COVID-19
Deborah Birx Came Directly from USAID
From the Brownstone Institute
Deborah Birx, who became the White House Coronavirus Task Force Coordinator on February 27, 2020, came directly from USAID – the department everyone now knows to be a front for CIA propaganda and regime change operations. [ref]
She served as U.S. Special Representative for Global Health Diplomacy, a joint USAID and State Department office that had ” developed a strategic approach to accomplish their shared mission that focuses on robust diplomacy and development as central to solving global problems.” [ref]
Almost exactly five years ago, the public was told that Deborah Birx was appointed by Vice President Mike Pence who, on February 26, 2020, took over coordination of the U.S. government’s response to the novel coronavirus. [ref]
The announcement said:
Ambassador Birx is a world-renowned global health official and physician. She will be detailed to the Office of the Vice President and will report to Vice President Mike Pence. She will also join the Task Force led by Health and Human Services Secretary Alex Azar. She will be supported by the National Security Council staff. [ref]
This announcement contains hints that Birx was not chosen by public health agencies or officials. Rather, she appears to be coming from the national security apparatus, and “will be supported by the National Security Council staff.”
Further supporting this supposition, on March 11, 2020, at a Heritage Foundation Talk, Trump’s National Security Advisor, Robert O’Brien, when discussing what the White House and NSC were doing about the virus, said:
We brought into the White House Debi Birx, a fantastic physician and ambassador from the State Department. We appreciate Secretary Pompeo immediately moving her over to the White House at our, well at the President’s, request. [min. 21:43 – 21:56]
In other words, Birx was “moved over to the White House” by the Secretary of State, at the request of the National Security Council.
The National Security Council Was in Charge of the U.S. Government’s Covid Response
These facts about Deborah Birx’s appointment to the Task Force are consistent with the government pandemic planning documents that show the NSC – not the HHS, CDC, NIAID, or any other public health agency – was in charge of the U.S. government’s Covid response policy.
Investigating Deborah Birx’s Role in the Covid Response
In August 2022 I published a series of articles investigating how Deborah Birx got the job on the Task Force, the bogus science she promoted, and her relationship with the public health officials on the Task Force.
Here are excerpts from, and links to, those articles:
How Did Deborah Birx Get the Job?
Deborah Birx, an immunologist and Army Colonel who worked for the Department of Defense and US Military on AIDS research, served as Directory of the CDC’s Division of Global HIV/AIDS and as the US Global AIDS Coordinator [ref], was appointed White House Coronavirus Response Coordinator on February 27th, 2020.
She had no training or experience in epidemiology, novel pathogen pandemic response, or airborne respiratory viruses like the coronavirus.
She was offered the position by Matt Pottinger, Deputy National Security Advisor for China, who told Birx that if she did not take the job American lives could be lost.
In her “excruciating story” of the pandemic, Silent Invasion, Deborah Birx does not even try to make coherent scientific or public health policy arguments in favor of the Chinese-style totalitarian measures she advocated. Instead, she provides self-contradictory assertions – some downright false and others long disproven in the scientific literature.
We know Birx was not working with President Trump, although she was on a task force ostensibly representing the White House. Trump did not appoint her, nor did the leaders of the Task Force, as Scott Atlas recounts in his revelatory book on White House pandemic activity, A Plague Upon Our House. When Atlas asked Task Force members how Birx was appointed, he was surprised to find that “no one seemed to know.” (Atlas, p. 82)
Yet, somehow, Deborah Birx – a former military AIDS researcher and government AIDS ambassador with no training, experience, or publications in epidemiology or public health policy – found herself leading a White House Task Force on which she had the power to literally subvert the policy prescriptions of the President of the United States.
It is my (as yet unproven) theory that the lab-leak cabal, for which Birx was a primary agent in the US government, wanted to impose strict lockdowns all over the world.
Whatever their motives, the goal seems very clear: Get as many countries as possible to lock down for as long as possible, at least until vaccines become available.
But locking down entire countries full of healthy populations was never an accepted or ethically/medically/scientifically supported pandemic response, and people might object to such draconian measures. So Birx+cabal had to create enough panic to make it happen.
Given this connection between the U.S. government’s Covid response, the CIA-adjacent USAID, and the National Security Council, maybe those who say they are interested in full transparency can answer the questions presented here:
Hey, Jim Jordan: Ask Fauci Who His Bosses Were!
And the crucial questions raised by the Covid Dossier.
Republished from the author’s Substack
Author
From LifeSiteNews
Freedom Convoy leader Tamara Lich said she is “disappointed” in the Canadian “justice system” that her and convoy co-leader Chris Barber’s verdict for their mischief trial, which supposed to have been released in two weeks, has now been delayed to an unknown date.
In a X post late Thursday, Lich shared the news with her followers, noting, “We just received news that our March 12th verdict date is unfortunately being postponed.”
“At the end of our criminal (longest) mischief trial last August, when Her Honour set the verdict date, she let us know the court system assigned her a full trial schedule to help clear the backlog from the Covid years,” wrote Lich.
“This is the sad state of the justice system in Canada. While we are disappointed in yet another delay in our case, we know the importance of the upcoming decision not just for us, but for all Canadians.”
Lich said that as soon as she is told when the new verdict date will be, she will let everyone know.
