparency-lawsuit-over-fda-records-of-pfizer-vaccine-authorization, 7 January 2022. Note: regarding the Pfizer-BioNTech and the Moderna COVID-19 “vaccines”, “mRNA” and “modRNA” are interchangeable descriptive words for these injectables.

The FDA press release of 11 December 2020, announcing the agency’s granting of the EUA for the Pfizer-BioNTech modRNA COVID-19 “vaccine” BNT162b2 is here: https://www.fda.gov/news-events/press-annoucenments/fda-takes-key-action-fight-against-covid-19-issuing-emergency-use-authorization-first-covid-19, “FDA Takes Key Action in Fight Against COVID-19 By Issuing Emergency Use Authorization for First COVID-19 Vaccine.” A screenshot from this press release is below:

Note the phrase, “Follows Thorough Evaluation…”. It is now known that this manifestly was NOT performed before the EUA was granted.

Regarding the invalidity of the 11 December 2020 EUA that was granted to Pfizer-BioNTech for BNT162b2 to be used “to prevent COVID-19 infection” in the United States: Yours Truly begins here: https://www.thefocalpoints.com/p/fda-authorization-of-pfizer-covid. “FDA VRBPAC December 11, 2020 Decision on Pfizer mRNA Found Invalid”, Nicolas Hulscher, MPH, 17 May 2025. There are several screenshots from this article, below:

Regarding the delaying by the FDA and the CDC of important information regarding the incidence of myocarditis following COVID-19 “vaccination”, and these agencies (and, also, Pfizer-BioNTech and Moderna) failing to issue Black Box Warnings about this on the Package Inserts for their modRNA COVID-19 “vaccines” (BNT162b2 [Pfizer-BioNTech] and mRNA-1273 [Moderna]), please see: https://www.thefocalpoints.com/p/us-fda-and-cdc-delayed-health-advisory, “US FDA and CDC Delayed Health Advisory on COVID-19 mRNA Vaccine Myocarditis for Months, Failed to Issue Black Box Warning for Years”, Peter A. McCullough, MD, MPH, 18 May 2025. A screenshot from this article is below:

The above slide image is from the FDA’s VRBPAC meeting of 22 October 2020. This meeting was held seven weeks prior to the 11 December 2020 granting of the EUA for BNT162b2. The FDA therefore KNEW before 11 December 2020 that BNT162b2 could cause myocarditis — but went ahead and issue the EUA anyway.

Yours Truly has written extensively on the manufacturing process for BNT162b2, and on associated topics. Please see: https://www.theqtree.com/2023/11/06/the-infamous-process-2-manufacturing-method-for-the-pfizer-biontech-modrna-covid-19-vaccines/

Also: https://www.theqtree.com/2024/02/01/an-open-letter-to-medical-professionals-who-took-the-covid-19-vaccines/

And: https://www.theqtree.com/2024/11/15/health-friday-11-15-2024-open-thread-hold-them-accountable-edition/

The FDA’s VRBPAC members will meet on Thursday 22 May 2025 to make “recommendations” regarding the “2025-2026 COVID-19 Vaccine Formulas.” Public comment is accepted until 11:59PM on Friday 23 May. To submit comments electronically, please see: https://www.federalregister.gov/2025/05/08/2025-080803/vaccines-and-related-biological-products-advisory-committee-notice-of-meeting-establishment-of-a; scroll down this page to the section “Electronic Submissions.”

But wait, there’s more! The “new” leadership of the FDA and the CDC, Dr. Vinay Prasad and Dr. Martin Makary wrote an article which was just published in the New England Journal of Medicine: https://doi.org/10.1056/NEJMsb2506929, “An Evidence-Based Approach to COVID-19 Vaccination”, Vinay Prasad, MD, MPH, and Martin A. Makary, MD, MPH, 20 May 2025. This article is NOT an “opinion piece” — Drs. Prasad and Makary make it clear that they are going to implement this “new approach” to COVID-19 “vaccination” through the FDA and the CDC.

In Yours Truly’s opinion, this “new approach” has many items to question. For example: the granting of FDA authorization for “new formula” COVID-19 “vaccines”, authorization based on lab-performed experiments on the “new formula” ingredients that produce certain numbers of “antibody titers” that might “correspond” to “effectiveness.” There would be no clinical trials at all, performed either on lab rats or on humans. This “lab-experiments with Petri dishes results” authorization method is outlined in “Option 4” of the FDA vaccine authorization / full approval guidelines that the agency adopted in 2022. This “lab-experiments with Petri dishes results” method will now be used for “new formula” COVID-19 “vaccines” for persons age 65 and over; and for persons under age 65 with compromised immune systems or who are part of “vulnerable” or “at risk” populations — such as, for example, pregnant women. Please see, regarding the “Option 4”: https://www.fda.gov/media/159452/download, “VRBPAC Briefing Document”, 28 June 2022. A screenshot of “Option 4” is below:

For another example: COVID-19 “vaccination” will still be “recommended” for pregnant women and for women who have just given birth. This flies in the face of the mounting, and published, evidence that COVID-19 “vaccination” during pregnancy can, and does, result in miscarriages, stillbirths, live births but the infant has medical issues, and so on. In addition, COVID-19 “vaccine” antibodies show up in the breast milk that “vaccinated” new mothers nurse their infants with.

