Our mission, as God-fearing and God-loving patriots, is to defend this Constitutional Republic and to increase its greatness, in all good things and ways, by using our voices in free but courteous speech, by discussing the happenings of the world and coming to a profound understanding of those things, and by sharing and promulgating these Truths on both this platform and others.
The above free image of a handwritten letter from 1889 is courtesy of Colourbox and Google Images.
Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. As this post speaks of the disasters of COVID-19 and of the COVID-19 BTI (Bioweapon Toxin Injections, aka the “vaccines”), it is dedicated to the memory of Yours Truly’s “fully vaccinated and boosted” late brother, Sam; to her late cousin, Bill; and to all persons, of whatever age or location, who have passed away from the negative effects (direct or indirect) of the COVID-19 “vaccines” they had in the their bodies. However, the discussion is not limited to what is presented today: It is an Open Thread.
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.
Herewith, the letter:
Dear Incoming President Donald J. Trump and Incoming Secretary of Health and Human Services Robert F. Kennedy, Jr.:
Greetings. This letter is from an independent researcher who has been writing about the COVID-19 virus and the COVID-19 “vaccines” for over four years.
The COVID-19 virus is, by now, a part of human life on this planet. It will continue to mutate and infect humans. The failed COVID-19 “vaccines” were developed and mandated for use on humans to “prevent” infection by this virus. The COVID-19 “vaccines” are not “safe and effective” as they are claimed to be by the CDC, the FDA, and many medical organizations. In fact, these injectables induce thousands of types of medical conditions; can aggravate existing medical conditions; re-establish previously-controlled medical conditions; induce COVID-19 infection; and more, among those who have COVID-19 “vaccines” in their bodies. For further information, please see the Appendix 1. List of Adverse Events of Special Interest section of the following document, given to the FDA by Pfizer-BioNTech on 30 April 2021, regarding the company’s modRNA COVID-19 “vaccine” BNT162b2: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-Feb-2021.”
It is now known that the COVID-19 virus was a lab-created biological weapon (bioweapon); and that the COVID-19 “vaccines”are lab-created and -enhanced biological weapons (bioweapons.) There were, and are, numerous entities and persons involved in the creation of this virus and these “vaccines” that must now be brought to justice for their activities. Among these activities was the deliberate withholding of vital information from you, President Trump, as then-President of United States, during “Operation Warp Speed”, which was part of the White House Coronavirus Task Force in your first administration. Please refer to: https://oversight.house.gov/wp-content/uploads/2024/12/2024.12.04-SSCP-FINAL-REPORT-ANS.pdf, “After Action Review of the COVID-19 Pandemic: The Lessons Learned and a Path Forward”, by the Select Subcommittee on the Coronavirus Pandemic, Chairman Brad Wenstrup, for more information regarding the development of the COVID-19 virus and of the COVID-19 “vaccines.”
To gain more knowledge regarding the disaster of the COVID-19 virus and the COVID-19 “vaccines”, please refer to: https://kirschsubstack.com/p/game-over-medicare-data-shows-the, “GAME OVER: Medicare data shows the COVID vaccines increase your risk of dying”, by Steve Kirsch, 2 February 2023; and, also:
The following website lists links to contracts between the United States government and Pfizer-BioNTech related to the COVID-19 issue: www.keionline.org/covid-contracts, “COVID-19 Contracts.” These contracts involve the Department of Defense; the Department of Health and Human Services; the Administration for Strategic Preparedness and Response (ASPR); the Biomedical Advanced Research and Development Authority (BARDA); the National Institutes of Health (NIH); and the National Institute for Allergies and Infectious Diseases (NIAID.) There are also links to contracts between the United States government and other companies related to COVID-19. These include companies such as, Glaxo-Smith-Kline; Johnson & Johnson; Moderna; and Novavax, among many others.
The following paper details how the dangerous lipid nanoparticles in the modRNA COVID-19 “vaccines” spread the ingredients of these “vaccines” throughout the body, inducing changes body-wide, particularly in the heart: https://doi.org/10.1038/s41587-024-02528-1, “Nanocarrier imaging at single-cell resolution across entire mouse bodies with deep learning”, Hendrik Dietz, et al., 14 January 2025. Please see the image of the Abstract from this paper, below:
Please also see the image below, from the blog post by Dr. Jessica Rose, PhD, which discusses the above paper (https://jessicar.substack.com/p/lnp-spike-mrna-induction-of-changes, “LNP spike mRNA induction of changes in proteins related to vasculature formation and maintenance (collagen) in the heart”, 15 January 2025):
President Trump and Mr. Kennedy, Jr.: The double disaster of the lab-created bioweapon called the COVID-19 virus, and the disaster of the lab-created and -enhanced bioweapons called the COVID-19 “vaccines”, must not ever be allowed to occur again. The entities and persons involved in the creation of this double disaster must be held accountable. In addition: The use of the COVID-19 “vaccines” must be stopped immediately, for all age groups, until complete, detailed, and proper clinical trials are held regarding these products, with all data fully collected, analyzed, and published for the public to see.And,President Trump: Mr. President, it is also incredibly important that those who deliberately withheld from you, or minimized to you, information that you needed to know during “Operation Warp Speed” in your previous administration, be held accountable.
It is also imperative that all medical professional organizations, state medical licensing boards, and specialty medical certification granting organizations, which currently require their applicants, licensees, and certification holders, to be COVID-19 “vaccinated”, to use only FDA-approved prophylactics and/or treatments for COVID-19, and to urge these products on their patients, be enjoined to end these requirements. Furthermore, access to, and use of, prophylactic and/or treatment options for COVID-19 that are safe and effective, such as, Ivermectin, Hydroxychloroquine, Quercetin, Zinc, and Vitamin D, must become available to all persons, including to persons with COVID-19 infection, whether they are hospitalized or not. In addition, medical professionals who choose to treat patients with the products listed above must not become subject to “professional discipline” protocols, or to have their License to Practice Medicine and/or their specialty medicine certifications restricted or revoked.
With Peace, Good Energy, and great Respect, from an independent COVID-19 researcher,
The above free vintage image of a medical doctor performing an exam on the larynx of a patient is courtesy of Google Images.
Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. Since today’s post speaks of the disaster of the COVID-19 virus itself, and of the COVID-19 BTI (aka the “vaccines”), it is dedicated to the memory of Yours Truly’s COVID-19 “fully vaccinated and boosted” late brother, Sam; to her late cousin, Bill; and, to all persons, of whatever age or location, who have passed away from the negative effects, direct or indirect, of the COVID-19 “vaccines” that they had in their bodies.
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.
This week’s Health Friday post concerns the ingredients and mechanisms of the COVID-19 BTI in the inducement of cancer in “vaccinated” persons. There is also a role to play here for the COVID-19 virus itself.
Yours Truly begins with examples of studies that prove the COVID-19 BTI (aka the “vaccines”) induce cancer: https://doi.org/10.1016/j.fct.2022.113008. “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs”. Stephanie Seneff, Peter A. McCullough, et al., June 2022. Below are Table 6 and Table 7 from this paper:
And, from this paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC9876036/, “Potential health risks of mRNA-based vaccine therapy: A hypothesis”, K Acevedo-Whitehouse and R Bruno, 25 January 2023. Below are two screenshots from the paper:
Another paper, which details damage in the “vaccinated” person’s body to the p53 tumor suppressor protein, plus damage to / interference with, the type I Interferon response (also called type I IFN response), is here: https://doi.org/10.7759/cureus.50703, “SARS-CoV-2 Vaccination and the Multi-Hit Hypothesis of Oncogenesis”, R.P. Angues and Y.P. Bustos, 17 December 2023. Below is the salient graphic from this paper:
**** Note that cancer can be fostered and/or metastasized by either COVID-19 “vaccination”, or by the COVID-19 virus itself. More on that later on in today’s post.
One important item that links all of the above is what the COVID-19 “vaccines” do to the p53 protein in the human body. P53 (also called TP53, or Tumor Protein 53) prevents the formation of cancer in the body. Please see: https://en.wikipedia.org/wiki/P53. The modRNA COVID-19 “vaccines” manufactured by Pfizer-BioNTech damage the p53 in the “vaccinated” person’s body, (which then interferes with and/or “disables”, the ability of p53 to “detect” and prevent the formation of cancer tumors in the “vaccinated” person’s body) via the SV40 African Green Monkey cancer promoter gene code piece that is present in this company’s modRNA COVID-19 “vaccines.“
Scientific researchers have been experimenting for years with the SV40 cancer promoter and its interaction to interfere with and/or to suppress, the p53 tumor suppressor protein. Here are examples of published papers on the topic:
One: https://doi.org/10.1128/mcb.19.4.2746. “New Insights into the Mechanism of Inhibition of p53 by Simian Virus 40 Large T Antigen”, Hilary M. Sheppard, et al., April 1999. Below are two images from this paper:
Note that the “monkey – human” amino acid percentage of “identicalness” of p53 is much higher than that of the “mouse – human” percentage.
