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Last year, the National Center for Advancing Translational Services (NCATS) launched the Rare Diseases Are Not Rare! Challenge. Check out the video and all the winners here!

The Dysautonomia Foundation has produced a variety of informational videos that will help you better understand FD, it's challenges and the work that is being done to benefit the FD community and all people at risk of carrying the FD gene.

No Tears - Life with FD

December 4, 2018
No Tears: Life With FD is the Dysautonomia Foundation's comic strip devoted to amusement and awareness about FD and the Foundation.


In The News


Looking for more?

Find out more about current research in our latest newsletter. 

See a full list of current research projects and published papers from the Dysautonomia Center at NYU.