Why do the FDA / CDC continue to ignore the evidence-based facts that Ivermectin, Hydroxychloroquine, Zinc, and Vitamin D both prevent and treat COVID-19 infections?

Three screenshots from the Prasad and Makary article are below:

NOTE THE LAST SENTENCE OF THE ABOVE IMAGE: “Ultimately, these studies alone can provide reassurance that the American repeat-boosters-in-perpetuity strategy is evidence-based.”

Let’s take a look at the combined Figure 2 and Figure 3 image:

Which makes it plain, in Figure 2, that the COVID-19 “vaccines” will be “recommended” for people who “fit” the diagnosis parameters of multiple types of medical conditions, including pregnant women and women who have just given birth — in other words, these groups of people may well be subjected to multiple types of “convincing” strategies to get them to agree to take these “vaccines.” Who made the decisions on the types of “risk factors” for the “increased at-risk” groups?

And, there’s this tweet, from Dr. Martin Makary, of August 2023:

There is published, irrefutable evidence that the COVID-19 “vaccines” can cause death among the “vaccinated.” Please see: https://www.thefocalpoints.com/p/the-causal-link-between-covid-19, “The Causal Link Between COVID-19 Vaccination and Death”, Nicolas Hulscher, MPH, 21 May 2025. There is an embedded interview between Mr. Hulscher and Dr. Idriss J. Aberkane, PhD, on this subject. A screenshot from the Hulscher article is below:

It appears to be unclear, in Yours Truly’s opinion, about where this “new approach to COVID-19 vaccination” fits in as regards the “Generation Gold Standard” that was announced a few weeks ago. Does the federal government control “new” COVID-19 “vaccine” development processes? Where does Big Pharma (Pfizer-BioNTech, Moderna, Novavax) come in? Is that what “Sponsor-Driven” clinical trials means (see the above image)?

However, here’s the real situation: In Yours Truly’s opinion, given that the initial EUA granted by the FDA to the Pfizer-BioNTech BNT162b2 on 11 December 2020 was invalid — that means, by extension, that every other EUA (and “Full Approval”) of the modRNA COVID-19 “vaccines” is also invalid: which would include any “formula” that is “recommended” for the “2025-2026 COVID-19 Vaccine”. Which would also, in Yours Truly’s opinion, invalidate any “Full Approval” of the Novavax COVID-19 “vaccine”, since the foundation of that injectable is the same Wuhan Hu1 SARS-CoV-2 virus that was used as the foundation for BNT162b2.

FLASH! — Meanwhile, the FDA just granted “Full Approval” to the Novavax company’s injectable on 19 May 2025, under the name “NUVAXOVID”: https://ir.novavax.com/press-releases/2025-05-19-U-S-FDA-Approves-BLA-for-Novavax-COVID-19-Vaccine.

FLASH! 2 — The VRBPAC members voted unanimously today to “recommend” that the “2025-2026 COVID-19 Vaccine Formula” injectables contain the JN.1 Omicron variant of the original SARS-CoV-2 virus. This is the same strain that was “recommended” for the “2024-2025 COVID-19 Vaccine Formula” injectables. The decision today by VRBPAC will be implemented according to the Dr. Prasad and Dr. Makary “new approach” method, as outlined above in today’s post. This means that persons age 65 and older, and that persons under age 65 who fall into one of the “increased risk” categories (Figure 2, above in the post) will be “encouraged” to get “vaccinated.” The exact formulation of the “2025-2026 COVID-19 Vaccine Formula” for the Pfizer-BioNTech and the Moderna injectables will be based, as was their other COVID-19 “vaccines” on the modRNA (aka mRNA)-based platform. The Novavax (now called NUVAXOVID) “2025-2026 vaccine” product will be based on the company’s previous “inactivated protein”-based platform. It is unclear whether the NUVAXOVID “2025-2026 vaccine” product will be authorized for persons under age 65 and/or who have underlying “increased risk” conditions. Please see: https://www.cidrap.umn.edu/covid-19/fda-vaccine-advisers-recommend-sticking-jn1-strain-next-covid-vaccines, 22 May 2025; and, https://cen.acs.org/pharmaceuticals/vaccines/FDA39s-new-COVID-19-vaccine/103/web/2025/05?sc=230901_cenrssfeed_eng_latestnewsrss_cen, 22 May 2025. A screenshot from the C&EN / ACS article is below, highlighting items related to the Dr. Prasad and Dr. Makary “new approach” article:

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

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

Illustration from 19th century.

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

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

Vaccination Certificate 1867

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

KMAG 20250226 Open Thread, Mad Cows & Raw Milk

I wrote this almost 2 decades ago. Most of the reference documents have been removed, archived or changed. However the basics remain the same.

Raw milk is a product whose safety CAN be assured by means other than pasteurization. The first is herd isolation and constant testing of the herd for diseases such as tuberculosis and brucellosis. The second is a very high standard of cleanliness during milking, the third is the testing of the milk itself. If you wish to drink raw milk, as some do then you KNOW the seller and check his facilities and testing procedures.

Unfortunately this type of program would uncover a whole can of worms the USDA/FDA and more importantly the International Corporate Cartel wants buried very DEEP. It is for that same reason the USDA and the Bush Admin. squashed the attempts of Creekstone to do its own BSE testing for Mad Cow disease.


Here is a bit about the BSE cover-up most people are unaware of and why the USDA/FDA want NO TESTING.

