Finn David Neel was born July 5th 2016 at 6:23pm. Ever since he has entered our lives he has been the most amazing little person; full of life, energy, laughter, and fun! On July 20th 2016 Finn was diagnosed with Cystic Fibrosis. With the support of our family, friends, Dr. Neil Aaron, and the Phoenix Children's Hospital team, we have been able to tackle this disease!
We hope that you will consider joining Finn's Troopers as we walk to spread awareness,, and find a cure for Cystic Fibrosis! Thank you so much for all of your love and support!
Here are some fun facts about Finn:
-Finn loves "Mickey Mouse Clubhouse."
-Finn's favorite Disney character is Donald Duck
-Finn loves to dance
-Finn knows how to stand, crawl, scoot, laugh, roll-over, cooes, and give high-fives
-Finn's favorite foods are pineapple, oranges, and bananas
-Finn has the best smile in the world
We can't wait to have you march with us! See you in April!
Important note on Attendance at Foundation Events:
Infections can exacerbate CF symptoms and worsen lung function, so we ask attendees at Foundation-sponsored events to observe the following best practices to reduce the risk of germ transmission:
Regularly wash hands with soap and water or with an alcohol-based hand gel.
Cover coughs and sneezes with a tissue or your inner elbow.
Maintain a safe 6-foot distance from anyone with a cold or infection.
To further reduce the risk of cross-infection, the Foundation’s attendance policy recommends that all people with CF maintain a safe 6-foot distance from each other at all times while attending an outdoor Foundation-sponsored event. All Great Strides walks are non-smoking events.