by Yolanda Hadid with Michele Bender ‧ RELEASE DATE: Sept. 12, 2017
A well-meaning and often compelling story of one woman’s relentless pursuit of an effective treatment for the devastating...
A Real Housewives of Beverly Hills star recounts her arduous battle with Lyme disease.
In this no-holds-barred memoir, Dutch-born former model and reality star Hadid tracks the debilitating symptoms that led to and progressively expanded beyond her eventual diagnosis for this chronic illness. In 2012, as filming was beginning for her first season on the Real Housewives and after having been misdiagnosed for close to two years, her condition became severe, dramatically curbing her professional and social lives and requiring prolonged periods of bed rest. The agonizing symptoms included intense joint pain and swelling, migraines, brain fog, blurred vision, and confronting an unseemly assortment of parasites. Over the next several years, Hadid’s journey would evolve into a desperate search for effective treatments, if not an outright cure. She visited dozens of medical and holistic treatment facilities throughout the world and underwent countless tests and procedures. Through expansive research and experience, the author effectively leverages her celebrity status as a persuasive spokesperson communicating the hardships endured by multitudes of sufferers who lack the financial means or insurance coverage to explore these potential resources. Yet this is also a Hollywood celebrity story, and readers who may not be fans of the Real Housewives series, with its reputation for tabloid-provoking drama, might question Hadid’s wisdom for having signed on to the program, feeling less sympathy for the intense media scrutiny that she and her family were forced to endure. Though her suffering has served as a grounding experience for the author to rise above the fray, it seems unlikely she or her children—two of whom were also diagnosed with Lyme disease—all celebrated runway models, are ready to step away from the limelight anytime soon.
A well-meaning and often compelling story of one woman’s relentless pursuit of an effective treatment for the devastating chronic effects of Lyme disease that should expand public awareness for this deeply misunderstood condition.Pub Date: Sept. 12, 2017
ISBN: 978-1-250-12165-3
Page Count: 320
Publisher: St. Martin's
Review Posted Online: July 3, 2017
Kirkus Reviews Issue: July 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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