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

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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.

Join us, learn more, and support our cause.

 

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.

For locations, visit the Screening Centers page.

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