My Nonprofit Reviews

Cystic Fibrosis is a disease that does not take a break- everyday our sons daughters, siblings, mothers, fathers need to take dozens of pills, inhale meds that take large chunks of time out of their day, do therapies to loosen mucus and help clear their lungs and this is when they are "healthy". Take A Breather Foundation gives moments, experiences that allow the child with Cf and their family to do just that, slow down and take a breather and just enjoy being a family together. TAB sent my 2 sons and their sister and my husband and I to a Flyers game. May not sound like much but believe me - IT WAS! Not only was our family treated like royalty, we were able to just take that Sunday and laugh and enjoy the whole day together. making memories! We were picked up in a limo and had fantastic seats- our boys were on the players bench during warmups , got to sit on the ice during the 3rd period, meet players. It was an amazing day and one we still talk about and will always remember. TAB went above and beyond to make sure our Flyer fanatic boys had an experience they would never forget! Our family can't thank them enough.
The Gregory Family
Bucks County, Pa.