From Regitiger on CTH:
a. the alpha C19 virus had a spreading factor somewhere between 2 and 4. The reason this is not a fixed number will be easier to understand in following bullet points. Keep this in mind. You will gain a full realization that r naught isn’t very useful or precise. More or less a method to determine upper and lower limits of a particular virus in a specific moment in a range of time and location/circumstances
b. In less than 14 months, alpha c19 (a RNA virus, corona type, with a very poor error checking mechanism) was measured to have achieved a KNOWN 40,000 mutations, of of which had more or less conserved the RNA payload functions. The Spike protein had experienced the majority of the genomic shift. This pressure to shift was due to 1) the nature of the c19 virus and how it was engineered in a wuhan lab…the genomic shift was more or less a linear change over time/dwell time in the global human pool of hosts.. 2) the natural human immune response of hosts ..which isn’t strange at all. So you have two things at play here. The c19 virus is sensitive in the spike protein to select new functions from the pressure of the human pool hosts immune dynamics. Again, for this 14 months where no mRNA vax was introduced into the human pool, the r naught (or rather upper and lower limits) remained linear as between 2 and 4.
c. around March 2021, one of the major 5 clades of mutations/variants, was determined to have developed a more efficient anchoring ability to the ace2 receptor. This was the first delta variant. it was detected first in India. Bear in mind at no time prior to this, did any mRNA or any other “vax” make its way into the human population. So it emerged as a product of human immune pressure. Again, showing just how sensitive this c19 virus can achieve new functions. However, the r naught even for THIS NEW VARIANT DELTA REMAINED at the upper and lower r naught of 2 to 4. So in understanding how the CDC defines it’s nomenclature, it is declared merely “of interest”…Not especially worrisome. No more risky or dangerous than any other variant and close enough to alpha (like at the others in the prior mutation).
d. However, England (UK) had introduced mRNA jabs at scale on or around late Jan-Feb 2021. (there is a time lag for mRNA to “train” the human response to detect spike pathogen particles…about 20-30 days). Add to that that it took about another 2 months for UK to have established a sizeable population size that had received at least the one mRNA jab. So in effect, you can add about 2-3 months to the Jan 2021 date of the campaign before the jabs have any statistically measurable effects. So we can call that July -Aug 2021 time line. Keep this date in mind.
e. Around July – Aug 2021 the CDC and WHO announced a more viral and pathogenic variant of delta was detected in the UK. it was a direct descendant of early delta located first in India. It “got there” by international travel. (one does not bike ride, swim, or take the rail from india to England…)
f. This “NEW” delta (and higher function variant) had no achieved a supremely more efficient means to anchor to the ace2 receptor. Essentially the c19 virus has a factor of two TIMES more structures with which to attach. More spike features that lock efficiently into the ace2 receptor means more opportunity. It has the effect of creating more human hosts in a classic sense. Thus the r naught limit changes by a factor of around 2….so it goes from 2-4 to 4-8!!! This means that delta can pass from one person to as many as 8 other on average and unlikely less than 4! That means delta becomes the dominant strain simple due to attrition. It literally outcompetes all other variants. (although those variants dont’ actually vanish..they are simply not the dominant and more risky variant…but still problematic. When you understand that there is no true cure for c19 (and any of its variants), there are literally 55,000 plus variants going around right now. They will all get you sick. Some more likely than others. Some far less likely. it’s like a galaxy of tiny variations of the same alpha parent. (if you understand the modern seasonal flu is composed of multiple variations AND ARE ALL direct descedants from the spainish flu of 1917/18 you begin to fully understand why these bugs do not just go away…they just shift, become more diversified..but each of the variant do co-exist..Some having higher affinity for selection than other. Same thing (but far more pervasive) with the RNA c19 virus! it will literally be with the human civilization forever! With any hope, it will transfer to endemic properties. But I doubt it. And here is why I have this INFORMED OPINION.