The “Hudson, Colvin” paper from 2016 details how SV40 suppresses p53, allowing tumors to form and grow: https://doi.org/10.1093/ilar/ilw001, “Transgenic Mouse Models of SV40-Induced Cancer”, Amanda L. Hudson, Emily K. Colvin, 31 March 2016. Below are images from this paper:
And, the Drayman, et al., 2016 paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC5288138/, “p53 elevation in human cells halt SV40 infection by inhibiting T-ag expression”, Nir Drayman, et al., 21 July 2016. Below is Figure 7 from this paper:
The point here is that the p53 tumor suppressor does a good job of preventing SV40 cancer promoter cells from infecting the body and establishing oncogenic (cancer tumor) cells. And, that this knowledge has been around for some time.
Which brings one back to the Pfizer-BioNTech modRNA COVID-19 BTI (aka the “vaccines”), and the discovery of “loose DNA” and of amounts of the SV40 cancer promoter gene code piece in these injectables. It is inconceivable that Pfizer-BioNTech did not know of the ability of the p53 protein in the human body to detect SV40 and then to prevent it from establishing oncogenic cells. It is also, in Yours Truly’s opinion, inconceivable that Pfizer-BioNTech can try to explain away this discovery by some kind of “Oops, we’re sorry, we didn’t mean to leave that stuff in the formulation of the product” hyperbole. The “loose DNA” (and, by extension, the SV40 cancer promoter gene code piece) are present in all the modRNA COVID-19 “vaccines” made by this company in the summer of 2020, when Pfizer-BioNTech “suddenly” switched the manufacturing process for BNT162b2 from the original “Process 1” method (not using an “extracts of E. coli bath” in the process), to the “Process 2” method (using an “extracts of E. coli bath” in the process) for use in the BNT162b2 (truncated and data-falsified) “clinical trials” going on at that time for this injectable; and which “Process 2” method has been used to manufacture the modRNA COVID-19 “vaccines” by this company since. Please also see here: www.theqtree.com/2023/11/06/the-infamous-process-2-manufacturing-method-for-the-pfizer-biontech-modrna-covid-19-vaccines/; the actual documentation that the company provided to the FDA regarding this change of manufacturing process is detailed.
Another piece to this situation is the fact that the modRNA COVID-19 BTI (aka the “vaccines”) contain dangerous lipid nanoparticles that quickly spread the contents (and, by extension, the mechanisms) of this injectables throughout the “vaccinated” person’s body. In addition, these lipid nanoparticles (ALC-0159 and ALC-0315 in the Pfizer-BioNTech BTI; and, SM-102 in the Moderna BTI) are specifically developed to evade the body’s natural “are you a friend or a foe” detection and elimination mechanisms. This is in addition to other excipients (adjuvants) in these injectables, such as PEG2000-DMG. Yours Truly has written extensively on these items and how they work to undermine / interfere with, the “vaccinated” body’s natural immune processes. Finally, there is the N1-Methylpseudouridine in BOTH the Pfizer-BioNTech AND the Moderna COVID-19 BTI. This lab-created compound was specifically developed to replace (remove) the natural Uridine RNA in the “vaccinated” body with “fake Uridine” plus a form of methane. In the specific case of N1-Methylpseudouridine, the consequences to the “vaccinated” body, BOTH in the physical AND in the psychological aspects, is profoundly negative. These are all aside from the addition of the SV40 cancer promoter in the Pfizer-BioNTech COVID-19 “vaccines.”
Going back to the graphic from the “Angues and Bustos” paper regarding the fact that BOTH the COVID-19 itself, AND the COVID-19 BTI (aka the “vaccines”) can cause cancer. Below is a repeat of the graphic:
Notice the Impaired type I IFN response (type I Interferon) on the lower right of the graphic. This is another ingredient / mechanism of the COVID-19 virus itself (likely) AND of the COVID-19 BTI (definitely), the workings of which have also been studied and known for years. An example of a paper that speaks to this is here: https://pmc.ncbi.nlm.nih.gov/articles/PMC4666791/, “The Type I Interferons: Basic Concepts and Clinical Relevance in Immune-Mediated Inflammatory Diseases”, Consuelo M Lopez-Padilla, Timothy B Niewold, PMC published 15 January 2017. Two images from this paper are below:
Three points here, in Yours Truly’s opinion, regarding those who lab-created the COVID-19 virus itself, and those who lab-created the COVID-19 BTI (aka the “vaccines”): One: they knew exactly what things would: interfere with the body’s type I Interferon responses; interfere with and/or destroy elements of the body’s natural immune system (CD4 – CD8 cells, IgG3 cells, and so on); evade or interfere with, the body’s natural p53 tumor suppressor response to detect and eliminate the SV40 cancer promoter that would be present in the Pfizer-BioNTech COVID-19 BTI; cross the Blood-Brain Barrier; and more. Two: they made sure that the COVID-19 virus itself is not “just another flu virus”, but, rather, a bioweapon that was lab-created from years of stunningly-detailed research and experimentation to wreak as much potential damage as possible on the person who contracts an infection of the virus itself. And, Three: they made sure that this created bioweapon virus would be the foundation of the COVID-19 “vaccines”; while, at the same time, limiting or denying access to simple and effective items that can successfully counteract the virus itself, such as Ivermectin, Hydroxychloroquine, Zinc, Vitamin D, and Quercetin.
While it is true that the survival rate for non-COVID-19 “vaccinated” persons who contract a COVID-19 virus itself infection and recover is 99% for ages 0 to 65 years, and between 94% – 95% for ages 65 and above, an infection from the COVID-19 virus itself can still potentially damage the body. However, those who lab-created the COVID-19 virus itself did not reckon completely with the human body’s natural immune system’s ability to detect, fight off, and eliminate this bioweapon. In Yours Truly’s opinion, the COVID-19 “vaccines” were lab-created to “finish the job” in this regard: injections which were then “mandated” for people to take, to “keep themselves and others safe from the virus.” With the disastrous results that are now presenting worldwide.
There are several items that can support / supplement the p53 of the body. Here are some examples:
Phenethyl isothiocyanate in the diet: www.nature.com/articles/cdd201648, “Reactivation of mutant p53 by a dietary-related compound phenethyl isothiocyanate inhibits tumor growth”, M Aggarwal, et al., 3 June 2016. This compound is also called “PEITC.” Natural sources of phenethyl include broccoli, watercress, cabbage, turnips, and radishes. More information can be found here: www.sciencedirect.com/topics/chemistry/phenethyl-isothiocyanate.
Finally, there is the phenomenon of shedding of the COVID-19 virus itself, and of the COVID-19 “vaccines.” It is not known at this time exactly what ingredients of these are shed. What IS known is that it is indeed happening, and that this shedding is negatively affecting the health of the people who are “shed upon.” A comprehensive article that explains this issue is here: https://pierrekorymedicalmusings.com/p/newly-published-study-shows-shedding, “Newly Published Study Shows Shedding of Covid mRNA Vaccine Products”. Pierre Kory, MD, 9 December 2024.
It is of the utmost importance that all people have, and maintain, the highest degree possible of general health; and, in particular, the health of their natural immune system.
THERE. MUST. BE. JUSTICE.
FLASH! Sunday 12 January 2025: ADDENDUM: Please see below, copied (and expanded here) from the main discussion thread today:
“WOLF MOON AND ALL — KEVIN McKERNAN FOUND THE MOAD REGARDING THE PFIZER-BIONTECH COVID-19 “VACCINES” AND TURBO-CANCERS:
The following is a “quick and dirty” summary. Yours Truly will append a “Flash! News” addendum to the body of the Health Friday post of two ago on the p53 cancer tumor suppressor gene and how SV40 interferes with it.
Summary:
One: Dr. Kevin McKernan ran the gene sequence from the cancer tumor biopsies and compared them to the gene sequence in the Pfizer-BioNTech COVID-19 “vaccine.” There was a match. He also found traces of the Pfizer-BioNTech COVID-19 “vaccines” in the cancer tumors.
Two: At least one sequence match was made a year AFTER the patient had been COVID-19 vaxxed.
