GAZELLE WEST Vol. 1, Issue 2 | Page 28

HEALTH & WELLNESS KELLY’S STORY THE IN-BETWEEN SPACE By VIRGINIA KERR When I first met Kelly Ellison, I was in the public restroom at KMOVTV in St. Louis where I worked as a TV host, getting ready for the station’s weekday program, Great Day St. Louis. She walked in with an amazing smile and an even better energy. I didn’t notice there was anything “wrong” at first. I asked why she was there. She said, “To talk about scleroderma.” 28 Oh right. I was on that segment. I had to look at my notes 10 times just to remember how to say that word. Scleroderma. It makes me feel better now when I hear Kelly tell her story, and she says, “At first, I couldn’t even say scleroderma much less explain what it was.” That was in 2007, when she finally received the correct diagnosis. A well-established team leader at Edward Jones at the time, she was going from doctor to doctor for all kinds of symptoms. Digestive issues, itching, swollen hands and feet, weight loss, fatigue...the one symptom she forgot to tell them about was cold hands and feet. That symptom combined with the others might have helped them figure it out sooner. When she finally got the answer, she was still not sure what she had. She can now explain that it is an over production of collagen that causes the skin and connective tissue to harden and build up around the lungs, digestive system and even the heart. It can kill you. GAZELLE WEST There are different levels, and Kelly has the worst kind. The kind that usually takes your life within five to 10 years. Her symptoms started 10 years ago. In the bathroom that day I wasn’t aware of her prognosis. I just knew I wanted to be around her. She had a light. A joy that you could tell she wanted to share. Somehow, in that two-minute exchange she revealed she was a Christian and she knew God was using her to help other people who have scleroderma or know someone who does. She was there to tell the world – well…the Great Day audience... she had started The Relief Foundation to help those affected by scleroderma. We became friends on Facebook, and I watched her post pictures and videos of how she found clever ways to overcome challenges. We met to catch up and celebrate her 44th birthday. She’s sporting a new hairdo. She had to cut her hair very short because she could no longer brush and curl it. The skin on her hands became so tight it hardened her fingers. They curl under, and she can’t move them. The pigment of her skin is fading in spots. She pulls back her sleeve and lets me feel her arm. It’s smooth like a stone.