Familial Dysautonomia: the leader in FD treatment and research
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- 2026 United Airlines NYC Half Marathon
- 2026 FD Journal
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- 2025 FD Journal
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- 2024 FD Journal
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- TEARLESS Art Exhibit 2019
Dear Friends,
The FD Annual Journal is a treasured tradition, dating back to 1955. Although our FD community reaches far and wide, we come together each year within the pages of the Journal to honor special people in our lives and to remember those who are no longer with us. This year, the Journal will include a special "Violet" Section, honoring Dr. Horacio Kaufmann's first decade as Director of the NYU Dysautonomia Center. We invite you to add a Violet Page in tribute to Dr. Kaufmann and his tremendous dedication to all those affected by FD. Please join us by contributing to the 2019 Journal. Your gift will fund the Foundation's important work:
- Ensuring that those living with FD have access to the best medical care;
- Funding cutting-edge research into FD and the FD gene;
- Offering support to families caring for a loved one with FD;
- Educating the Jewish community about FD and genetic testing.
To reserve your page, please mail in a completed form or visit our website by January 15, 2019.
Thank you for your support!
Lanie Etkind
Executive Director
Step 1
Design your submission
Full page: 4 1/2 x 7 inches
Half page: 4 1/2 x 3 1/2 inches
Quarter page: 4 1/2 x 1 3/4
Step 2
Fill in and submit the Journal form
Click here for our Journal form
Fax, email or mail the form
Fax, email or mail your artwork
Step 3
Submit Payment
Mail a check
Use our online form page
Call us with your credit card
©2026 Familial Dysautonomia Foundation, Inc.
| Disclaimer | Privacy Policy | Medical Disclosure
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.
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.