My Nonprofit Reviews

My name is Shana and I was diagnosed with Cystic Fibrosis when I was a baby, so I’ve never known life without CF. Several months ago at my CF clinic, my social worker told me about this amazing organization, the Take a Breather Foundation, and how they were going to give me a “breather” from CF whatever it may be. Well the child in me who had never been choose to go to Disney World for the first time.

A couple of weeks ago, my boyfriend and I went on our trip and I couldn’t have asked for a more amazing trip. Take a Breather did an AMAZING job organizing everything. They were also in great communication with me up until the day of the trip to assure I had everything I needed. Even when we were a month out and it turned out I was going to need assistance of wheelchair at the airports and when traveling around the parks they were so incredible in making sure I had everything I needed.

From all the transportation, the hotel, meal plan, to our hopper tickets for the parks, truly everything they organized was perfect. They really live up to giving people with CF a “breather” from everyday life. I will forever be grateful to them. Highly recommended Take a Breather and all that they do.