My Nonprofit Reviews

We are an “AFE grieving family”. Our beautiful daughter-in-law, Jacie Cochran, was lost to this condition during the birth of our miraculous grandson a little over three years ago. The Amniotic Fluid Embolism Foundation swooped in almost immediately to attempt to explain what had happened and to support our son through the shocking, unfamiliar, and incredibly difficult days that have followed. We are so very impressed by and appreciative of them. We will continue to call upon them when we have questions, comments, ideas, and/or issues as we continue to move forward and we have no doubt that the AFE Foundation will always be our most relied upon support system, the most trusted source of valuable needed information, and will someday #endAFE!

This group’s online support has been very comforting to me. We lost our daughter in law to an AFE recently, in July of 2020. Before this, we hadn’t heard of this silent killer. This organization has been a provider of support and information to my son, myself and several others of us over the past few months and we are very appreciative of their work.