My Xtreme Hike Story

Pacific NW + Hiking + CF = Why I Hike

I was born and raised in Washington State. My heart is in Oregon (also where I got married). I love hiking (usually with my doggo). And ever since our younger sister, Lisa, was diagnosed with cystic fibrosis (CF)*, it has been our family mission to fight and fundraise until CF stands for Cure Found. CF is a genetic disease affecting multiple organs that Lisa has been fighting her whole life. We are grateful that Lisa has been able to live a relatively healthy life due in no small part to the incredible advancements in CF research and treatments over the past decades. In 2018 she earned her Master’s degree, in 2022 she got married, and in 2023 she welcomed a baby boy. We are overjoyed. 

And yet, we won’t rest until it’s done; until CF stands for Cure Found. Our family team, Amsler's Army, fundraises every year and this year we are prioritizing our efforts through the Cystic Fibrosis XTREME HIKE event. My brother, Mitchell, my husband, Scott, and I will be hiking a challenging 20+ mile trail through Mt. Hood (outside of Portland, OR). By the end of the hiking day on AUGUST 10th, we hope to be physically exhausted, but heart-filled and hopeful, and $7500 (our team goal) closer to a cure. 

I wanted to share this cool thing we are doing so you can send us some good energy vibes! If you are interested in donating, here are some things that might help to know:

• ​Any amount at any time is so appreciated. Click on any of us to donate.
• 100% of your donation is tax deductible. 
• The CF Foundation https://www.cff.org/ puts 90% of every dollar raised directly towards CF research, life saving treatments, and a cure.

Please spread the word and feel free to reach out if you have any questions! Thank you for your support!

Love, Kelly, Scott and Mitchell

*There is currently no cure for cystic fibrosis. By participating in Xtreme Hike, we are helping to end this disease for thousands of people impacted by CF.

Cystic fibrosis affects the lungs, pancreas, and other organs. The symptoms can vary from person to person, and as people with CF live longer than ever before, their disease can become more complicated, leading to serious health issues. 

The Cystic Fibrosis Foundation has made extraordinary progress — including fostering the development of more than a dozen CF treatments — but these treatments are not a cure and not everyone can benefit from them. We must keep going.

Your support makes a difference.

By donating to our fundraising goal, you will help advance our mission for a cure for all. Please consider joining us and helping make CF stand for Cure Found.