The National ALS Registry is a program to collect, manage and analyze data about persons with ALS (PALS).
It includes data from existing national databases and information provided by persons with ALS who choose to
participate. Researchers can use Registry data to look for disease pattern changes over time and try to
identify whether there are common risk factors among PALS. Additionally, the Registry provides updated
links for participant resources like ALS clinical trials. Persons living with ALS can add their information
to the Registry by clicking the button at the top left of this page.
Selected states and metropolitan areas are also gathering data about ALS. Data from these smaller-scale registries
will be used to evaluate the completeness and accuracy of the data in the National ALS Registry.
In 2008, Congress enacted the ALS Registry Act to gather and organize information about who gets ALS and the potential causes of ALS.
The Agency for Toxic Substances and Disease Registry (ATSDR) is charged with developing and managing the Registry.
ALS Registry Act (Public Law 110-373)