New Board and Council Members Bring Expertise and Insights to the NFED

The National Foundation for Ectodermal Dysplasias (NFED) is thrilled to announce the addition of new leadership experts. Joining our Board of Directors, Patient Care Council, and Scientific Advisory Council, these four exceptional leaders will bring knowledge, experience and insights to advance the foundation’s mission of supporting and serving individuals and families affected by ectodermal dysplasias.

Four Key Takeaways from NFED’s 2017 Annual Impact Report

As a nonprofit organization serving the ectodermal dysplasias community committed to transparency, we are happy to share with you our 2017 Annual IMPACT Report. Here we report on just a few of the many activities and accomplishments from 2017.