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USGabbard Drops Receipts Detailing US-Funded Biolabs In Ukraine
Today, I’m releasing never before seen intelligence revealing new evidence of past US government funding for more than 120 biolabs in over 30 countries, including Ukraine.
In support of President Trump‘s Executive Order to end federal funding of dangerous gain of function research around the world, and increase transparency and accountability, ODNI will continue working with partners across the Administration to identify where these labs are, what pathogens they contain, and what “research” is being conducted.
Outgoing Director of National Intelligence Tulsi Gabbard on Friday declassified a set of internal intelligence slides documenting a long-running US program that has funded a worldwide network of biolabs that handle dangerous pathogens - including dozens in Ukraine.
Gabbard, who is set to leave her post at the ene of this month, said that the documents are "new evidence of longstanding United States government funding for more than 120 biolabs in over 30 countries," with over 40 of those in Ukraine, adding that this information has been "knowingly withheld from the American people." She accused US officials, along with Dr. Anthony Fauci and the Biden administration's national security team, of having "lied to the American people about the existence" of the labs.
"Now, despite the obvious potential for catastrophic global impact that research on dangerous pathogens in biolabs can have, politicians and so-called health professionals like Dr. Fauci, as well as entities within the Biden administration’s national security team, lied repeatedly to the American people about the existence of U.S.-funded and supported biolabs," Gabbard said, adding "Not only did they lie, they threatened those who attempted to expose the truth."
The slides, declassified April 23 and released Friday, describe facilities supported under the Defense Department's Cooperative Threat Reduction program, a post-Cold War effort begun in the 1990s to secure pathogens and weapons materials left over from the Soviet Union. In Ukraine, the program has operated since 2005, investing roughly $200 million to upgrade Ukrainian-run public-health and veterinary labs, according to Pentagon fact sheets. One newly declassified slide reflects a prior intelligence assessment that a veterinary lab in Kharkiv likely held dangerous pathogens and was vulnerable to Russian seizure or damage.
Gabbard tied the release to Executive Order 14292, which President Trump signed in May 2025 to end federal funding of gain-of-function research, and said she had directed the intelligence community to step up collection on the labs. The release is part of a wave of declassifications in her final weeks; an ODNI official has said she is working to release documents on the origins of COVID-19 before her departure.
The existence of the U.S.-funded labs has been public for years: the Pentagon published fact sheets on the program, the U.S. Embassy in Kyiv described it in 2020, and Under Secretary of State Victoria Nuland acknowledged Ukraine's "biological research facilities" in Senate testimony in March 2022 - in what Glenn Greenwald framed at the time as "with palpable pen-twirling discomfort and in halting speech, a glaring contrast to her normally cocky style of speaking in obfuscatory State Department officialese - acknowledged: “uh, Ukraine has, uh, biological research facilities.” Any hope to depict such "facilities” as benign or banal was immediately destroyed by the warning she quickly added: “we are now in fact quite concerned that Russian troops, Russian forces, may be seeking to, uh, gain control of [those labs], so we are working with the Ukrainiahhhns [sic] on how they can prevent any of those research materials from falling into the hands of Russian forces should they approach”
U.S. Under Secretary of State Victoria Nuland says Washington is working with Ukraine to prevent biological research facilities from falling into Russian hands. She just confirmed every conspiracy theory about the existence of those labs.
Why was an Epstein-associated fucking spook taking money from USAID and the Pentagon to research viruses in Ukraine?
I'll tell you exactly why.
DARPA, DTRA, USAID, and the CIA are all part of a biodefense mafia ring. It all started in 1969 when Nixon gave a speech on ending the US offensive bioweapon program, which culminated in the signing of the Biological Weapons Convention (or Biological and Toxin Weapons Convention, the BTWC), a treaty that prohibited further development of offensive bioweapons.
The treaty contained a loophole. It permitted pretty much all of the same exact Gain-of-Function research as was conducted under offensive biowarfare programs. All they had to do to avoid violating the treaty was euphemistically switch the names of the programs from biowarfare to biodefense, and say they were preemptively engineering deadly pathogens in order to vaccinate against them, just in case terrorists or anyone not signatory to the BTWC released a bioweapon. But the key point here is that the treaty is completely toothless and essentially has no force to actually stop the dangerous research in question.
