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Hope: Linear Morphea
The rash started spreading up my arm and over my joints, it started to scar.

Pink Daisy by Sherrill Knaggs, ISN Artist When I was twelve, I got this rash on my left arm that would not go away. My mom took me to the doctor and for three months he treated it as ringworm.

The rash started spreading up my arm and over my joints, it started to scar. The rash looked like a long line of bruises going up just one side of my arm. The scar on my hand and elbow looked like a burn scar.

A year after the doctor started treating me for ringworm, he finally sent me to Denver and from Denver they sent me to Kansas City and there they finally diagnosed it as linear morphea.

I have not had any other outbreaks of it anywhere else on my body. It has stayed in one place. I have to keep lotion on it to keep the scar from drying out and cracking. But other than that, there is nothing else that I do for it.

To Contact the Author
Hope
Email Withheld
Story edited 09-19-06 JTD
Story posted 10-26-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Juvenile Scleroderma
Linear Scleroderma
Morphea Scleroderma
Morphea 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 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
Mila: Morphea Now I am twenty-five years old, and that spot has grown throughout my right leg and on one side of my belly button...
(Español/Spanish) Mila: Morfea Hoy en día tengo 25 años y esa mancha está en toda mi pierna derecha y al lado de mi ombligo...
(Español/Spanish) (Update) Jeins: Esclerodermia Sistemica Difusa y Dermatopolimiositis Ya había escrito mi historia hace 3 años cuando recién estaba pasando por la enfermedad. Para quienes no lo saben tengo esclerodermia y dermatomiositis desde los 19 años.
Alana: Scleroderma (Peru) I cannot open my mouth completely, I have lost strength in my hands, I have breathing problems, my face looks different, my skin is really tight and I have lost my appetite...
(Español/Spanish) Alana: Paciente Nuevo con Esclerodermia (Peru) Le dije que ya no podía abrir la boca completamente, he perdido la fuerza de las manos, tengo problemas respiratorios, mi rosto está diferente, mi piel está dura y he perdido casi el apetito...
Kristy C: Generalized Morphea The only place where I do not have any morphea is my face, which I am very thankful for...
(Update) Raymond: Surviving Son of Scleroderma Patient On October 19th, the Herbert family lost another member of the family to scleroderma. My uncle Edmond has passed on...
More New Stories: November 2008
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