Views: 13
The Truth Shall Set You Free- “Liberty, when it begins to take root, is a plant of rapid growth.”
166 166Category: Biden Pandemic
166
Views: 16
So where are the free COVID tests coming from? Many think that they’re made in the USA and coming from American companies. Well not really. China and other countries with American locations.
What they didn’t mention is that many of these companies are foreign organizations that simply have small offices or manufacturing centers in the United States, and that much of the supplies are being imported from the foreign principals.
Access Bio is based in South Korea.
Advin is based in India.
iHealth is a California-based subsidiary of Andon Health of China.
Kwell Laboratories is based in South Korea
Sekisui is based in Japan.
In total, more than $312 million, through a contract branded to “reduce our reliance on overseas manufacturing” is being distributed to foreign companies. And $167 million has been awarded to the China-based iHealth, which has received *billions* of dollars from the U.S. government for their Covid tests.
Article originally was at The Dossier
160Pass it on.
Views: 26
Bombshell. Mayo Clinic on Hydroxychloroquine. Last year a demoted secretary tried to pass themself off as a Scientific Medical expert and claimed that two of the most prestigious hospitals in the world were kook hospitals. One being the Mayo Clinic. Guess what the Mayo Clinic posted on their website.
Hydroxychloroquine is used to treat malaria. It is also used to prevent malaria infection in areas or regions where it is known that other medicines (eg, chloroquine) may not work. Hydroxychloroquine may also be used to treat coronavirus (COVID-19) in certain hospitalized patients.
Using this medicine alone or with other medicines (eg, azithromycin) may increase your risk of heart rhythm problems (eg, QT prolongation, ventricular fibrillation, ventricular tachycardia). Hydroxychloroquine should only be used for COVID-19 in a hospital or during clinical trials. Do not take any medicine that contains hydroxychloroquine unless prescribed by your doctor.
165Pass it on.
Views: 25
The Biden administration tried to censor this Stanford doctor, but he won in court.
By Rikki Schlott.
This is a continuation/follow up to an article from Phoenix.
A federal court of appeals ruled earlier this month that the White House, surgeon general, CDC and FBI “likely violated the First Amendment” by exerting a pressure campaign on social media companies to censor COVID-19 skeptics — including Stanford epidemiologist Dr. Jay Bhattacharya.
“I think this ruling is akin to the second Enlightenment,” Bhattacharya told The Post. “It’s a ruling that says there’s a democracy of ideas. The issue is not whether the ideas are wrong or right. The question is who gets to control what ideas are expressed in the public square?”
The court ordered that the Biden administration and other federal agencies “shall take no actions, formal or informal, directly or indirectly” to coerce social media companies “to remove, delete, suppress or reduce” free speech.
Bhattacharya, a professor of medicine, economics and health research policy at Stanford University, co-authored the Great Barrington Declaration in the fall of 2020 with professors from Harvard and Oxford.
The epidemiologists advocated for “focused protection” — safeguarding the most vulnerable Americans while cautiously allowing others to function as normally as possible — rather than broad pandemic lockdowns.
“We were just acting as scientists, but almost immediately we were censored,” said Bhattacharya, director of Stanford’s Center for Demography and Economics of Health and Aging. “Google de-boosted us. Our Facebook page was removed. It was just a crazy time.
“The kinds of things that the federal government was telling social media companies to censor included us — along with millions of other posts from countless other people who were criticizing government COVID policy,” he added.
A New Orleans-based three-judge panel found that the federal government “likely coerced or significantly encouraged social-media platforms to moderate content” by vaguely threatening adverse regulatory consequences if social media companies did not suppress certain viewpoints on the pandemic.
“The government had a vast censorship enterprise,” Bhattacharya said. “It was systematically used to threaten and coerce and jawbone and tell all these social media companies, ‘You better listen to us: Censor these people, censor these ideas, or else.’”
It was later revealed that then-NIH director Dr. Francis Collins called for a “swift and devastating takedown” of Bhattacharya and his co-authors — whom Collins dubbed “fringe epidemiologists” — in an email to Dr. Anthony Fauci.
Subsequent reporting from Elon Musk’s so-called Twitter Files — internal documents and communications released by Musk, after he bought the platform, to expose Twitter’s inner workings — revealed that Bhattachrya’s profile was being suppressed on the platform.
