I Have Freeman-sheldon Syndrome Friedreich Ataxia


Freeman-Sheldon Syndrome Friedreich Ataxia anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Freeman-Sheldon Syndrome Friedreich Ataxia. You're not alone.

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 Hi, My name is Michel Beaudet, I'm 47, have FA and live in Quebec, Canada. I'm sending this message to invite people to join a...
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This is an experience group where everyone says: I Have Freeman-sheldon Syndrome Friedreich Ataxia. It features support, personal stories and experiences, advice, chat, talk, forums, videos, pictures and resources from real people, just like you. It's free to join, and the people in this group would love to meet you! If you've had this experience, or plan on having it in the future, simply click 'Me Too' or 'Plan To' and add it to your experiences. As you add more experiences, we're better able to recommend interesting people to you that share many of your personal experiences.

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