FOR CORONACOASTER: COVID-19 News, Info, Discussion /// Tracking the Spread of the Virus and its Effects

Hi, WHITE.
This is quite a long answer, maybe I have overdone it, IDK..but it's my best thoughts.

There are several areas of concern as I see it. The ones I know about:
(VAX + SARS2): Neuro-degenerative disease (ongoing concern, watching Kevin McCairn's experiments)
(VAX + SARS2): Amyloid/clotting
(VAX + SARS2): Vascular/endothelial disease (related to Amyloid, imo)
(MOSTLY VAX-ONLY CONCERN NOW): Cancer.
(MOSTLY VAX-ONLY CONCERN NOW): Auto-immune disease.
(MOSTLY VAX-ONLY CONCERN NOW): Direct damage to heart, kidneys, liver.
(MOSTLY VAX-ONLY CONCERN NOW): Immune system damage (T-Cell exhaustion, imprinting, ADE,...)



The last four, I class as mostly concern with the vaxxes for the following reasons:
Cancer:
-------
1) 'PRRA' is the nuclear translocation signal, i.e. what gets it in to the area where DNA resides.
- Omicron has lost 'PRRA' to become 'HRRA', so less risk of DNA impact.
- Vaxxes still have Wuhan-1 spike with 'PRRA'.
2) Carcinogenic excipients like SM102 only in the vax.


Auto-immune:
------------
The auto-immunity issue would include diseases like MS, Transverse Myelitis, Arthritis, etc.
Why the vax, not so much Omicron?
1) Repeated exposure to spike (which shares human protein similarities, i.e. mimicry) is a concern.
2) Exposure via non-usual pathways (injection) as opposed to the mucus membranes and gut-lung axis
- ASIDE:there is a complex interaction between sympathetic and parasympathetic immunity when we expose ourselves via the gut/lung.
- Trinity, our illustrious forum owner, had some discussion about peanut allergies only ever being seen after peanut oil was used in childhood vaccines.
3) mRNA which distributes throughout the body (even brain), and continues to produce spike for an unknown duration, whereas Omicron has lost much of its ability to infect heart/kidney/liver cells..
- Myocarditis being the obvious one here: immune cells kill heart tissue b/c it's producing spike??
- Also, remember the non-viral autoimmune liver diease wave in children (many transplants needed)?
4) Spike and Ab production after vaccination far exceeds a natural infection.. so we end up risking more autoimmune reaction

Direct damage to heart, liver, kidneys:
---------------------------------------
Again, why the vax and not Omicron?
Omicron lost 'PRRA' so much less invasion of these organs/tissues.
Remaining entry route to these cells is blocked by HCQ/Cathepsin blockers - it's treatable.
Syncytia is also reduced in Omicron, I think.

Immune-system damage:
---------------------
Very complex, but my feeling is that T-Cell exhaustion and imprinting from repeated vaxxing is an abuse of the immune system which leaves it less responsive to future threats.
Yes, repeated infections could do the same I suppose, but I am more concerned about a very narrow and MONOTONOUS response by ALL the injecteds driving this problem towards variants that use prior vaccination as a tool to assist infection (ADE).



Now, looking at the first three areas (concern is BOTH vax and Omicron):

Neurodegen:
-----------
I am watching Kevin McCairn's experiments as he is trying combinations of disease and vaccine on rats/primates to see if there is a key combination that may set off a prion-type cascade.
The results of Prion predictions from PLAAC onn the Spikes were that the vaxxes were the main culprit for Prion disease compared to Omicron, but consider that the Omicron Nucleocapsid still has large prion-genic regions!
The results from WALTZ algorithm showed that the vax and Omicron spike both had large propensity for Amyloid formation.

Amyloid/Clotting:
-----------------
See above for Omicron's general amyloid propensity.
Morticians still pulling extraordinary clots/blockages from the deceased.
I fear both vax and disease spikes are a big culprit, still.

Vascular/Endothelial disease:
------------------------------
Clearly something about both vax and Omicron damages the vasclar endothelium.

[link to www.cbc.ca (secure)]

Regina researchers believe new COVID-19 subvariants could be behind spike in wastewater viral load

My calculations verify Igor's. I think it's correct..:

>>This is a statistically significant difference, and implies a dose-dependent relationship between chance of miscarriage and amount of mRNA injected (30ug Pfizer vs. 100ug Original Moderna or 50ug Moderna Booster )...



---------------

CDC's Data:
[link to www.cdc.gov (secure)]
(See Page 32.)

---------------

My Spreadsheet, for confirmation of a 5.2xS.D. excursion from the 'null hypothesis' of:
"no difference in miscarriage rates <20wk between Moderna and Pfizer doses":
[link to ibb.co (secure)]


Whoa...

Many thanks to ParamedicUK and Uncle Doom for the encouragement...

I've got another stonker here...Just started a thread on it..Would welcome any input from diffster/others...

Many thanks to ParamedicUK and Uncle Doom for the encouragement...

I've got another stonker here...Just started a thread on it..Would welcome any input from diffster/others...

S-man

Am I missing something here?

