As we look back on 2024, we are filled with gratitude and hope. This year, more families reached out to the NFED than ever before—a 29% increase—and our community now spans 121 countries. Behind every number is a person with a story: children smiling with new confidence after receiving their first set of dentures, a family embraced at our conference after a new diagnosis, and a young adult bravely sharing with lawmakers and researchers as they advocate for critical legislation through the Ensuring Lasting Smiles Act (ELSA).
Thanks to your support, we sustained vital programs while staying true to our highly relational approach to our community. We launched new mental health resources, moved research forward, and supported families navigating a life-changing clinical trial.
Because of you, families find hope, answers, and connection. Together, we are building a brighter future for everyone affected by ectodermal dysplasias. We couldn’t be more thankful!
Please take a moment to visit the 2024 Impact Report Landing Page, full of videos, digital flipbook, and compelling stories and graphics!
