by Judith Heumann with Kristen Joiner ‧ RELEASE DATE: Feb. 25, 2020
A welcome account of politics in action, and for the best of causes.
A driving force in the passage of the Americans With Disabilities Act looks back on a long career of activism.
“An Occupation Army of Cripples Has Taken Over the San Francisco Federal Building.” So shouted a newspaper headline in the wake of one particularly vocal protest. According to disability rights activist Heumann, that was fine. “People weren’t used to thinking of us as fighters—when they thought about us at all,” she observes. Until the 1980s, disabled people were largely made invisible, with no easy means of access to the systems of transportation, employment, and other goods that the rest of the population often takes for granted. The author, who was paralyzed after a bout of childhood polio, might have been shunted off to an institution, as one doctor recommended, which was the usual practice in 1949. Instead, her parents, orphans of the Holocaust, resisted. The system did not make much allowance for her outside such an institution. At first, she was taught by a teacher who came to her home for two and a half hours a week, then sent to “Health Conservation 21,” a New York school system program in which students were expected to remain “until we were twenty-one years old, at which point we were supposed to enter a sheltered workshop.” Instead, Heumann distinguished herself academically and got involved in the drafting of legislation that would effectively add disability to the classes of protected citizens under the Civil Rights Act of 1964. To do so, she had to make the case that “discrimination against disabled people existed,” something that many people did not wish to acknowledge. Then she had to find allies inside government on top of battling a host of foes, including conservative politicians and businesses “worried about what ADA would cost, in time and money.” Heumann prevailed, and following passage of the ADA after years of agitation, she worked for the World Bank and was appointed a representative of the Obama administration to advance civil rights for disabled persons internationally.
A welcome account of politics in action, and for the best of causes.Pub Date: Feb. 25, 2020
ISBN: 978-0-8070-1929-0
Page Count: 232
Publisher: Beacon Press
Review Posted Online: Nov. 19, 2019
Kirkus Reviews Issue: Dec. 15, 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 Elie Wiesel ; edited by Alan Rosen
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by Elie Wiesel ; illustrated by Mark Podwal
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by Elie Wiesel ; translated by Marion Wiesel
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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