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My Great Strides Story

Makaylea Cortes
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Makaylea Cortes

My life took an unexpected turn at age six when I was diagnosed with cystic fibrosis. Suddenly, 'normal' childhood experiences were intertwined with daily treatments, hospitalizations, and the constant awareness of my lungs' limitations. But CF hasn't defined me. It's been a part of my story, a catalyst for strength, and a driving force behind my commitment to keep moving forward. This journey has been challenging, but it has also been filled with incredible people, moments of joy, and a deep appreciation for the gift of life. I believe a cure is within reach, and I'm dedicated to doing my part to make that a reality for myself, my son, and my husband. 

There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality.

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.  

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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$295
raised of $350 goal
 

Achievements

Leader

Team Salty Kisses

$295
$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.