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My Breathe Team Story

Brittany Dixon

Fundraising for 2026 runDisney Princess Half Marathon Weekend

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Brittany Dixon

There is currently no cure for cystic fibrosis and too many people with CF die young. I’m running 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. 

 

While my family doesn’t have a direct diagnosis of cystic fibrosis, we know firsthand what it means to fight for breath. My nephew was born with a congenital diaphragmatic hernia — a rare, life-threatening condition where the diaphragm doesn’t fully form, allowing organs to move into the chest and severely restrict lung development. From his very first moments, breathing was not something he could take for granted.

Watching your family member struggle for every breath changes you. It gives you a deep respect for families who live every day with chronic lung disease — including those battling cystic fibrosis. While the causes may be different, the fight for oxygen, strength, and normalcy is shared.

That’s why I’m running this Disney race to raise $1,500 for cystic fibrosis research and support. I may not have CF in my family, but I understand what it means to fight for breath — and I run to honor every child and family who faces that fight daily.


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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$240
raised of $1,500 goal
 

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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.