Familial Dysautonomia Foundation

Our Story

The Familial Dysautonomia Foundation was established in 1951 by dedicated parents seeking to improve the lives of children diagnosed with Familial Dysautonomia (FD). This organization has been at the forefront of research and advocacy, ensuring that those affected by FD receive the care they need.

Impact

Thanks to the foundation's efforts, the life expectancy of individuals with FD has dramatically increased from just 5 years to 40 years. The foundation has also established the world’s only two treatment centers dedicated exclusively to FD care and research.

Why Donate?

Your contributions to the Familial Dysautonomia Foundation directly support groundbreaking research and essential medical care for individuals affected by FD. Every donation helps improve quality of life and advances scientific understanding of this rare disorder.

Get Involved

Join the fight against Familial Dysautonomia by donating today! Your support can make a significant difference in the lives of those affected by this condition. Whether through cryptocurrency or cash, every contribution counts!