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My Great Strides Story

Kay Church

Fundraising for Oklahoma City Great Strides 2026

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Kay Church

Ten years ago, when Dylan was just four weeks old, we heard the words “cystic fibrosis.” In that moment, our world shifted. We didn’t know exactly what the journey ahead would look like — only that it would require courage, resilience, and more strength than we thought possible.

Today, Dylan is 10 years old. She is brave. She is strong. She is full of joy and determination. And every single day, she shows us what it means to fight with heart.

Team Dylan walks to raise awareness, support life-changing research, and push closer to a cure for cystic fibrosis. We walk for the treatments that help her thrive today — and for the breakthroughs that will give her an even brighter tomorrow.

We would be honored to have you join us. Donate if you’re able. Order a shirt and wear it proudly. Come walk beside us.

Because every step we take together is a step toward hope. There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality.

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.  

Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.

Will you help us end cystic fibrosis?

By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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$0
raised of $350 goal
 

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Team Dylan

$15
$3,500

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Attendance Policy

The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.