Andrew and Cece’s Army
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Our superhero, Andrew was born November 2013 with an intestinal blockage that required surgery immediately after delivery. As he recovered, we learned that Andrew has two copies of the df508 mutation and has cystic fibrosis. After 12 weeks in the NICU and two intestinal surgeries, Andrew is growing and thriving. He loves cars (and trains, playing outside, and playing with superheroes and Legos. Most days you would never know that he is sick, but he works hard doing his breathing treatments and taking his medicines every day to stay as healthy as possible!
Cecilia, Our newest CF Fighter, had a much easier start to her life with CF. We work hard to keep her as healthy as possible!! She gives great snuggles and loves to laugh and play with her big brother and sister! She loves Me-me (Mickey Mouse) and Go (Frozen).
We are hopeful that through funding for continued research, Andrew and others with CF will be able to live a long and healthy life!
Please join us in raising money for a cure for CF.
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ATTENDANCE POLICY:
Due to the COVID-19 pandemic, indoor events sponsored by the CF Foundation are strictly prohibited at this time. Scheduled outdoor events must adhere to strict requirements to minimize the risk of COVID-19 infection. Events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
IMPORTANT NOTE ON ATTENDANCE AT OUTDOOR FOUNDATION EVENTS:
To minimize the risk of COVID-19 infection, attendees at CF Foundation events must adhere to the following requirements:
Persons with CF should consult their physician before participation in any in-person event as they may be at an increased risk for severe illness from COVID-19. People with CF should maintain a safe 6-foot distance from persons outside of their household at all times.