“It’s akin to the efforts by governments to suppress the printing press when it first was invented, when books represented an enormous threat to power,” Bhattacharya said, referring to efforts by King Henry VIII and the Catholic Church to curb use of the printing press in the 16th century.
“There’s an analogous fight that’s currently going on with social media, which makes it vastly easier for anybody to express their ideas, and very powerful people find that incredibly threatening.”
The September 8 ruling affirmed but narrowed a lower court order, issued on July 4 by US District Judge Terry Doughty, which found that the Biden administration and other federal agencies “engaged in a years-long pressure campaign [on social media outlets] designed to ensure that the censorship aligned with the government’s preferred viewpoints” and that “the platforms, in capitulation to state-sponsored pressure, changed their moderation policies.”
Bhattacharya says the first victory, although in a lower court, was the most exciting to him.
“I was just absolutely thrilled, especially to have it on July 4th,” he said. “I think that judge was sending a message by issuing this ruling on July 4th that we’re going to restore free speech in this country.”
The Biden administration appealed to the Supreme Court on Thursday — a move that Bhattacharya anticipated.
But he believes it’s “unlikely” the Supreme Court will overturn the Fifth Circuit’s decision.
He feels his is a landmark case in curbing the influence the government has over social media — on matters that extend far beyond just COVID-19 and lockdowns.
169Pass it on.
Views: 40
COVID-19 symptoms have now become more mild and are nearly indistinguishable from allergies or the common cold, often affecting the upper respiratory tract, a number of doctors have said.
They note that some of the notable COVID-19 symptoms, including a cough or a loss of taste or smell, are less common among patients.
“It isn’t the same typical symptoms that we were seeing before. It’s a lot of congestion, sometimes sneezing, usually a mild sore throat,” Dr. Erick Eiting, vice chair of operations for emergency medicine at New York’s Mount Sinai, told NBC News on Sept. 16.
“Just about everyone who I’ve seen has had really mild symptoms,” Dr. Eiting said, referring to urgent care COVID-19 patients. “The only way that we knew that it was COVID was because we happened to be testing them.”
A study published in The Lancet shows that symptoms for COVID-19 have become milder since the omicron variant emerged and supplanted the delta variant in late 2021. Hospital admissions have also declined since then, along with initial symptoms such as a loss of taste or smell, according to the paper.
“The SARS-CoV-2 variant of concern, omicron, appears to be less severe than delta,” the abstract states, noting that there has been a “lower rate of hospital admission during omicron prevalence than during delta prevalence.”
Dr. Dan Barouch, director of the Center for Virology and Vaccine Research at Boston’s Beth Israel Deaconess Medical Center in Boston, told NBC News that the mild symptoms are, in part, due to previous immunity.
“Overall, the severity of COVID is much lower than it was a year ago and two years ago. That’s not because the variants are less robust. It’s because the immune responses are higher,” the doctor said.
Several doctors who spoke to the network said COVID-19 now commonly starts with a sore throat.
Dr. Michael Daignault, an emergency physician in California, told the network that “especially since July, when this recent mini-surge started, younger people that have upper respiratory symptoms … 99 percent of the time they go home with supportive care.”
The upper respiratory tract includes the nose, nasal cavity, mouth, throat, and voice box. The lower respiratory tract includes the trachea, lungs, and bronchial tubes.
Dr. Grace McComsey, with Case Western University, said that with the onset of the sore throat, some COVID-19 patients had “a burning sensation like they never had, even with strep in the past.”
“Then, as soon as the congestion happens, it seems like the throat gets better,” she said, estimating that about 10 to 20 percent of patients lose their sense of taste or smell now.
181Pass it on.
Views: 49
Researchers “alarmed” to find DNA contamination in Pfizer covid-19 vaccine.
A researcher testifies before a South Carolina Senate hearing about the discovery of DNA contamination found in Pfizer’s mRNA vaccine
Phillip Buckhaults, a cancer genomics expert, and professor at the University of South Carolina has testified before a South Carolina Senate Medical Affairs Ad-Hoc Committee saying that Pfizer’s mRNA vaccine is contaminated with billions of tiny DNA fragments.
Buckhaults, who has a PhD in biochemistry and molecular biology, said “there is a very real hazard” that these fragments of foreign DNA can insert themselves into a person’s own genome and become a “permanent fixture of the cell.”