g. there is a very high confidence assessment that mRNA has produced Delta and will continue to unnaturally accelerate this c19 virus to achieve even more efficiency. The double cleavage furin shape isn’t the only thing this c19 virus can shift toward. It can and probably will develop multi cell targeting capability. We call this an auto immune disease producing virus. Much like HIV/AIDS. it is far less likely that c19 would have ever achieved a serious delta feature with natural immune response pressuring it. We know this based on past historical evidence. Again, spanish flu informs us well. As do many other viruses. They all end up achieving high transmission factors but becomes less lethal over time. This is due to two factors. 1) the overall immune response from the human host develops over time and thus the virus is no longer novel. The explains the bell curve we often see from various orgs. Initially, everyone is at risk and cases go out the roof…people get sick and some die…but then it hits a peak…(the global human response is moderating the virus…AND the virus is being forced to select new functions..it’s sort of dance between humans and the virus. Typically, human immune response “wins” forcing the virus “into a corner” where only those features that can escape do. But even with the best immune response, take as a global pandemic, there is still going to be an imperfect outcome…We can think of this as the virus features are conserved in the evolutionary trajectory. Viruses are not perfect, but neither are our immune responses. So there is a equilibrium achieved. Then after the peak, cases drop. This is normally associated with evidence that herd immunity is the governing force in the life cycle.
h. Around late Dec 2020 until June – July 2021, we saw that global bell curve hit a peak and then dive rapidly as cases literally collapsed off a cliff. This was evidence that the global human immune response was taking shape and responsible for the decline in cases, severity, hospitalizations and even death. And although the delta parent have selected in or around april-march 2021, the data showed it was no more of a threat than any of the other mutations and variants. It did not actually have the distinctions of a twin dual cleavage furin site at the spike protein structure.
i. to repeat, it was the correlation between mRNA jabs in the UK that delta PLUS emerged. This was not coincidental. And it is not purely anecdotal to suggest the link. Alas, DELTA PLUS IN INDIA NEVER HAPPENED. One would scientifically EXPECT AND PREDICT THAT DELTA PLUS would emerge as it had in the UK for all other countries that had previously detected Delta initially, earlier. But we do not see that at all. We ONLY see DELTA PLUS emerging in those countries where mRNA was introduced. With a population size of India, one could reasonable assume this delta original would achieve delta plus features in record time. For lots of reasons and not simply because of the population size. it is a densely populated country!! And it was the country of origin for Delta initial. So it had more opportunity and time and dwell time to select for delta plus features. But it did not. It remained delta initial and then the cases dropped..rapidly…like a bump in the data chart. Alas, WE KNOW INDIA NEVER HAS INTRODUCED ANY mRNA VAX gene therapy to any of its citizens. Not one. Rather they used ivermectim as a mitigation drug for prevention!!!! UK and all other countries DID JUST THE OPPOSITE…No therpeutic drugs of any significance to prevent the c19 illness and they dropped the mother of all bio weapon enhancers into their populations: the mRNA boost.
tldr: c19 was engineered to create a pandemic to give global bodies the terror weapon they needed to being control and concentration of all power.
the mRNA “vax” was designed to boost the c19 virus into NEW capabilities that it could never achieve “in the wild”.
WE KNOW.
FPCHmom
September 29, 2021 3:55 pm
Alex Berenson just posted a very good, informative email from a reader of his in Australia about what is going on with information about covid in Australia, which helps to explain why the authoritarianism is winning there.
https://alexberenson.substack.com/p/the-diabolically-brilliant-politics
The title is – The (diabolically) brilliant politics of scaring the elderly.
CtC,
India was using Ivermectin (cases started dropping), then dropped it in favor of shots (cases then rose), then went back to Ivermectin (cases dropped again).
Timeline this sequence in with the timeline you outlined.
Is Delta + in India, and when?
Does Ivermectin crush Delta + as well as any other variants?
Mark...MnRA