An astute and valuable resource for both cancer physicians and patients.
A couple share their up-close and personal story of trouncing cancer.
In this memoir, the Marshalls take readers to the front lines of their triumphant battle against a cancer that invaded not only the wife’s body, but also their 22-year marriage. Liza was 43 years old when she was diagnosed with triple negative breast cancer, one of the most virulent and deadly forms of the disease. Ironically, her husband, John, was a world-renowned oncologist who had witnessed more than 1,700 of his 2,500 patients die. He voices strong opinions about the state of medical care in America in these pages. The book stands out among other first-person accounts about surviving cancer because of the authors’ striking frankness throughout the 340 pages. That’s not to say that the story is a downer. Although the account is flat-out honest and holds back nothing, the Marshalls inject lighter touches that balance the gravity of the situation. (“A brief history of my breasts. There were two of them.”) The couple’s emotional experiences at times diverge. A telling moment was their shopping trip to choose a wig for Liza. She and the couple’s children embraced the excursion as a fun family adventure. But John was roiling inside because the trip made Liza’s disease more real than he could handle. He notes that cancer is an entire family experience and that “whatever skeletons are hiding in the closet rattle louder.” A rare blowup happened when Liza wanted an expensive medication for her unrelenting nausea. John retorted: “Do you know how much that drug costs?” The Marshalls’ book is exceptional because it is multifaceted, deeply insightful, and brings readers right into the room. Liza delivers extensive details, including that her diagnosis came a few days before Thanksgiving at 2 p.m. Monday, Nov. 20, 2006. After months of agonizing tests, she opted for surgery, chemotherapy, and radiation and participated in a clinical trial, with John largely supporting her selections. He was against or had mixed feelings about other choices but stayed silent because he felt they should be her decisions. Ultimately, the treatments were successful and Liza remains cancer-free.
An astute and valuable resource for both cancer physicians and patients.Pub Date: April 6, 2021
ISBN: 978-1-64687-048-6
Page Count: 340
Publisher: Ideapress Publishing
Review Posted Online: Jan. 15, 2021
Review Program: Kirkus Indie
An absorbing, wide-ranging story of humans’ relationship with the water.
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. 4, 2020
Kirkus Reviews Issue: Feb. 1, 2020
BOOK REVIEW
BOOK REVIEW
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
BOOK REVIEW
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