Walk with our team to Cure Cystic Fibrosis
Raelyn's Roses
Fundraising for Central Florida Great Strides 2026
Raelyn's Roses
Raelyn's Fight
Ten days.
That's how long we had before our world changed forever.
At just 10 days old, Raelyn was diagnosed with cystic fibrosis. Instead of simply enjoying those early newborn days, we were learning how to care for a child with a lifelong, life-threatening disease.
Now at 6 years old, Raelyn is pure joy. She is happy, loving, and full of life. She has the biggest heart and is always looking for ways to help others. Her imagination is incredible, and she brings light into every room she walks into.
But cystic fibrosis doesn't take a day off.
Behind her smile is a routine that never stops-breathing treatments with a nebulizer and vest machine, enzymes with every meal, inhalers, and medications. When she gets sick, everything becomes harder, heavier, and more exhausting.
And as a parent, watching your child struggle to breathe… it's a feeling that never gets easier.
There are days when this disease takes a toll on all of us. Days filled with worry, fear, and exhaustion. Days where we're reminded just how fragile things can be.
But there are also the good days.
The days where she laughs, plays, creates, and just gets to be a kid.
Those are the days we hold onto the tightest. Because with cystic fibrosis, we live in a space of uncertainty-we never truly know when things could change or when her health might decline.
Raelyn is stronger than this disease. She shows us every single day what courage really looks like.
We are fighting for her future.
We are raising funds for the Cystic Fibrosis Foundation to support research, better treatments, and one day-a cure. A future where children like Raelyn don't have to fight so hard just to breathe.
If you're able, please donate, share her story, or simply keep her in your thoughts.
Because no child should have to fight this hard.
And no parent should have to watch.
Thank you for standing with Raelyn.
Ten days.
That's how long we had before our world changed forever.
At just 10 days old, Raelyn was diagnosed with cystic fibrosis. Instead of simply enjoying those early newborn days, we were learning how to care for a child with a lifelong, life-threatening disease.
Now at 6 years old, Raelyn is pure joy. She is happy, loving, and full of life. She has the biggest heart and is always looking for ways to help others. Her imagination is incredible, and she brings light into every room she walks into.
But cystic fibrosis doesn't take a day off.
Behind her smile is a routine that never stops-breathing treatments with a nebulizer and vest machine, enzymes with every meal, inhalers, and medications. When she gets sick, everything becomes harder, heavier, and more exhausting.
And as a parent, watching your child struggle to breathe… it's a feeling that never gets easier.
There are days when this disease takes a toll on all of us. Days filled with worry, fear, and exhaustion. Days where we're reminded just how fragile things can be.
But there are also the good days.
The days where she laughs, plays, creates, and just gets to be a kid.
Those are the days we hold onto the tightest. Because with cystic fibrosis, we live in a space of uncertainty-we never truly know when things could change or when her health might decline.
Raelyn is stronger than this disease. She shows us every single day what courage really looks like.
We are fighting for her future.
We are raising funds for the Cystic Fibrosis Foundation to support research, better treatments, and one day-a cure. A future where children like Raelyn don't have to fight so hard just to breathe.
If you're able, please donate, share her story, or simply keep her in your thoughts.
Because no child should have to fight this hard.
And no parent should have to watch.
Thank you for standing with Raelyn.
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