Ask Your Legislators in Washington D.C. to Support and Become an Original Cosponsor of the Ensuring Lasting Smiles Act (ELSA)

Wed, 11 Jul 2018 04:00:00 GMT

We're tired of people affected by congenital anomalies not getting the medically necessary care and treatment(s) they need.

The National Foundation for Ectodermal Dysplasias along with 70+ ELSA supporting organizations have made it a priority to get the Ensuring Lasting Smiles Act (ELSA) passed. This federal, bipartisan legislation requires a group health plan, and a health insurance issuer offering group or individual health insurance coverage, to provide coverage for medically necessary outpatient and inpatient items and services related to the diagnosis and treatment of a congenital anomaly or birth defect.

The Ensuring Last Smiles Act will be reintroduced in the U.S. Senate and U.S. House in the near future. It has gained tremendous bipartisan support since 2018, but it will need to pass both chambers of Congress and be signed into law by the President before the 118th Congress ends in December 2024. This process starts with you - please ask your U.S. Senators and U.S. Representative to support and become an Original Cosponsor of ELSA for its reintroduction.

Will you reach out to your members of Congress and ask for their support? You can email them our prepared letter, post a prepared message to their Twitter and Facebook pages, and call them. We've made it easy - it only takes a few minutes! Start by clicking on the "Take Action" button and enter your address.

Please take action today! Use this web tool to contact your U.S. Senators and Representative. Then share this web tool with your family and friends so they can do the same.

Current Actions

Ask Your Legislators in Washington D.C. to Support and Become an Original Cosponsor of the Ensuring Lasting Smiles Act (ELSA)