“We do not believe any group of men adequate enough or wise enough to operate without scrutiny or without criticism. We know that the only way to avoid error is to detect it, that the only way to detect it is to be free to inquire. We know that in secrecy error undetected will flourish and subvert.” –J. Robert Oppenheimer
The above 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 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 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 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.
The above free vintage image of a lock being picked is courtesy of Google Images.
Health Friday is a series related to Big Pharma, vaccines, general health, and associated topics. Since today’s offering is related to the COVID-19 disaster — the SARS-CoV-2 (COVID-19) virus itself; and, to the COVID-19 “vaccines” — it is dedicated to the memory of Yours Truly’s “vaccinated” late brother Sam, and her late cousin Bill; and to all persons of any age who have died as a result of either an infection from the COVID-19 virus itself, or to the negative effects (direct or indirect) of the COVID-19 “vaccines” that they took. 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 post includes several “puzzle pieces.” Each one is integral to the whole. Please bear with me. There is a General Summary at the end of the post.
To Begin: A post from our host, Wolf Moon: www.theqtree.com/2023/05/01/pfizer-and-moderna-vaccines-both-contain-the-prrarsv-key-to-the-cell-nucleus/. This post is one of several on the topic of the “PRRARSV Backdoor Key” that is present in both the Pfizer-BioNTech and in the Moderna modRNA COVID-19 “vaccines.” One of the papers cited in the post is “the Mehedi paper”, found here: https://doi.org/10.3389/fmicb.2023.1073789. “Nuclear translocation of spike mRNA is a novel feature of SARS-CoV-2”, Masfique Mehedi, et al., 26 January 2023. This paper proves that the PRRARSV code in the SARS-CoV-2 virus genome is only there, and not in either the SARS-CoV virus genome or the MERS-CoV virus genome. There are links to other important papers in the Wolf Moon post. Yours Truly is grateful to our host for doing serious investigation into this subject.
There has been speculation that the PRRARSV code may be related to snake venom. This also has been discussed by our good host in other of his posts on the subject. While Yours Truly believes that some type of snake venom that contains all or some of the PRRARSV code may be in play, she has an additional hypothesis on the PRRARSV code presence in the modRNA COVID-19 “vaccines” — and in the SARS-CoV-2 virus itself.
And, Now: May I present — the Pangolin (PAN-go-lin.)
Pangolins are shy, nocturnal mammals that are covered with scales; they are also called “scaly anteaters.” They resemble anteaters in body shape and length; however, Pangolins are covered with hard, keratin-like scales from the head to the tip of the tail. During the day, they remain in their burrows; at night, they emerge to hunt for and eat ants and termites. Their living habitat ranges from areas in Africa to India to southern Asia. As their meat, scales, and other body parts, are consumed as exotic foods, or are used in folk and traditional medicine in certain areas of the world, the Pangolin is listed as an endangered species. It is illegal to hunt or trap Pangolins, or to keep them as pets. However, because of their meat, scales, and other body parts, Pangolins are among the most-trafficked animals in the world (https://en.wikipedia.org/wiki/Pangolin.)
The above image of a Pangolin is courtesy of the International Fund for Animal Welfare and Goggle Images.
Pangolins, like other animals, have coronaviruses. And here is where the story gets interesting. One such Pangolin coronavirus is “pangolin-CoV MP789.” It appears that the RBD (Receptor Binding Domain) is this virus has an “uncanny” similarity to the RBD of the SARS-CoV-2 virus. In fact, it is been posited that the RBD of the SARS-CoV-2 virus resulted from a “recombination” of those of the bat-CoV RaTG13 virus and the pangolin-CoV MP789 virus. Below is Figure 1 of the “Morales-Espinosa, et al. paper” on this subject:
The “Morales-Espinosa, et al. paper” is found here: https://pmc.ncbi.nlm.nih.gov/articles/PMC7450963/, “The receptor binding domain of SARS-CoV-2 spike protein is the result of an ancestral recombination between the bat-CoV RatG13 and the pangolin-CoV MP789”, Rosario Morales-Espinosa, et al., 27 August 2020.
There is a plethora of scientific papers, articles, and scientific/medical blog posts related to the “probable” or “hypothetical” or “uncanny” similarity between Pangolin-CoV and SARS-CoV-2. Yours Truly will provide a sampling, below. Most of these papers, articles, and blog posts were written between 2020 and late 2022.
One: A scientific article by researchers in the CCP: www.cell.com/current-biology/pdf/S0960-9822(20)30360-2.pdf, “Probable Pangolin Origin of SARS-CoV-2 Associated with COVID-19 outbreak”, Tao Zhang, et al., 6 April 2020. A screenshot of part of the Conclusion of this article is below:
Two: Another 2020 paper, this one with an important mention in the Results section regarding the very high similarity of the S proteins in the pangolin-CoV genome and the SARS-CoV-2 genome: https://doi.org/10.1371/journal.ppat.1008421, “Are pangolins the intermediate host of the 2019 novel coronavirus (SARS-CoV-2)?”, by Ping Liu, et al., 14 May 2020. A screenshot of the section of the Results is below:
Three: Another scientific paper from 2020: https://doi.org/10.1101/2020.0707.184374. “Single source of pangolin CoVs with a near identical spike RBD to SARS-CoV-2”, Chan, Y.A., and Zhan, S.H., 31 October 2020. A screenshot from this paper is below:
Recall that it is only recently that the “the SARS-CoV-2 virus came from nature”, “the SARS-CoV-2 virus came from the ‘wet markets’ in Wuhan” claims have been proven incorrect. While there are still scientific papers and articles being published to “prove” the “came from nature” claims, what these papers and articles do not seem to explore, in Yours Truly’s opinion, are the Gain-of-Function experiments with various coronaviruses (including the pangolin-CoVs) that took place at the Wuhan Institute of Virology in the process of lab-creating the SARS-CoV-2 virus itself. These Gain-of-Function experiments used elements found in nature (bat coronaviruses, civet coronaviruses, pangolin coronaviruses, rabbit coronaviruses, monkey coronaviruses, etc.) to “build” the SARS-CoV-2 virus itself. Here, for example, is a 2022 scientific article regarding the claims that the virus came from nature: www.science.org/content/article/evidence-suggests-pandemic-came-nature-not-lab-panel-says, “Evidence suggests pandemic came from nature, not a lab, panel says”, 10 October 2022, by Jon Cohen.
Which leads into the discussion of the Wuhan Institute of Virology’s experiments with pangolin coronaviruses.
It is obvious that the Wuhan Institute of Virology conducted coronavirus experiments with bats, civets, monkeys, and pangolins, in the process of creating the SARS-CoV-2 virus.
Which leads to the next discussion, regarding PRRARSV and the furin cleavage site in the SARS-CoV-2 virus genome. Bear with Yours Truly here: this is an important piece of the puzzle.