Fearmongering about bioweapons was a cash cow and provided job security to virologists and bacteriologists and lucrative contracts to companies that sold huge lots of highly toxic vaccines to our military, like the Anthrax vaccines that caused Gulf War Syndrome. The Defense Threat Reduction Agency, for their part, had a component of the Nunn-Lugar Cooperative Threat Reduction program called the CBEP or BTRP (Cooperative Biological Engagement Program or Biological Threat Reduction Program - it's the same program, they just renamed it), where they partnered with countries with known current or former bioweapon stockpiles to destroy their stockpiles, just like the other components of the CTR for reducing stockpiles of other types of WMDs.
The key thing is that the CBEP/BTRP also gave DTRA a foot in the door to fund NGOs, like Metabiota and EcoHealth Alliance, to subcontract grants to foreign biolabs to conduct dangerous GOF research that would otherwise have been done in American BSL-3 or BSL-4 labs with oversight and FOIA accessibility. Edward Hammond knew about the expanding BSL-3 and BSL-4 lab capacity in the US throughout the 2000s and called it into question.
Not only were his concerns rebuffed by perennial biodefense mafia apologist Gigi Kwik Gronvall, a woman whose name sounds like Tolkien's idea of a name for a bridge troll, but immediately after the hearing in 2007, Nathan Wolfe founded Global Viral, the biolabs in the US quietly shuttered, and all of the work that was scrutinized by Edward Hammond was quietly outsourced to countries with no FOIA oversight where almost none of the lab staff speak English.
In 2014, there was a GOF research moratorium under the Obama administration specifically forbidding enhanced flu, SARS, MERS, et cetera.
Virologists threw a conniption fit because the gravy train was put on hold. Around that time, the head of EcoHealth Alliance, Peter Daszak, held a meeting where he said:
"Until an infectious disease crisis is very real, present, and at an emergency threshold, it is often largely ignored. To sustain the funding base beyond the crisis, he said, we need to increase public understanding of the need for MCMs such as a pan-influenza or pan-coronavirus vaccine. A key driver is the media, and the economics follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of process."
"Medical Countermeasures" (or MCM) is not a pharmaceutical term. It is military biodefense jargon and refers to the use of rapid-deployment vaccines and other measures to counter a foreign bioweapon attack.
Medical countermeasures, or MCMs, are FDA-regulated products (biologics, drugs, devices) that may be used in the event of a potential public health emergency stemming from a terrorist attack with a biological, chemical, or radiological/nuclear material, or a naturally occurring emerging disease.
The Defense Advanced Research Projects Agency (DARPA) is authorized to conduct a separate extramural program of basic and applied research in chemical and biological defense and, over the past 5 years, has included work on medical biodefense countermeasures. DARPA was established in 1958 to permit more flexible approaches to long-horizon, highrisk, high-payoff research within DoD. Its research program is shaped, in part, by the expertise and interests of program managers, who are recruited for 4-year periods. Programs do not necessarily continue beyond the tenure of their program managers. Some of the promising DARPA-funded projects on medical countermeasures have been transferred to the science and technology base of the Chemical and Biological Defense Program for further work.
In March 2016, a paper was published by Dr. Ralph Baric, an EcoHealth Alliance gain of function collaborator working at UNC, in PNAS titled “SARS-like WIV1-CoV Poised for Human Emergence.” In the article, the authors of the paper describe in detail how they used, designed, and constructed fulllength and chimeric viruses to determine if they would replicate in human airway cultures. This specific paper is relevant because it compares and documents the effectiveness of different variations gof coronavirus spike proteins at infecting human cells specifically by binding to ACE2 receptor, which was a critical and necessary step to design and engineer the SARS-COV2 virus. While 4 employed at EcoHealth Alliance, I met both Dr. Shi Zhengli and Dr. Ralph Baric, where they presented their work on the design and engineering of SARS-CoV2 (coronavirus gain of function research), and the use of highly specialized humanized mice models, which were necessary to successfully build SARS-COV2. These facts are supported by numerous recorded presentations by Dr. Peter Daszak and Dr. Ralph Baric from 2015- 2019. Some of which, I personally attended while employed at EcoHealth Alliance. 5 Additionally, the specific gain of function work described in this paper was presented by Dr. Peter Daszak to In-Q-Tel, a DoD and CIA venture capital firm. In the slides presented to In-Q-Tel, which I personally helped create at EcoHealth, describe the use of USAID – EPT – PREDICT funding to collect coronavirus samples from bats globally, where they are then analyzed to identify their most dangerous features to humans, and recombined to make new coronaviruses like SARS-COV2. Then, these viruses are tested on humanized mice to validate lethality and transmissibility. EcoHealth Alliance then used Dr. Baric’s work for testing experimental vaccines, treatments, and therapeutics against the newly engineered SARS-COV2 strain to determine which countermeasures would be the most effective at mitigating the disease in humanized mice. Reference: Menachery, V. D., Yount Jr, B. L., Sims, A. C., Debbink, K., Agnihothram, S. S., Gralinski, L. E., ... & Baric, R. S. (2016). SARS-like WIV1-CoV poised for human emergence. Proceedings of the National Academy of Sciences, 113(11), 3048-3053.
