by David Passieri, St. Ignatius
On October 19, 2022 the advisory committee to the Centers for Disease Control and Prevention (CDC) voted unanimously to take the first step toward adding the Pfizer and Moderna experimental mRNA medical therapeutics to the recommended immunization schedule for American children, without FDA approval. No sane person disputes the mounting evidence that these products have been a complete failure. The “vaccine” provides no immunity. It is, after all, nothing more than a medical therapeutic, and is not effective. Most Americans personally know people who received multiple injections and still got sick. What’s the point of getting a shot that doesn’t provide immunity? The simple truth is this. The Emergency Use Authorization (EUA), which is soon to end, provides liability protections to these manufacturers. Yet, the protections can continue beyond the expiration of the EUA, under one condition: The CDC adds the “vaccine” to the pediatric immunization schedule which automatically extends forever the liability protections for these SARS CoV-2 mRNA manufacturers. That means that no one can sue Pfizer or Moderna for injury or death, even if children are forced to get the shot to go to school. Sweden, Norway, France, Finland, Iceland, Germany and Denmark have restricted Moderna mRNA therapeutics to anyone under the age of 18 because it is not safe. We will see an exodus from the government school system that is so rapid and immense that the system will simply collapse if the CDC takes the final step of mandating these ineffective and unsafe injections for school attendance.