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

Download Slide Deck for Webinar 

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