He said it’s a plausible mechanism for what might be “causing some of the rare but serious side effects like death from cardiac arrest” in people following mRNA vaccination.
Buckhaults is not an alarmist and has been reluctant to go public with his findings for fear of frightening people.
He himself was vaccinated three times with Pfizer’s covid vaccine and recommended it to family and friends. He described the mRNA platform technology as “revolutionary” and said the vaccine has saved many lives.
“I’m a real fan of this platform,” Buckhaults told the Senate. “I think it has the potential to treat cancers, I really believe that this platform is revolutionary. In your lifetime, there will be mRNA vaccines against antigens in your unique cancer. But they’ve got to get this problem fixed.”
Buckhaults is most concerned about the “very real theoretical risk of future cancer in some people, depending on where this foreign piece of DNA lands in the genome, it can interrupt a tumour suppressor gene or activate an oncogene.”
“I’m kind of alarmed about this DNA being in the vaccine… DNA is a long-lived information storage device. It’s what you were born with, you’re going to die with and pass on to your kids. … So alterations to the DNA…well, they stick around,” he said.
Buckhaults believes the vaccines were deployed in good faith, but given the panic and urgency of the crisis, “there were a lot of shortcuts taken.” He puts it down to incompetence not malice, quoting Hanlon’s razor…
“…. which is never attribute malice to that which can be better explained by incompetence. There could be malice underneath, but I’m trying to see just incompetence to be gracious,” he told the Senate.
How did the vials end up contaminated with DNA?
Buckhaults explained how two different manufacturing processes were used to make Pfizer’s vaccine.
The initial production of Pfizer’s covid vaccine used a method called Polymerase Chain Reaction (PCR) to amplify the DNA template that was then used for production of the mRNA. This method, called PROCESS 1, can be used to make a highly pure mRNA product.
However, in order to upscale the process for large-scale distribution of the vaccine to the population for its “emergency authorisation” supply, Pfizer switched to a different method – PROCESS 2 – to amplify the mRNA.
PROCESS 2 used bacteria to make large quantities of “DNA plasmid” (circular DNA instructions), which would be used to make the mRNA. Hence, the final product contained both plasmid DNA and mRNA.
The switch from PROCESS 1 to PROCESS 2, ultimately resulted in the contamination of the vaccine (see red circles).
Pfizer tried to deal with the problem by adding an enzyme (DNAse) to chop up the plasmid into millions of tiny fragments.
But Buckhaults said it made the situation worse because the more fragments you have, the greater the chance that one of the fragments inserts itself into the genome and disrupts a vital gene.
“[Pfizer] chopped them up to try to make them go away, but they actually increased the hazard of genome modification in the process,” explained Buckhaults.
“I don’t think there was anything nefarious here, I just think it was kind of a dumb oversight,” he added. “They just didn’t think about the hazard of genome modification…it’s not all that expensive to add another process to get it out.”
A BMJ investigation found that batches of vaccine derived from PROCESS 2, were shown to have substantially lower mRNA integrity, and some say these vaccines have been associated with greater adverse events.
Buckhault’s research is not an outlier. Genomics expert Kevin McKernan has also reported plasmid DNA contamination in both Pfizer and Moderna bivalent covid-19 vaccines, in amounts that far exceeded the safety limit set by the FDA.
FDA safety limits
The FDA acknowledges that there are risks to having residual DNA left in vaccines:
Residual DNA might be a risk to your final product because of oncogenic and/or infectivity potential. There are several potential mechanisms by which residual DNA could be oncogenic, including the integration and expression of encoded oncogenes or insertional mutagenesis following DNA integration. Residual DNA also might be capable of transmitting viral infections if retroviral proviruses, integrated copies of DNA viruses, or extrachromosomal genomes are present.
In its guidance to industry, the FDA says:
The risks of oncogenicity and infectivity of your cell-substrate DNA can be lessened by decreasing its biological activity. This can be accomplished by decreasing the amount of residual DNA and reducing the size of the DNA (e.g., by DNAse treatment or other methods) to below the size of a functional gene (based on current evidence, approximately 200 base pairs). Chemical inactivation can decrease both the size and biological activity of DNA.
The problem with this advice said Buckhaults, is that it applies to the manufacturing of traditional vaccines, which contain what is known as “naked DNA.”
