Living with Syringomyelia: Questions and Support
in Health ·
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!
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!