The ALS Network – Your 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: Preservation of Vital Capacity as a Goal of ALS Drug Development: The NP001 Story
Please watch our ASK ME educational webinar, "Preservation of Vital Capacity as a Goal of ALS Drug Development: The NP001 Story" featuring Michael McGrath, MD, PhD, Professor of Medicine, Laboratory Medicine, and Pathology, UCSF.
ASK ME: ALS Research and Care in 2025
Please watch our ASK ME educational webinar, "ALS Research and Care in 2025" featuring Clive Svendsen, PhD, Executive Director, Regenerative Medicine Institute at Cedars-Sinai Medical Center and Chair, ALS Network Scientific Advisory Committee, and Catherine Lomen-Hoerth, MD, PhD, Clinic Director, ALS Treatment and Research Center at UCSF Medical Center.