There’s only one way that this can happen, IMO — it’s the SV40 African Green Monkey cancer promoter gene code piece that’s in the Pfizer-BioNTech COVID-19 “vaccines.” The SV40 promoter interferes with the body’s p53 cancer suppressor protein.”
Yours Truly will amplify on the above.
First: IN ADDITION to SV40 interfering with the p53 cancer suppressor protein in the COVID-19 “vaccinated” person’s body, there is ALSO the damage / destruction of the crucial immune system IgG3“fight it off” cells, instead fostering the increase of IgG4 “tolerate but never clear” cells. This “class switch” affects the entire body, “depressing” the natural immune “are you a friend or foe” mechanisms.
Second: The N1-Methylpseudouridine in the Pfizer-BioNTech AND in the Moderna modRNA COVID-19 BTI (aka the “vaccines”) replaces the RNA of the natural Uridine in the “vaccinated” person’s body. This ALSO interferes with / damages, the multiple body-brain interactions and mechanisms that natural Uridine regulates.
Third: There is ALSO the phenomenon of COVID-19 “vaccine” shedding by “vaccinated” persons to consider in this scenario. There are increasing reports of the negative effects that the ingredients (and, by extension, the mechanisms) of the COVID-19 “vaccines” do to non-“vaccinated” persons via this shedding. There is, in Yours Truly’s opinion, real potential for the SV40 cancer promoter that is in the Pfizer-BioNTech COVID-19 “vaccines” to be shed from persons who have taken this “vaccine” onto other people, including onto non-“vaccinated” persons.
Below are two other screenshots from the Slay News article:
The above image of a Mental Health word graphic is courtesy of Google Images.
Health Friday is a series about Big Pharma, vaccines, general health, and associated topics. Since today’s post speaks to the COVID-19 disaster, it is dedicated to Yours Truly’s COVID-19 “fully vaccinated and boosted” late brother, Sam; to her late cousin, Bill; and to all others who have died, or have become injured or disabled, directly or indirectly, due to the negative effects of the COVID-19 BTI (Bioweapon Toxin Injections, aka the “vaccines”) they had put into their bodies.
There are Important Wolf Moon Notifications, the Rules of our late, good Wheatie, and certain caveats by Yours Truly, of which readers should be aware. They are linked here. The discussion is not limited to what is presented today: It is an Open Thread.
This post is an Opinion Piece. Yours Truly will be making statements that, hopefully, can start a dialogue on what one believes is an important topic.
To Begin: There are approximately eight billion human beings on Earth at this time. Approximately five billion of these human beings have taken at least one dose of a COVID-19 BTI (aka the “vaccines.”)This means that approximately 61% of the entire population of the Earth has been COVID-19 “vaccinated.” Approximately one billion of these COVID-19 “vaccinated” human beings are already dead, or “vaccine”-injured, or “vaccine”-disabled. Please refer to this tweet, which contains a video clip from a recent interview between Ed Dowd and Brett Weinstein: https://x.com/_BlakeHabyan/status/1872735868709941748, which discusses this situation. This number will increase as time goes on, and as more COVID-19 “vaccinated” persons succumb to “vaccine”-induced injuries, “vaccine”-induced disabilities, or die from the negative effects of these injections. In addition, Yours Truly believes it can be fairly argued that what may be called the “ripple effects” among all persons in the world from the COVID-19 BTI (aka the “vaccines”), including among persons who are not “vaccinated”, will eventually be felt by every person on the planet.
Yours Truly will state at the outset that she is neither a medical professional, nor a mental-health professional. However, she has taken psychology and sociology courses in the process of earning two BFA degrees and an MA degree. She has also researched into the effects of the COVID-19 BTI (Bioweapon Toxin Injections, aka “vaccines”) on the body and brain of the “vaccinated” since March 2020. One will use terms “COVID-19 BTI” and “COVID-19 vaccines” interchangeably.
Note the accumulations of BNT162b2 in the Brain, the Adrenal Glands, and in the Pituitary Gland. Note especially the accumulations in the Liver. The Liver is where the body produces Uridine, which is crucial for all kinds of body functions, including the regulation of mood. This is all part of what is called the “Brain-Gut Connection.” The human gut (stomach, intestines, liver, etc.), and, importantly, Uridine, sends “signals” to the brain, which processes these signals and “translates” them into body functions, emotional reactions, mood states, cognitive processes, and more. The N-1 Methylpseudouridine in the modRNA COVID-19 “vaccines” literally replaces the RNA of the body’s natural Uridine with a combination of “fake Uridine” (which evades the body’s “are you a friend or a foe” recognition and elimination mechanisms), plus a form of methane.
There is an increasing number of scientific papers, articles, and editorial pieces regarding the negative effects on the brain, its components and mechanisms, and on its emotional-psychological functions, after COVID-19 “vaccination.” These negative effects range from inducement of “autism-like” behavior, to inducement of psychosis, to reports of suicide attempts and depression, and more. Examples of such writings include: https://doi.org/10.1007/s11064-023-04089-2. “Prenatal Exposure to COVID-19 mRNA Vaccine BNT162b2 Induces Autism-Like Behaviors in Male Neonatal Rats: Insight into WNT and BDNF Signaling Perturbations”, Mumin Alper Erdogan, et al., Epub 10 January 2024; www.psychiatrist.com/pcc/psychosis-associated-covid-19-vaccination/, Abdulsamad A. Aljeshi, MBBS, FRCPC, et al., 17 February 2022; https://pmc.ncbi.nlm.nih.gov/articles/PMC8716269/, “P.0707 Suicide attempt and depression after COVID-19 vaccination: a case report”, IA Gencan, et al., 30 December 2021; and, https://doi.org/10.1007/s10072-021-05662-9, “Spectrum of neurological complications following COVID-19 vaccination”, Ravinda K Garg, Vimal K Paliwal, 31 October 2021. Below is Figure 1. from the Garg and Paliwal paper:
Note that the neurological issues induced by COVID-19 “vaccination” are not confined to “vaccination” by the modRNA COVID-19 BTI; they also occur after “vaccination” with the adenovirus DNA COVID-19 BTI by AstraZeneca.
There are also studies that have been conducted regarding the mental health of persons who have what is called Long COVID; for example: https://scholarcommons.towerhealth.org/t-med/vol3/iss2/2/ “Examining the Mental Health Impact: Investigating the Association between Suicide and Long Covid Syndrome”, Nicole Ann E. Villa, et al., June 2024 (click on the article title at the URL link and the PDF will load.)
However, there is also a myriad of other mental-health issues that arise regarding COVID-19. For example: What about a person who is COVID-19 “fully vaccinated and boosted” who then passes away from “died suddenly”? What mental-health effects does this produce in the deceased’s survivors? — such as, grief — shock — denial — anger — and more? For example: What about a COVID-19 “fully vaccinated and boosted” person, who has previously-diagnosed mental-health issues that were under control, but then after “vaccination” presents with symptoms of aggravation of these issues? — such as, onset of new psychosis — loss of interest in daily activities — anxiety — and more? For example: What about a COVID-19 “fully vaccinated and boosted” person who then presents with a disability? — the mental-health issues that can arise from this, and the issues that can arise among the affected person’s family members? — such as, anxiety — grief (over lost abilities and opportunities) — anger — depression — and more? For example: What about non-COVID-19 “vaccinated” persons who have friends and family who are “vaccinated”, and who are starting to see the negative effects of these “vaccines” present in their loved ones? — such as, “anticipatory grief” — anger — sadness (especially if the non-“vaccinated” person tried to warn them)?
There are, in addition, the hormones that the body will release when under stress, in danger, in grief, and similar situations, among them cortisol and adrenaline. These hormones, once released into the body, interact with the Gut-Brain connection organs, and with the Vagus Nerve, which is an important component of the whole. For some further information on the Vagus Nerve, and its importance in good health please see: https://marica1776.com/2023/03/17/53289, “The Glass Wall Part 3 — The Body Needs a Healthy Vagus Nerve.”
