Running for my Husband
Megan Johnson
Fundraising for 2026 Disneyland® Half Marathon
Megan Johnson
This is my second race with the Breathe Team and I'm so excited to get to do this all over again!
I had heard of cystic fibrosis but didn't know a whole lot about it until I met my husband, Levi. He's taught me a lot, but I've also tried to educate myself and learn the best ways to support him in his journey with this disease.
Levi is my whole world, and I can't fathom the day that I won't have him in my life. Unfortunately, with cystic fibrosis it's a very real likelihood I will outlive the love of my life.
I won't delve too much into his personal story, as that is his journey to share. Just know he is doing really well in his current health and quickly approaching 30 years old!
I'm running this event not only for my husband but for everyone who fights cystic fibrosis every day!
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.
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.
I had heard of cystic fibrosis but didn't know a whole lot about it until I met my husband, Levi. He's taught me a lot, but I've also tried to educate myself and learn the best ways to support him in his journey with this disease.
Levi is my whole world, and I can't fathom the day that I won't have him in my life. Unfortunately, with cystic fibrosis it's a very real likelihood I will outlive the love of my life.
I won't delve too much into his personal story, as that is his journey to share. Just know he is doing really well in his current health and quickly approaching 30 years old!
I'm running this event not only for my husband but for everyone who fights cystic fibrosis every day!
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.
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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