How scientists and citizens banded together to lift the death sentence from AIDS.
It may be hard for anyone not alive at the time to comprehend how devastatingly the AIDS epidemic announced itself in the early 1980s and how resolute the Ronald Reagan government was in doing nothing about it. Emblematic was Jesse Helms, the North Carolina segregationist senator who argued in support of an amendment bearing his name to prohibit research and treatment funding, which he said would “promote, encourage, or condone homosexual activities.” Other bills introduced at the time included a suite that, among other things, “sought to bar people with AIDS from practicing in the health care industry, even as X-ray technicians.” Matters in the government did not begin to turn around, writes documentarian/journalist France (Our Fathers: The Secret Life of the Catholic Church in an Age of Scandal, 2004), until the Democrats took the White House, following a testy exchange with activists in which candidate Bill Clinton “cast himself as a better friend to people with AIDS than people with AIDS themselves.” It was those activists and their unflagging efforts, France documents, that kept the matter of AIDS and funding for its treatment in the public eye and on the political table, and while the long battle exhausted many—as France writes, there was a second epidemic of drug use, attributable to the self-medication of the traumatized—it was also extraordinarily effective in rallying both public and scientific/medical support. The result was a transformation of the disease—not just a physical one, with medications developed and made available that could “regenerate a person’s immune system,” but also a social one, with much of the stigma lifted from the ill. All this, as the author notes in closing, was accomplished by angry, vocal people out in the streets—a very good lesson for activists engaged in other issues today.
A lucid, urgent updating of Randy Shilts’ And the Band Played On (1987) and a fine work of social history.Pub Date: Nov. 29, 2016
ISBN: 978-0-307-70063-6
Page Count: 640
Publisher: Knopf
Review Posted Online: Sept. 20, 2016
Kirkus Reviews Issue: Oct. 1, 2016
Categories: GENERAL HISTORY | HEALTH & FITNESS | UNITED STATES | HISTORY
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BOOK REVIEW
BOOK REVIEW
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
Categories: BIOGRAPHY & MEMOIR | HOLOCAUST | HISTORY | GENERAL BIOGRAPHY & MEMOIR | GENERAL HISTORY
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A dense, absorbing investigation into the medical community's exploitation of a dying woman and her family's struggle to salvage truth and dignity decades later.
In a well-paced, vibrant narrative, Popular Science contributor and Culture Dish blogger Skloot (Creative Writing/Univ. of Memphis) demonstrates that for every human cell put under a microscope, a complex life story is inexorably attached, to which doctors, researchers and laboratories have often been woefully insensitive and unaccountable. In 1951, Henrietta Lacks, an African-American mother of five, was diagnosed with what proved to be a fatal form of cervical cancer. At Johns Hopkins, the doctors harvested cells from her cervix without her permission and distributed them to labs around the globe, where they were multiplied and used for a diverse array of treatments. Known as HeLa cells, they became one of the world's most ubiquitous sources for medical research of everything from hormones, steroids and vitamins to gene mapping, in vitro fertilization, even the polio vaccine—all without the knowledge, must less consent, of the Lacks family. Skloot spent a decade interviewing every relative of Lacks she could find, excavating difficult memories and long-simmering outrage that had lay dormant since their loved one's sorrowful demise. Equal parts intimate biography and brutal clinical reportage, Skloot's graceful narrative adeptly navigates the wrenching Lack family recollections and the sobering, overarching realities of poverty and pre–civil-rights racism. The author's style is matched by a methodical scientific rigor and manifest expertise in the field.
Skloot's meticulous, riveting account strikes a humanistic balance between sociological history, venerable portraiture and Petri dish politics.Pub Date: Feb. 9, 2010
ISBN: 978-1-4000-5217-2
Page Count: 320
Publisher: Crown
Review Posted Online: Dec. 22, 2010
Kirkus Reviews Issue: Jan. 1, 2010
Categories: GENERAL BIOGRAPHY & MEMOIR | BIOGRAPHY & MEMOIR | HEALTH & FITNESS
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