Making life easier for patients. Making strides toward a cure.
The Scleroderma Foundation Michigan Chapter is here to help.
Check out our new Applying for Disability Resource Guide!
Welcome to the Scleroderma Foundation Michigan Chapter website. Whether you're a scleroderma patient, have a friend or family member with scleroderma, or just want to learn more about the disease, we are so pleased you're here.
Click around to find information on scleroderma and its effects, strategies for coping with the disease, links for support, and news about fun and educational events sponsored by our chapter.
The mission of the Scleroderma Foundation is focused on three critical goals:
- SUPPORT: To help patients and their families cope with scleroderma through mutual support programs, peer counseling, physician referrals, and educational information.
- EDUCATION: To promote public awareness and education through patient and health professional seminars, literature, and publicity campaigns.
- RESEARCH: To stimulate and support research to improve treatment and ultimately find the cause of and cure for scleroderma.
We're here for you—and we'd love to hear from you.
Want to volunteer, donate, or learn more about the chapter and its events? Feel free to contact us; we're here to help in any way we can.
Laura Dyas, Executive Director
Scleroderma Foundation Michigan Chapter
23999 Telegraph Rd.
Southfield, MI 48033
People making a difference.
There are so many scleroderma patients in Michigan who need support from our chapter. The members of our Board strive to ensure that each and every one gets the help they need, and to raise awareness of our chapter's mission.
Board of Directors
Interested in joining our Board? Please fill out our recruitment questionnaire.
Medical Advisory Board
Sincerest thanks to our generous sponsors.