
Gaslighting…


Defenders of federal officials, including President Biden, who declared one year ago that people who received the COVID-19 vaccines would not contract the disease argue “the science” changes over time.
But the White House coronavirus response coordinator at the time the vaccines were developed and rolled out said in an interview Friday she wasn’t surprised that people who were quadruple vaccinated, including Biden and Dr. Anthony Fauci, contracted the disease.
“I knew these vaccines were not going to protect against infection and I think we overplayed the vaccines,” Birx told the Fox News Channel’s Neil Cavuto.
Birx, who is promoting a new book in which she confesses she manipulated data and quietly altered CDC guidance without authorization, was responding to the question of what she would say to unvaccinated people who in light of the ineffectiveness of the vaccines in preventing COVID might ask why they should bother getting the shots.
Arecent New York Times/Siena College poll showing 64 percent of Democrats preferring a new standard-bearer in 2024 rocked the White House and the political landscape, but it should not have come as a big surprise. After all, President Joe Biden continues to fall short of the promises that drew many Democrats, including myself, to his candidacy in 2020: his pledge for a new strategy combatting Covid-19.
Consider the Food and Drug Administration’s recent decision allowing pharmacists to play doctor and prescribe Pfizer’s anti-viral treatment Paxlovid, which Biden himself, having contracted Covid-19, is now taking. The agency claims this is meant to increase access to the medicine, which must be taken as soon as symptoms arise. But the drug’s fact sheet is a tangled web of restrictions that will make it impractical for most pharmacies to take the risk. Why is the FDA encouraging this?
The answer is plain to anyone who has been following the plight of independent doctors during the pandemic. Our public health agencies — heavily influenced by the pharmaceutical industry and beholden to Biden’s “vaccine first” approach — are committed to diminishing the medical profession and centralizing authority with bureaucrats in Washington, D.C. They have prosecuted a relentless campaign to reduce physicians to cogs in a health care system that is aggressively transforming all medical professionals from providers to prescribers.
The problems with Paxlovid are no secret. FDA granted Pfizer emergency use authorization for the drug after a single trial with questionable results. The medicine has many contraindications, meaning it can’t be taken by someone who simultaneously would be taking certain anti-depressants, anti-seizure, anti-psychotic, cholesterol, or blood pressure medications. Furthermore, many Americans cannot take Paxlovid, given that nearly half of adults have cardiovascular disease.
The risks are plain to see in FDA’s guidance, which recommends referring the patient to a doctor if “sufficient information is not available to assess renal and hepatic function” or “potential drug interactions.” Numerous contraindications are listed, and caution is advised throughout. The burden is on the patient to furnish medical records to prove that he or she doesn’t have any significant kidney or liver disease, drug sensitivities, or other medications that could cause serious adverse events.
President Trump’s former Covid-19 adviser Dr. Deborah Birx has made several stunning admissions of late – first telling the Daily Mail that Covid-19 “came out of the box ready to infect” when it hit Wuhan, China in 2019 – and that it may have been created by Chinese scientists who were “working on coronavirus vaccines.”
But it goes further than that.
As Fox News’ Jesse Waters lays out, Birx admitted in her new book that she and Dr. Anthony Fauci were essentially shooting from the hip when it came to national directives such as “two weeks to stop the spread,” and social distancing requirements.
According to Waters, Birx “admitted to making things up,” adding that she and Fauci “were lying to the president and to the American people about their COVID protocols.”
With the first lie; ’15 days to stop the spread’ – Birx writes “No sooner had we convinced the Trump administration to implement our version of the two-week shutdown than I was trying to figure out how to extend it.”
“So that 15 days to slow the spread was just a sneaky way to get their hooks into us, so they could lock us down for longer,” Waters opines. “And if you dared to leave your house, Birx told us, the only way to stay safe was to social distance.”
To that end, Birx writes that she “I had settled on 10 (feet) knowing that even that was too many, but I figured that ten would at least be palatable for most Americans – high enough to allow for most gatherings of immediate family but not enough for large dinner parties and, critically, large weddings, birthday parties, and other mass social events…”
Dr. Stephanie Seneff and many others have been suspicious of the actual safety and efficacy of the COVID-19 vaccines from the moment they started to be administered to the population.
Research into this novel technology made her very concerned that the vaccine could cause incurable prion diseases and prion-like diseases within the population in five to 10 years, or even further down the line.
“To have [almost] 100 percent success rate with [a] few months of testing, it just seems completely reckless to me,” she said on the call with The Epoch Times.
In 2021, months after the rollout of the mRNA Pfizer and Moderna COVID-19 vaccines, Seneff published a peer-reviewed paper with Dr. Greg Nigh (pdf).
In the study, she and Nigh declared that a vaccine that produced the spike protein of the SARS-CoV-2 virus could be a health concern as the spike protein has a prion region that is able to interact with proteins on human cells.
Prions are common proteins that naturally exist in the human brain. However, in the case of prion diseases, the prion will come into contact with a misfolded (pathogenic) prion, and just like a set of dominoes, the single contact will cause all other normal prions to become pathogenic, slowly killing the individual.
Awful as it sounds, it generally is a slow kill, often taking decades after the first exposure for symptoms to appear.
Examples of prion diseases include Creutzfeldt Jakob disease (CJD), an incurable and fatal disease.

Top doctors and scientists at the leading U.S. public health agencies are “frustrated, exasperated and alarmed” about the direction of the agencies they work for, according to the authors of a Substack post published last week.