Refer back to the images of page 7 and page 8 of the Appendix 1. in the BNT162b2 report above, regarding accumulations of BNT162b2 in the organs of the “vaccinated” lab rats in the study performed. The Brain, the Adrenal Glands, the Pituitary Gland, and the Liver all perform immensely important functions and regulation processes for the entire body — including in cognitive and emotional/psychological processes and regulation. It is clear that the modRNA COVID-19 BTI accumulate in, and attack, these very important areas of the “vaccinated” person’s body. **** And there is also this: Researchers at Yale University have found out that the spike protein from the COVID-19 BTI remain the body of the “vaccinated” person for as long as 700 days post-injection — https://alexberenson.substack.com/p/urgent-yale-researchers-have-found, “URGENT: Yale researchers have found Covid spike protein in the blood of people never infected with Covid — years after they got mRNA jabs”, 19 December 2024. This as-yet-unpublished study, called the “LISTEN study”, was headed by Dr. Akiko Iwasaki, a COVID-19 “vaccine” proponent. The findings are shocking. In addition to the COVID-19 spike protein being found in the blood of “vaccinated” persons for as long as 700 days post-injection (and that these “vaccinated” persons had never tested positive for COVID-19 infection), it was found that their CD4 immune system cells were compromised; also, that the DNA in the plasmids of the “vaccine” can indeed integrate into the genome of the “vaccinated” person’s body.
The implications of this the LISTEN study results are profound. It appears that the COVID-19 “vaccinated” person’s body literally manufactures spike protein for a very long time post-“vaccine” injection. However, at the same time, it is also known that whatever “immunity” that is “conferred” by COVID-19 “vaccination” dissipates after a matter of weeks or months. Thus, it is possible that, while the “immunity” conferred by these “vaccines” is short-lived, the body’s manufacturing of continuous amounts of spike protein from these “vaccines” is ongoing. The implications of the negative impacts of these “vaccines” on the mechanisms and processes of the Brain, the Adrenal Glands, the Pituitary Gland, and the Liver, especially with repeated “vaccine” injections, are likely incalculable.
Meanwhile, what can COVID-19 “vaccinated” persons (and, also, non-COVID-19 “vaccinated” persons) do to support their personal mental health in the era of COVID? The answer is unique to each individual. Some may have psychological counseling. Some will decide to make healthy changes to their diet, or to incorporate daily exercise. Others may consult their personal physician. Still others may craft a program of their own. Yet others will turn to meditation, and/or to a spiritual Force or Supreme Being to guide them. Some will consult with alternative medicine practitioners. And so on. However, what will not work is to turn to drug or alcohol abuse. What will not work is unhealthy or harming behavior to the self or to others. Here are two online resources, among many others, that provide helpful information: www.helpguide.org/mental-health/grief/coping-with-grief-and-loss. by Melinda Smith, M.A., et al.; and, www.anxietycentre.com/, which has many free articles, videos, and other resources.
The issue of mental health in the era of COVID is one that is an unfolding situation. It deserves deep and ongoing investigation. Today’s Opinion Piece can hopefully be part of the conversation about this issue.
The above image of a year-end wrap up countdown is courtesy of The Productive Woman and Google Images.
Health Friday is a series related to Big Pharma, vaccines, general health, and associated topics. Since today’s post mentions the COVID-19 virus itself, and the COVID-19 BTI (Bioweapon Toxic Injections, aka the “vaccines”), it is dedicated to the memory of Yours Truly’s “fully vaccinated and boosted” late brother, Sam; to her late cousin Bill; and, to all persons, of whatever age or location, who have passed away from the negative effects of the COVID-19 “vaccines” that they had in their bodies.
There are Important Wolf Moon Notifications, the Rules of our late, good Wheatie, and certain caveats by Yours Truly, of which readers should be aware. These are linked here. The discussion is not limited to what is presented in today’s post: It is an Open Thread.
Yours Truly will begin the Health Friday 2024 Year-End Wrap Up Edition with these:
And, many people who did “shut up and obey” are starting to realize that they have likely permanently damaged their bodies (and brains) via the multiple negative effects of the COVID-19 BTI (Bioweapon Toxin Injections, aka the COVID-19 “vaccines”) that they had put into their bodies.
And, some new information to help round out the year 2024:
From Steve Kirsch’s blog: https://kirschsubstack.com/p/the-cfr-from-the-pfizer-trial-show. “The CFR from the Pfizer trial show the vaccines make you 14X more likely to die from COVID”, 24 December 2024. Mr. Kirsch performed a statistical analysis of the Supplementary Table S4 of this 2021 paper: https://doi.org/10.1056/NEJMoa2110345, “Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months”, Philip R. Dormitzer, M.D., Ph.D., et al, published 15 September 2021. There are over 25 authors of this paper. Most of them are affiliated with Pfizer-BioNTech, the developer (along with several other entities, such as the United States Department of Defense, United States Army) and manufacturer (along with the United States Department of Defense, United States Army) of BNT162b2. Apparently, the CDC never performed its own analysis of the data presented in the paper. Mr. Kirsch performed the first real analysis. Here is his conclusion (from his blog post):
CFR = Case Fatality Rate. Below is the Supplementary Table S4 from the paper:
Note that “Unblinding” means that Pfizer-BioNTech offered to give BNT162b2 injections to “Blinded” subjects in the C4591001 clinical trial. Most of the “Unblinded” participants accepted the offer and took the injections. This also means that data collected from the “Blinded” subjects after they took the injections is potentially compromised. However, even with this caveat, the data on the Supplementary Table S4 confirm that persons who took BNT162b2 had adverse events that the “Placebo” (“Blinded”) group did not have.
From Mole at Substack, an important post regarding “educated hesitancy” about “new drugs and novel vaccines”: https://mole.substack.com/p/c-and-c-today-new-peer-reviewed-study, “C&C today: new peer-reviewed study tears jabs a new one”, 23 December 2024. The paper referred to is here: https://journals.sagepub.com/10.1077/09246479241292008. “Pharmaceutical product recall and educated hesitancy towards new drugs and novel vaccines”, Peter Rhodes and Peter I Perry, 6 November 2024. Below is a graphic from this paper, followed by the Conclusion:
And, to finish the 2024 wrap-up, the link to Katherine Watt’s Substack blog, Bailiwick News, listing and detailing the multiple signed (and, in some cases, also not redacted) agreements between the United States Department of Defense, United States Army, regarding the development, manufacturing, and distribution for administration, of the Pfizer-BioNTech COVID-19 BTI (Bioweapon Toxin Injection, aka COVID-19 “vaccine”) BNT162b2: https://bailiwicknews.com/p/on-contracts-consortium-agreement. “On contracts: consortium agreement; base agreement; technical direction letter-statement of work; project agreement”, 9 December 2024 (repost of her 28 April 2023 post.) The post is long and very detailed. It is worth reading through. There is much information in the documents that blows the lid off the cooperation between the Defense Department / United States Army, and Pfizer-BioNTech. This is, in Yours Truly’s opinion, a chain of documents that must be brought to the attention of both Robert F. Kennedy, Jr., (as the incoming Secretary of Health and Human Services); and, incoming President of the United States Donald J. Trump, on 20 January 2025, after President Trump is inaugurated the 47th President of the United States.
THERE. MUST. BE. JUSTICE.
Yours Truly urges all readers to build and maintain the highest possible degree of general health, and also the health of their natural immune systems. One also urges all readers who may be COVID-19 “vaccinated” to seriously consider investigating, and following, a COVID-19 “vaccine” detoxification / mitigation protocol, such as the ones listed on the FLCCC website: https://covid19criticalcare.com/.
Yours Truly wishes all readers a healthy New Year 2025! Peace, Good Energy, Respect: PAVACA
The above free image of a Christmas gift exchange is courtesy of Google Images.
Health Friday is a series of posts related to Big Pharma, vaccines, general health, and associated topics. The discussion is not limited to what is presented today: It is an Open Thread.
There are Important Wolf Moon Notifications, the Rules of the our late, good Wheatie, and certain caveats by Yours Truly, of which readers should be aware. They are linked here.
Today’s Health Friday is a Holiday Exchange for ideas, recipes, “life hacks”, “this is what my grandmother did when the family had a cold”, exercise hints, and so on, related to building and maintaining sound general health and a strong immune system. Advice and information from readers regarding items from Western medicine, Homeopathy, Naturopathic Medicine, Herbal medicines, Chinese medicine, Ayurvedic medicine, folk and traditional medicine, “Let thy food be thy medicine” recipes, personal experiences, “these are what I take on a daily basis”, books and articles, and the like — all are welcome. So, grab a cup of coffee or tea, come on over by the Christmas tree, and let’s exchange health ideas gifts!
To start the exchange rolling, Yours Truly provides the following:
“My Aunt Mary’s Daily Tonic“
Ingredients: 1 Tablespoon apple cider vinegar; 1 Tablespoon honey; 2 teaspoons lemon juice; a sprinkle of cinnamon; 1/3 cup very hot (not boiling) water.
Method: Muddle the apple cider vinegar, the honey, the lemon juice, and the cinnamon in a glass. Add the very hot water and stir gently. Drink as soon as it cools down just a little. (Please don’t “quaff” the mixture — take it in sips. I think cider vinegar tonic is tough to take all at once!)
