by Sharon Rondeau
(Oct. 22, 2021) — In his opening monologue Thursday night, Fox News host Sean Hannity recited a litany of factors impacting the U.S. economy under the Biden regime, including a crisis in supply chains; inflation; a “looming recession;” violence in Afghanistan following the Taliban’s takeover in mid-August; and Biden’s “rigid vaccine mandate” applying to federal employees and ostensibly to all U.S. companies with 100 or more employees.
Hannity pointed out with video evidence that during the presidential campaign, Biden pledged never to issue a COVID-19 vaccine mandate. Nevertheless, Biden has taken to blaming “the unvaccinated” for an increase in cases over the summer.
The Centers for Disease Control and Prevention (CDC) has reported that vaccinated individuals can not only experience COVID-19, but also transmit it to others.
“Why is there no other option, like many states and localities have adopted?” Hannity asked of the mandates. “…We’ve had that debate, and for whatever reason, I don’t know, millions of Americans are willing to lose their job, lose their benefits, abandon their retirement, because that’s how strongly they believe in their position. Many of these people have rare conditions that forbids them from getting the vaccine. [sic] Others have natural immunity, and they believe the science of natural immunity.”
He referenced a study from Israel which is yet to be peer-reviewed, reporting that “800,000 people…it seems natural immunity is better than the vaccine.”
“Time will tell; let’s follow the science,” Hannity concluded.
As a result of looming vaccination deadlines for many public and private employees, Hannity said, even more damage will be done to the flailing economy as jobs are shed. He suggested that “a simple option” would be to administer a “weekly” COVID test to those who decline to take the vaccine.
Hannity also questioned why the Biden regime does not promote monoclonal antibodies, a treatment found to be highly effective in COVID-19 patients, including former President Donald Trump.
Notably, Hannity did not mention what could be the most widespread rationale for Americans’ rejection of the vaccines: more than 700,000 adverse events, including more than 16,000 deaths believed to be associated with vaccine administration, and nearly 25,000 permanent disability cases reported, according to government statistics.
The number of reported adverse events is said by several sources to be between 1% and 10% of the actual numbers of such incidents based on a 2011 Harvard Pilgrim Health Care study completed for the U.S. Department of Health and Human Services (HHS).
Attorney Thomas Renz, who represents plaintiffs in two lawsuits opposing the vaccines filed earlier this year, claims that whistleblower reports show that the number of vaccine-associated deaths is more than four times that which appears in the VAERS database.
Not only is the government not releasing accurate numbers, Renz claims, but it has also suppressed the use of therapeutics which some physicians say they have used effectively with thousands of COVID patients.
According to two physicians, dozens of members of Congress requested and were given the decades-old ivermectin for COVID. Ivermectin is an FDA-approved therapeutic for parasitic infections which is recommended by the CDC for all “refugees” entering the U.S. from “all Middle Eastern, Asian, North African, Latin American, and Caribbean” nations.
Biden’s mandate does not apply to Congress, the federal judiciary, or their staffs.
As if in lockstep, the media and social media have rushed to discredit the use or prescription of therapeutics to include censorship of medical professionals who report success with them and “fact-checking” of social-media posts funded, at times, by Facebook itself.
Some of those hospitalized as a result of the virus are subjected to denial of “basic human rights,” including requested therapeutics, according to Dr. Elizabeth Lee Vliet, whose foundation is working to assist patients’ families in their quest for legal redress and the administration of alternative therapeutics.
McCullough has objected to the government medical establishment’s failure to provide safety advisories on the vaccines and the disbanding of the Data & Safety Medical Board to monitor reports of adverse events. An October 11 inquiry sent to three representatives at the National Institutes of Health by The Post & Email about the existence of a DSMB for coronavirus vaccines received no response.
On July 2, 2020, the Trump administration announced “Operation Warp Speed” with the purpose of producing COVID vaccines in an abbreviated time frame along with “diagnostics and therapeutics.” When vaccine distribution began last December, Americans’ expectations were high that the vaccines, as with others developed for smallpox and measles, would bring an end to the pandemic which disrupted the world economy, physical and mental health, and children’s education.
According to several sources, including Dr. Peter R. Breggin, vaccines for the SARS virus, of which COVID-19 is one, were in development years ago, and the major pharmaceutical companies seized upon the opportunity to mass-produce them for a world traumatized by the fear of a deadly virus which had already reportedly claimed millions of lives.
According to some sources, there is no fully-approved COVID-19 vaccine in the United States. All three currently in use — Moderna, Pfizer and Johnson & Johnson (Janssen) — remain under Emergency News Authorization (EUA). On August 23, the FDA issued a preliminary Biologics License Application (BLA) approval for the Pfizer “Comirnaty” vaccine which by some accounts is not yet available in the United States.
“Today, the U.S. Food and Drug Administration approved the first COVID-19 vaccine,” the press release reads. “The vaccine has been known as the Pfizer-BioNTech COVID-19 Vaccine, and will now be marketed as Comirnaty (koe-mir’-na-tee), for the prevention of COVID-19 disease in individuals 16 years of age and older. The vaccine also continues to be available under emergency use authorization (EUA), including for individuals 12 through 15 years of age and for the administration of a third dose in certain immunocompromised individuals.”
A “fact-check” on the issue by USA Today reads, in part:
Once the FDA approves vaccines, companies are permitted to market them under brand names, according to Scott Pauley, a press officer for the Centers for Disease Control and Prevention. Manufacturers may also then advertise their shots.
Because hundreds of millions of Pfizer doses were manufactured before the FDA’s full approval, some vials administered now may not have a Comirnaty label. But that doesn’t change what’s in the shot.
As with the proven forgery of Barack Obama’s long-form birth certificate by a five-year forensic investigation and the fraud employed in multiple states during the 2020 election, the media has maintained a virtual blackout on reports of adverse events to the COVID-19 vaccines. Rather, some media personalities have promoted the vaccines in what appear to be free advertisements for the manufacturers.
In contrast in July, Fox News’s Tucker Carlson Channel interviewed the mother of a previously-healthy, now-13-year-old girl who became permanently disabled after taking the vaccination during a clinical trial with her parents’ consent.
The morning show “Fox & Friends” has also aired a limited number of interviews with individuals describing severe side effects from the injections.
Updated, 12:39 p.m. EDT