Leading the worldwide fight to treat and cure Tay-Sachs, Canavan, GM1 and Sandhoff diseases
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Kathleen M Flynn Joins NTSAD as New CEO final.pdf
Modified on 28 May 2020 992 downloads
2020 May 28 Press Release NTSAD Hosts Largest and Virtual Family Conference.pdf
Boston, Mass.– National Tay-Sachs & Allied Diseases (NTSAD) kicked off its 42nd Annual Family Conference with a record-breaking turnout of nearly 400 individuals, including individuals and families affected by Tay-Sachs, Canavan, GM1, and Sandhoff, all rare genetic diseases. The four-day event moved from an in-person gathering in Denver, Colorado to a virtual event because of the Covid 19 pandemic.
Modified on 14 December 2018 1366 downloads
2018 Dec 13 Press Release Axovant Licenses GM2 and GM1 Gene Therapies.pdf
Modified on 21 September 2015 7826 downloads
NTSAD_2015 Research Grants final corrected.pdf
National Tay-Sachs & Allied Diseases Announces Research Initiative Grant Recipients
Nation’s first patient advocacy organization awards five grants totaling $266,000
September 18, 2015—BOSTON, MA—National Tay-Sachs & Allied Diseases Association (NTSAD), the nation’s first patient advocacy organization, today announced the awardees of its 2015 Innovative Research Grants. Reflecting an ongoing commitment to fund research aligned with its mission to lead the fight to treat and cure Tay-Sachs (TSD), GM-1, Sandhoff, Canavan (CD) and other related genetic diseases, NTSAD has solicited proposals for basic, translational or clinical research projects. This year’s grants include projects related to newborn screening, gene therapy delivery methods, animal models and international patient registries.
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NTSAD-CAC-Press-Release.pdf
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