…Before the BSE crisis about 350,000 tons of MBM feed was sold in Britain a year, and relatively little was exported. After the ban the UK government did inform the EU, but there was a surge in exports to Europe. Then, as European states – informed of the danger – banned British feed, exporters opened up new markets, including North America, the Middle East and Asia.

Dr Stephen Dealler, a microbiologist and BSE expert, said: “It was a terrible mistake… Look at the controls they are now trying to apply to stop BSE in France and other EU countries. It is going to be much harder in African and Middle Eastern countries.”

Evidence to the British BSE inquiry headed by Lord Phillips shows that British officials washed their hands of moral responsibility over the dangers of MBM spreading BSE to infection-free countries, the approach was to inform international bodies, leaving it to member states to decide whether to import UK feed and prevent it being fed to cattle.…

Report: BSE contaminated feed exported for Eight years after UK ban

Page not archived. http://www.independent.co.uk/life-style/health-and-wellbeing/health-news/exports-of-bsecontaminated-cattle-feed-continued-for-eight-years-after-uk-ban-626507.html

While danger spread; government response is marked by denial and delay as new diseases tear through cattle, wildlife – and people

June 1, 2002 Rocky Mountain News (Denver, CO) by Lou Kilzer

… It took the United States 10 years to follow Britain’s lead and ban the feeding of cattle-derived meat and bone meal (MBM) back to cattle. But the U.S. allows – indeed, actively promotes – the export of MBM to other countries. The Food and Drug Administration (FDA) makes no requirement that warning labels against feeding it to cattle be placed on the product.

One country that exports over a million cattle a year to the United States – Mexico – is just now adopting the ban on MBM as cattle feed. And the enforcement of that ban is suspect.

The FDA has allowed hundreds of meat-processing facilities to fudge on its MBM rules, handing out a handful of warning letters and taking little action to force compliance…

There is a small chance that mad cow disease.. (BSE), is already in this country, according to a risk assessment released today by Harvard University. The risk assessment concluded that even if BSE had entered this country, it wouldn’t become a major public health problem, although human illnesses could occur”.Harvard Risk Assessment 12/3/2001 http://www.organicconsumers.org/madcow/danger6102.cfm

Quantitative assessment of the BSE risk from meat and bone meal in MBM export, pet food, etc. non-ruminant feed mill mixed feed mill non-ruminant: http://www.svepm.org.uk/posters/2007/De%20Vos.pdf — Page not archived

After disease detectives in Great Britain determined that mad cow (BSE), was spread by feeding cattle infected meal, British officials banned the practice. But they didn’t ban the export of feed, spreading BSE to continental Europe and Japan…At the height of the BSE epidemic, the UK exported 500,000 tons, including 168,000 metric tons of MBM (meat and bone meal) between 1990 and 1996. It also exported 3.2 million cattle to 36 countries. A Harvard study said that the exact amount sent to the U.S. was unknown, but it noted that at least 69 tons of “mammalian meal and flour” and 334 cattle were shipped here during the period. https://web.archive.org/web/20020813043834/http://www.organicconsumers.org/madcow/danger6102.cfm

Back to why the USDA/FDA does not want raw milk.


AOL September 30, 2024 
Why Are People Drinking Raw Milk? Experts Explain The Benefits—And Extreme Risks

by Susan Choung

….is raw milk safe to drink even? The FDA and food safety experts caution against consuming unpasteurized dairy but that doesn’t stop A-list celebs, like Gwyneth Paltrow from adding raw cream to her coffee every morning.

She lives in California, where the sale of raw milk is legal, provided it has a warning label. (FYI: Her purveyor for raw milk has been linked to at least 165 salmonella cases, the largest outbreak in the U.S. in over a decade.) [So why in hades has it not been shut down? – GC]

And talk about politics making strange bedfellows: Former presidential candidate Robert F. Kennedy Jr.said, “I only drink raw milk,” in a video clip that made rounds on Twitter/X. Pesky government food regulations be damned!….

Here are some of the pros (notice the fight has been a very long one)


published in Magazine Digest – June 1938 Armchair Science is a British Medical Journal

Raw Milk Vs. Pasteurized Milk

Pasteurization’s great claim to popularity is the widespread belief, fostered by its supporters, that tuberculosis in children is caused by the harmful germs found in raw milk. Scientists have examined and tested thousands of milk samples, and experiments have been carried out on hundreds of animals in regard to this problem of disease-carrying by milk. But the one vital fact that seems to have been completely missed is that it is CLEAN, raw milk that is wanted. If this can be guaranteed, no other form of food for children can, or should, be allowed to take its place.

Dirty milk, of course, is like any other form of impure food — a definite menace. But Certified Grade A Milk, produced under Government supervision and guaranteed absolutely clean, is available practically all over the country and is the dairy-farmer’s answer to the pasteurization zealots.

Recent figures published regarding the spread of tuberculosis by milk show, among other facts, that over a period of five years, during which time 70 children belonging to a special organization received a pint of raw milk daily. One case only of the disease occurred. During a similar period when pasteurized milk had been given, 14 cases were reported.

Besides destroying part of the vitamin C contained in raw milk and encouraging growth of harmful bacteria, pasteurization turns the sugar of milk, known as lactose, into beta-lactose — which is far more soluble and therefore more rapidly absorbed in the system, with the result that the child soon becomes hungry again.

