In the beginning of 2023 our niece was diagnosed with Friedreich's Ataxia at 5 years old. This diagnosis came after months of testing and two years of physical therapy to improve her gross motor skills. Then a few months later our nephew, then age 2, was also diagnosed with FA. Family, friends, neighbors, and communities came together to support their family. This is when our mission began.
Families For Friedreich's Ataxia Foundation was founded in the spring of 2024 to support, empower, and advocate for individuals and families living with Friedreich's Ataxia by providing financial assistance and bringing awareness to FA.
Learn more about our organization and how you can get involved today!
Copyright © 2025 Families For FA - All Rights Reserved.
Powered by GoDaddy
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.