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The ALS Association Greater San Diego Chapter


Latest News

The ALS Association Endorses Legislation to Preserve Access to Speech Generating Devices and Eye Tracking Technology
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Call for Research Proposal: Drug Development Contract
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Message from Barbara J. Newhouse, President and CEO
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What is the National ALS Registry?
The National ALS Registry is a program to collect, manage, and analyze data about people with ALS.  It is important to include as many people with the diease as possible to get the most accurate information.  

Why should I join the National ALS Registry?
Learning more about ALS is a vital step in the battle to defeat ALS.  The Agency for Toxic Substances and Disease Registry (ASTDR) has developed the National ALS Registry to gather information from people who are living with ALS.  This information will help doctors and researchers learn more as they work toward a cure. 


For more information on the National ALS Registry or to join the National ALS Registry, click here or go to:

National Registry Image.jpg




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OUR MISSION: Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig's Disease and their families to live fuller lives by providing them with compassionate care and support.


The ALS Association, Greater San Diego Chapter
(858) 271-5547  7920 Silverton Ave. - Suite E - San Diego, CA 92126
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