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Becky: Morphea and Fibromyalgia
I am a very health-minded person,
and am really angry that by body appears to be attacking itself.

Flowers for Becky by Shelley Ensz I am a forty-two-year old mother of two teens, and have been married for twenty years.

I was finally diagnosed with fibromyalgia in 1998, myofascial pain syndrome and osteoarthritis in 2001, and just recently discovered I have mitral valve prolapse.

I also have what appears to be a bruise on the inside of my forearm, and appears to have an inflamed vein coming out of the bruise. My primary care physician referred me to a dermatologist, who took one look at the "bruise" and said that he was sure it was morphea. A biopsy was taken, along with bloodwork to see if this condition is systemic.

I am so glad I found this website. It has been so informative and comforting.

At first I was so upset. I felt betrayed by my body. I am a very health-minded person, and am really angry that by body appears to be attacking itself. I will get the results of the testing in two weeks, but the doctor seemed very sure of his diagnosis. The muscle in my forearm has already atrophied, and it has only been four weeks!

Thank goodness for my wonderful husband and sons, as they seem to be taking it all in stride. I have a very upbeat attitude, and will just take things as they come, trying to keep the blues away! If you have anything in common with my disease, let me know. And, as always, keep your chin up, we can handle this!

To Contact the Author
Becky
Old Email: rjschuck99@hotmail.com
Story submitted 5-14-02
Story posted 5-25-02
New email needed 05-01-08 SLE

Story Artist: Shelley Ensz
Story Editor: Judith Devlin
LINKS
Fibromyalgia
Morphea
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 !
ISN's Voices of Scleroderma Volume 2
The story on this page is featured in our book, Voices of Scleroderma Volume 2 ! International Scleroderma Network.
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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