Felicia Sisler

Hi, my name is Felicia and above is our son, Cason. 

Cason was 2 weeks old when we had the sweat test done to confirm his blood screening test that infants gets after 24 hours of birth. Many dr appts, medication, and breathing treatments keep Cason healthy. You would never know from his smile, laugh, and fun personality. Cystic fibrosis is what you would call an invisible disease. You never know the fight someone is fighting :)

Some cf information;

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 us!
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.