CA Taxpayers Can Now Fund ALS Research – Use Code 447 on CA Income Tax Returns

Learn More

The ALS Network – Your connection to care, research, and advocacy.

Get Services

We connect need with support, questions with answers, thought leaders with new ideas, research to funding, and advocates to challenge the status quo.

+
People with ALS served per year

Care Services

Our team of professional Care Managers provide expert advice and assistance for people with ALS, free of charge.

How We Can Help

Research

We invest in research that will lead to better treatments and cures. We can also help connect you to clinical trials.

Learn More
$M
Raised for ALS Research
+
Actions Taken Nationwide

Advocacy

Our advocacy efforts advance important public policy initiatives that benefit our ALS community.

TAKE ACTION

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.

Donate

One-time or monthly donations help us provide free services to people living with ALS.

Volunteer

Enthusiastic volunteers are key to our success! Volunteers can contribute in many ways - through their time, knowledge, skills and leadership.

Fundraise

You can host an event to help support the ALS community and push towards treatments and cures. It's easy to get started!

Participate

Sign up for one of our fundraising events and start or join a team to raise money for ALS Network!

Advocate

As an ALS advocate, you can help change the laws and policies that affect thousands of people with ALS and their families.

Celebrate

Establish a lasting legacy in honor or memory of someone special's battle with ALS using our easy tribute fund web pages.

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.

Find a Connection Group
Margie Petrakis 2016 CV Walk

ASK ME: ALS Research and Care in 2025

Please join us virtually on Tuesday, February 25 for ASK ME: ALS Research and Care in 2025 at 5:00pm PST / 3:00pm HST. This event will feature leading ALS researchers and physicians who will discuss recent scientific advancements, answer your questions, and preview what to expect in the year ahead. During this informative program, you will hear from 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, who will share updates from the 2025 ALS Network Research Summit and the impact on care and research in 2025. 
RSVP TODAY

2024 Los Angeles Walk & Roll to Cure ALS Livestream

Join us for the 24th annual Los Angeles Walk & Roll to Cure ALS IN PERSON and ONLINE via our Livestream, thanks to our Accessibility and Inclusivity Sponsor, Mitsubishi Tanabe Pharma America!

Watch here
Video
Play Video

News & Stories

Browse ALL Posts
2025 February ENewsletter

February 2025 | Monthly eNewsletter from ALS Network

ALSN ALSU Logo (800 X 533 Px)

15 ALS Nonprofits Collaborate to Form ALS United: A New Era of Innovation and Impact

02 2025 BHM Research Paper Springer Nature Link(1)

Springer Nature Link: Racial Disparities in the Diagnosis and Prognosis of ALS Patients in the United States

Stay up-to-date on ALS care, research, and advocacy, as well as upcoming activities and events, and learn more about the many ways ALS Network is helping the ALS community.

Sign Up for Our Newsletter