Booklvr
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About Me
I'm Canadian. I was diagnosed with M.E. about 5 years ago. It's been tough. I am disabled now but I am still able to work part-time, from home. Recently my GP thought I had MS due to lesions found on my brain (MRI). I had some hope from that, actually, because I thought I could finally get treatment and maybe even go into remission. Then I saw the neurologist and he said it is not MS. I never thought I'd be upset that I DON'T have MS. Having ME is so devastating. Now I'm back to the drawing board with M.E. I'm scared, frustrated, confused. I'm hoping to connect with others here who are experiencing the same things and maybe start feeling supported. I also hope to support others when they have tough times through this horrendous disease.
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Discussion Comment
Booklvr commented on the discussion fumble fingers?.
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New Friend
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Discussion Comment
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New Friend
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Discussion Comment
Booklvr commented on the discussion Is M.E. really a neurological disease?.
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Joined New Group
Booklvr joined the group Chronic Fatigue Syndrome.
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New Friend
