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Faye: Morphea Scleroderma
And because I had no problems walking, they lost interest.

Flowers for Faye by Sherrill Knaggs, ISN Artist My name is Faye, and I am Scottish. Here is my story. At the age of about six or seven, I developed what looked like a bruise on the front of my left thigh. It started off as a small purplish spot. My mother was very worried when it did not go away, so I was taken back and forth to the hospital.

Many a doctor scratched their head as no one seemed to know what this strange thing was. "Could it be leprosy?" I was asked. "Have you any pain?" "No," I replied. And because I had no problems walking they lost interest. I was later told it was a rare skin condition called morphea, and from then on I have been left in the dark.

My mum thinks that I was knocked hard on my leg while out playing, and that is what caused it.

I do not recall the time scale as it is all a bit of a blur now, but the bruise grew to full size in my teenage years and has now, thankfully, stopped growing. It is about seven inches long and four inches wide. It is shaped like a picture of a rabbit, of all things!

I have lost some of my thigh muscle as it has grown, but I am in perfect health. For this I am grateful! I can walk, run, swim and ski. It does not stop me from doing anything at all. But sometimes at night I get aching pains and I worry about people staring at me when I am in my swim wear, but that is no big deal. I do get very tired and very stressed easily which I have been learning to control over the years.

I am now twenty-nine, living in Sydney, Australia, and getting married in February, so I have lots to look forward too!

If anybody wants to write to me I would be really interested to hear similar stories.

To Contact the Author
Faye
Email: polmuir@hotmail.com
Story posted 12-5-03

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Morphea
Juvenile 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!
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(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...
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More New Stories: August-November 2009
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