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Submission declined on 19 May 2026 by Devonian Wombat (talk). This draft's references do not show that the subject meets Wikipedia's criteria for inclusion for organizations and companies. The draft requires multiple published secondary sources that:
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This draft has been resubmitted and is currently awaiting re-review. |
This draft is not adequately supported by reliable sources. Wikipedia's verifiability policy requires that all content be supported by reliable sources.
Declined by Dan arndt 3 months ago.
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| Founded | 1991 |
|---|---|
| Type | Nonprofit organization |
| Legal status | 501(c)(3) |
| Headquarters | Woodland Hills, California, U.S. |
| Staff | ~60 (2024)[1] |
| Website | alsnetwork |
Formerly called | The ALS Association Golden West Chapter/ALS Golden West |
The ALS Network (previously named the ALS Association Golden West Chapter and briefly named ALS Golden West) is a nonprofit 501(c)(3) organization in the United States focused on services for people living with Amyotrophic Lateral Sclerosis (ALS), funding ALS research, and supporting public policy related to the disease. The organization was founded in 1991 as the Golden West Chapter of the ALS Association and became independent in 2023, after which they adopted the name ALS Network in 2024. The organization operates across California, Hawaii, and beyond.[3]
ALS Network states that its mission is "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."[4]
ALS Network provides care management to individuals with ALS and their families, often in collaboration with ALS specialty clinics, with services provided at no cost to people living with ALS and caregivers. Care managers support medical referrals, equipment loans, insurance navigation, home safety assessments, psychosocial support, and coordination with multidisciplinary teams.
The care program includes access to various ALS multidisciplinary treatment centers and affiliated clinics, and coordinates monthly Connect, Support, Chat groups for specific communities.[11]
ALS Network funds ALS research with an emphasis on innovative and community-informed projects. In 2024 and 2025, the organization established a Scientific Advisory Committee and a Community Research Committee. They have also launched various drug-repurposing initiatives with academic and national lab partner.
Each January, the ALS Network hosts an annual webinar highlighting outcomes of the year's ALS Network Research Summit, which includes scientific presentations and discussions related to ALS research, presented by participants from California, Hawaii, the U.S., and beyond.[12]
The organization participates in local, state, and federal advocacy efforts related to ALS research funding, healthcare access, and disability policy.[13]
Each May, the organization celebrates ALS Awareness Month in collaboration with local government offices. In 2025, ALS Awareness Month proclamations were signed by: California Governor Newsom, Thousand Oaks Mayor David Newman, Hawaii Governor Josh Green, Hawaii County Mayor Kimo Alameda, and Maui Mayor Richard Bissen.[14]
Throughout the years, the ALS Network has supported legislation related to ALS research, caregiving, veterans’ benefits, and healthcare access, including:[15][16]
ALS Network hosts community awareness and peer-to-peer fundraising events in key areas throughout the nation in California, Hawaii, Massachusetts, and more, with events including the Walk & Roll to Cure ALS and endurance events.
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