When we received the diagnosis that our 12 week old baby had Neuroendocrine cell Hyperplasia of Infancy, a 1 in 6 million lung disease, we were on the hunt for answers. Was it genetic? Was it enviromental? Was it an immune response? Every avenue we traveled down led to an empty hallway of "we don't know." That research was limited because of the rarity of her condition. A condition that wasn't even discovered until 20 years prior. Without research funding, possible causes will never be uncovered and cures will never be discovered!

Our hope is to reach our goal of 1000 dollars before September 29th towards lung disease research!