Hello Family and Friends,
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. Will you join me and support my fundraising goal?
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. Will you join me? Please consider donating to my Great Strides fundraising campaign today!
Team Ryan's Renegades has raised more than $100,000 over the past 19 years and we could not have accomplished this without the tremendous love and support of our family and friends. We hope that you will consider supporting us again this year. If you can't give a monetary donation then perhaps you want to come and walk with us on May 19th in Frederick, Maryland.
To give you an update on Ryan: He is 19 years old and is a sophmore at the University of Maryland, College Park, He is currently using his social media platforms to spread awareness of Cystic Fibrosis, his love of fitness and his growing faith. He has gained quite a following and has inspired many across the world.
Thanks to the work of the CF foundation and to the lifesaving effects of Trikafta he has dared to dream big and go after those dreams.
We are at a pivotal moment in the history of cystic fibrosis and your support matters. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting groundbreaking research and medical progress towards a cure. Please help me reach my fundraising goal!
We are truly thankful for the continued support of Ryan's Renegades.
Alex, Gina and Ryan
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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.