Health Friday 9.19.2025 Open Thread: Remove the COVID-19 “Vaccines” from the Market and from Use. Now.

The free header image for today’s offering is courtesy of Dreamstime.com/ and Google Images.

Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks of the disaster of the COVID-19 “vaccines” (Bioweapon Toxin Injections), Yours Truly dedicates it to all those persons who have taken these “vaccines” and have since suffered injuries, illnesses, or disabilities, resulting from them; and, to the memory of all those persons who have taken these “vaccines” but who then passed away due to their deleterious effects. The foregoing is not a kind of “boilerplate” — it is to help ensure that those who have suffered from taking these “vaccines” are not forgotten.

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, except perhaps for AI-generated images in certain of the linked URLs in the post. If readers wish to post AI-generated content in the discussion thread for today’s offering, they must cite their source. Thank you.

Yours Truly begins here: https://www.theburningplatform.com/2025/09/07/the-massive-covid-vaccine-deception/, “THE MASSIVE COVID VACCINE DECEPTION”, by Camus. Please see the screenshots below of portions of the statements by HHS Secretary Robert F. Kennedy, Jr.:

“For the first six weeks, the vaccine is ineffective.” Not so fast. The following is proof that the COVID-19 “vaccines” are “effective” not in the “official government statements” ways (“prevention of COVID-19”; “reducing risk of severe infection and death from COVID-19”, etc.), but instead in the multiple negative ways in which these injectables were designed to be, and are still designed to be, from the moment they are injected into a person’s body. Please note: the list below is not exhaustive. The following are examples of what may be termed the “Actual Efficacy” of the modRNA COVID-19 “vaccines”:

They kill: https://kirschsubstack.com/p/new-analysis-of-the-czech-covid-vaccines, “New analysis of the Czech COVID vaccine data reveals that the mRNA shots were deadly for all ages. They should be pulled from the market.”, 28 August 2025. Please see the screenshot from this article, below, which shows that death occurred in COVID-19 “vaccinated” persons in the Czech Republic within a month after said “vaccination“:

The death rates from COVID-19 “vaccination” began to rise on 1 June 2021, the start date of the statistical analysis timefrane on the chart above.

They cause myocarditis and/or pericarditis among the COVID-19 “vaccinated“: The “primary source material” proof on this situation is furnished by Pfizer-BioNTech itself — the BNT162b2 Post-authorization report that the company gave to the FDA on 30 April 2021. The report is found here: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENTS REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021”, by Worldwide Safety, Pfizer-BioNTech. The APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST section begins on Page 30 of this report. This section lists the 1,291 types of serious adverse events reported among persons who took BNT162b2 between 11 December 2020 (the date that the FDA granted the initial Emergency Use Authorization (EUA) for this modRNA COVID-19 “vaccine”), and the end of February 2021 — a span of only 79 days (11.2 weeks.) Please see Page 6 of the APPENDIX 1 section (Page 35 of the report), where “Myocarditis” listed; and, Page 7 of the same section (Page 36 of the report), where “Pericarditis” is listed. Screenshots of the salient portions of each page are below; first, of Page 6:

And, of Page 7:

They cause permanent alteration of the DNA of the LINE-1 cells of the COVID-19 “vaccinated” person’s body (this permanent alteration is accomplished within 48 hours after “vaccination”): Please see: https://doi.org/10.3390/cimb44030073, “Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 Vaccine BNT162b2 In Vitro in Human Liver Cell Line”, Markus Alden, Yang De Marinis, et al., 22 February 2022. Figure 2 from this paper is below. BNT162b2 is reverse transcribed into LINE-1 human liver cells within 48 hours post-“vaccination”, resulting in permanent alteration of the DNA of these cells:

They cross the Blood-Brain Barrier and facilitate entry of the spike protein into the cerebral arteries: Please see https://doi.org/10.1016/j.jocn.2025.111223, “Expression of SARS-CoV-2 spike protein in cerebral Arteries: Implications for hemhorragic stroke Post-mRNA vaccination.”, Nakao Ota, et al., June 2025. A screenshot of the Highlights section of this paper is below:

They replace all of the RNA of the natural Uridine in the “vaccinated” person’s body with the lab-created compound, N1-Methylpseudouridine. This replacement “turns off” the functions of the natural Uridine. The N1-Methylpseudouridine then acts as a “facilitator” for the spread of the ingredients of the modRNA COVID-19 “vaccines” throughout the body; and, via the vagus nerve (which natural Uridine helps to regulate the functions and mechanisms thereof), into the brain. Please see https://www.nature.com/articles/s41467-024-51301-0, “N1-Methylpseudouridine and pseudouridine modifications modulate mRNA decoding during translation”, Kristin S Koutmou, et al., 16 September 2024. A screenshot of a portion of the Introduction of this paper is below:

“Substitute” the RNA of the Uridine is a fancy way of saying, “Destroys the RNA, then replaces it with N1-Methylpseudouridine.”