Ralph Baric at UNC Chapel Hill partnered with Shi Zhengli at the WIV on bat coronaviruses for many years, and he shared his viral recombinant genetic engineering techniques with her.
If this was supposed to be CIA intelligence work, using NGOs and middlemen for surveillance of Chinese biolabs suspected of doing bioweapon research, why were the technology transfers going in the wrong direction, from the US to China?
The head of mRNA vaccine manufacturer Moderna, Stephane Bancel, was formerly the head of BioMerieux, in France. The founder of BioMerieux, Alain Merieux, was the man principally responsible for the French-Chinese partnership to build the BSL-4 lab at the Wuhan Institute of Virology in the first place.
The institute is home to the China Centre for Virus Culture Collection, the largest virus bank in Asia which preserves more than 1,500 strains, according to its website.
The complex contains Asia's first maximum security lab equipped to handle Class 4 pathogens (P4)—dangerous viruses that pose a high risk of person-to-person transmission, such as Ebola.
The 300-million-yuan ($42 million) lab was completed in 2015, and finally opened in 2018, with the founder of a French bioindustrial firm, Alain Merieux, acting as a consultant in its construction.
France thought that the partnership would be a foot in the door to conduct joint French-Chinese virus research at the lab, but then, to no one's surprise, China closed their doors to basically everyone. Except, of course, for the Western NGOs feeding them grant money.
The funding relationship here is circular and RICO-like. DTRA and USAID funded the virus research via middlemen like EcoHealth Alliance and Metabiota. DARPA and BARDA funded Moderna and mRNA vaccine research, and Dan Wattendorf, the main cheerleader for mRNA vaccines at DARPA, now works for the Gates Foundation. The Pentagon paid for the virus. The Pentagon paid for the vaccine.
The COVID-19 vaccines were acquired under an Other Transaction Authority contract as "Medical Countermeasures", allowing them to bypass any sort of requirement for proper clinical trials and certification. The FDA and the clinical trial runners actually committed fraud by authorizing the vaccines, for two reasons.
One, the vaccines were never legally pharmaceuticals in the first place, but were acquired as "military prototypes to demonstrate mass production and processes". Usually, OTA contracts are used by the DOD to acquire limited runs of prototypes of things like sensor turrets and night vision goggles, not tens of billions of dollars of vaccines. The PREP act not only authorized all of this bullshit, but gave the manufacturers total immunity.
Two, the vaccine manufacturers switched from one process to another. They conducted clinical trials for one process, falsified their fucking Western Blots, and then switched to another, cheaper recombinant process with lots of junk and impurities ending up in the vials. Also, SARS-CoV-2 Spike is a horrifying prion-like protein that causes vascular amyloidosis and slowly turns your blood plasma into a hydrogel-like substance that fluoresces strongly on Thioflavin T staining due to all the amyloid-fibrin "fibrinaloid" gunk in it.
The Covid mRNA vaccines were acquired and authorized through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction.
These mechanisms did not require the application of, or adherence to, any laws or regulations related to vaccine development or manufacturing.
The FDA’s Emergency Use Authorization for the vaccines was based on clinical trials and manufacturing processes conducted with no binding legal standards, no legally proscribed safety oversight or regulation, and no legal redress from the manufacturer for potential harms. (This last point is being challenged in multiple court cases, so far to no avail.)
Other Transaction Authority/Agreement (OTA): A Military Acquisition Pathway
The agreement between the US government, represented by the Department of Defense (DoD), and Pfizer, representing the BioNTech/Pfizer partnership, in July 2020, for the purchase of a “vaccine to prevent COVID-19” was not an ordinary acquisition contract.
It was an agreement under Other Transaction Authority (OTA) – an acquisition pathway that, according to Department of Defense guidelines, has been used since 1958 to “permit a federal agency to enter into transactions other than contracts, grants, or cooperative agreements.”
