There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. I walk for Oliver, my son, who was diagnosed with Cystic Fibrosis at one week old. Life has been a rollercoaster of emotions, doctors appointments, and learning every day about this disease. But this is why we are striving for a cure with all of you!
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind. We are a big CF family.
Oliver is our spunky almost 4 year old, with so much light in his eyes. He never lets CF stop him and takes on this disease with everything in his mighty being!
Please support me!
Together, we can make CF stand for Cure Found. Any and all help matters!
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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.