“Last words—it doesn’t happen like the movies. That’s not how patients die.” — Bob Parker
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It should be clear, as we argued in the first part of this two-part post, that the word “suicide” is not always appropriate. In this second part of our post, we offer a candidate word.
I hope others might be inspired to hold frank and open conversations about fundamental questions most of us will face. It would be so much less lonely for us all.
Your emotional reaction to a dread disease diagnosis can have major implications for whether your treatment preferences will be accepted.
Patients may not be aware that their health care system is faith-based, and rarely understand the restrictions that their health systems have implemented — until they need this care.
Changes to Bill C-7 (Canada) have released people with dementia from a cruel trap by letting them make provisions in advance to end their lives.
“We have a long way to go to educate the public about choices in dying, about defining ‘life’, and about making the end less agonizing for patients and their families.”
When a friend once confessed, “Jim, I don’t think I could do what you’re doing,” I immediately blurted, “I don’t think I could not do what I’m doing!”
I know well Judaism’s ban on euthanasia. But when I understood that my father would take his own life, I knew without a doubt that I would be by his side.
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