Madison Reporter

Dr. Pierre Kory, the former chief of critical care at the University of Wisconsin Hospital said a patient told him of a neurologist who said he wasn’t “allowed to talk about” the fact his “whole practice is full of vaccine injuries.”

“A jab-injured patient of mine told me today that when she recently told a neurologist at Scripps that her facial spasms were from the shot, the doc replied: ‘ "Our whole practice is full of vaccine injuries but we are not allowed to talk about it,’” Kory posted on X (formerly known as Twitter).

Kory also previous served as head of the main medical-surgical intensive care unit (ICU) at the university’s hospital.

He currently is president of the Front Line COVID-19 Critical Care (FLCCC) Alliance, a 501(c)3 that recommends treating COVID-19 infection with alternative modalities, such as ivermectin and hydroxychloroquine.

There have been 1,585,094 adverse events reported by people after taking the “COVID-19” MRNA injection, according to the Vaccine Adverse Event Reporting System (VAERS).

That includes 35,911 deaths, 208, 190 hospitalizations, and 27,414 reports of myocarditis and/or pericarditis.

The MRNA injections are more commonly known as “COVID-19 vaccines.” Dr. David Martin, founder and chairman of M-CAM Inc, said the “vaccines” are actually gene therapy.

“It is not a vaccine. What is this doing? It’s sending a strand of synthetic RNA into the human being and is invoking within the human being, the creation of the S1 spike protein, which is a pathogen,” Martin told the Weston A. Price Foundation. “It’s a toxin inside of human beings. This is not only not keeping you from getting sick, it’s making your body produce the thing that makes you sick.”

VAERS is a U.S. government database that collects and monitors reports of adverse events or side effects following vaccination, helping to track and assess the safety of vaccines. The system is owned and operated by multiple U.S. federal agencies, primarily the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA), in collaboration with the Department of Health and Human Services (HHS). 

By the admission of its creators, VAERS also underreports adverse events. 

“‘Underreporting’ refers to the fact that VAERS receives reports for only a small fraction of actual adverse events,” says the VAERS website. “The degree of underreporting varies widely.”