My late Aunt Mary drank this tonic for decades. She believed that it “cleaned the intestines.” Well, it must have been beneficial for her — she lived to be 96 years old. I will say that I change the amounts of the first three ingredients when I prepare the mixture to: 2 teaspoons apple cider vinegar; 2 teaspoons honey; 1 teaspoon lemon juice (the cinnamon amount and the water amount remain the same.) I suspect that this tonic is / was, probably used by many other people, and is known by various names. My Aunt Mary also used a fabulous, easy recipe for baked salmon and peas (her mother was from County Mayo), which I remember eating but I don’t have the recipe. She firmly believed that eating salmon could cure or prevent many diseases.
https://dspiked.com/NOTE: This product contains Shilijit (Shilijat) and also Ginko Biloba. Both of these can cause significant interactions with prescription drugs for diabetes, for blood clotting, and for other health issues. Please search www.webmd.com/ for Shilijat and for Ginko Biloba, and read the “Side Effects“, “Precautions“, and “Interactions” sections for these items.
Where There is No Doctor: A Village Health Care Handbook, David Werner, et al. (any edition.)
Where There is No Dentist, Murray Dickson.
Vintage editions of Baby and Child Care, (very vintage editions are called The Common Sense Book of Baby and Child Care) by Dr. Benjamin Spock, MD. (Yours Truly used a vintage edition of this book “back in the day.” I recall that there were some interesting practical suggestions, such as, how to make “emergency baby formula” if someone with an infant was stranded somewhere and waiting for evacuation and/or had no access to either a doctor or to baby supplies.)
Yours Truly sends warm Holiday Greetings to one and all. Here’s to healthy, strong New Year 2025!
The above royalty-free image of vintage vaccine vials and syringes is courtesy of Shutterstock and Google Images.
This post is a STOP PRESS offering. It details what is, in Yours Truly’s opinion, indisputable confirmation that the ingredients (and, by extension, the mechanisms) of the COVID-19 BTI (Bioweapon Toxin Injections, aka the COVID-19 “vaccines”) do indeed shedonto other persons, including onto non-“vaccinated” persons; and, that this shedding can result in multiple negative effects.
Since this post relates to the COVID-19 BTI (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 who have passed away as a result (direct or indirect) of the COVID-19 BTI they have taken.
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. The discussion is not limited to what is presented in this post.
There. Must. Be. Justice.
Yours Truly begins with the following blog post by Dr. Pierre Kory: https://pierrekorymedicalmusings.com/p/newly-published-study-shows-shedding, “Newly-Published Study Shows Shedding Of Covid mRNA Vaccine Products”, 9 December 2024. The study referred to is here: https://doi.org/10.56098/tp99wn15, “Menstrual Abnormalities Strongly Associated with Proximity to COVID-19 Vaccinated Individuals”, Sue E. Peters, PhD, James A. Thorp, MD, et al., 7 December 2024. This paper is HUGELY important as regards not only proof that the COVID-19 BTI (the COVID-19 “vaccines”) do indeed shed, but ALSO that there are multiple negative effects of this shedding for females who are in their childbearing years. Several screenshots from the paper are below, starting with the Abstract:
Then, a diagram of the non-COVID-19 “vaccinated” subgroup of females in the study:
Followed by a table listing the menstrual abnormalities reported among the non-COVID-19 “vaccinated” females who were in close proximity to COVID1-19 “vaccinated” persons:
Finally, the Conclusion of the paper:
The “exposure radius” for the cohort set of non-COVID-19 “vaccinated” females was 6 feet (or shorter) to COVID-19 “vaccinated” persons. These females reported the same types of menstrual issues that have been reported by COVID-19 “vaccinated” females.
Dr. Kory cites another paper, by independent researcher Helene Banoun, from 2023, which is also important to the situation. It is here: https://doi.org/10.3390/ijms241310514, “mRNA: Vaccine or Gene Therapy? The Safety Regulatory Issues”, Helene Banoun, 21 June 2023.
There is now MUCH more than meets the eye regarding the shedding of the COVID-19 BTI (the COVID-19 “vaccines”), as found here (and also cited by Dr. Kory): www.midwesterndoctor.com/p/covid-19-vaccine-shedding-experiences, “What We’ve Learned from Over a Thousand Vaccine Shedding Reports”, by A Midwestern Doctor.
Back to the blog post by Dr. Pierre Kory: It is long and detailed, but Dr. Kory and A Midwestern Doctor have compiled an enormous amount of information about the COVID-19 BTI shedding phenomenon. Dr. Kory’s post has a list of chapters that have organized the material. Following are some screenshots from his post:
The above screenshot is from the Peters, Thorp, et al., paper cited above, listing items related to the development and implementation of the COVID-19 BTI (the COVID-19 “vaccines”.) It is important to understand that the Pfizer-BioNTech “clinical trial” (C4591001) was stopped at six months, in order for the company to give the data collected up to that point to the FDA in the fall of 2020. [Yours Truly: The six month timeframe was between late April (the start of the “clinical trial”) and late October-early November of 2020.] This was done by Pfizer-BioNTech so that their “flagship” COVID-19 BTI (“vaccine”), BNT162b2, could get through the “review process” by the FDA prior to securing that agency’s initial EUA for the use of BNT162b2 in the United States (this initial EUA was granted by the FDA on 11 December 2020.) [Yours Truly: C4591001 was “resumed” after the initial EUA was granted, under various “subsection trials” listed on clinicaltrials.gov/.] It is important to understand that Pfizer-BioNTech KNEW that shedding of BNT162b2 could occur — which is why the company asked that subjects in the C4591001 clinical trial report any exposure to pregnant females, or to the partner of a pregnant female “prior to the time of conception” (translation: the company ALSO KNEW that the fertility of MALES can be damaged by BNT162b2.)
Dr. Kory and A Midwestern Doctor did a thorough job of collating and organizing the details of the over 1,000 reports they received regarding shedding of the COVID-19 BTI (the COVID-19 “vaccines”.) What follows is a description of some of these details.
The exosomes that “shuttle” the COVID-19 BTI spike protein can be exhaled; they can be on the surface of the skin; and, they can be “transferred” during sexual intercourse.
**** The post by Dr. Kory contains several sections in addition to the Chapters section. Some of the sections include:
“Evidence For Person-to-Person Shedding“
“Routes of Exposure” (exhalation; hugging [non-sexual]; sexual intercourse; skin-to-skin)
“Most Common Symptoms” of COVID-19 BTI (the “vaccines”) shedding: in females: menstrual abnormalities, including pregnancy termination; other types of gynecological issues; in men: groin pain; ingeneral: headache; tinnitus; nose bleeds; painless bruising; dizziness; brain fog; immune-suppression symptoms; Shingles; skin rashes
“Less Frequent Symptoms“: Atrial fibrillation; muscle pain; seizures; insomnia; vision / eye problems, including microclots to the eyes.
“Rarer Symptoms“: blood clots; cancers; and, anxiety, among them.
**** Below is a screenshot of the graphic from Dr. Kory’s post, listing the symptoms:
**** Dr. Kory adds an important caveat, the “Clinical Guidance” section of his post. A screenshot from this section is below:
Yours Truly has written about the importance for non-COVID-19 “vaccinated” persons to NOT make themselves into “hermits”, to NOT stay away from “vaccinated” friends and family, and so on. On the other hand, in addition to the above from Dr. Kory, it may be worthwhile to wash the hands frequently; and, to consider using disposable gloves when putting gas into the car, or perhaps in a healthcare setting, and the like. It is also imperative for people to have, and to maintain, their general health and the health of their immune system at the best level possible.
**** And, continuing from there, part of the “Protection Strategies” section:
Yours Truly here. Now that it is confirmed that the COVID-19 BTI (the COVID-19 “vaccines”) do indeed shed, and can shed onto non-“vaccinated” persons, questions arise: Does this mean that any of the N1-Methylpseudouridine in the COVID-19 BTI can also shed via the “shuttle service” of the exosomes? What about the lipid nanoparticles in these injectables? And, since nobody really knows how long the COVID-19 BTI work in the body of the “vaccinated” person, how long does this shedding continue? What about shedding among COVID-19 “vaccinated” persons — are they constantly exposing other “vaccinated” persons to the ingredients (and mechanisms) of these injectables?
The above free vintage image of DNA strands is courtesy of Shutterstock via Google Images.
