We have provided some materials and resources to help you advocate and prepare for meetings with your legislators. Advocating for ELSA? Let everyone know!| National Foundation for Ectodermal Dysplasias
April 4th was an extraordinary day for families affected by ectodermal dysplasias and congenital anomalies! You could almost hear the cries of victory and feel the joy of our advocates, families and staff who watched the live stream of the House of Representatives where they announced that ELSA had passed. Read about the exciting vote and what's next for the bill in the U.S. Senate.| National Foundation for Ectodermal Dysplasias -
The Ensuring Lasting Smiles Act (ELSA) would require all private insurance group and individual health care plans to cover medically necessary services| National Foundation for Ectodermal Dysplasias