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Giving Tuesday

Embrace the spirit of the season and give to The ALS Association before the end of the year.

Embrace the spirit of the season and give to The ALS Association before the end of the year.

GIVE NOW
The Minnesota/North Dakota/South Dakota Chapter supports people living with ALS and their loved ones through services and education. We leave no stone unturned in search for the cure of this progressive neurodegenerative disease.
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.
Get Involved With Us
Help create a world without ALS by getting involved in the way that best suits YOU! When you fundraise with friends and family you take us closer to discovering a cure.

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Black Woods Blizzard Tour

Mark your calendars. The 2017 Black Woods Blizzard Tour will be held February 1-4. Join us as we ride to support those living with ALS and their families. Secure your spot today.

Get Started

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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. 

Read the Latest Issue

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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.

Learn More
Discover More Ways to Help Fight ALS
November is National Family Caregivers Month
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Resources

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
Stay Connected With Us

Sign up to receive the latest news in ALS and learn how you can continue making a difference in the search to treat and cure this disease.

You Can Help Create A World Without ALS

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.