The ALS Association

The ALS Association is the only non-profit organization fighting Lou Gehrig's Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.

OUR MISSION
To lead the fight to cure and treat ALS through
global, cutting-edge research, and to empower
people with Lou Gehrig’s Disease and their
families to live fuller lives by providing them
with compassionate care and support.

OUR VISION
In the quest to create a world without ALS, our vision is to care for and support all people living with Lou Gehrig’s Disease as we leave no stone unturned in our relentless search for a cure.

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