HSAN Research

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Donate To The Dysautonomia Foundation

Your contribution to the HSAN Research Fund can make a difference!
Help us provide the best possible scientific and medical research for the benefit of people with HSAN

HSAN (hereditary sensory and autonomic neuropathy) disorders are characterized by reduced sensation, autonomic dysfunction and progressive loss of function of peripheral nerves. There are five types of HSAN (familial dysautonomia is HSAN type 3).
 
The Dysautonomia Foundation supports research leading to better understanding and treatment of HSAN disorders. Doctors and researchers at our Dysautonomia Center at NYU Langone Medical Center conduct clinical research for the benefit of people suffering with HSAN.
 
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 HSAN disorders.

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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.

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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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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.