On November 1, a young woman named Brittany Maynard ended her life with a fatal dose of medication, legally prescribed by her doctor. It was her way of wresting control from a terrible disease that had taken over her life and made her dying a slow, debilitating, painful, and excruciating journey.

Just six months ago, she had received a diagnosis of an aggressive and incurable brain cancer. She was given six months to live, and her doctors duly informed her that the dying process would involve increasingly frequent and severe seizures, symptoms of stroke, brain swelling, and severe headaches and neck pain, along with distressing side effects of medication to control her symptoms. As a result of this dire prognosis, Brittany, her husband, and her mother moved from San Francisco to Portland to take advantage of Oregon’s physician-assisted suicide put into law by the Death with Dignity Act.





of life. It promotes hospice as an excellent alternative to dying in a hospital’s intensive care unit. But what if hospice care can’t provide any semblance of quality of life or a peaceful death? Death with Dignity laws go one step further, proclaiming that each person should have the right to not only allow death to come when it calls, but also to hasten death in order to avoid any lingering, suffering, and expense.
