A young lady named
EVA has truly been an inspiration. I stumbled across her blog sometime ago and have been following her ever since. She has CF and has survived one double lung transplant. She has been waiting for a second double lung transplant (her body rejected the first) and it saddens me to say that time is working against her fight. Eva should be a role model for all of us. I try to teach my family to live life and treat each day and our family as a gift. Life is too precious to focus on things that truly don't matter. Don't sweat the small stuff...right?
Eva has just posted a video on her blog and at her young age, she has known how to Live & Love and truly understands what's important in life. Please send some prayers for strength for her and her family. I will be very honest that her video is real and is heartbreaking.
* CF is short for Cystic Fybrosis. I have studied a lot about cystic fybrosis because both of my boys had to be tested for it, Antonio when he was 2 and Shane at 1. Shane had a lot of breathing issues and many of the symptoms that are similiar to CF patients. My friends may remember me talking about it often during the time he had the sweat test and the wait for the results. Through my research I realize the need to find a cure for CF and the importance of spreading the word about the importance and critical need for becoming an organ donor. I thank God that Shane tested negative for CF and that his breathing issues have improved.
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