The ALS Association today applauded the reintroduction of the Accelerating Access to Critical Therapies for ALS (ACT for ALS) Reauthorization Act (H.R. 8205), bipartisan legislation to extend and ...

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ALS is life‑changing, but new treatments, specialized care, and innovative research are bringing real hope. See how advances at University of Utah Health are shaping the future of ALS care.

In recognition of National Caregivers Day, caregivers for people living with amyotrophic lateral sclerosis (ALS) across ...

There is no cure for this neurogenerative disease. CBS News Chief Medical Correspondent Dr. Jon Lapook sat down with a ...

Dentsu Lab’s Project Humanity is building interfaces that translate minute muscle signals and brainwaves into full digital ...

A new book, “Letters to ALS,” shares personal stories from people living with ALS, families, and professionals. ALS is a ...

A dream came true for a Utah man living with ALS and confined to a wheelchair, thanks to the determination of family and friends who helped him reach the famous Delicate Arch.

ALS advocate and founder Leah Stavenhagen has died at 33, almost five years after she launched Her ALS Story and nearly seven years after she was diagnosed with amyotrophic lateral sclerosis (ALS).

ALS caregivers in Canada face significant stress, anxiety, and burnout. ALS Canada now offers free national virtual counseling, support groups, and resources. Caregivers can access up to four free ...

Advocate and nonprofit founder Leah Stavenhagen has died at 33, nearly seven years after she was diagnosed with amyotrophic lateral sclerosis (ALS) Her death was announced on Sunday, Feb. 22, with an ...