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At the time, a third sister, Margaret Mary Gough, was admitted to ICU at St. Elizabeth Fort Thomas Hospital with respiratory problems after testing positive for COVID-19 following her first dose of the vaccine.
Sister Nancy initially expressed hope that Sister Margaret Mary was recovering, saying that she is “[c]urrently in ICU, but we think she will be moved from there. She’s doing so much better. She had serious respiratory issues.”
But yesterday, through the monastery’s official Facebook page, she too was confirmed to have died, on February 10, “from complications of the COVID virus.” One other sister recovered in ICU and was able to return to the monastery.
In an apparent attempt to quell fears about the dangers of the vaccine, Dr. Steven Feagins, the Hamilton County public health director, explained that strong side-effects are “actually way more common than you might think.”
He added that, in cases where the patient suffers side-effects, he recommends simply delaying the second dose: “Whenever you get it, you get it, so we consider the 21 days [between jabs] minimum,” he said.
The remaining sisters are set to receive their second dose of the vaccine in May.
Since the launch of the Pfizer-BioNTech COVID-19 vaccine, the latest data from the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) has recorded a total of 929 deaths from December 15, 2020, up to February 12, 2021, accounting for almost 6% of 15,923 adverse events on the system’s report.
1,869 people were hospitalized, 616 of whom were considered to have suffered a life-threatening reaction.
Roughly 66.5 million doses have been administered in the U.S. of either one of the mRNA-based COVID-19 vaccinations offered by Pfizer-BioNTech and Moderna. Both were given emergency use authorization by the Food and Drug Administration (FDA) in December, and, until they are fully licensed by the regulator, are considered experimental.
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During LifeSiteNews’ “Unmasking COVID-19” conference, Dr. Sheri Tenpenny, Dr. Eric Nepute and Dr. Pam Popper joined LifeSite’s Stephen Kokx in a panel discussion focused on the science regarding the vaccines, and whether it is right to regard them as the chief protection against COVID-19. The medics decried even calling the injections “vaccines,” since they did not meet the standards necessary for the term, and warned about the risk of the experimental products themselves attacking the body’s immune response system.
Tenpenny argued that the currently available vaccines do not merit the name vaccine since they don’t “meet any of the standards by which a vaccine is supposed to work: to prevent the spread of infection, to keep you from getting sick, to keep you from being hospitalized, to decrease the amount of illness, to protect people from this contagion that’s out there. It doesn’t meet any of those standards.”
Describing the vaccine manufacturers as having “skipped all the steps” of normal testing and development procedures, Popper noted that “we have no possible hope that this could actually be either safe or effective.”
The U.K.’s Medicines and Healthcare products Regulatory Agency (MHRA), which authorized the use of both the Pfizer-BioNTech and Oxford/AstraZeneca developed COVID vaccines for use in Britain, reported that, between December 8 and February 14, it “has received 197 U.K. reports of suspected ADRs to the Pfizer-BioNTech vaccine in which the patient died shortly after vaccination, 205 reports for the Oxford University/AstraZeneca vaccine, and 4 where the brand of vaccine was unspecified.”
“The majority of these reports were in elderly people or people with underlying illness,” the MHRA added.
Italy, too, reported major health concerns regarding the AstraZeneca vaccine after the Tribuna di Treviso newspaper reported “dozens and dozens” of teachers and professors in the Treviso region were too ill to teach on Monday morning, having received the vaccine over the weekend. Consequently, two middle schools had to close during the week due to a lack of staff.
Despite the numerous side-effects reported by those who received the vaccine, Michele Mongillo, the director of prevention and public health for the Veneto Region maintained an optimistic position on the effect of AstraZeneca’s abortion-tainted vaccine: “We have begun the vaccination with AstraZeneca this week; there have been a few local reactions, especially fever. Over six thousand doses were given, and a few cases of local reactions were reported to our offices. It’s a temporary phenomenon, and on the bright side it shows that the immune system is reacting to the vaccine.”
Meanwhile, in France, the same AstraZeneca vaccine has caused so many adverse side-effects that the French vaccination task force (Conseil d’orientation de la stratégie vaccinale) has recommended “a staggering of the vaccination schedule for people working in the same care unit” as well as “the systematic intake of paracetamol just before the injection and in the two following days.”
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