webmn.alsa.orgThe ALS Association Minnesota/North Dakota/South Dakota Chapter

ALS Ice Bucket Challenge Progress Sign up | Login | Find local services | Search Close | Menu Close Minnesota North Dakota South Dakota Chapter Find local services Certified Centers & Clinics Support Groups Calendar of Events View Ice Bucket Progress Donate Certified Centers & Clinics Support Groups Calendar of Events About ALS About Us Our Research Local Care Services Advocate Get Involved Donate The ALS community is challenging everyone to do anything and everything they can to cure ALS. Learn More The ALS community is challenging everyone to do anything and everything they can to cure ALS. Learn More 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 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. Find Services Take Action Raise Awareness Latest Research Find Services Take Action Raise Awareness Latest Research 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. What is Respite? Being a family caregiver, while a fulfilling role, can consume a great deal of physical, mental, and emotional energy. Respite simply means an interval of rest or relief. The ALS Association will reimburse a partner agency in your area to step in as caregiver for up to 18 hours each month so that you can take a break. Learn More Today Connecting ALS Have you heard about our new podcast addressing the disease from virtually all angles? New episodes of Connecting ALS are released each month. Subscribe today! Subscribe 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 Discover More Ways to Help Fight ALS Advancing Global ALS Research Find Out How 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 In The News ALS Community Responds to FDA Guidance Document with Call for More Urgency, Flexibility November 7, 2019 Show Appreciation to a Caregiver During National Family Caregivers Month November 1, 2019 ALS Association Contributes $3.3 Million to Fund Groundbreaking Genome-Sequencing Database October 22, 2019 High School Students Spread Awareness and Raise Money for ALS Research October 11, 2019 Read the Latest Chapter News 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. Join Us 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. Give Now Give Now Give Monthly Give In Honor Or Memory End Hide -- Learn About Other Ways to Give Privacy Policy | Link Policy | Important Information | Contact Us | Manage Your Profile 1919 University Ave W Suite 175 St. Paul, MN 55104 (888) 672-0484 All content and works posted on this website are owned and copyrighted by The ALS Association. ©2020 Lou Gehrig® used with permission of the Rip Van Winkle Foundation / www.LouGehrig.com...