Overwhelmed With Love and Belonging!

By Terri Andrews I was born in a little rural area in Alabama in 1959. Not much was known about ectodermal dysplasia nor the type of ectodermal dysplasias I was born with called ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. If I received any type of major treatment or surgery, I had to travel at least 100 miles, which was not…

The True Meaning In Life Is To Plant Trees, Under Whose Shade You Never Expect To Sit!

 By Ashli Matus-George Allyson Kelso’s Aunt Founder, Rally for Ally When Ally was born on December 22, 2004 in Oxnard, CA, it was an exciting time.  A new baby, Christmas for her three-year-old big sister, Morgan. My then fiancé, Tom, and I were recently engaged and planning a wedding, Kristin had a thriving career, and…

Support Each Other: We are Family!

By Josh Long Why do we donate our time and money to the NFED?  Because the NFED is family!  Two years ago, we attended our first Family Conference in Orlando, Fla. through a very generous NFED scholarship.  The conference was a life-changing event for our entire family. We had mom, dad, son, daughter, grandma and grandpa in attendance. …

A Chance Meeting Changed my Life!

    By Frank Farrington, D.D.S., M.S. Affiliated with the Medical College of VCU, Dept. of Pediatric Dentistry, Richmond, VA Why have I stayed involved with the NFED and the Scientific Advisory Council, Patient Care Council, and the Board of Directors for so many years?  The answer is very simple. When you are on the faculty of a…

She Was One of the Founding Families as a Toddler in 1981. Today, She’s an Advocate for the Community.

Hi there, My name is JoAnna Nix and I volunteered last fall to help represent the NFED at my local Combined Federal Campaign (CFC) and State Campaigns.  The NFED is known as the Skin and Dental Dysfunction Foundation #10604 by the CFC. Being a government employee, I’ve seen that government workers really do care about their communities and want…