Project Veritas: Former DARPA Fellow Pens Letter Exposing Gov’t Secrets

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U.S. Marine Corps Major Joseph Murphy wrote a letter in August of 2021 with important evidentiary attachments that have now been obtained by Project Veritas. The documents further verify previously released information, according to Project Veritas founder James O’Keefe.

Murphy, formerly a fellow with DARPA, has exposed additional “incriminating documents…hidden in a top-secret shared drive” concerning the gain-of-function research on bat-borne coronaviruses and the link between NIH and EcoHealth Alliance to the Wuhan Institute of Virology. According to Murphy, the documents were placed in the folder in July 2021. To this day, Fauci denies involvement in gain-of-function research and/or contracts.

In the August 13, 2021 letter with attachments obtained by Project Veritas, Murphy discusses information and documents to which he was privy during his time as a fellow for DARPA. Project Veritas emphasizes in its video that Maj. Murphy is “not the source of its reporting” and has done “nothing wrong.”

Murphy explains that the EcoHealth alliance submitted a proposal for a two-phase, $14,209,245 project named DEFUSE—Defusing the Threat of Bat-borne Coronaviruses (2018) to the Defense Advanced Research Projects Agency (DARPA) to conduct gain-of-function research of bat-borne coronaviruses. The purpose of the research was allegedly designed to “innoculate bats in Yunnan, China caves where confirmed SARS-CoVs were found. Ostensibly doing this would prevent another SARS CoV pandemic; the bats’ immune systems would be reinforced to prevent a deadly SARS-CoV from emerging.” Ultimately, the proposal was rejected because the risks were not well-considered at the time.

DARPA says no to DEFUSE

Murphy states that SARS-CoV-2 or, in his words, “SARS-CoV-WIV” (Wuhan Institute of Virology) is:

“less a virus than it is engineered spike proteins hitchhiking a ride on SARSr-CoV quasispecies swarm…it is a synthetic spike protein chimera engineered to attach to human ACE2 receptors and inserted into a recombinant bat SARSr-CoV backbone.”

Murphy also explains that EcoHealth and the “NIAID under the direction of Dr. Fauci, went ahead with the research in Wuhan, China and at several sites across the U.S.” Incidentally, the Obama administration and the NIH announced a moratorium on funding for gain-of-function research on October 17, 2014. The moratorium was lifted in 2017.

As previously mentioned above, the virus was accidentally released before it was “fully attenuated.” That means it was released before it mutated sufficiently “to be non-pathogenic…presumably to bats and humans,” as explained by mRNA developer Dr. Robert Malone.

Significantly, in the same article, Dr. Malone questions the logic of a construct where researchers would “choose a chimera that attaches to the human ACE2 receptors as the target?” Malone explains:

“Warning- tortuous logic curves ahead…”

“Once again seeking to provide the benefit of the doubt, I suspect that the logic must have been that by vaccinating the bats with such a construct, this would reduce the risk of developing a human-adapted, ACE2-binding SARS-related virus in same bats. But if this is the case, then the logic is really convoluted. One would first develop a human-adapted SARS-like virus which binds human ACE2, then attenuate this virus, then find a way to aerosolize it, then infect the bats. And apparently, somehow, before the attenuation step to adapt the human-adapted virus to infect the bats, there was a lab leak.”

One of the more remarkable disclosures was Murphy’s reflection pertaining to whether government officials who received the report adequately understood “the significance of what [he] communicated” and that important “decisions with regards to the vaccines do not appear to be informed by analysis of the documents.” He goes on to say that SARS-CoV-2:

“matches the SARS vaccine variants the NIH-EcoHealth program was making in Wuhan; that the DOD rejected the program proposal because vaccines would be ineffective and because the spike proteins being inserted into the variants were deemed too dangerous (gain-of-function); and that the DOD now mandates vaccines that copy the spike protein previously deemed too dangerous. To me, and to those who were informed by analysis, this situation meets no-go or abort criteria with regards to the vaccines until the toxicity of the spike protein can be investigated. There’s also information within the documents about which drugs effectively treat the program’s SARS-CoVs.” (bold lettering added)

Murphy also emphasizes the vaccine’s poor efficacy in protecting against coronavirus, explaining that the…

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