There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. We walk for them. We walk for Ella. Will you join us? All you need to do to become a member of our team is click on the "Join our Team" button. Then come out and walk in the sunshine with us!
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. At 12, Ella was eligable for a ground breaking medication called Trikafta! It has completly changed her life. Trikafta alters the effect Cystic Fibrosis has on the body at a cellular level. It has allowed her to live a more normal and carefree life without having to be weighted down by her endless medications and breathing treatment regimen. It has even enabled her to compete and excel in new types of sports that require more stamina, like wrestling! Without Trikafta, Ella would never have found the love, comradery and confidence that wrestling has brought into her life.
Please help us reach our fundraising goal by donating now!
By becoming a member of team "Team La La" or by making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF like Ella, by supporting the search for a cure. Until it's done!
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families, and this year the walk is just 3 days before Ella's 16th birthday!! So, naturally that means there will be cake!!
We are always looking for new memebrs to join our team! We are a small team fighting the fight against a very strong competitor. Come and be apart of our victory, not only for Ella but for all the Cystic Fibrosis fighters of the world!!
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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.