#FDMatch22: Our FD Stories
#FDMatch22 Crowdfunding Campaign has a tremendous impact on the FD Foundation and on the community we serve by raising funds to ensure the Foundation’s continued efforts to enhance and extend the lives of people affected by FD.
This year's #FDMatch22 celebrates Our FD Stories, spotlighting individuals and families who are making tremendous strides towards—and benefiting from—the patient care, medical research, and life-enhancing programs and services provided by the Foundation and made possible by YOUR support.
In the coming weeks, we will share a series of “FD Stories”, so please continue to check this site to view the latest story and track our fundraising progress!
If you would like to become a Matching Donor please contact Lanie Etkind at Letkind@famdys.org
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.
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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The FD Foundation does not offer medical advice. We always recommend that you contact the Dysautonomia Center (link here) or your personal physician.