I am being honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding professionals in Austin. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of curing cystic fibrosis (CF) and providing all people with CF the opportunity to lead long, fulfilling lives.

How did I get involved? Miles Falck! This incredible kid was diagnosed with CF when he was a baby, and I can't imagine a world where he doesn't grow up to be Spiderman, a garbage truck operator, firefighter, dog trainer, or whatever he decides he loves next. Don't worry, leading up to the event, I will share all of my favorite photos of this guy to brighten your day, including the one below (don't worry, the axe isn't real!)



Please help me meet my fundraising goal by making a donation. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.

More info about CF:
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!