PAVACA’s Top 12 List of Damages the COVID-19 “Vaccines” Can Do to the “Vaccine” Recipient

The above is an image of Father Christmas from a vintage postcard.

The following may be a bit “heavy” — please regard it as a kind of rich “Christmas Pudding” of COVID-19 “vaccine” knowledge base. Not a “lump of coal!”

Just in time for Christmas, Yours Truly presents a list of what she considers to be the “Top 12” types of damage that the COVID-19 “vaccines” can do to the body of the “vaccine” recipient. This list has been gathered from the 1600+ hours of investigating “all things COVID-19” that Yours Truly has done since March 2020. Therefore, it is only her opinion. People who read through the report that Pfizer-BioNTech gave to the FDA on 30 April 2021, regarding the over 1,000 serious adverse events medical conditions that the company’s COVID-19 “vaccine”, BNT162b2, caused in persons who took this “vaccine” IN FEWER THAN THREE MONTHS after the FDA granted the initial EUA for this “vaccine” in December 2020 for its use in the United States, may come up with “Top Lists” of their own. The report can be found here: https://phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf, BNT162b2 5.3.6 Cumulative Analysis of Post-authorization Adverse Events Reports. The APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST, found at the end of the report, lists these serious adverse events conditions reports that BNT162b2 caused in “vaccinated” persons.

However, what is NOT opinion is that the FDA then knew, on 30 April 2021, that the Pfizer-BioNTech “flagship” COVID-19 “vaccine” BNT162b2 (actually, an untried gene therapy injection), was capable of damaging the body of the “vaccine” recipient in over 1,000 different ways, including the ways on Yours Truly’s “Top 12 List..” However, instead of performing its regulatory (and moral and ethical) obligations to immediately pull BNT162b2 off the market and out of use until the situation could be further investigated, the FDA chose to CONTINUE the EUA that it granted in December 2020 for BNT162b2. Not only that, but the FDA went ahead and granted “full approval” for the use of the European version of BNT162b2, called COMIRNATY, in the United States. Not only that, but the FDA granted EUA’s for the Pfizer-BioNTech COVID-19 “bivalent vaccine” to be used in the United States. Finally, in the spring of 2023, the FDA quietly stopped all use of BNT162b2 in the United States — in Yours Truly’s opinion, after mounting reports of serious adverse events, including deaths, being caused by this “vaccine” were beginning to circulate widely and to be confirmed by professional researchers and by doctors — and substituted the use of the Pfizer-BioNTech (and the Moderna) “booster vaccines” for the Omicron variant. In the summer of 2023, the FDA granted EUA’s for both the Pfizer-BioNTech and for the Moderna “2023-2024 Formula COVID-19 Vaccine”, which had only been tested on mice.

Here is Yours Truly’s “Top 12 List”: The first nine, from the APPENDIX 1. cited above:

Death: neonatal and Sudden unexplained death in epilepsy (page 3 and page 8); Myocarditis and Pericarditis (page 6 and page 7); Stroke (Cerebral artery embolism page 2; Cerebral thrombosis, page 2); Thrombotic Stroke (page 9), among other types; THIRTY different types of Autoimmune disorders (page 2); FORTY different types of Herpes disorders (page 4 and page 5); THIRTY-PLUS different types of Liver disorders (page 4); TWENTY-FIVE different types of Immune System disorders (page 5); SIXTEEN different types of Neurological (brain and/or central nervous system) disorders (page 6); and, COVID-19 and COVID-19 Pneumonia (page 3).

As an example, here is a handy-dandy image of page 4 of the APPENDIX 1., with Yours Truly’s notes:

To round out the “Top 12 List” of COVID-19 “vaccine” damage to the body of the recipient, there are these three:

One: Heart tissue and lung tissue damage / destruction: Please refer to: https://doctors4covidethics.org/wp-content/uploads/2022/08/causality-article.pdf, by Michael Palmer, MD, and Sucharit Bhakdi, MD; Two: Fetal / Neonatal disorders, including 1p36 deletion syndrome (also listed on page 1 of the APPENDIX 1.): Please refer to the following regarding 1p36 deletion syndrome: https://medlineplus.gov/genetics/condition/1p36-deletion-syndrome/ (more on this condition below); and, Three: Cancer induced with the assistance of the SV40 cancer promoter DNA that has been recently discovered in the Pfizer-BioNTech COVID-19 “vaccines” (more on this below): Please refer to the following: https://osf.io/preprints/osf/mjc97, “DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events”, David Speicher, Jessica Rose, Kevin McKernan, et al. From lines 94-95 of this paper: “McKernan, et al., found SV40 promoter-enhancer-ori [DNA], and SV40 polyA signal sequences in the Pfizer vaccines.” The SV40 promoter-enhancer DNA is also in the Pfizer-BioNTech COVID-19 “vaccines” that were used in the United States: https://rumble.com/v3r1pqf-vaccine-adulteration-wkevin-mckernan-byram-bridle-chris-martenson-steve-kir.html, beginning at 3:32 in the video. Please also refer to the letter of December 2023 from Florida Surgeon General, Dr. Joseph Ladapo, to the directors of the FDA and the CDC: www.floridahealth.gov/about/_documents/12-06-2023-DOH-Letter-to-FDA-RFI-on-COVID-19-Vaccines.pdf. Yours Truly will posit that, since the modRNA + its spike protein and the “Process 2” manufacturing method for the current “2023-2024 Formula COVID-19 Vaccine” by this company in use in the United States are both based on its original “vaccine” formulations (BNT162b2 and the “booster and bivalent vaccines”), it appears that this opens up the possibility that the SV40 promoter-enhancer DNA is present in this “vaccine” also. Important: The SV40 promoter-enhancer DNA in the Pfizer-BioNTech COVID-19 “vaccines” is not the entire code, only a part of it. In and of itself, this “partial code” likely would not cause cancer; however, it can be involved in the general damage / destruction that the COVID-19 “vaccines” do to the “vaccine” recipient’s body, which can, in turn, be involved in the onset of cancer, or the re-emergence of cancer already in remission, in that person’s body. In addition, Pfizer-BioNTech DID NOT TELL the Canadian health authorities, nor, apparently, the FDA in the United States, about the SV40 issue.

About the 1p36 deletion syndrome caused by the modRNA COVID-19 “vaccines”: This is particularly troubling, since it effects UNBORN children and THE SPERM AND THE EGGS OF THE “VACCINATED” PARENTS. 1p36 deletion syndrome is a multi-faceted condition that negatively affects fetal development. Infants born with this condition have severe intellectual difficulties; weak muscle tone; have vision, hearing, and heart issues; and either do not speak, or can only speak a limited vocabulary; among other things. Please refer to the MedlinePlus link, above, for further information. It has been proven that large amounts of the dangerous lipid nanoparticles AND the enhanced spike protein + its modRNA in the Pfizer-BioNTech COVID-19 “vaccine” migrate to, and lodge in, two important areas of the recipient’s body — the OVARIES and the TESTES. Please refer to the image below, directly from Pfizer-BioNTech, on page 8 of a document that the company gave to the FDA on 21 January 2021. The document is called BNT162b2 2.6.5 Pharmacokinetics Tabulated Summary. It is available through https://phmpt.org/.

Please also refer to this graphic, which shows what the modRNA COVID-19 “vaccines” do in the pregnant mother’s body and in the body her unborn child or her nursling child (this is from a CDC presentation):

1p36 deletion syndrome is “...caused by a deletion of genetic material from a specific region in the short (p) arm of chromosome 1…Most cases of 1p36 deletion syndrome are not inherited.” (per the MedlinePlus link, above.) Think about that.

Three “Christmas Bonuses” to to along with the “Top 12 List”: One: The COVID-19 “vaccines” can, and do, cause onset of psychosis in “vaccinated” persons. Please refer to the following: https://doi.org/10.24869/psyd.2022.377, “First Episode of Psychosis Following the COVID-19 Vaccination — A Case Series”, Tonka Borovina, et al.; Two: The risk of mortality increases for the “vaccinated” person for each injection they take of a COVID-19 “vaccine.” Please refer to the following: www.theburningplatform.com/2023/12/10/newly-leaked-data-shows-just-how-dangerous-the-covid-vaccines-are/; and, Three: The damage / destruction of the “vaccine” recipient’s immune system and connections to what is called “turbo-cancers” that this induces. Please refer to the following: https://jessicar.substack.com/p/igg4-and-cancer-a-mechanism-of-action; and, to https://vigilantnews.com/post/turbo-cancer-death-from-turbo-cancers-were-in-trouble-says-dr-ryan-cole/.