PRRARSV is located at the S1-S2 furin cleavage site on the SARS-CoV-2 virus genome, from a scientific paper in September 2020: https://doi.org/10.1016/j.lfs.2020.118056, “Structural features of coronavirus SARS-CoV-2 spike protein: Targets for vaccination”. by Ariane Sternberg and Cord Naujokat, 15 September 2020. A screenshot from section 2 of this paper is below:
The redoubtable Walter M Chesnut expands on this, and how PRRARSV assists in the translocation of the modRNA spike protein in the SARS-CoV-2 virus into every cell in the human body: https://wmcresearch.substack.com/p/prrarsv-the-furin-cleavage-site-a. “PRRARSV—The Furin Cleavage Site: A Nuclear Localization Signal that Translocates the Spike and its mRNA to the Nucleus Inducing H3.3 histone Deposition and Rapid Aging”, 10 April 2023. Below is the National Cancer Institute definition of a histone (www.cancer.gov/publications/dictionaries/cancer-terms/def/histone):
In other words, the PRRARSV present in the SARS-CoV-2 virus enters the cell, assists the spike protein of the SARS-CoV-2 virus to enter the nucleus of the cell, and interferes with the H3.3 histone in the DNA of the cell.
There are four “inserts” that were introduced into the SARs-CoV-2 virus genomeduring the process that lab-created the SARS-CoV-2 virus. These four “inserts” were first isolated and described in the “Pradhan paper” from 2020. This paper was Retracted and suppressed almost as soon as it appeared. However, it can be found here: https://medicalveritas/org/wp-content/uploads/2020/02/Pradhan-et-al-Coronavirus-HIV-paper.pdf. A screenshot of Table 1. from the paper is below. The “PRRAR” code is “Insert 4”:
In addition, Figure 2. of this paper has the SARS-CoV-2 virus genome spelled out, with the position of each of the four “inserts.”
This leads to further proof that the PRRARSV code is indeed part of the SARS-CoV-2 virus itself. For example: https://jessicar.substack.com/p/it-turns-out-that-the-prrarsv-motif, “It turns out that the “PRRRARSV” motif is more than a furin-cleavage site”, 1 October 2022. Dr. Rose performed her own analysis of the PRRARSV code in the SARS-CoV-2 virus genome. She proves that the PRRARSV code is indeed the fourth “insert” into the virus genome. A screenshot of her analysis is below:
What does this all mean? It means the following:
General Summary:
One: The Pangolin, a shy, nocturnal mammal that is covered in keratin-like scales and eats ants and termites, also is prone to having a coronavirus, called pangolin-CoV. This virus has a genome code that is “quite similar” in some ways to the SARS-CoV-2 virus itself genome code. One of these “similarities” is a genome code called “RRSV” or “PRRAR”, depending on the research paper on the topic.
Two: There are four “unique inserts” in the SARS-CoV-2 virus itself genome. The fourth “insert” is the PRRARSV code. The PRRARSV code interferes with the important H3.3 histone in the DNA of every cell in the body of the person who is infected by SARS-CoV-2 (the COVID-19 virus) or who is infected with the SARS-CoV-2 virus itself.
Three: The PRRARSV code was possibly derived from experiments with a type of snake venom; unless otherwise proven, it certainly was derived from experiments with the pangolin-CoV genome code.
Four: The experiments with the PRRARSV code were conducted at the Wuhan Institute of Virology in the process of the lab-creation of the SARS-CoV-2 virus itself.
Five: Since the COVID-19 “vaccines” use the Wuhan Hu1 SARS-CoV-2 virus itself as the basis for these injectables, the PRRARSV code is therefore present in these “vaccines.” This means that all persons who have ever taken a COVID-19 “vaccine” have been exposed to the PRRARSV code. To date, nobody knows exactly how long the ingredients and mechanisms of the COVID-19 “vaccines” remain at work in the “vaccinated” person’s body. In fact, the COVID-19 “vaccines” are designed to trick the “vaccinated” person’s body into thinking it has a COVID-19 virus infection, forcing the “vaccinated” person’s body to make large amounts of antibodies to fight off the “fake COVID-19 infection”: www.brandeis.edu/magazine/2020/fall/inquiry/vaccine.html, “On the cusp of a COVID-19 Vaccine”, by Lawrence Goodman. A screenshot from the article is below, quoting Dr. Drew Weissman of the University of Pennsylvania Perelman School of Medicine:
Six: Un-vaccinated” persons who contract a COVID-19 virus itself infection, and are therefore exposed to the PRRARSV code, can still mitigate and/or defeat the effects of the damage done by the virus itself if the person has a healthy immune system. On the other hand, COVID-19 “vaccinated” persons, in addition to being exposed to the PRRARSV code present in the “vaccines”, are also exposed to the other ingredients in the “vaccines”, such as N1-Methylpseudourdine. N1-Methylpseudouridine replaces the natural Uridine in the “vaccinated” person’s body, and also evades the natural immune system components and mechanisms in the COVID-19 “vaccinated” person’s body. COVID-19 “vaccinated” persons therefore have their natural immune systems damaged or destroyed, making it difficult or even impossible to mitigate and/or defeat the damage done by the “vaccines.”
Yours Truly will posit, based on the research and writing that she has been engaged in about the COVID-19 virus itself, and the COVID-19 “vaccines”, since March 2020: that any un-“vaccinated” person, of any age, who has had a COVID-19 virus itself infection; or, any person, of any age, who has had a COVID-19 “vaccine” put into their body — has been injured by the negative effects of the virus itself, or by the negative effects of the “vaccines.” In addition, COVID-19 virus itself infected persons, and COVID-19 “vaccinated” persons, have died from the effects of the infection or the “vaccine.” One will also say that the COVID-19 “vaccines” have added ingredients and mechanisms that make these injectables more dangerous and deadly than the COVID-19 virus itself. Finally, the outcomes of infection by the COVID-19 virusitself, andthe negative outcomes from taking the COVID-19 “vaccines”, were, and are, planned and intentional.
It is now, in Yours Truly’s opinion, imperative that all persons make it their business to have and to maintain their natural immune system in the best possible condition.
It is now time to bring to account all of the multiple agencies, scientists, and other entities involvement (including the United States military) in the development of the lab-created SARS-CoV-2 virus itself: of the COVID-19 “vaccines”; and in the processes that resulted in the granting of Emergency Use Authorization and/or Full Approval of these “vaccines” without proper protocol adherence to rigorous testing and clinical trials for the said “vaccines.” It is now time to stop all further use of any COVID-19 “vaccine” until the above accountability is fully undertaken and finished, It is now time for all government agencies, medical organizations, and medical practitioners to recognize that Ivermectin and Hydroxycholoquine are inexpensive and vastly effective treatments for COVID-19 infection and for COVID-19 infection prophylaxis. It is now time to stop the use of Paxlovid and Remdesivir as “officially approved” treatment for COVID-19 infection, as both of these drugs have significant negative side effects, including a high “rebound COVID infection” rate for Paxlovid, and kidney damage and/or death for Remdesivir; and to substitute the use of Ivermectin or Hydroxycholoquine.
The above free image of Justice is courtesy of Pixabay 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 in today’s offering: It is an Open Thread.
As today’s Health Friday post is related to the COVID-19 disaster (the virus itself, and the COVID-19 “vaccines”; and, to the governmental and Big Pharma tyranny over the lives and livelihoods of millions of people “in the name of Science” related to the COVID-19 disaster), it is dedicated to the memory of Yours Truly’s COVID-19 “vaccinated” late brother Sam, and her late cousin Bill; and to the memory of all other persons of any age who have passed away since 11 December 2020, either directly or indirectly, due to the COVID-19 “vaccines” they have taken. May they rest in eternal Peace.
