Our chapter continues to provide free programs and services to support families affected by ALS.
Our chapter continues to provide free programs and services to support families affected by ALS.
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Walk to Defeat ALS
More than 180 walks take place in communities across the country February through November. Walk to Defeat ALS draws people of all ages and athletic abilities coming together to honor a loved one with the disease, to remember those who’ve passed and to show their support for the cause.
Host your own event to support our Chapter
Hold a golf tournament, run a marathon, or donate your birthday to raise funds that will help create a world without ALS.
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Celebrate a Loved One with ALS
Pay tribute to a friend or loved one affected by ALS. Each tribute is a personalized online fund designed to honor or memorialize someone special. Your Community of Hope fund creates a lasting legacy.
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Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.
Let us help you and your family cope with the day-to-day challenges of living with ALS.
For People with ALS
Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.
For Researchers
Caring for someone with ALS is hard work. We offer resources and support to help you.
For Caregivers-
Enhancing State Advocacy Efforts, A Win-Win for the ALS Community
March 14, 2022 -
Join Us as We Walk to Defeat ALS
March 10, 2022 -
ALS Association Submits Public Comments in FDA Review of Tofersen
March 8, 2022 -
More Than Just Food: The Dietitian's Critical Role in ALS Care
March 7, 2022 -
Enhanced State Advocacy Efforts Bring Fight Against ALS to Statehouses
March 3, 2022
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Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.