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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 by Date Posted
Stories in Other Languages
Difficult Diagnosis and Undiagnosed
Eosinophilic Fasciitis
Interstitial Cystitis
Sjögren's Syndrome

References

(1) audioAudio pronunciations for this page are from Mirriam-Webster Online Dictionary.
 
Go to Difficult Diagnosis
 

SCLERO.ORG is operated by the International Scleroderma Network, which is a full-service U.S. nonprofit 501(c)(3) established in 2002. We provide stellar worldwide research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension. Donate or Shop Now.

Questions? Post a message in Sclero Forums or email us directly at isn@sclero.org. Or call our Scleroderma Hotline (English only), Toll Free in U.S. 1-800-564-7099 or Direct at 1-952-831-3091. Ask for our Welcoming Email.

Our headquarters postal mailing address is: International Scleroderma Network (ISN), 7455 France Ave So #266, Edina, MN 55435-4702, United States.

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