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 * About Us
   * Our Mission, Vision, and Values
   * What We Do
   * Where We Serve
   * Our Impact
   * Financial Information & Institutional Effectiveness
   * Leadership
   * News & Stories
   * Calendar of Activities & Events
   * Contact Us
 * Understanding ALS
   * What is ALS?
   * Who Gets ALS?
   * Symptoms and Diagnosis
   * Genetic Testing for ALS
   * ALS Glossary
 * Services
   * Our Care Services
   * Newly Diagnosed
   * ALS Clinics and Centers
   * Emotional Support
   * Treatments and Therapies
   * ASK ME – Educational Webinars
   * Living With ALS
     * Resource Guides for Daily Living
     * Caregiver Support
     * Speech and ALS
     * Managing Speech Changes
     * Financial Information for People With ALS
     * Medicare and Home Health Information
     * ALS Registry
     * Emergency Preparedness for People with ALS
     * Nutrition and ALS
   * Resources for Military & Veterans
   * For Caregivers
   * Support for Families
   * Recursos en Español
   * Bereavement Support
 * Research
   * Our Approach
   * Research We Fund
   * Clinical Trials
   * Our Experts
 * Advocacy
   * Become an Advocate
   * Public Policy Priorities
 * Get Involved
   * Community Outreach Events
   * Create a Fundraiser
   * Volunteer
   * Sign Up for Our Newsletter
 * Give
   * Donate Now
   * Ways to Give
     * Gifts in Tribute
     * Leave a Legacy
     * Donor Advised Funds
     * Donate a Vehicle
     * Workplace Giving
     * Matching Gifts
     * Donor Bill of Rights


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 * About Us
   * Our Mission, Vision, and Values
   * What We Do
   * Where We Serve
   * Our Impact
   * Financial Information & Institutional Effectiveness
   * Leadership
   * News & Stories
   * Calendar of Activities & Events
   * Contact Us
 * Understanding ALS
   * What is ALS?
   * Who Gets ALS?
   * Symptoms and Diagnosis
   * Genetic Testing for ALS
   * ALS Glossary
 * Services
   * Our Care Services
   * Newly Diagnosed
   * ALS Clinics and Centers
   * Emotional Support
   * Treatments and Therapies
   * ASK ME – Educational Webinars
   * Living With ALS
     * Resource Guides for Daily Living
     * Caregiver Support
     * Speech and ALS
     * Managing Speech Changes
     * Financial Information for People With ALS
     * Medicare and Home Health Information
     * ALS Registry
     * Emergency Preparedness for People with ALS
     * Nutrition and ALS
   * Resources for Military & Veterans
   * For Caregivers
   * Support for Families
   * Recursos en Español
   * Bereavement Support
 * Research
   * Our Approach
   * Research We Fund
   * Clinical Trials
   * Our Experts
 * Advocacy
   * Become an Advocate
   * Public Policy Priorities
 * Get Involved
   * Community Outreach Events
   * Create a Fundraiser
   * Volunteer
   * Sign Up for Our Newsletter
 * Give
   * Donate Now
   * Ways to Give
     * Gifts in Tribute
     * Leave a Legacy
     * Donor Advised Funds
     * Donate a Vehicle
     * Workplace Giving
     * Matching Gifts
     * Donor Bill of Rights

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Walkers, rollers, runners, and riders join us at an upcoming event to help cure
ALS!

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THE ALS NETWORK – YOUR CONNECTION TO CARE, RESEARCH, AND ADVOCACY.

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Newly Diagnosed? Start Here
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WE CONNECT NEED WITH SUPPORT, QUESTIONS WITH ANSWERS, THOUGHT LEADERS WITH NEW
IDEAS, RESEARCH TO FUNDING, AND ADVOCATES TO CHALLENGE THE STATUS QUO.


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People with ALS served per year


CARE SERVICES

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

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RESEARCH

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help connect you to clinical trials.

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ADVOCACY

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

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SUPPORT OUR MISSION

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.

DONATE

One-time or monthly donations help us provide free services to people living
with ALS.

VOLUNTEER

Enthusiastic volunteers are key to our success! Volunteers can contribute in
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PARTICIPATE

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Establish a lasting legacy in honor or memory of someone special's battle with
ALS using our easy tribute fund web pages.


CONNECT, SUPPORT, CHAT

Connection 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.

Find a Connection Group

Play Video


2024 BAY AREA PENINSULA WALK & ROLL TO CURE ALS LIVESTREAM

Join us for the 25th annual Bay Area Peninsula Walk & Roll to Cure ALS IN PERSON
and ONLINE via our Livestream, thanks to our Accessibility and Inclusivity
Sponsor, Mitsubishi Tanabe Pharma America!

Since 2000, Bay Area Walk participants and supporters have raised funds to power
the ALS Network’s mission-critical activities related to care, research and
advocacy.


Watch here


ASK ME: FINDING HOPE - A PHYSICIAN'S PERSPECTIVE ON EMOTIONS AND MANAGING ALS

Join us for our ASK ME educational webinar, "Finding Hope: A Physician’s
Perspective on Emotions and Managing ALS" featuring Jeffrey Rosenfeld, MD, PhD,
of the Neuromuscular ALS/NMD Multidisciplinary Clinic at Loma Linda University
Health on Wednesday, November 13 at 5:00 PM PST/3:00 PM HST.
RSVP TODAY




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ALS NETWORK ANNOUNCES RESEARCH GRANT AWARDED TO AUTTX, LLC.

KION: 25TH ANNIVERSARY OF THE ALS NETWORK’S MONTEREY BAY WALK & ROLL TO CURE ALS

BENITOLINK: ALS WALK HAPPING OCT. 19




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