Walk with our team to Cure Cystic Fibrosis

TeamJax
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TeamJax

My almost 8 year old Grandson Jaxson was diagnosed with Cystic Fibrosis as a newborn. Since then he has had 10 hospital stays at C.S. Mott Children's Hospital in Ann Arbor. Each hospital stay lasts 14 days. As his Grandma, I would love to see continued medical advancements for my little guy, and one day a cure for all who suffer from CF. While many incredible advancements have been made, the goal is for CF to stand for Cure Found. Thank you in advance for your donation!!

There is currently no cure for cystic fibrosis and too many people with CF die young. I'm walking to help change that reality.
CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.
Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Will you help us end cystic fibrosis?
By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.