Posted on 04/12/2021 3:32:12 PM PDT by ransomnote
Dr. Tenpenny has written, “According to the Coronavirus Vaccine Tracker, as of Dec. 26, 2020, 83 vaccines are in Phase 1, 2 or 3 human and animal clinical trials, with 18 approaching the final stages of testing.
Never before have so many companies tested so many different vaccines at the same time, against a virus that has not been isolated. Of those in the trials, five vaccines are now early use, with three vaccines approved for clinical use Pfizer, Moderna and AstraZeneca.”
“Are you willing to be injected with something unknown and never tested before in humans?” she asks.
After all, humans are now the guinea pigs for these injections.
Tenpenny warns that those who have taken the vaccine will begin to become sick and many will die within 3-6 months.
People are perfectly capable of reading and absorbing information without performing the research firsthand; else the very reason for professional journals would not exist.
Dipstick.
There are all kinds of potential issues.
But you’re brushing them under the rug.
https://www.mdpi.com/2076-393X/9/1/36/htm
It is generally thought that the sole function of viral membrane fusion proteins is to allow the viruses to bind to the host cells for the purpose of viral entry into the cells, so that the genetic materials can be released and the viral replication and amplification can take place.
However, recent observations suggest that the SARS-CoV-2 spike protein can by itself trigger cell signaling that can lead to various biological processes. It is reasonable to assume that such events, in some cases, result in the pathogenesis of certain diseases.
Our laboratory only tested the effects of the SARS-CoV-2 spike protein in lung vascular cells and those implicated in the development of PAH. However, this protein may also affect the cells of systemic and coronary vasculatures, eliciting other cardiovascular diseases such as coronary artery disease, systemic hypertension, and stroke. In addition to cardiovascular cells, other cells that express ACE2 have the potential to be affected by the SARS-CoV-2 spike protein, which may cause adverse pathological events.
Thus, it is important to consider the possibility that the SARS-CoV-2 spike protein produced by the new COVID-19 vaccines triggers cell signaling events that promote PAH, other cardiovascular complications, and/or complications in other tissues/organs in certain individuals (Figure 3). We will need to monitor carefully the long-term consequences of COVID-19 vaccines that introduce the spike protein into the human body.
Furthermore, while human data on the possible long-term consequences of spike protein-based COVID-19 vaccines will not be available soon, it is imperative that appropriate experimental animal models are employed as soon as possible to ensure that the SARS-CoV-2 spike protein does not elicit any signs of the pathogenesis of PAH or any other chronic pathological conditions.
Way to misrepresent the hell out of the subject.
Tell me the number of other vaccines which are based on a single protein from the microorganism being vaccinated against.
Over 700 million vaccine dose have been delivered in the world.
700 MILLION!
Yet you’ll believe they were all deadly and no one knows.
700 MILLION.
Sounds to me like the worse advice I've ever heard given on C-19.
On the third day of symptoms, I lost my smell and taste. That to me was confirmation that I likely had C-19. I had seen that a doctor in the area had written a letter to President Trump saying that he was having good results with early treatment of C-19 using the Zelenko Protocol.
I drove two hours to the appointment, the two of us were tested and then we saw the doctor. The next morning after starting treatment (12 hours later), my chest congestion was noticeably better.
Two days later, we both had smell and taste back, basically all symptoms were gone. But even two weeks later, by taking a deep breath there was still discomfort. That took a while to clear up but it is indication that this is nothing to screw around waiting for test results.
So how did the medical profession kill so many people when this can be easily treated in the first few days? The idiots in ER would test people who came in and then send them home to wait results! Yes, they really are that ignorant. In their defense, they were following the recommendations of Fruad Fauci and his co-conspirators who did NOT want the public knowing there are early treatment options.
The last I heard from Dr Tyson he was approaching 5000 patients treated (positive tested C-19 patients) with TWO mortalities. That rate is probably better than the average doctor who has a few thousand flu infected patients.
