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Walter M Chesnut: @parsifaler
Walter M Chesnut: @parsifaler
@Parsifaler
Apr 4 • 11 tweets •
Parsifaler/status/1510789756690571270
It has been proposed that Alzheimer's disease might be a 'whole body' problem, as
amyloid-beta can travel, cancer-like, to brain from other parts of body.
Normal mice that had been joined (via bloodstreams) to genetically modified
partners for a
3) year "contracted" Alzheimer's disease. The researcher song says the amyloid-beta
traveled from the genetically-modified mice to the brains of their normal partners,
where it accumulated and began to inflict damage.
Not only did the normal mice develop plaques, but also a
4) pathology similar to "TANGLES" -- twisted protein strands that form inside brain
cells (please note, per image, this is PRECISELY what the Spike Protein induces),
disrupting their function and eventually killing them from the inside-out. Other signs
of Alzheimer's-like damage
6) amyloid-beta is produced in blood platelets, blood vessels and muscles, and its
precursor protein is found in several other organs. But until these experiments, it was
unclear if amyloid-beta from outside the brain could contribute to Alzheimer's
disease.
Which brings us to
Studies of nerve biopsy or cardiac autopsy specimens from patients with ATTR and
AL amyloidoses show atrophy of cells near amyloid fibril aggregates. In addition to
the stress or toxicity attributable to amyloid fibrils
By the way. Who discovered this? Department of Neurology and Centre for Clinical
Neuroscience, Daping Hospital, THIRD
The proposed therapeutics to deal with this pathology sound quite familiar: (1)
reducing or preventing the production of causative proteins; (2) preventing the
causative proteins from participating in the process of amyloid fibril
And this is what is MOST ALARMING and should cause the world to go FULL
IMMEDIATE STOP ON ALL SPIKE PROTEIN THERAPIES. PLEASE READ (1)
AGAIN!
11) We need to make ourselves well, before we make ourselves ever more ill.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347239/
https://www.sciencedaily.com/releases/2017/10/171031084808.htm
https://www.nature.com/articles/mp2017204
https://www.biorxiv.org/content/10.1101/2021.12.16.472920v1.full
Oligomerization of the SARS-CoV S glycoprotein: dimerization of the N…
Viral envelope glycoproteins are oligomeric and the quaternary structure is critical
for their membrane fusion activity. Typically the transmembrane glycoproteins of
class I fusion proteins contain t…
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092807/
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