While starting to work on the Kynurenine piece part II, I stumbled upon this PDF from Public Health Ontario.
It has your usual public healthcare messaging and observations that have been obvious for months (BA. 4 and 5 are coming to dominate, and reinfections add to all-cause mortality, a really duh moment for me). Nevertheless, this isn’t why I am sharing this.
The following is.
They are all saying the quiet part out loud. Current vaccines do little to protect against infection, don’t provide sterilizing immunity, reinfections are starting to take a toll on the physiology of many, adverse outcomes increasing, but the second point is the one that should caught your eye.
Reinfections leading to “Acquired Immune Dysregulation” (what I call PAID, but I prefer Dysfunction). At least they are recognizing that SARS-CoV-2 (and it is the fucking vaccine fueling this dysregulation/dysfunction) is slowly killing the immune system of some people. The more reinfections, the higher your chances of acquiring such dysfunction.
Higher viral loads, more antibiotics use, and the “all cause mortality” increase all comes down to the modulation of the immune system to produce what I came to refer as a molecular IED.
To understand what the hell is going on.
The one below came to be the most important paper in this whole thing.
Old diseases will keep coming back, worse outcomes for these diseases with “odd, uncommon” death causes will keep coming, and they will ask themselves how, or why it happened. As a matter of fact, right now there are 3 registered monkeypox d eaths in the world. 2 in Spain, one in Brazil.
2 for encephalitis, one for sepsis. If you read the PAID hypothesis (Part II about Toll Like Receptor especially) you will understand the how. I
And since we are talking about Reinfection, hospitalization and vaccines. Real-world data on that. Not a fan of Eric, but data is data.
Also, while my Subscriber numbers are relatively low compared to others, I have a higher number of PhDs, scientists and other eyes on me, so I want someone with connections to confirm to me if Pfizer is pouring money on NR4A receptors. I need some corroboration. E-mail me with a throwaway account.
The big questions I have are: "Do never-injected adults who acquired broad spectrum durable immunity suffer same risk of reinfections and immune dysfunction as the fully-injected?" and "If I had a mild infection from the strain that was circulating in Feb. 2020, and got what was called Omicron in Dec. 2021, basically a day in bed with a mild fever, watching Netflix, is the Omicron infection I had considered to be 'reinfection', or a 'different infection'?" and "If my acquired immunity to the Feb. 2020 strain couldn't fully protect me against Dec. 2021 Omicron, how the heck is a fourth shot of mRNA coding for a two years out of date spike protein going to protect anyone else from whatever Omicron strain we are supposed to worry about in 2022?"
Ooh that's not good! Official confirmation, and why genuinely safe & effective antiviral stacks are needed urgently. It's a pity the most in need are also the most clueless and most likely to queue for the next booster snake oil.
I've put a call out about the NR4A receptors.