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Karen H: Eosinophilic Fasciitis
My symptoms first began as pain in my shoulders.
Pink Watsonia by Sherrill Knaggs, ISN Ar I have been living with Eosinophilic Fasciitis (EF) for about eight months now. My symptoms first began as pain in my shoulders. I went to my doctor who said I needed physical therapy.

Soon after, I started noticing swelling in my upper arms. It was a large, hard knot. I could feel heat coming from it. After several visits to several different doctors, a rheumatologist ordered a muscle biopsy which revealed my results.

By then I was having severe pain in both shoulders, wrists, hips, knees, and ankles. I was treated with Prednisone which greatly resolved my pain for a while. I have now had to come off of it due to osteoporosis. I am experiencing extreme fatigue and muscle pain on a daily basis.

I have somehow continued to work but it is becoming increasingly harder to do my job. I am still in the process of being treated and am not sure how long this disease will last. I am only thirty years old and I have three children. I would love to be able to get on with my life. I do not want to give up my career that I have worked so hard for but I am not sure how much longer I can live like this.

I hope this story helps someone else like the ones I read have helped me. Since this seems to be so rare it is a comfort knowing that someone else can relate to what I am going through.

To Contact the Author
Karen H.
Email: Withheld by request
Story edited 11-20-06 JTD
Story posted 11-27-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin
LINKS
Diseases Similar to Scleroderma
Eosinophilic Fasciitis
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
Maria T: Daughter of Deceased Scleroderma Patient (Italy) He, upon looking at my mom's face and hands diagnosed her with sclerodermia, in fact he took care of her until the end...
(Italiano) Maria T: Figlia di una Paziente Defunta di Sclerodemia (Italia) Lui, come vide a mia madre disse "tu hai la sclerodermia", guardandole le mani e la faccia...
(Update) Dee B: Limited Scleroderma/CREST Syndrome (South Africa) There is so much I want to add to my original letter after reading more of other peoples stories. I am certainly not getting better but wish I was...
Tessa: Morphea The nurse just told me that I have morphea and knew nothing about it and she told me to look online for information...
More New Stories: August-November 2009
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Go to Karen M.R.: Diffuse Scleroderma and Fibromyalgia
 
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