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September 2014
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tay-sachs Press Releases

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By Matthew Forbes Romer Foundation
Foundation is Focused on Education & Research of Children’s Genetic Diseases of the Brain; Event will Celebrate Honorees, Entertain Attendees with ‘The Capitol Steps’ Comedy Show, and Update Guests on This Year’s New and Exciting Progra

By NTSAD
First human trial for Tay-Sachs, Canavan and other rare enzyme deficiency diseases plans to begin in early 2013 thanks to NTSAD, the nation's oldest patient advocacy organization, which leads efforts to find a cure or treatment.

By National Tay-Sachs & Allied Diseases Association
NTSAD Family Conference will bring together 300-plus people from around the world; To focus on research findings, family support and practical tips

By National Tay-Sachs & Allied Diseases Association
Leading the Fight to Treat and Cure Tay-Sachs, Canavan and Related Fatal Genetic Diseases in Children, NTSAD Provides Families with Group and Individual Support, Research Updates and Education During Four-Day Event

By Mathew Forbes Romer Foundation
Emotional Event Celebrates Boca Raton Rabbi and Massachusetts Doctor for Their Work; Honors Numerous Children and Their Families Afflicted with Fatal Genetic Diseases

By www.twitter.com/taysachs
An International Health Care Campaign To Help Fight Disease Was Launched On Twitter at www.twitter.com/taysachs.



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