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Persistence of the Spike Protein May be Inducing Systemic Autoimmune Disease MIMICKING Sjogren’s, Arthritis, Vasculitis, Diabetes, etc.
A perfect bioweapon? Sowing the body with the seeds of self-destruction via most efficient endothelial delivery.
THIS IS MY MOST IMPORTANT WORK TO DATE.
An illustration of Sjogren’s Syndrome
A paper was posted January 26 which has now caused me to revise my Spike Protein Progeria Disease hypothesis. Until I read this paper, I hypothesized that the Spike invaded the endothelium (Spike Protein Endothelial Disease) and then the organs leading to a Progeria Syndrome. However, I now need to revise the Progeria Syndrome part of the hypothesis.
My updated hypothesis is related to Progeria.
What I believe is now occurring is that the Spike Protein is a designed viral fragment that has been attached to a coronavirus as a delivery mechanism. This viral fragment causes ARDS, multiple organ failure and death in a very few due to the initial phase of the Syndrome it induces. This is what I have called SPED. Spike Protein Endothelial Disease.
The second phase of this Syndrome I had initially thought was a Progeria syndrome. I now no longer believe that to be the case. However, Phase II would certainly be PART of a Progeria syndrome. I now believe that, given recent evidence, Phase II is the induction of a SYSTEMIC AUTOIMMUNE DISEASE which I will call Spike Protein Autoimmune Syndrome.
So, how does the Spike Protein cause this Syndrome? By the PERSISTENCE OF THE SPIKE PROTEIN within the body.
Let us look at how viruses can induce autoimmune disease.
The persistence of a virus, over time, ACTIVATES autoreactive B and T cells which are present in the body. They do this via, among other mechanisms, molecular mimicry. They also do this via VIRAL PERSISTENCE. The constant presence of a virus will eventually cause the body to attack those cells in which the virus persists.
Yet, what is a virus? It is an organism which is composed of proteins. For example, SARS-CoV-2 has N, E, M and the infamous S proteins. It also has 16 non-structural and 11 accessory proteins.
However, the VIRUS ITSELF does not activate the autoreactive B and T cells. The PROTEINS in the virus activate the autoreactive B and T cells. Complete virus is not found in those with Long COVID. The Spike Protein IS. The spike has also been proven to travel via nanotubes from cell to cell, evading the immune system – yet “planting” itself in ever more cells.
Now. DEPENDING ON WHERE THE TARGET ANTIGEN IS the body’s immune system will attack. Of course, the Spike Protein is a TARGET ANTIGEN. So – if it is in a very wide variety of organ cells – well, you can do the math.
This is why the finding from the following paper is so critical:
Results In total, 641,704 patients with COVID-19 were included. Comparing the incidence rates in the COVID-19 (IR=15.05, 95% CI: 14.69-15.42) and matched control groups (IR=10.55, 95% CI: 10.25-10.86), we found a 42.63% higher likelihood of acquiring autoimmunity for patients who had suffered from COVID-19. This estimate was similar for common autoimmune diseases, such as Hashimoto thyroiditis, rheumatoid arthritis, or Sjögren syndrome. The highest IRR was observed for autoimmune disease of the vasculitis group. Patients with a more severe course of COVID-19 were at a greater risk for incident autoimmune diseases.
Incident autoimmune diseases in association with a SARS-CoV-2 infection: A matched cohort study
I believe what we will discover is that people are NOT developing Sjogren’s, Arthritis, Diabetes, Vasculitis etc. PER SE. WHAT THEY ARE DEVELOPING IS A SYSTEMIC AUTOIMMUNE DISEASE INDUCED BY THE SPIKE PROTEIN WHICH MIMICKS THESE AUTOIMMUNE DISEASES!!!!!
I cannot stress this enough.
If this is indeed correct, and I am almost certain it is, then it will bring to the fore the importance of clearing the body of the spike protein. Let’s hope that the Spike’s mRNA has not been retrotranscribed into our DNA. That would pose a problem I cannot yet fathom how to solve.
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