I'm honored to share that I’ve been selected by the Cystic Fibrosis Foundation to be recognized at a special event celebrating professionals making a difference in our community. As part of this recognition, I’ve committed to raising funds to support the Foundation’s mission: finding a cure for cystic fibrosis (CF) and helping everyone with CF live long, full lives.
 

I’d love your support in helping me reach my fundraising goal. Your donation—big or small—has the power to move us closer to ending this disease for good. It’s a real chance to be part of something historic.
 

CF is a progressive, genetic disease that impacts about 40,000 people in the U.S., affecting the lungs, pancreas, and other organs. Not long ago, kids with CF often didn’t live long enough to start school. Thanks to incredible progress driven by the CF Foundation, the median life expectancy is now over 50. Still, there’s more work to do—many people with CF don’t benefit from current treatments, and we won’t stop until everyone has a path to a cure.
 

Cystic fibrosis (CF) is a genetic disease that affects about 40,000 people in the U.S., impacting the lungs and other organs. Just 60 years ago, most children with CF didn’t live to attend elementary school. Today, thanks to research and care supported by the CF Foundation, the median life expectancy is over 50. While major progress has been made, not everyone benefits from current treatments. The Foundation’s mission is clear: to find a cure for every person with CF and ensure no one is left behind.


To learn more or donate, visit www.cff.org. Thank you so much for donating and  helping support being this great cause with me.