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Miles for Breath

Kristina Lamarre

Fundraising for BMW Berlin Marathon 2026

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Kristina Lamarre

Hi Everyone,
This fall, I’ll be running the Berlin Marathon through one of the most iconic, global cities in the world. I’m proud to be running in support of the Cystic Fibrosis Foundation and the thousands of children and adults fighting CF each day. Currently, there isn’t a cure for CF, but treatments have improved dramatically and life expectancy has steadily increased since the 1950s.
Cystic fibrosis remains a life-shortening, progressive disease that primarily affects the lungs and digestive system. Daily treatment is complex, time-consuming (treatment takes 2-3 hours daily), and physically demanding. Beyond the physical toll, individuals with CF experience depression and anxiety at rates 2 to 3x higher than the general population. The constant treatment burden, fear of infection, and uncertainty about the future weigh heavily on patients.

Here in Boston, we are fortunate to have two of the oldest and most respected institutions serving patients with CF: Boston Children's Hospital and Brigham and Women's Hospital. These hospitals provide comprehensive clinical care, access to cutting-edge therapies, and clinical trials that are advancing treatment and bringing hope to families locally and around the world.

The Cystic Fibrosis Foundation funds groundbreaking research, supports a national network of accredited care centers, provides patient support services, and advocates for access to high-quality care and therapies. Because of this work, people with CF are living longer than ever; however there is still so much to do. 

Every mile I train is for stronger lungs, living longer lives, and continued progress toward a cure. If you are able to give,  I would be so grateful. Together, we can make a meaningful impact. 
I'm very excited to be running my second Abbott World Marathon Major run in support of CF and chasing my second star!
💙🏃🏾‍♀️🌟🌟

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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$100
raised of $4,000 goal
 

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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.