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Betty W: Morphea
I had spots of it on my hand,
on the top part of my arms and on the top part of my leg.

Snowflake for Betty W. by Sherrill Knaggs, ISN Artist When I was sixteen years of age I was diagnosed with morphea. I had spots of morphea on my hand, on the top part of my arms and on the top part of my leg.

The dermatologist took a biopsy of my hand and diagnosed this to be morphea. I was told they knew very little about this disease. He said if I had to have it I had the best kind, some kinds would get into your internal organs.

That was in 1984. Twenty-two years later I am fine except for some ugly spots on these places but they have lightened. Needless to say, I was very frightened as I did not know what to expect and neither did the doctor. He did say it was very rare.

I feel blessed that it ran its course without too much damage to my skin. Hopefully after this long it will never return.

To Contact the Author
Betty
New Email needed 04-19-08 SLE
Old Email: bwood7@centurytel.net
Story edited 07-12-06 JTD
Story posted 08-23-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin
LINKS
Morphea
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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