I was diagnosed with cystic fibrosis at just five months old. Before I could even walk or speak, my life was already shaped by a disease that would challenge every breath I take.

But cystic fibrosis does not define me, it fuels me.

Today, I am a second-grade teacher, pouring love and energy into my students every single day. I’m also a dancer and dance teacher, finding joy and freedom in movement, something that hasn’t always come easily to me. Over the years, I’ve volunteered, created my own clothing line to spread awareness, and even written a memoir to share my journey in hopes of inspiring others.

On the outside, my life may look full, and it is, but behind the scenes, the fight never stops.

Even with advancements in medicine, including being on the CF modulator Alyftrek, I am still battling ongoing health challenges. There are still hard days. Days where breathing feels heavy. Days where my body reminds me that this disease is relentless.

And that’s why I walk.

I walk for the little girl I once was, whose future felt uncertain.
I walk for my students, so I can continue to show up for them.
I walk for every person and family impacted by cystic fibrosis.
And I walk because there is still no cure.

Your donation is more than just a gift, it’s hope. It’s more time. It’s more birthdays, more dances, more moments that matter. It’s a step closer to a future where no child has to grow up fighting to breathe.

If my story has touched your heart, I ask you to stand with me. Help me keep going. Help all of us keep going.

Together, we can change the ending of this story.