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July 16, 2022

Much of the growth in military ethics education and training stems from the flagrant illegal orders and unethical medical conduct brought out during the Nuremberg trials.  “Just following orders” would not exonerate a soldier or an officer for complying with direct or tangentially illegal or unethical orders.  It was the crimes of Dr. Josef Mengele that galvanized the war crimes tribunal to lay down ten standards with which future physicians must conform when carrying out experiments on human subjects.

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The principle of voluntary informed consent is to protect the right of the individual to control his own body, be he a prisoner or a front-line soldier.

Immunizations required for military service are governed by military regulations.  For decades, Food and Drug Administration (FDA)–approved immunizations are required for military service — boot camp, officer candidate schools, service academies.  FDA-approved immunizations or prophylaxes are required when deployment is to a biologically hazardous region (against malaria, parasitic infested waters, etc.) or when conditions of imminent threat exist, such as when an enemy is reported to have deployed anthrax in a combat zone.  You can check all of them out here

The president declared: “It is the policy of my administration to halt the spread of coronavirus disease 2019 [COVID-19] … by relying on the best available data and science-based public health measures.”

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Specifically:

As of the date of this order, one of the COVID-19 vaccines, the Pfizer-BioNTech COVID-19 Vaccine, also known as Comirnaty, has received approval from the Food and Drug Administration (FDA), and two others, the Moderna COVID-19 Vaccine and the Janssen COVID-19 Vaccine, have been authorized by the FDA for emergency use.

Sec. 2 of the executive order mandated coronavirus vaccination for federal employees, negating voluntary informed consent, without explaining the difference between the terms “FDA-approved” and “Emergency Use Authorization.” 

“FDA approval” from the Food and Drug Administration is an independent, scientifically reviewed approval for medical products, drugs, and vaccines.  Approval is based on substantial clinical data and evidence; the product is deemed safe, effective, and able to be produced within federal quality standards.  Emergency Use Authorization (EUA) is a mechanism used by the FDA to facilitate making products available quickly during a public health emergency, when there is no other adequate and approved medical product available.

Did the secretary of defense inform his service members of the difference between FDA approval and EUA?  Were service members informed that the FDA suddenly proscribed coronavirus therapeutics, curatives, and prophylaxes before any EUA “vaccines” were released?

The secretary of defense memo stated, “Mandatory vaccination against COVID-19 will only use COVID-19 vaccines that receive full licensure from the Food and Drug Administration (FDA), in accordance with FDA-approved labeling and guidance.”