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Breather
- Other
- Narberth, PA
About this business
To fulfill wishes for children who have been touched by Cystic Fibrosis. Our goal is to give these children, along with their families the opportunity to "take a breather" from CF and focus on creating magical memories that will stay with them for a lifetime. Memories that will strengthen their hearts and minds as they battle the psychological, emotional and economic turmoil that accompanies life with Cystic Fibrosis.
Location details
107 Forrest Ave., Suite 105, Narberth, PA, 00007, United States
Get directions| Weekday | Schedule | Status |
|---|---|---|
| Mon | 9:00 a.m. to 6:00 p.m. | |
| Tue | 9:00 a.m. to 6:00 p.m. | |
| Wed | 9:00 a.m. to 6:00 p.m. | |
| Thu | 9:00 a.m. to 6:00 p.m. | |
| Fri | 9:00 a.m. to 6:00 p.m. | |
| Sat | Closed | |
| Sun | Closed |
We would like to take a moment to thank Matt and Molly and family!! We were planning a TAB wish for our son with them and due to an unexpected change in health for our son, what we were planning which was a long weekend to OCMD, would not be able to occur due to the PICC line he was having placed and needing to have for the whole summer. But they worked everything out so he could go the next weekend before he got the PICC line!! We all had a wonderful time.... It was amazing!! Our son Jordan(CF and CFRD) is 17 and his brothe... read more
I would like to thank The Take A Breather Foundation for the AMAZING wish they granted to my sons, Colin and Sean Randles. As most of you may know, the salt water is a natural therapy for those living with CF. We have been blessed to live by the beach and now the boys get to enjoy their own surfboards in the Spring!! They will find peace on the waves and we could not be more grateful for the kindness of TAB!! The boys also get to use their new Apple computer to stay on top of their studies as well as stay connected to others... read more
The Take A Breather Foundation sent my daughter Maddy to see Hamilton on Broadway in NYC. Words can not express how much this trip has meant to her. It lived up to every high expectation and more. It is hard to believe our family received such an amazing experience. Maddy has been in the hospital a lot lately. She was in patient at Children's Hospital of Philadelphia 5 times in the span of 6 months. She is a freshman in high school, in a new school. She has missed over 60 days of school. She was supposed to go on a field tri... read more
Business response:
So glad we were able to fulfill Maddy's Wish to see Hamilton: An American Musical
I wanted to thank all the people who works for and supports Take A Breather Foundation. The trip to Orlando was one that my family will never forget. Makena my daughter who has Cystic Fibrosis was made to feel like royalty. Her special wish to meet Minnie Mouse was the high point of the trip. When Minnie walked into the VIP lounge at Magic Kingdom her heart lit up so much that she cried a little bit which made Mom and Dad do the same. Those of us who have loved ones with CF know the struggles they go through on a daily basis... read more
Business response:
Loved hearing you had such a good time! We are so happy to get to be a part of making her wish come true!
Frequently asked questions about Breather
How is Breather rated?
Breather has a 5 star rating with 80 reviews.
When is Breather open?
Breather is closed now. It will open at 9:00 a.m.
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