Renowned Scientist Nancy S. Wexler Shares Extraordinary Personal and Scientific Journey in New Memoir, My Life, My Science: Pursuing a Cure for Huntington’s Disease

New York, May 06, 2026 (GLOBE NEWSWIRE) -- One of the most influential figures in modern genetic research, Nancy S. Wexler, PhD, led the pioneering fieldwork that helped make possible the discovery of the gene responsible for Huntington’s disease, a fatal, hereditary neurodegenerative disorder. Now she brings her personal journey to a wide audience in her memoir, My Life, My Science: Pursuing a Cure for Huntington’s Disease, available nationwide.

For decades, Wexler has stood on the frontlines of the genetic revolution, engaging with such hot-button issues as the ethical use of genetic information and the promise and peril of predictive gene testing. During the search for the Huntington’s disease gene, she helped create new forms of collaboration while encouraging and mentoring several generations of researchers, especially women.

But her scientific mission began with a personal revelation. At age 23, she learned that her mother Leonore’s jerky movements and gradual withdrawal into depression and anxiety were due to a hereditary illness, the same disease that had killed Leonore’s father and all three of her brothers. Wexler also learned that she and her sister each faced a 50–50 chance of developing it themselves. Rather than retreat, she embarked on a lifelong quest to understand and ultimately defeat the disease.

Wexler draws readers into her experiences moving among the halls of government, university labs, lecture halls, and the impoverished barrios and stilt villages around Lake Maracaibo, Venezuela—home to the largest concentration of Huntington’s disease in the world. She returned there with a team every year for 22 years to help unravel the mysteries of the disease. In her memoir, she shares both the rewards and the toll of that quest, including her private struggles over whether to have children and her gradual realization that she, too, was developing the disease she had spent her life trying to cure.

Now living with Huntington’s, Wexler offers an unflinching account of resilience, purpose, and hope.

“This book is the story of a life shaped by urgency—the need to understand a disease that affects my family and that of so many others,” said Nancy Wexler. “Science gave me a way to fight back, but it was love—for my mother, my family, and this community—that sustained me.”

The memoir also highlights the role of family, including her father, psychoanalyst Milton Wexler, who established what is now the Huntington’s Disease Foundation, and her sister, historian Alice R. Wexler, with whom she collaborated on this book, along with writer Mark Hampton.

All author royalties from My Life, My Science support the Huntington’s Disease Foundation’s ongoing efforts to fund research and improve the lives of those affected by the disease.

Praised as “a lesson in courage, fortitude, heroism, and above all…love” by Carol Burnett, the book offers a powerful window into both the scientific process and the human realities behind it.

About the Author

Nancy S. Wexler, PhD, is the Higgins Professor of Neuropsychology at Columbia University Vagelos College of Physicians and Surgeons and president of the Huntington’s Disease Foundation. Her work identifying the genetic basis of Huntington’s disease has earned numerous honors, including the Lasker Award for Public Service and the Cold Spring Harbor Double Helix Medal.

Book Details

My Life, My Science: Pursuing a Cure for Huntington’s Disease
By Nancy S. Wexler, PhD, in collaboration with Mark Hampton and Alice R. Wexler
Publication Date: March 10, 2026
Publisher: Cold Spring Harbor Laboratory Press
Available via Amazon and Cold Spring Harbor Laboratory Press

Media Opportunities

Nancy S. Wexler and Alice R. Wexler are available for interviews.

Attachments

Myrna Manners
Nancy Wexler, Renowned Author
7189867255
mmanners@mannerspr.com

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