Probably pasteurization’s worst offence is that it makes insoluable the major part of the calcium contained in raw milk. This frequently leads to rickets, bad teeth, and nervous troubles, for sufficient calcium content is vital to children; and with the loss of phosphorus also associated with calcium, bone and breain formation suffer serious setbacks.

Pasteurization also destroys 20 percent of the iodine present in raw milk, causes constipation and generally takes from the milk its most vital qualities

Looks like pasteurized milk is great news for Big Pharma and the supplement manufacturers.

The Health Benefits of Raw Milk from Grass-Fed Animals

By naturopathic physician, Ron Schmid, ND 2002

My testimony was framed to respond to objections to raw milk raised by the state health department and to document the benefits of raw milk. To quote from that testimony:

“The state epidemiologist writes that ‘It has yet to be demonstrated that raw milk has any beneficial health effects. . . ‘ He cites articles attached to his letter. In one article, ‘Unpasteurized Milk, The Hazards of a Health Fetish’ (Journal of the American Medical Association, 10/19/84), the authors make a series of misstatements about the research of Francis Pottenger before concluding that raw milk has no health benefits. I detail these charges as follows in the paper I’ve given the members of the Committee.

“Now what Pottenger actually did in some of his experiments is this. He used four groups of cats. All received for one-third of the diet raw meat. The other two-thirds of the diet consisted in either raw milk or various heat-treated milks. The raw milk/raw meat diet produced many generations of healthy cats. Those fed pasteurized milk showed skeletal changes, decreased reproductive capacity and infectious and degenerative diseases.

“Now just who was Francis Pottenger? He was the son of the physician who founded the once famous Pottenger Sanatorium for treatment of tuberculosis in Monrovia, California. He completed his residency at Los Angeles County Hospital in 1930 and became a full-time assistant at the Sanatorium. From 1932 to 1942, he also conducted what became known as the Pottenger Cat Study.

“In 1940, he founded the Francis M Pottenger, Jr. Hospital at Monrovia. Until closing in 1960, the hospital specialized in treating non-tubercular diseases of the lung, especially asthma.

“Dr. Pottenger was a regular and prolific contributor to the medical and scientific literature. He served as president of several professional organizations, including the Los Angeles County Medical Association, the American Academy of Applied Nutrition and the American Therapeutic Society. He was a member of a long list of other professional organizations.

“Pottenger’s experiments met the most rigorous scientific standards. His outstanding credentials earned him the support of prominent physicians. Alvin Foord, MD, Professor of Pathology at the University of Southern California and pathologist at the Huntington Memorial Hospital in Pasadena, co-supervised with Pottenger all pathological and chemical findings of the study.

“One particular question that Pottenger addressed in his study is one that modern science has largely ignored. It has to do with the nutritive value of heat-labile elements-nutrients destroyed by heat and available only in raw foods.

“In his article ‘Clinical Evidences of the Value of Raw Milk,’ Pottenger writes: ‘Some of the factors transmitted by milk are thermo-labile [sensitive to heat]. Though their destruction may not produce death, their deficiency may prevent proper development of the child. This may show in the development of an inadequate skeleton or a decrease in resistance. . . . delay in development of osseous centers is noted more frequently in those children. . . receiving heat treated milk. It is particularly absent from the raw milk fed children. . . . I am basing this discussion on analysis of 150 children whose parents have consulted me because of respiratory allergies. Many other workers. . . have also shown that treating milk by heating interferes with its proper assimilation and nutritional qualities. . . . The best milk from a nutritional standpoint is raw milk. . . . Heat-treating milk interferes with calcium metabolism causing. . . delay in bone age and small bones. . . . The interference with calcium metabolism as shown in the bones is only a physiological index of disturbed metabolism throughout the body.’

“I have prescribed raw milk from grass-fed animals to my patients for nearly fifteen years. Time and again I have seen allergies clear up and dramatically improved health. Particularly in children, middle ear infections usually disappear and do not recur on raw milk. Both children and adults unable to drink pasteurized milk without problems have thrived on raw milk. In hundreds-perhaps thousands-of my patients using raw milk, not one has ever developed a salmonella, campylobacter, or other raw-milk-related infection.

“In the letter cited above, the state epidemiologist states that ‘The processes of certification and/or inspection do not guarantee that raw milk will not be contaminated with pathogenic organisms.’ He also lists a host of microorganisms that are alleged to be transmitted by raw milk, not mentioning that, as the literature accompanying his letter makes clear, the only organisms even potentially associated with the consumption of certified raw milk are salmonella and campylobacter. And in one of the articles he cites, ‘The Hazard in Consuming Raw Milk’ (in The Western Journal of Medicine), the authors actually state that ‘Salmonella and campylobacter diseases in humans are generally not serious. But in persons with compromised health (particularly those with malignant conditions and immunosuppressed by disease or therapy), these infections may be serious.’

“So, the gist of the state’s argument against certified raw milk is that it might possibly on isolated occasions cause serious disease in some people whose immune systems have been compromised by the toxic effects of chemotherapy. And because of this very slight risk, those of us who might choose to drink certified raw milk for the benefits I have catalogued should be denied that right.”

Here is the REASON the FDA went on the attack.


Please read the whole thing because it is really eye opening what has been done to the actual safety of our food.

