Walk with our team to Cure Cystic Fibrosis

EASTON’S ARMY

Easton was diagnosed with Cystic Fibrosis at birth. He was born with Meconium Ileus, which required a life-saving surgery at 3 days old. So far in Easton's 22 months of life, he has been hospitalized 3 times. In order to stay healthy, he requires multiple treatments each day and several medications, including a minimum of 20 pills per day.

There is currently no cure for cystic fibrosis and too many people with CF die young. I'm walking 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 \u2013 a cure for everyone with CF.