About Us
Finding Inspiration at Every Turn
We believe in the importance of community and empowerment for everyone living with scleroderma and their supporters while driving research that will lead to a better quality of life and ultimately a cure.
Our Story
The Scleroderma Foundation of Greater Chicago has been serving the scleroderma community and fighting for a cure for more than 40 years. This cause is very personal for us. What started as a grassroots organization around one family's dining table has evolved into a multi-state organization and a national leader in both patient support and research funding.
Our team is deeply committed to our mission and has been a driving force in advancing the cause both locally and nationwide. With your help, we will continue to expand our services and make sure that everyone living with scleroderma feels empowered to live their best life, while we fight for a cure.
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Meet our Team
Stephanie Somers Gresh
Executive Director
Stephanie has been involved with the Scleroderma Foundation of Greater Chicago since 2009. When scleroderma affected her own family, she decided to start fundraising and help bring awareness to the disease. She remains deeply committed to the cause and continues looking for ways to improve the lives of all those living with scleroderma.
Dennis Brock
Administrative Assistant
Dennis joined the Scleroderma Foundation of Greater Chicago team in early 2023. Originally, from the North East, he is also a recent addition to the Chicago area. He is passionate about helping others, serving his wider community, and learning about history.
Our team also includes countless volunteers that help us achieve our mission! We are so grateful for all of you!
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Our Partners
We are proud to collaborate with these organizations in order to move our mission forward and provide the best possible services to the scleroderma community.
