The above free vintage image of a medical doctor performing an exam on the larynx of a patient is courtesy of Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. Since today’s post speaks of the disaster of the COVID-19 virus itself, and of the COVID-19 BTI (aka the “vaccines”), it is dedicated to the memory of Yours Truly’s COVID-19 “fully vaccinated and boosted” late brother, Sam; to her late cousin, Bill; and, to all persons, of whatever age or location, who have passed away from the negative effects, direct or indirect, of the COVID-19 “vaccines” that they had in their bodies.

There are Important Wolf Moon Notifications, the Rules of our late, good Wheatie, and certain caveats from Yours Truly, of which readers should be aware. They are linked here.

This week’s Health Friday post concerns the ingredients and mechanisms of the COVID-19 BTI in the inducement of cancer in “vaccinated” persons. There is also a role to play here for the COVID-19 virus itself.

Yours Truly begins with examples of studies that prove the COVID-19 BTI (aka the “vaccines”) induce cancer: https://doi.org/10.1016/j.fct.2022.113008. “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs”. Stephanie Seneff, Peter A. McCullough, et al., June 2022. Below are Table 6 and Table 7 from this paper:

And, from this paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC9876036/, “Potential health risks of mRNA-based vaccine therapy: A hypothesis”, K Acevedo-Whitehouse and R Bruno, 25 January 2023. Below are two screenshots from the paper:

Another paper, which details damage in the “vaccinated” person’s body to the p53 tumor suppressor protein, plus damage to / interference with, the type I Interferon response (also called type I IFN response), is here: https://doi.org/10.7759/cureus.50703, “SARS-CoV-2 Vaccination and the Multi-Hit Hypothesis of Oncogenesis”, R.P. Angues and Y.P. Bustos, 17 December 2023. Below is the salient graphic from this paper:

**** Note that cancer can be fostered and/or metastasized by either COVID-19 “vaccination”, or by the COVID-19 virus itself. More on that later on in today’s post.

And, to “tie it all together” regarding the confirmation of the presence of “loose DNA” and the SV40 African Green Monkey cancer promoter gene piece in the modRNA COVID-19 “vaccines”, this paper, by three high school students who worked in an FDA-supervised lab in Maryland: https://jhss.scholasticahq.com/article/127890-a-rapid-detection-method-of-replication-competent-plasmid-dna-from-covid-19-mrna-vaccines-for-quality-control, TJ Wang, A Kim, K Kim, 29 December 2024. The Wang, Kim, and Kim paper is further discussed here: https://blog.maryannedemasi.com/p/exclusive-fda-lab-uncovers-excess, “EXCLUSIVE: FDA lab uncovers excess DNA contamination in COVID-19 vaccines”, 2 January 2025. By the way, the Wang, Kim, and Kim paper was peer-reviewed prior to publication.

One important item that links all of the above is what the COVID-19 “vaccines” do to the p53 protein in the human body. P53 (also called TP53, or Tumor Protein 53) prevents the formation of cancer in the body. Please see: https://en.wikipedia.org/wiki/P53. The modRNA COVID-19 “vaccines” manufactured by Pfizer-BioNTech damage the p53 in the “vaccinated” person’s body, (which then interferes with and/or “disables”, the ability of p53 to “detect” and prevent the formation of cancer tumors in the “vaccinated” person’s body) via the SV40 African Green Monkey cancer promoter gene code piece that is present in this company’s modRNA COVID-19 “vaccines.“

Scientific researchers have been experimenting for years with the SV40 cancer promoter and its interaction to interfere with and/or to suppress, the p53 tumor suppressor protein. Here are examples of published papers on the topic:

One: https://doi.org/10.1128/mcb.19.4.2746. “New Insights into the Mechanism of Inhibition of p53 by Simian Virus 40 Large T Antigen”, Hilary M. Sheppard, et al., April 1999. Below are two images from this paper:

Note that the “monkey – human” amino acid percentage of “identicalness” of p53 is much higher than that of the “mouse – human” percentage.

The “Hudson, Colvin” paper from 2016 details how SV40 suppresses p53, allowing tumors to form and grow: https://doi.org/10.1093/ilar/ilw001, “Transgenic Mouse Models of SV40-Induced Cancer”, Amanda L. Hudson, Emily K. Colvin, 31 March 2016. Below are images from this paper:

And, the Drayman, et al., 2016 paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC5288138/, “p53 elevation in human cells halt SV40 infection by inhibiting T-ag expression”, Nir Drayman, et al., 21 July 2016. Below is Figure 7 from this paper:

The point here is that the p53 tumor suppressor does a good job of preventing SV40 cancer promoter cells from infecting the body and establishing oncogenic (cancer tumor) cells. And, that this knowledge has been around for some time.

