Andrea Hudson
🌸✨She’s tiny, but she’s mighty.✨🌸
This little warrior lives with cystic fibrosis—a diagnosis that brings challenges most of us will never understand. But every single day, there she is, with a big smile that lights up the room, a giggle that melts hearts, and a strength that’s nothing short of inspiring. 💜
She takes her treatments like a champ. She dances through her breathing treatments, sings (dolly ‘partner’, Disney princess songs, Sia, etc) during her nebulizer time, and somehow finds the magic to inspire her family even on hard days. She’s not just fighting CF—she’s living her childhood with joy, courage, and grace.
To know her is to believe in hope. 💫
To love her is to believe in miracles. 💕
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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