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Ely E: Linear Scleroderma

Italian

Clowning Around by Shelley EnszWhere to begin? I have linear scleroderma and I have had it for about twelve years. Now I am twenty-five so I discovered that I had it when I was very young, just thirteen.

My mother realized that I had a dark surfacing line on my stomach that had some pus. She took me to the dermatologist who discovered another spot that ran through my left leg from the stomach towards the back. Not convinced, he sent me to a specialist. This doctor looked at everything, and analyzed the spot, but he first did a biopsy to check the subcutaneous tissue, and right there and then told me to consider myself lucky, since the illness was in abortive phase. That is, the spots would remain, but no other problems, in theory. He told me it was a strange disease that would be cured with very expensive therapy.

Just today twelve years have passed, and there is always a dark mark that has faded with the years nonetheless. Perhaps my veins are more pronounced than those of a normal person, but I am fine. I am not giving up, it doesn’t matter how dangerous this illness is.

I would like to add something to the discourse on causes of scleroderma. My mother, when pregnant, worked until the eighth month at a dye factory for wool, therefore there were chemicals around her. I cannot even explain the smell to you! If, like I have read here, a reason for it can be chemicals, I would like to reflect on this with you.

To Contact the Author
Ely
Email: el84ena95@yahoo.it
Story edited 07-14-09 JTD
Story posted 07-14-09 SLE

Story Artist: Shelley Ensz
Story Translator: Alba León
Story Editor: Judith Thompson Devlin
LINKS
Italian:
Ely E: Sclerodermia Lineare
Sclerodermia Lineare

English:
Causes of Scleroderma
Juvenile Scleroderma
Juvenile Scleroderma Stories
Linear Scleroderma
Linear Stories
Medical: Diseases and Symptoms
Scleroderma Experts (Worldwide)
Sclero Forums
Symptoms of Scleroderma
Types of Scleroderma
What is Scleroderma?
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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