Dear Friends, Multiple System Atrophy New Jersey (MSA NJ) is a non-profit organization, which provides support for patients […]
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Familial dysautonomia is rarer than most rare diseases, but this little known genetic disorder has become a gateway […]
At FD Day 2016, patients and family members came together for a 1-day intensive conference in New York […]
History The photography competition began in 2009 when we set the challenge for people with familial dysautonomia […]
You either heard about FD Day or came to FD Day. Every year we tell you what is […]
Only you know how what it feels like to grow up with FD, and this is a chance […]
At the 2016 International Congress on MSA, over 130 experts in the field came together for a 2-day […]
Professor Vaughan Macefield, Deputy Dean in the School of Medicine at Western Sydney University and Professor of Integrative […]
In the Hound of the Baskervilles, Sherlock Holmes is investigating the mysterious death of a superstitious British baronet […]
Your brain senses every single move you make. It accepts information coming in from different senses including vision, touch […]
