Posted on 01/06/2022 5:31:07 PM PST by Hojczyk
It is the nature of the retrovirus. The virus cannot multiply by itself. It must send its RNA to your cells, and then your cells will multiply its RNA and will also turn its RNA into more virus proteins.
In my case, ever since I have had my thyroid removed, I have had zero colds or flu bouts for the past 20 years. All of a sudden, the dreaded stomach flu of winter or feverish bouts are no more. Reactions to flu vaccines, none, and same with small pox injections which create zero scabbing my case.
The medical field has this colonist mentality. It won’t want to hear about your medicine or patient testimony, they want to sell you THEIR pills. This is so obvious.
But we know that now. There are pre-treatments:
-PJ
Read later.
That’s very interesting.
Medical science knows a whole lot less about the human body than it pretends to and when they encounter someone with a really unusual condition, they don’t even want to bother.
Been there, doing that.
During my searching around, I have not run across any reports of the symptoms for Coxsackievirus infection.
I do think, that there is some probability that, some of the vaccines are leading to the SARS-CoV-2 Spike Protein being “expressed” on the surface of some cells that
a) are NOT supposed to be participating as host cells, and/or
b) are participating in locations (heart, kidney examples),
that may lead to significant concentrations of inflammation.
That inflammation happening, because the immune system *record keeping* (some portion thereof, that stores patterns) may be
c) considered by the immune system, to be at fault along with,
or
d) found by the immune system, to be a bit confused when discovering,
said participants sporting the Spike Protein(s).
Scenario:
Immune system finds a SARS-CoV-2 Spike Protein at the surface of what otherwise has been recorded to be a Known Good One [type of] Cell.
Immune system re that Cell, does one of the following
e) tosses out the “Known Good One” record status, or
f) temporarily sets a bypass switch to ignore the “Known Good One” record status, or
g) makes no change to the “Known Good One” record status;
and then, the immune system either
h) attends to the Spike Protein, or
i) attends to the combination of the Spike Protein and participant cell.
IF the participant cell is NOT protected by some recorded status (Known Good One), then, possibly, an auto-immune event may occur, either temporarily or as an initial incident for a longer haul.
For conditions (c) and (d) above, the immune system memory storage system may have some Storage First Aid process that cleans, resets/restores the particular memory storage area.
This scenario, is a way for me to explain what I have been observing among reports by people re their personal experience and symptoms.
How does the Spike Protein leave the cell after it is created by the ribosomes? The ribosomes of the dendrite cells will translate the messenger RNA into the Spike Protein which is broken up by the protezome and presented on the MHC-1 and MHC-2 complex molecules on the surface of the host cell’s membrane. The Spike Protein is completely contained and no way does it float around in the blood stream. Those who say the Spike Proteins are running around in the blood stream don’t know what they are talking about.
Sit down, relax and watch the video:
https://www.youtube.com/watch?v=SQztlqblgVI
How does the Spike Protein leave the cell after it is created by the ribosomes?
Hmm . . . Re that consideration, I did not propose that; nor have I proposed that the Spike Proteins are running loose.
I set up conditions for my Scenario . . . “and then, the immune system either”
[clarifying a bit, my writing:]
h) attends to the Spike Protein (ie ignoring the host cell), or
i) attends to the combination of the Spike Protein and participant cell (not ignoring the host cell).
That said, I am watching Mobeen Syed, MD’s video - tx.
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