Meet Zoe

Single Greatest Night honorees got together for lunch this week (thanks Carabbas!) and we were joined by a couple of the team ambassadors, Zoe and Cammie. I should back up and tell you about how our teams are structured, and why. Each of us 40+ honorees are all divided between 4 different teams to provide help each other fundraise and provide a competitive incentive as we go through November. Each team is named after an child ambassador from Jacksonville with CF. I am a proud member of Team Zoe (and we’re the top fundraising team so far!).
Zoe is an adorable 5-year-old girl, the youngest of 8 kids. She was diagnosed with CF just before her first birthday, but you wouldn’t know it by meeting her. Zoe is a little shy, but she is very into princesses, Hello Kitty and most things pink. Zoe’s mom, Jada, is an avid blogger. She chronicles the family and Zoe’s journey with CF on the blog, Zoe for Life. (I’ve also added it to my blogroll if you want to check it out.

Single Greatest Night honorees got together for lunch yesterday (thanks Carabbas!) and we were joined by a couple of the team ambassadors, Zoe and Cammie. I should back up and tell you about how our teams are structured, and why. Each of us 40+ honorees are all divided between 4 different teams to provide help each other fundraise and provide a competitive incentive as we go through November. Each team is named after an child ambassador from Jacksonville with CF. I am a proud member of Team Zoe (and we’re the top fundraising team so far!).

Zoe is an adorable 5-year-old girl, the youngest of 8 kids. She was diagnosed with CF just before her first birthday, but you wouldn’t know it by meeting her. Zoe is a little shy, but she is very into princesses, Hello Kitty and most things pink. Zoe’s mom, Jada, is an avid blogger. She chronicles the family and Zoe’s journey with CF on the blog, Zoe for Life. (I’ve also added it to my blogroll if you want to check it out.)

It was great to sit down with other members of Team Zoe and meet Zoe, her brother Austin and their mom Jada over lunch. Zoe spent most of the lunch coloring in her Hello Kitty color book, but she did wow us with some Princess trivia (Who is the only princess to have 3 different names?) and gave us all purple bracelets that read “Cure Cystic Fibrosis.” Here are a few pictures we took with Zoe after lunch.

Team Zoe
An almost smile from Zoe!

The CF bracelets Zoe gave us (and her own)
The CF bracelets Zoe gave us (and her own)
Zoe and her brother Austin
Zoe and her brother Austin

Meeting Zoe and her family gave me another unforgettable connection to CF. Lately my giving back efforts haven’t gone much further than running in a charity race, donating blood or giving money to a friend’s fundraising efforts…but getting involved with CFF and Single Greatest Night has been one of the best things I’ve done since I came to Jacksonville. It’s amazingly powerful to interact with kids like Zoe and be able to share their stories with all of you. Most of us take for granted the breaths we take, yet there are 30,000 children and adults in America who are fighting a disease that can make each breath a struggle. Next time you take a deep breath, I hope you think of Zoe and her fight.

To help my efforts to raise money for the Cystic Fibrosis Foundation, please consider donating by clicking here.

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Meet Zoe