IMPORTANT UPDATE: The safety of the ALS community is always our top priority. Out of an abundance of caution, the Central & Southern Chapter has made changes to various chapter activities and events. Click Here for more information. We are continuing to evaluate our planned Chapter’s activities and events, in accordance with the Centers for Disease Control (CDC) and Ohio Department of Health guidelines. We are promoting everyday preventive health actions to all our participants and staff.
People living with ALS and their families remain desperate for champions to step up — to sustain and grow the day-to-day services they rely on, to bring innovation through assistive technology, to fund life-prolonging treatments, and ultimately, to find a cure for this devastating disease.
Please give generously this year-end to bring both help and hope to people facing this ravaging disease. Click here to give.
Legends of Ohio State Football-ALS Ice Bucket Challenge!
Tune in as sixty eight years of Buckeye football legacy join forces to combat ALS. Join us LIVE on YouTube, August 9 at noon as these giants of Buckeye Football are called forth one at a time to experience a bucket of icy water dumped on them by Brutus Buckeye or the Crew Cat to raise funds and awareness for ALS. Donate to your favorite football era by selecting the button below!
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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- Suzanne Schrag, Senior Director of Care Services and ALS Clinic Liaison
January 18, 2022 - Wil Armstrong: Riding Against the Wind to Fight ALS
January 14, 2022 - AAN Accepting Public Comments on Updated ALS Quality Measurement Set
January 13, 2022 - Meet Dr. John Novak, Neurologist and ALS Clinic Medical Director
January 11, 2022 - Extending Survival for People Living with ALS
January 4, 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.