National Foundation for Ectodermal Dysplasias
Director of Support
My experience at the NFED continues to be amazing with each family contact. I have the privilege of providing support and resources to your families. Not only do I get to share information with families, I learn a great deal in return.
Jodi Edgar Reinhardt
Director of Marketing and Communications
It is an honor to raise awareness and funds for these rare disorders. I enjoy meeting the families, hearing their stories and then being able to share them with others to increase understanding. Working together, we can achieve great things! I consider the NFED my second family and thank them for letting me share their lives and for all that they teach me.
Mary Fete, R.N., M.S.N., C.C.M.
I have the best of all worlds working at the NFED. My daily responsibilities include working with wonderful individuals and families to help them with treatment and health-related questions. I also am very fortunate to work with some of the best researchers in the world as we continue to make great strides in ectodermal dysplasia research. Give me a call. I would love to talk with you!
I had the most inspiring, enjoyable, first National Family Conference experience. I met so many great, enthusiastic, loving, caring, dedicated, smiling adults & children whom I am honored to call my new friends. Thank you for letting me be part of the NFED family! I am learning from yesterday, live for today, and hope for tomorrow. When life’s problems seem overwhelming, I look around and see what other people are coping with and decide not to be discouraged. For me, it is important to feed my faith and my fears will starve to death! When life gives me a hundred reasons to cry, I show life that I have a thousand reasons to smile. I don’t wait. I make memories today. I celebrate my life. Thank you for letting me join in celebrating your lives and making new memories!
Administrative Assistant to Programs
I am privileged to work for the NFED where everyone is a family. As a new member of the staff, I can’t wait to meet families and hear their stories, which will ultimately help me work with the program team for support, research and treatment of ectodermal dysplasias. I look forward to all the things that our individuals and families that are affected by ectodermal dysplasias will be teaching me in the present and future.