The ALS Association’s mission is to lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with ALS and their families to live fuller lives by providing them with compassionate care and support.

In the quest to create a world without ALS, their vision is to care for and support all people living with Amyotrophic Lateral Sclerosis as they leave no stone unturned in their relentless search for a cure.

They are committed to being the:

• Preeminent organization and catalyst in funding and promoting ALS research.
• Most comprehensive provider of care and support services to the Wisconsin community through their Chapter and Clinics.
• Leading advocate and voice for the Wisconsin community.
• Recognized authority and most trusted source of information and education about ALS.