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This board is for medical issues related to Scleroderma, i.e., symptoms, concerns, treatments, questions
jeffn, kathsherman, christel
You can talk about anything here
Tell us about yourself, when disagnosed, type of SD, treatment.
For Scleroderma patients on AP who want to share their story, i.e., when started, progress, any other treatment with AP, AND for those considering AP.
This section is for books you would recommend. Please list TITLE, AUTHOR, where to purchase if possible. No commentaries, please so we can keep an ongoing list.
This is to post pictures of anything that interests you that might interest others.