Team Ollie strong not only walks for others battling Cystic Fibrosis but specifically we walk for Oliver, our laughing little boy. Oliver will be three in May and he was diagnosed with Cystic Fibrosis at one week old. Oliver had his first hospital stay at almost one year old from this harsh life altering disease. He is our litter fighter and we will walk circles around the world to help find a cure for him and so many others. Olivers smile is contagious and he brings such a light and happiness to our life.
We want to help make it possible for Oliver and so many others to live a long, amazing life full of laughter, love, and adventure. Every step towards a cure is just what we need!
Want to join our team? Walk with us? Donate to the cause? Click the link below and you can do any of those!
Team Ollie Strong is so grateful for the support.
We are forever grateful for the support and hard work from the Cystic Fibrosis Foundation, and this is our chance to give back to them.
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.