Guest guest Posted September 7, 2009 Report Share Posted September 7, 2009 I will be meeting with our pediatric neurologist (who is from the MDA site) and MDA on Wednesday with my 4 year old who was diagnosed with CMT through genetic testing. Do any of you have suggestions regarding questions I should have or anything else that may be helpful? Also, my daughter was recently diagnosed with anemia and has some hearing loss in one ear. Could that be related to CMT or would that be completely separate? I would love to hear any thoughts. Thank you for your help with this new journey I am on! Amy Quote Link to comment Share on other sites More sharing options...
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