When Dr Fareed testified in December to the US Senate, YOUTUBE removed the video. The deep state cannot have doctors saying that with early treatment, C-19 can be cured with almost 100% effectiveness with almost all staying home, NOT hospitalized.
The Marine slogan: “Improvise, Adapt, and Overcome” should have been the motto of our physicians in the pandemic.
It certainly wasn’t.
Is you is, or is you ain’t, overlooking something?
The spike protein affects for example the ACE2 receptor.
The ACE2 receptor signals the cell to push out a bunch of inflammatory-signaling proteins.
Riddle me this.
On a single SARS-2 COVID19 virion, how many spikes are there?
Because, ya know, a single virion can only itself attach to, merge with (furin cleavage site on the spike protein), and inject RNA into one cell.
So the rest of the spikes on each virion are *wasted*.
But if you inject a truckload of mRNA into cells, and that mRNA tells each cell to turn out a bunch of individual spike protein units, each individual unit can stimulate another cell’s ACE2 receptor: so the effect in terms of host cell lysis/destruction, the mRNA is not as bad as a real infection, but in terms of cell signaling / inflammatory response, it has the potential to be much worse.
The other element I don’t hear people talking about is antibody-dependent enhancement. This is relevant, because back in the days when the coof was isolated in Wuhan, and hadn’t come to the US, people said ADE had been observed in other (IIRC) coronaviruses, I think maybe including SARS-1; and it was posited that ADE was responsible for the “walk down the street and suddenly fall down dead” seen in Wuhan.
You’d have to dig more details, to find things like which sets of viruses exhibit this side effect, and also whether the effect depends more on antibodies to which specific antigens are on the virus’s surface, but I don’t think it can automatically be dismissed by a curt wave of the hand.
Remind me again of how Pfizer, Moderna, and Astra-Zeneca are doing all this solely at their own expense, assuming all risks including liability for harm, and not charging a penny?
As a virile man of good stock I will do my part to help repopulate the human population.
I didn’t say they are all deadly.
I said the risks haven’t been properly assessed to my satisfaction.
” if you inject a truckload of mRNA into cells, and that mRNA tells each cell to turn out a bunch of individual spike protein units, each individual unit can stimulate another cell’s ACE2 receptor: so the effect in terms of host cell lysis/destruction, the mRNA is not as bad as a real infection, but in terms of cell signaling / inflammatory response, it has the potential to be much worse.”
“Potential”... but no evidence of that “potential” occurring.
But do you even care about evidence?
You’ve postulated something- and have no evidence of it occurring- but do you even care?
That kind of effect is the kind of thing a longer, broader, more carefully performed Phase 1 trial might be able to identify, long before tens to hundreds of millions of doses are administered to all ages, under an EUA for a vaccine which has a vanishingly small fatality rate for people under age 60.
Because you can’t unring a bell.
Troll.
LOL!
Of course anyone who points out your idiocy is a “troll”.
LOL!
Gee, have a high opinion of your idiocy don’t you.
You’re right. D.O.’s aren’t “quacks”. Some of the finest surgeons and anesthesiologist’s I’ve worked with are Osteopathic Doctors.
No, you’re just a troll by second nature.
” no evidence of that “potential” occurring.
But do you even care about evidence?”
LOL!
Of course you don’t. Can’t believe I gave you a chance to defend your lies. I knew you wouldn’t and couldn’t.
But I gave you the opportunity.
You’re a liar.
And a spectacularly unsuccessful troll.
What a self-professed coward!
It’s your cowardice that impresses me, and others, not your dishonesty.
Even more lame.
Maybe you’re sobering up and that’s why you lack even as much as your usual limpidity.
” no evidence of that “potential” occurring.
But do you even care about evidence?”
LOL!
Of course you don’t. Can’t believe I gave you a chance to defend your lies. I knew you wouldn’t and couldn’t.
But I gave you the opportunity.
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