#ebkids #cure4eb #ebawareness ebkids.org debra.org ebresearch.org This is Nicky, he has the Recessive Dystrophic form of Epidermolysis Bullosa (RDEB). Like his page here --> https://www.facebook.com/NickyLivingWithEB/ I have a rare condition called Epidermolysis Bullosa. There is no cure. But with awareness, someday there might be. Will you help me? Can you tell ONE person a fact about EB today? You could save my life. Epidermolysis Bullosa Awareness.