A new peer-reviewed study has quietly revealed one of the most consequential biological findings of the pandemic era — and the authors never acknowledge it: Every single vaccinated participant in the study had fibrinolysis-resistant, ThT-positive amyloid microclots circulating in their blood.
The house of cards will fall. It is only a matter of time. All of the scum in the government responsible for this and their Neo-Malthusian, anti-natalist plutocrat buddies need to be perp-walked in front of the whole world.
There is no difference between the Mob and all these institutions, they have been completely captured. This couldn't be any more corrupt.
Most politicians and officials dirtied their hands, so they will probably never want to seriously acknowledge this.
A new peer-reviewed study has quietly revealed one of the most consequential biological findings of the pandemic era — and the authors never acknowledge it: Every single vaccinated participant in the study had fibrinolysis-resistant, ThT-positive amyloid microclots circulating in their blood.
It's so wild to me that excess deaths are still up by an alarming amount and all these institutions decided to do is try and stop publicizing all cause mortality statistics.
In a few years this will become more and more apparent. When endless numbers of people get Creutzfeldt–Jakob like symptoms.
For anyone who hasn't been keeping up: Having avoided the COVID vaccine means very little. It's the spike protein, which has the furin cleavage site, that catalyzes these amyloids, and it is on the virus itself.
Furthermore, these amyloids are stable in the environment for years. Considering that there are people whose bodies are still producing spike protein, as well as others who have suffered a prion cascade, it is very easy to get enough of these amyloids in your body from the environment to start a cascade.
These neurodegenerative diseases take quite some time to get spotted. You can go a decade without symptoms, and by the time your nerves start acting up, your brain is already full of holes.
There is no difference between the Mob and all these institutions, they have been completely captured. This couldn't be any more corrupt.
Most politicians and officials dirtied their hands, so they will probably never want to seriously acknowledge this.
It's so wild to me that excess deaths are still up by an alarming amount and all these institutions decided to do is try and stop publicizing all cause mortality statistics.
In a few years this will become more and more apparent. When endless numbers of people get Creutzfeldt–Jakob like symptoms.
For anyone who hasn't been keeping up: Having avoided the COVID vaccine means very little. It's the spike protein, which has the furin cleavage site, that catalyzes these amyloids, and it is on the virus itself.
Furthermore, these amyloids are stable in the environment for years. Considering that there are people whose bodies are still producing spike protein, as well as others who have suffered a prion cascade, it is very easy to get enough of these amyloids in your body from the environment to start a cascade.
These neurodegenerative diseases take quite some time to get spotted. You can go a decade without symptoms, and by the time your nerves start acting up, your brain is already full of holes.
Severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2)-induced infection, the cause of coronavirus disease 2019 (COVID-19), is characterized by unprecedented clinical pathologies. Phenotypic vascular characteristics are strongly associated with various coagulopathies that may result in either bleeding and thrombocytopenia or hypercoagulation and thrombosis [1,2]. Various circulating and dysregulated inflammatory coagulation biomarkers, including fibrin(ogen), D-dimer, P-selectin and von Willebrand Factor (VWF), C-reactive protein (CRP), and various cytokines, directly bind to endothelial receptors. Endotheliopathies are therefore a key clinical feature of the condition [3,4]. During the progression of the various stages of the COVID-19, markers of viral replication, as well as VWF and fibrinogen depletion with increased D-dimer levels and dysregulated P-selectin levels, followed by a cytokine storm, are likely to be indicative of a poor prognosis [5–8]. This poor prognosis is further worsened as together with a substantial deposition of microclots in the lungs [9–11]. Plasma of COVID-19 patients also carries a massive load of preformed amyloid clots [5], and there are also numerous reports of damage to erythrocytes [12–14], platelets, and dysregulation of inflammatory biomarkers [5–8].
The virulence of the pathogen is closely linked to its membrane proteins. One such protein, found on the COVID-19 virus, is the spike protein, which is a membrane glycoprotein. The spike proteins are the key factors for virus attachment to target cells, as they bind to the angiotensin-converting 2 (ACE2) surface receptors [15]. Spike proteins are class I viral fusion proteins [16]. They are present as protruding homotrimers on the viral surface and mediate virus entry into the target host cells [17]. A singular spike protein is between 180 and 200 kDa in size and contains an extracellular N-terminal, a transmembrane domain fixed in the membrane of the virus, and a short intracellular C-terminal segment [16,18]. Spike proteins are coated with polysaccharide molecules that serve as camouflage. This helps evade surveillance by the host immune system during entry [18]. The S1 subunit is responsible for receptor binding [19], with subunit 2 (S2), a carboxyl-terminal subunit, responsible for viral fusion and entry [20] (see Figure 1).
