Tag: Comirnaty

Health Friday Open Thread 12.13.2024: The DNA in the Pfizer-BioNTech modRNA COVID-19 Bioweapon Toxin Injections (aka the COVID-19 “Vaccines”)

The above free vintage image of DNA strands is courtesy of Shutterstock via Google Images.

Health Friday is a series of posts related to Big Pharma, vaccines, general health, and associated topics. Since today’s post is related to the modRNA COVID-19 “vaccines”, it is dedicated to the memory of Yours Truly’s COVID-19 “vaccinated” late brother, Sam, and to her late cousin Bill; and to all persons, of whatever age or location, who have passed away from the negative effects (direct or indirect) of the COVID-19 “vaccines” that they took.

There are Important Wolf Moon Notifications, the Rules of our late, good Wheatie, and certain Yours Truly caveats, of which readers should be aware. They are linked here. The discussion today is not limited to what is presented below: It is an Open Thread.

Above all — There. Must. Be. Justice.

To Begin: Yours Truly will now change the name of the COVID-19 “vaccines” to reflect what they really are — dangerous and deadly bioweapons injections:

COVID-19 Bioweapon Toxin Injections (COVID-19 BTI). They are NOT “vaccines.” The FDA, the CDC, and the makers of these injections/injectables KNOW THIS. If Yours Truly refers to these injectables as “vaccines”, it is for “convenience-recognition” only, e.g., as in scientific papers or in media headlines.

Today’s post is a confirmation and an amplification regarding the discovery of large amounts of “free” DNA residue in vials of the Pfizer-BioNTech modRNA COVID-19 modRNA BTI, BNT162b2. The trail begins here: https://jessicar.substack.com/p/a-new-paper-confirms-presence-of, A new paper confirms presence of DNA in COVID-19 shot vials, settles issues pertaining to DNA quantification models, shows spike persistence and exosomal shuttling (shedding), by Jessica Rose, PhD., 4 December 2024. Yours Truly will address this article and the paper that it cites, in addition to some earlier papers by other researchers on the topic. The “weave” of today’s post is somewhat dense — the depth of the perfidy behind BNT162b2 is wide and deep. Please bear with me.

The paper to which Dr. Rose refers is here: https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/, Ulrike Kammerer et al., 3 December 2024. Read the paper’s title again — there are TWO types of DNA elements in the Pfizer-BioNTech COVID-19 BTI, BNT162b2: what may be called “loose” DNA, plus an SV40 African Green Monkey cancer promoter-enhancer genome code sequence. The salient graphics regarding this from the paper are below:

The Kammerer, et al., paper is hugely important. The multitude of tests and assays that were performed on the samples from the Pfizer-BioNTech modRNA COVID-19 BTI vials is not only incredibly thorough; it is also stunning. Several earlier hypotheses (and evidence from previous scientific papers and articles) regarding these injectables are now confirmed:

One: More of the ingredients of the Pfizer-BioNTech modRNA COVID-19 BTI are confirmed — “loose” DNA; the SV40 African Green Monkey cancer promoter-enhancer genome code sequence; the presence of HEK293 cells (aborted fetal cells); the presence of the antibiotic, Neomycin (a drug that treats bacterial infections); and, ORI replicons in the plasmids in the injectable. ORI replicons are the things that “teach” the “vaccinated” person’s body to make copies of the spike protein — in other words, a type of self-amplifying modRNA mechanism is introduced into the body. Plasmids are tiny DNA molecules that are inside a cell; plasmids are not chromosomal DNA and can independently reproduce themselves. An image of plasmids inside a cell is below (courtesy https://en.wikipedia.org/wiki/Plasmid):

Two: The amount of “loose” DNA in BNT162b2 is well above EMA (European Medicines Agency) limits. A screenshot of Figure 2. section D, of the Kammerer, et al., paper, below, clearly shows this:

Three: The presence of the DNA plasmids and of the SV40 African Green Monkey cancer promoter-enhancer gene code sequence were NOT disclosed to the FDA by Pfizer-BioNTech prior to that agency’s granting of the initial EUA for BNT162b2 on 11 December 2020 for this injectable’s use in the United States. The salient statement from the Kammerer, et al., paper, on this is below:

Yours Truly will note that the FDA also granted “full approval” of BNT162b2 in 2022, under the brand name COMIRNATY, and its “descendant clone” modRNA COVID-19 BTIs, including all “new formula” injections {such as the 2024-2025 COMIRNATY COVID-19 modRNA BTI.)

Four: There is a distinct possibility that BNT162b2 can “shed” from “vaccinated” persons onto other persons, via exosomal secretion. From the Discussion section of the Kammerer, et al., paper, below:

The COVID-19 modRNA BTIs are “shuttled” throughout the body of the person who takes these injectables. This “shuttling”, in part, is performed by exosomes. Exosomes are tiny elements that are formed by lipid bilayers and function as a kind of “shuttle service” within the body, carrying proteins, lipids, and other items to and from body organs, including to the skin. Please refer to: https://pubmed.ncbi.nlm.nih.gov/35436552/, “Innate immune suppression by SARS-CoV-2 mRNA vaccines: The role of G-quadruplexes, exosomes, and MicroRNAs”, Stephanie Seneff, et al., 15 April 2022.

Scientific researchers have been experimenting with SV40 African Green Monkey cancer promoter-enchancer gene code since at least 1997. Please see: https://doi.org/10.1128/JVI.71.1.427-436.1997, “Direct modulation of simian virus 40 late gene expression by thyroid hormone and its receptor”, Fengrong Zuo, Tod Gulick, et al. Below is a graphic of the SV40 gene code experiment, followed by a portion of the Discussion section of this paper:

Research has been performed regarding SV40-induced cancers, via “methylation.” Please refer to: https://doi.org/10.1038/sj.cr.7290295, “Epigenetic changes in virus associated human cancers”, Hsin Pai Li, et al., 1 April 2005.

Two papers by Kevin McKernan have researched much of the information that the Kammerer, et al., paper has confirmed. One McKernan paper is here: https://doi.org/10.31219/osf.io/b9t7m, “Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose”, Kevin McKernan, et al., 10 April 2023. A graphic from this paper is below:

Please note that there are two separate SV40 elements in this graphic: the SV40 enhancer and the SV40 “signal” in the poly-A “tail” of BNT162b2.

The other McKernan paper is here, regarding DNA fragments in BOTH the Pfizer-BioNTech AND in the Moderna modRNA COVID-19 BTIs: https://doi.org/10.31219/osf.io/mjc97, “DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose relationship with serious adverse events”, Kevin McKernan, et al., 19 October 2023.

Yours Truly now turns to the “primary source document” for BNT162b2, the International Patent declaration document for this injectable. It is found here: https://patents.google.com/patent/WO2021213945A1/en, published on 28 October 2021. Note: The patent number in the Kammerer, et al., paper (WO2021214204) is a another identifier for this patent. It is difficult to access the actual patent document by using this identifier on a search — the above Google URL is easy to find. Another patent number for BNT162b2, WO2021213924, is similarly difficult to find. Yours Truly suspects that these other patent documents and information were “subsumed” into WO2021213945A1.