Health Friday is a series of posts related to Big Pharma, vaccines, general health, and associated topics. Since today’s post is related to the modRNA COVID-19 “vaccines”, it is dedicated to the memory of Yours Truly’s COVID-19 “vaccinated” late brother, Sam, and to her late cousin Bill; and to all persons, of whatever age or location, who have passed away from the negative effects (direct or indirect) of the COVID-19 “vaccines” that they took.
There are Important Wolf Moon Notifications, the Rules of our late, good Wheatie, and certain Yours Truly caveats, of which readers should be aware. They are linked here. The discussion today is not limited to what is presented below: It is an Open Thread.
Above all — There. Must. Be. Justice.
To Begin: Yours Truly will now change the name of the COVID-19 “vaccines” to reflect what they really are — dangerous and deadly bioweapons injections:
COVID-19 Bioweapon Toxin Injections (COVID-19 BTI). They are NOT “vaccines.” The FDA, the CDC, and the makers of these injections/injectables KNOW THIS. If Yours Truly refers to these injectables as “vaccines”, it is for “convenience-recognition” only, e.g., as in scientific papers or in media headlines.
Today’s post is a confirmation and an amplification regarding the discovery of large amounts of “free” DNA residue in vials of the Pfizer-BioNTech modRNA COVID-19 modRNA BTI, BNT162b2. The trail begins here: https://jessicar.substack.com/p/a-new-paper-confirms-presence-of, A new paper confirms presence of DNA in COVID-19 shot vials, settles issues pertaining to DNA quantification models, shows spike persistence and exosomal shuttling (shedding), by Jessica Rose, PhD., 4 December 2024. Yours Truly will address this article and the paper that it cites, in addition to some earlier papers by other researchers on the topic. The “weave” of today’s post is somewhat dense — the depth of the perfidy behind BNT162b2 is wide and deep. Please bear with me.
The Kammerer, et al., paper is hugely important. The multitude of tests and assays that were performed on the samples from the Pfizer-BioNTech modRNA COVID-19 BTI vials is not only incredibly thorough; it is also stunning. Several earlier hypotheses (and evidence from previous scientific papers and articles) regarding these injectables are now confirmed:
One: More of the ingredients of the Pfizer-BioNTech modRNA COVID-19 BTI are confirmed — “loose” DNA; the SV40 African Green Monkey cancer promoter-enhancer genome code sequence; the presence of HEK293 cells (aborted fetal cells); the presence of the antibiotic, Neomycin (a drug that treats bacterial infections); and, ORI replicons in the plasmids in the injectable. ORI replicons are the things that “teach” the “vaccinated” person’s body to make copies of the spike protein — in other words, a type of self-amplifying modRNA mechanism is introduced into the body. Plasmids are tiny DNA molecules that are inside a cell; plasmids are not chromosomal DNA and can independently reproduce themselves. An image of plasmids inside a cell is below (courtesy https://en.wikipedia.org/wiki/Plasmid):
Two: The amount of “loose” DNA in BNT162b2 is well above EMA (European Medicines Agency) limits. A screenshot of Figure 2. section D, of the Kammerer, et al., paper, below, clearly shows this:
Three: The presence of the DNA plasmids and of the SV40 African Green Monkey cancer promoter-enhancer gene code sequence were NOT disclosed to the FDA by Pfizer-BioNTech prior to that agency’s granting of the initial EUA for BNT162b2 on 11 December 2020 for this injectable’s use in the United States. The salient statement from the Kammerer, et al., paper, on this is below:
Yours Truly will note that the FDA also granted “full approval” of BNT162b2 in 2022, under the brand name COMIRNATY, and its “descendant clone” modRNA COVID-19 BTIs, including all “new formula” injections {such as the 2024-2025 COMIRNATY COVID-19 modRNA BTI.)
Four: There is a distinct possibility that BNT162b2 can “shed” from “vaccinated” persons onto other persons, via exosomal secretion. From the Discussion section of the Kammerer, et al., paper, below:
The COVID-19 modRNA BTIs are “shuttled” throughout the body of the person who takes these injectables. This “shuttling”, in part, is performed by exosomes. Exosomes are tiny elements that are formed by lipid bilayers and function as a kind of “shuttle service” within the body, carrying proteins, lipids, and other items to and from body organs, including to the skin. Please refer to: https://pubmed.ncbi.nlm.nih.gov/35436552/, “Innate immune suppression by SARS-CoV-2 mRNA vaccines: The role of G-quadruplexes, exosomes, and MicroRNAs”, Stephanie Seneff, et al., 15 April 2022.
Scientific researchers have been experimenting with SV40 African Green Monkey cancer promoter-enchancer gene code since at least 1997. Please see: https://doi.org/10.1128/JVI.71.1.427-436.1997, “Direct modulation of simian virus 40 late gene expression by thyroid hormone and its receptor”, Fengrong Zuo, Tod Gulick, et al. Below is a graphic of the SV40 gene code experiment, followed by a portion of the Discussion section of this paper:
Research has been performed regarding SV40-induced cancers, via “methylation.” Please refer to: https://doi.org/10.1038/sj.cr.7290295, “Epigenetic changes in virus associated human cancers”, Hsin Pai Li, et al., 1 April 2005.
Two papers by Kevin McKernan have researched much of the information that the Kammerer, et al., paper has confirmed. One McKernan paper is here: https://doi.org/10.31219/osf.io/b9t7m, “Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose”, Kevin McKernan, et al., 10 April 2023. A graphic from this paper is below:
Please note that there are two separate SV40 elements in this graphic: the SV40 enhancer and the SV40 “signal” in the poly-A “tail” of BNT162b2.
The other McKernan paper is here, regarding DNA fragments in BOTH the Pfizer-BioNTech AND in the Moderna modRNA COVID-19 BTIs: https://doi.org/10.31219/osf.io/mjc97, “DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose relationship with serious adverse events”, Kevin McKernan, et al., 19 October 2023.
Yours Truly now turns to the “primary source document” for BNT162b2, the International Patent declarationdocument for this injectable. It is found here: https://patents.google.com/patent/WO2021213945A1/en, published on 28 October 2021. Note: The patent number in the Kammerer, et al., paper (WO2021214204) is a another identifier for this patent. It is difficult to access the actual patent document by using this identifier on a search — the above Google URL is easy to find. Another patent number for BNT162b2, WO2021213924, is similarly difficult to find. Yours Truly suspects that these other patent documents and information were “subsumed” into WO2021213945A1.
Yours Truly found listed in the above document, among many other items:
One: That BNT162b2 targets the “vaccinated” person’s CD 4 and CD8 cells. Please see the screenshot, below, from the International Patent declaration:
Two: That BNT162b2 uses ** either ** N1-Methylpseudouridine, orpseudouridine, or5-methyl-uridine, to replace the natural Uridine in the “vaccinated” person’s body. Please see the screenshot, below, from the International Patent declaration:
The reason why, in Yours Truly’s opinion, there are THREE different types of “fake” Uridine that can be used in BNT262b2 is because Pfizer-BioNTech wanted to have “maximum leeway” to choose any of these three types for use in various formulations and/or lots of BNT162b2. That’s why the words “in one embodiment” are used throughout the patent document. This “leeway” would also theoretically apply to any “descendant clone” modRNA COVID-19 BTI made by this company.
**** Three: Regarding the Kammerer, et al., paper: These researchers used “Sequence ID 16” (SEQ ID 16) in the BNT162b2 International Patent declaration as the basis for their tests and assays regarding the presence of “loose” DNA and the presence of the SV40 African Green Monkey cancer promoter-enhancer gene code piece. Below is a screenshot of the mention of this sequence, and the BNT162b2 patent that was used, by Kammerer, et al.
Yours Truly read through the patent document and found the only area that appears to match SEQ ID 16. A screenshot of this, from the patent document, is below:
From here, Yours Truly found a long list of the actual spike protein gene codes (S protein) in SEQ ID 16. This sequence begins with “hAg-Kozak“, which is important as regards “loose” DNA and the SV40 cancer promoter gene piece code. Please see the screenshot of the hAg-Kozak code, followed by a portion of the spike protein codes, below:
The hAg-Kozak codes are a kind of nucleic acid “pattern” that functions as a “protein initiation site” in mRNA applications (paraphrased from the hAg-Kozak entry at Wikipedia.)
Finally, a screenshot follows of the FI element and Poly-A tail gene codes in SEQ ID 16:
Recall that the Poly-A tail is the “signal” for the SV40 cancer promoter gene code piece in the McKernan paper, cited above.
