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Five Canadian students personally affected by ALS each received $2,500 from ALS Canada's Kevin Daly Bursary.

A filmmaker with amyotrophic lateral sclerosis (ALS) is working with his friends to finish a documentary about death.

Patients' personal preferences and not disease severity were linked to requests for medically assisted death in people with ALS in a study.

Columnist Juliet Taylor shares what she wishes she'd known about the emotional weight of being a caregiver before ALS entered the picture.

Columnist Kristin Neva has lived for 16 years with grief and stress, but here writes about finding moments that push ALS into the background.

An ALS study testing PHENOGENE-1A as an add-on to riluzole has completed enrollment and randomization of about 105 adults.

More than 2,000 people joined the third annual ALS Nexus Conference to learn about innovations in care and discuss community goals.

Diagnosed with ALS, a mother of six discovered her purpose, dignity, and community through MDA's support and accessibility resources.

A very different approach to ALS treatment is now entering an early-stage clinical trial 🔗 https://bit.ly/4xh5dGn

People with ALS who are exposed to high levels of certain pollutants predisease have worse survival outcomes, according to a study.