We’re proud of where we’ve been

But we’re not done yet.

Donate To The Dysautonomia Foundation

Your contribution can make a difference!
Help us provide the best possible medical care and research
for the benefit of people with FD

The Dysautonomia Foundation is the leading source of support for FD treatment, research, public awareness and social services for the benefit of people with FD. We have established the world's only two FD treatment centers and the world's only FD clinical research laboratory, and we have endowed the world's only two professorships for the study of FD.
We are hoping that you will join us in our mission by making a contribution. The Dysautonomia Foundation is a 501(c)3 public charity, and all contributions are tax deductible to the extent permitted by law. Your contribution, no matter how much, can make a difference as we try to help improve the quality of life and life expectancy for people with familial dysautonomia.



Send a card & show someone you care 

Tribute cards can be sent in honor of any person or occasion, or in memory of a loved one. 
The card will be inscribed with your special message. Most cards are sent within one to two business days from the date you make your donation.
Your card will not only show someone special that you care, it will also support treatment and research for familial dysautonomia (FD).



Make a Donation or Send a Card



Please be assured that your transaction is secure and none of your credit card information will be stored in our records. Your privacy is important to us. We will not share your information with any other organization and you will not be added to any third-party mailing lists. 


The Dysautonomia Foundation is a registered 501(c)3 non-profit organization. 
Contributions are tax deductible to the extent permitted by law.

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©2022 Familial Dysautonomia Foundation, Inc.
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Photos by Rick Guidotti, POSITIVE EXPOSURE EIN 13-6145280

315 W 39th St, Suite 701, New York, NY 10018


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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.

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.

Privacy Policy
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.

If you conduct a transaction on our website for the purpose of a charitable contribution, we will not record or store any of your credit card information on our servers or in our records. All credit card transactions are conducted through secure web pages.

If you make an online contribution to one of our events or fundraisers, we may ask your permission to list your name and/or the amount of your contribution and/or the name of the organization you represent (if applicable) as a sponsor of the event or as a contributor to the event. We will not list any of your personal information without your consent.

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.