“…While I believe a meaningful, uniform, universal ID system for all livestock with adequate tracking will evolve, as a state animal health official, I would be less than responsible if I did not encourage industry and government to move quickly to get a handle on our ability to traceback animals today for diseases such as brucellosis, tuberculosis, and others that present risks of exacerbation and the extreme costs associated with such…” Dr. Sam Holland, State Veterinarian, South Dakota from REPORT OF THE COMMITTEE ON LIVESTOCK IDENTIFICATION – 2005

Why the sudden need to stampede the USA into a track back system?

This is an example of the USDA’s response to one disease over the last decade. The chart shows how USDA cut back testing after WTO was created and the VP of Cargill wrote the WTO Agreement on Agriculture 1995.

Note the significant drop in Government testing!

UCD VET VIEWS CALIFORNIA CATTLEMAN,  JULY-AUGUST 2002

Summary of Tuberculosis Surveillance in California Cattle

Number of Cattle Tested……..1995…..1996…..1997…….1998…….1999……2000…..2001
By Animal Health Officials…10,576…5,100 ….2,861 …..3,530…..1,425 ….1,967…..2,500
By Private Veterinarians …15,921…17,100…19,930…18,189…22,863…19,930…19,587
Submissions at Slaughter……….39……….58 ………64………..39………..58……….64………385

What about the danger of Bovine Tuberculosis in the USA since the passage of WTO and the lifting of tariffs and quarrantine mandated by WTO?

Bovine TB was confirmed in three dairy herds during 2002-2003.[California] ….Although the source of the infections was not confirmed, the investigations indicate TB was most likely imported in infected cattle…. http://www.cdfa.ca.gov/ahfss/Animal_Health/pdfs/Tb_in_California_2006.pdf — archived page removed

“The high prevalence of bovine tuberculosis in Mexican cattle was discussed. A multiagency investigation in New York city identified 35 cases of human M. bovis infection. Fresh cheese from Mexico was identified as the likely source of infection” (Winters et al., 2005). http://www.nzfsa.govt.nz/science/riskprofiles/FW0320_Mbovis_in_meat_final_May_2006.pdf — archived page removed


What was the USDA’s response to “The high prevalence of bovine tuberculosis in Mexican cattle”

in April 2001, the USDA’s Veterinary Services published an interim rule requiring Mexican feeder steers to originate from herds that had recently been tested for TB. The USDA then agreed to grant waivers to the whole-herd testing…http://www.boergoats.com/clean/articles/texasanimalhealthcommission/mexicancattle2002-03-07.htm

Page not found. Updated to: Federal Import Requirements for Mexican Feeder Cattle in Effect April 1, 2002: USDA Increases Mexican Cattle Surveillance https://web.archive.org/web/20040929195955/http://www.boergoats.com/clean/articles/texasanimalhealthcommission/mexicancattle2002-03-07.htm

(I guess we did enough screaming.)


Texas imports a million cattle a year from Mexico. The cattle port-of-entry at Santa Teresa, NM is the largest entry.

Cattle crossing facilities on the U.S. side of the border are operated primarily by private firms… at Santa Teresa, NM, Chihuahuan cattle producers [Mexican] operate both sides of the cattle port-of-entry… https://web.archive.org/web/20011117084712/http://www.ers.usda.gov/publications/Agoutlook/june2001/AO282d.pdf

SO what happened after the waivers of whole herd testing was granted”

For Mexican Feeder Cattle in Effect April 1, 2002… Dr. Logan… said, the disease is extremely rare in U.S. herds. However, more TB-lesioned cattle are being detected at slaughter, and ear tags indicate that many of these animals are of Mexican origin. https://web.archive.org/web/20030413013230/http://www.tahc.state.tx.us/news/pr/2002/302TBMx.pdf

Summary of Selected Disease Events April–June 2007

Oklahoma
On May 1, 2007, the Oklahoma Department of Agriculture reported a case of bovine tuberculosis (TB) discovered as a result of slaughter surveillance…. Subsequent testing of the index herd identified a TB- positive cow with a Colorado ID tag… The herd has been depopulated…Bovine TB was last reported in Oklahoma in 1982, and Oklahoma has been classified by the USDA as tuberculosis-free since 1984.

New Mexico
On June 14, 2007, the State of New Mexico confirmed that a dairy herd in Curry County was infected with bovine tuberculosis…Two infected herds were confirmed with TB in late 2002, .

Additionally, it is anticipated that both New Mexico and California will lose their TB “free” status in 2008, from AGENCY STRATEGIC PLAN: FOR THE FISCAL YEARS 2009-2013 BY TEXAS ANIMAL HEALTH COMMISSION

What is the USDA/FDA position on testing by non-government (or non corporate cartel) entities???

The USDA is abandoning a known effective method of disease prevention, the first-point testing program, where the live cows in a herd are tested, in favor of a method that allows the disease more time to spread since the cows are at the end of their life before testing is done. Also Texas complains of the USDA shutting down disease testing labs by withdrawing funding. This is in line with the USDA’s refusal to allow Creekstone to test 100% of their slaughtered cattle for BSE and Japan’s response of increasing their cattle herds. See: http://www.cornucopia.org/2008/09/appeals-court-prevents-company-from-testing-for-mad-cow-disease/

Government targeting of independents.

The Henshaws were not allowed to test their animals or to even SEE the government test results.

