National ALS Registry Background & History
The ALS Association is the leading organization championing the establishment of a national ALS patient registry that will identify cases of ALS in the United States and collect information that will advance research into the cause, treatment and cure for Lou Gehrig’s Disease.
Each person battling ALS is a hero.
Family, friends, and all those who observe the way ALS patients fight this disease see their courage, resolve, and dignity. Registering and taking the surveys can help make a difference in the lives of those living with ALS today and for generations to come.