By the way, the “primary source document” regarding the fact that N1-Methylpseudouridine destroys all of the natural RNA of the Uridine in the “vaccinated” person’s body (along with details and descriptions of the other ingredients in BNT162b2, such as the inclusion of lipid nanoparticles) is found in the Worldwide Patent declaration for BNT162b2 by Pfizer-BioNTech. This document was published on 28 October 2021. It is found here: https://patents.google.com/patent/WO2021213945A1/en, “CORONAVIRUS VACCINE”, by Pfizer-BioNTech. Click on “Download PDF” for the entire document.

They cause serious Central Nervous System (CNS) issues, since they cross the Blood-Brain Barrier: Multiple CNS issues result from modRNA COVID-19 “vaccination”; among them, new-onset Multiple Sclerosis. Again, the “primary source document” for this is the 5.3.6 Post-Authorization report cited above. Please see the salient portion of Page 6 of the APPENDIX 1. section of this report (Page 35 of the report), below:

Please also see: https://doi.org/10.1016/j.jneuroim.2021.577785, “New diagnosis of multiple sclerosis in the setting of mRNA COVID-19 vaccine exposure”, Karlo Toljan, et al., 9 December 2021. A screenshot of section 3.2 Case 2 from this paper is below:

They accumulate COVID-19 “vaccine” ingredients (modRNA, spike protein, lipid nanoparticles, and all the other elements of this injectable) in every organ and area of the “vaccinated” body: Please see another “primary source document” from Pfizer-BioNTech regarding this situation. The document is found here: https://icandecide.org/wp-content/uploads/2022/03/125742_S1_M2_26_pharmkin-tabulated-summary.pdf, “BNT162b2 2.6.5 Pharmacokinetics Tabulated Summary”, by Pfizer-BioBNTech. The company gave this document to the FDA on 21 January 2021. Page 7 and Page 8 of the document are below; first, Page 7:

And, Page 8:

Please note that these accumulations begin to occur within 30 minutes after injection with BNT162b2. Please also note that the formulation used in the Wistar lab rats experiments above is the same formulation that was granted the initial FDA Emergency Use Authorization for use in the United States on 11 December 2020; and was subsequently FDA-approved under the name COMIRNATY.

In terms of the “waning efficacy” of the COVID-19 “vaccines”: It was shown in the large Penn State University study of 2022 that COVID-19 “vaccine efficacy” wanes badly by the fifth month after “vaccination”; in fact, the “efficacy” begins to wane well before that. Please see https://doi.org/10.1186/s12879-022-07418-y, “SARS-CoV-2 vaccine effectiveness against infection, symptomatic and severe COVID-19: a systematic review and meta-analysis”, Paddy Ssentengo, et al., 7 May 2022. A screenshot of the Results section of this paper is below:

VE = Vaccine Effectiveness

It is also known that the COVID-19 “vaccines” do not prevent COVID-19 infection; they do not prevent death from COVID-19 infection in “vaccinated” persons; they do not prevent the spread of the virus; and, that any “efficacy” from these injectables wanes almost completely well before seven months post-“vaccination.” In short, the COVID-19 “vaccines” are ineffective in what they were / are “officially” designed to do. On the other hand, these injectables are “effective” in causing “vaccine”-induced injuries, illnesses, disabilities, and death.

HHS Secretary Kennedy, Jr.: All COVID-19 “vaccines” must be pulled off the market and removed from use. Now. There is no rational reason why these injectables are still being authorized, approved, or administered. The Amendment 12 to the PREP Act regarding COVID-19 Medical Countermeasures, signed by former HHS Secretary Xavier Becerra in December 2024, must be rescinded. Bring those who lab-created the COVID-19 “vaccines” brought to account. Get Ivermectin, Hydroxychloroquine, Vitamin C, Vitamin D, Azithromycin / Doxycycline, Zinc, NAC, and Quercetin all FDA-approved for prevention and treatment of COVID-19 infection. Get these items made readily available to the general public and also to medical professionals.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA