The Dysautonomia Center welcomes guest writer Alyson Brenner who shares her story on the journey to reduce sedative medications for her […]
FD
Tackling rare diseases requires a well-planned strategy. The Center is kick-starting a new clinical project as part of […]
Life is very unpredictable at times, but imagine how it must feel like to have no control over […]
The human brain weighs less than 2% of our total body weight, yet consumes 20% of the body’s […]
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 […]
When NYU recruited Dr. Shay Bess, they wanted him to tackle the most complex spine cases. The […]
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