Short Bio |
I was diagnosed with CMT in Jan after going 9 months with a probability of ALS. My new Neurologist (CMT specialist) thought the CMT was masking a Neuromuscular disorder and in Sept said I have LGMD. Having to get myself informed on my diseases via the internet because my Neurologists gave me very little data. I have just started wearing AFOs to help with the CMT.
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How long have you or the person that you are caring for had MD? |
Just diagnosed Sept 2021 but been symptomatic for over 2 years
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