….The claim is that the USDA did this because of Pseudorabies, yet the government did not follow it’s own standard operating procedures of testing as outlined in the USDA’s own documents. The USDA spilled bodily fluids from the slaughtered pigs all over the road where any disease could be transmitted to other farms and other animals. Slaughter is not required for testing for Pseudorabies. These issues seriously puts into question the validity of the disease claim and/or the competence of the government officials involved…. https://web.archive.org/web/20080922034213/http://nonais.org/2006/09/29/henshaw-incident/

The Faillice family had similar treatment from the USDA. When the standard test results were all negative and the animals had all been slaughtered, an experimental testing procedure was used and then the samples “lost” and “Destroyed” Of interest was the fact the Faillice family lived in England and were Experts on Mad Cow disease. (sorry about no direct link you would have to read the book Mad Sheep

https://web.archive.org/web/20081012080005/http://www.chelseagreen.com/bookstore/item/mad_sheep:hardcover/reviews

There is a darn good reason to bury this report because it gives very good evidence that the USDA and FDA are intentionally allowing disease into this country and ALLOWING it to go unchecked by shutting down testing labs and NOT testing at farms.

Without the increase in food borne disease and the media’s propaganda spreading fear, there would be not reason to implement the new “Food Safety” law passed Congress during the December 2010 lameduck session. Senator Burr, after promising NC farmers he would not vote for the bill, was a co-sponsor. The new Law is specifically designed to wipe out independent farmers as similar laws have done in the European Union. The FDA has already stated it will “harmonize” with EU and other international laws per an agreement signed by Bush and the WTO AoA treaty.

Those treaties and the NEW Law are NOT designed to do a blasted thing about actual food safety. They are only there to help the International Cartels remove “barriers” to trade…. and to remove the independent farmer competition.

From the original before it was modified under the same date of course

TEXAS ANIMAL HEALTH COMMISSION 2009 – 2013 AGENCY STRATEGIC PLAN

https://web.archive.org/web/20080821223653/http://www.tahc.state.tx.us/agency/TAHC_Strategic_Plan_2009-2013.pdf

The surveillance element or function is the most intensive of the six functions with respect to resources and personnel. Surveillance includes all activities designed and implemented to identify and locate any possible focus of infection or exposure to diseases of animal/poultry health significance in the livestock, poultry and exotic animal population. TAHC surveys animal populations for possible disease problems by collecting blood samples at livestock markets, on farms or ranches, and at slaughter plants…. Additionally, TAHC foreign animal disease diagnosticians investigate all reports of potential foreign animal diseases in order to achieve early diagnosis of a foreign animal disease, should it be introduced into the state.

USDA is moving toward supporting fewer labs nationwide, with the remaining labs serving as regional labs and supporting larger geographic areas….. If this funding is not maintained, this lab will be closed and the out-of-state samples will not be processed by remaining TAHC laboratories….

The first-point testing program is the “early warning system” for the brucellosis program, enabling detection of infection prior to sale of cattle within the state. With the discontinuation of first-point testing, slaughter testing will become the primary method for brucellosis surveillance. There is a key difference between first-point testing and slaughter testing. An animal identified through first-point testing as possibly infected is alive. This allows the agency to collect additional samples (blood, milk and tissue) and conduct additional diagnostic serologic and culture tests to determine if the animal is in fact infected with Brucella abortus. An animal identified through slaughter testing as possibly infected is no longer living and therefore additional testing of that animal is not possible. As a result, the process to be followed requires the identification of the herd the animal came from and conducting a whole herd test to determine whether or not infection is present in the herd. The traceability back to the original owner or farm of origin is also much higher in a first-point test positive versus a slaughter positive, because the animals are individually identified with permanent identification devices, are identified to an owner at the time of testing and market records improve traceability of the animals. …


..All states are expected to collaboratively participate in cooperative disease control and eradication programs or face significant animal movement restrictions from USDA and other states. Movement restrictions would significantly reduce the marketability of Texas animals and increase the cost of market access.

[NAFTA and WTO trade agreements impact]
…New national disease control programs, emergency management responsibilities, and trade agreements with foreign countries have a significant impact on TAHC. These new or expanded programs continue to stretch TAHC’s already stressed resources to their limits.

[foreign diseases  imported due to trade agreements  and  the Agreement on the Application of Sanitary and Phytosanitary Measures]

…The responsibilities of TAHC have significantly increased as programs for disease control and surveillance have expanded, animal and premises identification systems have been initiated, and participation in emergency planning and response activities impacting animal health require more agency resources. Additionally, new disease challenges are emerging. Some are domestic diseases that are increasing in significance. Others are foreign diseases that may be imported as result of the exponential increases in international importations of animals and animal products. Our industries and our economy are threatened by diseases and pests that heretofore we only read about in disease text books or heard about in lectures….

Since 1999, there have been seven foreign animal diseases diagnosed within the United States (West Nile Virus, Exotic Newcastle Disease, High Pathogenic Avian Influenza, Hemorrhagic Disease of Rabbits, Monkey Pox, Bovine Spongiform Encephalopathy, and Wildebeest Associated Malignant Catarrhal Fever). Unfortunately, there does not appear to be an end in sight for outbreaks of foreign or domestic diseases and these diverse activities related to disease control and eradication….

As usual the situation is not nearly as cut and dried as the government and its propaganda arm, the Mass Media would paint it.

