by Fed Up Texas Chick, The Tenpenny Report:

“Approving a vaccine, utilizing novel RNA technology without extensive testing is extremely dangerous. The vaccine could be a bioweapon and even more dangerous than the original infection.”

Introduction

Dr. Tenpenny was one of the first people to say this in 2021 when she wrote 40 Mechanisms of Injury. Long ago, she said that injecting synthetically made SARS-CoV-2 spike protein into the entire population greatly increased the risk of long-term side effects, and that risks of developing an autoimmune illness will remain for an unknown period of time. With B-cell priming and  irreversible genetic manipulation, the risk for developing chronic illness is great.  The spike protein can bind to the surface of the vaccine recipient’s cells. This spike protein then becomes a potential receptor for other more aggressive or more dangerous infectious agents. SARS-CoV-2 is the only coronavirus with a prion-like domain found in the receptor-binding domain of the S1 region of the spike protein. SARS-CoV-2 demonstrates a 10- to 20-fold higher affinity for ACE2 receptor, their primary binding site, than SARS-CoV and other common coronaviruses.