by Diane Rehm ‧ RELEASE DATE: Feb. 5, 2020
Thoughtful conversations with friends and foes of the death-with-dignity movement.
In a companion to a TV documentary, the longtime NPR host and podcaster interviews terminally ill patients and others about end-of-life choices.
One in five Americans lives in a jurisdiction that allows terminally ill adults to request “medical aid in dying,” the term many experts prefer to “assisted suicide.” Rehm (On My Own, 2016, etc.) became a champion of the swiftly growing right-to-die movement after her first husband, ravaged by Parkinson’s disease, begged doctors in vain for help ending his life. In the gently probing interviews collected here, the author discusses the pros and cons with people who have seen the effects at close range: patients, relatives, physicians, clergy, hospice administrators, and others. An African Methodist Episcopal pastor explains why he opposed the death-with-dignity law in Washington, D.C., given its potential for use against blacks. Dan Diaz recalls the upheavals his wife, Brittany, faced when they moved to Oregon so she could end her life after a diagnosis of terminal cancer; amid the devastating news, she had to find a house to rent and get a new driver’s license and voter registration card to establish residency. Other interviews in the book, which features a foreword by John Grisham, focus on a variety of relevant questions: Who qualifies for medical aid in dying? What life-ending medicines do doctors prescribe? How long does it take to die after you ingest them? Several contributors give similar answers to the same question, which at times grows repetitious but suggests the variations around the country. For gravely ill patients, a vital point is that securing aid in dying involves paperwork, a waiting period, and finding two doctors willing to help. These safeguards can have heartbreaking results for anyone who puts off making a decision. The approval process takes an average of about one month, notes the president of the group Compassion & Choices, “and about half the people die before that.”
Thoughtful conversations with friends and foes of the death-with-dignity movement.Pub Date: Feb. 5, 2020
ISBN: 978-0-525-65475-9
Page Count: 256
Publisher: Knopf
Review Posted Online: Nov. 9, 2019
Kirkus Reviews Issue: Dec. 1, 2019
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by Elie Wiesel & translated by Marion Wiesel ‧ RELEASE DATE: Jan. 16, 2006
The author's youthfulness helps to assure the inevitable comparison with the Anne Frank diary although over and above the...
Elie Wiesel spent his early years in a small Transylvanian town as one of four children.
He was the only one of the family to survive what Francois Maurois, in his introduction, calls the "human holocaust" of the persecution of the Jews, which began with the restrictions, the singularization of the yellow star, the enclosure within the ghetto, and went on to the mass deportations to the ovens of Auschwitz and Buchenwald. There are unforgettable and horrifying scenes here in this spare and sombre memoir of this experience of the hanging of a child, of his first farewell with his father who leaves him an inheritance of a knife and a spoon, and of his last goodbye at Buchenwald his father's corpse is already cold let alone the long months of survival under unconscionable conditions.
Pub Date: Jan. 16, 2006
ISBN: 0374500010
Page Count: 120
Publisher: Hill & Wang
Review Posted Online: Oct. 7, 2011
Kirkus Reviews Issue: Jan. 15, 2006
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by Paul Kalanithi ‧ RELEASE DATE: Jan. 19, 2016
A moving meditation on mortality by a gifted writer whose dual perspectives of physician and patient provide a singular...
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A neurosurgeon with a passion for literature tragically finds his perfect subject after his diagnosis of terminal lung cancer.
Writing isn’t brain surgery, but it’s rare when someone adept at the latter is also so accomplished at the former. Searching for meaning and purpose in his life, Kalanithi pursued a doctorate in literature and had felt certain that he wouldn’t enter the field of medicine, in which his father and other members of his family excelled. “But I couldn’t let go of the question,” he writes, after realizing that his goals “didn’t quite fit in an English department.” “Where did biology, morality, literature and philosophy intersect?” So he decided to set aside his doctoral dissertation and belatedly prepare for medical school, which “would allow me a chance to find answers that are not in books, to find a different sort of sublime, to forge relationships with the suffering, and to keep following the question of what makes human life meaningful, even in the face of death and decay.” The author’s empathy undoubtedly made him an exceptional doctor, and the precision of his prose—as well as the moral purpose underscoring it—suggests that he could have written a good book on any subject he chose. Part of what makes this book so essential is the fact that it was written under a death sentence following the diagnosis that upended his life, just as he was preparing to end his residency and attract offers at the top of his profession. Kalanithi learned he might have 10 years to live or perhaps five. Should he return to neurosurgery (he could and did), or should he write (he also did)? Should he and his wife have a baby? They did, eight months before he died, which was less than two years after the original diagnosis. “The fact of death is unsettling,” he understates. “Yet there is no other way to live.”
A moving meditation on mortality by a gifted writer whose dual perspectives of physician and patient provide a singular clarity.Pub Date: Jan. 19, 2016
ISBN: 978-0-8129-8840-6
Page Count: 248
Publisher: Random House
Review Posted Online: Sept. 29, 2015
Kirkus Reviews Issue: Oct. 15, 2015
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