Adam Klein

My Great Strides Story

My daughter Lexi is 20 years old fighting CF. 20 years ago her life expectancy was very short. The work of the foundation helps develop treatments that continue to improve the length and quality of life for CF patients. Lexi is one of 10% that don’t qualify for modulator treatments due to her genetic mutation. Please consider making a donation to help improve treatments for Lexi and others.

CF Facts

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.