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My Great Strides Story

Don Luteran

Fundraising for Central Florida Great Strides

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Don Luteran

Lauren's Light: Teaching and Fighting

I write this message to readers as a way to share all that I have been through in my life with Cystic Fibrosis. I have been defined by this disease since I was born. Every breath was a battle, every day a careful balancing act of treatments, medications, and the ever-present uncertainty of what the future held. But then everything changed.

When I took my first dose of Trikafta back in 2019, it was as if someone had opened a door I didn’t even know existed. For the first time, I could breathe—truly breathe—without the weight of CF pressing down on me. And with that breath, a new dream took shape: teaching.

Before Trikafta, I never imagined I could handle the exhaustion and demands of a full-time job, let alone one that required constant energy and enthusiasm. But now, standing in front of my second-grade classroom, I knew—teaching hadn’t just become possible. It had saved me.

Each morning, I am met with wide-eyed students eager to learn, their laughter filling all the walls of the room. Their joy gives me a sense of purpose, their curiosity fuels me, and their endless questions remind me why I fight so hard to be here.

I don't share my personal life to my students, specifically, cystic fibrosis, but I try to share wisdom in other ways. I teach them about perseverance when a math problem seems impossible, about patience when frustration bubbles up, about kindness in the smallest moments. Every lesson carries a piece of my journey, woven into the fabric of my classroom.

Before Trikafta, I had been surviving. Teaching had given me something more. It had given me a reason to wake up every morning with excitement, to pour myself into something greater, to live the life I never thought I could have.

And with every lesson taught, every story read, and every tiny hand raised in curiosity, I knew—this was where I was meant to be. Giving back to others, making little Lauren proud, and breathing easy.. always.


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.  

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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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.