NORD is pleased to share the RareAction Network’s Summer 2017 State Policy Legislative Tracker. This document shows, state-by-state, which legislation we are tracking to help improve the lives of people and families with rare diseases. Together, we are taking action in 42 states and the District of Columbia. Let’s keep going – together, we are strong!
For questions related to these bills, or regarding other pieces of legislation that are not featured in the Spring 2017 tracker, contact [email protected].
Sign Up: Join the Action
If you have not already done so, be sure to become a member of the RareAction Network by joining today. By signing up to become a member, you will receive NORD’s Advocacy Alerts and information about ways to get involved in your state.
Learn more about the RareAction Network by visiting rareaction.org.