Take a Breather Foundation: A Cystic Fibrosis Wish Organization

Meet the Take a Breather Foundation. Their goal is “to allow children living with cystic fibrosis, along with their families, to ‘take a breather’ from CF and focus on creating lasting memories that will stay with them for a lifetime.”

“Our name is actually our mission. We provide a ‘breather’ for these children.”

To learn more about cystic fibrosis, click here: http://bit.ly/1QltnFs

Stay updated on all the latest CF news here: http://bit.ly/1jNDqsz

One comment

  1. Brigid Walker says:

    There is not a day that goes by that I miss Ashleigh. She passed away a and a few weeks before my first child was born. I felt guilty because i did not get to see her on those last days of her life but, I did get to attend her wedding. Her Husband and I worked together. The time i did get to spend with her was the most fun. And, I thank that Lord that she was my friend even though it was only for a few years. I will never forget her smile. We named our Christmas Tree top Angel after her. And, my children know to call the angel Ashleigh.

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