The ethic of informed medical consent includes the right of individuals to accept or to decline a pharmaceutical product or medical intervention.  This right has been universally affirmed as a human right by ethicists, medical societies, Virginia regulation, institutional patient bills of rights, and the United Nations Universal Declaration of Human Rights.  Phase III clinical trials for the available COVID-19 shots will not be completed until 2023, and as these are new pharmaceutical products, long-term safety profiles are not available.  Specifically, it is not known whether these experimental products may cause autoimmune disease, allergy, cancer, reproductive harm, or cardiac, vascular or neurodevelopment disorders.  In June 2021, the CDC reported a “likely association” between injection with the mRNA COVID-19 shot and heart inflammation.  The FDA subsequently required that a warning about myocarditis and pericarditis be added to the manufacturer’s insert (myocarditis and pericarditis are inflammatory conditions that can lead to cardiac arrhythmia and death).  Individuals have the right to decide whether the risks associated with this pharmaceutical product are ones they are willing to accept for themselves or their child(ren).  Furthermore, vaccinated individuals are still capable of contracting the SARS-CoV2 virus and transmitting it to others.  The natural immunity of those individuals who have recovered from COVID-19 has been shown to be robust and durable.