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.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: