That two weeks or two months of lockdown would prevent the feared deaths from ever occurring was a false hope.
Our Federal and state governments implemented unprecedented measures beginning in March to stem the spread of COVID-19. Informed consent provides a foundation of medical ethics. Did our elected officials and public health experts get our informed consent for policies that have put 30 million Americans out of work?
Medical experiments have often been performed on unsuspecting subjects, like the infamous Tuskegee Experiment. The U.S. Public Health Service in 1932 began studying the health effects of syphilis on African- American men recruited with a promise of free health care. Even after penicillin emerged as a treatment, the study participants still only received placebos and went untreated until public revelation in 1972.
Informed consent became the ethical dividing line. According to the American Medical Association, “The process of informed consent occurs when communication between a patient and physician results in the patient’s authorization or agreement to undergo a specific medical intervention.” A patient should be provided information on “the burdens, risks, and expected benefits of all options, including foregoing treatment.”
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