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MISSION: The Scleroderma Foundation mission is to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families and support networks. VISION: Our vision is to be a relentless force in finding a cure and improving the lives of people affected by scleroderma. Check out our EVENTS PAGE to see what's happening and how you can get involved. To donate directly, please mail checks to: |
DANVERS, Mass. – January 11, 2022 – The Scleroderma Foundation, a national nonprofit that advances medical research, promotes disease awareness and provides support and education to people with scleroderma and their families and support networks, today announced that it will now be known as the National Scleroderma Foundation to help reach and educate a larger audience and connect more people in the scleroderma community with the resources they need.
The National Scleroderma Foundation also relaunched its website and unveiled a new logo to accompany the name change. The National Scleroderma Foundation helps connect the community of 300,000 Americans living with scleroderma and funds innovative research to discover the cause, understand the mechanism, and overcome the disease forever.
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| Social media outlets such as Facebook, Instagram and Twitter can often serve as an important communications tool for Scleroderma sufferers and supporters alike. We'll continue to update our website with timely information, but other outlets allow for a more interactive experience while you keep in touch with family, friends, and other Scleroderma Chapters across the country. |
 @sclerodermasefl |
 @sclerodermasefl |
 @sclerodermasefl |
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