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Old 06-05-2012, 12:22 PM
lolah lolah is offline
Junior Member
 
Join Date: Jun 2012
Posts: 6
10 yr Member
lolah lolah is offline
Junior Member
 
Join Date: Jun 2012
Posts: 6
10 yr Member
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Quote:
Originally Posted by norahs View Post
Until I was diagnosed I had never heard of "erthromelalgia" and because it is pretty rare there are few with it. Although I wouldn't wish this on anyone it would mean a lot to me to have someone to talk to that shares my situation and pain.

I also have PN, Raynaud's which my doctor believes are a result of the EM. There are other sites with EM sufferers but I like this site so much just thought I would check with you all.

Thank you.
I am new here, and I know this is an old post but I thought I'd share my two cents, anyway. I was diagnosed with EM approximately 2 months ago. I have it in my upper body, which is even more rare. Face, neck, ears, etc.
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