Scleroderma Patient Stories
We feature the world's largest collection of scleroderma patient and caregiver stories, in many languages.
The stories from this site form the basis for the ISN's Voices of Scleroderma book series. (Also see What is Scleroderma? and Types of Scleroderma)
Limited SD Stories
Overlap Patient Stories
Morphea Stories (Italiano)
English Stories by Type (Main listing)
English Stories Alphabetically by First Name
Stories in Other Languages
Difficult Diagnosis and Undiagnosed
See ISN News
for recent donors, including memorials for
Patricia Ann Black, Gayle Hedlin, Janet Paulmenn and Lilian Stiles.
SCLERO.ORG is the world leader for trustworthy research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension. We are a service of the nonprofit International Scleroderma Network (ISN), which is a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team, or Volunteer. Donations may also be mailed to:
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA
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TOLL FREE HOTLINE 800-564-7099
Free to U.S. and Canadian Callers. Ask for our Free Info Packet by mail or email!
Scleroderma, Pulmonary Arterial Hypertension, and related illnesses.
The most important thing in the world to know about scleroderma is sclero.org!