National Amyotrophic Lateral Sclerosis (ALS) Registry

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THE NATIONAL ALS REGISTRY
You can make a difference in the fight against ALS. Joining the National ALS Registry offers the chance to participate in research and be counted.
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Patients and Caregivers
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Learn more about the National ALS Registry, Biorepository, and other ALS research projects and support.

Researchers and Clinicians
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Discover how you can use the National ALS Registry and Biorepository data for research, funding opportunities, and clinical training resources (Free CEUs).

Partners
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Information for National ALS Registry partners and organizations.

General Public
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Learn more about the disease and the history of the National ALS Registry.

Page last reviewed: May 7, 2020
Content source: Agency for Toxic Substances and Disease Registry