I was diagnosed with scleroderma in February 2007. I was not feeling very well in 2006 contributing me not feeling well to just getting old. My joints were starting to swell and by winter my fingers and my toes were going...
Scleroderma, Systemic anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Scleroderma, Systemic. You're not alone.
Other experience groups that have been combined into this group include: None yet.
This is an experience group where everyone says: I Have Scleroderma, Systemic. It features support, personal stories and experiences, advice, chat, talk, forums, videos, pictures and resources from real people, just like you.
It's free to join, and the people in this group would love to meet you! If you've had this experience, or plan on having it in the future, simply click 'Me Too' or 'Plan To' and add it to your experiences. As you add more experiences, we're better able to
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