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My Breathe Team Story

Michael Yancey

Fundraising for 2027 runDisney Springtime Surprise

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Michael Yancey


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

Cystic fibrosis isn't just something people live with; it's something they battle every single day. While I get to choose when I lace up my running shoes, they don't get to choose when their next treatment is, when breathing becomes difficult, or what challenges tomorrow may bring.





Why am I running?



I've seen firsthand the impact CF can have on individuals and the people who love them. Friends and family have been affected by this disease, and watching the daily challenges they face has given me a deep appreciation for the strength, resilience, and hope it takes to keep fighting.



Today, though, this race has become even more personal.

I have the privilege of being "Uncle Mikey" to two of the most incredible kids -Dane (10), and Hollis (8).

They both live with cystic fibrosis, but you would never know it by the way they embrace life. Some of my favorite days are the ones I get to spend with them-whether we're building LEGO creations that somehow take over the entire house or squeezing in a workout together (because somehow these two think going to the gym is fun!).


Dane and Hollis inspire me every single day. They show everyone around them that cystic fibrosis doesn't define who they are or what they're capable of. But I also know there are countless treatments, medications, and doctor's appointments behind the scenes that no child should ever have to endure.



Running has taught me that every mile has a purpose. For me, this race is about so much more than crossing a finish line.



Every person born with CF is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road still 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.



I want Dane and Hollis-and every person living with cystic fibrosis-to grow up in a world where "CF" no longer stands for Cystic Fibrosis.



It stands for Cure Found.







Will you help us end cystic fibrosis?



Every donation, no matter the amount, helps fund groundbreaking research, life-changing care, and brings us one step closer to a world where no one has to face cystic fibrosis. Every mile I run is for Dane, Hollis, and everyone still fighting this disease.


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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.