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Gunner Capps

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Gunner Capps

Hi! My name is Gunner Capps, and I'm 22 months old-almost 2, which basically makes me a big deal. I was born with cystic fibrosis, so my start in life came with some extra challenges. I spent 75 days in the NICU (that's like... forever in baby time) and had a few surgeries before I even learned to crawl. These days, I take 30 enzymes a day just so I can chow down like a champ. Life might throw me curveballs, but I throw them right back-with a giggle, a smile, and maybe a little toddler mischief too!

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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$2,773
raised of $2,500 goal
 

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Team Gunner

$3,801
$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.