Forums

This forum is for discussing the Coronavirus pandemic, and how it coincides with Friedreich's Ataxia. Ask questions, share tips for self-isolation, etc. Please note that Friedreich's Ataxia News Today is not a resource for medical advice. However, we can share news and patient and caregiver perspectives.

Significant relationships (either with friends, family, or romantic partners) is a difficult subject on its own, but adding FA into the mix seems complicated and may be overwhelming. Here we can discuss any topics regarding relationships here.

This forum is for sharing and discussing any scientific study. If you have a question about something you read, please ask the community here. Also to discuss anything that may alleviate the symptoms of FA.

This forum serves as a place where anyone impacted by Friedreich’s Ataxia (FA) -- both patients and caregivers -- can share stories and life advice with one another. Often, living with a rare disorder like FA feels lonely. Facing troubles that seem unique to you causes isolation and loneliness. We seek to eliminate that by connecting people in the Friedreich’s Ataxia community to share their own stories, tips, successes, and troubles with one another in this forum by opening up a dialogue between those in the FA community!

This forum is designed for patients, caregivers, family and friends who would like more information on different FA resources. These resources can include support groups, press releases, events and more!