In 2008 a beautiful little girl who had recently come into my life was diagnosed with Cystic Fibrosis. She is the daughter of my husband’s childhood friend and someone we have both watched grow up. This diagnosis and her and her family’s reaction to it have impacted my life in ways I never knew it would. I’m not even sure they realize how they have impacted me! As I learn more about the disease and try to contribute to their cause whenever possible, I find myself very aware of how precious life is. Below are the links to the Breathe for Olivia website and Facebook page. Please take a look and keep her and all those out there fighting for a cure and a cause close to your heart!
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