Which brings one back to the Pfizer-BioNTech modRNA COVID-19 BTI (aka the “vaccines”), and the discovery of “loose DNA” and of amounts of the SV40 cancer promoter gene code piece in these injectables. It is inconceivable that Pfizer-BioNTech did not know of the ability of the p53 protein in the human body to detect SV40 and then to prevent it from establishing oncogenic cells. It is also, in Yours Truly’s opinion, inconceivable that Pfizer-BioNTech can try to explain away this discovery by some kind of “Oops, we’re sorry, we didn’t mean to leave that stuff in the formulation of the product” hyperbole. The “loose DNA” (and, by extension, the SV40 cancer promoter gene code piece) are present in all the modRNA COVID-19 “vaccines” made by this company in the summer of 2020, when Pfizer-BioNTech “suddenly” switched the manufacturing process for BNT162b2 from the original “Process 1” method (not using an “extracts of E. coli bath” in the process), to the “Process 2” method (using an “extracts of E. coli bath” in the process) for use in the BNT162b2 (truncated and data-falsified) “clinical trials” going on at that time for this injectable; and which “Process 2” method has been used to manufacture the modRNA COVID-19 “vaccines” by this company since. Please also see here: www.theqtree.com/2023/11/06/the-infamous-process-2-manufacturing-method-for-the-pfizer-biontech-modrna-covid-19-vaccines/; the actual documentation that the company provided to the FDA regarding this change of manufacturing process is detailed.

Another piece to this situation is the fact that the modRNA COVID-19 BTI (aka the “vaccines”) contain dangerous lipid nanoparticles that quickly spread the contents (and, by extension, the mechanisms) of this injectables throughout the “vaccinated” person’s body. In addition, these lipid nanoparticles (ALC-0159 and ALC-0315 in the Pfizer-BioNTech BTI; and, SM-102 in the Moderna BTI) are specifically developed to evade the body’s natural “are you a friend or a foe” detection and elimination mechanisms. This is in addition to other excipients (adjuvants) in these injectables, such as PEG2000-DMG. Yours Truly has written extensively on these items and how they work to undermine / interfere with, the “vaccinated” body’s natural immune processes. Finally, there is the N1-Methylpseudouridine in BOTH the Pfizer-BioNTech AND the Moderna COVID-19 BTI. This lab-created compound was specifically developed to replace (remove) the natural Uridine RNA in the “vaccinated” body with “fake Uridine” plus a form of methane. In the specific case of N1-Methylpseudouridine, the consequences to the “vaccinated” body, BOTH in the physical AND in the psychological aspects, is profoundly negative. These are all aside from the addition of the SV40 cancer promoter in the Pfizer-BioNTech COVID-19 “vaccines.”

Going back to the graphic from the “Angues and Bustos” paper regarding the fact that BOTH the COVID-19 itself, AND the COVID-19 BTI (aka the “vaccines”) can cause cancer. Below is a repeat of the graphic:

Notice the Impaired type I IFN response (type I Interferon) on the lower right of the graphic. This is another ingredient / mechanism of the COVID-19 virus itself (likely) AND of the COVID-19 BTI (definitely), the workings of which have also been studied and known for years. An example of a paper that speaks to this is here: https://pmc.ncbi.nlm.nih.gov/articles/PMC4666791/, “The Type I Interferons: Basic Concepts and Clinical Relevance in Immune-Mediated Inflammatory Diseases”, Consuelo M Lopez-Padilla, Timothy B Niewold, PMC published 15 January 2017. Two images from this paper are below:

Please also see: https://wmcresearch.substack.com/p/a-unifying-theory-of-covid-19-pathogenesis, “A Unifying Theory of COVID-19 Pathogenesis, Combining Senescent, Cardiovascular, Oncogenic and Neurodegenerative Pathologies”, 4 April 2022.

Three points here, in Yours Truly’s opinion, regarding those who lab-created the COVID-19 virus itself, and those who lab-created the COVID-19 BTI (aka the “vaccines”): One: they knew exactly what things would: interfere with the body’s type I Interferon responses; interfere with and/or destroy elements of the body’s natural immune system (CD4 – CD8 cells, IgG3 cells, and so on); evade or interfere with, the body’s natural p53 tumor suppressor response to detect and eliminate the SV40 cancer promoter that would be present in the Pfizer-BioNTech COVID-19 BTI; cross the Blood-Brain Barrier; and more. Two: they made sure that the COVID-19 virus itself is not “just another flu virus”, but, rather, a bioweapon that was lab-created from years of stunningly-detailed research and experimentation to wreak as much potential damage as possible on the person who contracts an infection of the virus itself. And, Three: they made sure that this created bioweapon virus would be the foundation of the COVID-19 “vaccines”; while, at the same time, limiting or denying access to simple and effective items that can successfully counteract the virus itself, such as Ivermectin, Hydroxychloroquine, Zinc, Vitamin D, and Quercetin.

While it is true that the survival rate for non-COVID-19 “vaccinated” persons who contract a COVID-19 virus itself infection and recover is 99% for ages 0 to 65 years, and between 94% – 95% for ages 65 and above, an infection from the COVID-19 virus itself can still potentially damage the body. However, those who lab-created the COVID-19 virus itself did not reckon completely with the human body’s natural immune system’s ability to detect, fight off, and eliminate this bioweapon. In Yours Truly’s opinion, the COVID-19 “vaccines” were lab-created to “finish the job” in this regard: injections which were then “mandated” for people to take, to “keep themselves and others safe from the virus.” With the disastrous results that are now presenting worldwide.

