It’s heartwarming to hear about the incredible experience Matt J. and his wife Erin had during their hockey breather from cystic fibrosis, especially as Philadelphia Flyers fans. The VIP treatment, including a road trip to Pittsburgh and rink-side seats, added a special touch to their adventure.
Starting with an exciting away game and culminating in a home game with VIP access, Matt and Erin were able to immerse themselves in the thrilling world of hockey, creating memories that will undoubtedly last a lifetime. We are thrilled to have provided Matt, a devoted Flyers superfan, with an opportunity to enjoy the game he loves while spending quality time with his family.
The road trip to Pittsburgh added an extra layer of enjoyment, allowing them to explore the city before cheering on their team to victory. A few days later, the experience of sitting rink-side during the game in Philadelphia surely added to the excitement and made the entire event even more memorable.
A special thank you to Erin for sharing your kind words. We are honored to have played a part in creating this unforgettable experience for Matt, and we hope it provided a well-deserved breather from the challenges of cystic fibrosis. Here’s to many more victorious moments for Matt and his family!
“I wanted to reach out to say how thankful I am for the generous gift you gave my husband, Matt, and in turn, me as well. You granted his wish in far more ways than we ever imagined, and I could not be more grateful. We had such a wonderful time in Pittsburgh and at both hockey games, which were only made more perfect since our boys in orange and black were winners.
Matt was the happiest I have seen in a long time, and his excitement and energy could be felt the entire long weekend and even in the days leading up to our trip.
I cannot stress how much fun we had, and all because of you! The generosity of this Foundation is truly amazing, and I have listened to Matt rave about it, especially Molly. It means so much to me to know that there is an organization which aims to help those suffering from CF. In a world where many do not know or understand what CF is, it is comforting to have people on our team.
If there is anything I can do to help the Foundation in the future, please don’t hesitate to let me know. Again, I cannot say how much this meant to us. Some time away where we could just relax, enjoy life and take a breath was exactly what we needed! I hope vou all enioy the holidavs and I wish vou all the best :)”
Erin J.
