My Team CF Story

BIG News!

I am thrilled to announce that I will be running in the 2024 Chicago Marathon with the Cystic Fibrosis Foundation! 

This cause is very close to my heart as my niece, Ellie, was born on February 12, 2021, and was diagnosed with Cystic Fibrosis. She has been diagnosed with the rare mutation, phe157x, which makes her one of only five individuals in the CF database with this specific mutation. Despite the challenges she faces, Ellie is an incredible little girl - feisty, funny, strong, and fearless! 

Determined to make a difference in the lives of those affected by Cystic Fibrosis, including Ellie. To achieve this, I need your support! 

By participating in the marathon, I aim to raise funds for the Cystic Fibrosis Foundation, which supports groundbreaking research, medical advancements, and provides vital resources for individuals, like Ellie, living with CF.

Your generous donations will help improve the quality of life for CF patients, fund critical research, and bring us one step closer to finding a cure. Every contribution, no matter the size, can make a significant impact! 

Together, let's make a difference and create a future where Ellie and all other CF warriors can live their lives to the fullest. 

Your support means the world to me and to all those affected by Cystic Fibrosis.

Thank you in advance for your generosity, love, and encouragement! Let's run towards a brighter future together! 

#ChicagoMarathon2024 #CysticFibrosisAwareness #FundraisingForACure #RunningForEllie