Eileen


Hi everyone, my name is Eileen and I am 30 years old. I was diagnosed with Scleroderma about a year and a half ago. I also have Raynauds phenom. Now as I think back, I started to have symptoms around the age of 26. My hands and feet used to swell up and I couldn't close my hands to make a fist anymore. I didn't really think anything of it so I let it go and kept putting off going to the doctor until Chirstmas of 2000. A cousin of mine, who works in a hospital, had noticed my hands and asked me what was wrong with them. I told her I didn't know so she made me make an appointment with my family doctor. I went to see my family doctor and they didn't know exactly what was wrong with me. They took blood test after blood test and finally referred me to a Rhuematoligist. My Rhuematoligist asked me about what kind of symptoms I had had and took one look at my hands and arms and told me that I had Scleroderma. That was Februaury of 2001. So far it hasn't been too painful, but it is progressing fast. At first it was only affecting my hands (curling of the fingers) and my arms (tightening of the skin), but about 4 months ago I had a CT scan done and now it's affecting my lungs. I also have problems with my flexibility. I'm currently taking predisone and darvacet for the pain, protonix for the heart burn and now with the lung disease they have put me on cytoxan. I'm not in too much pain, but without the medications I feel as if I can't get out of bed sometimes. The littlest things that I used to be able to do, like picking something up off of the ground are now a real challenge. Some times even putting on my socks takes a lot of work.
My Rhuematoligist tells me how impressed he is with my positive out look on the whole thing. I tell him it's because I believe that God only gives you what he thinks you can handle and I have the support of my family and friends. I also figure that since I'm not feeling too bad that I can still lead a normal life right now. If anyone would like to talk about this disease, please feel free to leave me an email. In the subject line put "Scleroderma" so that way I won't delete it. Thank you for taking the time to read my story and I would like to hear from anyone else out there with this disease so I could learn more about it.

Thanks again,
Eileen =0)  leen1212@aol.com

 
  

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