Marching For Millie
Gemma Cochrane
Fundraising for Palm Beach & Treasure Coast Great Strides 2026
Gemma Cochrane
Hi everyone!
I'm Millie, and I'm 16 years old living with Cystic Fibrosis. Every day, I fight this disease, but I believe in a future where CF no longer exists - and that's why I'm asking you to join me in making a difference.
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.
We invite you to join Marching for Millie, as we walk to support the Cystic Fibrosis Foundation in their mission to find a cure!
Together, we can make a difference - one step at a time. Let's walk, raise money, and bring hope to those battling Cystic Fibrosis. Every step we take, and every dollar we raise, brings us closer to a world without CF. So, whether you walk beside us, or donate, your support means the world.
Join us in making an impact. Let's March for Millie, and for a future without CF.
Thank you for your support!
Love, Millie
I'm Millie, and I'm 16 years old living with Cystic Fibrosis. Every day, I fight this disease, but I believe in a future where CF no longer exists - and that's why I'm asking you to join me in making a difference.
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.
We invite you to join Marching for Millie, as we walk to support the Cystic Fibrosis Foundation in their mission to find a cure!
Together, we can make a difference - one step at a time. Let's walk, raise money, and bring hope to those battling Cystic Fibrosis. Every step we take, and every dollar we raise, brings us closer to a world without CF. So, whether you walk beside us, or donate, your support means the world.
Join us in making an impact. Let's March for Millie, and for a future without CF.
Thank you for your support!
Love, Millie
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