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Getting involved in the FA Community
When I was first diagnosed 15 years ago, I wanted to get involved right away by meeting others with FA. At that time, however, there weren’t many resources to do so.
Thankfully, today, things are different, and there are endless ways to connect with FAers all over, whether it is through social media platforms, online support groups, Bionews, the Friedreich’s Ataxia Research Alliance (FARA), and more!
How have you become involved in the FA community? Were you able to make real and life-long connections?
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