Nancy Sabin Wexler

About the Author

Nancy Sabin Wexler is a pioneering psychologist and geneticist whose groundbreaking research has transformed the understanding and treatment of Huntington’s disease, a devastating neurodegenerative disorder. As president of the Hereditary Disease Foundation, she has spearheaded international efforts to map the gene responsible for the condition, leading to the 1993 discovery of the HTT gene mutation. Her personal journey, marked by the loss of her mother and three aunts to the disease, fueled a lifelong commitment to scientific advocacy and patient support. In her memoir 'My Life, My Science: Pursuing a Cure for Huntington’s Disease,' Wexler intertwines intimate family stories with the rigors of scientific inquiry, offering an inspiring narrative of resilience, discovery, and hope for future therapies. Her work continues to bridge the gap between laboratory breakthroughs and compassionate care, influencing global health policy and research ethics.