My Great Strides Story
Great Strides is NEXT weekend! Please consider donating, buying a t-shirt, or joining us in person at 9:30 am on Saturday, May 4th at Q2 Arena!
Miles loves most things that he does, and loves to say so.
He loves to play hide and seek, and giggle loudly about how no one can see him.
He loves to play with cars, and insists by his next birthday “he will get to drive.”
He loves playing with his little brother and telling him how sweet he is.
Miles also loves to reassure people. He likes to tell his doctors and nurses they are doing a great job while he is being tested. All his mother and I want to do is reassure him (and make him giggle).
Cystic fibrosis has no cure. Advances in treatment have been remarkable, but finishing the job, for everyone, is a lifelong task.
Your support, and reassurance, go a long way.
Check out Miles for Miles 2024 merch: https://www.bonfire.com/store/miles-for-miles/
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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.