Next book

DEAD GIRLS

ESSAYS ON SURVIVING AN AMERICAN OBSESSION

An illuminating study on the role women play in the media and in their own lives.

In this engrossing debut collection of essays, Bolin (Creative Nonfiction/Univ. of Memphis) looks at two things: America’s cultural obsession with dead girls in works of literature and on TV and Los Angeles from the perspective of both a newcomer and a veteran.

“Our refusal to address warning signs that are so common they have become cliché means we are not failing to prevent violence but choosing not to,” writes the author, the former nonfiction editor of Electric Literature’s literary magazine, Okey-Panky. In fact, according to Bolin, Americans demonstrate a specific fascination with watching women die on screen, seeing them lose control over their lives to abusive husbands and societies, and, most crucially to her story, investigating the circumstances around their murders. To study these phenomena, the author explores shows like Twin Peaks, True Detectives, and Pretty Little Liars, among others. “If you watch enough hours of murder shows,” she writes, “you experience a peculiar sense of déjà vu…the same murders are recounted again and again across shows.” Interwoven with these analyses of pop culture is the story of the author’s arrival in LA, broke, friendless, and with not much awareness of life under the sunny Californian sky. She drew many impressions of the city from the work of Joan Didion and Raymond Chandler, among others, who have painted a picture of a unique, bewildering city: “I was impressed by the unnerving sense of a city that sprang up overnight and sprawled like an invasive species over the landscape.” Bolin’s LA story becomes exemplary of her insights about female-obsession culture, from her wacky roommates to her boyfriends to her eventual private and public writing practices. The author’s voice is eerily enthralling, systematically on point, and quite funny, though at times readers may not fully understand the motives behind their laughter.

An illuminating study on the role women play in the media and in their own lives.

Pub Date: June 26, 2018

ISBN: 978-0-06-265714-5

Page Count: 288

Publisher: Morrow/HarperCollins

Review Posted Online: April 3, 2018

Kirkus Reviews Issue: April 15, 2018

Awards & Accolades

Likes

  • Readers Vote
  • 18


Our Verdict

  • Our Verdict
  • GET IT


Google Rating

  • google rating
  • google rating
  • google rating
  • google rating
  • google rating

  • Kirkus Reviews'
    Best Books Of 2016


  • New York Times Bestseller


  • Pulitzer Prize Finalist

Next book

WHEN BREATH BECOMES AIR

A moving meditation on mortality by a gifted writer whose dual perspectives of physician and patient provide a singular...

Awards & Accolades

Likes

  • Readers Vote
  • 18


Our Verdict

  • Our Verdict
  • GET IT


Google Rating

  • google rating
  • google rating
  • google rating
  • google rating
  • google rating

  • Kirkus Reviews'
    Best Books Of 2016


  • New York Times Bestseller


  • Pulitzer Prize Finalist

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

Next book

THE IMMORTAL LIFE OF HENRIETTA LACKS

Skloot's meticulous, riveting account strikes a humanistic balance between sociological history, venerable portraiture and...

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

Close Quickview