Thank you to everyone who attended the 25th annual Bay Area Peninsula Walk & Roll to Cure ALS today! Over 150 registered participants have helped raise over $122,000 towards our goal of $250,000! All proceeds raised will advance the ALS Network’s mission in finding effective prevention strategies, treatments and cures for ALS. We thank every single one of you who came out to support #ourALScommunity. If we missed you at the walk you can still donate today at alswalkbayarea.org.
ALS Network
Non-profit Organization Management
Woodland Hills, CA 1,049 followers
Everything we do advances the search for effective treatments and cures. It is only together that we will end ALS.
About us
We connect need with support, questions with answers, thought leaders with new ideas, research to funding, and advocates to challenge the status quo. For more information about the ALS Network, please visit www.alsnetwork.org or send an email to [email protected].
- Website
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https://alsnetwork.org
External link for ALS Network
- Industry
- Non-profit Organization Management
- Company size
- 11-50 employees
- Headquarters
- Woodland Hills, CA
- Type
- Nonprofit
Locations
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Primary
PO Box 7082
Woodland Hills, CA 91365, US
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PO Box 11284
Honolulu, HI 96828, US
Employees at ALS Network
Updates
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Tune in to ALS Network's livestream of the Bay Area Walk & Roll to Cure ALS happening now! Join us virtually from wherever you are and watch our special program! Watch now at: https://lnkd.in/gim-VVws
ALS Network Bay Area Peninsula Walk and Roll
https://www.youtube.com/
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TODAY (10/5) is the ALS Network's 25th annual Bay Area Peninsula Walk & Roll to Cure ALS! Check-in begins at 10 am at Coyote Point Recreation Area. We can't wait to see you! And if you can't make it in person, be sure to tune into our livestream at https://lnkd.in/gBGVPYPg, courtesy of our Accessibility and Inclusivity Sponsor, Mitsubishi Tanabe Pharma America. Please make a gift in support of #ourALScommunity at alswalkbayarea.org
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TOMORROW (10/5) is our 25th annual Bay Area Peninsula Walk & Roll to Cure ALS. Join ALS Network on Saturday, October 5 at Coyote Point Recreation Area. Check out our schedule of events and click the link in bio or visit alswalkbayarea.org for more event details and FAQ. Want to participate but can’t attend? The walk will be available via our Livestream thanks to our Accessibility and Inclusivity Sponsor, Mitsubishi Tanabe Pharma America at https://lnkd.in/gBGVPYPg All funds raised support the local mission priorities of the ALS Network in care services, public policy, and research.
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Social media is a powerful tool that helps create and sustain relationships with timely communication. The ALS Network has a robust presence across many social media platforms and channels. If you are participating in an ALS Network Walk & Roll to Cure ALS or Endure to Cure ALS event, we invite you to follow our event-specific social accounts on Facebook and Instagram. Like, share and comment on our posts to help spread our mission. Follow us on Instagram, Facebook, Linkedin, X, and YouTube to stay connected with #ourALScommunity, to raise #ALS awareness and support. Learn more and get links to all of ALS Network's social media pages: https://ow.ly/82jy50TCNb7.
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Please join us for Connect, Support, Chat: Trach and Vent on Thursday, October 10 at 1:00 PM PDT/10:00 AM HST. Contact ALS Network Care Managers Robin Eller, RCP at [email protected] or Kathleen Kelsey, RCP at [email protected] for more information on how to participate.
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The ALS Network commends Office of California Governor Gavin Newsom for signing AB 2613 into law! This bill creates the Jacqueline Marie Zbur Rare Disease Advisory Council (RDAC), ensuring that Californians with ALS and other rare diseases have a strong voice in shaping healthcare policies that impact their lives. Huge thanks to Assembly Member Rick Zbur for leading this critical effort and supporting the 1-in-10 Californians living with a rare disease.
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Please join us for Connect, Support, Chat: Living with ALS Under 50 on Tuesday, October 15 at 4:00 PM PDT/1:00 PM HST. Please contact Care Managers Emma Karavardanyan, M.A. at [email protected] or Shannan Sonnicksen, LCSW, MPH, at [email protected] for more information about how to participate
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We invite you to join us for Connect, Support, Chat: For Caregivers of ALS Clients Affected by FTD on Wednesday, October 9 at 3:00 PM HST. For more information and to register via Zoom, please contact Rex Like, MA, ALS Network Care Manager, at [email protected].
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We are honored to have joined in celebrating the debut album of Broadway actor and Essey award winner, Aaron Lazar in Hollywood this past weekend. It was truly an event filled with love, music, and inspirational remarks. The star-studded album titled “Impossible Dream” features several Broadway stars celebrating the fighting spirit of #ourALScommunity, which includes Aaron himself, who has been living with #ALS since 2022, to dream the impossible in the face of adversity. ALS Network is grateful to Aaron Lazar, producers Kitt Wakeley and Jonathan Estabrooks, and the entire Impossible Dream album team for their support of our mission-critical activities in care services, research developments, and advocacy efforts. A portion of sales support the ALS Network and #ouralscommunity. You can order your copy today at https://lnkd.in/grCbR7fv.