Yours Truly found listed in the above document, among many other items:

One: That BNT162b2 targets the “vaccinated” person’s CD 4 and CD8 cells. Please see the screenshot, below, from the International Patent declaration:

Two: That BNT162b2 uses ** either ** N1-Methylpseudouridine, or pseudouridine, or 5-methyl-uridine, to replace the natural Uridine in the “vaccinated” person’s body. Please see the screenshot, below, from the International Patent declaration:

The reason why, in Yours Truly’s opinion, there are THREE different types of “fake” Uridine that can be used in BNT262b2 is because Pfizer-BioNTech wanted to have “maximum leeway” to choose any of these three types for use in various formulations and/or lots of BNT162b2. That’s why the words “in one embodiment” are used throughout the patent document. This “leeway” would also theoretically apply to any “descendant clone” modRNA COVID-19 BTI made by this company.

**** Three: Regarding the Kammerer, et al., paper: These researchers used “Sequence ID 16” (SEQ ID 16) in the BNT162b2 International Patent declaration as the basis for their tests and assays regarding the presence of “loose” DNA and the presence of the SV40 African Green Monkey cancer promoter-enhancer gene code piece. Below is a screenshot of the mention of this sequence, and the BNT162b2 patent that was used, by Kammerer, et al.

Yours Truly read through the patent document and found the only area that appears to match SEQ ID 16. A screenshot of this, from the patent document, is below:

From here, Yours Truly found a long list of the actual spike protein gene codes (S protein) in SEQ ID 16. This sequence begins with “hAg-Kozak“, which is important as regards “loose” DNA and the SV40 cancer promoter gene piece code. Please see the screenshot of the hAg-Kozak code, followed by a portion of the spike protein codes, below:

The hAg-Kozak codes are a kind of nucleic acid “pattern” that functions as a “protein initiation site” in mRNA applications (paraphrased from the hAg-Kozak entry at Wikipedia.)

Finally, a screenshot follows of the FI element and Poly-A tail gene codes in SEQ ID 16:

Recall that the Poly-A tail is the “signal” for the SV40 cancer promoter gene code piece in the McKernan paper, cited above.

Our gracious host, Wolf Moon, points out that the FI element is this, per the link here: https://assets.publishing.service.gov.uk/media/65e702542f2b3bd5107cd85f/FOI_22-1116_-_attachment.pdf:

FI element (nucleotides 3864 to 4158): The 3′-UTR is a combination of two sequence elements derived from the “amino terminal enhancer of split” (AES) mRNA (called F) and the mitochondrial encoded 12S ribosomal RNA (called I). These were identified by an ex vivo selection process for sequences that confer RNA stability and augment total protein expression9

Wolf Moon continues: “So basically these are gene sequences that were found to work well as linkers which enhance production of the desired target (the spike protein), and are thus tacked onto the sequence for the spike. IMO they are a lot like the SV40 sequence for DNA, but they work at the mRNA level.”

Further discussion of the TWO separate SV40 cancer promoter elements in BNT162b2 are found in another item cited by the Kammerer, et al., paper: https://anandamide.substack.com/p/pfizer-and-moderna-bivalent-vaccines, “Pfizer and Moderna bivalent vaccines contain 20 – 35% expression vector and are transformation competent in E. coli”, 8 March 2023. A screenshot of their assessment of the SV40 cancer promoter and “signal” placements in BNT162b2 is below:

In Yours Truly’s opinion: What we have here was / is NOT a case of Pfizer-BioNTech saying, “Oops, forgot to remove the loose DNA from BNT162b2 before it was / is put into the vials”; NOR was it / is it, a case of, “Oops, forgot to remove the SV40 elements from the product before it was / is put into the vials.” Instead, it is deliberate inclusion of BOTH the “loose” DNA AND of the SV40 African Green Monkey cancer promoter-enhancer gene code piece into BNT162b2. It says it right there in the International Patent declaration for BNT162b2, the SEQ ID 16 listings. Since BNT162b2 is the basis for the “descendant clone” COVID-19 modRNA BTI by this company, plus the fact that all of these products are manufactured using the “Process 2” method (“marinating” the ingredients of the injectable in E. coli), Yours Truly will posit that it can be assumed that “loose” DNA and the SV40 promoter-enhancer gene codes are present in these “descendant clone” injectables, even if they are present in lesser amounts.

For more information regarding the “shedding” of modRNA COVID-19 BTI, please see: www.theqtree.com/2024/03/25/the-elephant-in-the-room-shedding-of-both-the-covid-19-virus-itself-and-the-covid-19-vaccines/.

For more information on the Process 2 manufacturing method that Pfizer-BioNTech and Moderna use to produce BNT162b2 and mRNA-1273 respectively (and their respective “descendant clone” modRNA COVID-19 BTI), please see: www.theqtree.com/2023/11/06/the-infamous-process-2-manufacturing-method-for-the-pfizer-biontech-moderna-covid-19-vaccines/.

IT IS TIME TO STOP ALL USE OF BNT162b2 (COMIRNATY), OF mRNA-1273 (SPIKEVAX), AND THEIR “2024-2025 FORMULA COVID-19 VACCINES” IMMEDIATELY.

THERE. MUST. BE. JUSTICE.

Peace, Good Energy, Respect: PAVACA

Health Friday 10.18.2024: Special Edition: Neurological Effects of the COVID-19 “Vaccines”– Physical and Psychological

The above word-cloud image about memory loss is courtesy of Google Images.

This post is part of Health Friday, a series devoted to Big Pharma, vaccines, general health, and associated topics. Today’s offering, a Special Edition, is in honor of Yours Truly’s “fully vaccinated and boosted” brother, who was just diagnosed with “sudden-onset dementia.” Yours Truly will make it clear that one is not a medical doctor; one is not treating my brother; and, this post is a “narrative primer” on negative neurological effects from the COVID-19 “vaccines”, the Pfizer-BioNTech COMIRNATY (BNT162b2) modRNA COVID-19 “vaccine” in particular.

There are Important Wolf Moon Notifications; the Rules of our late, good Wheatie; and, certain extra items that readers should be familiar with. They are all linked here.

For purposes of today’s post, the trail begins here: https://mole.substack.com/p/who-monkey-pox-is-side-effect-of-covid/comments, “WHO: Monkeypox Is ‘Side Effect’ of Covid ‘Vaccine'”, 12 October 2024.

