

My Xtreme Hike Story
Jennifer Morris
Jennifer Morris
In 2013 my niece Rylee was diagnosed with Cystic Fibrosis shortly after birth. A few years later, Rylee’s mom and my sister, Johnie was also diagnosed with this horrible disease. Rylee has spent over 100 nights in the hospital. She takes medications daily and never misses a breathing treatment. She is incredibly brave and resilient. I think she gets this from her mom!
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. This August, I will hike over 20 miles through Mt. Hood National Forest in the CFF Xtreme Hike Challenge.
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.
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. This August, I will hike over 20 miles through Mt. Hood National Forest in the CFF Xtreme Hike Challenge.
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