The National ALS Registry may be the single largest ALS research project ever created. It is designed to identify ALS cases from throughout the United States. The Registry is collecting critical information about the disease that may improve care for people with ALS and help us learn what causes the disease, how it can be treated and even prevented.
Learn more about the National ALS Registry today, and find out how this research can help, including by informing people living with ALS about new and ongoing clinical trials. Visit https://wwwn.cdc.gov/als/Default.aspx for more info.