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

We Care for Rare

If your family is now faced with the diagnosis of Canavan, GM1 Gangliosidosis, Sandhoff or Tay-Sachs disease, know that you are not alone. 

NTSAD's Family Services Team is here to help you get what you need in this moment in time. Help us get to know you and your family by completing this form hereand we will be in touch with you.

You can also request to join the NTSAD Family Support Group on Facebook. This group is private and only for affected individuals and their families. 

Learn about Rare Families below.

Find support and learn more.

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