To provide Wishes for children living with Cystic Fibrosis.


We've started locally in our community, in the greater Philadelphia area, with the Narberth CF Run. The vision of our foundation is to expand our reach to serve children living with cystic fibrosis nationally.


To increase our capacity of fulfilling the wishes of children living with cystic fibrosis we partner with like-minded organizations including Give Kids the World, Something mAAgic Foundation and CFF Accredited Care Centers.


We take steps to ensure that our Wish Program is not only needed, but is also sustainable. The Foundation positions itself to exist for the long term. Partnerships are created with extensive analysis, and we are committed to providing each one until cystic fibrosis stands for Cure Found.


We are governed by a volunteer board of directors, all of whom have a direct connection to Cystic Fibrosis and chaired by Matt McCloskey, 45 and living with Cystic Fibrosis.


The Take A Breather Foundation is a 501(c)(3) tax exempt, non-profit charitable foundation formed in 2012. Our IRS 990 Filings can be found on this page and in our public filing on Guidestar. 

Full Legal Name

Take A Breather Foundation, Inc.

Tax I.D. Number


Frequently Requested Documents

2013 Form 990
2012 Form 990
501(c)(3) Determination Letter

Contact Us

Take A Breather Foundation
355 Lancaster Ave., Suite 200
Haverford, PA 19041

Phone: 610-642-9474
Email: info@takeabreather.net

Public Profile