Hardcover. "An intimate and eloquent memoir of scientific discovery, social policy-making, and self-reflection that is as inspiring as it is harrowing. With verve, wit, and passion, Wexler tells her story of creating a new model for biomedical research while racing to find a cure for the lethal family disease she herself will one day inherit." -- Dr. Sanjay Gupta, neurosurgeon, CNN medical reporter, and author "Nancy Wexler's story is a lesson in courage, fortitude, heroism, and above all . love. I read it in one gulp. My heart is full." -- Carol Burnett, actor and writer When Nancy Wexler was 23, her father revealed that the mysterious illness inexorably diminishing her mother had a name. Huntington's disease, a fatal, hereditary, neurodegenerative disorder. Newly aware she had a fifty-fifty chance of developing the same condition, Wexler could have retreated. Instead, she immersed herself in what has become a lifetime's pursuit of the causes of the disease and a cure. She pioneered groundbreaking fieldwork that enabled the identification of the responsible gene. She took charge of what is now the Huntington's Disease Foundation and made it a force to be reckoned with. And when the human genome became a focus of scientific study, she was an eloquent voice for patients in disease gene research and insistent advocate for ethical use of genome sequence information. Now living with Huntington's disease, Nancy Wexler has drawn on decades of letters, research notes, and vivid memories to describe her remarkable life with warmth, wit, and unsparing honesty. She takes us from a privileged but shadowed California childhood to the shores of Venezuela's Lake Maracaibo, where she and colleagues earned the community trust that enabled them to collect blood samples and construct pedigrees, to the innovative consortium of research laboratories where those samples revealed the malevolent gene, to the halls of Congress where she pressed legislators for resources, and the boardrooms where philanthropists were persuaded into action. In this book, Wexler tells a unique story about the intertwining of personal stakes and professional passions, a testament to her courage, persistence, and belief that science can change destinies--one life, one family, one gene at a time. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.

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Detalles bibliogr�ficos

T�tulo: My Life, My Science: Pursuing a Cure for Huntington's Disease (Hardcover)
Editor: Cold Spring Harbor Laboratory Press
Fecha de publicaci�n: 2026
Idioma: Ingl�s
ISBN 10: 1621825450
ISBN 13: 9781621825456
Encuadernaci�n: Hardcover
Estado: new

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Sinopsis

"An intimate and eloquent memoir of scientific discovery, social policy-making, and self-reflection that is as inspiring as it is harrowing. With verve, wit, and passion, Wexler tells her story of creating a new model for biomedical research while racing to find a cure for the lethal family disease she herself will one day inherit."
-- Dr. Sanjay Gupta, neurosurgeon, CNN medical reporter, and author

"Nancy Wexler's story is a lesson in courage, fortitude, heroism, and above all ... love. I read it in one gulp. My heart is full."
-- Carol Burnett, actor and writer

When Nancy Wexler was 23, her father revealed that the mysterious illness inexorably diminishing her mother had a name. Huntington's disease, a fatal, hereditary, neurodegenerative disorder. Newly aware she had a fifty-fifty chance of developing the same condition, Wexler could have retreated. Instead, she immersed herself in what has become a lifetime's pursuit of the causes of the disease and a cure.

She pioneered groundbreaking fieldwork that enabled the identification of the responsible gene. She took charge of what is now the Huntington's Disease Foundation and made it a force to be reckoned with. And when the human genome became a focus of scientific study, she was an eloquent voice for patients in disease gene research and insistent advocate for ethical use of genome sequence information.

Now living with Huntington's disease, Nancy Wexler has drawn on decades of letters, research notes, and vivid memories to describe her remarkable life with warmth, wit, and unsparing honesty.

She takes us from a privileged but shadowed California childhood to the shores of Venezuela's Lake Maracaibo, where she and colleagues earned the community trust that enabled them to collect blood samples and construct pedigrees, to the innovative consortium of research laboratories where those samples revealed the malevolent gene, to the halls of Congress where she pressed legislators for resources, and the boardrooms where philanthropists were persuaded into action.

In this book, Wexler tells a unique story about the intertwining of personal stakes and professional passions, a testament to her courage, persistence, and belief that science can change destinies--one life, one family, one gene at a time.

Acerca del autor

Nancy Sabin Wexler, PhD, is a pioneering neuropsychologist, geneticist, and advocate best known for her leadership in the discovery of the gene causing Huntington's disease. As Higgins Professor of Neuropsychology at Columbia University and President of the Huntington's Disease Foundation, she has spent over four decades at the forefront of human genetics, bridging research and patient advocacy. Wexler's achievements have been recognized with the Benjamin Franklin Medal in Life Science, the Albert J. Lasker Award for Public Service, and election to the National Academy of Arts and Sciences. Wexler currently resides in New York, NY.

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