Please join us in the walk to find a cure for Cystic Fibrosis.
It’s that time of the year again! Update on Cason:: After going over 2 years without an admission, we had a small hiccup where we were unable to get his Trikafta for a little over a month and he declined rapidly and ended up in the hospital. If this wasn’t a sign that this drug is a MIRACLE, then I don’t know what is. He got a quick tune up, and Children’s helped us get assistance for his Trikafta and he is thriving once again. BUT, that doesn't mean we're out of the woods. We will fight until we find a cure! Cason is active in football, baseball, basketball, K-kids at school and is outside playing sports with his friends with any downtime!! I'm so grateful for that.
If you’re are in a place and are able to donate-great. If not, that is totally okay. You can help us just as much with bringing awareness to find a cure AND joining us for the Cystic Fibrosis walk for a cure on May 4th, 2024.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. I walk for them and hope you will support me in my efforts.
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today in honor of #TeamCasonKyle
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. Your gift is 100-percent tax deductible.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.