Fawn and Auburn are honored to serve on this year’s LOL4CFF committee. After competing in previous years, they decided it was time to pour their hearts into the event and help make an even greater impact.

Join us October 2 at 6:30 PM at The Casey as we come together to laugh and support the cystic fibrosis community.

Auburn has spent 36 years fighting cystic fibrosis. After years of hospital stays and declining lung function, she received a double lung transplant 10 years ago when her lungs were functioning at just 15%.

But a transplant isn’t a cure. Auburn continues to manage the lasting effects of CF, taking more than 30 medications each day, and is now awaiting a kidney transplant.

Thanks to the Cystic Fibrosis Foundation and generous donors like you, Auburn is thriving.

Your support helps fund research, treatments, and resources that give people living with CF more time and more possibilities.

Thank you for helping us make a difference.

With gratitude,
Auburn & Fawn