May is ALS Awareness Month
As a community defined by care, resilience, shared purpose, and a pioneering spirit, the ALS Network celebrates the Power of Community this May because together, we shape what comes next.
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: Cutting-Edge ALS Research – 2026 Packard Center Symposium Review
Please watch our ASK ME webinar, "Cutting-Edge ALS Research – 2026 Packard Center Symposium Review.” Hosted by Steve Goclowski, Vice President, Care Services, ALS Network, this informative presentation features Sarah Dougherty, PhD, Senior Director of Research, ALS Network, and Christine Vande Velde, PhD, Scientific Director, Robert Packard Center for ALS Research at Johns Hopkins.
