Fighting for effective treatments and cures, and helping people with ALS to live their lives to the fullest.

Everything we do advances the search for effective treatments and cures for ALS

Raised for ALS Research


Our research program fuels global collaboration to expedite the discovery of treatments and cures for ALS.

People with ALS Served

Care Services

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

Actions Taken Nationwide


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

OUR NEXT ASK ME WEBINAR ALS Research and Care in 2023

We invite you to join us on Tuesday, January 31 from 5:00 PM PST - 6:30 PM PST (3:00 PM HST - 4:30 PM HST) to learn about the outcomes from our 13th Annual California ALS Research Summit and the impact on care and research in 2023. 

Join a Support Group

Support 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.

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RECENT ASK ME WEBINAR ALS from the Caregivers Perspective

In honor of National Family Caregivers Month, please watch our ASK ME educational webinar, “ALS from the Caregiver’s Perspective,” as we discuss ALS from the perspective of two women who each cared for a person living with ALS.

Panelists included Mari Fuentes, who cared for her husband, filmmaker Anton Maillie, and Trish Rice, who cared for her son, writer and poet Ryan Farnsworth. We are grateful to both Mari and Trish, who continue to honor their loved ones by supporting our mission and the ALS community.


News & Stories


2023 MLK Day of Service

Brainstorm Logo

BrainStorm Cell Therapeutics Partners to Provide Public Access to Biospecimens from NurOwn’s Phase 3 ALS Study

FILE - Singer Roberta Flack poses for a portrait in New York on Oct. 10, 2018. A representative for Roberta Flack has announced that the legendary singer has ALS, commonly known as Lou Gehrig’s disease, and can no longer sing. (Photo by Matt Licari/Invision/AP, File)

Roberta Flack reveals ALS diagnosis, making it “impossible to sing”

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