Posted on 05/22/2021 7:56:02 AM PDT by Enterprise
“I personally, this is my own personal opinion, believe it’s the spike protein,” she said. “I believe that there’s billions of spike proteins and it’s a protein that then can last longer. And some people have said they think it’s the messenger RNA. Messenger RNA is pretty unstable. And so I don’t think it would last very long. But if you were having close personal contact with people like a spouse and you were hugging or kissing or having sex with someone or like with the grandchild probably sitting in Grandma or Grandpa’s lap, something is being transmitted that is causing horrible problems and not just bleeding problems.”
She went onto explain that we simply don’t know for sure how it’s being transmitted or even what’s being transmitted. It could even be the 5G theory that many have discussed. Until we know more, it’s best to finally use social distancing for something useful when around vaccinated people.
(Excerpt) Read more at thelibertydaily.com ...
I just don’t know...Do the antibodies show up in the blood?
.
I agree with you on the 5G data.
Not worried at all about this.
Generally, whatever Gov’t/Mainstream media tells me what is to be in my best interest, I take the opposite approach.
Lockdown? No lockdowns
Masks? No Masks
Jabs? No Jabs
I take care of my body, eat healthy, get sunshine, live in a free state “South Dakota” and TRUST my immune system.
Johns Hopkins University confirms that “self-spreading” vaccines are real.
I would think they do. When I went to have a Covid-19 antibodies test, they drew blood for it.
> “Then there’s the American Red Cross refusing to allow COVID19-vaccinated persons to donate blood” <
That’s not strictly true. The Red Cross allows Covid-vaccinated people to donate whole blood and platelets. But not convalescent plasma.
https://www.redcrossblood.org/donate-blood/dlp/coronavirus—covid-19—and-blood-donation.html
Is that a standard, boilerplate admonition? Does that show up in other studies of vaccines or treatments, like radiation therapy or vaccines where the actual virus (dead?) is used?
If it is an accurate quote... Dr. Sherri would have been better off keeping her crazy and unsubstantiated thoughts about 5G to herself. It is not unlike like some people who believe that they are being witty who would be better off counting to ten before they hit the post button. It is very likely that as a a long time senior hazmat officer that I have had ten or more times the number of vaccinations that you have. But I and at approximately half of my former coworkers and subordinates have no intention of taking the experimental Covid “vaccines”. Does that make us “anti-vaxers”?
Even if these shots were 100% safe, I would still refuse it due to the use of aborted baby cell lines.
Satan hit the mother load with these “vaccines” It amazes me how easily people are led to the path of destruction.
None. Stop being so obtuse. YOU made the point that because this women was making money off what she had to say, what she had to say was “tainted” by that money. AND MY ONLY POINT IS YOUR RULE MUST ALSO APPLY TO THE VAX PRODUCERS.
“Very Unreliable”
Yes, she is all over the map. The 2/3 comment was so naive, so uninformed that it really jumped out. She’s all over the map with her comments and, like Biden, wanders all over and frequently starts statements she doesn’t finish. She does not come across as a person who went through medical school.
“That said, I would NEVER get any of the vaccines for it and, as I’ve already HAD the virus, studies are showing that’s as good (better) than the vaccine.”
I remember a time when we did not need a study to understand that surviving a virus was as good or better than a vaccine.
Now they recommend vaccine even if you have recovered from covid. What could our immune system hope to learn from the vaccine that it did not learn from the virus itself?
This whole vaccine push is wrapped in absolute nonsense.
“It could even be the 5G theory that many have discussed.”
This tells you everything you need to know about this so-called expert.
Some people live in a fantasy world of malign conspiracy.
It’s a mental illness.
Forgot to say your post #25 was great, I recommend everyone read it.
The big elephant in the room is exactly what you stated, what shuts down production. I have not heard a good answer.
LOL - liberals do NOT believe in fair play... if they did they would not be liberals...
> Johns Hopkins University confirms that “self-spreading” vaccines are real. <
I found that interesting. So I followed your link to the ‘Tatty Journal’. They cite a Johns Hopkins study, and provide a link to that study. But their link just goes to the Johns Hopkins homepage. It does not go any study!
So I did a quick search. A number of sites talk about this “self-spreading” vaccine topic. And they all reference Johns Hopkins. But none of them link to any Johns Hopkins study. What’s going on here?
I think you have the wrong person.
I never injected money into Tenpenny’s stupidity.
This coherent enough?
From the International Journal of Vaccination Theory, Practice, and Research
https://ijvtpr.com/index.php/IJVTPR/article/view/23/36
-There has been considerable chatter on the Internet about the possibility of vaccinated people causing disease in unvaccinated people in close proximity. While this may seem hard to believe, there is a plausible process by which it could occur through the release of exosomes from dendritic cells in the spleen containing misfolded spike proteins, in complex with other prion reconformed proteins. These exosomescan travel to distant places. It is not impossible to imagine that they are being released from the lungs and inhaled by a nearby person. Extracellular vesicles, including exosomes, have been detected in sputum, mucus, epithelial lining fluid, and bronchoalveolar lavage fluid in association with respiratory diseases (Lucchetti et al., 2021).A Phase 1/2/3 study undertaken by BioNTech on the Pfizer mRNA vaccine implied in their study protocol that they anticipated the possibility of secondary exposure to the vaccine (BioNTech, 2020). The protocol included the requirement that “exposure during pregnancy” should be reported by the study participants. They then gave examples of “environmental exposure during pregnancy” which included exposure “to the study intervention by inhalation or skin contact.” They even suggested two levels of indirect exposure: “A male family member or healthcare provider who has been exposed to the study intervention by inhalation or skin contact then exposes his female partner prior toor around the time of conception.
