Tough Like Teagan

️ HOLIDAY LAKE, LET’S COME TOGETHER AND SHOW SOME LOVE! ️ Sometimes a family finds themselves facing something they never expected, and in those moments, having a community behind them can mean more than we realize. Please bid on items in the silent auction to support this family as they travel to be with their precious daughter during this very difficult time.  No family should have to face something like this alone.  So, Holiday Lake, let’s rally around them!  

Nicole’s precious granddaughter, Baby Teagan, is only 5 months old and is battling a rare skin condition, EB. This sweet little girl goes through so much each and every day, with ongoing medical care and countless doctor appointments — some requiring trips all the way to Chicago.  EB-Epidermolysis Bullosa is a life threatening rare genetic disorder that affects the body's largest organ:  the skin.  
Children with EB are often called "Butterfly Children" because their skin is as fragile as the wings of a butterfly.  With skin this fragile, everyday activities like eating, sleeping, walking and playing become monumental tasks.  At this time, there is no cure.
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