by John Dittmer ‧ RELEASE DATE: May 1, 2009
A stark reminder not just of the actions of a group of idealistic activists but of the violence and turmoil of the nation’s...
Civil-rights historian Dittmer (History/DePauw Univ.; Local People: The Struggle for Civil Rights in Mississippi, 1994) focuses on one of the lesser-known groups involved in the struggle.
The author acknowledges that his coverage of the Medical Committee for Human Rights in the Bancroft Prize–winning Local People was inadequate. Here he tells the full story of this activist health-care organization, linking its aims and accomplishments with larger struggles. The MCHR, founded by left-wing, white, mostly Jewish doctors and joined by African-Americans, had a dual mission—to provide medical care for civil-rights workers in Mississippi during Freedom Summer (1964) and to reform the South’s Jim Crow health-care system. Dittmer reveals the motivations of many of the organization’s leaders, and he paints a disturbing picture of the shameful treatment of both black doctors and patients in the South. In the early chapters he writes vividly of the challenges facing civil-rights workers and of the brutality—beatings, jailings, killings—inflicted on them. The narrative pace slows when the author shifts attention to the political controversies and internal ideological disputes that led to the group’s decline. Dittmer documents the disintegration of the MCHR following the Voting Rights Act of 1965 and the rise of the black-militant movement. Northern white liberals began to question their role in the organization, and a rift was growing between those who saw it as the medical arm of the civil-rights movement and those who believed its mission should be to address the health-care needs of all poor people, regardless of race. By the late ’60s the MCHR had become a cash-strapped loose federation of largely independent local chapters. The author argues that it should be remembered for its role in desegregating Southern hospitals and medical societies, creating comprehensive community-health centers, shaping health-care legislation and providing a model for subsequent activist health organizations, such as Partners in Health.
A stark reminder not just of the actions of a group of idealistic activists but of the violence and turmoil of the nation’s not-so-distant past.Pub Date: May 1, 2009
ISBN: 978-1-59691-567-1
Page Count: 384
Publisher: Bloomsbury
Review Posted Online: May 19, 2010
Kirkus Reviews Issue: March 15, 2009
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by John Dittmer
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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