The World Health Organization (WHO) has a website, www.vigiaccess.org/, that lists “side effects” reported in persons who took COVID-19 “vaccines.” The Mole article describes how the VigiAccess search was performed to find “Monkeypox” as a “side effect” of the Pfizer-BioNTech COVID-19 “vaccine”, BNT162b2. A screenshot of the search protocol is below:

Yours Truly performed a VigiAccess search for reported memory problems (dementia is considered to be a form of “memory impairment.”) This is what I did:

Went to www.vigiaccess.com/

Clicked on “Search database”

Typed “BioNTech” into the Search box

Clicked on “Pfizer BioNTech COVID-19 Vaccine” on the list that came up

Clicked “OK” on the “Dialog” box

Under “Reported potential side effects”, I clicked on “Nervous system disorders” — and found a long list. A screenshot of a portion of this list shows “Memory impairment”:

These are only the reported cases of conditions that are considered to be “side effects” of BNT162b2. It can be argued that there are many multiples more “side effects” cases from BNT162b2 that are not reported for some reason. Yours Truly also performed searches on the VigiAccess list under “Psychiatric disorders”, and under “Metabolism and nutrition disorders”, as certain other details were given to one in phone conversations related to the situation which raised interest.

The balance of today’s post will be presented in a “quasi-scientific paper” form. With the exceptions of some in-line references, scientific paper, blog and/or article citations will be numbered in the text with [“number”], and listed at the end of the post. Hypotheses and opinions of Yours Truly (H/O) will be delineated by Bold text with Italics. A General Summary will be included at the end of the post.

First: A Short Narrative Summary of What Occurs When a Person is Injected with the Pfizer-BioNTech modRNA “Vaccine” COMIRNATY: The “vaccine” here is the 2024-2025 Formula COMIRNATY COVID-19 “vaccine” (which, by the way, contains elements of BNT162b2, the original Pfizer-BioNTech modRNA COVID-19 “vaccine.”) Each “vaccine” dose is either supplied in a single-dose vial, with the dose to be administered withdrawn for injection; or, is in a pre-filled syringe ready for administration. (H/O) Upon “vaccination”, the person’s body immediately sends an “enemy detected” signal to the brain. The person’s body may react from fainting to chills to nausea, among other physical responses: see Sections 5.1 and 5.2 of the COMIRNATY 2024-2025 Fact Sheet, below [1]:

The lipid nanoparticles in the “vaccine” quickly begin to spread the contents of the injection throughout the “vaccinated” person’s body. This process is called biodistribution. Images of page 7 and page 8 of the January 2021 Pfizer-BioNTech Pharmacokinetics Tabulated Summary of the company’s modRNA COVID-19 “vaccine”, BNT162b2, are below [2]. Yours Truly will again emphasize that BNT162b2 is the basis for all of the Pfizer-BioNTech modRNA COVID-19 “vaccines”, including the COMIRNATY 2024-2025 Formula.

Note the accumulations in the Brain, the Liver, and the Large Intestine.

Note the accumulations in the Pituitary Gland, the Thymus Gland, and the Small Intestine. The intestines produce 90% of the body’s Serotonin. Serotonin is a neurotransmitter that is involved in the emotional / psychological / cognitive processes of the brain (per Wikipedia.)

Why is there accumulation of BNT162b2 in the Pituitary Gland? This small organ, called the “master gland” of the body, produces or directs many important hormones. Together with the hypothalamus, the pituitary gland work together to serve as the “brain’s central command center to control vital bodily functions”, according to Yours Truly’s online search at the Cleveland Clinic. These functions include breathing, stress response, reproduction, blood pressure, and more. (H/O): BNT162b2 and/or COMIRNATY is a “vaccine” to supposedly “prevent” a COVID-19 virus infection, not to work like a sort of pituitary gland treatment vehicle.

At least one of the lipid nanoparticles (LNPs) in COMIRNATY, ALC-0159 (but listed under its chemical component name), affects the thymus gland of the “vaccinated” person’s body. The thymus gland is “the primary lymphoid organ of the immune system” (per Wikipedia). The Abstract of a paper [3] that explains how ALC-0159 and other PEG-based LNPs work in the body is below:

While the lipid nanoparticles (LNPs) in COMIRNATY are spreading the ingredients of this “vaccine” throughout the “vaccinated” person’s body, the “vaccine” is using the PRRARSV “backdoor key” (an element which is only in the SARS-CoV-2 virus; and therefore, by extension, the modRNA COVID-19 “vaccines”) to facilitate entry of the “vaccine” ingredients into every cell in the “vaccinated” person’s body [4},[5]. (H/O) At the same time, the ingredients and mechanisms of COMIRNATY (BNT162b2) are beginning to work on inducing accelerated aging in the “vaccinated” person’s body, all the way down to the mitochondrial level [6]. Dao-Fu Dai, et al., wrote a paper in 2014 on how oxidative stress affects the mitochondria and the aging process [7].

N1-Methylpseudouridine is present in all versions of COMIRNATY (BNT162b2), starting with the “original version” of this “vaccine”, BNT162b2. N1-Methylpseudouridine is a synthetic form of Uridine. Uridine is an important nucleoside for neurological processes, for the central nervous system, and other body processes. It is found only in RNA. Below is the Abstract of the Yueyuan Yang, et al., paper that the mechanism of Uridine in the body [8]:

The importance of Uridine cannot be minimized. This RNA element is produced in the Liver. Uridine helps to regulate mood; it also assists in the release of dopamine in the brain. Dopamine is a neurotransmitter that “affects emotions, behavior, and movement” (per WebMD.)

The purpose of N1-Methylpseudouridine in COMIRNATY is twofold: One, to “supersede” / “overwrite” the mechanisms of the natural Uridine in the “vaccinated” person’s body; and, Two, to enhance the mechanism of COMIRNATY in “mRNA switches in cells” of the “vaccinated” person’s body (Callum JC Parr, et al.) [9]. Below is the Abstract of this paper:

Yours Truly will blow the lid off the deliberate inclusion of N1-Methylpseudouridine in BNT162b2 (COMIRNATY.) This chemical was specifically added to the “vaccine” to replace the processes of natural Uridine; and, to evade the body’s natural immune system’s “enemy detection and elimination” elements and mechanisms. Below are screenshots from the Global Patent for BNT162b2, 28 October 2021 [10}:

Note that this appears to be a tacit admission that Gain-of-Function experiments were performed to create the modRNA in BNT162b2.

Note that this appears to be an admission that self-amplifying RNA (saRNA) can be used in Pfizer-BioNTech COVID-19 “vaccines.”

In addition to the “replacing” of uridine with N1-Methylspeudouridine in the body of the person “vaccinated” with COMIRNATY, the DNA of that person’s body is also being changed; please see Slide 14 of this article for a graphic of how the modRNA COVID-19 “vaccines” change the DNA.