Normally, low levels of naked DNA in a vaccine would not be a problem because the bits of DNA are chewed up by tissue enzymes before they’ve had a chance to get inside cells. However, the DNA in Pfizer’s vaccine is not “naked.”
It is wrapped up in lipid nanoparticles (LNPs) – essentially fat globules – that help transport the genetic material (mRNA and plasmid DNA) inside the cells where the DNA can migrate to the nucleus and insert itself into the genome.
That’s why Buckhaults told the Senate that the FDA’s rules for safe levels of DNA in vaccines does not apply to the new mRNA platform technology.
“The fact that there is a regulatory threshold for the amount of DNA allowed in a vaccine is a throwback to an era when we were talking about [traditional] vaccines…but they inappropriately applied that regulatory limit to this new kind of vaccine where everything is encapsulated in this lipid nanoparticle — this was an inappropriate application of an old school regulation to a new kind of vaccine,” said Buckhaults.
What now?
Buckhaults said that vaccinated people need to be tested to see if any of the foreign DNA has integrated into the genome of their stem cells. This is easily detectable because the foreign DNA has a unique signature. Buckhaults said “It leaves a calling card.”
“This is not terribly expensive to do these kinds of tests,” he added, “But there has to be a system where professors are not going to be penalised for producing results that are counter to what the party line is supposed to be.”
Senator Billy Garrett asked whether Buckhaults could test for DNA contamination in the new covid boosters that the Biden administration just recommended for all Americans aged 6 months or older.
“I would like to do that,” said Buckhaults. “It takes about three hours to check a vial of vaccine to see if it’s got this in it – about 100 bucks of reagents.”
“And I will not get the vaccine again myself unless I get a batch and find out that it’s free of DNA,” he added.
While the Senators offered to intervene if Buckhaults received any retribution or harassment in response to his testimony at the hearing, they did appear helpless in their ability to bring about meaningful change.
Senator Richard Cash said, “We are not going to have any authority over the FDA to force Pfizer to do something. I mean, that’s a federal issue.”
Buckhaults told the Senate that he emailed the FDA about the contamination problem but had not received a reply.
The FDA has been approached for comment.
217Pass it on.
Views: 43
Dr. Birx ‘We Don’t Need to Mandate’ Masks. Recently the good doctor has been going from network to network being critical of Tony the Fauch. Sadly when he was killing millions of people worldwide, she was silent. But now she seems to have had a change of heart.
“Four years in, we don’t need to mandate. We need to actually empower people with the information that they need for themselves and their families because every family is different. And by the way, outside is safe, and playgrounds are safe.”
We are seeing a panic across the country with some hospitals and colleges, but for the most part the vast majority of Americans are ignoring the cultists cry for masking.
But in closing Dr. Birx had something interesting to say about the vaccines.
“So, you could switch them out (vaccines) and make them quickly, and instead of doing that, we’re basing vaccines on old variants rather than the new variants, and we know today exactly who needs to be immunized,”
191Pass it on.
Views: 7
Just putting this out there. COVID news updates.
“There is so little data available on the safety of this latest booster, the FDA’s actions create an unnecessary risk to the public’s health.” —Dr. Pierre Kory
Let’s start there with what our doctors are saying about the safety of the new COVID shots that were recently approved by the FDA and blessed by the CDC.
It is our moral and ethical imperative to report to you the most reliable information and scientific data available of which you must be aware so that you can make the best and most informed decisions possible to preserve your health.
Dr. Kory, chief medical officer of the FLCCC and Dr. Paul Marik, the FLCCC’s chief scientific officer, want you to be fully aware of the lack of trustworthy science for the safety and efficacy of these injections before you decide whether or not you wish to receive a shot.
“Our government continues to look for shortcuts in approving vaccines under the guise of an emergency while putting the public at risk of more injuries from these boosters that have not been through the extensive review and testing that is required outside of the EUA,” said Dr. Marik.
He’s right. Pfizer and Moderna—with the full-throated assent of the FDA— have leveraged the (unnecessary) Emergency Use Authorization (EUA) that remains in effect—despite there being no emergency— in order to push these new shots to market—for a low-risk illness that produces mild symptoms for most people.
There is no emergency (except for the vaccine purveyors’ urgent desire to fill their pockets with more and more $$$.)
Meanwhile, what do YOU get? Let’s see.
💉 You get a “vaccine” for a strain of COVID that is quickly becoming extinct.
