13 Scleroderma Foundation Resources to Help You

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4. My Voice

This page showcases some stories from teens and children who live with scleroderma. Remember, you’re not alone!

 

5. Discussion Board

A 24/7 on-line support group and discussion community with members and patients from all over the world.

 

6. Weekly eLetter

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.

According to the Scleroderma Foundation, while there is no proven cure for scleroderma, much can be done to prevent, minimize, or alleviate its effects and symptoms. 

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