Meanwhile, the newly-COMIRNATY-“vaccinated” person’s body, having “detected” an “enemy within the gates” (the “vaccine”), is sending out “all-out effort” signals to the body’s natural immune system to manufacture large amounts of cells to “fight off” the “detected enemy.” These natural immune system cells include CD4 cells, CD8 cells, IgG3 cells, and lymphocytes. However, the ingredients and mechanisms of the “vaccine” hamper, damage, and/literally destroy these natural immune system cells, via the “class switch” [11]; while, at the same time, inducing oxidative stress and cell death at the mitochondrial level all over within the “vaccinated” person’s body; and, also, inducing a state (of a still-unknown timeframe) of “faux SARS-CoV-2 infection” in the “vaccinated” person’s body [12]. A screenshot from this University of Maryland Medical System is below; note the last sentence:

The “rationale” behind the development and use of the modRNA COVID-19 “vaccines” is that the human body is not capable, of itself, to detect and “fight off” an infection by the SARS-CoV-2 virus; the body must have “assistance” in the form of the modRNA COVID-19 “vaccines” and their mechanisms. (H/O) However, it can be fairly argued that, given the multiple Adverse Events reports regarding COMIRNATY to VAERS and to VigiAccess, that this “vaccines” needs much more thorough R&D processes, testing on lab animals and then on humans, and extensive data collection and analyses, before this “rationale” can be fully proven. Pfizer-BioNTech rushed BNT162b2 into production, into securing the initial Emergency Use Authorization from the FDA in December 2020, and into this modRNA COVID-19 “vaccine” being used on the general public, before any of the above were fully undertaken. Pfizer-BioNTech and the FDA knew, back in April 2021, that BNT62b2 could, and did, cause hundreds of serious Adverse Events [13].

Second: Physical Neurological Effects of the COVID-19 “Vaccines”: These negative effects are somewhat “easier” to identify, as they can present with unmistakable symptoms. From the Appendix 1. List of Adverse Events of Special Interest in the 5.3.6 Cumulative Analysis document on BNT162b2 that was cited above, some examples: Page 2: Brain stem embolism; Brain stem mycoplasmal (encephalitis); Central nervous system lupus; Cerebellar artery thrombosis; Cerebral venous thrombosis. Page 3: Demyelination; Embolic stroke; Encephalitis autoimmune; Encephalitis post-immunisation. Page 4: Epilepsy; Epileptic psychosis; Grey matter heterotopia; Guillain-Barre syndrome. Page 5: IIIrd nerve paralysis; Immune-mediated encephalitis; IVth nerve paresis. Page 6: Meningitis; Multiple sclerosis; Neuritis; Neuromyelitis optica spectrum disorder; Neuropsychiatric lupus. Page 9: Thrombotic stroke; XIth nerve paralysis.

Bell’s Palsy is also reported after BNT162b2 “vaccination” [14].

In other words, COMIRNATY (and BNT162b2) damage multiple mechanisms and processes of the brain that result in physical medical conditions and/or illnesses. This “vaccine” damages the sheath coverings of the nerves, including of the spinal cord (Demyelination.) This “vaccine” causes brain inflammations of various types (Encephalitis.) This “vaccine” causes stroke. This “vaccine” causes nerve paralysis. And more. (H/O) This “vaccine” can also potentially aggravate existing physical neurological conditions and/or illnesses, including ones that were under control before the patient was COVID-19 vaccinated.”

There is also what may be considered a “hybrid” condition, since it involves both physical and psychological symptoms, and since can be brought on by either an infection by the COVID-19 virus itself, or by COVID-19 “vaccination”: Long COVID (also called Long Vax.) Long COVID appears to be an “overraction of the immune system” [15]. Physical symptoms include blood pressure swings, fatigue, and “brain fog.” Psychological symptoms include depression, anxiety, and even PTSD [16]. The FLCCC Alliance has articles on Long COVID / Long Vax.

Third: Psychological Effects of the COVID-19 “Vaccines”: The Blood-Brain Barrier (BBB) consists of “closely-spaced cells” that act as a protective barrier to keep many substances from reaching the brain. Below is the National Cancer Institute definition of the Blood-Brain Barrier [17]:

However, COMIRNATY (and the BNT162b2 before it) were specifically developed to cross the Blood-Brain Barrier and to damage glial cells of the brain, down to the mitochondrial level [18]. A screenshot of section 4. Conclusions of this paper is below:

Recall that COMIRNATY (and the BNT162b2 before it) contain the lipid nanoparticle, ALC-0159. This lipid nanoparticle, one of the four within the “vaccine”, assists in the spread of the “vaccine” to all areas of the “vaccinated” person’s body, including into the brain.

Does the crossing of the Blood-Brain Barrier by COMIRNATY (and the BNT162b2 before it) also affect the psychological processes of the brain? The answer is, Yes: and, most likely, via the use of the N1-Methylpseudouridine in this “vaccine.” Recall that natural uridine, (which is one of the nucleosides that make up the RNA of the body) is produced by the liver. Uridine influences the brain by assisting in regulating mood, behavior, movement, and more. N1-Methylpseudouridine was deliberately included in COMIRNATY (and the BNT162b2 before it) to replace the natural uridine in the “vaccinated” person’s body with a created “faux uridine” (see the screenshots from the BNT162b2 Global Patent document, above in the post.) This chemical was chosen because it was “more effective” than the other two chemicals listed in the Global Patent documentation screenshot above in the post.

The Roh, et al., paper of 28 May 2024 traced a potential association between COVID-19 “vaccination” and the onset of Alzheimer’s disease (AD) and also of Mild Cognitive Impairment (MCI) [19]. A screenshot from this paper is below:

While there is not yet a proven association between MCI and the onset of dementia, the potential is higher for onset of dementia in persons who have MCI [20].

At the same time, there is documented proof that COVID-19 “vaccination” can cause psychosis. Examples of papers published on this topic are: the “Aljeshi paper” [21]; the “Borodina, et al., paper” [22];, the “Lazarevna, et al.” paper [23]; the “Morz paper” [24]; and, the “Laxmi and Grover paper” (psychosis diagnosed months after COVID-19 “vaccination” [25].

Yours Truly will again emphasize that one is not a medical doctor; nor am I treating my brother. (H/O) However, I believe there is sufficient evidence to at least consider the possibility that COMIRNATY (BNT162b2) modRNA COVID-19 “vaccinated” persons are at risk of numerous negative effects to the brain, both physical and psychological, induced by this “vaccine”; AND, since it is unknown exactly how long the elements and mechanisms of COMIRNATY (BNT162b2) work in the “vaccinated” person’s body, the possibility also exists that the potential for any physical or psychological neurological negative effects from this “vaccine” may actually increase with additional injections of COMIRNATY (BNT162b2.)