It’s a PDF ... on page 47
You will have to download the file... publication is from 2018.
Might be interested in this discussion of prion disease. Sorry about the lost formatting.
https://ijvtpr.com/index.php/IJVTPR/article/view/23/36
A Possible Link to Prion Diseases and NeurodegenerationPrion diseases are a collection of neurodegenerative diseases that are induced through the misfolding of important bodily proteins, which form toxic oligomers that eventually precipitate out as fibrils causing widespread damage to neurons. Stanley Prusiner first coined the name `prion’ to describe these misfolded proteins (Prusiner, 1982). The best-known prion disease is MADCOW disease (bovine spongiform encephalopathy), which became an epidemic in European cattle beginning in the 1980s. The CDC web site on prion diseases states that “prion diseases are usually rapidly progressive and always fatal.”(Centers for Disease Control and Prevention, 2018). It is now believed that many neurodegenerative diseases, including Alzheimer’s, Parkinson’s disease, and amyotrophic lateral sclerosis (ALS) may be prion diseases, and researchers have identified specificproteinaceous infectious particles linked to these diseases (Weickenmeier et al., 2019).Furthermore, researchers have identified a signature motif linked to susceptibility to misfolding into toxic oligomers, called the glycine zipper motif. It is characterized by a pattern of two glycine residues spaced by three intervening amino acids, represented as GxxxG. The bovine prion linked to MADCOW has a spectacular sequence of ten GxxxGs in a row (see uniprot.org/uniprot/P10279).More generally, the GxxxG motif is a common feature of transmembrane proteins, and the glycines play an essential role in cross-linking α-helices in the protein (Mueller et al., 2014). Prionproteins become toxic when the α-helices misfold as β-sheets, and the protein is then impaired in its ability to enter the membrane (Prusiner, 1982). Glycines within the glycine zipper transmembrane motifs in the amyloid-β precursor protein (APP) play a central role in the misfolding of amyloid-β linked to Alzheimer’s disease (Decock et al., 2016). APP contains a total of four GxxxG motifs.When considering that the SARS-CoV-2 spike protein is a transmembrane protein, and that it contains fiveGxxxG motifs in its sequence (see uniprot.org/uniprot/P0DTC2), it becomes extremely plausible that it could behave as a prion. One of the GxxxG sequences is present within its membrane fusion domain. Recall that the mRNA vaccines are designed with an altered sequencethat replaces two adjacent amino acids in the fusion domain with a pair of prolines. This is done intentionally in order to force the protein to remain in its open state and make it harder for it to fuse with the membrane. This seems to us like a dangerous step towards misfolding potentially leading to prion disease.A paper published by J. Bart Classen (2021) proposed that the spike protein in the mRNA vaccines could cause prion-like diseases, in part through its ability to bind to many known proteins andinduce their misfolding into potential prions. Idrees and Kumar (2021) have proposed that the spike protein’s S1 component is prone to act as a functional amyloid and form toxic aggregates. These authors wrote that S1 has the ability “to form amyloid and toxic aggregates that can act as seeds to aggregate many of the misfolded brain proteins and can ultimately lead to neurodegeneration.”According to Tetz and Tetz (2020), the form of the spike protein in SARS-CoV-2 has prion regions that are not present inthe spike proteins for other coronaviruses. While this was reported in a non-peer-reviewed article, the authors had published a previous paper in 2018 identifying prion-like regions in multiple eukaryotic viruses, so they have considerable expertise in this area (Tetz and Tetz, 2018).A final point here relates to information about the Pfizer vaccine in particular. The European Medicines Agency (EMA) Public Assessment Report is a document submitted to gain approval to market the vaccine in Europe. It describes in detail a review of the manufacturing process as well as a wide range of associated testing data. One concerning revelation is the presence of “fragmented species” of RNA in the injection solution. These are RNA fragments resulting from early termination of the process of transcription from the DNA template. These fragments, if translated by the cell following injection, would generate incomplete spike proteins, again resulting in altered and unpredictable three-dimensional structure and a physiological impact that is at best neutral and at worst detrimental to cellular functioning. There were considerably more of these fragmented forms of RNA found in the commercially manufactured products than in the products used in clinical trials. The latter wereproduced via a much more tightly controlled manufacturing process.Pfizer claims the RNA fragments “likely... will not result in expressed proteins” due to their assumed rapid degradation within the cell. No data was presented to rule out protein expression, though, leaving the reviewers to comment, “These [fragmented RNA] forms are poorly characterised, and the limited data provided for protein expression do not fully address the uncertainties relating to the risk of translating proteins/peptides other thanthe intended spike protein” (EMA 2020). To our knowledge no data has been forthcoming since that time.While we are not asserting that non-spike proteins generated from fragmented RNA would be misfolded or otherwise pathological, we believe they would at least contribute to the cellular stress that promotes prion-associated conformational changes in the spike protein that is present
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