CuriousGirl
Member
- Joined
- Nov 7, 2010
- Messages
- 26
- Diagnosis
- 10/2012
- Country
- US
- State
- CA
- City
- sacramento
after 3 years of emg's, nerve conduction studies, mri's, blah blah blah. i haven't been diagnosed with pma definately, but neurologist suggested it may be pma or hiriyama syndrome.
i've been taking a look at the pma support group, but there're no postings since january 2011. what happened to everybody? i'd really like to be a part of the support group, but .......
i've been taking a look at the pma support group, but there're no postings since january 2011. what happened to everybody? i'd really like to be a part of the support group, but .......