Sheri Strahl, MPH, MBA begins tenure as President & CEO of ALS Network

At the ALS Network, we connect people living with ALS in California and Hawaii with the resources they need to live a longer, more comfortable life.

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

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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.

Research

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

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Raised for ALS Research
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Actions Taken Nationwide

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.

Margie Petrakis 2016 CV Walk
UPCOMING WEBINAR

ALS Network Town Hall

Please join us on Thursday, March 7 at 5:00 PM PST / 3:00 PM HST for an opportunity to meet our new president & CEO, Sheri Strahl, MPH, MBA, and learn more about the ALS Network.

Watch Our Latest ASK ME Webinar

Please watch our ASK ME educational webinar, “ALS Research and Care in 2024” featuring Clive Svendsen, PhD, Director, Cedars-Sinai Regenerative Medicine Institute and Chair, California ALS Research Network, and Jill Goslinga, MD, MPH Assistant Professor, Neurology at UCSF Weill Institute for Neuroscience who will share updates from the 2024 California ALS Research Summit and the impact on care and research in 2024. You will also have a chance to see presentations from the 2024 Barber ALS Research Award winners.

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News & Stories

2024 February ENewsletter

February 2024 | Monthly eNewsletter from ALS Network

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Aaron Lazar Says He Won’t ‘Fight’ ALS After His Diagnosis: ‘There’s Nothing to Beat’

Broadway Aaron Lazar

Aaron Lazar’s ‘Impossible Dream’: Healing from A.L.S.

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.