On July 15, 2016, our dear friend Emily's daughter Elodie was born with a rare genetic disorder called Epidermolysis Bullosa ("EB"). This devastating disease means that Elodie is missing a critical protein that helps bind the layers of the skin together, making her skin extremely fragile, and causing internal and external wounds. The only option to care for Elodie is through a twice-daily bandaging process that is both painful and extensive. Today there are no cures or even treatments for this disease, and children face lives that are cut far too short. Yet even despite the suffering that she endures each day, Elodie is the sweetest and most adorable little girl in the world. She inspires us to fight each day to bring her - and other Butterfly Children - a much needed treatment. One day in the not so distant future, we envision a world free of EB, and we will continue to Plunge until that dream becomes a reality. We invite you to make a splash with us by taking the Virtual Plunge for Elodie and making a donation; every dollar makes a difference! 100% of donations benefit the EB Research Partnership, the largest non-profit dedicated to funding research aimed at treating and ultimately curing EB. Visit plungeforelodie.org for more information.