💉 You get a shot whose ingredients are linked to clotting, which leads to lack of oxygen in body tissues.
💉 You run the risk of acquiring pathophysiologic abnormalities triggered by the spike protein, which lead to myriad damages to a number of organ systems.
💉 You get a ticket to a lottery to win a chance to become one of 65 million people worldwide suffering debilitating vaccine injuries.
💉 You get exposed to ad after ad after ad trying to guilt-shame you into getting a dangerous injection for a fading strain of COVID by warning you that not doing so will place your loved ones in harm’s way. It’s simply not true, but many doctors remain afraid to talk to their patients about it for fear of reprisals by their employers, licensing bodies and medical boards. ***
“The ‘system’ does not encourage independent thinking when it comes to treatment. They want everyone to follow the same protocols — and many healthcare providers do, as they’re afraid of the repercussions,” said Dr. Joe Varon, a critical care physician and one of the co-founders of the FLCCC. “If there’s one thing that the FLCCC is proud of, it is that we never give up. If one thing doesn’t work, we go and find something else. That’s what makes us different, and what makes us a complete alternative to what’s out there in healthcare.”
100%, Joe. An alternative to the current healthcare system is critical—especially now— given that the FDA’s recommendation for this new booster was based on data submitted by the companies that have a financial interest in the approval. There was no independent or peer review of this data.
“There is the almost unfathomable rise of 6 standard deviations from the norm in disability rates coinciding with the COVID-shots rollout in late 2020 followed by their mandating on the American labor force,” said Dr. Kory, who addressed rising cases of vaccine injuries, the continuing war on ivermectin and Big Pharma on the Kevin Wall radio program this week. (Hear Dr. Kory starting at about 15:00.) “Most dispiriting of all is that the vast majority of the vaccine-injured were highly functional before these spike protein exposures or injections.”
BOTTOM LINE: Educate yourself thoroughly about the COVID shots before deciding what’s best for you and your family.
***A one-year-old California law that allowed for the punishment of physicians who provided “misinformation” to their patients—specifically regarding COVID-19 and the vaccines— will soon be voted on for repeal. Under the law, if doctors violated “scientific consensus” and official “standards of care”, they could be cited for unprofessional conduct and subject to board disciplinary action. Many physicians claimed the law violated their First Amendment rights, and prompted several lawsuits challenging its constitutionality.
Lawmakers in both Florida and South Carolina have, in official proceedings, voiced their concern over the safety, efficacy and need for the current COVID shots.
In South Carolina, attorney Aaron Siri testified in a pandemic preparedness listening session about COVID vaccine “safety” (an oxymoron?). And in Florida, Surgeon General Joseph Ladapo warned healthy adults under the age of 65 against taking a new COVID-19 booster.
“With the amount of immunity that’s in the community — with virtually every walking human being having some degree of immunity, and with the questions we have about safety and about effectiveness, especially about safety, my judgment is that it’s not a good decision for young people and for people who are not at high risk at this point in the pandemic,” said Dr. Ladapo.
Keep talking, gentlemen. Keep talking.
GREAT NEWS!
Ohio House Bill 73 advanced to the next important step in the Ohio legislature and will soon be considered by the Senate Health Committee. Testimony will be heard by the committee followed by a vote to advance the bill to the entire Ohio Senate.
The Dave and Angie Patient and Health Provider Protection Act, if passed into law, will protect the rights of doctors to prescribe repurposed drugs. This encouraging progress on bipartisan legislation will ensure access to essential treatments that were arbitrarily restricted during the pandemic.
Our own Dr. Paul Marik, who testified on HB73 before the Ohio House Health Provider Services Committee, said this about the bill’s advancement in the Senate: “The bill is not only critical to the future of the practice of medicine in Ohio, but sets an example for the nation to follow.”
“We are seeing an increase in the number of cases of COVID. That’s the bad news. The good news is that not a single patient has had to go to the hospital because of COVID.” —Dr. Joe Varon.
Dr. Joseph Varon and Dr. Katarina Lindley joined host Betsy Ashton this week for the FLCCC Weekly Webinar to discuss what they are seeing at their practices in terms of COVID, long COVID and vaccine injury/“long vax”. No need to panic, FLCCC protocols are focused on prevention, treatment and recovery!
