Over twelve years ago my beautiful daughter entered the world, and it was love at first sight. We knew that Ella was going to be born with Cystic Fibrosis due to each of us going through genetic screening and eventually having an amnio done to get the full result. If anyone actually knows the type of man that I am, I am a person who thrives on obtaining information and gaining knowledge. Utilizing these skills to pursue my passion in medicine. I am the kind of man and father who will do anything possible to obtain any and all information needed to ensure my daughter gets the best possible health care available as well as learning and using the best possible preventative measures to allow my daughter to live a happy and healthy life.
So come on out and meet this beautiful bundle of joy. You may be asked to sing lyrics from the hit movie Frozen, Moana or dance like a crazy person, but everyone will be having a great time. Ella and I are truly thankful for everyones support over the past several years and I hope you can join in on a little piece of Ella's joyful and sassy attitude.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.