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Amanda Takes A Breather from CF at Disney

“I was able to Take a Breather because of the Take a Breather Foundation. To be able to get out of my “normal” routine and forget about the troubles of Cystic Fibrosis was an unforgettable experience. My family and I were able to go to Disney where I could make some precious memories with my babies and forget about how sick I always am and the many hospital stays. Without Take A Breather this would not be possible. Many CFers could benefit from this. I know that this opportunity has also given me a new sense of life. I feel very refreshed and ready to tackle CF even harder!” – Amanda