This area features articles that appear in "The Voice" written by real kids living with scleroderma. It's a place to care and share, and know that you're not alone.
| Date |
My Article |
| March, 2008 |
 Alivia Watson
"I was diagnosed with Raynaud’s when I was 4.
My doctor told my mom and dad that I may have
scleroderma. He kept a good watch on me for three
years, and when I was 7 he told my mom and dad that
I had systemic sclerosis." |
| September, 2007 |
 Cynthia Cervantes
"My experience with scleroderma began more than a year ago when I suddenly would get weak, my body ached, and my vision was getting worse." |
| March, 2007 |
 Samantha Murray, National Youth Ambassador for the Scleroderma Foundation
"Kids aren’t supposed to get this disease—it’s for grownups, mostly women like my mom’s age." |
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