About Us
The ALS Association’s vision is to create a world without ALS.
The ALS Association’s mission is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
What is ALS?
ALS (amyotrophic lateral sclerosis) is a degenerative disease of the central nervous system. ALS results in the progressive weakness of voluntary muscles which often leads to total paralysis. There is no known cause or cure for ALS. People with ALS typically live between two and five years after being diagnosed.
How does The ALS Association help?
We fulfill our mission by offering programs, services, and equipment free of charge to anyone affected by ALS residing in Minnesota, North Dakota, and South Dakota. Our work is funded by individual donations and the money raised by our special events.
Durable Medical Equipment Loan Pool
Communication and Assistive Device Program
Funding for these programs comes from individual donations and money raised through our special events.
The ALS Association’s vision is to create a world without ALS.
The ALS Association’s mission is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
What is ALS…
Issue Areas Include
- Disability
- Health & Medicine
Location
- 1919 University Avenue West, St. Paul, MN 55104, United States
Suite 175