FI element (nucleotides 3864 to 4158): The 3′-UTR is a combination of two sequence elements derived from the “amino terminal enhancer of split” (AES) mRNA (called F) and the mitochondrial encoded 12S ribosomal RNA (called I). These were identified by an ex vivo selection process for sequences that confer RNA stability and augment total protein expression9
Wolf Moon continues: “So basically these are gene sequences that were found to work well as linkers which enhance production of the desired target (the spike protein), and are thus tacked onto the sequence for the spike. IMO they are a lot like the SV40 sequence for DNA, but they work at the mRNA level.”
Further discussion of the TWO separate SV40 cancer promoter elements in BNT162b2 are found in another item cited by the Kammerer, et al., paper: https://anandamide.substack.com/p/pfizer-and-moderna-bivalent-vaccines, “Pfizer and Moderna bivalent vaccines contain 20 – 35% expression vector and are transformation competent in E. coli”, 8 March 2023. A screenshot of their assessment of the SV40 cancer promoter and “signal” placements in BNT162b2 is below:
In Yours Truly’s opinion: What we have here was / is NOT a case of Pfizer-BioNTech saying, “Oops, forgot to remove the loose DNA from BNT162b2 before it was / is put into the vials”; NOR was it / is it, a case of, “Oops, forgot to remove the SV40 elements from the product before it was / is put into the vials.” Instead, it is deliberate inclusion of BOTH the “loose” DNA AND of the SV40 African Green Monkey cancer promoter-enhancer gene code piece into BNT162b2. It says it right there in the International Patent declaration for BNT162b2, the SEQ ID 16 listings. Since BNT162b2 is the basis for the “descendant clone” COVID-19 modRNA BTI by this company, plus the fact that all of these products are manufactured using the “Process 2” method (“marinating” the ingredients of the injectable in E. coli), Yours Truly will posit that it can be assumed that “loose” DNA and the SV40 promoter-enhancer gene codes are present in these “descendant clone” injectables, even if they are present in lesser amounts.
Health Friday is a series of posts related to Big Pharma, vaccines, general health, and associated topics. Since today’s post is related to the COVID-19 virus itself, and to the COVID-19 “vaccines”, it is dedicated to the memory of Yours Truly’s COVID-19 “vaccinated” late brother, Sam, and to her late cousin, Bill; and to all people, of any age or location, who have passed away from the negative effects (direct or indirect) of the COVID-19 “vaccines” that they took. The discussion today is not limited to what is presented in the post: It is an Open Thread.
Today’s Health Friday post is about what the COVID-19 “vaccines” do to the “vaccinated” person’s natural immune system. It is also about what the COVID-19 virus itself does to a person’s natural immune system. The bottom lines are: One: the modRNA COVID-19 “vaccines” severely damage or evendestroy the natural immune system of the person who takes these “vaccines”, with the damage or destruction increasing with each additional injection of them. Two: the COVID-19 virus itselfcandamage the natural immune system. Three: it is more possible to repair and support the immune system of a person who is non-COVID-19 “vaccinated.”
Actually, Yours Truly respectfully disagrees with the title of the above book: in her opinion, it should read: Bill Gates I Want to Kill Three-Quarters of You, and Control the Survivors.
There. Must. Be. Justice.
There are several aspects that make up today’s post. *** Yours Truly is firmly convinced that the SARS-CoV-2 virus itself was designed and lab-created, AND the modRNA COVID-19 “vaccines” were / are designed and lab-created, as bioweapons. These lab-created bioweapons attack the immune system of the human body; damage and/or destroy important components of the immune system of the human body; and, in the case of the modRNA “vaccines”, keep this damage and/or destruction going for an indefinite period of time in the “vaccinated” person’s body. Also — Yours Truly will present evidence that — wait for it — the pangolin-CoV MP789 virus genome is an integral part of the situation.
To begin: The 5.3.6 Postmarketing Experience document that Pfizer-BioNTech submitted to the FDA on 30 April 2021: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received Through 28-Feb-2021. Below are two screenshots from the Appendix 1: List of Adverse Events of Special Interest section of this document:
The above are autoimmune and immune-mediated medical conditions that were reported in the first two months after the rollout of the Pfizer-BioNTech modRNA COVID-19 “vaccine” BNT162b2 among persons who took this “vaccine” during that period. Notes: BNT162b2 is the basis of all subsequent formulations of the COVID-19 “vaccine” injectables by this company (since 2022, marketed under the brand name COMIRNATY); and, there are other listings of autoimmune and immune-mediated conditions in the Appendix 1. of the above report.
Yours Truly now turns to a 2021 paper by Stephanie Seneff, PhD: https://doi.org/10.56098/ijvtpr.v2i1.23, “Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19”, 10 May 2021. Dr. Seneff points out that only the spike protein was used for the modRNA in the Pfizer-BioNTech and in the Moderna COVID-19 “vaccines” (BNT162b2 and mRNA-1273, respectively.) A screenshot from this paper is below, listing the “firsts” regarding the modRNA COVID-19 “vaccines”:
Dr. Seneff references a 2020 paper by Lu, et al., regarding an important discovery about the SARS-CoV-2 virus itself: https://pmc.ncbi.nlm.nih.gov/articles/PMC7429369/, “A COVID-19 mRNA Vaccine Encoding SARS-CoV-2 Like Particles Induces a Strong Antiviral-like Response in Mice.” The authors make it clear that there are three separate-but-important components in the SARS-CoV-2 virus itself: the membrane (M); the envelope (E); and, the spike protein (S). Another screenshot from the Seneff paper is below, regarding this issue:
Why is it important to know that Pfizer-BioNTech and Moderna chose only the spike protein of the SARS-CoV-2 virus itself as the basis for their respective modRNA COVID-19 “vaccines”? Yours Truly hypothesizes that, in so doing, it was then possible for them to create a modRNA that would have the most potential to damage the persons taking these respective modRNA COVID-19 “vaccines.” The Lu, et al., 2020 paper, cited above, also describes how the authors created various “prototype” COVID-19 “vaccines.” These “prototype vaccines” were lab-produced using various ingredients — one of which was — wait for it — N1-Methylpseudouridine; as well as one “prototype vaccine” that used Uridine. The authors concluded that N1-Methylpseudouridine was “superior” in creating “neutralizing antibodies.” Please refer to Figure 1. and its description underneath from this paper, where N1-Methylpseudouridine is used in the “Lane 5 proto-type vaccine” of the experiments. In Yours Truly’ opinion, it is within the realm of possibility that Pfizer-BioNTech, or Moderna, or both, knew of the Lu, et al., research.
Below are screenshots of section 11 Description of the Pfizer-BioNTech (COMIRNATY) “2024-2025 Formula COVID-19 vaccine”; and, of section 11 Description of the Moderna (SPIKEVAX) “2024-2025 Formula COVID-19 vaccine.” There is no mention in either one of the membrane or of the envelope of the original Wuhan Hu1 SARS-CoV-2 virus; there is only the mention of the spike protein:
The modRNA COVID-19 “vaccines” damage and/or destroy crucial IgG3 immune system cells in the “vaccinated” person’s body (the “fight it off” element), and instead foster the increase of IgG4 immune system cells (the “tolerate but never clear” element). Please refer to the Jessica Rose, PhD, post at the top of today’s post. Below is another figure from her post, from the Supplementary Materials of this 2022 paper (cited in the post): www.science.org/doi/10.1126/sciimmunol.ade2798, “Class switch toward noninflammatory, spike-specific IgG4 antibodies after repeated SARS-CoV-2 mRNA vaccination”, Pascal Irrgang, et al., 22 December 2022. This image, from Figure 2: Figure S1 of the paper, clearly shows the decimation of IgG3 (“fight it off”) immune system cells, and the increase of IgG4 (“tolerate it”) immune system cells, after repeated modRNA COVID-19 “vaccinations”:
And, also from the Irrgang, et al., paper:
Those who are COVID-19 “vaccinated”, especially if they take repeated injections of these “vaccines”, are the slowest to “clear” a COVID-19 infection:https://pmc.ncbi.nlm.nih.gov/articles/PMC9258747/, “Duration of Shedding of Culturable Virus in SARS-CoV-2 Omicron (BA.1) Infection”, Julie Boucau, Ph.D., et al., published in the New England Journal of Medicine, 21 July 2022. The salient figure from this Letter to the Editor is below:
Please refer to the second and third column percentages. These “tell the tale.”
This leads to the next part of today’s post: the SARS-CoV-2 virus itself, which is the foundation of the modRNA COVID-19 “vaccines.”
