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Living with Syringomyelia: Questions and Support

Started by Kevin Davis9 · Nov 7, 2008 · 👁 3 views · 0 replies

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Kevin Davis9 NewcomerOP

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joined Nov 2008

#1 · Nov 7, 2008

Hey there,
does anyone happen to know if there’s an association for people living with syringomyelia based here in the States? I’ve been scouring the web for ages and coming up totally empty-handed, so I would be seriously grateful for any leads or info you guys might have!

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