Familial Dysautonomia: the leader in FD treatment and research
Thank you for joining us (virtually) for our 35th annual International FD Day Conference!
On Sunday, June 7, 2020 world-renowned physicians and scientists gathered to share the latest updates on FD research and medical care. More than 260 families representing almost 450 members of the FD community from 9 countries and 25 US states registered to attend.
Questions about the PFDD meeting? Please contact pfddinfo@famdys.org
If you weren't able to join us live, you can still experience FD Day by clicking on one of the buttons below.
View the 2019-2020 Research Booklet
Watch the FD Day Welcome and Introduction
Watch the FD Day Clinical Session and Q&A
Watch the FD Day Dystinguished Awards
Watch the FD Day Research Session and Q&A
Watch the FD Day Closing Remarks
©2022 Familial Dysautonomia Foundation, Inc.
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Photos by Rick Guidotti, POSITIVE EXPOSURE
EIN 13-6145280
Website Disclaimer
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.
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Privacy Policy
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Medical Disclosure
The FD Foundation does not offer medical advice. We always recommend that you contact the Dysautonomia Center (link here) or your personal physician.