My Great Strides Story
My great niece lives with Cystic Fibrosis. Please join us in helping find a cure. Team ”Little Line’s Leprechaun Lungs” will be participating in the Great Strides Walk for Cystic Fibrosis on Saturday June 3, 2023. Please join us.
Here is a note from Adeline's Mom & Dad, “As a parent, one of the hardest things to hear is that your child has an incurable disease and that that disease might take your child away from you. As Adaline's parents, we can't stand for this. We walk for a cure, raise awareness for a cure, raise funds for a cure. There is nothing that can or will stop us from doing everything we can to protect and provide the fullest, happiest, healthiest life for our daughter. Please join us. Let Adaline know how loved and supported she is by not only her parents, but by you too!”
Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. They are moms, dads, sisters, brothers, daughters, sons, and friends who face the sobering prospect of a shortened lifespan. I walk for them.
Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
You can support me!
Please help me make "CF" stand for cure found by joining my team and donating today! Every little bit helps individuals like me live healthier, happier, and fuller lives. Thank you!!!
By supporting my fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
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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:
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