“We do not believe any group of men adequate enough or wise enough to operate without scrutiny or without criticism. We know that the only way to avoid error is to detect it, that the only way to detect it is to be free to inquire. We know that in secrecy error undetected will flourish and subvert.” –J. Robert Oppenheimer
The above image is courtesy of Lincolnton, NC, and Google Images.
Health Friday is a series regarding Big Pharma, vaccines, general health, and associated topics.
There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: 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 to today’s discussion thread, they must cite their source. Thank you.
Today’s offering is slightly different from others in this series. It is an honor and a privilege for Yours Truly to present today’s post on this day, 4 July 2025, the 249th birthday of the representative republic known as the United States of America.
Facsimile of the United States Declaration of Independence made by William Stone in 1823.
The above image of Declaration of Independence is courtesy of iStock and Google Images.
Our good TradeBait2 has posted many articles on the board regarding the signers of the Declaration of Independence. These amazing men understood what it meant to sign a document in which they stated, “And for the support of this Declaration, with a firm reliance on the protection of divine Providence, we mutually pledge to each other our Lives, our Fortunes, and our sacred Honor.” They were not perfect individuals, but they understood how high the stakes were. They were ready to deal with whatever would happen to them. Many of them lost their own lives, the lives of family members, their land, their homes, and much more, because of the document that they signed. We, the citizens of the United States of America today, honor and remember them for their courage and for their sacrifices in laying the foundation for breaking the tyrannical stranglehold of British Monarchy in order to create a new and free country. It is the responsibility of American citizens to fight enemies, “both foreign and domestic.”
Regarding health, the United States of America is beginning to recover from the disaster of the lab-created bioweapons called COVID-19 virus itself and the COVID-19 “vaccines”: a disaster that was unleashed on the globe in the fall of 2019, and in the development of which both the United States Defense Department and the United States National Institutes of Health were involved. Millions of Americans became infected with the virus; thousands died from the complications and from “hospital protocols” (the use of Remdesivir, ventilators, Paxlovid, molnupiravir, and so on.) Thousands more have died from the dangerous, deadly effects of the COVID-19 “vaccines” that were injected into their bodies. Millions of Americans have COVID-19 “vaccine”-induced injuries, illnesses, or disabilities (https://openvaers.com/.) People are seeing their COVID-19 “vaccinated” loved ones, friends, and colleagues succumb to the dangerous, deadly effects of these injectables. Thankfully, more information and confirmation regarding the dangers and deadliness of these “vaccines” are coming into public view by the day. The American people are indebted to many courageous medical professionals who have labored, and continue to labor, to expose the truth about both the COVID-19 virus itself and the COVID-19 “vaccines” — Dr. Robert Malone, MD; Dr. Ryan Cole, MD; Dr. Peter A. McCullough, MD; Dr. Pierre Kory, MD; Dr. Stephanie Seneff, PhD; Dr. Jessica Rose, PhD; among others. The United States Department of Health and Human Services, under the current Secretary, Robert F. Kennedy, Jr., is taking steps to curtail the imposition of these “vaccines.” The cheap and effective preventative and treatment for COVID-19, Ivermectin, is finally being made available to the public — now, it needs FDA approval, which it still does not have. Many persons involved in the lab-creation of the COVID-19 disaster must be held to account.
There is one COVID-19 “vaccine”-related news item that Yours Truly will present in today’s offering: the coordinated plot by https://www.bio.org/ to remove current HHS Secretary Robert F. Kennedy, Jr.; and, to “redesign” the FDA into the vassal of Big Pharma that it was for many years previous to January 2025, the start of the second administration of President Donald Trump47. BIO.org partners closely with the United States Defense Department in the development of vaccines and other technologies. Please see the screenshots below from the company’s website.
The Partnering with the Department of Defense webpage also has three embedded videos, related to “rapid development of vaccines” and “how to work with the DoD.”
Regarding the coordinated effort by BIO.org to remove Secretary Kennedy, Jr., and related items, please see the screenshots below. The first one is from Yours Truly on The Q Tree. The rest of the screenshots are from the PDF of the BIO.org Vaccine Policy Steering Committee meeting that occurred on 3 April 2025. The link to the Substack article by Dr. Rose is: https://jessicar.substack.com/p/the-plot-to-remove-rfk-by-big-pharma.
The BIO.org meeting was held on 3 April 2025. Yours Truly corrects a date mistake in The Q Tree comment screenshot, above.
