Diane Coleman, President and CEO of Not Dead Yet, looks at the lack of resources available in the health care system as the nation prepares for overwhelming COVID-19 cases and discusses hoe the disabled will be significantly endangered.
A dialogue about the right to die in interview format between the blog editor and a woman who has lived over four decades as a paraplegic.
This week’s post discusses the 2018 VSED death of Rosemary Bowen at age 94, based on the 16-minute film about her experience.
In this third part of a series analyzing the arguments against medical-assistance-in-dying (MAID) by opponents of physician-assistance in hastening a person’s death in the face of a terminal illness, Lamar Hankins looks at a major reference for most MAID opposition articles – a 2008 Michigan Law Review article, “Physician-Assisted Suicide in Oregon: A Medical Perspective,” by psychiatrist Herbert Hendin and neurologist Kathleen Foley. Both oppose what they term “assisted suicide.”
Disability rights groups that oppose self-determination for people who seek physician-assisted dying (PAD ) argue that such people should not have the right to decide for themselves when their lives are no longer tenable. Nevertheless, the disability rights groups do make points related to PAD that are worth considering; for one, they have helped me realize that over the last ten years I have become disabled.
In Part 2 of this post about dementia, disability, and advance directives, Lamar Hankins challenges Dresser’s assertion that an advance directive that calls for allowing a person to die in the later stages of dementia should be ignored in favor of her view of what care is appropriate.
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.
In Part 1, I began explaining why the disability rights group Not Dead Yet opposes Death With Dignity laws and the right to die. I also provided the most recent data from Oregon’s experience with its DWDA to refute some of the claims of Not Dead Yet.
All of the arguments made against the DWD laws by Not Dead Yet are false or misleading.
