“Meaning matters just as much as medicine at the end of life.” — Dr. Michelle Riba
“There at the End: Voices from Final Exit Network: A Celebration of 20 Years” shares powerful testimonies from individuals connected to Final Exit Network (FEN), showcasing the organization’s dedication to supporting mentally competent adults suffering from terminal conditions in their right to choose death.
A new workbook by a Minneapolis cardiologist offers guidance and reflective prompts to prepare for conversations with loved ones about end-of-life topics.
The article contrasts the end-of-life experiences of Grandma Lilly, who suffers in ICU, with Grandpa Joe, who dies peacefully surrounded by loved ones, highlighting the choices in dying.
A woman’s terminal cancer diagnosis leads her to organize farewells with loved ones, ensuring her affairs are in order, resulting in what her family calls a “Good Death.”
The article explores the complexities and contradictions in the concept of a “good death,” questioning the reliance on medication and the preconceived ideals, urging a flexible, adaptive approach to end-of-life care.
In Part 1 of this post, Michele Bograd explores the concept of the “good death,” highlighting the influence of personal beliefs, social privilege, and structural inequalities in shaping end-of-life experiences as an end-of-life doula.
“Look at this book and let’s talk,” I imagine people saying. Or, “Read the story on page (X) and know that’s what I envision for myself.”
Research points to rise in deep grief as more families are left wondering what more could have been done.
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