4. My Voice
This page showcases some stories from teens and children who live with scleroderma. Remember, you’re not alone!
A 24/7 on-line support group and discussion community with members and patients from all over the world.
The Scleroderma Foundation has an electronic newsletter out every Friday. This way you can stay up-to-date with all the latest updates on scleroderma research, resources, and other news.
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