As the year comes to a close, we’re deeply grateful to you for being part of this unstoppable community driving progress toward a cure. The Scleroderma Research Foundation exists for...
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As the year comes to a close, we’re deeply grateful to you for being part of this unstoppable community driving progress toward a cure. The Scleroderma Research Foundation exists for...
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On July 18, Strike Out Scleroderma Day returned to T-Mobile Park, bringing members of the scleroderma community together for a day of scleroderma awareness and baseball. Over 30 members of...
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“I #SayScleroderma because although it is rare and may feel isolating, it is not one to be alone with," says Ryan M. (dx 2019). "There is a global community that...
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We’re committed to significantly increasing our scleroderma research investments in the years to come. But to do that, we need your help. Please make a gift today to help us...
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For Scout L., her mother Jackie’s experience with scleroderma is why she chooses to #SayScleroderma: to help drive research that leads to better, more personalized treatments. "Scleroderma affects people in...
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As someone living with scleroderma, Tiffany P. believes in the power of research to drive change. This month, she’s joining us to #SayScleroderma and share why scleroderma research matters to...
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Let's talk about scleroderma—because understanding this disease is key to spreading awareness. It’s Scleroderma Awareness Month, which is a time to shine a light on this challenging disease and the...
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It’s Scleroderma Awareness Month–are you ready to spread the word? Why #SayScleroderma? Because everyone should know what this disease is and does. Because no one should have to live with...
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The countdown is on ⏳ Scleroderma Awareness Month kicks off soon in June! We are gearing up for the most action-packed awareness month of the year, where we come together…
