NTSAD advocates for comprehensive, high-quality genetic carrier screening for anyone planning a pregnancy or who is already pregnant, regardless of their ethnicity or family history of genetic diseases. Below are documents that provide general information and various carrier screening resources for professionals, as well as families. More information regarding carrier screening can also be found in the family services section of our website under carrier screening.
National Tay-Sachs & Allied Diseases Association (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.
The National Tay-Sachs & Allied Diseases Association (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.
Community Connections
Get the latest news from NTSAD about our Community, the research that provides hope, and what is happening in the world of rare disease.
Community Connections
Get the latest news from NTSAD about our Community, the research that provides hope, and what is happening in the world of rare disease.
192 South Street, Suite 300
Boston, MA 02111
(617) 277-4463
info@ntsad.org
Tax ID
#13-1912877
National Tay-Sachs & Allied Diseases Association
2001 Beacon Street, Suite 204, Boston, MA 02135
(617) 277-4463 | info@ntsad.org
Tax ID
#13-1912877
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