In 2012, geneticists thought that Chikungunya Virus had two open reading frames (ORFs).
They believed the nucleotides and codons in Chikungaya were at a 3:1 ratio.
They believed “UAG” to be a single codon in the termination point, consisting of three nucleotides.
But sometimes it “overshot” what was assumed to be the 3′ UTR.
Nobody could explain why, “but sure, let’s CRISPR you anyway.”
DARPA was working on their secretive P3 Pandemic Prevention Program back in 2017, which went something like, we’re going to have this “universal cure” ready to roll out to everyone within 60 days.
Why is that bad? “your body becomes the bioreactor.” Do you remember how right before this there was all this talk about how “in the future” they would be able to induce your body to “make medicine” ? That’s related to their discovery that yeast could be coaxed into making almost any type of cell including healthy RBCs.
(Well no kidding, silly. That’s what happens when you eat yeast.)
So what if the “drug” is bad and they can’t shut the “bioreactor” off ?
Thats’s why the P3 program is secretive and I was banned for retweeting/mentioning Darpa and Moderna’s early 2019 trials – all of which had already been underway since 2017 under Defense Advanced Research Projects Agency grant HR0011-17-2-0069 and Gates Foundation grant OPP1066832.
Now if you read up on those grants, you will learn that they were originally paid out in the pursuit of an “hiv’ vaccine and/or for DARPA’s P3 Pandemic “Prevention” program starting in 2017.
These payments started shifting to efforts related to Chikungunya.
And then by 2020 the money was being spent on their “covid” fiasco.
Under those same grant numbers that were opened in 2016, 2017(?)
Despite its name, “sars-cov-2” does not resemble “sars-cov” at all.
Why? Because of its “10 Open Reading Frames,” ORF1 through ORF10.
We didn’t know about those before 2019. We thought that most genetic strings were eh, give or take, 61 or 62 or 63 “codons” long with a 5′ UTR start codon, two ORFs aka EXONS, and a 3′ stop codon.
In the case of “HIV” , pol/env/gag resided roughly in those two ORFs, and then “NEF” as I previously mentioned, would have been in the “stop codon.” My previous hypothesis was that neomycin/kanamycin/etfak would destroy NEF in the HIV ORF, rendering the mRNA chain of HIV replication incompetent (99 out of 100 of them already are replication incompetent, in the region where “protease inhibitors” target and my hypothesis is that it would render it close to 100/100, e.g. a functional cure if not an actual cure. I disagree that the resulting replication incompetent mRNA are infectious or represent “viral load”).
The University of Washington is sitting on a new “hiv pcr test” that proves this. It is likely that numerous individuals previously believed to be “hiv positive” are already in a functional remission of sorts. But the CDC/DHHS and Gilead Sciences jointly co-own the patents on an HIV drug called “truvada” , which they claim allows “hiv positive” people to have sex with “hiv negative” people without transmitting “hiv.” There is a pending class action lawsuit against Gilead Sciences in which it is alleged Truvada destroys plaintiffs bones and organs.
That would be really awkward for the CDC/DHHS if it turns out millions of people didn’t need the medicine – or that “hiv viral load” isn’t what they thought it was, and they encouraged millions of people to engage in unprotected sex, assuring them it was “safe and effective” and that “undetectable = untransmissible.”
What if, “oh hahah oops, the “3′ stop codon’ at the “end” of the “second” orf was actually … the middle of the gene … and that there were eight more of them than previously discovered?
Can DARPA shut off the “bioreactor” they turned you into with mRNA?
This was no such thing as “stop” and “superstop,” this was a codon that was in a codon position normally associated with a 3′ UTR stop codon, except in the case of Chikungaya, it’s still well into mid-codon.
It is not the stop codon.
Does it contain a “non essential protein” ? Yes. NLuc, nano-luc.
Analogous to “NEF” in “HIV”, if I have that correct.
Which begs the question of whether NEF is HIV’s stop codon and whether that illness also consists of heretofore undiscovered ORFs.
In a 3:1 ratio, UAG is a single codon consisting of 3 nucleotides.
In a 1:1 ratio, U, A, and G are three codons consisting of 1 nucleotide.
And while previously thought to consist of two Open Reading Frames at ORF1 and ORF2..
… there are 10 of them …
“covid-19” is a botched hiv vaccine / chikungaya vaccine. Defense Advanced Research Projects Agency grant HR0011-17-2-0069 and Gates Foundation grant OPP1066832 are the paper trail proving it.
That’s the best information DARPA and Moderna had available when they started pursuing an mRNA Chikungunya vaccine in 2015.
Back in 2013, the U.S. Department of Defense’s Defense Advanced Research Projects Agency (DARPA) awarded Moderna up to $25 million to develop antibody-producing drugs against infectious diseases and other biological threats. The scope of the grant was expanded in 2015 to support vaccines projects, including this Chikungunya candidate.
Here’s a really pretty chart with a nice graphic and everything explaining the two ORFs and how the vaccine’s going to work.
