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My Great Strides Story

Caleb Curran
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Caleb Curran

My name is Caleb and I am 4 years old. I was diagnosed with CF when I was just a few months old. My mommy and Uncle Matt also have CF. I’ve had a tough past year with 10 admissions in 2024 but am hoping for a better year this year. Hopefully my new medications help to keep me healthy. These medications wouldn’t be possible without the fundraising done by everyone. 

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.

Comments

$150
raised of $100 goal
 

Achievements

Leader

Team Caleb’s Crazy Crew

$150
$1,500

Recent Donations

Attendance Policy

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.