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My Breathe Team Story

Jonathan Shea

Fundraising for BMW Berlin Marathon 2026

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Jonathan Shea

My name is Jonathan Shea and for the past three years, I have had the privilege of being part of the Cystic Fibrosis Foundation family, most recently having run the 2025 Boston Marathon with the team.

This year, I am running the 2026 Berlin Marathon alongside my brother Ken, and our four friends Trevor, Carter, Braydon, and Jude, all proud Boston College High School graduates and Eagles. 

Together, we are combining our efforts to fight Cystic Fibrosis and raise awareness about this life-altering disease. The CFF is an extraordinary organization and I could not be more honored to be representing them again as part of the "Breathe Team."

Thank you to everyone, in advance, who helps us support this incredible cause. 

- Jon

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There is currently no cure for cystic fibrosis and too many people with CF die young. 

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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$150
raised of $4,000 goal
 

Achievements

Member of

Team Eagles in Berlin

$575
$24,000

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.