Like many rare disease organizations, the National Foundation for Ectodermal Dysplasias (NFED) stepped up to serve as a catalyst for research that is otherwise likely to be neglected by mainstream science. Now, with more than 30 years of leadership, the NFED is driving the charge to develop effective treatments and—most importantly—cures.
Research has been an integral part of our mission from the very beginning. Since the launch of the Research Fund in 1987, we’ve provided more than $1.2 million in direct funding to researchers and contributed $3.6 million to research overall. Research studies have focused on the classification of ectodermal dysplasias as well as several of the 100+ different syndromes, and, when combined with our investment in grants, conferences and salaries, we’ve seen incredible results:
- Identified the genes for several ectodermal dysplasias
- Developed treatment protocols for life-threatening skin erosions in the p63 syndromes
- Significantly expanded what we know about the ectodermal dysplasias and officially documented it in scientific literature
- Brought a potential treatment to human clinical trials for the most common type of ectodermal dysplasia!
Throughout our decades of research, the power of collaboration can’t be overlooked. Researchers, academics and health professionals from medical and dental communities have continually pooled their resources and expertise to advance knowledge and care of ectodermal dysplasias. From their dedication has come a sense of community, and from partnerships have come innovation. We’ve come together for a range of conferences and gatherings over the years:
- Skin Erosion Workshop (2002)
- International Research Symposium on Ankyloblepaharon-Ectodermal Defect-Cleft Lip and/or Palate (AEC) Syndrome (2006)
- International Conference on Ectodermal Dysplasia Classification (2008)
- Goltz Research Conference (2013 and 2015)
Families and individuals affected by ectodermal dysplasias are at the heart of everything that we do, including research. Without their participation in research studies—sometimes for many years—and their willingness to join the Ectodermal Dysplasias International Registry, progress would not be possible.
Without scientific research, there can be no better treatment protocols for this present generation and no potential for a cure for future generations. I simply can’t accept that, knowing that I have the ability to positively affect the future by participating in research.Virginia Higgins, AEC research volunteer
Erin & Shannon’s Story
Our Strong Families
Shaping Our Future: Boost the Cure!
The NFED has been the sole force in the world to blaze this trail toward a cure. Despite the long history of ectodermal dysplasias, research focus and expansion has only taken place in the last three decades. We are proud of the extraordinary successes we have achieved in a relatively short amount of time and with a small amount of money.
Lives have been saved. Treatments have been developed. Hope has been given. Now is the time to invest in leading edge research that results in longer, healthier and happier lives.Donate to Develop Cures