A slim, worthwhile handbook to tackling a new cancer diagnosis.

Cancer: What I Wish I Had Known When I Was First Diagnosed

TIPS AND ADVICE FROM A SURVIVOR

A cancer survivor offers practical solutions for navigating a diagnosis of malignancy.

When she found a lump in her breast, Michele Ryan had just quit her stressful job in favor of staying home with her 3-year-old son. Four years after her cancer diagnosis, her husband was given his own cancer diagnosis, and he died within a year. Ryan’s story opens with a powerful account of her quick transition from career woman to cancer patient, and then it turns immediately to the book’s point: to help others traverse a new cancer diagnosis via humor, practicality and education. With a warm, reassuring tone, she begins with concrete advice—bring a friend, a pen and paper to every doctor’s visit; confirm statistics found on the Internet; enlist someone trustworthy to organize bills and handle insurance issues and appointments. She shares tips that only a cancer patient would know; for example, avoid scents, including pungent foods, if receiving chemotherapy. Ryan’s compassion informs each suggestion, including how to handle asking for or even accepting help. Her solution? Email a list of needs—laundry, transportation, food, pet-care needs—to nearby friends and family, thus avoiding the need to ask directly. Ryan addresses the body, mind and spirit. She offers strategies for managing depression and explaining the situation to children, and she helps prepare readers for the varied reactions and levels of support they might receive from family and friends. She also says that shopping for a wig can be fun—no more bad-hair days. As a 10-year survivor, the author doesn’t leave much unsaid. Her book can be read quickly but is an invaluable resource for encouragement from a brave woman with a lighthearted approach.

A slim, worthwhile handbook to tackling a new cancer diagnosis.

Pub Date: Feb. 20, 2014

ISBN: 978-1-4944-7231-3

Page Count: 84

Publisher: CreateSpace

Review Posted Online: May 7, 2014

Kirkus Reviews Issue: June 1, 2014

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

THE IMMORTAL LIFE OF HENRIETTA LACKS

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

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An absorbing, wide-ranging story of humans’ relationship with the water.

WHY WE SWIM

A study of swimming as sport, survival method, basis for community, and route to physical and mental well-being.

For Bay Area writer Tsui (American Chinatown: A People's History of Five Neighborhoods, 2009), swimming is in her blood. As she recounts, her parents met in a Hong Kong swimming pool, and she often visited the beach as a child and competed on a swim team in high school. Midway through the engaging narrative, the author explains how she rejoined the team at age 40, just as her 6-year-old was signing up for the first time. Chronicling her interviews with scientists and swimmers alike, Tsui notes the many health benefits of swimming, some of which are mental. Swimmers often achieve the “flow” state and get their best ideas while in the water. Her travels took her from the California coast, where she dove for abalone and swam from Alcatraz back to San Francisco, to Tokyo, where she heard about the “samurai swimming” martial arts tradition. In Iceland, she met Guðlaugur Friðþórsson, a local celebrity who, in 1984, survived six hours in a winter sea after his fishing vessel capsized, earning him the nickname “the human seal.” Although humans are generally adapted to life on land, the author discovered that some have extra advantages in the water. The Bajau people of Indonesia, for instance, can do 10-minute free dives while hunting because their spleens are 50% larger than average. For most, though, it’s simply a matter of practice. Tsui discussed swimming with Dara Torres, who became the oldest Olympic swimmer at age 41, and swam with Kim Chambers, one of the few people to complete the daunting Oceans Seven marathon swim challenge. Drawing on personal experience, history, biology, and social science, the author conveys the appeal of “an unflinching giving-over to an element” and makes a convincing case for broader access to swimming education (372,000 people still drown annually).

An absorbing, wide-ranging story of humans’ relationship with the water.

Pub Date: April 14, 2020

ISBN: 978-1-61620-786-1

Page Count: 288

Publisher: Algonquin

Review Posted Online: Jan. 5, 2020

Kirkus Reviews Issue: Feb. 1, 2020

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