ALS is a progressive neurodegenerative disease and we need your help to find a cure.
ALS is a progressive neurodegenerative disease and we need your help to find a cure.
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We're Moving!
Our Chapter headquarters will be relocating from Minneapolis to St. Paul, MN, in February, 2019. Click below for more on why we're so excited about our new space!
Have you seen our eNewsletter?
Check it out! Our chapter eNewsletter, the Source, is full of information about our programs and services, events, volunteer opportunities, and the latest in ALS research. Make sure you stay up to date with all that's going on here at the Chapter and throughout the ALS community.
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Volunteer
Our programs and services for people living with ALS and their families would not be possible without volunteers. Whether you are looking to volunteer one day a year at a special event or weekly for a family affected by ALS, we have something for you.
Get Involved
Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.
Let us help you and your family cope with the day-to-day challenges of living with ALS.
For People with ALS
Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.
For Researchers
Caring for someone with ALS is hard work. We offer resources and support to help you.
For Caregivers- New Report Highlights Heightened Risk of ALS in Military
March 21, 2019 - New Education Guides Help to Lessen Fear, Uncertainty for Youngest Affected by ALS
March 11, 2019 - ALS Disability Insurance Access Act Reintroduced in 116th Congress
March 1, 2019 - ALS Disability Insurance Access Act Reintroduced
February 27, 2019
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Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.