Viewing 0 reply threads
  • Author
    Posts
    • #16960

      Hearing Friedreich’s Ataxia for the first time can be an overwhelming time experiencing the emotions of a new diagnosis and trying to determine next steps. It is important to recognize that you are not alone. The FA Community is an active and supportive one.

      FARA (Friedreich’s Ataxia Research Alliance) has created this packet as a resource and guide for newly diagnosed families. It is also a good tool for any existing patients:
      https://www.curefa.org/pdf/living-with/NewlyDiagnosedPacket.pdf

Viewing 0 reply threads
  • You must be logged in to reply to this topic.

©2022 KLEO Template a premium and multipurpose theme from Seventh Queen

CONTACT US

We're not around right now. But you can send us an email and we'll get back to you, asap.

Sending

Log in with your credentials

or    

Forgot your details?

Create Account

Verify you are not a robot