Emmer Mackillop

My Great Strides Story

Two years ago, a beautiful red-haired girl joined our family. When she was only a few weeks old, it became apparent that she was unwell, but we didn't know what was wrong. After many trips to the pediatrician and a few specialists, she was diagnosed with cystic fibrosis and began receiving treatment from the Dallas Children's Center for Cystic Fibrosis. She's doing well now thanks to some of the treatments developed through past research. I'm so grateful for the people who came before us so that our daughter can have hope and a longer life.

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.