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Theresa C: CREST/Limited Scleroderma
I have been told to stop this kind of work, but it's all I know.

Red Flowers by Sherrill Knaggs, ISN Artist My name is Theresa. I am fifty years old and I was diagnosed with CREST in September of 1996. I had no idea what 'CREST' was until my doctor told me to go home and look it up on the Internet, which I did.

It started with my hands and feet being very sensitive to cold and heat. They turn white with cold and bright red with heat. It's very painful. I also noticed that I was having problems with shortness of breath and acid reflux. I was given inhalers, which I use twice a day, everyday, and medication for acid reflux. The skin around my fingers is often dry, cracks open and take awhile to heal. I also have painful stiff joints in my fingers, hips, arms and knees.

I come home from work and go straight to bed because of the pain. I am a cake decorator and I am really not ready to give up working even though my job causes a great deal of my pain due to the constant squeezing of icing bags and going in and out of the refrigerators. I have been told to stop this kind of work, but it's all I know. I did manage to stay at home for six weeks, but I could not handle thinking about my situation, so I went back to work.

The thing that keeps me going is not the medicine that does not work or being told by my doctors that there are no silver bullets for curing this illness, it's my faith in God. He rules my life and gives me the strength to get up on cold rainy days when I ache and am in pain. He pushes and pulls me through each and every day to encourage others who are worse off than me. On my down days of tears and pain, He gives me rest for my soul and spirit.

I do not know what my outlook is. I only know that I am constantly in pain. Being busy is the only way out. So I work and teach Bible study for children at my church.

Thank you for letting me share my story.

To Contact the Author
Theresa
New email address needed 08-08-06 SLE
Old Email Prefix: theresacollins
Story posted 9-19-02

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Acid Reflux
CREST
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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