There are several items that can support / supplement the p53 of the body. Here are some examples:

Green tea compound: www.sciencedaily.com/releases/2021/02/210212094113.htm, “Green tea compound aids p53, ‘guardian of the genome’ and tumor suppressor”, Chunyu Wang, et al., 12 February 2021.

Capsaicin: https://jeccr.biomedcentral.com/articles/10.1186/s13046-016-0417-9, “Reactivation of mutant p53 by capsaicin, the major constituent of peppers”, Gabriella D’Orazi, et al., 6 September 2016.

Phenethyl isothiocyanate in the diet: www.nature.com/articles/cdd201648, “Reactivation of mutant p53 by a dietary-related compound phenethyl isothiocyanate inhibits tumor growth”, M Aggarwal, et al., 3 June 2016. This compound is also called “PEITC.” Natural sources of phenethyl include broccoli, watercress, cabbage, turnips, and radishes. More information can be found here: www.sciencedirect.com/topics/chemistry/phenethyl-isothiocyanate.

Finally, there is the phenomenon of shedding of the COVID-19 virus itself, and of the COVID-19 “vaccines.” It is not known at this time exactly what ingredients of these are shed. What IS known is that it is indeed happening, and that this shedding is negatively affecting the health of the people who are “shed upon.” A comprehensive article that explains this issue is here: https://pierrekorymedicalmusings.com/p/newly-published-study-shows-shedding, “Newly Published Study Shows Shedding of Covid mRNA Vaccine Products”. Pierre Kory, MD, 9 December 2024.

It is of the utmost importance that all people have, and maintain, the highest degree possible of general health; and, in particular, the health of their natural immune system.

THERE. MUST. BE. JUSTICE.

FLASH! Sunday 12 January 2025: ADDENDUM: Please see below, copied (and expanded here) from the main discussion thread today:

“WOLF MOON AND ALL — KEVIN McKERNAN FOUND THE MOAD REGARDING THE PFIZER-BIONTECH COVID-19 “VACCINES” AND TURBO-CANCERS:

The following is a “quick and dirty” summary. Yours Truly will append a “Flash! News” addendum to the body of the Health Friday post of two ago on the p53 cancer tumor suppressor gene and how SV40 interferes with it.

Summary:

One: Dr. Kevin McKernan ran the gene sequence from the cancer tumor biopsies and compared them to the gene sequence in the Pfizer-BioNTech COVID-19 “vaccine.” There was a match. He also found traces of the Pfizer-BioNTech COVID-19 “vaccines” in the cancer tumors.

Two: At least one sequence match was made a year AFTER the patient had been COVID-19 vaxxed.

The article that talks about this: https://slaynews.com/news/top-scientist-sounds-alarm-traces-covid-vaccines-found-cancer-tumors/, “Top Scientist Sounds Alarm as Traces of Covid ‘vaccines’ Found in Cancer Tumors”, by Frank Bergman, 11 January 2025. There is a video in the article of an interview with COVID researcher John Beaudoin on this situation.

Screenshot from the above article:

There’s only one way that this can happen, IMO — it’s the SV40 African Green Monkey cancer promoter gene code piece that’s in the Pfizer-BioNTech COVID-19 “vaccines.” The SV40 promoter interferes with the body’s p53 cancer suppressor protein.”

Yours Truly will amplify on the above.

First: IN ADDITION to SV40 interfering with the p53 cancer suppressor protein in the COVID-19 “vaccinated” person’s body, there is ALSO the damage / destruction of the crucial immune system IgG3 “fight it off” cells, instead fostering the increase of IgG4 “tolerate but never clear” cells. This “class switch” affects the entire body, “depressing” the natural immune “are you a friend or foe” mechanisms.

Second: The N1-Methylpseudouridine in the Pfizer-BioNTech AND in the Moderna modRNA COVID-19 BTI (aka the “vaccines”) replaces the RNA of the natural Uridine in the “vaccinated” person’s body. This ALSO interferes with / damages, the multiple body-brain interactions and mechanisms that natural Uridine regulates.

Third: There is ALSO the phenomenon of COVID-19 “vaccine” shedding by “vaccinated” persons to consider in this scenario. There are increasing reports of the negative effects that the ingredients (and, by extension, the mechanisms) of the COVID-19 “vaccines” do to non-“vaccinated” persons via this shedding. There is, in Yours Truly’s opinion, real potential for the SV40 cancer promoter that is in the Pfizer-BioNTech COVID-19 “vaccines” to be shed from persons who have taken this “vaccine” onto other people, including onto non-“vaccinated” persons.

Below are two other screenshots from the Slay News article:

Links to two other articles from Slay News that are germane to the 11 January article: https://slaynews.com/news/top-surgeon-warns-aggressive-cancers-mutating-covid-vaxxed/, 27 October 2024 (with a video by British cancer surgeon, Dr. James Royle); and, https://slaynews.com/news/renowned-oncologist-evil-covid-vaccines-caused-turbo-cancer-explosion/, 17 December 2024 (an interview with British oncologist, Dr. Angus Dalgleish.)

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA