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.