The Leader in Global ALS Research
The ALS Association has committed more than $67 million for ALS Research. Read More »
Honor Lou Gehrig's Legacy
The ALS Registry
The National ALS Registry may be the single largest ALS research project ever created. Read More »
Fight ALS with a Third Party Event
Create Your Own Event and Raise Funds for The ALS Association. Read More »
In The Spotlight
Summertime Means Vacation Time
Traveling offers many exciting opportunities but if you have difficulty getting around, traveling brings additional challenges. Read tips for travelling with ALS.
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.