No Longer Feel Isolated With AEC Syndrome

Learn about the Brown family’s journey when their daughter, Erin, was diagnosed with Ankyloblepharon-Ectodermal Defects-Clefting (AEC) syndrome. They also talk about how their NFED family has been a tremendous help over the last 5 years.

Expanding Our Volunteer Team in 2017

Service and giving are qualities that are greatly cherished by all of us at the NFED.     You, as a volunteer, help our organization by lending a kind helping hand – and our only payment to you are wages of love, gratitude and knowing that you are making a significant impact on lives.  Everyone has such busy…