THE ADMINISTRATION OF 8,900,000 DOSES OF mRNA INOCULANT BASED ON FINDINGS IGNORED FROM 23 PEOPLE

A Rush To Jab Unsupported By "The Science"

The Gateway Pundit (h/t Caddy) has just published an article that is stunning in its implications. According to The Gateway Pundit the Biden administration approved the manufacture and distribution of the mRNA inoculant based on the “safety” findings from a study in which 23 people participated; 11 were between the ages of 18 and 55 and 12 were between the ages of 65 and 85. This study was made publicly available following a successful suit by Judicial Watch.

Here is the very short and very pertinent summary of what that study revealed.

The Pfizer study investigated the frequency of local (injection site) effects including pain, redness, and swelling. In brief, the most reported finding was pain at the injection site which was reported in far more people in the 18-55 year old group than in the group of 65-85 year olds.

The Pfizer study also recorded systemic effects: fever, fatigue, headache, chills, vomiting, diarrhea, muscle pain, and joint pain. What is most interesting is that following the first dose virtually no one in the 65-85 year old group experienced any systemic effects, however, systemic effects were widespread in the 18-55 year old group. Furthermore, the appearance of systemic effects in the 18-55 year old group was dose related from the first to the second dose. In other words more people experienced adverse systemic effects following the second dose than following the first dose. Reports of fever and muscle continued to increase in frequency following the third dose in this group.

The appearance of adverse systemic effects following the second dose also increased in the 65-85 year old group but not close to the magnitude and the extent of the response seen in those 18-55 year olds.

From a public health policy perspective as well as a matter of sound science these findings should have sounded alarms, instead they were ignored by the Biden administration over the objections of Marion Gruber, PhD, a 32 year veteran at the FDA and the Director of the FDA’s Office of Vaccine Research and Review and her Deputy, Dr. Phil Krause both of whom left the FDA reportedly because of undue political pressure from the Biden Administration and Dr. Fauci to approve Pfizer vaccine boosters for all Americans 16 and over.

Gruber and Krause were not alone in their objections to the pressure from Biden and Fauci. The FDA’s own vaccine advisory panel, comprised of the leading vaccine experts in the U.S. voted overwhelmingly 16-2 not to authorize the boosters for those under the age of 65. Nevertheless, the FDA approved the Pfizer mRNA inoculant for all ages and dosing began.

Those of you who have been with Larry’s Letters for a while may remember that I called attention to an obvious dose related increase in myo/pericarditis among those who were between the ages of 14 and 24 - part of the very same age group at greatest risk of adverse systemic effects in the Pfizer study.

Granted, myo/pericarditis are not the same as the systemic effects reported in the Pfizer study of 23 people upon which the decision was made to inoculate the nation with a poorly understood inoculant. However, a systemic effect is a systemic effect and the mRNA “stuff” that Pfizer and the Biden administration has forced and continues to force on the nation causes them.

”The Science” was not followed — it was ignored and it is still being ignored today.

”A false witness will not go unpunished, and he who breathes out lies will perish.”

Proverbs 19:9

Union, Kentucky

2 September 2023