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ALS ASSOCIATION | AMYOTROPHIC LATERAL SCLEROSIS ASSOCIATION

The Association’s network plays a lead role in advocating for increased public and private support of ALS research and public policy initiatives that responds to the needs of people with ALS. Our organization’s public policy efforts in Washington, D.C. have raised the profile of ALS at the White House, among members of Congress, and within federal agencies, including the National Institutes of Health, Centers for Medicare and Medicaid Services, Food and Drug Administration, Department of Defense, Department of Veterans Affairs, Social Security Administration, and Centers for Disease Control and Prevention.

Last assured

09/05/2024

Physical Address

1300 Wilson Boulevard, Arlington, VA 22209

Hours

Mon. - Fri., 9 am - 5 pm

Fax

7812558811

Fax

Voice

8662576663

Toll Free

Application process

Call, email or visit the website

Fee

No fee

Eligibility

Persons with ALS,PLS, PMA and PBP diagnosis

Agency info

AMYOTROPHIC LATERAL SCLEROSIS ASSOCIATION

The mission of The ALS Association is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.