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Little Sweet Pea Closet is donating a portion of their sales during National EB Awareness Week, October 25th-31st, 2014, in honor of Ava, who passed away from Epidermolysis Bullosa (EB) in 2012. You can donate directly in her honor below.

Thank you for your donation. We appreciate your support!

debra is the only national not for profit that supports the research for a cure and treatments for, while providing services and programs to those who suffer from the rare and painful genetic disorder, Epidermolysis Bullosa (EB). Today, there is no cure or treatment. EB makes the skin so fragile that the slightest friction causes blisters and skin tears. The eyes, mouth, throat and other internal organs are also affected. Your support is very much appreciated. 

 
 
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