02/27/2026
Huntington’s disease (HD) is a rare, fatal, genetic disorder that causes progressive breakdown of nerve cells in the brain, deteriorating a person’s physical and mental abilities usually beginning between ages 30 and 50.
It leads to devastating physical, cognitive, and psychiatric symptoms — including involuntary “dance-like” movements (chorea), dementia, and profound personality changes.
Cold Spring Harbor Laboratory’s 2019 Double Helix Medal honoree, Nancy Wexler, learned at 23 that she was at risk for Huntington’s disease. She turned that moment into a life’s mission — leading groundbreaking research in a Venezuelan community that helped identify the HD gene mutation and paved the way for today’s genetic test.
Coming March 10 from Cold Spring Harbor Laboratory Press, renowned geneticist Nancy Wexler shares her extraordinary personal and scientific journey in "My Life, My Science: Pursuing a Cure for Huntington’s Disease".
A powerful story of persistence, discovery, and hope. Available for pre-order from Amazon now: https://amz.cx/3c1w
Because breakthroughs in rare disease begin with basic biology.