Figure 2. S-protein proteolysis by NE renders amyloid-like fibrils. Thermostability of (A) SARS-CoV-2 S-protein, (B) NE, (C) S-protein+NE, measured by DSF. Dashed line in (C) is the mathematical sum of S-protein and NE, respectively, from (A) and (B) supporting cleavage of S-protein by NE. MALDI-ToF spectra of C18 isolated peptides of (D) S-protein, (E) NE, and (F) S-protein+NE (6 h, 37 °C). TEM micrographs of (G) S-protein alone depicting the expected trimers, (H) NE alone, and (I) S-protein+NE coincubated at pH 8.4, 24 h, 37 °C.
Most importantly, we discovered amyloid-like fibril formation upon proteolytic cleavage using TEM. Neither NE nor SARS-CoV-2 S-protein incubated alone formed fibrils (Figure 2G–H). Fibrils were found only after co-incubation of the two proteins (Figure 2I). The fibrils showed unusual morphology with evident branching (Figure 2I), suggesting involvement of proteolytically nicked S-protein within the fibril, rendering nodes for branching of different amyloidogenic sequences (Figures 2I and S5).
When Spike is proteolytically cleaved and broken down, it forms small peptide fragments (protein debris) which are, themselves, amyloidogenic.
Do people realize that an airborne prion disease, with a virus modified so that its proteins cross the blood-brain barrier and cause CJD, would be literally the most insanely lethal bioweapon ever devised? You could give it high transmissibility and relatively low virulence, everyone would seem perfectly fine, and then a decade later, they drop dead from Mad Cow Disease. Completely doable with current technology. Actually, completely doable like decades ago.
Do people realize that an airborne prion disease, with a virus modified so that its proteins cross the blood-brain barrier and cause CJD, would be literally the most insanely lethal bioweapon ever devised? You could give it high transmissibility and relatively low virulence, everyone would seem perfectly fine, and then a decade later, they drop dead from Mad Cow Disease. Completely doable with current technology. Actually, completely doable like decades ago.
Potentially. I’m hearing some reports that basically everyone who was exposed to Spike, vax or virus, has the ol’ jelly-blood. Elevated levels of amyloid and fibrin accumulations. Those fibrous white clots that coroners have been pulling out of people are giant cell-free hunks of protein, almost like a biopolymer. Normal blood clots have platelets in them, and they undergo fibrinolysis, dissociate, and dissolve over time. These resist enzymatic breakdown and just keep getting bigger by autocatalysis until they block the blood vessels. Not good.
There are some groups experimenting with filtering blood plasma, with some success, like using HELP apheresis or DFPP (plasmapheresis), but that’s quite expensive and difficult. It’s like putting someone on dialysis. They’re taking blood plasma out, filtering it extracorporeally, and putting it back in, removing the amyloids. Even then, if there are small bits of amyloid left over, they can just keep accumulating even more over time by autocatalysis, so it ends up being a continuous process of repeat treatments. I think the real solution would be some kind of targeted protein biologic that binds and removes Spike and its debris, as a follow-on to the plasmapheresis.
Amyloid fibril formation is basically a continuous chemical reaction of proteins clumping into strands of unusable, indigestible junk. It's one of the main limiting factors in human lifespan: most supercentenarians die of progressive amyloidosis if they manage to escape the usual killers of old people like cancer, diabetes, high blood pressure, heart failure, et cetera. Alzheimer's disease is thought to involve tauopathy where misfolded tau proteins accumulate in the brain. Protein misfolding is a real bitch of a pathology, and viral proteins that induce misfolding in human proteins are a total nightmare.
Amyloid fibril formation is basically a continuous chemical reaction of proteins clumping into strands of unusable, indigestible junk. It's one of the main limiting factors in human lifespan: most supercentenarians die of progressive amyloidosis if they manage to escape the usual killers of old people like cancer, diabetes, high blood pressure, heart failure, et cetera. Alzheimer's disease is thought to involve tauopathy where misfolded tau proteins accumulate in the brain. Protein misfolding is a real bitch of a pathology, and viral proteins that induce misfolding in human proteins are a total nightmare.
