Well that title is a handful, isn’t it.
I just want to first say how odd it is that General Practitioners all over the world haven’t been singing AMYLOIDOSIS at the tops of their lungs for months. This, to me, is such a perfect fit.Walter Chestnut wrote this up as well. Many times. I applaud you for seeing what I did not.
What is amyloidosis? Amyloidosis comprises diseases that result from protein aggregation of fibrous proteins called amyloids. These amyloids can be formed as the by-product of inflammatory responses and infection in the human body and can also be iatrogenic.
I think humans really need to stop. Like, really STOP. With all the bullshit criminal behaviour. Against nature. Against each other. Against science. Protein mis-folding is very serious. No cure. I wrote this up. Adverse event reports of Creutzfeldt-Jacob Disease are up to 41.As usual, reaching for band-aid solutions instead of root causes and destroying the source of the problem. Man. I digress.
This is a crystal structure that was resolved from work you can read about here. I chose it for no particular reason - to illustrate the beta-sheet alignment that gives the fibrils their visual appearance that you can observe using cryo-transmission electron microscopy.
A paper was published on May 17, 2022 entitled: “Amyloidogenesis of SARS-CoV-2 Spike Protein” and it nails this down in my opinion. They propose that the protease neutrophil elastase (NE) which is overexpressed at sites of inflammation, cut the spike protein into amyloidogenic bits. This means that those amyloidogenic bits produce amyloid deposits. Those amyloid deposits look like this (right) using negative stain transmission electron microscopy (TEM):
Richard Hirschman found fibrous clots in some of the bodies he had embalmed. He’s an embalmer, don’t worry. He referred to these structures as “white stringy fibrous tissue”.
These amyloid deposits don’t get broken down and disrupt the normal functioning of cells and tissues affected, and unfortunately, can affect pretty much all tissues. This, in my opinion, is the reason for the carditis’s we are seeing. Amyloid deposits in the myocardium, pericardium and endocardium. Amyloid cardiomyopathy.
Make no mistake: these shots are massively dangerous. You truly take an enormous risk by getting injected with this modified spike protein, in my opinion. It absolutely has associations with prion-like illnesses with demonstrable amyloidygenic properties.
I leave my readers to decide for themselves what they think is going on here, but I strongly believe that these modified spike proteins were made to be destructive. It cannot be that intelligent experimentalists did not know the potential dangers associated with what they created. The modifications are too precise and targetted. These prion-like proteins work entirely against an optimally-functioning human physiological being, and they could be the link between all adverse events and disease symptoms we are seeing in adverse event data and clinically: neurological, (CJD), immunological, cardiovascular, hepatological, etc…
One thing that does bother me is that people are playing with amyloid fibrils and applying it to tech. The authors listed in reference 1 (some of the players) are funded by the Wellcome Trust.
The amyloid fibril has been increasingly examined for its potential role in forming nanotubular scaffolding for bionanotechnology. 
Risk factors for amyloidosis include age (60+), gender (male), race (African descent), genetic predisposition and chronic infectious or inflammatory diseases.
I don’t think there’s any doubt that these modified spike proteins are amyloidygenic, thus being one of the big reasons for the atypical numbers and diversity of adverse event reports in VAERS, the Yellowcard and the EUDRA systems. (I still think the lipid nanoparticles are bad news, as well.)
I leave you with some Amyloidosis adverse event data from VAERS. I included diagnostic markers like “D-dimer” and “Transthyretin” as well.
It’s never Lupus.
Rambaran RN, Serpell LC. Amyloid fibrils: abnormal protein assembly. Prion. 2008;2(3):112-117. doi:10.4161/pri.2.3.7488.
There are typically 350 cases per year in the U.S. so if we consider the upder-reporting factor of only 9, we have exceeded our background for the year.
Attended the Better Way Conference this weekend. Wow, what an experience. I have to admit though specific adverse events were not discussed in detail, simply because we needed weeks for this conference rather than 3 days. It was a pleasure to see you on screen and listen to your wise words. I do have a brother-in- law who now has new onset Parkinsons , age 65. I believe it began after his first jab, but I cannot ask, as my sister has told me not to discuss anything covid with her. “if I am going to die, I am going to die”. My brother-in-law has now taken his booster. So many never connecting the dots. Neither are their “specialists”. On another note, a person called Tim Hume, tweeted “Davos for Covid truthers and antivaxxers is playing out in the English city of Bath right now”. As Del Bigtree said, any publicity about the conference is publicity💕💕
This of course is very frightening, and does not surprise me one bit. How one wishes to see into the future re what will one day have been learned about why some vaxxed and boosted individuals seem (at least so far) to have avoided the ghastly vaxx-induced illnesses and disabilities that others have not. Is it a case, as some suspect, of a monstrous, planned experiment wherein various batches of the stuff were intentionally made more or less toxic, to yield info for the future reference of madmen? Or is there something genetically built into some of us that makes us resistant to the vaxx's harmful effects? Down the road, we will know so much more -- much too late for so very many. And yes, this madness must stop! But how to make it stop when behind the shape-shifting fear-porn juggernaut are so many of the world's powerful who seemingly will stop at nothing.