Shannon Miller

My Great Strides Story

Hey everyone! Thank you for your continued support over the years in my journey with CF. If you know me at all you know how passionate I am about raising CF awareness and raising money for research. There has been a lot of progress in CF research since I was born in 1980. There is more research to be done because there isn’t a cure yet. 

Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. They are moms, dads, sisters, brothers, daughters, sons, and friends who face the sobering prospect of a shortened lifespan. I walk for them. 

Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.

You can support me!

By supporting my fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history. You can join team Shannonigans too and help fundraise and make a world of difference in the lives of people with CF. 

Thank you so much!!