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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)

Systemic Scleroderma:

CREST Stories

Diffuse Stories

Limited SD Stories

Overlap Patient Stories

Localized Scleroderma:

Linear Stories

Morphea Stories

Morphea Stories (Italiano)

Others

English Stories by Type (Main listing)

English Stories Alphabetically by First Name

Stories in Other Languages

Difficult Diagnosis and Undiagnosed

Eosinophilic Fasciitis

Interstitial Cystitis

Sjögren's Syndrome

Go to Scleroderma Videos
 
Recent Donors
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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Scleroderma, Pulmonary Arterial Hypertension, and related illnesses.
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