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Doris: Morphea
I have spent over $2000.00 on different creams, ointments and pills to no avail.

Pottery by Sherrill Knaggs, ISN Artist I was diagnosed with morphea in 2006. It started with itching that would not stop and now after a year and a half later it is still itching and painful with more blotches appearing weekly.

I have spent over two thousand dollars on different creams, ointments and pills to no avail.

What I found that gives me the most relief is Vicks Vapor Rub, put directly on the sores. I am able to sleep almost all night.

To Contact the Author
Doris
New email address needed 08-06-09 SLE
Old Email Prefix: sis2ten
Story edited 02-05-08 JTD
Story posted 02-05-08 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin
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ISN Artist: Sherrill Knaggs (In Loving Memory)
Sherrill Knaggs Sherrill Knaggs, ISN Artist, created the digital photo to illustrate the story on this page. Sherrill lived in New Zealand. Her story was featured in ISN's book, Voices of Scleroderma Volume 2.
ISN Story Editor: Judith Thompson Devlin
Judith Rose ThompsonJudith Thompson Devlin is the ISN Story Editor for this story. She is also lead editor of the ISN's wonderful Voices of Scleroderma book series!
New Personal Stories
Maria T: Daughter of Deceased Scleroderma Patient (Italy) He, upon looking at my mom's face and hands diagnosed her with sclerodermia, in fact he took care of her until the end...
(Italiano) Maria T: Figlia di una Paziente Defunta di Sclerodemia (Italia) Lui, come vide a mia madre disse "tu hai la sclerodermia", guardandole le mani e la faccia...
(Update) Dee B: Limited Scleroderma/CREST Syndrome (South Africa) There is so much I want to add to my original letter after reading more of other peoples stories. I am certainly not getting better but wish I was...
Tessa: Morphea The nurse just told me that I have morphea and knew nothing about it and she told me to look online for information...
More New Stories: August-November 2009
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Go to Dorne: Overlap and Possibly CREST
 
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