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Carolina: Linear Scleroderma

Truth is I was diagnosed about ten years ago.

Cherry Blossom by Sherrill Knaggs, ISN Artist Truth is I was diagnosed about ten years ago. After multiple exams, many visits to different dermatologists and immunologists I was diagnosed with localized linear scleroderma.

This began when I was about twelve years old, with little spots on my right leg thigh. As time went by it disseminated throughout my leg and reached my foot. At that time (I am talking of about 1997) I was treated with methotrexate once a week and folic acid the rest of the week.

I was also told to exercise, but not to put pressure on my knee, which meant I could not do a lot of jumping: no jogging on hard surfaces, no basketball, mostly swimming and cycling so my muscles would not suffer more atrophy.

After two years the treatment ended and scleroderma did not advance to muscle or bone, but along the years I have found more spots on the same leg.

In spite of the initial diagnosis, I think that as time went by, linear scleroderma has turned into morphea, because the characteristics are more similar.

I would like to be in contact with other people in a similar situation so they can tell me which treatments they have followed, etc.

To Contact the Author
Carolina
Email: carolita0184@hotmail.com
Story edited 06-09-06 JTD
Story posted 09-26-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Translator: Alba León
Story Editor: Judith Thompson Devlin
LINKS
(Español/Spanish) Carolina: Esclerodermia Lineal

Linear Scleroderma
Linear Scleroderma Stories
Types of Scleroderma
What is Scleroderma?
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 Translator and Editor: Alba León
Alba Leon, ISN TranslatorAlba León is the ISN Translator for this page. She is studying international relations in Mexico City.
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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