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Do We Have The Right To Die If We're Terminally Ill? - Diane Rehm | Modern Wisdom Podcast 288

Diane Rehm is a former radio presenter, producer and an author. Talking about the end of life is uncomfortable, but watching someone you love be forced to live on through pain is even worse. Diane has interviewed hundreds of people on the topic of assisted dying from Doctors to Priests, terminally ill patients and ethicists. Expect to learn why Right To Die Laws are so complex, problematic and applied differently across the world. what the difference is between euthanasia and assisted dying, how to broach the subject with someone you love and much more... Sponsors: Get 50% discount on your FitBook Membership at https://fitbook.co.uk/modernwisdom (use code MODERNWISDOM) Extra Stuff: Buy When My Time Comes - https://amzn.to/3uBEFRd Follow Diane on Twitter - https://twitter.com/drshow Get my free Ultimate Life Hacks List to 10x your daily productivity → https://chriswillx.com/lifehacks/ To support me on Patreon (thank you): https://www.patreon.com/modernwisdom #righttodie #euthanasia #assisteddying - Listen to all episodes online. Search "Modern Wisdom" on any Podcast App or click here: iTunes: https://apple.co/2MNqIgw Spotify: https://spoti.fi/2LSimPn Stitcher: https://www.stitcher.com/podcast/modern-wisdom - Get in touch in the comments below or head to... Instagram: https://www.instagram.com/chriswillx Twitter: https://www.twitter.com/chriswillx Email: modernwisdompodcast@gmail.com

Diane RehmguestChris Williamsonhost
Feb 27, 202151mWatch on YouTube ↗

CHAPTERS

  1. 0:00 – 0:48

    Why Diane Rehm took on the “last taboo” of death

    Diane Rehm explains that the book emerged from her documentary project and reflects a curated set of interviews from across the U.S. She frames end-of-life autonomy as a subject society avoids, but one that demands honest discussion.

  2. 0:48 – 3:05

    Personal losses that shaped her views on choosing the end

    Rehm recounts multiple family experiences with suffering and self-inflicted death, grounding her advocacy in lived history rather than theory. These stories form the emotional and moral backdrop for her belief that individuals should have agency at the end of life.

  3. 3:05 – 5:29

    What a “good death” looks like—and why planning matters

    Rehm describes her preferred end-of-life scenario: at home, with loved ones, able to say goodbye. She argues that avoidance of death talk leads to defaults like hospital deaths with invasive interventions, rather than intentional, humane endings.

  4. 5:29 – 7:29

    How medical aid in dying works in parts of the United States

    Rehm outlines the legal framework in the states and DC where medical aid in dying is permitted. She emphasizes safeguards: prognosis requirements, second opinions, and assessments to reduce coercion, with the final act performed by the patient.

  5. 7:29 – 10:36

    When it’s not legal: the cost and inequity of “moving to die”

    The conversation turns to what happens outside permitted jurisdictions, highlighting practical barriers that make access unequal. Rehm uses Brittany Maynard’s case to show how relocation, expenses, and time constraints shape who can exercise this choice.

  6. 10:36 – 11:50

    Europe, Switzerland, and the line between assisted dying and euthanasia

    Rehm and Williamson compare international approaches and clarify key terminology. They distinguish assisted dying (patient self-administers) from euthanasia (physician administers), noting different legal and ethical boundaries.

  7. 11:50 – 16:18

    Gray areas, technicalities, and the ALS self-administration dilemma

    Williamson probes ethical inconsistencies and practical quirks—especially cases where “self-administration” becomes a legal fiction. Rehm describes how jurisdictions try to reconcile autonomy with rules that prevent doctors from delivering the final dose.

  8. 16:18 – 21:00

    Arguments against medical aid in dying—and where mistrust comes from

    Rehm summarizes key opposition blocs and their reasoning, emphasizing that objections are not monolithic. She highlights religious doctrine, medical paternalism, disability-rights concerns, and historic injustice driving distrust in healthcare systems.

  9. 21:00 – 23:53

    Withdrawing treatment vs hastening death: different paths, similar outcomes

    The discussion distinguishes stopping treatment from taking medication intended to end life. Rehm shares her husband’s Parkinson’s decline and his decision to voluntarily stop eating and drinking, portraying it as a harsh alternative when legal aid isn’t available.

  10. 23:53 – 27:10

    DNR failures, 911 realities, and “death cafes” as community preparedness

    A story about a Do-Not-Resuscitate order being ignored in practice illustrates how systems default toward intervention. Rehm argues that beyond legal documents, community awareness and repeated conversations help ensure wishes are respected.

  11. 27:10 – 32:03

    Aid in dying vs suicide—and why control can be the real “medicine”

    Rehm differentiates terminal-illness aid in dying from non-medical suicide, emphasizing intent, context, and suffering. She notes that many who obtain the medication never use it—because having the option restores peace and perceived control.

  12. 32:03 – 41:37

    When to have the conversation—and how to actually start it with family

    Williamson admits he has never discussed end-of-life wishes with his parents, prompting Rehm to insist that waiting for a crisis is too late. She offers scripts and a realistic model: multiple, gradual discussions that normalize planning without panic.

  13. 41:37 – 51:38

    Why the topic matters: legal risk, personal regret, and making meaning of mortality

    Rehm recounts being warned not to help her husband due to legal jeopardy, underscoring how law can constrain compassion. The episode closes with practical resources and Williamson’s broader philosophy: confronting death to live more deliberately today.

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