We host a variety of events around the country to help raise awareness and critical funds for ALS research and care. Help us create a world without ALS by getting involved today in the way that best suits YOU!
ALS Nexus brings together leaders in the ALS community to connect, collaborate, and change the future of ALS. This is more than a conference – it’s an opportunity to spark new ideas and accelerate progress towards our goal of making ALS a livable disease until we can cure it.
Join us as we welcome Cindy’s Angels. A Texas nonprofit whose mission is to provide estate planning services—simple wills, power of attorney, and directives to start—to ALS warriors.
This lab will cover various topics, including adaptive equipment, communication in ALS, feeding tubes, and dysphagia. It promises to be an informative session for Caregivers, hosted by experts from OT, SLP, and Dietitian programs. Click here to register for the event. For more information, contact Tanya Peterson at tanya.peterson@als.org or call (616) 276-3383.
Join us on May 11th to celebrate Lou Gehrig Day with the Buffalo Bisons. Don't miss your chance to experience the excitement and help us raise funds for people living with ALS and their families.
Navigating ALS is a special series for newly diagnosed families. In our next session, we'll review the importance of balancing nutrition and a healthy di,et and the benefits for people living with ALS.
Join us on June 9th to celebrate ALS Awareness Night & Walk to Defeat ALS Kickoff with the Erie Seawolves. Don't miss your chance to experience the excitement and help us raise funds for people living with ALS and their families.
For questions, please contact Anna Patsch by emailing anna.patsch@als.org.
Join us on May 27th to celebrate Lou Gehrig Day with the Vermont Lake Monsters. Don't miss your chance to experience the excitement and help us raise funds for people living with ALS and their families.