We’re stronger together.

Come see for yourself.

FD Day Annual Conference

FD Day is the biggest source of information about FD – all in one place.

For FD Families, Caregivers and Friends. Registration and attendance are FREE.

We are in the fight against FD together. With your help, we will accelerate breakthroughs patients can feel in their everyday lives.

At FD Day, you’ll find:
Latest News: The Dysautonomia Center team will provide updates on treatments, clinical trials and research.
Special Panels: Informative presentations on subjects of interest to all.
Entertainment and fun for kids.
Dinner party for FD adults.
And more!

Check back for more updates and to register early!

Registration dates will be announced soon.

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The information provided in the Dysautonomia Foundation web site is intended to educate the reader about certain medical conditions and certain possible treatments. It is not a substitute for examination, diagnosis, and medical care provided by a licensed and qualified health professional. If you believe you, or your child, or someone you know, suffer from the conditions described herein, please see your health care provider. Do not attempt to treat yourself, your child, or anyone else without proper medical supervision.

The Foundation provides linked sites only for the convenience of the visitor. The Foundation does not control nor does it warrant the accuracy of any information provided by these linked sites. Individually identifiable user information is not collected through this site unless voluntarily submitted to the Foundation by the user. Linked sites may have different privacy policies. Any User information submitted directly to the Foundation will not be shared with other parties without the express written consent of the User.

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The Familial Dysautonomia Foundation will not share or sell any personal information (name, address, email address, phone numbers) that you submit through this website or offline with any third party organization without your explicit consent.

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