While no one knows the cause of amyotrophic lateral sclerosis (#ALS), people living with the disease and their families now have a role in finding a cause and cure, in part by registering for a new national ALS database. The National ALS Registry – run by the Center for Disease Control’s Agency for Toxic Substances and Disease Registry – is a new program to collect, manage and analyze data about people with ALS. The goal is to gather information to better understand the disease and improve care for people with ALS. Read more: bit.ly/1v8qvRM.
Posted on: Mon, 22 Sep 2014 13:35:51 +0000