It appears that BIO.org is making it clear that they want “the good old HHS and good old FDA back”, and will do all they can to have this happen. It also appears that BIO.org believes that Dr. Martin Makary (current Commissioner of the FDA) is “manageable.” This may be a result of Dr. Makary’s recommendation for pregnant women to get COVID-19 “vaccinated.”
This is the same Dr. Martin Makary and his FDA that granted “Fast Track” approval in April 2025 for the H5N1 Avian Influenza “vaccine”, ARCT-2304, a self-amplifying RNA (saRNA) “vaccine.” Please see: https://www.contagionlive.com/view/fda-grants-fast-track-status-to-arct-2304-for-h5n1-influenza-protection, 10 April 2025. Surely Dr. Makary understands that saRNA, once injected into the body, turns that “vaccinated” body into a “literal interior Xerox machine” for manufacturing the modRNA of an injected saRNA “vaccine”, and that this “literal interior Xerox machine” effect can be permanent?
It appears that BIO.org is planning to foment distrust and disagreement between President Trump47 and Secretary Kennedy, Jr.
It also appears that BIO.org is planning to “work with” the United States Senate in coordinating the removal of Secretary Kennedy, Jr.
It is Yours Truly’ opinion that every United States Senator needs to see the BIO.org meeting document from April 2025; either the document itself; or, the link to the Dr. Jessica Rose article, above.
It is up to We, the People of the United States, to stop the efforts of BIO.org, of Big Pharma, of the World Health Organization, of the United Nations, of the American Medical Association, and other entities and persons, in hobbling, let alone taking away, health freedom in America.
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 ToxinWeapons.
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:
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.
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”?
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.
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.
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:
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:
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The Strategy I See Behind the New “Universal Vaccine Platform”
Some of you have to be asking yourselves why Robert F. Kennedy Jr. seems to have gone from being an opponent of vaccines, to being a proponent of them. I will try to explain.
To begin with, it helps to read the following document (H/T to PAVACA for producing these images). You can use this link, or the images below it.
HHS, NIH Launch Next-Generation Universal Vaccine Platform for Pandemic-Prone Viruses
It is hard for me to put into words, how much of a change this really is. But let me give you a quick “TL;DR” list of the big-ticket items.
Big Pharma is completely cut out of this platform – it’s US government owned and driven.
The vaccines are designed to be resistant to evolution of the pathogens they protect against. The vaxxes themselves are immune to “scariants”.
The vaccines completely abandon mRNA, cDNA, recombinant antigen, spike protein, lipid nanoparticle, and all genetic and related technologies.
The vaccines abandon Fauci’s always-failing strategy of targeting current variants, and instead seek to handle both current and future variants.
The result is fewer and less frequent shots. The better the shot, the more this is true.
The vaccines must pass rigorous safety standards, or otherwise fail to be approved.
The vaccines change direction and focus, from smaller subunits to whole-virus immunity.
The vaccines are potentially capable of inhibiting transmission.
IMO this is not just about changing the vaccines – it’s about changing minds in government science.
Most scientists, sadly, are sheep. They have neither the courage nor the inclination to challenge anything in the current scientific narrative – particularly as reported by our toxic media. If the media says “most scientists believe X”, then most scientists think this is true, and won’t bother to check, much less actively disagree.
The evil media has trained us all to believe certain myths.
There will be more and more exotic diseases coming at us from nature
There will need to be more and more vaccines, and more and more injections of them
Vaccines get better by using newer technology, not by working better for people
Vaccine hesitancy is a bad thing, and must be prevented at all costs
Vaccines are all safe, and rumors that any are bad, are dangerous
Apparently, despite the iron fist of Faucism, somebody in NIAID was thinking in ways that lead in the opposite direction from where Pfizer was taking us. I suspect that these forces sat tight, waited for “reinforcements to arrive” (Trump, RFKJ, and Dr. Jay), and had their proposal working up the chain of command as soon as Trump won.
Will this vaccine approach work? IMO it will work better than mRNA. Whether it works well enough to pass Kennedy’s new standard, based on comparison to placebos and true controls, is another question.
For the sake of those who still want vaccines, I hope so.
I suspect that these vaccines will be safer than mRNA, but not completely safe – particularly with a pathogen like COVID. As long as these vaccines are not mandated, I’m OK with their existence. In any case, the vaccines will have to prove themselves safe and effective.
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:
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.
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.
