Recently, Derek Humphry wrote about the words we use to discuss end-of-life concerns in the US, focusing on the appropriateness of the term “suicide.” He did so, in part, to stimulate a discussion about the words we use. Like Humphry, I have no personal problem with the use of the term suicide–it accurately describes death by our own hand–but I resist it for several reasons.
End-of-life pain can be complex and not all such pain is easily or satisfactorily controlled. FEN member Craig Phillips shares his experiences with pain control while working as a volunteer in a hospice.
Thanks to everyone who made suggestions to deal with Jane’s presumptive problems (see previous post). If Jane had an independent social worker–one not in her healthcare system–that person might respond to Jane’s difficulties with something like the following:
Many people with debilitating and irreversible health conditions do not have supportive family and friends. They include include people with metastatic cancer, irreversible neurological conditions, and multiple medical problems that have taken away any enjoyment and quality of life as determined by them. They no longer want to continue living because they know that their condition will only worsen, and for them it is already beyond bad. There is no realistic hope that their lives will improve. Most of the time, family members and friends are able to see the suffering in their loved one’s life and understand a desire to end the suffering. But this is not always the case, as illustrated in this post.
A Dutch contribution to how we look at death and dying is provided by Cornelis J. “Jack” van Dyjk.
With this post, I begin a multi-part series about the views of those who oppose medical-assistance-in-dying (MAID) or have written critically about MAID laws. I think there are some good ideas that we can learn from these critics to help us improve MAID laws, though that is not their intent. They will oppose MAID under any law, no matter how carefully written.
A Washington state man, Aaron McQ, described his illness (a rare form of ALS) as “terrifying . . . like waking up every morning in quicksand.” He agreed to discuss his experience with Kaiser News to help provide more understanding about how users feel after qualifying for PAD. Over 3,000 terminally ill residents in the US have used PAD laws since Oregon’s first took effect twenty years ago. This is one man’s experience.
This post lays out a process for making a dementia directive to be used when or if we become unable to make our own views known because of mental incapacity. If you are willing to live with dementia through the end of the disease, this post will not be of use to you.
The Society for Humanistic Judaism (SHJ) supports the right of all people to decide when their lives should end. This post looks at the SHJ’s position on physician-assisted death.
A former Dominican priest shares his thoughts on ending life gracefully after a fruitful time on this earth.