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, and which are all linked here.
Donald Trump was just overwhelmingly re-elected to be the next President of the United States. It appears that he will appoint Robert F. Kennedy, Jr., to be Secretary of the Department of Health and Human Services. Mr. Kennedy, Jr., has vowed to end the “stranglehold” that the FDA, the CDC, Big Pharma, and “Establishment Medicine” have imposed on the American people for decades. It also appears that he plans to re-organize the FDA into an agency that actually does its job in protecting the health of the American people. One of his efforts, in Yours Truly’s opinion, needs to be investigating the exact “reorganization” changes that the FDA began to implement within that agency on 1 October 2024: www.fda.gov/about-fda/fda-organization/fda-modernization-efforts-establishing-unified-human-foods-program-new-model-field-operations-and.
In addition, there is much to be accomplished regarding holding multiple persons, agencies, and other entities accountable for the damage that has already been done to the general public health of Americans, in addition to the health of people all over the world, due to the COVID-19 disaster. While Yours Truly is notadvocating a “re-do” of the French Revolution, there must be ways to hold these multiple persons, agencies, and other entities to account. Please see www.midwesterndoctor.com/p/new-data-exposes-the-corruption-behind, “New Data Exposes the Corruption Behind the COVID Response”, 12 November 2024. A screenshot of the start of this blog post is below:
The following Listsbarely scratch the surface:
List One: Dr. Anthony Fauci (former head of the NIAID); Dr. Francis Collins (former head of NIH); Dr. Deborah Birx (White House Coronavirus response team under then-President Trump); Dr, Stephen Hahn (former Commissioner of the FDA); Dr. Robert Califf (current Commissioner of the FDA); Dr. Robert Redfield and Dr. Rochelle Walensky (former Directors of the CDC); Dr. Mandy Cohen (current Director of the CDC); Ralph Baric, Ph.D. (UNC, Chapel Hill); Peter Daszak, Ph.D. (EcoHealth Alliance); and, Dr. Eric Rubin (VRBPAC committee, FDA “We’re never gonna know if it’s effective unless we start giving it” — related to the committee’s recommendation to give the COVID-19 “vaccines” to children.) If Dr. Zheng-li Shi (Wuhan Institute of Virology) can be extradited from Communist China, that would be a good addition to the list.
The above article contains a link to the archived CDC document.
Regarding Dr. Anthony Fauci: Please watch the short video clip of leaked testimony from a Congressional hearing in which Dr. Fauci spoke. Listen to his comments. Listen to them again. At 0:23 in the clip, Dr. Fauci states: “And it’s been proven that when you make it difficult for people in their lives, they lose their ideological bullshit and they get vaccinated.” (Bolding mine). The video clip is here: https://x.com/LisaLu/status/1855788234392932353.
List Two: Albert Bourla, DVM (CEO of PfizerUSA); Stephane Bancel (CEO of Moderna); Alex Gorsky (former CEO of Johnson & Johnson.)
List Three: Alex Azar (former), and Xavier Becerra (current), Secretaries of the Department of Health and Human Services; Kathy Hochul, Governor of New York; Tom Wolf, former Governor of Pennsylvania; Gretchen Whitmer, Governor of Michigan.
List Four: United States Department of Defense Secretaries Patrick M. Shanahan, Mark Esper, Christoper C. Miller (former, 2018-2021); and, Lloyd Austin (current). United States Army Chiefs of Staff Gen. Mark A. Milley, Gen. James C. McConville (2015 through August 2023); and, Gen. Randy A. George (current.) These, all in relation to the United States Defense Department’s and the United States Army’s previous and (likely) current involvement in the development, manufacture, and distribution of the Pfizer-BioNTech modRNA COVID-19 “vaccines”; and, to the forced “mandate” that all US military personnel be COVID-19 “vaccinated.” www.documentcloud.com/downloads/22028603-pfizer-base-agreement, July 2018; www.hhs.gov/sites/default/files/pfizer-inc-covid-19-vaccine-contract.pdf, 21 July 2021; www.law.cornell.edu/uscode/text/10/4022.
List Five: Bill Gates; Kelly L. Moore, MD, MPH (director of https://immunize.org/); Mark Green (former), and Samantha Power (current), Administrators of the United States Agency for International Development (www.usaid.gov/; also via https://usaidmomentum.org/.)
Readers are invited to add names to these lists, and/or to create other lists.
The above image of lab equipment is courtesy of Google Images and Public Domain Pictures.
Today’s offering for Health Friday concerns what is called self-amplifying RNA (saRNA.) As the presentation includes discussion of saRNA COVID-19 “vaccines”, this post is dedicated to the memory of Yours Truly’s cousin Bill, who “died suddenly and unexpectedly” in September 2023.
Readers already know about the Important Wolf Moon Notifications, the importance of Civil Discussion, the Rules of our late, good Wheatie, and the caveats regarding Health Friday posts by Yours Truly. Links to these items can be found here. NOTE: Since this post is detailed and there are multiple areas to cover, Yours Truly has added Summaries of certain sections, and a General Summary at the end.
Before one begins: It is well known that the modRNA and the viral vector COVID-19 “vaccines” currently in use have been, and are, a disaster on multiple fronts. Not only do they induce literally thousands of negative medical and psychological effects in the bodies of those who took them and who take them now; these “vaccines” also cause death. The numbers of COVID-19 “vaccinated” persons presenting with COVID-19 “vaccine”-induced illnesses, injuries, disabilities, or “died suddenly and unexpectedly” are increasing by the month. Nobody knows exactly how long, or in what amount, the elements and mechanisms of the COVID-19 “vaccines” work in the “vaccinated” person’s body: what IS known, is that whatever “protection” is conferred by these “vaccines” is short-lived, while, at the same time, the “vaccine” mechanisms linger on in the body for an indeterminate period of time. Yours Truly has written extensively for this board regarding this situation. For further information, please see websites such as these: https://kirschsubstack.com/ (Steve Kirsch); https://petermcculloughmd.substack.com/ (Peter McCullough, MD); and, https://phinancetechnologies.com/HumanityProjects/Projects.htm#Nav_ExcessDeaths (Ed Dowd, statistician.)
At the same time, the development of new types of COVID-19 “vaccines”, as well as new types of “vaccine delivery” (intranasal, oral, and aerosol, for examples) goes on apace. One of the “newest” types of COVID-19 “vaccines” uses what is called self-amplifying RNA, or saRNA.
The concept of saRNA is the use of a small amount of RNA (or mRNA) in an injectable. Once introduced into the body of the patient, the saRNA theoretically goes to work, “re-creating itself.” (Think RNA or mRNA being turned into a “Xerox copier” inside the “vaccinated” person’s body.) The “goal” of saRNA is for the agent to “re-create itself” inside the “vaccinated” person’s body for a certain amount of time and in some amount. The patient’s body is “instructed” by the saRNA to “recognize” and produce antibodies against certain “enemies”, such as viruses. The theory is that a smaller amount of saRNA initially introduced into the body, followed by the “Xerox copier effect”, then followed by “instructing” the body to “recognize” and fight off certain “enemies”, will make saRNA a “more effective use” of mRNA in injectables.
