SCLERO.ORG is retiring 4-24-2021. Thank you for the memories! You'll still find us in the Wayback Machine, and we'll carry your stories in our hearts forever.

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)


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

SCLERO.ORG is the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses. We are a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team. Donations may also be mailed to:

International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA
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