Unstoppable Joy: Aubrey’s CF Journey with Laughter, Love, and a Whole Lot of Cartwheels

Aubrey, 2020

Spend just a few minutes with Aubrey, and you'll quickly learn she’s not one to sit still — unless it’s to crush you in a card game during treatments. 💁‍♀️ Born in January 2014 and diagnosed with cystic fibrosis just three weeks later, Aubrey has grown up knowing what CF means… but she’s never let it define her.

From a young age, Aubrey has been blessed with minimal hospital stays and relatively few illnesses — something her family doesn’t take for granted for a single second. Her journey hasn’t been without its challenges, but through it all, she has embraced life with wide arms and an even wider smile.

Aubrey’s passions are as full of energy as she is: gymnastics, volleyball, swimming, cheer, art, and anything that involves movement or creativity. If it involves sunshine, cartwheels, or glitter? Even better. 🌈

She loves camping trips, hanging out with friends and family, and playing with her “babies.” And when it’s time for treatments, you’ll find her curled up with her iPad or favorite TV show — never complaining, always making the best of it.

Whether she’s doing flips in the yard or cannonballs at the pool, Aubrey radiates joy. Her smile is contagious, her spirit is fierce, and her love for life is impossible to miss.

Aubrey reminds us that living with CF doesn’t have to mean living in fear. It can mean living loudly — with laughter, movement, connection, and courage. She is sunshine with a side of sass, and she’s one of the unforgettable faces of CF.