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Keith H: Eosinophilic Fasciitis
It took several tests and blood work
and several specialists to determine the problem.

Yellow Tiger Moth Airplane by Sherrill Knaggs, ISN Artist I recently discovered that I have a rare skin disease called eosinophilic fasciitis (EF), a skin and muscle disease which causes tightness of the skin, and sometimes a reddish coloration of the skin in areas. It can also cause symptoms of rheumatoid arthritis, which is what I have.

I'm forty-one years old, and my symptoms started right before Christmas of last year. It took a few rounds of tests and blood work and several specialists to determine the problem.

I had extremely high white blood cells (eosinophilic) and the doctors could not figure out why, until a red spot showed up on my leg. They took a biopsy of that spot, and that is when they diagnosed eosinophilic fasciitis (EF). I also have swelling in my lower legs and in my hands with extreme tightness in the joints. I have been taking prednisone for the pain and swelling and it has helped a great deal.

I have been on short term disability. I am getting ready to take another drug methotrexate and vitamins. They will keep me under observation with blood work and regular visits and who knows what else.

I will be going into physical therapy. My hands are still a big problem, with lots of tightness, and in my knees and ankles as well. It looks like there is no cure, but only treatment. With a little luck, it will go into remission.

Thanks for letting me post my message. I hope this helps.

To Contact the Author
Keith H.
Email: ziggy_40@msn.com
Story edited 03-30-05
Story posted 03-30-05 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Eosinophilic Fascitis
Diseases Similar to Scleroderma
Rheumatoid Arthritis
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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