Sary Chea
Hello,
I have decided to join the Breathe Team in dedication to my little hero Beckett.
He is strong, resilient, silly and has such a kind soul. He has gone through so much for only being 8 years old. Chad and I try to look at the bigger picture when times get tough, but as a parent, we can't help but to stress and overthink. Beckett always finds the silver lining in every situation and aways finds a way to help us see life through his eyes. He is wise beyond his years. He doesn't complain about having to do his daily breathing treatments or about taking his medications. He understands this is part of this daily routine. But we hope in the future that one day, his "norm" and others living with this genetic disorder would be able to live freely without having to do their daily routine just to get through the day and maintain.
The Cystic Fibrosis Foundation has help aided so much with the research and advances in medication. We hope one day CF could stand for Cure Found.
But all of it would not have been possible without your support and dedication.
Thank you in advance for your support and participation to this event, you are helping to make a difference for people living with CF!
Love - Sary
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