Ryan & Sean

Take a Breather from CF at Disney World

"None of us will ever forget our magical trip to Disney"

 

Take a Breather provided my family and I with the trip of a lifetime which we couldn't have otherwise afforded. In August of 2012, we enjoyed an all expense paid trip to Disney World. Everything was top shelf and we continue to talk about the trip over a year later.

suffer from the effects of Cystic Fibrosis but our whole family is immersed each and every day in fighting this disease. This non-profit provides families like mine with opportunities to focus on something truly pleasurable beyond the world of CF, and they do it with the absolute highest levels of class, compassion and generosity.

The preparation, care and attention to detail that goes into providing CF patients with these gifts is truly a labor of love for this family oriented charity. I simply cannot say enough good things about it!!