Resources and Support | The ALS Association

Our nationwide network of ALS Association care teams and other partners provide people living with ALS and their family and loved ones with support in communities across the country.

The professionals in this network offer many care and support programs that were designed with one thing in mind – enhancing quality of life and supporting families impacted by ALS.

Programs

Our programs and services are dedicated to providing those living with ALS and their loved ones with the information, support and tools they need, free of charge.

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Resources

If you’ve been diagnosed with ALS—or care for someone who has—quickly and easily access information pertaining to a variety of subjects related to ALS.

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Centers and Clinics

We collaborate with some of the best ALS physicians and clinics across the United States to help ensure that people living with ALS have access to specialized care, based on best practices.

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Support Groups

Support groups are a great resource for people to maintain control over their lives, to give and take the wisdom and experience that comes from living with a devastating illness.

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Webinars

With expert speakers, real-world insights, and a community that understands, our educational webinars are designed to meet the real needs of individuals living with ALS, their families, and caregivers.

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For Caregivers

Caregiving for someone with ALS has a broad and lasting impact, in both daily life and long-term well-being. Find resources specifically tailored for ALS caregivers.

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For Veterans

We’re dedicated to providing resources that will improve the lives of military veterans living with ALS, and funding research that will help us understand the link between military service and ALS.

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