Take a Breather Foundation: A Cystic Fibrosis Wish Organization

0
(0)

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

How useful was this post?

Click on a star to rate it!

Average rating 0 / 5. Vote count: 0

No votes so far! Be the first to rate this post.

As you found this post useful...

Follow us on social media!

We are sorry that this post was not useful for you!

Let us improve this post!

Tell us how we can improve this post?

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.

Leave a Comment

Your email address will not be published. Required fields are marked *