National Amyotrophic Lateral Sclerosis (ALS) Registry

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Information for ALS Researchers
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What is The National ALS Registry?

Learn more about what we do and ALS.

Brad Dusek (pictured) Taking on ALS (Video).

Join the National ALS Registry

ALS research counts on you! Be counted and join the fight against ALS.

Log in to your Dashboard

Tell your story and take the risk factor surveys and help researchers learn more about ALS.

ALS Registry Dashboard

View the latest information on ALS statistics in the U.S. and how the Registry is advancing research.

ALS Clinical Trials & Studies
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View the clinical trials and studies the Registry has helped to recruit for and how you can be notified.

National ALS Biorepository
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Donate your blood and saliva at no cost to you and help ALS researchers learn more about this disease.

Research Funded by the Registry
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Learn how the Registry advances ALS research by funding grants.

Publications & Reports
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Read the latest publications by the Registry and its partners.

Registry Newsletter & ALS Act
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Sign up to receive newsletters from the Registry.

Registry Partners
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Information about Registry partners and organizations.

Annual Research Meetings
Conferences & Events
Frequently Asked Questions