“Fear is a liar. So—faith over fear. Do the things you always do when you get sick and find a doctor you trust.” advised Dr. Kat Lindley.
In this new episode of ‘Whole Body Health’, Dr. JP Saleeby describes how hormones, drugs and supplements can support or interfere with your thyroid. Dr. Saleeby also explains why it is important to check your thyroid hormones if you have long COVID or post-vaccine syndrome.
In this episode of Long (COVID) Story Short, our Dr. Been reviews an early pandemic study.
This is a study of COVID-19 confirmed hospitalized patients. Researchers found two groups of individuals with biomarker profiles: the first had high fibrinogen levels in relation to C-Reactive proteins (CRP) and the second had an increase in D-Dimers in relation to CRP. These molecules generally increase in relation to CRP; however, here the researchers found that the fibrinogen and D-Dimers increased while the CRP stayed low. These cohorts were associated with higher likelihood of neurological long COVID. Dr. Been takes us through both the findings and the mechanisms.
The FLCCC protocols save lives all around the world!
From the very start in March 2020, through sharing the FLCCC Alliance COVID-19 protocols, this doctor was able to share life-saving information with hundreds of his contacts, his extended family (USA, Philippines, UK, Canada, Israel), close friends, former patients, relatives and former classmates locally and overseas. The protocols prevented infection, severe infection and untimely death for ALL of his contacts. Watch his MyStory now.
154Pass it on.
Views: 3
NYC must reinstate 10 Dept. of Education employees fired for refusing COVID vaccine, judge rules.
(The Center Square) — A New York state judge has ruled that 10 New York City teachers who were fired for refusing to get the COVID-19 vaccine were wrongfully dismissed.
In the ruling, state Supreme Court Judge Ralph J. Porzio said the city’s denial of religious accommodations from getting vaccinated employees was “unlawful, arbitrary and capricious” and ordered the teachers to be reinstated with back pay.
“This court sees no rational basis for not allowing unvaccinated classroom teachers in amongst an admitted population of primarily unvaccinated students,” he wrote in the 22-page ruling.
During the pandemic, New York City imposed some of the strictest COVID-19 vaccine mandates in the country, enforcing rules for public and private sector workers.
More than 1,750 city workers were fired for refusing to get vaccinated, including 36 members of the New York City Police Department and more than 950 public school employees.
Several unions sued the city over the mandate, and last October, Porzio ruled that the city’s policy was enacted “illegally” and workers who were fired for refusing to comply must be “immediately reinstated” with back pay. The city appealed the judge’s ruling.
The article was originally found at The Center Square.
96Pass it on.
Views: 13
Emails Show Tony the Fauch Was Aware of Wuhan Lab Funding.
B Wednesday, 06 September 2023
Newly released emails show that since at least January 2020, Dr. Anthony Fauci was aware of extensive research on coronaviruses conducted at the Wuhan Institute of Virology.
U.S. Right to Know obtained the emails via a Freedom of Information Act request. They show that the head of the U.S. response to the COVID-19 pandemic was corresponding with other officials about the lab’s findings.
The institute, indirectly funded by the National Institute of Allergy and Infectious Diseases through EcoHealth Alliance’s coronavirus research projects in China, has been at the center of theories on the virus’ origin.
Fauci was heading NIAID at the time of the now-released correspondence between him and his chief of staff, Greg Folkers, who informed Fauci that Wuhan discovered 52 novel coronaviruses related to SARS, the species to which SARS-CoV-2 belongs. SARS-CoV-2 is the virus that causes COVID-19.
The research also included the sampling of over 12,000 animals, the discovery of the Swine Acute Diarrheal Syndrome Virus, and the detection of the closest cousin virus to SARS-CoV-2.
Folkers said the Wuhan lab used genetically modified mice, whose organs were made close to humans’, to test some of the viruses. The novel coronaviruses reportedly caused SARS-like diseases in the mice.
In addition, the aide highlighted research from the University of North Carolina that found some novel coronaviruses could bind to human lung, heart, and blood vessel cells.
A spokesperson for the House Committee on Oversight and Accountability’s select subcommittee on the coronavirus pandemic told the Washington Examiner that the emails were concerning.
“Dr. Fauci’s involvement in downplaying the lab-leak theory continues to raise more questions and concerns regarding his actions. Americans deserve to hear answers from Dr. Fauci himself,” the panel spokesperson said.
146
