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Another Diagnosis Option
So I was diagnosed with Freidriech’s Ataxia (FA) from genetic testing and have just gone along with. But lately, I have been finding some of the symptoms I supposed have been getting I have not. This questions the results I got from the genetic testing. Did they get it wrong? I had my parents tested, and neither one have the gene that is supposed to have come together and passed to me. I have an older brother and he is completely fine.
Does anyone have any suggestions for me in seeking a second diagnosis?
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