As reported by LifeSiteNews, Lich and Barber’s verdict was supposed to have been announced on March 12.
They both face a possible 10-year prison sentence. LifeSiteNews reported extensively on their trial.
Lich and Barber’s trial concluded back in September of 2024, more than a year after it began. It was only originally scheduled to last 16 days.
Last week, Lich shared a heartwarming letter she received from a child, who told her to “keep fighting” for everyone and that “God will protect” her from the “enemy.”
As reported by LifeSiteNews, Lich recently spelled out how much the Canadian government has spent prosecuting her and Barber for their role in the protests. She said at least $5 million in “taxpayer dollars” has been spent thus far, with her and Barber’s legal costs being above $750,000.
Lich was arrested on February 17, 2022, in Ottawa. Barber was arrested the same day.
In early 2022, the Freedom Convoy saw thousands of Canadians from coast to coast come to Ottawa to demand an end to COVID mandates in all forms. Despite the peaceful nature of the protest, Prime Minister Justin Trudeau’s government enacted the never-before-used Emergencies Act (EA) on February 14, 2022.
During the clear-out of protesters after the EA was put in place, one protester, an elderly lady, was trampled by a police horse, and one conservative female reporter was beaten by police and shot with a tear gas canister.
Trudeau revoked the EA on February 23.
The EA controversially allowed the government to freeze the bank accounts of protesters, conscript tow truck drivers, and arrest people for participating in assemblies the government deemed illegal.
From LifeSiteNews
For his first major action since taking office just two weeks ago, Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. has issued a 90-day stop-work order to American biotech company Vaxart Inc., which had been contracted during the Biden administration to develop a new “oral COVID-19 vaccine.”
Kennedy’s order came just as 10,000 individuals were scheduled to begin clinical trials on Monday.
HHS will utilize the 90-day hiatus to review Vaxart’s initial findings to determine the future of the human trials and continued drug development.
Approximately $460 million had been allotted to Vaxart by HHS to develop its new COVID-19 “vaccine,” of which $240 million had been authorized for the preliminary study, according to a report by Fox News Digital, which broke the story.
“While it is crucial that the Department [of] Health and Human Services support pandemic preparedness, four years of the Biden administration’s failed oversight have made it necessary to review agreements for vaccine production, including Vaxart’s,” Kennedy told Fox News Digital.
“I look forward to working with Vaxart and medical experts to ensure this work produces safe, effective, and fiscal-minded vaccine technology,” added Kennedy.
“If anyone was worried that RFK would not address vaccine damage, this is proof he’s only getting started,” declared the producers of the 2022 Died Suddenly film, which questioned the motives behind the development and mandating of the first round of COVID-19 shots and the startling number of deaths attributed to them.
There appears to be plenty of justification for pausing and even terminating Vaxart’s continued development of its “oral COVID-19 vaccine”
According to a report by The Defender’s John-Michael Dumais and published by LifeSiteNews in June, “Vaxart’s pill, VXA-CoV2-1, uses an adenovirus vector to infect epithelial cells in the lower small intestine. The vaccine delivers the genetic material to create the spike protein. The company boasts that a special coating allows the oral pill to survive the low pH in the stomach.”
“Johnson & Johnson’s (J&J) and AstraZeneca’s COVID-19 vaccines also used adenovirus vectors,” noted Dumais, who explained:
The use of J&J’s vaccine was paused in April 2021 due to reports of thrombosis with thrombocytopenia syndrome (TTS), a severe blood clotting disorder. In July 2021, the FDA warned about the risk of Guillain-Barré syndrome with the J&J vaccine after approximately 100 cases were reported among 12.8 million vaccine recipients. With existing doses of the J&J vaccine having expired in May 2023, the vaccine is no longer in use.
AstraZeneca’s COVID-19 vaccine also caused blood clots, resulting in temporary pauses in its use in several countries. With declining demand, it was also removed from the market in May 2023.
Vaxart’s oral COVID-19 development project is part of the Biden administration’s $4.7 billion Project NextGen initiative, launched in 2023 to accelerate the development of new COVID “vaccines.”
Vaxart’s “vaccine” was funded through a contract with the Biomedical Advanced Research and Development Authority (BARDA), which falls under the umbrella of HHS’s Administration for Strategic Preparedness and Response.
The pausing of Vaxart’s COVID-19 “vaccine” development can be seen as Kennedy’s first important move to fulfill his stated mission as HHS secretary.
Shortly after Robert F. Kennedy Jr. was sworn in as secretary of the Department of Health and Human Services (HHS), President Donald Trump signed an executive order titled Establishing The President’s Make America Healthy Again Commission (MAHA EO) to investigate and address the root causes of America’s escalating health crisis.
Chaired by Kennedy, the commission has four main policy directives to reverse chronic disease: Empower Americans through transparency and open-source data and avoid conflicts of interest in all federally funded health research; prioritize gold-standard research on why Americans are getting sick in all health-related research funded by the federal government; work with farmers to ensure that U.S. food is the healthy, abundant, and affordable; and ensure expanded treatment options and health coverage flexibility for beneficial lifestyle changes and disease prevention.
The MAHA EO came at a time when many Americans have lost trust in the nation’s healthcare system and are increasingly skeptical as to whether they are receiving honest answers about the causes of the country’s health crisis and how to improve it.
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