The ALS Network – Your family of support and connection to care, research, and advocacy.
We connect need with support, questions with answers, thought leaders with new ideas, research to funding, and advocates to challenge the status quo.
Care Services
Our team of professional Care Managers provide expert advice and assistance for people with ALS, free of charge.
Research
We invest in research that will lead to better treatments and cures. We can also help connect you to clinical trials.
Advocacy
Our advocacy efforts advance important public policy initiatives that benefit our ALS community.
Support Our Mission
To partner with the ALS community as we drive the discovery of prevention strategies, treatments, and cures for ALS; provide access to quality care and connection; and promote initiatives to improve health outcomes.
Connect, Support, Chat
Connection groups are a great place for people living with ALS and their loved ones to share their personal experiences and learn more about strategies for preserving independence and maximizing quality of life.
ASK ME: ACT for ALS - Progress, Impact, and What's Next
Please watch our ASK ME educational webinar, "ACT for ALS - Progress, Impact, and What's Next.” This free online program will provide an accessible overview of the landmark legislation and what it means for the ALS community today — and what comes next. Attendees will also have the opportunity to ask questions following the presentation.
ASK ME: ALS Research and Care in 2026
Please watch our ASK ME educational webinar, "ALS Research and Care in 2026,” featuring leading ALS researchers and physicians who will share recent scientific advancements, answer your questions, and provide a preview of what to expect in the year ahead, including updates from the 2026 ALS Network Research Summit and insights on their impact on ALS care and research.