Analysis of the real problems with US food safety:


Peanut Quality – How did the Food Inspection Fail?


Legislators overlook serious flaw in USDA’s HACCP food – Policy


See John Munsell’s comment in this article: “Who needs Al-Qaeda when you have got E. coli?


One E. coli O157:H7 Outbreak I Think I could have Prevented

As Robert Kennedy has pointed out, it is not just vaccines that are a problem.

Placeholder Open Thread 11.27.2024: PRRARSV Part 2: Pangolin Addenda Edition

This image has an empty alt attribute; its file name is vintage-laboratory-work-stockcake.jpg

The above free vintage image of a scientist at work is courtesy of StockCake and Google Images.

As Gail Combs is apparently still in “locked out” mode for publishing posts (via WordPress, or **some other entity**), our host, Wolf Moon, gave the go-ahead for Yours Truly to do a Placeholder Open Thread for today. I am indebted to our host for this opportunity, as further information has surfaced regarding the role of the pangolin-CoV MP789 virus in the lab-creation of the SARS-CoV-2 (COVID-19) virus itself. Since today’s post concerns the COVID-19 virus itself, and the COVID-19 “vaccines”, it is dedicated to the memory of Yours Truly’s COVID-19 “vaccinated” brother Sam, and to her cousin Bill; and to all persons, of whatever age and location, who have passed away from the negative effects of the COVID-19 “vaccines” that they had in their bodies. However, the discussion is not limited to what is presented here: It is an Open Thread. Bear with me: there are a couple of surprising details coming up. There is a General Summary at the end of the post.

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. They are linked here.

To Begin: What will be called the “Part 1 Presentation” of the role of the PRRARSV genome code of the pangolin-CoV MP789 in the lab-creation of the SARS-CoV-2 virus itself is here: www.theqtree.com/2024/11/22/health-friday-11-22-2024-open-thread-lets-talk-about-prrarsv-the-backdoor-key/. Yours Truly presented evidence that: One: the pangolin-CoV MP789 virus genome code has “an uncanny similarity” to the PRRARSV genome code that was inserted into the genome code of the SARS-CoV-2 virus itself; Two: that this insertion occurred during the lab-creation process for the genome code of the SARS-CoV-2 virus itself; Three: that this insertion is at or very near the S1-S2 furin cleavage site in the genome code of the SARS-CoV-2 virus itself; Four: that the bat-coronavirus RaTG13 coronavirus also has a role to play in the lab-creation of the genome code of the SARS-CoV-2 virus itself, although the pangolin-CoV MP789 coronavirus genome code has more “areas of similarity” to the SARS-CoV-2 virus genome code; and, Five: that taxpayer-funded Gain-of-Function experiments were {most likely] used to perform all of the above, and most likely, at the Wuhan Institute of Virology.

In 2020, the year after the SARS-CoV-2 virus itself was beginning to ravage the world, and when COVID-19 “vaccines” had not yet been granted Emergency Use Authorizations by the FDA in the United States, by the EMA (European Medicines Agency), or by other agencies, a plethora of scientific papers and articles were written and published: papers and articles in which the researchers attempted to pinpoint exactly how the SARS-CoV-2 virus itself came into being. Many of these papers and articles examined the role(s) that various animal coronaviruses may have played in the emergence of the SARS-CoV-2 virus itself: for examples, by “natural evolution”; or, by “recombination” of coronavirus genomes among animals via cross-infection; or, by a “sudden appearance.” These investigations and their published results pre-date the confirmation within the past 18 months that Gain-of-Function experiments at lab facilities, most notably the Wuhan Institute of Virology, were the foundation of the lab-created disaster called the SARS-CoV-2 virus itself (links to Congressional reports on this situation are in the “Part 1 Presentation” Health Friday post, see above.) One such year 2020 scientific paper is the “Dimonaco, et al.” paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC7823979/, “Computational Analysis of SARS-CoV-2 and SARS-Like Coronavirus Diversity in Human, Bat and Pangolin Populations”, Nicholas J. Dimonaco, et al., 30 December 2020. A screenshot of the Abstract of this paper is below:

The Health Friday post cited above discusses Yours Truly’s hypothesis that the pangolin-CoV MP789 coronavirus genome code was chosen, along with the important but actually less-similar bat coronavirus RaTG13 genome code, as the main virus genome that were used to create the SARS-CoV-2 virus itself genome. Today’s post, in Yours Truly’s opinion, presents evidence that “clinches the deal” on the choice of the pangolin-CoV MP789 genome code as the primary one for insertion into the SARS-CoV-2 virus itself genome code — however, the evidence comes from a surprising source.

The trail to this source begins here, an article by Stella Paul: https://brownstone.org/articles/why-are-hospitals-still-using-remdesivir/, 30 May 2023. The Paul article, in turn, was linked from this Vigilant Fox article: https://vigilantfox.news/p/9-shocking-covid-truths-theyll-never, 23 November 2024. This, in turn, led first, to here: www.fda.gov/consumers/consumer-updates/know-your-treatment-options-covid-19 (this article has no mention whatsoever of effective alternate treatment options for COVID-19, such as Ivermectin or Hydroxycholoquine); which, then, led to here: www.fda.gov/drugs/emergency-preparedness-drugs/coronavirus-covid-19-drugs. Which, in this last link, led to: mention of a “new” COVID-19pre-exposuretreatment drug that can only be used under certain circumstances, such as in persons with already-compromised immune systems; and only can be administered by infusion (IV): PEMGARDA, a monoclonal antibody treatment that also functions as an antiviral.

