I don't believe they're trying to help.

So based on my research... I can't conclude anything but have a few speculations. (self.conspiracy)

submitted 5 hours ago * by Catsarenotreptilians

You can go ahead and hunt for the papers, I'm not bother linking them, this is going to be a short post.

I believe they were working on combating HIV gp120, this is what the "gain of function" research was actually working on...

HIV gp120 is literally what's causing 90% of people's issues. Go ahead and go to duck duck go and search "Covid GP120" don't put hiv, you will get some creepy results.

HIV gp120 is cytotoxic itself, and in the brain, is known to cause brain fog in HIV positive individuals.

The vaccine is clearly a rush to get something into the brain/past the blood brain barrier (BBB), and its pretty clear that its gp120.

Now the exact's around all of this are VERY confusing.

Theoretically, this medical catastrophe could be worse than we could imagine. They want to force your body to have an immune response against the covid spike protein (gp120 is what makes covid spike protein so bad, based upon all my research)/gp120, either for good or for bad.

There is also the other fact that its proven that a decent amount of the gp120 makes it into the reproductive tract.

They are not hiding the fact that there will be an explosion in Alzheimer's patients in the future, obviously due to a large elderly popuation but its odd that they aren't even sugar coating this.

All the prion stuff, including from covid itself, and the vaccine, is centered around the spike protein/gp120 being the cause of protein misfolding.

The other scary part:

https://miningawareness.wordpress.com/2021/08/24/covid-19-neurodegenerative-disease-risk-from-pfizer-mrna-vaccine-prions-cjd-alzheimers-parkinsons-disease/

This isn't the greatest resource/information source, but if this is true, this is fucked up:

“COVID-19 RNA Based Vaccines and the Risk of Prion Disease by J. Bart Classen, MD* Republished Citation: Classen JB. COVID-19 RNA Based Vaccines and the Risk of Prion Disease; Microbiol Infect Dis. 2021; 5(1): 1-3. ISSN 2639-9858 * Classen Immunotherapies, Inc., 3637 Rockdale Road, Manchester, MD 21102 Keywords: COVID-19, Vaccines, Diabetes, Immunity, prion

ABSTRACT Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARS-CoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing.

In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients. The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations.

The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations.

https://web.archive.org/web/20210210033730/https://scivisionpub.com/pdfs/covid19-rna-based-vaccines-and-the-risk-of-prion-disease-1503.pdf

Here's a link, its been scrubbed... Coincidental. /s

" The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration."

https://pubmed.ncbi.nlm.nih.gov/15370273/

HIV-1 gp120 and immune network

"It has been demonstrated that the immunodominant V3 loop of HIV-1 gp120 and its flanking regions bear sequence and structural homology to the framework and complementarity-determining regions of human immunoglobulins. It has been proposed that the Ig-like domain of gp120 might encode idiotypes and in this way permit HIV-1 entry into the immune regulatory network. This notion is strongly supported by results demonstrating that the anti-V3 loop and anti-Ig antibodies of healthy individuals share complementary structure and that V3 reactive antibodies are present in HIV-negative sera. This might be the mechanism by which HIV induces immunological abnormalities, "

Did you read that, this study is about HIV-1 gp120, reread that last bolded sentence.

Now, I will leave you with the list of Anthony Fauci's patents: Do a quick search on the webpage for "gp120", you might be surprised. https://patents.justia.com/inventor/anthony-s-fauci

TL;DR: theoretical: Fauci funded gp120 gain of function research in China, it escaped, they are trying to prevent worldwide prion issues/or compromised immune systems/etc. Someone seems to own a lot of patents on gp120 function. You may recognize him.

EDIT: I won't be shocked if this get shadowbanned/hidden. :c