How The Stand Together Conference is Unique This Year

This year’s summer event is going to look a little different than other years. Find out what you can expect when you attend the Stand Together Advocacy Conference and how you’ll leave empowered to advocate for yourself at home and on Capitol Hill!

Financial Consultant Gives Heart and Time to Help Her Son’s Tribe

Marianne Vermeer’s “guardian angel” of a dentist encouraged her to get involved with the NFED. She jumped all in becoming an active volunteer and member of the Board of Directors. Read about the powerful moment she had as a volunteer and what she’s learned about children with ectodermal dysplasia.

Finding Success in the Water, in Law and in Love

Lawrence Dillon read John Baker’s ectodermal dysplasia story and discovered they had similar journeys. The champion swimmer and attorney talks about how he, too, has successfully navigated a lifetime of “being different” by facing it head on.

Best Practices for Treating Your Ectodermal Dysplasia Teeth

You have many different treatment options for teeth affected by ectodermal dysplasia. It can be overwhelming to know what’s the best thing to do for you or your child. Learn from our dental experts which treatments to consider to achieve an age-appropriate dentition.

Developing a Non-Invasive Way to Diagnose XLHED Prenatally

The NFED is funding research to help scientists develop a new way to diagnose XLHED prenatally. Because it’s non-invasive, it would not pose any risks for the pregnant mother. Learn about the procedure and how it would help mothers who are considering the EDELIFE clinical trial.