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Take A Breather Foundation fulfills wishes for children living with Cystic Fibrosis.
Take A Breather Foundation fulfills wishes for children battling cystic fibrosis (CF). Our goal is to give these children, along with their families, the opportunity to "take a breather" from CF and focus on creating magical memories that will stay with them for a lifetime. Memories that will strengthen their hearts and minds as they battle the psychological, emotional and economic turmoil that accompanies life with Cystic Fibrosis.
Cystic fibrosis is a hereditary disease that destroys the lungs, pancreas and other organs. Children spend long amounts of time in the hospital where they receive IV antibiotics to fight off life threatening lung infections. There is no cure and the average life expectancy is late 30's.
- Matt McCloskey
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