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Rachel received a treadmill from the foundation.
At one point in my life I was a very healthy person. I an active, athletic and determined girl. Up until I was diagnosed I have never been in the hospital for one single thing, except for my birth of course. Suddenly one July morning in 1997, I woke up to very swollen ankles and feet. It was very unusual, my mother took me to the doctor and they referred me to a Nephrologist. The Nephrologist decided to do a biopsy of my kidneys. The biopsy showed that I had FSGS, (at the age of 17). Immediately I was started on high doses of prednisone. As a 17 year old girl, this was very difficult for me. I was told that I would have 5 to 10 years before I would need a kidney transplant. Four years later at the age of 21 I lost my kidney function. I went on hemo dialysis for about three months. Fortunately, my aunt was tested for kidney donation and matched. I received a transplant on October 31, 2001. I was very lucky to have received a kidney so fast. However, this was not the last of my problems. My disease returned to the transplanted kidney. They once again told me that my new kidney will last 5 to 10 years, depending on how aggressive the disease attacks the new kidney. Almost 6 years later I received the news from my doctor, my kidney was failing. It was functioning at 20% and was going to decrease rapidly. In June of 2007 at the age of 27 I began peritoneal dialysis. I have been on dialysis ever since and have had no luck so far with finding a kidney. I have been placed on a couple of different transplant lists and I now play the waiting game.
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