My Breathe Team Page
Kyle Nicholson
Kyle Nicholson
Hey there! My name is Kyle and I'm stoked to be a part of the Breathe Team for the '25 CHI Marathon! My lifelong best friend, Nick, was diagnosed with Cystic Fibrosis as a baby and has been a fighter ever since. Growing up, I didn't quite understand the daily battles and challenges Nick, and every CF warrior faces. That's a testament to how tough CF fighters are and how they carry themselves every single day. Nick is the embodiment of positivity and toughness in the face of adversity as he takes every hurdle in stride. At 36 years old, Nick's CF journey is so inspiring to myself, and everyone he meets.
Nick and I have traveled the world together and started a non-profit music festival (@rocktheranchsc) that gives back to some amazing charities (CFF being one of those!). I had the honor of a lifetime officiating his wedding to his bride, Kendra. Most recently, I've been able to cheer them on as they welcomed their beautiful baby girl into the world in October.
There is currently no cure for Cystic Fibrosis and too many people with CF die young. Nick lives every day to the fullest and I will continue the fight until CF stands for "Cure Found". I’m running to raise money and help change that reality. Nick inspires me daily and I'm here to channel my all into the race for him and all the other CF fighters!
Every person born with cystic fibrosis is on a unique journey and experiences this 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.
Nick and I have traveled the world together and started a non-profit music festival (@rocktheranchsc) that gives back to some amazing charities (CFF being one of those!). I had the honor of a lifetime officiating his wedding to his bride, Kendra. Most recently, I've been able to cheer them on as they welcomed their beautiful baby girl into the world in October.
There is currently no cure for Cystic Fibrosis and too many people with CF die young. Nick lives every day to the fullest and I will continue the fight until CF stands for "Cure Found". I’m running to raise money and help change that reality. Nick inspires me daily and I'm here to channel my all into the race for him and all the other CF fighters!
Every person born with cystic fibrosis is on a unique journey and experiences this 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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