Jim Waun, a retired anesthesiologist, shares some of his personal experiences that led him to support the Death With Dignity movement and the Final Exit Network (FEN), and he explains how FEN’s Exit Guide program works.
In his 2006 book about death with dignity and the right to die (The Future of Assisted Suicide and Euthanasia), Neil Gorsuch leveled several criticisms, by implication, against Oregon’s Death With Dignity Act (DWDA), a law that deals not at all with assisted suicide or euthanasia. Under the Oregon law, a person desiring a hastened death in the face of terminal illness may take his own life with a lethal prescription drug or drugs, unassisted by another person. Nevertheless, Gorsuch argues that we can’t determine the value of the DWDA for other jurisdictions without knowing how Oregon’s law is working in practice, and he asserts that we don’t have enough information about that.
A former Dominican priest shares his thoughts on ending life gracefully after a fruitful time on this earth.
The idea suggested by some disability rights advocates, that most of us will be disabled in one way or another by the time we reach the end of our lives, has been borne out in my experience. Virtually everyone I have known who has died has met, days or weeks or months before their deaths, the definition of disability under the Americans with Disabilities Act. How can we assure that those who are disabled are not coerced into ending their lives too soon?
Understanding disagreements between DWD advocates and disability rights advocates may be a way to find some common ground between the two groups. This is Part 1 of a multi-part series exploring the issues.
All of the Death With Dignity (DWD) laws now in the US are modeled after the Oregon law that went into effect in 1997. The other jurisdictions that have adopted such a law include Washington, Vermont, Washington, D.C., Colorado, California, and Hawaii. A judicial decision in Montana allows DWD to be practiced with cooperating doctors.
Missing from all of these laws is the right of people who have specific kinds of incurable, debilitating, painful, or extremely distressing medical conditions, but are not necessarily within six months of dying, to use these laws.
The American Association of Suicidology recognizes that the practice of physician aid in dying, also called physician assisted suicide, Death with Dignity, and medical aid in dying, is distinct from the behavior that has been traditionally and ordinarily described as “suicide,” the tragic event our organization works so hard to prevent. Although there may be overlap between the two categories, legal physician assisted deaths should not be considered to be cases of suicide and are therefore a matter outside the central focus of the AAS.
No, it is not an obituary for a specific individual. It is an obituary that recognizes and celebrates taking control of one’s end-of-life suffering.
When a family member provides care in the home for someone with a disability, when does this responsibility become a burden on the caregiver? Is being a burden asking too much of a family member? These and related questions are discussed in this week’s post.
In 2017, the District of Columbia (DC) became the seventh jurisdiction in the United States to legalize medical aid in dying, which gives terminally ill patients the option of how and when they die. The new DC statute is nearly identical to earlier enacted medical aid in dying statutes in California, Colorado, Oregon, Vermont, and Washington State. Only Montana legalized medical aid in dying through a court decision, but subsequently, proponents of the act have failed in every attempt to legalize medical aid in dying through constitutional or statutory litigation.