Basically,saRNA COVID-19 “vaccines” turn the “vaccinated” person’s body into a “Xerox copier” (which, apparently, the “vaccinated” person’s body CANNOT stop, slow down, or mitigate) for the ingredients (and, by extension, the mechanisms) of the saRNA “vaccine.” Today’s post is a primer about saRNA COVID-19 “vaccines.”
****** Summary: In other words, saRNA injectables **may**, at some point down the road, have **some** benefits. In the meantime — NONE of these types of injectables (GEMCOVAC, Kostaive) have been SUFFICIENTLY AND THOROUGHLY INVESTIGATED AND TESTED FOR USE ON HUMANS. But they are being approved ANYWAY, and are being injected into the bodies of unsuspecting persons who buy into the “Look, this shot has less mRNA than the ones you took before, and it’ll work better!” hype.
****** Look closely at the above graphic. It appears that the basic schema of saRNA is a “double-layer” of saRNA “replicons” that create a “subgenomic RNA.” This, in turn, creates the “Xerox copier” response which forces the body of the saRNA “vaccinated” person to endlessly produce immune system response— and for “at least” as long as 28 days after such “vaccination.”
Please see this paper regarding a discussion of saRNA “vaccine” design: https://doi.org/10.1016/j.tibtech.2023.05.007, “Rise of the RNA machines — self-amplification in RNA vaccine design”, Jerome D.G. Comes, et al., 14 June 2023. Below is the Abstract of this paper:
Note the language about “,…at least in theory” advantage of saRNA “vaccines.” Also note the last sentence — saRNA can “persist for a month.” In fact,nobody really knows how long saRNA elements will “persist” in the body of the person who takes this type of “vaccine” — NO long-term clinical trial or study has been performed using this technology.
On 28 November 2023, the Japanese Government approved the use of the saRNA COVID-19 “vaccine”, ARCT-154 (also called LUNAR-COVID-19 and Kostaive) for “active immunization” (translation: “prevention”) against COVID-19 for persons age 18 and older. Kostaive was developed by CSL / Arcturus (remember this company? Yours Truly took the lid off it here: www.theqtree.com/2024/08/02/the-hhs-gave-the-go-ahead-to-use-an-h5n1-vaccine-but-the-ama-just-issued-new-cpt-codes-for-an-h5n8-vaccine/.) This “vaccine” was to have supplies ready for administration by physicians or hospitals by mid-December 2023.
CSL / Arcturus, the Japanese government, and media outlets were quick to herald this “first-ever saRNA COVID-19 “vaccine.” Except — there already was an saRNA COVID-19 “vaccine” approved and in use, since 2022, in India: GEMCOVAC. Perhaps what CSL / Arcturus, the Japanese government, and media outlets should have mentioned the fact that Kostaive is modRNA-based from the J.1. Omicron SARS-CoV-2 variant (along with other “familiar” manufacturing methods, see below in today’s post); whereas GEMCOVAC based on an “ancestral variant” (in other words, the Beta variant) of the original Wuhan Hu1 SARS-CoV-2 virus.
Before Yours Truly presents information on Kostaive, she will first discuss GEMOCOVAC. This is in order to present further background information on saRNA technology as applied in COVID-19 “vaccines.” Stay with me — this is all germane to the situation:
Looking at GEMCOVAC, one can get the beginning of a picture of how saRNA COVID-19 “vaccines” work. The “latest version” of this “vaccine” is called GEMCOVAC-OM. Below is a portion of the SmPC pdf for this product (https://gemcovac.com; scroll down the page to GEMCOVAC-OM SmPC (pdf) and click “Download”):
The BA.1. Omicron variant of SARS-Co-V-2 is the basis for this “vaccine.” It is not strictly modRNA (however, recall that ALL of the “descendant variants” of the original Wuhan Hu1 SARS-CoV-2 virus contain elements of that original lab-created virus).
Of the excipients (in other words, the adjuvants): per Wikipedia, DOTAP (1,2-Dioleoyl-3-trimethylammonium propane) is a chemical used in fabric softeners, but also is used as a lipid nanoparticle in vaccines. Squalene: below is Page 1 of the FisherScientific MSDS Safety Data Sheet for this chemical (www.fishersci.com/):
Continuing: for polysorbate 80, again from Fisher Scientific, Page 1 of the MSDS Safety Data Sheet:
And, here is the Mechanism of Action for GEMCOVAC-OM, from the Package Insert (see the link above):
Note the language, “…which is reported to interact with host cells receptors (ACE-2.)” (Italics mine.) The developer and manufacturer (GENNOVA) of this “vaccine” can’t exactly quantify how the product works.
Yours Truly now turns to Kostaive, (ARCT-154) the saRNA COVID-19 “vaccine” that was approved by the Japanese government in November 2023.
Note the language in the above regarding “…the potential for extended duration of protection while using lower doses of mRNA compared to existing mRNA vaccines.” (Italics mine) Again, nobody knows exactly how long this “extended duration” period is; nobody knows exactly how much “Xerox copying” of the altered mRNA in Kostaive occurs during this period in the “vaccinated” person’s body; and, nobody knows exactly what effects this “Xerox copying” of the altered mRNA in Kostaive will have in the “vaccinated” person’s body. In other words, anyone who takes Kostaive, or any saRNA “vaccine”, in Yours Truly’s opinion, is being used a “human lab rat” — just as people were used / are still being used, as “human lab rats” for the modRNA COVID-19 “vaccines.”
And, here is the Report of the Deliberation Results (which contains the information about Kostaive that led to its approval) from the Japanese Ministry of Health, Labour, and Welfare: www.pmda.go.jp/files/000269813.pdf. This report is an interesting read. There are numerous “blacked-out” areas, reminding one of the blacked-out areas in certain publicly-released Pfizer-BioNTech reports that the company gave to the FDA regarding that company’s modRNA COVID-19 “vaccine” BNT162b2. HOWEVER, section 2.1 Active Substance for Kostaive states that this saRNA “vaccine” contains elements from the original Wuhan Hu1 SARS-CoV-2 virus, plus elements from the Omicron variant strain. More information on this is found on Page 4 of the document. Below is a portion of this page:
Looking at the above, starting with the D614G mutation, the Abstract from the Zhang, et al. paper on this (https://doi.org/10.1038/s41467-020-19808-4, “SARS-CoV-2 spike-protein D614G mutation increases virion spike density and infectivity”, Lizhou Zhang, et al., 26 November 2020. The paper was researched and published before any COVID-19 “vaccine” was authorized for use):
In other words, the D614G element causes the SARS-CoV-2 virus to be more infective.
Looking at V987P, part of the section Full-Length S Glycoprotein Vaccines from this paper: https://doi.org/10.3389/fimmu.2021/701501, “SARs-CoV-2 Vaccines Based on the Spike Glycoprotein and Implications of New Viral Variants”, Daniel Martinez-Flores, et al., 11 July 2021):
In other words, if V987P was “good enough” for Pfizer-BioNTech and for Moderna to use in their modRNA COVID-19 “vaccines”, it apparently was “good enough” to be used in Kostaive.
The K986P protein used in Kostaive: please see here: www.rcsb.org/structure/6zp1. This viral protein, along with V987P above, are BOTH on the Arg S1/S2 cleavage site on the SARS-CoV-2 virus genome. (FURIN CLEAVAGE SITE, anyone?)