General Summary: One: The Pfizer-BioNTech modRNA COVID-19 “vaccine” COMIRNATY (and, the company’s modRNA COVID-19 “vaccine” BNT162b2 before it) can induce multiple negative physical and psychological neurological side effects and/or Adverse Events conditions in persons who take these “vaccines.” Two: COMIRNATY (and BNT162b2) contain dangerous lipid nanoparticles, among them, ALC-0159, which quickly spread the ingredients of this “vaccine” throughout the “vaccinated” person’s body, including to the brain, the intestines, and the pituitary gland. Three: COMIRNATY (and BNT162b2) contain the lab-created chemical, N1-Methylpseudouridine, which replaces the natural Uridine in the “vaccinated” person’s RNA. Four: Pfizer-BioNTech included N1-Methylpseudouridine in the formulation COMIRNATY (and BNT162b2) and stated this in the company’s Global Patent documentation for this “vaccine.” Five: Pfizer-BioNTech tacitly admitted that Gain-of-Function experiments were performed in the development of BNT162b2, per the Global Patent documentation for this “vaccine.” Six: Pfizer-BioNTech admitted that self-amplifying RNA (saRNA) can be used in COVID-19 “vaccines”, per the Global Patent documentation for this “vaccine.”

In addition, the following may be of interest: One: A blog article by Alex Swanson, M.S., on uridine, 30 November 2020; and, Two: The FLCCC protocol on recovering from COVID-19 “vaccination.”

The list of citations follows. Peace, Good Energy, Respect: PAVACA

[1] www.fda.gov/media/151707/download, Full Prescribing Information for COMIRNATYR (COVID-19 Vaccine, mRNA) suspension for injection, for intramuscular use 2024-2025 Formula

[2] https://icandecide.org/wp-content/uploads/2022/03/125742_S1_M2_26_pharmkin-tabulated-summary.pdf, BNT162b2 2.6.5 Pharmacokinetics Tabulated Summary, FDA-time stamped 21 January 2021

[3] https://doi.org/10.1038/s41541-023-00788-z, Polyethylene glycol (PEG)-associated immune responses triggered by clinically relevant lipid nanoparticles in rats, Haiyang Wang, et al., 2 Nov. 2023

[4] www.thailandmedical.news/news/breaking-u-s-nih-study-finds-that-sars-cov-2-spike-proteins-and-mrnas-can-translocate-into-the-nucleus-of-host-cells-unlike-any-other-coronaviruses, 1 Oct. 2022

[5] https://doi.org/10.1101/2022.09.27.509633, Nuclear translocation of spike mRNA and protein is a novel pathogenic feature of SARS-CoV-2, Sarah Sattar, et al., 27 Sept. 2022

[6] www.theqtree.com/2023/10/28/the-covid-19-virus-and-the-modrna-covid-19-vaccines-induce-accelerated-aging/

[7] https://doi.org/10.1186/2046-2395-3-6, Mitochondrial oxidative stress in aging and healthspan, Dao-Fu Dai, et al., 2014

[8] www.ncbi.nlm.nih.gov/pmc/articles/PMC10937367/, Uridine and its role in metabolic diseases, tumors, and neurodegenerative diseases, Yueyuan Yang, et al., 29 Feb. 2024

[9] https://pubmed.ncbi.nlm.nih.gov/32090264/, N1-Methylpseudouridine substitution enhances the performance of synthetic mRNA switches in cells, Callum JC Parr, et al., 6 Apr. 2020

[10] https://patents.google.com/WO2021213945A1/en, CORONAVIRUS VACCINE Global Patent document, 28 Oct. 2021

[11] https://jessicar.substack.com/p/igg4-cd4s-and-why-the-lnp-mrna-platform, IgG4s, CD4s and why the LNP/mRNA platform should be prohibited, 14 Aug. 2023

[12] www.umms.org/coronavirus/covid-vaccine/mrna, Understanding the COVID Vaccine and mRNA, 30 Sept. 2022 (NOTE: This link no longer works as of 17 October 2024. There is a new link: www.umms.org/health-services/covid-19/about-the-vaccines.)

[13] www.phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf, BNT162b2 5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports; please see Appendix 1. List of Adverse Events of Special Interest. FDA time stamped 30 Apr. 2021

[14] https://doi.org/10.1016/S1473-3099(21)00451-5, Bell’s palsy following vaccination with mRNA (BNT162b2) and inactivated (CoronaVac) SARS-CoV-2 vaccines: a case series and nested case-control study, Eric Yuk Fai Wan, PhD, et al. 16 Aug. 2021

[15] www.science.org/content/article/rare-link-between-coronavirus-vaccines-and-long-covid-illness-starts-gain-acceptance, Gretchen Vogel and Jennifer Couzin-Frankel, 3 July 2023

[16] www.nhsinform.scot/long-term-effects-of-covid-19-long-covid/about-long-covid/signs-and-symptoms-of-long-covid/

[17] www.cancer.gov/publications/dictionaries/cancer-terms/def/blood-brain-barrier

[18] https://doi.org/10.1101/2022.03.02.482639, Decoding COVID-19 mRNA Vaccine Immunometabolism in Central Nervous System: human brain normal glial and glioma cells by Raman imaging, H. Abramczyk, et al., 2 Mar. 2022

[19] https://doi.org/10.1093/qjmed/hcae103, A potential association between COVID-19 vaccination and development of alzheimer’s disease, Jee Hoon Roh, et al., 28 May 2024

[20] www.alz.org/alzheimers-dementia/what-is-dementia/related_conditions/mild-cognitive-impairment

[21] www.psychiatrist.com/pcc/psychosis-associated-covid-19-vaccination/, Abdulsamad A. Aljeshi, et al. Case report and disucssion, read-only, 17 Feb. 2022

[22] https://doi.org/10.24869/psyd.2022.377, First Episode of Psychosis Following the COVID-19 Vaccination – A Case Series, Tonka Borodina, et al., 18 May 2022

[23] https://doi.org/10.3389/fpsyt.2024.1360338, New-onset psychosis following COVID-19 vaccination: a systematic review, Marija Lazarevna, et al., 11 Apr. 2024

[24] https://doi.org/10.3390/vaccines10101651, A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against COVID-19, Michael Morz, 1 Oct. 2022

[25] https://doi.org/10.4103/indianjpsychiatry.indianjpsychiatry_607_22, Unmasking of schizophrenia following COVID-19 vaccination, Laxmi, Raj; Grover, Sandeep, Mar. 2023

Big Pharma – Government – University Collusion on COVID Vaccines

Newly Uncovered COVID Vaccine Contracts Lead Unexpectedly to Academic Corruption and Shill Science Attacks on Honest, Skeptical Scientists

A Gail Combs deep dive into a tangent of Karen Kingston’s latest revelation on Pfizer Comirnaty vaccine deaths and injuries, leads back to the war against truth-telling doctors and scientists – this time by their own CORRUPT university employers.

PREFACE by Wolf Moon

Remember people saying that there was no such thing as the “FDA-approved” Comirnaty version of the Pfizer vaccine in existence?

Well, it turns out that REAL, LIVE COMIRNATY is out there, it has already killed over 50 people [in VAERS – yeah – do the math – x20 (1000), x40 (2000), or x100 (5000)], and – now even more shocking – there was some kind of bureaucratic screw-up in the contract and approval process which makes Pfizer LIABLE for all the deaths and injuries.

