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Carla: Morphea Scleroderma
It's not life threatening, mostly just an annoyance.
But I am fearful that it could spread to other areas.

Dressing Room for Carla by Shelley Ensz My name is Carla. I am a twenty-nine-year-old mother of three. I have localized morphea on my lower back.

It first appeared when I was in junior high, and has grown slowly since then. It started out as a spot on my back that looked just like a bruise that would not go away, and was accompanied by lower back pain. It now spans from one side of me to the other, with one main lesion in the center, which branches out and has other spots around it.

It still looks just like a bruise, and if people see it they usually gasp and say, "What happened?" Luckily, it's not difficult to hide since it's on my back. Most of the time I do not even think about it, it's not life threatening, mostly just an annoyance. But I am fearful that it could spread to other areas.

I was diagnosed early on, but have never had any treatments. I would really like to stop it from getting any larger. Does any one know of successful treatments for this type of morphea?

I would love to talk with others with similar morphea conditions. For a long time I have felt like some what of a freak, and did not even think about searching on the Internet about it until recently.

Thanks for listening, and God Bless.

To Contact the Author
Carla M.
E-mail: mamacarla3@yahoo.com
Story posted 1-8-02
LINKS
Morphea Scleroderma
Types of Scleroderma
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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