Fundraising to find a cure for Cystic Fibrosis for our little man
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Save the Date for the 2019 Chillin' & Grillin' for a Cure on Sunday September 22nd from 12-5pm
Yellow Finch Lane in Frankfort
Join us for a day of fun at an outdoor fundraiser to raise money for the Cystic Fibrosis Foundation! Invite your friends and family and join us for Kids Activities, Music, Food, Baskets and if you choose, test your culinary skills with our Wing cook-off and Cookie bake-off!  

Tickets are available for purchase online at $20 per person ages 3+ with a $75 family rate through 9/13. Afterwards, tickets will be available for $25 per person the day of the event. For the latest details, to purchase tickets and to register as a chef, go to

Sponsorship and volunteer opportunities available, email for more info.
Schedule of Events
12:00 - 1:00: ​Wing Cook-off tasting
12:00 - 1:30: Face painting / tattoos
12:00 - 4:00: Baskets / Auctions
  ​1:00 - 5:00: ​BBQ Food/Drinks
​  1:30 - 2:00: ​Storytelling
  2:00 - 3:00: Organized kids games
            3:30: Desserts
            3:30: ​Kids Horse Race
​            4:30: Basket winners announced

All Day:​
Bouncy, Drinks, Music, Photo Booth, T-shirt sales
Click here for event details
For the most part, Dean has been extremely healthy but then there are times when a persistent cough wracks his body 24/7 or when the extreme heat during a baseball game causes him to sweat more and lose more salt. Losing too much salt for Dean can lead to loss of appetite, tiredness, nausea, difficulty concentrating, weakness, dizziness, muscle cramps, headaches and dehydration (which in itself causes sputum to be thicker and increases the likelihood of infection). We combat this by giving him a ton of extra salt in foods and his favorite, using NUUN salt tabs in his water bottles. In true Dean form though, he doesn't notice the heat or complain about it, he just wants to keep playing. And while we may cringe at the constant coughing, he says, "Look at my abs! I've got a six-pack." There have been more than a few days when I look into Dean's young face and wish I could take it all away and that we could all forget just what Cystic Fibrosis is but since that isn't my superpower, we do what we can and we fight hard, diligently keep him on his treatment regimen and we annual host the Chillin' & Grillin' for Cure.
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Eat. Pray. Dean · CURECF · INDEANSLIFETIME, OK #1047 · USA

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