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SARS-CoV-2 vaccines high ROS, Paxlovid high viral loads
And the many plagues inbound.
This will be a mixed post because I refuse to send 5 e-mails in one single day, for small but rather important information. First, about the favorite drug of the vaccinated and boosted.
This is one to be on the lookout for, because while it is rare, it is a natural mutation that significantly impacts the (proposed) efficacy of Paxlovid main ingredient, taken together with another post where I covered the mutations that will, in my opinion, arise from the widespread use of this poorly efficacious drug, we now have a solid base to watch and track. Leading us to paper number 2.
At long last, we get a juicy paper with information that I have been eager to learn, not only that but also we get a more honest approximation of the real rebound rate, which I estimate the real number to be close to 70%. The more important part of this one is the viral load.
The viral load in persons who experience rebound is at the same level as acute infection. By now any reader of my Substack is fairly and deeply aware of how much high viral loads can and do become a problem. Not only from a viral evolutionary perspective but from a long-term damage one, since most proteins in this virus have multiple purposes and can induce long-term changes. The more evidence we get, the more my first point on this drug being not only useless but dangerous becomes closer to truth and not merely assertion.
And talking about useless treatments.
Twitter Censors Top Israeli Biological Research Scientist After He Says Monkeypox Outbreak May Be Connected to mRNA Shots
I find it rather encouraging, when someone highly respected in his/her field spouts the same observations that I had weeks, sometimes months ago and I thought it was merely insanity from my mind. As a joke, he should not worry about monkeypox, because as I wrote quite a few times here many other diseases will come back because of what he is referring to, and because of the virus to a minor level.
I will get back to this (other diseases) shortly.
The following was once again one of those moments “we finally have this information”. Since the start of the vaccination campaign, I have been asking if the vaccines could create large amounts of ROS (
And we finally have that important information, a piece of the puzzle I have been eager to have. Getting the vaccine increases your ROS levels to such an extent that it takes the body more time to get back to base levels than with natural infection. There are also gender differences, which come down to hormone levels but I won’t cover this here.
The importance of this is simple, from a very basic, simplistic perspective (and you can find me writing about this since 2020) SARS-CoV-2 is an infection driven primarily by ROS, in a very simplistic explanation this is how it happens.
You get infected
Cellular rust (ROS) is formed
Your body needs to deal with that rust and much more, otherwise, disease progresses, you get sicker
The body uses the stores of nutrients and antioxidants you have to clean everything
Elevating the ROS to a high level before an infection, in a disease in which the severity is led primarily by the lack of the most important antioxidant in the body (Glutathione) seems counter-productive on a normal day. Poorly designed product from the get-go. With just this piece of information, you can connect the dots quite easily.
This helps explain a few different aspects of why the vaccine is “so much worse” than the viral infection when it comes to adverse effects and the development of any sort of disease short and long-term. From the start point, depending on each individual person's physiological state, you are already driven into a low antioxidant state, in which a breakthrough infection or poor diet (comorbidities apply) will further impede you from getting back to normal levels.
Pushing your body to produce toxic levels of Kynurenine metabolites, which add a metabolic explanation to why the vaccinated are pushed so, so, so heavy towards Th17 (a super inflammatory immune state).
Now back to the MonkeyPox point raised by the biologist. Weeks ago NYC had a case of polio, which was further traced to a Jewish community and an unvaccinated child.
New York State health officials say they have identified the polio virus in sewage water samples taken from two unique geographical locations in the New York City suburb of Orange county.
The samples were taken in June and July and indicate community spread, the state’s health department warned in a statement confirming their findings.
My guess would be that “two unique geographical locations” would mean a different, not connected sewer system, which would exclude contamination from a single source. Polio cases in highly vaccinated (with the safe versions of the vaccines btw, unlike the deattenuating one used in some of the poorer countries) keep increasing. It is a signal for me, something for the reader to bear in mind out of curiosity if the person wishes, not out of concern.
ACAM2000 per the news article has one of the worst safety profiles of any other vaccine, not only that, it has a myocarditis incidence of 3 ORDERS OF MAGNITUDE over the mRNA vaccines. Plus, per my last Pox piece, we know you only develop immunity against Poxviruses via T-cells. This legitimately feels like a lowkey eugenics attempt.
You can’t vaccinate immunocompromised people without prior clinical testing, and even at that, and we have this information with SARS-CoV-2, it is a shot in the dark most of the time, with 50/50 working or not. If anything this will just fuel more mutations and evolution.
In which I made the joke I will now start to refer to what SARS-CoV-2 did and created as “Non-Canonical Viral Evolution”.
As a last piece of news, this. As long as it is not H10N3 though, I won’t feel unbelievably worried, but this is something I forecasted months and months ago.
Another post coming later today.
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