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My Breathe Team Story

Jill Mccormack
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Jill McCormack

My beautiful daughter Paige was diagnosed with Cystic Fibrosis (CF) at just two weeks old. As the mother of a healthy three-year-old, the diagnosis was a complete shock, as my husband and I had no known history of CF. Over the past year, we've adapted to a new routine of treatments, medications, and vigilant hygiene. We became CF experts overnight and have worked closely with our clinic to ensure Paige receives the best care possible. Paige is thriving on Trikafta and does vest treatments twice daily. She is our strong, brave, and happy little fighter! 

I'm running the Marine Corps Marathon in honor of Paige. If you would like to donate to support my running journey, please donate below. As a parent, I will not stop fundraising and fighting for my daughter until there is a cure. 

 

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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raised of $1,000 goal
 

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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.