As Congress adjourns for the month-long August recess, it is important that our Chapters and advocates continue to reach out to their elected officials when they are home in their states and districts. Therefore, we are providing the following tools and guidance to help you build additional support for our cause and for the ALS Registry Act (S. 1382/HR 2295). Click on the links below for more information about each topic.

ALS Registry Act Update and links to cosponsors by state
August Recess tools:
Congressional District Meetings
Town Hall Meetings
Sample letter-to-the-editor and links to our Media Action Center
Advocacy Letters and Photographs to Senators
The tools above will help you continue to deliver our key messages throughout August and we encourage you to take advantage of these opportunities to fight for a treatment and cure for ALS.

Thank you for your continued advocacy! Together we are making a difference.

If you have any questions about this update or would like additional information, please contact the Advocacy Department at advocacy@alsa-national.org.