2018 National Conference Save the Date
The 2018 National Patient Education Conference will be held July 27-29 in Philadelphia! Will you join us?

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Stepping Out to Cure Scleroderma
Take a Step for Scleroderma

Find a "Stepping Out to Cure Scleroderma" walk/run near you today!

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Who We Are

The Scleroderma Foundation is a federally qualified 501(c)(3) nonprofit dedicated to serving the needs of the scleroderma community.  Our primary goal is to raise funds and awareness for our three-fold mission of support, education and research.  All donations are qualified charitable donations to the fullest extent of the law.  Our federal tax identification number is 52-1375827.  All donations are gratefully accepted. 

What is Scleroderma?

Scleroderma, or systemic sclerosis, is a chronic connective tissue disease generally classified as one of the autoimmune rheumatic diseases. The word “scleroderma” comes from two Greek words: “sclero” meaning hard, and “derma” meaning skin. Hardening of the skin is one of the most visible manifestations of the disease.

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Download Our Free Scleroderma Information Packet

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annual report cover
Click the image above to access a copy of our FY 2015-16 Annual Report

 

News

Visit the eLetter Archive to read the stories behind these headlines.
  • Thanksgiving Holiday Observance
  • Video: Drugs that Cause Scleroderma/Morphea
  • Scleroderma Researcher Profile – Monica Mukherjee, M.D., M.P.H.
  • Doctor of the Year – Maureen Mayes, M.D., M.P.H.
  • ATS Patient Voices 6
  • Open Enrollment Ends December 15 for 2018 Health Insurance Under ACA
  • Key Hemodynamic Differences Noted With Scleroderma-Associated PAH vs. Idiopathic PAH
  • Grassroots Advocacy Training Online – November 27
  • 2018 National Patient Education Conference
  • Giving Tuesday is November 28

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                                                               annual report cover

Click on image above to access our FY 2015-16 Annual Report!

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