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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.
107 Forrest Ave., Suite 105, Narberth, PA, 00007, United States
Get directionsWeekday | 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 |
Dear Matthew and the entire Take a Breather Foundation crew, Please accept our most sincere and exuberant thanks for our vacation on Lake Winnipesaukee. Your care, dedication and organization laid the groundwork for the best family vacation ever. It was a week filled with fun, excitement, challenges, and even a little education. Our cabin was excellent, the water perfect, and our fellow resort residents were warm and welcoming. Tommy experienced many firsts on this trip, including zip lining, climbing to the top of a fire to... read more
Take a Breather is an amazing foundation started by a family directly affected with this disease. They are a family much like everyone with CF is a family.. surrounded by love and a helping hand. Their care made CF like a bit easier for my daughter Sierra and making her wish come true!! Thank you so much to TAB!!!
The Take A Breather Foundation is a great organization! They sent me a MacBook Pro for school which was much needed. They we're super nice and helpful!! I definitely recommend them to anyone suffering from CF who may need a little escape from the realities of it. Not many CFers are granted wishes and TAB gives those a chance to receive something that they most certainly deserve. TAB is FABULOUS! =)
THERE ARE NO WORDS that could do justice for what this foundation has provided for our family. For years it's been my 8 year old daughter with CFs dream to go to Disney so she could meet the Disney princesses. Thanks to Take A Breather, our family of 5 was given the opportunity to make her wish come true. Our week in FL was more than we ever could have dreamed of, more than my husband and I could have ever done on our own. Our memories from this MAGICAL respite vacation will last forever. From the bottom of my heart, THANK Y... read more
You all have a great doundation i have a neice and nephew with cf my neice is twelve and just had a double lung transplant in ky she was only 11 the youngeat in ky to have one qith out that she wouldnt be here today
First off I would like to thank from the bottom of my heart The Take a Breather Foundation for giving my daughter Itzely(wish child) and our family the chance to spend a wonderful week in Florida...We visited Disney World,Sea World,and Universal Studios.This was such an amazing gesture and seeing how happy my daughter was is just amazing..You guys gave her something to look forward to..Thank you very much for the wonderful vacation you guys gave us..and for making her wish come true.
My daughter abigail is 10 years old. We would like to say thanks to Matt n Molly n family for making my daughter Abigail's wish come true.we just returned on Sunday from a week at Disney and can not be more greatful after the year we had. All the magical memories even tears it was so amazing n cannot thank yous enough.on behalf of the herrejon family and others we would like to say how much we love and appreciate everything you've done for our family n others with cystic fibrosis we love you for it .may God bless you all tha... read more
Breather has a 5 star rating with 80 reviews.
Breather is closed now. It will open at 9:00 a.m.
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