They’re not “mutations.”
The codon to nucleotide ratio was interpreted incorrectly.
And if you’re not sure what they represent, keep your god damned fucking needle to yourself.
And then, come January 2019:
Hey kids, the genome of Chikungaya is “poorly understood!” Let us modify your genes, for something we don’t fucking UNDERSTAND!
Got it everyone? Four months after “the biology of it is poorly understood” they’re over here cooking up batches of CRISPR and injecting people anyway.
You could have said something.
But you already know that if you’d explained the mishap, nobody on this planet in their right fucking mind would have gotten it.
In 2020, they were aware that Ivermectin treats chikungaya.
So they didn’t call this illness “chikungaya” to market their shot.
There was no need for an EUA, we had a treatment for it (ivermectin).
Which they concealed by lying about its name and its nature.
It’s not all bad news, “HIV positive” people have one of the lowest “covid-19” mortality rates out of ANY group.
Natural “covid-19” infection appears to damage the NEP, “NEF” in HIV, resulting in a weakened form of “HIV.” [ with potentially life threatening anemia/ARDS, I will get to that next]
In the case of the United States,
Withholding information about risks, lying about what the disease or the treatment even are, and censoring anyone who claims there are adverse effects is interference with my right to informed consent.
Threatening to weld me in my house, deny me public accommodations, groceries etc , and inciting others to shun, dissociate from me like a cult, or otherwise coerce me, is against my federally established civil right to “voluntary” participation.
When you “coerce” someone to have sex, its rape.
Coercion is force.
Both of these categories are a defacto conspiracy to deny civil rights established under CFR 45 46, to wit, the rights to informed consent and voluntary participation. This comes with up to a 10 year prison sentence or the death penalty in the event someone dies from your negligence or willful conduct, deceptive business practices, and racketeering.
There are called “Nuermburg Laws” elsewhere.
The unlawful, hostile, foreign occupation of the United States is not a peaceful or law abiding one. It is one that giddily violates Nuremburg and has an awful lot of willing and eager co-conspirators.
I am not a “traitor” to my home country or people: “i tried” even if you appear to be a lost cause at times.
Here is what I can tell you about p24: its like an immunological indicator lamp. It burns brightly in the presence of malaria, zika, chikungaya, HIV, just to name a few. It fades when the infection is cleared, as is the case with malaria.
Your Elisa p24 antibody test remains “hiv positive” unless you knock out the Non Essential Protein (NEP) which in the case of HIV is NEF.
p43 , p120, and p160 are multimers of p40, which means “they’re just clumps of p40 sticking to each other.” What is p40? Parasitic infection.
On the topic of “swine flu,” as I previously posted, the 1967 “marburg virus” outbreak occurred at the BSL-3 Paul Ehrlich Institute in Marburg DE, and at the same factory in Frankfort DE that produced Bio-N-Tech. 100% of the victims were occupational exposures from vaccine labs.
There is some vague mention that it possibly occurred in San Diego CA at the same time in news archives but no one goes into detail.
When Nixon and Agnew resigned, we got Gerald Ford for president, who nobody elected. You also got Joe Biden around this time. Ford made Saul Paul Ehrlich Jr his Surgeon General. This is Paul Ehrlich’s son (or grandson.) Furthermore, the Paul Ehrlich Institute has been an independent German Federal Agency since 1962. Ehrlich Jr failed to disclose his conflicts of interest with his family’s vaccine research and development business and he violated Hatch Act in failing to register as a foreign agent for his family owned German Federal Agency.
Ehrlich Jr’s first order of business was to approach Congress and the CDC in January of 1976 arguing to remove liability for vaccine manufacturers, for nooooooo reason at all, over the objections of the CDC. So they got rid of anyone sane at CDC.
Ehrlich Jr’s second order of business was to attempt to inject 212 million Americans with a “swine flu” vaccine his family’s vaccine business was involved in developing in March of 1976. It was halted for safety reasons after .. idk.. about 50 million people had received it
Ehrlich Jr’s testimony before Congress was considered when the 1984 NIDA/Vaccine Act was implemented – formally waiving vaccine liability. This should not have happened, as he had familial and financial conflict of interest. After that, the United States more or less became a Vaccineocracy. We had Searle/Pfizer’s Donald Rumsfield as our minister of war, we now have a CDC/FDA packed with pharma CEOS, DARPA is in bed with Moderna , which is in bed with Bill and Melinda and the University of Washington, and they think they have a free pass. Unless, of course , they’re violating federal law (CFR 45 46) and/or conspiracy to deny rights (and/or “under color of law.”)
And they absolutely are.
DARPA was instrumental in making Twitter and Facebook, and they silence their critics and continue to ban/ostracize/punish them.
If you did that to me for these people, cheered as I was censored, or thought it somehow “made sense” to imprison or murder anyone who resisted these people or attempted to speak about their deeds, you are insane. “Depart from me. I never knew you.”