COVID-19, January 8, 2021: Information and frequently asked questions regarding the COVID-19 vaccines have been addressed by the Foundation's Medical & Scientific Advisory Board. Read More What's New at the Scleroderma Foundation Greater Chicago ChapterThank you for making the 2020 virtual walks a success!
Although we missed seeing you all in person, we were blown away by what you all accomplished when you came together virtually to #WalkAloneTogether. From Springfield to Dixon and Highland Indiana to Highland Park Illinois, our supporters made the 2020 walk season one to remember, helping us raise more than $120,000! From all of us at the Scleroderma Foundation, thank you for your support and for joining us as we continue the fight for a cure!
Online Patient Education
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Our MissionImproving the lives of patients. Making strides toward a cure.The mission of the Scleroderma Foundation is focused on three critical goals:
Whether you're a scleroderma patient, have a loved one struggling with scleroderma, or just want to learn more about the disease, we have resources, education events and fundraisers you'll love! |
Contact InformationStephanie Somers Gresh, Executive Director Scleroderma Foundation Greater Chicago Chapter |
Board of Directors Mary Carns |
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Medical Advisory Board |
Online Patient Education
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Finding Joy Everyday Through the Arts: Real Ways to Improve Emotional Health During these uncertain times, Jennifer La Civita, PsyD of Adler University is here to show you practical, yet inspiring ways you can instill peace and calm by using the arts. You’ll learn easy, relaxing ways to soothe body, mind, and spirit. Find joy everyday! You don’t have to be an artist to benefit from this webinar! |
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Free Weekly Guided Relaxation Every Wednesday at 5:30pm CST Join the team at Yoga for Scleroderma for "Wednesday Wind Down," a free weekly guided relaxation. You can join from a land line, cell phone, or you can join on Zoom. You can also phone in, no internet needed: +1 (669) 900-6833 US
Meeting ID: 82635317704
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Patient Education Virtual University The Scleroderma Foundation's "Virtual University" Patient Education Series was offered in place of the 2020 National Patient Education Conference, which was cancelled as a result of the COVID-19 pandemic. This series of webinars, workshops and videos covers everything from managing symptoms to everyday living advice from individuals with scleroderma, physicians and specialists.
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Patient Support
Support groups provide a forum to share thoughts, concerns, information and connect with others who understand the experience of living with scleroderma. Find a support group in your area or connect with others on our online support community, Inspire.
Looking to start a new support group in your area? Contact us at 312-660-1131.
Diamond National Sponsors
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