Didion (We Tell Ourselves Stories in Order to Live: Collected Nonfiction, 2006, etc.) delivers a second masterpiece on grief, considering both her daughter’s death and her inevitable own.
In her 2005 book, The Year of Magical Thinking, the much-decorated journalist laid bare her emotions following the death of her husband, John Gregory Dunne. The same year that book was published, she also lost her adopted daughter, Quintana Roo, after a long hospitalization. Like Magical Thinking, this book is constructed out of close studies of particular memories and bits of medical lingo. Didion tests Quintana’s childhood poems and scribblings for hints of her own failings as a mother, and she voices her helplessness at the hands of doctors. “I put the word ‘diagnosis’ in quotes because I have not yet seen that case in which a ‘diagnosis’ led to a ‘cure,’ ” she writes. The author also ponders her own mortality, and she does so with heartbreaking specificity. A metal folding chair, as she describes it, is practically weaponized, ready to do her harm should she fall out of it; a fainting spell leaves her bleeding and helpless on the floor of her bedroom. Didion’s clipped, recursive sentences initially make the book feel arid and emotionally distant. But she’s profoundly aware of tone and style—a digression about novel-writing reveals her deep concern for the music sentences make—and the chapters become increasingly freighted with sorrow without displaying sentimentality. The book feels like an epitaph for both her daughter and herself, as she considers how much aging has demolished her preconceptions about growing old.
A slim, somber classic.Pub Date: Nov. 1, 2011
ISBN: 978-0-307-26767-2
Page Count: 208
Publisher: Knopf
Review Posted Online: April 5, 2011
Kirkus Reviews Issue: April 15, 2011
Categories: GENERAL BIOGRAPHY & MEMOIR | BIOGRAPHY & MEMOIR
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PERSPECTIVES
IN THE NEWS
PERSPECTIVES
The excruciating story of a young man on a quest for knowledge and experience, a search that eventually cooked his goose, told with the flair of a seasoned investigative reporter by Outside magazine contributing editor Krakauer (Eiger Dreams, 1990).
Chris McCandless loved the road, the unadorned life, the Tolstoyan call to asceticism. After graduating college, he took off on another of his long destinationless journeys, this time cutting all contact with his family and changing his name to Alex Supertramp. He was a gent of strong opinions, and he shared them with those he met: "You must lose your inclination for monotonous security and adopt a helter-skelter style of life''; "be nomadic.'' Ultimately, in 1992, his terms got him into mortal trouble when he ran up against something—the Alaskan wild—that didn't give a hoot about Supertramp's worldview; his decomposed corpse was found 16 weeks after he entered the bush. Many people felt McCandless was just a hubris-laden jerk with a death wish (he had discarded his map before going into the wild and brought no food but a bag of rice). Krakauer thought not. Admitting an interest that bordered on obsession, he dug deep into McCandless's life. He found a willful, reckless, moody boyhood; an ugly little secret that sundered the relationship between father and son; a moral absolutism that agitated the young man's soul and drove him to extremes; but he was no more a nutcase than other pilgrims. Writing in supple, electric prose, Krakauer tries to make sense of McCandless (while scrupulously avoiding off-the-rack psychoanalysis): his risky behavior and the rites associated with it, his asceticism, his love of wide open spaces, the flights of his soul.
Pub Date: Jan. 1, 1996
ISBN: 0-679-42850-X
Page Count: 320
Publisher: Villard
Review Posted Online: May 20, 2010
Kirkus Reviews Issue: Oct. 15, 1995
Categories: GENERAL BIOGRAPHY & MEMOIR | BIOGRAPHY & MEMOIR
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SEEN & HEARD
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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