It's that time of year an I'm back for my 7th SEASON, helping make CF stand for Cure Found! As Co-Chair for Team Jase, I couldn't be more excited to see another amazing gala come together, where over $250,000 annually is raised for Cystic Fibrosis.

By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Since first becoming involved in 2017.The life expectancy for the CF kids I've come to know, honor and love has increased by literal decades. They can now plan for college, families of their own, careers and making their dreams come true. Please consider joining us and help make medical history.

Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. 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.

To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!