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The National ALS Registry

Contact Information

Toll-Free
(800) 232-4636

Who We Are

The National Amyotrophic Lateral Sclerosis (ALS) Registry, part of the Centers for Disease Control and Prevention (CDC) offers individuals the chance to participate in research and be counted. Go to the website to join and be connected with resources to learn more about the disease, the history of National ALS Registry, and research projects and support.

Who We Serve

Service Area(s)
Nationwide

Cost & Payment Methods

Fee Structure
No Fee

Age Requirements
No Age Requirement

Available 24/7
Yes

Intake Process
Please join the registry through the site, sign up for the newsletters to receive up-to-date information.