Our goal with this organization is to help fund research for CDH that will ultimately eliminate this birth defect or at least make it a much more manageable diagnosis. We firmly believe that the brilliant minds working in this field will one day find a way to fix CDH in utero. This cannot happen though without necessary funding and increased awareness. From the morning after receiving this diagnosis in early April 2021, we were committed to doing everything we could to help our baby wage this war as well as raising awareness of this awful diagnosis. Even though our Molly isn’t physically here anymore, we are still fully committed to her and the fight that she and all of the other babies born with CDH unfairly take on.