Welcome to my Great Strides page! The Spencer Striders team is walking for its 18th year and we are excited to be walking in Jacksonville, FL for 2024. As many of you know, John and I formed this team after our daughter, Sophia was born in 2006. She was diagnosed with Cystic Fibrosis shortly after birth and the Sophia's Striders began walking. In 2008, our son Gianni was born and diagnosed with CF. We changed the team's name to Spencer Striders and kept on walking. Sophia and Gianni are doing well thanks to the great care they get at their CF clinic in Jacksonville and the amazing advancements in medicines and therapies developed under the direction of the Cystic Fibrosis Foundation. Every dollar we raise during Great Strides is a step closer to finding a cure for Cystic Fibrosis. Please join me in this fight!
The Spencer Striders will be walking in Jacksonville, FL. If you are local, please join my team and walk with us on May 18, 2024. If you are not local but would still like to support, please donate to the Spencer Striders!
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.
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
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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.