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My Breathe Team Story

Lindsay Stonebraker

Fundraising for Cowtown Marathon

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Lindsay Stonebraker

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.
 
In November 2009 my sister Courtney lost her battle with CF at the age of 26. I miss her smile, her laughter, even her cough, but most importantly I miss her loving spirit and positivity


My sisters and I love to keep her memory alive by continuing to raise money and awareness for the Cystic Fibrosis Foundation just like she asked.  In true Courtney fashion, she ALWAYS put others before herself and if they didn’t find a cure for her there is still hope for others living with the same disease.  Please help me honor Court by contributing to our Cowtown half Marathon Breathe team - Courtney’s Frunners.  Your love and support means the world to us. 💗🫶🏻 

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.

Comments

$425
raised of $1,000 goal
 

Achievements

Leader

Team Courtney's Frunners

$885
$5,000

Recent Donations

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.