The expected stillbirth rate in the U.K. is 1 in 1000.

These figures are massively higher.

Or have I got it wrong?

No difference between the jabs but both deadly???

Lost a good friend tonight.


A terrific doctor, worked tirelessly for the sick and the down-trodden. Was refused usage of our PAPR, but still went back into Uganda. His wife messaged us the sad news.


Mbe, I salute you.


Uganda has lost all and any control.

Lost a good friend tonight.


A terrific doctor, worked tirelessly for the sick and the down-trodden. Was refused usage of our PAPR, but still went back into Uganda. His wife messaged us the sad news.


Mbe, I salute you.


Uganda has lost all and any control.

Hi, WHITE.
This is quite a long answer, maybe I have overdone it, IDK..but it's my best thoughts.

There are several areas of concern as I see it. The ones I know about:
(VAX + SARS2): Neuro-degenerative disease (ongoing concern, watching Kevin McCairn's experiments)
(VAX + SARS2): Amyloid/clotting
(VAX + SARS2): Vascular/endothelial disease (related to Amyloid, imo)
(MOSTLY VAX-ONLY CONCERN NOW): Cancer.
(MOSTLY VAX-ONLY CONCERN NOW): Auto-immune disease.
(MOSTLY VAX-ONLY CONCERN NOW): Direct damage to heart, kidneys, liver.
(MOSTLY VAX-ONLY CONCERN NOW): Immune system damage (T-Cell exhaustion, imprinting, ADE,...)



The last four, I class as mostly concern with the vaxxes for the following reasons:
Cancer:
-------
1) 'PRRA' is the nuclear translocation signal, i.e. what gets it in to the area where DNA resides.
- Omicron has lost 'PRRA' to become 'HRRA', so less risk of DNA impact.
- Vaxxes still have Wuhan-1 spike with 'PRRA'.
2) Carcinogenic excipients like SM102 only in the vax.


Auto-immune:
------------
The auto-immunity issue would include diseases like MS, Transverse Myelitis, Arthritis, etc.
Why the vax, not so much Omicron?
1) Repeated exposure to spike (which shares human protein similarities, i.e. mimicry) is a concern.
2) Exposure via non-usual pathways (injection) as opposed to the mucus membranes and gut-lung axis
- ASIDE:there is a complex interaction between sympathetic and parasympathetic immunity when we expose ourselves via the gut/lung.
- Trinity, our illustrious forum owner, had some discussion about peanut allergies only ever being seen after peanut oil was used in childhood vaccines.
3) mRNA which distributes throughout the body (even brain), and continues to produce spike for an unknown duration, whereas Omicron has lost much of its ability to infect heart/kidney/liver cells..
- Myocarditis being the obvious one here: immune cells kill heart tissue b/c it's producing spike??
- Also, remember the non-viral autoimmune liver diease wave in children (many transplants needed)?
4) Spike and Ab production after vaccination far exceeds a natural infection.. so we end up risking more autoimmune reaction

Direct damage to heart, liver, kidneys:
---------------------------------------
Again, why the vax and not Omicron?
Omicron lost 'PRRA' so much less invasion of these organs/tissues.
Remaining entry route to these cells is blocked by HCQ/Cathepsin blockers - it's treatable.
Syncytia is also reduced in Omicron, I think.

Immune-system damage:
---------------------
Very complex, but my feeling is that T-Cell exhaustion and imprinting from repeated vaxxing is an abuse of the immune system which leaves it less responsive to future threats.
Yes, repeated infections could do the same I suppose, but I am more concerned about a very narrow and MONOTONOUS response by ALL the injecteds driving this problem towards variants that use prior vaccination as a tool to assist infection (ADE).



Now, looking at the first three areas (concern is BOTH vax and Omicron):

Neurodegen:
-----------
I am watching Kevin McCairn's experiments as he is trying combinations of disease and vaccine on rats/primates to see if there is a key combination that may set off a prion-type cascade.
The results of Prion predictions from PLAAC onn the Spikes were that the vaxxes were the main culprit for Prion disease compared to Omicron, but consider that the Omicron Nucleocapsid still has large prion-genic regions!
The results from WALTZ algorithm showed that the vax and Omicron spike both had large propensity for Amyloid formation.

Amyloid/Clotting:
-----------------
See above for Omicron's general amyloid propensity.
Morticians still pulling extraordinary clots/blockages from the deceased.
I fear both vax and disease spikes are a big culprit, still.

Vascular/Endothelial disease:
------------------------------
Clearly something about both vax and Omicron damages the vasclar endothelium.

Many thanks to ParamedicUK and Uncle Doom for the encouragement...

I've got another stonker here...Just started a thread on it..Would welcome any input from diffster/others...

i'll ask. is this cover for lack of med workers? an excuse for why health care system is failing?

Can anyone confirm statement in red at bottom?

Thanks S-man for your long explanation, in other word, once vaxxed or infected with the original spike protein, it is kind of like a death sentence with Omicron helping it speed up along the way.

I will search for this 'PRRA' and see if I can get more information, cheers. :-)

Hi S-man,
You can post your thread link here, this thread has nothing personal, most important is to share information, thanks.