The R682G, R683S, and R685S proteins used in Kostaive: please see here: https://doi.org/10.1038/s41467-022-32665-7, “Omicron SARS-CoV-2 mutations stabilize spike-up RBD conformation and lead to a non-RBM-binding monoclonal antibody escape”, Zhennan Zhao, et al., 24 August 2022. If appears that these proteins help to create a “one-RBD-up conformation.” Below is a portion of the Abstract of this paper:
In other words, these proteins increase the immune system attack from the Omicron SARS-CoV-2 variants by making Omicron “stick better” to the ACE2 receptor cells in the human body.
****** Summary: It appears, then, that Kostaive contains one protein from the original Wuhan Hu1 SARS-CoV-2 virus genome (D614G); two proteins from the “ancestral line” of the SARS-CoV-2 virus (K986P and V987P); and three proteins of the Omicron SARS-CoV-2 variant (R682G, R683S, and R685S.) See below in the post for more information on these items.
One more ingredient of Kostaive, mRNA-2105: This ingredient is derived from the Venezuelan Equine Encephalitis virus (VEEV.) Below is section 4.R.1. of the Deliberations Results document discussing this:
The question that immediately occurs regarding the above: How can Arcturus (the manufacturer of Kostaive) state that mRNA-2105 cannot be “incorporated into host cell DNA”? How is Arcturus absolutely sure that there is zero reverse transcription potential or ability in Kostaive? This is similar to the same statements from Pfizer-BioNTech about BNT162b2 “cannot change the DNA of the vaccinated individual” — which has been proven to be false (please see: here, Slide 14.)
****** Summary of the above: What Yours Truly is getting at here is that Kostaive appears to be the end-product of: ONE: a lab-created mixture of the dangerous D614G element from the original Wuhan Hu1 SARS-CoV-2 virus, plus, various elements of earlier SARS-CoV-2 mutations; TWO: NO long-term clinical trials, NO safety studies for Toxicity, use on pregnant women, etc.; THREE: the “Process 2”-type manufacturing method (“culturing” the lab-enhanced mRNA for the “vaccine” in a “bath” of E. coli); FOUR: using lipid nanoparticles, one of which (ATX-126) has never been used before in an injectable); FIVE: what appears to be a “pro-forma” Deliberation Results document on Kostaive that raises more questions than it answers; and, SIX: approval by the Japanese government for use on humans without a thorough investigation of the above. Related to point SIX: below is the list of Approval Conditions that were imposed along the approval of Kostaive for use in Japan, from the Deliberations Results document:
By the way, these Approval Conditions read very much like the ones that the FDA imposed on Pfizer-BioNTech along with that agency’s EUA for BNT162b2.
Regarding Kostaive itself, more particulars:
The ingredients of Kostaive are listed in section 2.2 Vaccine Product of the report. A screenshot of this section is below:
Kostaive contains at least three separate types of LNPs (lipid nanoparticles): ATX-126; DSPC; and, PEG2000-DMG. Below is a portion of the MSDS Safety Data Sheet for ATX-126:
Section 2.2.3 of the Deliberation Results document for Kostaive discusses the manufacturing process for Kostaive. It appears that Kostaive ALSO “switched” from a “Process A” manufacturing method over to a “Process B” manufacturing method. (Recall that the Pfizer-BioNTech BNT162b2 was “switched” from its “Process 1” manufacturing method over to a “Process 2” manufacturing method):
One more item from the Deliberation Results document for Kostaive, again on the ATX-126 lipid nanoparticle used in this “vaccine.” It confirms that this “novel excipient” (adjuvant) has not been used before in a “vaccine.”
Yours Truly will again emphasize that other sections of the DeliberationResults document on Kostaive make it clear that NO studies were performed for numerous items, such as Toxicity, potential for impairment of reproduction, and so on. By the way, buried in the document is a “passing reference mention” that the “Process B” manufacturing method for this “vaccine” uses E. coli as the “culturing medium” for the “enhanced” mRNA in the product. (The “Process 2” manufacturing method for BNT162b2 and its “descendant” COVID-19 “vaccines” also uses E. coli.) It also appears that the use of Kostaive on pregnant women in clinical trials was “inconclusive”; this “vaccine” should be taken by pregnant women only if the situation so warrants.
Also: Kostaive is to be taken as a “primary series” of two separate injections, 28 days apart; with a “booster” taken about three months later. The question that arises is: If it is true that the saRNA in Kostaive is active, including installing numberless “Xerox copiers” of itself in the “vaccinated” person’s body for AT LEAST 28 days AFTER the initial injection, WHY is there a need for ANOTHER injection around Day 28? And a “booster” after that?
******BUT — AND THIS IS A HUGE BUT — TAKE ANOTHER LOOK AT SECTION 2.2.1 OF THE DELIBERATION RESULTS DOCUMENT FOR KOSTAIVE:
Look at the “active ingredient” item, “zapomeran.” What is zapomeran? It is a “drug” that contains the RNA of the Venezuelan Equine Encephalitis Virus (VEEV or VEE) in an saRNA form. It is ALSO manufactured by ARCTURUS (CSL.) It is unclear if it is being used in other types of COVID-19 “vaccines” other than Kostaive. Please see: https://synapse.patsnap.com/drug/510bcf7ef75649278b284a94663c69f6. Scroll down the page to R&D Status to see that zapomeran has already been approved in the EU; Norway; Iceland; and Liechtenstein; but in what final form it is used, is also unclear. NOTE 1: It has been impossible to find a complete list of ingredients for zapomeran. One would not be surprised to learn that the names Kostaive and zapomeran may, in some respects, be “interchangeable.” NOTE 2: It is not easy to find information on zapomeran. Yours Truly has encountered “504 Bad Gateway” error messages when going back to recheck a couple of the links to zapomeran in this post.
Looking further into VEEV (or VEE), there is this article: https://ceh.vetmed.ucdavis.edu/health-topics/venezuelan-equine-encephalitis-vee, by Amy Young, 28 August 2020. This virus can affect horses, donkeys, or zebras. VEEV is transmitted to these animals by infected mosquitos that bite them. It can cause severe disease or death by infecting the brain and the central nervous system. Humans who contract VEEV can also become severely ill and can also die from it. Another paper, discussing the RNA of VEEV (VEE),by Sarah E. Hickson and Jennifer L. Hyde, is here.
****** VERY IMPORTANT:The SARS-CoV-2 spike proteins in zapomeran are the same ones that are in Kostaive. These were discussed above in the post. Turning to the nsP proteins (non-structural proteins) in zapomeran (hyperlinks to papers are embedded), as these elements are also apparently contained in Kostaive:
****** SUMMARY:IT APPEARS, THEN, THAT KOSTAIVE CONTAINS ZAPOMERAN, WHICH INCLUDES THE VENEZUELAN EQUINE ENCEPHALITIS RNA; PLUS, SIX LAB-ENHANCED/LAB-ISOLATED GENOME CODES OF SARS-CoV-2; AND, FOUR NON-STRUCTURAL PROTEINS, ONE OF WHICH IS A ROTAVIRUS TOXIN. KOSTAIVE ALSO CONTAINS DANGEROUS LIPID NANOPARTICLES (SUCH AS ATX-126.) THESE ARE ALL PRESENT IN THIS saRNA COVID-19 “VACCINE” PRODUCT. RECALL THAT LIPID NANOPARTICLES WILL HELP TO SPREAD A “VACCINE” THROUGHOUT THE ‘VACCINATED” PERSON’S BODY, INCLUDING CROSSING THE BLOOD-BRAIN BARRIER.
