Tris was born February 9, 2010 with 0 neutrophils. As her parents, we were unaware of what that news actually meant. When we began to research we quickly found that there were few resources out there for parents like us who were facing this situation. We are thrilled to begin fundraising for this foundation which began shortly after her birth. Our hope is that all those facing the unknowns of the severity of neutropenia will at least find hope that steps are being taken to help with this rare disease. We also hope that through this fundraising drive awareness is raised so that even more projects will be undertaken. We are fortunate that Tris has faced very few difficulties as a result of her condition but know that there are many who are not as lucky. This is our way of saying we are praying for all the parents like us and their babies.