The National Foundation for Ectodermal Dysplasias (NFED) is family! That’s a common refrain whenever we talk with someone connected to our mission and vision. And, it’s true. NFED staffer Kelley Atchison talks about the joys of family connections and the frustration of not having all of the answers. But, there’s hope, knowing we can do more together!
Experiencing the Magic of Ectodermal Dysplasias Research Collaboration
Bringing people together is what the National Foundation for Ectodermal Dysplasias does best—especially when advancing research. This is more than science; it’s about saving lives. Read what happened at our recent Complex Wound Healing Conference in Philadelphia.
Dermatologist Volunteers and Creates New Resources for Ectodermal Dysplasias
Long time National Foundation for Ectodermal Dysplasias (NFED) volunteer and pediatric dermatologist Dr. Elaine Siegfried said that mentoring the next generation of doctors about the ectodermal dysplasias is one of her passions. This month, we feature one of those new doctors in our volunteer spotlight. Dr. Rylee Moody graduated from medical school at Saint Louis…
We’re Hiring, Communications Coordinator!
Are you or someone you know passionate about communications and marketing with a desire to make a real difference? Do you believe in the power of storytelling to inspire change? The National Foundation for Ectodermal Dysplasias is looking for a dynamic Communications Coordinator to help us expand our reach and amplify our mission. As a…
We’re Hiring, Development Coordinator!
Are you passionate about nonprofit development and looking to make a meaningful impact? The National Foundation for Ectodermal Dysplasias (NFED) is excited to announce a full-time, remote opening for a Development Coordinator! This is a dynamic role where you’ll support our Director of Development and Communications in executing strategic plans that drive our mission forward….
Complex Wounds in Ectodermal Dysplasias, TP63 Syndromes: November Conference in Philadelphia
We understand that wound healing presents a significant challenge for individuals with TP63 syndromes. This is why we are thrilled to share that the National Foundation for Ectodermal Dysplasias (NFED) will host a wound healing conference in just a few weeks, November 3-5. The collaborative Complex Wounds in Ectodermal Dysplasias Conference will occur at the…
Living with EEC: A Journey of Resilience, Art, and Advocacy
Greta Geiger knows living with a rare genetic condition can be a challenge. It also can shape your journey in unexpected and profound ways. A graduate from Millsaps College, where she received an art scholarship, Greta is both an award-winning sculptor and an aspiring genetic counselor pursuing a Masters in Medical Genetics and Genomics at…
NFED Recruiting TP63 Research Project Subjects
The National Foundation for Ectodermal Dysplasias (NFED) and researchers at East Carolina University (Dr. Maranke Koster & Shirley Parraga) are recruiting research subjects to participate in a new collaborative research project.