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.

 

Yes. If you and your partner are carriers for the same recessive disease, there is a 25% chance with each pregnancy that your child will be affected with the disease as well as a 75% chance of having an unaffected child. Two carrier parents could have several healthy children before having an affected child.

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