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

Aaron's Fund


In 2019, Aaron's Fund was established in loving memory of Aaron Feinberg (1964-1970) as well as Morty and Marcia Feinberg, dedicated NTSAD parents and volunteers throughout their lives. The Fund’s goal is to support NTSAD in its unique role as a vital resource to patients, families, members of the medical and scientific community, and other key stakeholders to develop ways to prevent, detect, and treat rare genetic diseases. Aaron's Fund supports NTSAD’s research initiatives and family services, specifically the most critical need each year.

Donate Here.