Courtney Mackey

Hello everyone,

We are excited to begin our fundraising journey for Cystic Fibrosis again this year!

We continue our team Walking for Aluna! This team was created for my beautiful daughter Aluna who has Cystic Fibrosis. Please join our team and walk for awareness and a cure! We also ask for donations that will go to the CF Foundation!

This year we had increased challenges with Alunas health, with her first hospital stay other than her NICU stay. Multiple sicknesses and increased treatments! However, like always our little warrior showed her resilience, strength, and determination to push through the challenges! 

We would like to thank all the nurses, doctors, specialists, LNAs, volunteers, and every other amazing person that cares for our CF warriors and others in need! We appreciate you all! 

We also want to thank the CF foundation and hope to continue to raise money in hopes of continued research that will lead to a cure! Please help us support the CF Foundation, our incredible girl, and all CF warriors. 

Here’s some information from the CF foundation to help others better understand CF!

There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?

Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.  

Please support me!

We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!