This is my niece’s family and her son Elijah has Cystic Fibrosis!
I’m asking for help to help make his life easier.
Currently asking for donations for his team for our GREAT STRIDES 5K! As a princess performer my niece, Elijah’s mom donated hours of here time each year at walks like these. They bring together an amazing community and are such a positive event for the little ones fighting each day.
If you wish to donate, it’s tax deductible and your dollars will go to helping us find treatments and eventually a cure for Elijah along with thousands of others.
Please help my son live his best life possible. You can help by:
Joining our team (virtually)
Donating if you can (any amount helps)
Sharing my post
Thank you so much in advance!
Please feel free to message me or comment if you have any questions
My Great Strides Story
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!
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 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.