Leading the worldwide fight to treat and cure
Tay-Sachs, Canavan, GM1 and Sandhoff diseases

Support for Families

If your family is affected by a rare genetic disorder, you are not alone. NTSAD is here to help with resources that can help from the day of diagnosis through day-to-day care, tough end-of-life decisions and beyond. With an incredible network of families ready to offer advice and share their experiences to an unforgettable annual family conference, NTSAD is there for families and individuals coping with these diseases.
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