Why on Earth is a COVID-19 “vaccine” that contains the RNA of an equine brain inflammation virus (a virus that comes from infected mosquitos that bite equine animals) being used on humans? A “vaccine” that is engineered to create an unknown number of “Xerox copiers” of the “vaccine” elements into the body of the “vaccinated” person? A “vaccine” that contains six apparently lab-enhanced/lab-isolated genome codes from the SARS-CoV-2 virus or its variants? What does an equine brain inflammation virus have in common with SARS-CoV-2? What if a person who has already taken, say, five or six injections of a modRNA COVID-19 “vaccine” decides to take Kostaive? Could an saRNA COVID-19 “vaccine” somehow “interact” with the modRNA COVID-19 “vaccine” elements already in that person’s body?
****** GENERAL SUMMARY: saRNA “vaccines” for COVID-19 are already being used (GEMCOVAC in India); and are being approved for use (Kostaive in Japan.) The technology for saRNA is not fully developed and not fully tested; the COVID-19 “vaccines” that use saRNA contain “lab-enhanced”/”lab-isolated” genome codes of the SARS-CoV-2 virus or its variants; saRNA COVID-19 “vaccines” contain lipid nanoparticles — and, in the case of Kostaive, an LNP (ATX-126) that has never been used before in an injectable; that no studies have been performed on saRNA COVID-19 “vaccines” regarding Toxicity, the effects on reproductive potential, and so on; and, that Kostaive contains the RNA of the Venezuelan Equine Encephalitis Virus. And yet, these products are being hailed as “the vaccines of the future.” And, the people taking them are again being used as “human lab rats.”
The above image from an old medical-scientific journal is from PeopleImages, via Google Images.
This post is part of Health Friday, a series of offerings 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. However, since this presentation is about a COVID-19 “vaccine”, the post is dedicated to the memory of Yours Truly’s cousin Bill, who died “suddenly and unexpectedly” in September 2023.
To begin, there are Important Wolf Moon Notifications, with a couple of extra items:
Free Speech is practiced here: “Use it or lose it.”
The following are alternate Q Tree sites for certain circumstances:
The U Tree is for “argue it out” interactions. There is a “Featured” article at this site for use as a “Rescue Thread.”
The “third site”, in case the above two are inaccessible.
Civil discussion is practiced here. The excellent and timely Rules of our late, good Wheatie prevail:
One: No food fights.
Two: No running with scissors.
Three: If you bring snacks, bring enough for everyone.
Please follow the added Guidelines from Wolf Moon. Please do not give the modern-day version of Cato the Elder the opportunity to show “enmity” to the board.
The extra items: What Yours Truly presents in this series, as in her other blog posts to this board, is not medical advice — the are opinions and hypotheses based on her over 4 1/2 years (and continuing) of reading about, researching out, and writing about “all things COVID”, Big Pharma, and other health topics. Readers are encouraged to consult a healthcare practitioner regarding health concerns or conditions.
The Health Friday post today concerns the impending Retraction of a peer-reviewed and published paper that details long-term COVID-19 “vaccine”-induced injuries in North India. The paper was submitted to Springer for review and publishing on 9 January 2024; it was accepted (it had passed the peer-review process); and it was published on 13 May 2024. Here is a free-access version (to read the entire paper on Springer, one has to either access through an institution, or to pay for a copy): www.qeios.com/read/JK7IBA/pdf, “Long-Term Safety Analysis of the BBV152 Coronavirus Vaccine in Adolescents and Adults: Findings from a 1-Year Prospective Study in North India”, Upinder Kaur, et al., 13 May 2024. The study was conducted at Banaras Hindu University in India. BBV152 is another name for the COVAXIN COVID-19 “vaccine”, developed by Bharat BIotech of India in cooperation with Indian Council on Medical Research (ICMR) – National Institute of Virology. ICMR receives “royalty payments” for each dose of COVAXIN that is administered, as does Bharat Biotech (Sound familiar? — as in, the co-development, co-ownership of patents, and sharing of “royalty payments” between the NIAID and Moderna for the modRNA COVID-19, mRNA-1273?)
The Kaur, et al., paper referenced above was published by Springer on 13 May 2024. Almost immediately, the attacks began on the paper, the authors, and the publisher — with articles like this one: https://timesofindia.indiatimes.com/india/1-in-3-covaxin-recipients-hit-by-adverse-events-study/articleshow/110187284.cms, “1 in 3 Covaxin recipients hit by adverse events: Study”, 17 May 2024. On 18 May 2024, the ICMR demanded that Springer retract the paper (Yours Truly: nothing like causing panic in a government agency when the truth is published about a “vaccine” that the agency is pushing as “safe and effective,” especially when that agency is also getting “royalty payments” for the use of the “vaccine”, is there?). But, the attack on Springer and the authors didn’t end there. In July 2024, Bharat Biotech filed a lawsuit against Springer and the authors (some of the authors are students), demanding retraction of the paper and the payment of damages to Bharat Biotech of $600,000 US dollars (50 million Indian rupees.) In addition, the lawsuit accused the paper’s authors of defamation against the company, included with a demand for separate damages to be paid to the company for defamation. Despite sworn statements from the authors that no defamation was intended or written into the paper; and, despite the fact that Nitin Joshi, the editor of the Springer journal (Drug Safety) in which the study appeared, was one of the reviewers who approved the study for publishing, it was Joshi who notified the authors on 28 August 2024 that he was going to have the paper retracted. He confirmed this decision in an email to the authors on 17 September. However, as the defamation lawsuit is now in court, the study is still available on the internet.
What is BBV152/COVAXIN? It is an “inactivated whole virion vaccine” (whole virus vaccine) for “active immunization” against COVID-19. It is not an mRNA-based/modRNA-based COVID-19 “vaccine”, although it does use an “ancestral wave strain” of the original Wuhan Hu1 SARS-CoV-2 virus (in other words, a strain from the Wuhan Hu1 virus that occurred before the Beta, Delta, or Omicron strains.) The Package Insert for COVAXIN is here: www.bharatbiotech.com/images/covaxin/covaxin-pack-insert.pdf. Below is an image from the Package Insert:
Per Wikipedia, 363,774,435 persons in India had been “vaccinated” with at least one dose of COVAXIN as of 4 March 2023.
