
Over eleven years ago a beautiful daughter entered my 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 far, Ella has amazed us all. She continues to grow everyday and is considerably healthy on a constant basis. Though Ella needs enzymes for every meal, we are constantly greatful for how healthy Ella has been and can only benefit from this in the future.
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.
Thank you and See you Soon!
Will you join us?
Great Strides is a fun event that provides a fantastic opportunity for family, friends, students, and colleagues to come together to make a difference in the lives of people with CF.
To participate, just click on the "Join our Team" button. From there, you can make a donation and start fundraising.
By joining our Great Strides team and making a donation, you will be part of a tenacious and passionate group of people committed to ending this disease. Together, let’s make CF stand for Cure Found!
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
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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.