My Xtreme Hike Story

Why I’m Hiking

I didn’t know what Cystic Fibrosis was, and I’m sure many of you don’t either, until I met the girl who would be my future sister-in-law. Meeting Kelly for the first time I couldn’t have guessed how serious CF was or what craziness was going on side her lungs. All I knew is that Kelly was a fun, happy, always positive, and pretty girl that my brother seemed to like very much. So, when Nate told us that Kelly had a serious disease, my brain wouldn’t believe it. As far as I could see she might have a cough and have some low energy days, but all in all seemed mostly healthy. As the years went on and the CF progressed Kelly’s health started to decline. This was a terrifying time in all of our lives as we had to face the reality that we might lose someone who means so much to my family, as well and many others. Even with the advances in medicine that helped to prolong Kelly’s life (from only the estimated 18 years when she was born) she eventually had to be on Oxygen support 100% of the time and waited for a transplant that didn’t arrive until the ultimate last minute, 3 years after being accepted on to the wait list. I’m so incredibly happy to share that Kelly is living a full and healthy life, breathing deeply with her new lungs!

Cystic fibrosis is a rare, life-shortening, genetic disease found in about 30,000 people in the U.S., which causes persistent lung infections and limits the ability to breathe over time. Those living with this disease are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers – all struggling each day just to breathe and live normal, healthy lives.
Sixty years ago, most children with cystic fibrosis did not live long enough to attend elementary school, but thanks to Foundation-based research and care, many people with CF are now living into their forties – achieving milestones once thought not possible, such as attending college, pursuing careers, and having a family of their own.
While there has been significant progress in treating this disease, there is still no cure and too many lives are cut far too short. By participating in Xtreme Hike, I am helping add tomorrows to the lives of all people living with CF today. Those who participated in this hike and other fundraisers for the CF foundation helped to save my sister’s life, and now it’s time for me to repay the favor.
Please make a difference and support me by giving to my Xtreme Hike fundraising campaign today. Donate an amount that is meaningful to you, anything will help. Thank you!