This is the link to the FDA-issued document for healthcare professionals for PEMGARDA: www.fda.gov/media/177067/download (note: PEMGARDA is also called Pemivibart in this document.) There have been no studies performed for PEMGARDA regarding carcinogenicity, mutagenicity, or impairment of fertility (section 13 Nonclinical Toxicology of the FDA document.) Persons who have been prescribed PEMGARDA need to take the infusion (IV) of the drug every 3 months (page 15 of the FDA document.) Also, PEMGARDA is not to be used as a “substitute” for COVID-19 “vaccination” (page 15 of the FDA document.) More details from the section Limitations of Authorized Use of the FDA document are below:

There is a slew of other warnings (including Black Box warnings), cautions, and restrictions regarding PEMGARDA in the FDA document.

Here is a screenshot of section 12.4 Mechanism of Action of the FDA document on PEMGARDA (aka Pemivibart):

**** And now, for the pangolin-CoV connection: This is found in the FDA document on PEMGARDA, Table 2. Yours Truly is including screenshots of Table 2., below. Please look at the screenshots carefully. There are seven screenshots. This is the list of SARS-CoV-2 variants that PEMGARDA is ** allegedly ** supposed to help “guard against.” The bottom line here is: Virtually every SARS-CoV-2 variant is derived from a pangolin-CoV genome code (most likely that of pangolin-CoV MP789) that was “blended in” along with the bat-CoV RaTG13 genome code in the lab-creation of the original SARS-CoV-virus itself. The giveaway is “Pango lineage” at the top of the variants columns. (Note: due to screenshot size constraints, some of the variant lists are broken up: however, EVERY variant column clearly states Pango lineage at the top left.)

The question that comes to mind is: Why is PEMGARDA being promoted as a “pre-exposure prophylaxis” against a COVID-19 infection in immunocompromised persons; or, for that matter, for any person, COVID-19 “vaccinated” or not? The answer is that the FDA still does not recognize, authorize, or recommend, the use of Ivermectin, Hydroxycholorquine, Zinc, Quercetin, Vitamin D, or other “non-FDA-authorized or approved” drugs or treatments for prophylaxis for COVID-19 infection; or for COVID-19 infection treatment. While there may be need for PEMGARDA to be used for certain patients in narrow circumstances, it is Yours Truly’s opinion that it is vastly less expensive and effective to use Ivermectin, Hydroxycholorquine, Zinc, Quercetin, and Vitamin D in the large majority of situations to prevent infection by COVID-19.

Then, there is the issue of what Yours Truly will call “Universal Immune System Compromise from COVID-19 Vaccination.” It is her firm opinion that any person who has ever taken a COVID-19 “vaccine” has a compromised immune system. This is due to the ingredients and the mechanisms of the COVID-19 “vaccines” themselves; in which the critical IgG3 “fight it off” immune system cells of the “vaccinated” person are damaged and/or destroyed, and the growth of IgG4 “tolerate but never clear” cells is increased. This process increases with each successive COVID-19 “vaccine booster” injection (which would include injections of the “latest version” of said “vaccines.”) Please see: https://jessicar.substack.com/p/igg4-cd4s-and-why-the-lnpmrna-platform, “IgG4, CD4s and why the LNP/mRNA platform should be prohibited”, by Jessica Rose, Ph.D., 14 August 2023.

PEMGARDA (aka Pemivibart) is an expensive drug. For example, below is a screenshot from www.patientpower.info/ regarding the cost per treatment for PEMGARDA. This is the non-insurance covered cost:

Recall that the FDA document on PEMGARDA cited above states that persons who are prescribed to take this drug need to repeat the treatment every 3 months.

General Summary: One: Yours Truly presented the first of the hypothesis regarding the use of the pangolin-CoV MP789 in the lab-creation of the original SARS-CoV-2 virus itself (the original Wuhan Hu1 COVID-19 virus itself) in the Health Friday post of 15 November 2024. Two: there is a large amount of scientific papers and articles published in 2020, with researchers investigating various hypotheses regarding a “combination” of animal coronaviruses in nature that produced the original SARS-CoV-2 virus itself. This research was performed prior to the confirmation that the SARS-CoV-2 virus itself was the product of Gain-of-Function lab-creation, most likely at the Wuhan Institute of Virology, using coronaviruses from various animals, including the bat-CoV RaTG13 and the pangolin-CoV MP789. Four: the pangolin-CoV MP789 virus genome has the “closest overall match similarity” to the genome of the SARS-CoV-2 virus itself. Five: there is a new FDA “pre-exposure prophylaxis and antiviral” drug, PEMGARDA, that is administered by infusion (IV) only, and only for certain types of immunocompromised persons. Six: the FDA-issued Fact Sheet for PEMGARDA clearly shows, in Table 2. of the document, that the SARS-CoV-2 variants that PEMGARDA is to “guard against” are virtually all derived from what the document states is “Pango lineage.” Seven: the FDA still does not recognize, authorize, or approve, of the use of Ivermectin, Hydroxycholorquine, and other effective alternatives for COVID-19 infection prevention or treatment.

Peace, Good Energy, Respect: PAVACA