The ALS Association urges Congress to act swiftly to pass the ACT for ALS Reauthorization Act and sustain the momentum toward making ALS livable and curing it. Every day matters for people living with ...

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.

The ALS Association is now throwing its full weight behind the newly reintroduced ACT for ALS Reauthorization Act ( H.R. 8205 ), a bipartisan push to ensure that life-extending programs for people ...

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

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 ...

Every few months for the past three years, Jeff Vierstra has been receiving infusions in his spine that target and disable a ...

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 ...

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.

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 ...