I am walking for my son, Colton and raising money for the Cystic Fibrosis Foundation.
Colton is such a loving boy with a huge heart! He loves to joke and make himself and those around him laugh. He has really changed my outlook on life and continues to remind me not to take it or the little things for granted.
This foundation has helped Colton and our family so much that it only feels right to continue to give back to them!
They have done so much to improve treatments and the lives of all those living with CF. They truly are doing AMAZING things!
We cant wait to start the new drug this year that although is not a cure, it is the closest thing to it right now! And your donations made it possible!!!
Please join us if you can on May 6th! Sign up with our team Coltons CF Fighters. We would love to see anyone who can make it out!
If you are able to donate- please know how appreciative we are for any amount, big or small! A little goes a long way to help this AMAZING charity continue to come closer to a cure for CF!
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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.