Look – I don’t know about the latter part – that’s “the law”, which is basically filled with LIES at this point. Whether any of these people will ever answer for anything is highly debatable, in my opinion.

But that’s not where this goes.

Gail Combs started looking at this video, and discovered ANOTHER scandal – the fact that universities which are silencing and firing honest doctors and scientists are not doing so from some misperception or moral high ground. These universities are turning on honest doctors and scientists because the universities themselves are COMPROMISED – by money, corruption, and the involvement of OTHER scientists at those same universities in the “scamdemic”.

We don’t yet know how deep this goes, but we do know this – the universities are clearly in cover-up mode. It’s not just limited to the vaccines. Fauci’s horrifying executioner remdesivir was forwarded past Trump, thanks to “work” done at one such university.

Follow along with Gail and you’ll see the SHAME of what has happened to many American universities, once bastions of free thinking and HONESTY – now CORRUPT and enemies of TRUTH.

-Wolf

START HERE….

FDA Broke Pfizer’s EUA Shield: Liability Protection Gone, Time To Bring Down The Gavel (10 minutes)

Stew Peters Show, Published January 26, 2022

LINK: https://www.redvoicemedia.com/2022/01/fda-broke-pfizers-eua-shield-liability-protection-gone-time-to-bring-down-the-gavel/

LINK: https://rumble.com/vtcugv-fda-broke-pfizers-eua-shield-liability-protection-gone-time-to-bring-down-t.html

Stew Peters interviews former Pfizer employee and analyst Karen Kingston, who does deep dives into patents and contracts. She found the three major contracts for Moderna, J&J and Pfizer.

Stew: “Karen says she found contracts showing the DOD was in control of what data went to the FDA from vaccine trials. If that is true, then DOD not Big Pharm, was the central figure in any vaccine cover-up…. Military leaders maybe exposed as well…. When the FDA approved the Pfizer vax under the name Cormirnaty, it somehow broke their immunity shield.”

That is not exactly correct. DOD delegated it to Pfizer. With the Pfizer contract with the US Army, it appears that, it was delegated to Pfizer to have the ability to manipulate the data that was submitted to the FDA.

With the Moderna contract for example it shows HHS [US Dept of Health & Human Services] had the authority to manipulate the data that was submitted to the FDA. The contract date is 4/03/2020 for ½ billion $$$ with NIH subsidizing a lot of the contract. It was for producing 100 million mRNA vaccines. The contract (shown) states:

* Contractor shall submit draft FDA submission to BARDA at least 15 days prior to FDA submission

* BARDA will provide feedback to Contractor within 10 days of receipts

* The Contractor MUST address, in writing its consideration of all concerns raised by BARDA prior to FDA Submission.

NOTICE THE DATE 4/03/202. No wonder they wanted to kill HCQ in April!

April 7, 2020 Trump’s Critics Attack His Optimistic Case for Hydroxychloroquine

Karen goes on to say that the contract says that BARDA can provide EDITS to the Data and THAT gets submitted to the FDA. She has never seen anything like this before. This [editing] is why the data was so phenomenally positive. This explains why the Whistle Blowers at Ron Johnson’s Formun found the DOD data had been ‘edited’ to remove the tons of adverse events.

She also said a lot of that contract is redacted including the Key personnel at BARDA .

The J&J contract of an mRNA vaccine was signed 08-Apr-2015 and 60 out of the 90 pages are redacted.

She then goes into the most recent contract. It is a joint mission of Dept of Defense and Dept of Health & Human services who contract with Pfizer/BoiNTech “for the co-development and distribution (excluding China) of a potential mRNA-based Coronavirus vaccine aimed at preventing Covid-19 infection“….. LOTS OF REDACTION….

The Research Collaboration & License Agreement
by and between
PFIZER INC.
and
BIONTECH RNA PHARMACEUTICALS GmbH [Germany]
and
BIOTECH AG
July 20, 2018

Again the DATE July 20 2018 shows mRNA vaccines for the next outbreak of Covid WAS A DONE DEAL!

@5:00 Karen EXPLAINS the OOPS in the Contract. You can not have a contract for commercialization WITHOUT A FDA APPROVAL DATE!!! So how in Hades did they KNOW there would be FDA APPROVAL? This shows it was PRE-PLANNED IN 2018.

@7:00 She also found the Cormirnaty lots used in the USA and the VAERs data

LOT NUMBERS

FD7220
FE3592
FF2587
FF2588
FF2590
FF2593
FF8841

VAERS Dec 2021
Deaths = 51
Disabilities = 94
Hospitalizations 415

So who is BARDA?

Biomedical Advanced Research and Development Authority (BARDA)

WE ARE BARDA

The Biomedical Advanced Research and Development Authority (BARDA), within the Office of the Assistant Secretary for Preparedness and Response in the U.S. Department of Health and Human Services, provides an integrated, systematic approach to the development of the necessary vaccines, drugs, therapies, and diagnostic tools for public health medical emergencies such as chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks, pandemic influenza, and emerging infectious diseases.

Together with our industry partners, BARDA promotes the advanced development of medical countermeasures to protect Americans and respond to 21st century health security threats.


About NIH | National Institutes of Health (NIH)

A part of the U.S. Department of Health and Human Services, NIH is the largest biomedical research agency in the world

So there is your Fauci connection.

And that brings me to the digging I have been doing.

I start with the Chair of the COVID VACCINE ADVISORY BOARD, Hana El Sahly, M.D. of Baylor College of Medicine. She is the one who wrote the Remdesivir paper for Fauci, just in the nick of time so he could get that toxin approved for the use in hospitalized elderly Covid patients.

Baylor College rang a major bell with me. This Yahoo News articles shows why:

August 2, 2021

Dr. Peter McCullough Sued by Baylor After Appearance on Stew Peters Show…

Dr. Peter McCullough is being sued by the healthcare system that just mandated 40,000 employees to get the jab, and they’re doing it out of spite. Here’s the list of emails to those targeting him, if you wish to let them know how you feel….

I dare anybody to watch this and find anything wrong with anything that Peter McCullough is saying. He is basically admitting – at a time when social media was still removing people for saying as much – that the vaccines seemed to no longer be working. And NOW we know why – because of the delta variant.

LINK: https://www.redvoicemedia.com/2021/08/stew-peters-show-dr-peter-mccullough-destroys-vaxx-efficacy-narrative-united-pilots-file-suit-to-stop-mandate/

LINK: https://rumble.com/vlblnr-dr.-peter-mccullough-destroys-vaxx-efficacy-narrative-united-pilots-file-su.html


Dec 20 2021

Doctor fired for spreading COVID misinformation finds supportive Crowd in Bartlesville.

