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Rodriguez: Linear Scleroderma
I went to the ER and was unable to receive a diagnosis.

Shelly Beach and Pier by Sherrill Knaggs, ISN Artist I have lived with linear scleroderma since 1999. I was eighteen when I was first diagnosed and I was unaware of what I was in for. Being from a small city in Texas was even harder because at the time I was the only case and there was little information on linear scleroderma.

It was February 5,1999, when I first noticed the discoloration in my leg and how stiff my skin was. I went to the emergency room and was unable to receive a diagnosis.

Finally in April of 1999 a biopsy was conducted and I was diagnosed with linear scleroderma. I later moved to Pennsylvania with my brother to look into going to school, but my leg seemed to get worse.

I was then taken to a rheumatologist who started me on Methotrexate injections which later changed to pill form when I was referred to Dr. Alan Friedman in Houston, Texas.

I have lived with scleroderma for the past eight years and I have been off of Methotrexate for the past two years. Little by little pigmentation is coming back into my leg and there are times I still feel joint pain but I have gotten through it.

To Contact the Author
Rodriguez
Email: dragongrl237@aol.com
Story edited 03-17-07 JTD
Story posted 04-08-07 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin
LINKS
Linear Scleroderma
Medical: Diseases and Symptoms
Symptoms of Scleroderma
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 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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