Luchando por tratamientos y curas efectivos, y ayudando a las personas con ELA a vivir sus vidas al máximo.

Todo lo que hacemos avanza en la búsqueda de tratamientos y curas eficaces para la ELA

Criado para la investigación de ALS


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

People with ALS Served

Servicios de atención

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

Actions Taken Nationwide


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

NUESTRO PRÓXIMO SEMINARIO WEB PREGÚNTAME Investigación y atención de la ELA en 2023

Te invitamos a unirte a nosotros en Martes, 31 de enero de 5:00 p. m. PST - 6:30 p. m. PST (3:00 p. m. HST - 4:30 p. m. HST) to learn about the outcomes from our 13th Annual California ALS Research Summit and the impact on care and research in 2023. 

Únase a un grupo de apoyo

Los grupos de apoyo son un excelente lugar para que las personas que viven con ALS y sus seres queridos compartan sus experiencias personales y aprendan más sobre las estrategias para preservar la independencia y maximizar la calidad de vida.

294889170 418127147022498 1301934875654195080 N

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.



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.