Dr. Peter McCullough, a Dallas cardiologist who is largely discredited by the scientific community [Remember Dr McCullough is the MOST PUBLISHED AUTHOR OF SCIENTIFIC PAPERS IN THE USA.] for his assertions that the COVID-19 vaccines are unsafe and that early treatment options have been suppressed….

While McCullough said that doctors were probably afraid to show up to the event, one of Oklahoma’s top infectious disease physicians, Dr. Anuj Malik, director of infection prevention and control at Ascension St. John, said that the doctors he spoke to were not afraid to attend. They were just not interested in sitting through what would be seen as a “politically-motivated, ideological speech by a modern-day quack.”

Malik said. “With all due respect, none of McCullough’s ideas have been supported by any randomized, double-blind, controlled clinical trials,” [<=== THIS IS ALWAYS THE EXCUSE! NO data is allowed except that PAID FOR BY BIG PHARMA/NIH.]

McCullough shared what he said was a threatening letter from the American Board of Internal Medicine warning that he could lose his certification for spreading misinformation.
There is likely a good reason for his concern about losing certification. A Dallas County court granted a temporary restraining order against him in July on behalf of Baylor Scott & White Health for continuing to claim titles, including vice chief of internal medicine at Baylor University Medical Center, even after he was fired from Baylor in February.
In addition, an article in Medscape, an online global news source for physicians and healthcare professionals, reported that Texas A&M College of Medicine, Texas Christian University and University of North Texas Health Science Center School of Medicine have also cut ties with McCullough for spreading misinformation….

>

So the Baylor Connection made me curious.

And looky what I found! No wonder Baylor sued Dr McCollough in the hopes of shutting him up as they entice people to be lab rats!

June 8, 2021

Baylor launches clinical trial for COVID-19 vaccine booster


Researchers at the Vaccine and Treatment Evaluation Unit at Baylor College of Medicine have launched a clinical trial to study the safety and efficacy of a booster dose of the Moderna-mRNA-1273 COVID-19 vaccine…. The study is being conducted by the Infectious Disease Clinical Research Consortium in collaboration with the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health…. “It’s important to determine the magnitude of the immune response after a booster dose in persons who received different vaccines in their initial vaccine regimen. We will also be looking at the safety of a booster dose,” said Dr. Robert Atmar, professor of infectious diseases at Baylor and co-principal investigator of the national study.

This activity is supported by the Infectious Diseases Clinical Research Consortium (IDCRC) through the National Institute of Allergy and Infectious Diseases (NIAID) (UM1AI148684). The IDCRC, consisting of the Vaccine Treatment and Evaluation Units (VTEUs) and the IDCRC Leadership Group, was formed in 2019 to support the planning and implementation of infectious diseases clinical research that efficiently addresses the scientific priorities of NIAID.  The consortium includes infectious diseases leaders and clinical researchers from Emory University, University of Maryland School of Medicine, Baylor College of Medicine, Cincinnati Children’s Medical Center and University of Cincinnati, FHI360, Fred Hutchinson Cancer Research Center, Johns Hopkins University, Kaiser Permanente Washington Health Research Institute, New York University, Saint Louis University, Vanderbilt University Medical Center, University of Alabama at Birmingham, University of Rochester, University of Washington, and NIAID. For more information about the IDCRC, please visit www.IDCRC.org.

https://idcrc.org/_includes/images/group_fullv2.jpg

January 21, 2020, Rockville, MD [Above photo]

With presentations from members of the NIAID, the Infectious Diseases Clinical Research Consortium (IDCRC) Leadership Group, and VTEU PIs, the inaugural meeting of the IDCRC began with opening remarks from Anthony Fauci, MD, NIAID director. Session topics featured details on working with the NIAID, the Division of Microbiology and Infectious Diseases, and grants management. Breakout sessions facilitated thoughtful discuss on the consortium’s scientific agenda, flu, STIs, malaria, enteric, and emerging diseases, mentoring and career development, special populations, emerging lab sciences, and operations.

https://idcrc.org/about/index.html

Leadership Operations Center


The IDCRC institutions are leaders of influential infectious diseases, immunology and clinical research programs focused on vaccines and STIs at eight top academic institutions and affiliates across the country. The programs, faculty and collaborators at these institutions have exceptional NIH/NIAID network and international connectivity, a history of performing outstanding ID clinical research and the experience and capability of rapidly responding to ID threats.

Bio Robert Atmar


Dr. Atmar is a member of the Baylor Vaccine Research Center and the federally funded Vaccine Treatment and Evaluation Unit (VTEU). This research group performs Phase I to Phase IV studies of experimental and licensed vaccines, and Dr. Atmar serves as Principal Investigator or Co-Investigator for the clinical trials. Dr. Atmar and the research group have been involved in important studies that led to the licensure of live attenuated and high dose inactivated influenza virus vaccines. They also have performed many studies evaluating vaccines targeting pandemic influenza, including H5N1, H9N2 and H7N9 viruses, and they have evaluated methods to improve vaccine immunogenicity, including delivery of vaccine by different routes of administration, different dosages, and with different adjuvant preparations. The group has also evaluated vaccines targeting other pathogens, including those with importance to biodefense.

2,625 studies found in data base [Baylor College] and 4195 for just Baylor.
24,250 studies – Just college

224,279 studies – University

SEE:
https://clinicaltrials.gov/ct2/results/details?cond=&term=university&cntry=&state=&city=&dist=&Search=Search

>

So is there a Robert Atmar – Hana El Sahly connection???

PubMed(dot)Gov lets you search by author name. So I went looking to see if those two authored papers together.

Search for Atmar R
https://pubmed.ncbi.nlm.nih.gov/?term=Atmar+R&sort=date&size=50

AND WELL WELL WELLL the first two out of the BOX!!!

2022 Jan 26.

SARS-CoV-2 Omicron Variant Neutralization after mRNA-1273 Booster Vaccination.


Pajon R, Doria-Rose NA, Shen X, Schmidt SD, O’Dell S, McDanal C, Feng W, Tong J, Eaton A, Maglinao M, Tang H, Manning KE, Edara VV, Lai L, Ellis M, Moore KM, Floyd K, Foster SL, Posavad CM, Atmar RL, Lyke KE, Zhou T, Wang L, Zhang Y, Gaudinski MR, Black WP, Gordon I, Guech M, Ledgerwood JE, Misasi JN, Widge A, Sullivan NJ, Roberts PC, Beigel JH, Korber B, Baden LR, El Sahly H, Chalkias S, Zhou H, Feng J, Girard B, Das R, Aunins A, Edwards DK, Suthar MS, Mascola JR, Montefiori DC.

N Engl J Med.

And the Affiliations:

• Moderna, Cambridge, MA.
• National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, MD.
• Duke University Medical Center, Durham, NC.
• NIAID, Bethesda, MD.
• Emory University School of Medicine, Atlanta, GA.
• Fred Hutchinson Cancer Research Center, Seattle, WA.
• Baylor College of Medicine, Houston, TX.
• University of Maryland School of Medicine, Baltimore, MD.
• National Institutes of Health, Bethesda, MD.
• Los Alamos National Laboratory, Los Alamos, NM.
• Brigham and Women’s Hospital, Boston, MA.
…..

