Discussion in 'Latest ME/CFS Research' started by Jacque, Aug 9, 2013.
Small_Fiber_Neuropathy_and_FMS...docx (271 KB)
Mine too! I have an appointment for testing with a neurologist who specializes in small fiber neuropathy next month. Hope something good comes from it.
I'm sure I must have the same thing too. Let us know what type of testing the neurologist does liquid sky, I hope you can get some sort of treatment!
We all suffer here at PR but for those who DON'T have this...COUNT YOUR BLESSINGS!!!!
this link is not working for me. Am I missing something?
You can also try a Google Site Search
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