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 ...

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 ...

People living with amyotrophic lateral sclerosis (ALS) in the U.S. generally prefer care models where they can see multiple healthcare providers during the same visit, rather than only regularly ...

A global consortium to develop specially grown, patient-derived stem cell models will ensure Babraham Research Campus-based ...

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 ...

Breanna Olson said the tech was able to re-establish the expression and connection her ALS had eroded.

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

More than $10,000 has been raised for a local coach facing one of the toughest battles of his life. Tim Turner, a former ...

Columbia's Silence ALS program is testing spinal antisense therapy in a high‑risk patient; early EMG tests normalized.

The ALS Network today announced its support for the reintroduction of the Accelerating Access to Critical Therapies (ACT) for ALS Act (H.R.8205), bipartisan legislation led by Representative Mike ...

Joe Redmond has outlived his prognosis by years and now volunteers as a 'Pathfinder' to guide newly diagnosed patients ...