However, the COVAXIN Package Insertdoes not actually describe how the “vaccine” works (the “Mechanism of Action.”) Yours Truly found something along the lines of the necessary information here: www.clinicaltrialsarena.com/projects/covaxin-bbv152-for-the-treatment-of-covid-19/?cf-view&cf-closed, “COVAXIN (BBV152) for the Treatment of Covid-19, India”, 28 June 2022. Below is a screenshot from this article:
But, COVAXIN has been hailed by the Indian government about being “the first indigenous COVID-19 vaccine in India” (www.bharatbiotech.com/covaxin.html.) Why is ViroVax involved? (More on this later in the post.) Back to the Package Insert for COVAXIN. Below is a screenshot of the ingredients used in this “vaccine”:
Looking further into the ingredients list, starting with the NIV-2020-770 strain of SARS-CoV-2: please refer to this paper: www.ncbi.nlm.nih.gov/pmc/articles/PMC7825810/, “Safety and immunogenicity of an inactivated SARS-CoV-2 vaccine, BBV152: a double-blind, randomised Phase 1 trial”, Krishna Mohan Vadrevu, et al., May 2021. It appears that NIV-2020-770 (the “inactivated whole virion”) is part of the Asp614Gly variant chain of the SARS-CoV-2 virus. The Asp614Gly variant itself is apparently part of the “ancestral wave” of the original Wuhan Hu1 SARS-CoV-2 virus; and, it is “not as serious” as the Beta or the Delta waves of the virus. Please refer to this article: www.thelancet.com/pdfs/journals/langlo/PIIS2214-109X(22)00199-1.pdf, Vol.10, July 2022, a Comment “Decoding the next SARS-CoV-2 variant”, by Jeremy Nel and WD Francois Venter. Below is a screenshot of a portion from the Comment:
Thus, BBV152/COVAXIN cannot be considered to be one of the “most recent” types of COVID-19 “vaccines”, as it does not include any elements before the Beta, Delta, or Omicron variants.
The Aluminium Hydroxide Gel in the ingredients (it is an “excipient” [“adjuvant]”): this is also called “Algel-IMDG” and “Alhydroxiqium-II” — in other words, it is a hydrogel. It was invented by ViroVax LLC of Lawrence, Kansas, under the aegis of the EpscoR Idea Foundation (part of the National Science Foundation in the United States), and with funding by the NIAID. This is the ViroVax / United States government connection. Here is a screenshot from an article by the EpscoR Idea Foundation on this “success story” (www.epscorideafoundation.org/success-stories/kansas-adjuvant-developed-with-nih-funding-enhances-efficacy-of-indias-covid-19-vaccine):
Note that Alhydroxiqium-II targets the lymph nodes of the person who takes COVAXIN. So, while this excipient is not exactly a lipid nanoparticle (LNP), it, in Yours Truly’s opinion, basically functions like an LNP in targeting the lymph nodes for delivery of the “vaccine payload” of COVAXIN; and, by “stimulating” the “vaccinated” person’s natural immune system to go and “search” for invading pathogens. By the way, Aluminium Hydroxide Gel is not to be used in foods, drugs pesticides, or “biocidal” products — see the screenshot below, from the search on Fisher Scientific (ThermoFisher) about this chemical, Page 1:
HOWEVER, it appears that FisherScientific had a “change of heart” since December 2021 regarding the “Uses advised against” for Aluminium Hydroxide — below is their MSDS Safety Sheet as of February 2024, Page 1:
Here is another source for an MSDS Safety Sheet, this one specifically for Aluminium Hydroxide Gel:www.oxfordlabfinechem.com/msds/ALUMINIUMHYDROXIDEGEL.pdf. Please see section 3Hazards Identification; and section 11Toxicological Information Special Remarks on Other Toxic Effects on Humans. Below is part of the Special Remarks portion of section 11:
The TLR7/8 excipient (adjuvant) in COVAXIN: This one is used in immunotherapy, including in the treatment of HIV-1. Please see: https://doi.org/10.3389/fmicb.2023.1033448, “Novel TLR7/8 agonists promote activation of HIV-1 latent reservoirs and human T and NK cells”, Yangyang Li, et al., 26 January 2023. This begs the question, Why is an HIV-1 immunotherapy treatment element being used in a COVID-19 “vaccine?” This also, in Yours Truly’s opinion, removes any consideration of COVAXIN to be labeled a “vaccine” — it is actually a gene therapy/immunotherapy injectable.
And, the 2-Phenoxyethanol excipient (adjuvant) in COVAXIN. Below is a screenshot portion of the Fisher Scientific (ThermoFisher) MSDS Safety Sheet for this chemical, Page 1:
The Kaur, et al., paper, goes into detail regarding the types of reported serious adverse events that affected the study subject pool who took COVAXIN. Three pages of the Supplementary Table 1. from the paper are below. Note that these are details from subjects one year after “vaccination” with COVAXIN. Note also that another paper from December 2020 (by different authors) shows that the S1 protein of the SARS-CoV-2 virus itself crosses the Blood-Brain Barrier.
If Yours Truly is reading about this situation correctly, it appears that one of the “problems” with the Kaur, et al., paper, is that the subject pool of COVAXIN-“vaccinated” persons in North India who reported serious adverse events following “vaccination” to the study authors was “small.” One has to ask: How many COVAXIN-“vaccine”-induced serious adverse events would need to be reported before they would be considered “relevant” by the Indian government and by Bharat BioTech? — say, a “minimum” of 3 million adverse events reports? Is it “within acceptable limits” that COVAXIN-“vaccinated” persons in North India suffer a stroke or a heart attack after “vaccination” with this product? Is this another situation of “the known and potential benefits outweigh the known and potential risks” of taking a COVID-19 “vaccine”, which is the “official” position of the CDC and the FDA in the United States?
Yours Truly has gone into detail regarding the situation with BBV152/COVAXIN for several reasons: First, to enumerate the multiple potentials for “vaccine”-induced serious adverse effects from this COVID-19 “vaccine” product; Second, to highlight the persecution of the authors of a paper who sought to study and write about these potentials; Third, to highlight the persecution of the journal that peer-reviewed, approved, and published the paper;Fourth, to bring to light the involvement of the United States government (via the NSF and the NIAID) in the funding and development of an ingredient (excipient/adjuvant) in this “vaccine” intended for use in a foreign country; and, Fifth, to again emphasize how important it is that consumers “do their own due diligence” regarding information on drugs and/or injectables that they put into their bodies.
This is a very open-ended post. The goal is to get YOUR thoughts, opinions, and theories.
Without getting too deep, I can tell you that we are seeing a LOT of COVID in my world. It seems to be everywhere. But some apparent attempts to get masks going again are fizzling out fast, thank goodness.
So I’m curious what others are seeing. But beyond that, we’ve had almost 5 years of COVID in this world – maybe more.
Time for reassessment – particularly prior to the election.
Time for some fresh ground reports.
What think you about COVID?
Tell us what you’re seeing and thinking, please!!!
The above vintage image of a tired woman is courtesy of QuoteGram, via Google Images.
Today’s Health Friday post, as it relates to COVID-19 and the COVID-19 “vaccines”, is dedicated to the memory of Yours Truly’s cousin Bill, who died “suddenly and unexpectedly” in September 2023. Health Friday is a series of offerings related 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.
To begin, there are Important Wolf Moon Notifications, with a couple of extra items:
Free speech is practiced here: “Use it or lose it.”
The following are alternate Q Tree sites for certain circumstances:
The Rescue Thread at the U Tree: click on the Featured article there.
The Third site, in case the above two are not accessible.
Civil discussion is practiced here. The excellent and timely Rules of our late. good Wheatie prevail:
One: No food fights.
Two: No running with scissors.
Three: If you bring snacks, bring enough for everyone.