 2022 Jan 26.

Homologous and Heterologous Covid-19 Booster Vaccinations.

Atmar RL, Lyke KE, Deming ME, Jackson LA, Branche AR, El Sahly HM, Rostad CA, Martin JM, Johnston C, Rupp RE, Mulligan MJ, Brady RC, Frenck RW Jr, Bäcker M, Kottkamp AC, Babu TM, Rajakumar K, Edupuganti S, Dobrzynski D, Coler RN, Posavad CM, Archer JI, Crandon S, Nayak SU, Szydlo D, Zemanek JA, Dominguez Islas CP, Brown ER, Suthar MS, McElrath MJ, McDermott AB, O’Connell SE, Montefiori DC, Eaton A, Neuzil KM, Stephens DS, Roberts PC, Beigel JH; DMID 21-0012 Study Group.N Engl J Med.

Affiliation
• From the Departments of Medicine and Molecular Virology and Microbiology, Baylor College of Medicine, Houston (R.L.A., H.M.E.S.), and Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston (R.E.R.); the Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore (K.E.L., M.E.D., K.M.N.), and the Division of Microbiology and Infectious Diseases (S.C., S.U.N., P.C.R., J.H.B.) and the Vaccine Research Center (A.B.M., S.E.O.), National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda; Kaiser Permanente Washington Health Research Institute (L.A.J.), the Departments of Medicine (C.J., T.M.B., M.J. McElrath) and Laboratory Medicine and Pathology (C.J., C.M.P.), University of Washington, the Vaccine and Infectious Disease Division (C.J., C.M.P., C.P.D.I., E.R.B., M.J. McElrath) and the Statistical Center for HIV/AIDS Research and Prevention (D.S., J.A.Z.), Fred Hutchinson Cancer Research Center, and Seattle Children’s Research Institute (R.N.C.) and the Department of Pediatrics (R.N.C.), University of Washington School of Medicine, Seattle; the Department of Medicine, Division of Infectious Diseases, University of Rochester, Rochester (A.R.B., D.D.), NYU Langone Vaccine Center and Division of Infectious Diseases and Immunology, Department of Medicine, NYU Grossman School of Medicine, New York (M.J. Mulligan, A.C.K.), and NYU Langone Hospital-Long Island Vaccine Center Research Clinic and the Division of Infectious Disease, Department of Medicine, NYU Long Island School of Medicine, Mineola (M.B.) – all in New York; the Departments of Pediatrics (C.A.R.), Microbiology and Immunology (M.S.S.), and Medicine (S.E., D.S.S.), the Center for Childhood Infections and Vaccines (C.A.R.), Hope Clinic of Emory Vaccine Center (S.E.), Emory Vaccine Center, and Yerkes National Primate Research Center (M.S.S.), Emory University School of Medicine, Emory University, and Children’s Healthcare of Atlanta (C.A.R.) – all in Atlanta; the Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh (J.M.M., K.R.); Cincinnati Children’s Hospital Medical Center, Division of Infectious Diseases, University of Cincinnati College of Medicine, Cincinnati (R.C.B., R.W.F.); and FHI 360 (formerly Family Health International) (J.I.A.) and Duke Human Vaccine Institute (D.C.M.) and the Department of Surgery (D.C.M., A.E.), Duke University Medical Center, Durham, NC.

2021 Oct 15

Heterologous SARS-CoV-2 Booster Vaccinations – Preliminary Report.

Authors: Atmar RL,….. El Sahly HM…

EPub 2021 Sept 22
Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase.

El Sahly HM, … COVE Study Group. N Engl J Med. 2021 Nov 4….. Epub 2021 Sep 22….

PubMed lists: COVE Study Group [Corporate Author]

COVE STUDY GROUP:

Hana M. El Sahly, MD is principal investigator for Baylor and under her is listed
Jennifer A. Whitaker, C. Mary Healy, Christine Akamine, Wendy A Keitel, Robert L Atmar, Annette Nagel, Sandra Francisco, Thea Marie Cordero, Janet Brown, Jennifer Christensen, Caroline Doughty-Skierski, Connie Rangel, Carrie Kibler, Coni Cheesman, Lisreina Toro, Chanei Henry, Chianti Wade Bowers, Pedro Piedra, Kathy Bosworth, Kayla Burrell, Jesus Banay, Tykel Eddy, Trent Davis, Shetel Anassi, Yvette Rugeley, Olga Rybina-Willis
…..

So what about the OTHER 15 on the ‘Advisory Board’ I checked, none are in the COVE study group.

….

And one last Baylor – Atmar paper:

SARS-CoV-2 Vaccination During Pregnancy: A Complex Decision.

Wang EW, Parchem JG, Atmar RL, Clark EH.Open Forum Infect Dis.

2021 Apr 10

Abstract
As the first severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines passed UK and US regulatory milestones in late 2020 and early 2021, multiple professional societies offered recommendations to assist pregnant and breastfeeding people as they choose whether to undergo vaccination. Despite such guidance, the lack of data describing vaccine safety, immunogenicity, and efficacy in pregnant and breastfeeding people has made this decision challenging for many. However, even considering the paucity of data, the known risks of coronavirus disease 2019 during pregnancy likely outweigh the not yet fully elucidated risks of SARS-CoV-2 vaccines, which have reassuring safety and efficacy profiles among nonpregnant people.

The Chair of the FDA Vaccines and Related Biological Products Advisory Committee is so compromised she should NEVER have been anywhere near the approval process!

-GC

Summary

After viewing the tape of Dr. Peter McCullough on Stew Peters, I’m both shocked and disappointed that Baylor (IMO both the College of Medicine and the allied University) would do anything except DEFEND Dr. McCullough for simply speaking TRUTH when nobody else dared to say it.

At a time when all of social media was defending what now amounts to SCIENTIFIC ERROR, Baylor – a renowned institution – accused a TRUTH-TELLER of “misinformation” for being on the cutting edge.

To borrow from Trump…… “SAD!”

We know now that everything Dr. Peter McCullough said was not only true, but that the science he cited was LEADING EDGE – pointing in the direction of future findings.

It is not “misinformation” to state scientific and medical findings which are both TRUE and in the process of CHANGING narratives. That IS what science is supposed to do.

China won’t have to fire a SHOT to steal academic leadership from the United States, if Baylor – in TEXAS of all places – is going to hand them scientific superiority on a silver platter.

Get the politics and the self-dealing OUT OF YOUR SCIENCE, BAYLOR.

It is a TRAVESTY for you, Baylor, to let your “big money scientists” force out your TRUTH-TELLERS based on POLITICS and motivated by their own SCIENTIFIC MISJUDGMENTS.

W

A Book of Some Importance to Baptists