by Vanessa Grubbs ‧ RELEASE DATE: June 13, 2017
The book will appeal specifically to those personally affected by kidney disease but should also fascinate anyone interested...
A nephrologist’s memoir of navigating the kidney disease of a loved one.
Grubbs (Medicine/Zuckerberg San Francisco General Hospital) came by her medical specialty honestly: she fell in love with and later married a man with end-stage kidney disease; a few months into their relationship, she donated a kidney to him. The author’s absorbing first book leads with that personal interest story, but it doesn’t end there. Moving around, occasionally confusingly, in time, Grubbs explores how an African-American girl from a country town in North Carolina came to become a doctor and move to San Francisco. She darts in and out of her experiences in medical school and residency, occasionally landing in a room with one of her patients. While her husband, Robert, is sometimes overly romanticized, the author doesn’t sugarcoat much else in her life. Robert’s kidney replacement, which took place after a long period of dialysis, hardly ended his struggles. It took several surgeries and a considerable amount of luck before the transplanted kidney started working properly. Other medical crises, as well as conflicts between Grubbs and her husband regarding treatment, followed. Revealing details about the experiences of both patient and donor during kidney surgery will enlighten those inside and outside the loop of kidney disease. Along the path to a career in nephrology, Grubbs fell in love not just with her husband, but with the kidney as an organ, with its hundreds of strands “like interlaced fingers.” The author expresses clear, not always politically correct opinions about a medical system that she believes discriminates against blacks, encourages patients to continue dialysis even when it prolongs suffering, and spends money on patients not committed to their own care. Grubbs also includes a helpful appendix of frequently asked questions about kidney disease and treatment.
The book will appeal specifically to those personally affected by kidney disease but should also fascinate anyone interested in the state of health care in the United States.Pub Date: June 13, 2017
ISBN: 978-0-06-241817-3
Page Count: 288
Publisher: Amistad/HarperCollins
Review Posted Online: April 29, 2017
Kirkus Reviews Issue: May 15, 2017
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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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