Please follow the Added Guidelines as expressed. Please do not give the modern-day version of Cato the Elder the opportunity to show “enmity” to the board.
The extra items:
What Yours Truly presents in this series, as in her previous blog posts for this board, is not medical advice — they are opinions and hypotheses based on her over 4 1/2 years (and continuing) of reading about, researching about, and writing about, “all things COVID”, Big Pharma, and other health topics. Readers are encouraged to consult a healthcare practitioner regarding health concerns or conditions.
Note: If any reader of today’s post is also a subscriber to Mr. Kirsch’s Substack (https://kirschsubstack.com/), it would be much appreciated if the link to this post could be sent to him. Thank you.
Dear Mr. Steve Kirsch:
Greetings. The writer of this post is a regular reader of your Substack site. Many thanks for all your efforts in exposing the truth about the COVID-19 “vaccines.” This is a response to your blog post of 30 August 2024, The COVID shots are fueling the rise of ME/CFS cases. While it is true that ME/CFS can present symptoms that are similar to that of “Long COVID”, I suspect that there may well be other items in play. To start, I am including an image of the VAERS chart that is in your blog post:
The incidence reports of CFS (ME/CFS) after taking COVID-19 “vaccines” far outstrips all of the other vaccines listed.
ME/CFS conditions existed well before either the SARS-CoV-2 (COVID-19) virus itself, or the COVID-19 “vaccines” — per Wikipedia, Dr. Melvin Ramsay “published the first diagnostic criteria for ME” (Myalgic encephalomyelitis) in 1986. (Wikipedia search “history of ME/CFS”) However, cases of ME/CFS began to present in otherwise healthy people after they contracted a case of COVID-19 early on in the COVID-19 pandemic (before the COVID-19 “vaccines” were in use.) One such case is summarized here, in the Yale Medicine blog: Long COVID, ME/CFS and the Importance of Studying Infection-Associated Illnesses, 13 May 2024, by Osman Moneer. Below is a screenshot from the article:
Note: “Dr. Deborah F.” is not her real name.
There also may be a link between ME/CFS, Long COVID, and negative emotional-psychological outcomes: Infections, ME/CFS, Long COVID and Psychosis: Is There a Link?, 16 July 2023, by Cort Johnson. A screenshot from part of The Gist section of the article is below:
This opens up the question, What is in the COVID-19 virus itself, and therefore in the COVID-19 “vaccines”, that can induce ME/CFS (Post-viral Fatigue)? Yours Truly turns to the report that Pfizer-BioNTech gave to the FDA on 30 April 2021, regarding post-authorization Adverse Event Reports submitted to the company in people who took the first injection of the modRNA COVID-19 “vaccine” BNT162b2, between 12 December 2020 (the date on which the FDA granted the initial authorization for BNT162b2 to be used in the United States) and 28 February 2021. The report is here, via FOIA release: www.phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf. Page 30 of this report is the APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST. This is a nine-page listing of over 1,200 serious Adverse Events that occurred in people who were “vaccinated” with BNT162b2 during the report period. Page one of this list has two types of damage to the mitochondria reported: “Alanine aminotransferase increased”; and, “Antimitochondrial antibody positive”. Page three lists “Chronic fatigue syndrome.” Page five lists “Immune-mediated encephalitis” and “Immune-mediated encephalopathy.” Page seven lists “Post viral fatigue syndrome.” In other words, at least six types of mitochondrial, neurological. or “body-wide” issues that are induced by modRNA COVID-19 “vaccines”, which can present in various forms, including CFS or ME/CFS.
There is also a link between the Epstein-Barr Virus (EBV) and the COVID-19 “vaccines.” EBV can be an “adjunct” presenting condition related to ME/CFS. Yours Truly found one paper, by Japanese researchers, on EBV presenting after “vaccination” with BNT162b2 (the Pfizer-BioNTech COVID-19 “vaccine”, [Epstein-Barr virus-associated lymphoproliferative disorders after BNT162b2 mRNA COVID-19 vaccination], from 2023. Only the Abstract is available in English. It is below:
It is now known that the COVID-19 “vaccines” (actually, gene therapy injections) do the following to the “vaccinated” person’s body:
Cross the Blood-Brain barrier (BBB); interfere with / damage / destroy mitochondrial elements and mechanisms; can induce negative effects / interfere with neurological elements and mechanisms; can induce onset of psychological issues, including psychosis; interfere with / damage or destroy, elements and mechanisms of the natural immune system (citations below.) These negative effects, in Yours Truly’s opinion, all have a bearing on the causation and presentation of COVID-19 “vaccine”-induced or aggravated ME/CFS. In order for these to occur, again in Yours Truly’s opinion, certain specific elements had to have been “inserted” into the lab-created SARS-CoV-2 (COVID-19) virus itself (and, by extension, into the lab-enhanced COVID-19 “vaccines”) to induce these types of damage. Perhaps it was a specific element that interacts with the WASF3 protein; perhaps it was a specific element that interacts with a component of the Epstein-Barr virus. Perhaps it was a specific element that interacts / interferes with other aspects of Human Chromosome 13. Perhaps it was all of these. I believe that ongoing research into the actual ingredients of the modRNA of the COVID-19 “vaccines” will eventually reveal the answers.
In addition, there are the following lipid nanoparticle (LNP) ingredients in the modRNA COVID-19 “vaccines”:
For the Pfizer-BioNTech “vaccines”: ALC-0159, ALC-0315, and PEG2000-DMG; for the Moderna “vaccines”: SM-102, ALC-0315, and PEG2000-DMG. All of these lipid nanoparticles are dangerous. All of them are to be used for research only, not for use in diagnosis or therapeutics for humans or for animals. All of them specifically “evade” the “vaccinated” person’s natural immune system’s “Are you a friend or a foe?” recognition and elimination mechanisms. They facilitate “access” of the ingredients and mechanisms of these modRNA COVID-19 “vaccines” to induce damage / destruction of the IgG3 “fight it off” immune system cells in the “vaccinated” person’s body; and, at the same time, to increase the amount of IgG4 “tolerate and never clear” immune system cells. This process is called the “Class Switch” done by the modRNA COVID-19 “vaccines.” (Citations below.)
In Summary: The COVID-19 virus itself can induce multiple negative medical effects on persons who contract an infection of the virus, including ME/CFS. The COVID-19 “vaccines”, which contain elements of the COVID-19 virus itself (in addition to other lab “enhancements” for these “vaccines”, such as the lipid nanoparticles), can therefore also induce multiple negative medical effects in persons who take these injectables, including ME/CFS. In addition, both the COVID-19 virus itself, and, by extension, the COVID-19 “vaccines”, can induce and/or aggravate negative psychological conditions. I believe that these “vaccines” need to be banned outright immediately and removed from the market across the world, until and unless such time they are completely reformulated and thoroughly tested (including testing by independent labs) for human safety, efficacy, toxicity, mutagenesis potential, and reproductive effects potential.
It is my opinion that: One, that all people, COVID-19 “vaccinated” or not, follow a personal program to acquire and maintain the highest degree of natural immune system health as possible; and, Two, that all people investigate any vaccine that is recommended (or “mandated”), then, to decide whether or not to take the injectable(s.)
Citations regarding the In Summary above, the lipid nanoparticles, and the “Class Switch”:
