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Miguel: Linear Scleroderma

Spanish

Orange Day Lily by Sherrill Knaggs, ISN Artist Hello, my name is Miguel. I am twenty-seven years old and some months ago I went to see a doctor because I had a spot on my left leg. It didn't hurt, but my skin became very dry and started to harden in that area.

The doctor sent me to get a biopsy and as a result of it he diagnosed me with linear scleroderma. He gave me treatment with some pills, I can't remember the name.

My problem is I feel the illness is spreading as now my knee and ankle hurt. I went to see another doctor, who ordered blood tests to see whether my internal organs are at risk. The doctor found two more spots in my back.

Right now the best treatment I have is my wife. She is my angel, and thanks to her I feel much better. Now I only have to wait for the results and see what treatment the doctor will give me.

I am not feeling very well physically, but I am quite happy. I've found that the best remedy is to give and get love. Thank you and be safe.

To Contact the Author
Miguel
Email:Withheld by Request
Story edited 03-17-07 JTD
Story posted 04-10-07 SLE

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