There is currently no cure for cystic fibrosis, and far too many people with CF still die young. I’m walking with our Great Strides team, Miles for Myles, to help change that reality.

Myles was diagnosed with cystic fibrosis when he was just 3 weeks old. Today, he is 17 years old, a junior in high school, and living an active, healthy life. He plays lacrosse for his high school team and even runs his own grass-cutting service in our neighborhood.

Myles is able to enjoy these moments because of the life-saving medicines and treatments made possible through years of research, science, and generous support for the Cystic Fibrosis Foundation.

CF is a genetic, life-shortening disease that affects the lungs, pancreas, and other vital organs. It can make breathing difficult, increase the risk of life-threatening infections, and lead to serious lung damage. While incredible progress has been made, there is still a long road ahead for many people living with CF.

Every person with cystic fibrosis has a unique journey. Our dream is that everyone with CF has the chance to live a long, healthy life — and ultimately, that we find a cure.

Will you help us support that mission?

By donating to our Miles for Myles Great Strides team, you are helping advance the research and science needed to move us closer to a cure for everyone with cystic fibrosis. Every donation, no matter the size, makes a difference.

Thank you for supporting Myles, our family, and everyone fighting CF.