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The ALS Association Minnesota/North Dakota/South Dakota Chapter

 

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Enroll Today!

Learn more about the National ALS Registry and how to enroll. Read More »

  NEWS & EVENTS
 

Check out our upcoming events on our Events Page 

 

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Registration is 100% full for the 2012 Black Woods Blizzard Tour!

Click here to support a rider or to get more information  

 

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Registration is open for the 2012 Kolar Toyota Walleye Tournament!

click here for more information 

 

Kwik Trip Rewards ProgramKwik Trip Logo

There are many ways to give to The ALS Association, MN/ND/SD Chapter. One easy way is by designating us as the recipient of your Kwik Rewards when you apply for a personal Kwik Card from Kwik Trip. 
Read More>

 

New Minneapolis Family Caregiver Support Group

Family Caregiver Support Group
The ALS Association, MN/ND/SD Chapter Office

UNION PLAZA BUILDING
333 Washington Ave. N., Suite 105,

Minneapolis, MN 55401

3rd Wednesday, 7:00-8:00pm 

RSVP IS NECESSARY TO
ACCESS PARKING 
Contact: Jennifer Myhre, LICSW at 1-888-672-0484, or jennifer@alsmn.org.

 

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We're on Twitter @ALSA_MNNDSD!MN_Home_Twitter_Follow_Me 

 


WELCOME!

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Former MN Twins baseball player, Kent Hrbek and his wife, Jeanie.

We Are A Local Organization With National Support! 

We welcome you to browse through the many topics on our website, but we never want to forget our main focus - people dealing with the stages of ALS. 

 If you are a person with ALS (PALS) or a caregiver, family member of friend of a person with ALS please go to Local Care Services to find out how The Minnesota Chapter can help.  Please don't hesitate to contact us at any time.

The ALS Association is the only not-for-profit voluntary health organization dedicated solely to the fight against ALS. Read More >
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Make the ALS Promise

I’d like to invite you to join us in the promise to help create a world without ALS by starting an ALS Promise Fund. Your gift will establish an enduring tribute and provide a transformative impact on our shared vision of finding the cause and developing a cure for ALS.

The ALS Promise Fund is a special fund that is created to commemorate the life of a loved one by friends and family who know the heartache of ALS. They come together to make the ALS promise by sharing their story through a multi-media website and establishing a fund to celebrate the life of someone special in their life.  Every story is unique, but each conveys the triumph of the human spirit.

Please take a minute to visit the Promise Fund website at www.alspromise.org. If you’d like to find out more please contact Sue at sue@alsmn.org  or 612.672.0484.  

IRA Charitable Rollover

You may have heard that the Tax Relief Act was extended through 2011 and will provide the opportunity to rollover your IRA in support of The ALS Association. Read More>

MN_CharitiesReviewLogoCharities Review Council

The ALS Association, Minnesota Chapter, is an approved charitable organization by the Charities Review Council. Read More>

MN_CommPartners_OpenArmsMeet Our Community Partners!

Read how local organizations are supporting The MN/ND/SD Chapter.  Read More>

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Be Prepared for Disasters Decrease the impact of a disaster. Read More>

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Click here to view our 2011 Annual Report Page
 

Traveling with a Disability

MN_Travel_VeniceIf you have wondered what to consider when traveling, the Traveling with a Disability Presentation may be helpful. 
Read More> 

 Nutrition in ALSMN_MyPlate.gov logo

Interested in nutrition in ALS?  This webinar by a dietician at Mayo Clinic in Rochester provides information and tips on maintaining good nutrition in persons with ALS.  Read More>

 

MN_Joanne_DeckerLocal Artist with ALS Creates Note Cards for Chapter

For years I enjoyed expressing nature's beauty in my drawings of flowers, mountains, trees, clouds, lakes and sunsets. When I was diagnosed with ALS in 2002, I discontinued drawing because my hands were too weak to hold any drawing tools. Read More> 

 
 
 

 


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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.


The ALS Association, Minnesota/ North Dakota /South Dakota Chapter 
 

333 North Washington Ave,
Suite 105,
Minneapolis, MN 55401
(612)672-0484 / (888)672-0484

 

North Dakota Division
PO Box 10805,
Fargo, ND 58106-0805
(701)235.2399 / (888)672-0484


All content and works posted on this website are owned and copyrighted by The ALS Association. ©2011