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FOX11: LA’s Hailey Winslow on the 2024 Los Angeles Walk & Roll to Cure ALS

December 8, 2024 Comments Off on FOX11: LA’s Hailey Winslow on the 2024 Los Angeles Walk & Roll to Cure ALS

Our deepest gratitude to Hailey Winslow, Susan Hirasuna, and FOX 11 news for your thoughtful segment about the 24th annual Los Angeles Walk & Roll to Cure ALS. We cannot say thank you enough to Hailey for joining us at Dignity Health Sports Park as this year’s emcee, even taking the #ALSIceBucketChallenge, on behalf of…

December 2024 | Monthly eNewsletter from ALS Network

December 6, 2024 Comments Off on December 2024 | Monthly eNewsletter from ALS Network

Our December eNewsletter is in your inbox now, or you can view it online! This month, we celebrate our ALS Network family! Throughout this month, we will showcase members of the ALS community and their dedication to cure ALS together. Join us as we prepare for our LA Walk & Roll to Cure ALS this…

Honoring the Producers of the Impossible Dream Album

December 6, 2024 Comments Off on Honoring the Producers of the Impossible Dream Album

The ALS Network (formerly ALS Golden West) is proud to announce Kitt Wakeley, David Das, and the Producers of the Grammy Award-nominated album, Impossible Dream, as our 2025 Essey Spotlight Award Honorees. The list of esteemed honorees includes the following exceptional team of music industry professionals: Grammy Award winner Kitt Wakeley (pictured left above), David…

ALS Network Holiday Card Features Artwork of Gayle Garner Roski

December 5, 2024 Comments Off on ALS Network Holiday Card Features Artwork of Gayle Garner Roski

Before her passing from ALS in 2020, Gayle Garner Roski described watercolor as a “medium of magic.”  Gayle once explained she loved “watercolors because they have a way of being unpredictable, and yet they can transform us by taking an instant of time and holding it still, so that we may reflect on it and…

Help Shape ALS Network’s 2025 Advocacy Priorities

December 5, 2024 Comments Off on Help Shape ALS Network’s 2025 Advocacy Priorities

At the ALS Network, we deeply value the voices of people living with ALS, their caregivers, and others who have been impacted by this disease. Your experiences and insights are essential as we set our state and national advocacy priorities that truly reflect the needs of the ALS community. The ALS Network has developed an…

FOX 11: 24th annual Walk & Roll to Cure ALS happening in LA

December 5, 2024 Comments Off on FOX 11: 24th annual Walk & Roll to Cure ALS happening in LA

This weekend is the Walk & Roll to Cure ALS. ALS Network president and CEO Sheri Strahl joined FOX 11 to talk about the event and the work the nonprofit does to help raise funds and awareness for ALS. Thank you to Elex Michaelson and FOX 11 for taking the time to help us raise…

ALS Network Seeks Support For the ALS Community

December 2, 2024 Comments Off on ALS Network Seeks Support For the ALS Community

Giving Tuesday & Year-End Tax-Deductible Gifts Support Care, Research, and Advocacy Efforts December 2, 2024 – FOR IMMEDIATE RELEASE LOS ANGELES – Support from individual and corporate donors fuels the life-improving work of the ALS Network, formerly ALS Golden West. The ALS Network offers hope and help throughout the ALS community by providing localized, free…

Giving Tuesday: Stories from families helped by your support

December 2, 2024 Comments Off on Giving Tuesday: Stories from families helped by your support

On Giving Tuesday your support can create a lasting impact. Your gift will help provide care services, resources, and community connection; fuel groundbreaking research; and advance important public policy initiatives that benefit the ALS community. Learn more about the families helped by your support this Giving Tuesday. Meet Etzael Jimenez A donation to the ALS…

ALS NETWORK RECOGNIZES NATIONAL FAMILY CAREGIVERS MONTH

November 26, 2024 Comments Off on ALS NETWORK RECOGNIZES NATIONAL FAMILY CAREGIVERS MONTH

Each November, the ALS Network recognizes National Family Caregivers Month and pays tribute to the individuals who provide daily care and support to loved ones who are living with the challenges of ALS. Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s Disease, is a fatal, neurodegenerative illness that affects nerve cells in the brain…

California’s AB 2123 to offer caregivers in access to paid family leave

November 15, 2024 Comments Off on California’s AB 2123 to offer caregivers in access to paid family leave

Starting January 1, 2025, California Assembly Bill 2123 (AB 2123) will make it easier for family caregivers to access paid family leave (PFL). The law removes the requirement for employees to use up to two weeks of their vacation time before receiving PFL benefits, allowing caregivers to take up to eight weeks of leave without…