From all of us to all of you…thank you! Your kindness, your generosity, and your loving support make our kids and families – and the National Foundation for Ectodermal Dysplasias – Forever Strong! Watch our thank you video message.
What Makes A Child With Ectodermal Dysplasia Forever Strong?
Growing up isn’t easy, especially if you are a child affected by ectodermal dysplasia.
You are Strong!
As the challenging times continue, we know a few things are certain. You are strong. Together, we are stronger. Find about the exciting projects we are launching this summer to bring us together.
The Amazing Power of Helping Others!
Helping others can end up helping ourselves and our health. Find out ways you can help pay it forward!
Celebrating Our Superman’s Legacy
Our hearts broke when Dr. Frank Farrington recently passed after a long illness. We recall with much love and gratitude his amazing legacy after 40 years of service to the NFED and our families.
Tim Mickelson Joins NFED Team
We are excited to introduce you to the newest member of our team, Tim Mickleson. He will serve as the Director of Development. “Tim brings 30+ years of experience in the corporate and nonprofit world,” said Mary Fete, executive director of the National Foundation for Ectodermal Dysplasias. “We look forward to him leading our fundraising…
Donor Spotlight: Linda Marcus
Linda Marcus decided to become an NFED Smile Maker in honor of her grandson who is affected. Learn what she’s doing to support him and the Foundation.
Remembering Joanna Daniel Nix
NFED Founder Mary K. Richter recalls the beautiful person, Joanna (Daniel) Nix. Joanna was affected by EEC syndrome and was one of the NFED”s founding families.