Meet with your Members of Congress and their staff to urge them to:

• Increase federal funding for ALS - specific research from the Department of Defense and NIH.
• Develop a prescription drug benefit for Medicare beneficiaries.
• Support patients and caregivers.
  

PLEASE help by either:

• Meeting with your senator/representative in person on Advocacy Day; or
• Writing a letter to your senator/representative, giving us a copy to hand-deliver on Advocacy Day.

For More Information, contact Kate McNamee at
800-672-8857 or email mcnamee@als-ny.org.