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My Breathe Team Story

Lindsey Leonette

Fundraising for Disneyland® Halloween Half Marathon Weekend

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Lindsey Leonette

There is currently no cure for cystic fibrosis and too many people with CF die young. I'm running to help change that reality - to help change my reality!

I was diagnosed with cystic fibrosis when I was two months old. I'm participating in this event with my incredible (& very supportive) husband. We'll be running the half marathon! By God's grace, I have breath in my lungs to do so.

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 be a part of our shared dream forward - a cure for e v e r y o n e with CF.
Glory to God who is able to do exceedingly and abundantly more than we ask or think! (Eph. 3:20)

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$405
raised of $2,000 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.