They’re also embarrassed — about “bad science.” And many are leaving.
“It’s like a horror movie I’m being forced to watch and I can’t close my eyes,” said one senior official with the U.S. Food and Drug Administration (FDA). “People are getting bad advice and we can’t say anything.”
The comment was one of many culled from calls and text messages between officials and the article’s co-authors, Marty Makary M.D., M.P.H., and Tracy Beth Høeg M.D., Ph.D.
Makary and Høeg said the officials who spoke to them agreed to be quoted — but only anonymously, for fear of professional repercussions.
The National Institutes of Health (NIH) and the Centers for Disease Control and Prevention (CDC) are plagued with “low morale” and “high turnover,” officials told Makary and Høeg.
“At the NIH, doctors and scientists complain to us about low morale and lower staffing: The NIH’s Vaccine Research Center has had many of its senior scientists leave over the last year, including the director, deputy director and chief medical officer,” they wrote.
And it’s no better at the CDC, they said:
“The CDC has experienced a similar exodus. ‘There’s been a large amount of turnover. Morale is low,’ one high-level official at the CDC told us. ‘Things have become so political, so what are we there for?’ Another CDC scientist told us: ‘I used to be proud to tell people I work at the CDC. Now I’m embarrassed.’”
Officials complained the heads of their agencies “are using weak or flawed data to make critically important public health decisions, that such decisions are being driven by what’s politically palatable to people in Washington or to the Biden administration and that they have a myopic focus on one virus instead of overall health.”
One CDC scientist told Makary and Høeg about the shame and frustration within the agency over what happened to U.S. children during the pandemic.
The scientist said:
“CDC failed to balance the risks of COVID with other risks that come from closing schools. Learning loss, mental health exacerbations were obvious early on and those worsened as the guidance insisted on keeping schools virtual. CDC guidance worsened racial equity for generations to come. It failed this generation of children.”
The CDC also ignored natural immunity, according to some officials who declined to be named. “The vast majority of children have already had COVID, but this has made no difference in the blanket mandates for childhood vaccines.”
By mandating “vaccines and boosters for young healthy people, with no strong supporting data, these agencies are only further eroding public trust,” they added.
“I can’t tell you how many people at the FDA have told me, ‘I don’t like any of this, but I just need to make it to my retirement,’” one official told Makary and Høeg.
The Centers for Disease Control and Prevention (CDC) — the primary U.S. health protection agency — publicly pledges, among other things, to “base all public health decisions on the highest quality scientific data that is derived openly and objectively.”
The CDC’s “primary vehicle for scientific publication of timely, reliable, authoritative, accurate, objective, and useful public health information and recommendations,” according to the agency, is its Morbidity and Mortality Weekly Report (MMWR).
The CDC states that the MMWR readership consists predominantly of physicians, nurses, public health practitioners, epidemiologists and other scientists, researchers, educators and laboratorians.
However, these weekly reports also serve as the means by which the agency disseminates its scientific findings to a much wider readership through media outlets that inform hundreds of millions of people.
Though the CDC asserts its MMWRs reliably communicate accurate and objective public health information, the reports are not subject to peer review, and the data behind the scientific findings are not always available to the public.
Since Covid vaccines first became available more than a year and a half ago, women have been sounding alarms about the shots’ adverse effect on their menstruation.
For example, in an August 2021 article at The Grayzone that criticized the U.S. medical establishment’s failure to study the effects of the vaccines on women’s reproductive systems, Marcie Smith Parenti recounted disturbing experiences from her own circle of friends:
Their symptoms have included hemorrhagic bleeding lasting more than a month; heavy intermittent bleeding for four months; passing golf-ball size clots of blood; and extreme cramping, serious enough to land one friend in the ER.
On social media, the The Grayzone was accused of “fearmongering,” being “anti-vax,” and peddling “dangerous disinformation.” Meanwhile, the response of the FDA and CDC to women’s pleas might be best characterized as a bureaucratic shrug.
In August, NPR said the FDA and all three U.S. vaccine manufacturers claimed “they have not seen evidence that any of the vaccines cause menstrual irregularities.” The American College of Obstetricians and Gynecologists said it was “aware” of the complaints, but urged women to plunge forward with vaccinations anyway without regard to the timing of their cycles.
Now, however, a large-scale study adds substantial new confirmation of what thousands of women have been proclaiming since the jabs started. As NBC News reports:
“An analysis published Friday in the journal Science Advances found that 42% of people with regular menstrual cycles said they bled more heavily than usual after vaccination…14% reported a lighter period.“
The study also found many women who don’t typically menstruate—such as those beyond menopause and those on certain long-term contraceptives—experienced “breakthrough” or unexpected bleeding after receiving Covid vaccines.
The watchdog group Empower Oversight is taking action against the National Institutes of Health (NIH) for evading accountability in its legal obligations to disclose “requested” documentation under a Freedom of Information Act (FOIA).
According to Empower Oversight’s court filing, NIH improperly withheld information gathered in response to questions from Senators Chuck Grassley (R-Iowa), Marsha Blackburn (R-Tennessee) and Roger Marshall (R-Kansas).
Last year, the Senators asked about the agency’s decision, the request of Chinese researchers, to delete coronavirus genetic sequence information from an NIH database.
NIH has already admitted in the lawsuit that it failed to meet deadlines required by FOIA in responding to Empower Oversight’s request.
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