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National Tay-Sachs & Allied Diseases Association (NTSAD)

Description

National Tay-Sachs & Allied Diseases Association (NTSAD) leads worldwide efforts to find treatments, therapies, and eventually a cure for Tay-Sachs, Canavan, GM1, and Sandhoff diseases. We drive research, build connections, facilitate collaboration, and nurture community.

Supporting Families is the Center of Everything We Do

We provide more than 750 individuals and families from around the world with connection, resources, and individual support.

For more than 65 years, we’ve built an active and caring community of affected individuals, parents, siblings, grandparents, extended family, and friends. Every year, our Community meets at the Annual Family Conference to reconnect, support, and learn together.

Advancing Research, Providing Education, and Advocating for Our Community

We support research, promote carrier screening and prenatal testing, and raise awareness of rare genetic diseases. Clinicians, researchers, and industry members recognize the pivotal role NTSAD plays in accelerating the development of treatments, therapies, and cures.

Video About Us

Contact

Address
2001 Beacon Street, Suite 204 Boston,
Zip/Post Code
MA 02135
2001 Beacon Street, Suite 204 Boston,
Social Info

Rare Disease Watch

Our aim is to make complex information clear, accessible, and trustworthy. With concise reporting and consistent daily coverage, Rare Disease Watch helps professionals, patients, advocates, and families stay informed about what is changing in the rare disease landscape and why it matters.
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