So looks like xbb is going to be the big one that will run us over. Its here in nyc so i have to be extra careful, stay safe everybody.

Can anyone confirm statement in red at bottom?

SMAN, based on that low % difference, i don't think that is all CHINA knows then. wouldn't cause the freak out CHINA has done. it does point to covid escaping the lab too early.more evidence of what they were designing the virus for and that it was not completed.

WHITE - it's simply the mutation at position 681 of the spike.
In Omicron, the 'P' changed to an 'H'.

PRRA is necessary for the Furin Cleavage Site. Without 'PRRA', SARS2 cannot enter using ACE2/TMPRSS2.
That's why Omicron does not infect heart/kidney/liver cells too well.
(Also of note, PRRA is made by the sequence CT CCT->[P] CGG->[R] CGG->[R] GCA->[A] CGT AG - and this sequence appears in a Moderna Patent from 2016!
The Sequence also does not appear in ANY other eukaryotic or viral genomes - AT ALL!
It's obviously an insert. (Link to thread on this: Thread: SARS-CoV2 --Lab Origin-- The final word, and PROOF beyond reasonable doubt. )



Finally, if you just click on the bottom of my (quoted) post from the thread, it takes you to the thread itself, but here it is anyway:
Thread: Moderna causes 42% more miscarriages than Pfizer...

Can anyone confirm statement in red at bottom?

There was chatter about this early in the main covid thread!

VERY IMPORTANT TALK
=====================
This actually advances our knowledge hugely of what's going on at a microscopic scale with the vaccines! - And it explains a lot...

Arne Burkhardt's talk (German Pathologist of very high repute) -- reviewed with Kevin.
Slides from Autopsies, and some live Biopsies of vax injured; all associatted with vaccine (NOT SARS2, no nucleocapsid)..
[link to wtyl.live (secure)]

1h10m: The vascular endothelium and clots/blockages stain with Congo Red -> Amyloidosis.
1h15m: Strange fibers in the lungs also stain with Congo Red -> Amyloidosis. (also another case at 1h39m40s -amyloid).
1h18m: Analysis of the extracted 'clot' material: Has protrusions - "self-assembling proteins" - no cells (fibrocytes or red blood cells), just protein.
1h20m: Lung: clot-like structures in the veins, intravascular dark objects, foreign bodies, not wall-adherent (unattached). Stains for Spike and Amyloid.
1h22m: Endothelium is detached and inflammatory lymphocytes congregate.
1h27m: Compares what he's seeing to his early days seeing mesaortitis luetica (syphillis-caused aortic inflammation),
1h28m: Compares also to a toxic agent from chickpeas which affected the aorta!
1h31m: Coronary Arteries, Splenic Artery, Cerebral Base Artery, with spike protein embedded in the walls + inflammation..
1h32m30s: "These are now regular findings and for me (Burkhardt), are associated with the vaccine."
1h33m30s: Aorta showing separation between the wall and lining (wall defects, prolapses), and a slide with inflammation at the boundary - with Spike protein present.
1h34m: "Onion-skin Arteritis" Congo Red Deposits (-> Amyloid).
1h35m: Malignant Lymphomas, with spike protein!
1h35m20s: Large B-Cell lymphoma of the gastric mucosa. Immune reaction to the tumor, with spike being expressed in the surrounding white blood cells.
1h36m20s: This assiciation betwen spike and cancer cant be a coincidence, and one probably believes in a connection with the vaccine.
1h38m20s: Spike but NO NUCLEOCAPSID (so vax).
1h42m30s: Lymphocytes infiltrating the dura mater (brain lining). Almost all organs affected (Thyroid, Salivary, Vasculature, Skin, Liver, Kidney, Testes, Prostate, Muscle and Fat tissues, Dura)
1h43m: Autoimmune diseases Lichen Planus developed after vax.

BRAIN:
1h45m: Transfection-associated encephalitis (NB: Mad Cow is a transmissible Spongiform Encephalitis, as is CJD,...).
1h45m: Blood-vessel (intracerebral and sub-arachnoid) destruction, haemorrhages.
1h45m30s: Amyloid deposits in-brain.
1h46m: In-brain bleeding, punctiform lesions, bleeding INTO THE VESSEL WALL.
1h46m30s: "I am shocked to tell you I have seen vascular changes in almost every brain we have done, it cannot be swept under the table"

1h49m: Protein amyloid deposits in the half-destroyed vessel walls.
1h49m30s: Classic picture of a micro-aneurisym - she can burst at any time - with CongoRed stain (amyloid), due to disruption of the vessel wall elastic lamellae.
1h50m30s: Kevin: "we were right, folks.."
1h51m: Iron accumulates on the elastic lamellae.
1h51m20s: Calcification in the brain and similar in an artery of the Thyroid
-> "That knocked both of us off our feet. I have never seen that in my whole life. It has to be associated with the vaccine ('impf-assoziaten')".

THYROID:
1h51m51s: Plaque-like deposits of Congo Red (amyloid) - like observed in neurodegenerative diseases.