For GM2 Families on how to accelerate research Read More
NTSAD leads the worldwide fight to treat and cure Tay-Sachs, Canavan, GM1, and Sandhoff diseases by driving research, forging collaboration, and fostering community. Supporting families is the center of everything we do.
It is best to talk with your doctor or make an appointment with your genetics professional to discuss your interest in carrier screening. Each of these medical professionals can explain the screening, submit an order, and interpret the results for you.