A final note on the current “2023-2024 Formula COVID-19 Vaccines” by both Pfizer-BioNTech and by Moderna: These apparently do include the ingredients (although in smaller amounts) of the original modRNA COVID-19 “vaccines” made by each company (BNT162b2 by Pfizer-BioNTech; and, mRNA-1273 by Moderna), with additional elements of the Omicron XBB 1.5 variant lineage. Please refer to the following: www.fda.gov/media/167211/download, page 39 (Pfizer-BioNTech); www.fda.gov/media/167208/download, page 34 (Moderna); and, https://covid19.nih.gov/covid-19-vaccines.

As an aside, in case readers hear someone “congratulating themselves” for their taking either the Novavax or the Johnson & Johnson (Janssen) COVID-19 “vaccines”, because they believed that somehow these “vaccines” are “safer” than those of Pfizer-BioNTech or of Moderna: The Novavax COVID-19 “vaccine” uses the same modRNA + its spike protein as in the Pfizer-BioNTech and the Moderna COVID-19 “vaccines.” The difference with the Novavax COVID-19 “vaccine” is that the SARS-CoV-2 virus is “marinated” in an insect culture, with the resulting modRNA “harvested” and mixed with “adjuvants” made from soap tree bark; this “vaccine” also uses lipid nanoparticles (LNPs.). The Johnson & Johnson (Janssen) COVID-19 “vaccine” was removed from use (revoked) in the United States by the FDA in May 2023. However, persons who took this “vaccine” prior to May 2023, are at risk for Thrombosis and Thrombocytopenia, as listed on the “black letter warning” area on the (revoked) FDA Fact Sheet for Healthcare Providers for this “vaccine.” Please refer to the following: for the Novavax COVID-19 “vaccine”: www.fda.gov/media/159897/download, page 33; www.hackensackmeridianhealth.org/en/healthu/2022/08/09/novavax-vaccine-how-its-different-and-how-it-works; and, for the Johnson & Johnson (Janssen) revoked COVID-19 “vaccine”: www.fda.gov/media/146304/download, page 1.

Yours Truly will make it clear she believes that COVID-19, in its variants forms, is still a threat to health. Since one is a concerned citizen, not a healthcare practitioner, one can only offer the following thoughts:

First: it is of primary importance that all people have, and maintain, the best level of personal health and immunity that is possible; “un-vaccinated” people have a primary responsibility here to themselves. Second: It is of primary importance that all “un-vaccinated” people follow a protocol for prophylaxis against COVID-19, such as those outlined at https://covid19criticalcare.com/, and including judicious exposure to sunlight and daily mild to moderate exercise. Third: It is of primary importance that all people follow “common sense” approaches, such as washing the hands, and staying away from sick people if possible. Fourth: It is of importance that “vaccinated” people know about various protocols to try and mitigate the dangerous effects of the COVID-19 “vaccines” at work in their bodies; https://covid19criticalcare.com/treatment-protocols/. Fifth: It is of great importance to have and keep a positive connection with a Supreme Being.

“Then will you know the truth, and the truth shall set you free.” John 8:32

It is past time, in Yours Truly’s opinion, to bring to justice those who were/are involved in the development and manufacture of the COVID-19 “vaccines”; and those in the FDA / CDC / AMA, and other medical agencies and organizations, who either know, should have known, or knew of, the dangers of these “vaccines” — but still continue to push them. Some examples: Albert Bourla, DVM (CEO of Pfizer Inc.); Stephane Bancel (CEO of Moderna); Alex Gorsky (CEO of Johnson & Johnson until 2022); Anthony Fauci, MD (former head of the NIAID); Francis Collins, MD (former head of the NIH); Janet Woodcock, MD (former Acting Commissioner of the FDA); Rochelle Walensky, MD (former Director of the CDC); Peter Daszak, CEO of EcoHealth Alliance; Robert Califf, MD (current Commissioner of the FDA); Mandy Cohen, MD (current Director of the CDC); Jesse M. Ehrenfeld, MD, (current head of the AMA); and, Ralph Baric, PhD, of the Baric Lab at the University of North Carolina, Chapel Hill.

A link to a another of Yours Truly’s pieces on COVID-19 and the COVID-19 “vaccines”, that has a compilation: www.theqtree.com/2023/11/29/the-covid-19-vaccines-pave-the-way-for-turbo-cancers-and-a-note-on-the-virus-itself/

Best wishes for a good Christmas 2023 and New Year 2024. Peace, Good Energy, Respect: PAVACA