
Walk with our team to Cure Cystic Fibrosis
Fundraising for Lake Charles Great Strides 2026
McKee's Mission
💙 WELCOME TO MCKEE’S MISSION! 🫁
As parents, our greatest wish is for our children to live long, healthy, happy lives.
Our kids, Landon (16) and Karlee (10), both live with Cystic Fibrosis (CF) — a genetic disease that causes thick, sticky mucus to build up in the lungs and other organs. This can lead to chronic lung infections, difficulty breathing, digestive problems, and permanent lung damage.
Living with CF means daily treatments, medications, breathing treatments, airway clearance, doctor visits, and constant monitoring just to help them stay as healthy as possible. While CF is a lifelong disease, incredible advances in research have changed what the future can look like for many people living with CF.
Today, Landon and Karlee are taking Alyftrek, the newest medication approved for CF. We are incredibly thankful for the research that made this possible and for the hope these treatments give our children. 💙
But there is still no cure, and not everyone with CF can take these life-changing medications. There are still people waiting for treatments that will work for them and families hoping for a breakthrough.
That’s why we continue to fight.
Every donation helps fund research, develop new treatments, support people living with CF, and bring us closer to a cure for everyone.
👕 WANT TO WEAR YOUR SUPPORT?
Our McKee’s Mission T-shirts are available for purchase! Grab yours and help us spread awareness wherever you go. Click the link below to be able to purchase a McKee's Mission T-shirt. McKee's Mission Custom Ink Fundraising.
Whether you donate, purchase a shirt, share our page, or simply help spread awareness, you are helping us move closer to a future without CF.
Thank you for standing with our family and helping us fight for more time, more memories, and more tomorrows. 💙🫁
We won’t stop until there’s a cure!









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