The lab-created SARS-CoV-2 (COVID-19) virus itself attacks the body (and brain) of a person infected with this virus in several ways. One way is that the virus “attaches” itself to the ACE2 receptor cells of the body. ACE2 stands for “angiotensin-converting enzyme 2” cells. What these cells do is discussed here: www.cas.org/recources/cas-insights/ace2-covid-19-target, by Angela Zhou, 15 December 2022. A screenshot of this article is below:
The spike protein of the SARS-CoV-2 virus itself dysregulates (“downregulates”) the functions of the ACE2 receptor cells in the body of the infected person: https://doi.org/10.1101/2020.12.04.409144, “SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE2”, Yuyang Lei, et al., 4 December 2020. “Endothelial function” is the range of functions of the vascular endothelium. Endothelial cells release elements that control the opening and closing of the arteries.
Also, the COVID-19 virus itself “mimics” the proteolytic activation of human ENaC cells: https://doi.org/10.7554/eLife.58603. “SARS-CoV-2 strategically mimics proteolytic activation of human ENaC”, Praveen Anand, et al., 26 May 2020. ENaC stands for “Epithelial sodium channel” (an ion channel); this element has an important role in kidney function, the immune system, and vasculature. “Proteolysis” has to do with protein breakdown in the body.
The SARS-CoV-2 virus itself attacks, damages, and/or destroys, the CD4 cells of the human body. Please refer to: https://doi.org/10.1101/2020.09.25.20200329, “SARS-CoV-2 uses CD4 to infect T helper lymphocytes”, Natalia S Brunetti, et al.; paper published in 2020, version of record 31 July 2023. A screenshot of the Abstract from this paper is below:
Note that damaged CD4 cells are a component in HIV infection; also, note again that, since the original SARS-CoV-2 virus itself is the foundation for the modRNA COVID-19 “vaccines” by Pfizer-BioNTech and by Moderna, the “attack and damage” elements and mechanisms described above are present in said “vaccines.”
For further information regarding how the spike protein of the SARS-CoV-2 virus itself works in the human body, please refer to the ongoing research of Walter M Chesnut: https://wmcresearch.substack.com/.
And now, another visit with our shy, nocturnal scaly anteater, the Pangolin:
Yours Truly has written about this mammal, and of how the PRRARSV (or RRAR or RRARSV, depending on which scientific paper one reads) genome code in the original SARS-CoV-2 virus itself was lab-manipulated from the pangolin-CoV MP789 to include this code; for example: www.theqtree.com/2024/11/22/health-friday-11-22-2024-open-thread-lets-talk-about-prrarsv-the-backdoor-key/. It appears that the pangolin-CoV MP789 genome code was “mixed in” with the bat-CoV RaTG13 genome code in the lab experiments that created SARS-CoV-2. However, Yours Truly has discovered something else about pangolin-CoV MP789:It“binds” better to human ACE2 receptor cells, compared to the bat-CoV RaTG13!
It would appear, then, that the pangolin-CoV MP789 genome has much more to do with the lab-creation of the SARS-CoV-2 virus itself (and, by extension, the modRNA COVID-19 “vaccines”) than at first meets the eye. This is not to discount the use of genome code elements from the bat-CoV RaTG13 in the lab-creation process of the virus itself; nor to discount the other coronavirus code elements that were “mixed in” from monkey, civet, and other animal coronaviruses. In Yours Truly’s opinion, those who lab-created the SARS-CoV-2 virus itself were searching for a genome code that could most effectively attack and compromise human ACE2 receptor cells and the mechanisms of these cells. They found what they were looking for in the pangolin-CoV MP789 genome code. However, it is crucial to understand that those who lab-created the SARS-CoV-2 virus itself did not also add N1-Methylpseudouridine to it — this compound was added to the modRNA COVID-19 “vaccines.” And therein, again in Yours Truly’s opinion, lies an important difference between the SARS-CoV-2 (COVID-19) virus itself, and the presence of this virus in the modRNA-COVID-19 “vaccines.” It is the difference between a non-COVID-19 ” vaccinated” person being infected with the SARS-CoV-2 virus itself and recovering (even if there are complications), because the natural Uridine in the non-COVID-19″vaccinated” person’s body is still operative to help regulate many body functions and mechanisms that can assist in recovery; whereas, in the COVID-19 “vaccinated” person’s body, the natural Uridine has been replaced with N1-Methylpseudouridine (thereby literally erasing the potential for natural Uridine to work.)
Is it, then, a foregone conclusion that the natural immune system of the COVID-19 “vaccinated” person is so severely damaged, or even destroyed, especially with that person taking more and more injections of these “vaccines”, that there is no hope for any possible repair or restoration of it? In the case of the RNA of Uridine being replaced by N1-Methylpseudouridine, some things can be done to supplement the body: consuming Uridine-containing foods, such as beets, goat cheese, walnuts, and broccoli. There is some promising research on the use of a compound, called 5-FU, to help repair Uridine RNA: https://doi.org/10.3389/frnar.2023.1248236, “RNA damage: the forgotten target of clinical compounds”, by Nicole Simms and John R.P. Knight. In the case of damaged CD4 cells, there are natural methods to increase the body’s healthy CD4 cell count. Please refer to: www.medicalnewstoday.com/articles/how-to-boost-cd4-count-naturally, by Charlotte Lillis, 16 July 2024. Supplementation with Vitamin D, multivitamins, and probiotics are mentioned in this article.
Finally, Yours Truly firmly believes that the SARS-CoV-2 virus itself is not “just another virus” or “just another flu virus.” Au contraire: this virus itself was lab-created from a “palette” of animal coronaviruses (the pangolin-CoV MP789 in particular, with the bat-CoV RaTG13 close behind) to be as damaging as possible, even deadly, to the human body — in other words, a bioweapon. Yes, a non-COVID-19 “vaccinated” person may become infected with the SARS-CoV-2 virus itself, and recover well; however, there may be “residual damage” from the virus itself remaining for some period of time in their body. There is also the phenomenon of “COVID-19 vaccine shedding” from COVID-19 “vaccinated” persons onto others, including onto non-COVID-19 “vaccinated” persons, to consider: as these “vaccines” contain elements in them that make this virus, as well as the “vaccines” themselves, more dangerous and/or deadly. Does this mean that non-COVID-19 “vaccinated” persons should avoid contact with other persons, especially COVID-19 “vaccinated” persons? No — what it does mean, however, is that it is imperative to have, and maintain, the highest possible degree of health of the body’s natural immune system.
The above free vintage image of Thankfulness is courtesy of iStock and Google Images.
Health Friday is a series of posts devoted to Big Pharma, vaccines, general health, and associated topics. However, the discussion is not limited to what is presented today: It is an Open Thread.
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.
Today’s Health Friday post is devoted to Thankfulness. Beginning with:
Thankfulness for our gracious host, Wolf Moon, who provides The Q Tree as a haven of good cheer, encouragement, support, knowledge, and camaraderie to the online family that are denizens of this particular Tree. We are there for each other, in good times and in difficult times.
Thankfulness for the authors on this board, including our host, for their contributions and their expertise: for the Reminders of the Word of God; for the Physics lessons (Yours Truly’s eyes no longer glaze over at the mere mention of Physics or Astronomy); for the in-depth political / DeepState/ economic Analyses; for the adherence to Truth; for the Sharing of knowledge, of history, of research, of poetry; and so much more, that they bring.
Thankfulness for every commenter on this board, for their bonhomie and constancy.
Continuing with:
Thankfulness that Donald Trump, after surviving two assassination attempts, was re-elected President of the United States.
Thankfulness that there will be a chance that the corruption and deceit rampant in both houses of Congress, and in the White House, can be exposed and cleansed.
Thankfulness that breaches among individuals’ families and friends can be repaired; that our beloved country can be healed of divisiveness; that the United States of America can be restored to her rightful role as a Representative Republic, instead of as a “modern-day application” of the type of “despotic democracy” that helped to undermine, then ruin, ancient Greece.
Thankfulness that the entire truth behind the premeditated disaster of the COVID-19 itself and the COVID-19 “vaccines” can finally be brought to light; that the millions of “vaccinated” persons who are “vaccine”-injured or “vaccine”-disabled can be recognized, and their stories be told; that those who have passed away (either directly or indirectly) from the negative effects of the COVID-19 “vaccines” they took will not have died in vain; and, that Justice will be accomplished regarding those who created this virus, and those who developed these dangerous, deadly “vaccines” for worldwide use.
Thankfulness for this:
Thankfulness, above all, to the Supreme Being who is the Divine Force behind the Founding Fathers of this great land: the Founding Fathers who wrote the Declaration of Independence, the Constitution, and the original Bill of Rights.
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 genomecode; 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.
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 12.4Mechanism 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.
