Presenters – Becky Abbott and Beth Pond, Chairs, NFED Advocacy Committee
This webinar took place on Tuesday, May 16, 2017 and was recorded.
Watch Webinar
Our advocacy goal is to get a federal law passed that would guarantee that insurance companies would be mandated to pay health insurance benefits for necessary medical care and treatment due to a congenital anomaly…which includes the teeth and the bone that holds them.
In This Webinar, You Will Learn:
- How to educate our U.S. Senators and Representatives
- The importance of family-driven advocacy
- The importance of your story for your first time visiting legislators
- How to prepare for Ectodermal Dysplasias Advocacy Day on Capitol Hill on Wednesday, July 19th
- Tools on the NFED website
Why We Are Doing This Webinar:
We want to…
- Share our excitement
- Share advocacy experiences
- Help you prepare
- Walk you through a day on Capitol Hill
- Answer your questions
- Excite you to join us and be NFED Family Driven Advocacy Strong