Our daughter, Marley Kaye (MK), lives with cystic fibrosis (CF). MK’s CF journey began on June 26, 2025. Five days after she was born, her pediatrician called us to share the results of the genetic testing she received in the hospital at 24 hours old. Michael and I did not know we were carriers—we had never even heard of CF. Now, CF is our world. We want to work toward finding a cure and educating others about CF. We also want to celebrate MK’s bravery through every part of her CF journey. 

The CF Foundation’s mission is to cure CF and provide individuals with CF the opportunity to live long, fulfilling lives. The CF Foundation funds research and drug development, partners with the CF community, and advances high-quality, specialized care.

The CF Foundation hosts the “Walk to End CF” to bring awareness to and raise funds for its mission. Michael and I are so grateful that every dollar raised during this fundraiser will benefit MK and all other individuals with CF. Please feel free to view more information below and use this webpage to learn more about the CF Foundation, ways to donate, and how to join us for the walk on May 2.

We appreciate everyone supporting our team,“Marching for Marley Kaye” 🤍

-Michael and Hannah Land