Last fall, a group of Democrats introduced the Michigan Death With Dignity Act, which would legalize physician-assisted dying, also known as medical aid in dying [, assisted suicide and euthanasia]. Patients with a terminal condition, expected to die within six months, would be able to request that a participating doctor write them a prescription for drugs that, when self-administered and ingested, would allow the patient to die on the date of their choosing.
Terri Laws [pictured here] is an associate professor of African and African American studies at the University of Michigan-Dearborn.
Many Michiganders will see this legislation as reasonable and compassionate. To others, however, often people of color, this legislation is more complicated. Some fear doctors and insurance companies may deny them lifesaving treatments and steer them toward assisted suicide instead. Others are concerned that legalization will normalize this type of death as the “correct” way to approach the end of life, when their cultural beliefs and practices tell them otherwise. Central to these views are issues around equitable access to care — and of trust.