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AJ: Linear Scleroderma
I grew up being poked and prodded and
paraded in front of one specialist after another.

Straw Hat with Flowers, photography by Shelley EnszI have had linear scleroderma since 1968, when I was seven years old. I always felt like I WAS scleroderma, as I have never met anyone else with the same diagnosis.

I grew up being poked and prodded and paraded in front of one specialist after another. Sometimes whole classes of medical students were brought to look at me.

Scleroderma affected the left side of my body, wrecking havoc in a very short amount of time. My left leg is two and a half inches shorter than my right and much smaller.

Due in a very large part to my mother's persistence and nightly therapy, I have good use of my leg and arm. Also, I believe Dr. Claybaugh, who treated me at Wesley Hospital in Wichita Kansas, saved my life in more ways than one. Mainly by finally fixing on a diagnosis and listening to my mother and her thoughts and feelings regarding my illness.

I did not realize how much I had to say, I have never discussed scleroderma with anyone. Most doctors I have seen since my last visits with Dr. Claybaugh (1974?) do not even know how to spell scleroderma, let alone treat any problems I might have that are associated with this disorder.

I am so fortunate that my scleroderma stopped advancing with only small advances on my right side. But I can say that scleroderma affected my life and still affects me in ways incomprehensible to "normal" people. I remember wishing as a child that I had polio instead. People could spell it and while they did not understand it's dimensions, it was accepted in ways scleroderma never was. Weird, huh?

I am sorry for the little girl I was with scleroderma. I enjoyed no personal space, was so sick for so long. The agony of my limbs slowly drawing up is something I cannot describe accurately, and besides, it is a private matter. But I am also happy for the little girl who had the extreme luck of meeting a fine physician such as Dr. Claybaugh and the many physical therapists who were endlessly patient with a mad little girl who tried to hate them all.

Well, that is such a small part of my story, but I hope it finds it's way to a mother with a sick little girl. If it does, do not despair. I have a good life. I have a good job, own my own home, my own car. But the best thing of all, something the doctors warned my mother I would never have—two beautiful, healthy children!

To Contact the Author
AJ Miller
(AJ we need your new email address.)
Posted 3-1-99
LINKS
Linear 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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