University of Michigan Professor Creates Website to Provide Scleroderma Patients Resources and Support

Dinesh Khanna, a professor at the University of Michigan has worked heavily with the rare disease scleroderma. Michigan has its own Scleroderma Program, of which Khanna is the director. Through…

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“Stampede Scleroderma” Event for Systemic Sclerosis held at the Detroit Zoo Raised Over 130,000 Dollars for Research

Systemic Sclerosis Systemic Sclerosis (Systemic Scleroderma) is a rare disease which results in the hardening of the connective tissues in the body as well as the skin. It can affect…

Continue Reading “Stampede Scleroderma” Event for Systemic Sclerosis held at the Detroit Zoo Raised Over 130,000 Dollars for Research
Plan Now to Attend the 2018 Scleroderma National Patient Education Conference, July 27-29
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Plan Now to Attend the 2018 Scleroderma National Patient Education Conference, July 27-29

Finding a community is important for everyone -- but particularly if you have a chronic or rare disease. For the approximately 300,000 Americans with scleroderma, there's an active support group…

Continue Reading Plan Now to Attend the 2018 Scleroderma National Patient Education Conference, July 27-29