The Scleroderma Foundation of Greater Chicago serves people living with scleroderma, their families, caregivers, and healthcare partners by offering support, education, community connections, and resources to help them navigate diagnosis, care challenges, and life with this complex autoimmune disease.
Their vision is to build a world where individuals and families impacted by scleroderma feel understood, supported, and empowered to live their best lives while advancing toward improved treatments and, ultimately, a cure through collective awareness, education, and community engagement.
Their mission is to provide hope, support, education, advocacy, and community for people affected by scleroderma, fostering connection and understanding, and to raise awareness and funds that drive research, improve quality of life, and bring the community together in the fight against this rare disease.
Connect with your federal legislators to speak up for dermatological conditions today.