Today, Ashley begins her fourth month with a mystery cough. We have seen an allergist who found Ashley very interesting but couldn't find a thing wrong with her. We did find that she doesn't have any allergies yet nor does she have asthma. Then a week later an Ear Nose and Throat Specialists examined Ashley. Again, couldn't find a thing wrong with her but prescribed a steriod inhaler because we had tried everything that we could available over-the-counter. We did learn that Ashley's hearing is perfect, which is great because now she has no excuse for ignoring me. And because I am deaf in my left ear; I have an excuse for ignoring her. So what's wrong with Ashley...now that's a mystery still needing to be solved. Just this week I took Ashley to the pediatrician again because Ashley is now complaining of a headache. I am getting calls at work from the school just about once a day because Ashley is in the clinic complaining about not feeling well. But when I ask As...
Ashley has biliary atresia, a chronic life threatening liver disease. Her disease has no cure, and her only hope for a long life is a transplant. We are trying to raise money for her liver transplant and other medical needs. Because her disease is unpredictable, her medical needs are unpredictable. It is because of this and the fact that we are unable to get life insurance for Ashley that we ask for donations. If you feel it in your heart to donate to Ashley's fund, we will be grateful.