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My Great Strides Story

Brenna Kehoe

Fundraising for Boston Great Strides 2026

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Brenna Kehoe

Hi there! I’m raising money for the Cystic Fibrosis Foundation to support the incredible work this foundation is doing to support people like myself who live with this disease. There is currently no cure for cystic fibrosis and too many people with CF die young. For the third year I'm so proud to share that my team will be participating in the Boston Great Strides walk.

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 disease differently. Significant progress has been made - many of us have access to life changing treatments and medical care (shoutout to the Boston doctors and researchers). However a long road still lies ahead for far too many people fighting this terrible disease. There’s a sizable population that does not have access to modulators and other care needed to maintain a healthy life with this disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.

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. Any donation is greatly appreciated and extremely impactful. 

If you’re still reading, gold star for you. I appreciate you more than you know. Please donate and share this event far & wide! We don’t stop until CF stands for Cure Found. 

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$565
raised of $1,500 goal
 

Achievements

Leader

Team Brenna

$565
$3,500

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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.