The CEO Soak is on Thursday, Sept. 19 from 1 p.m. - 3 p.m. in St. Petersburg. People can sign up for the cause and help raise ...

For columnist Kristin Neva, whose husband, Todd, has ALS, everyday moments like her son's football game are filled with both ...

Prince Middleton and Kate Middleton shared their support on X for a new book written by late rugby star and ALS advocate Rob ...

A New York-based neurotech startup, Synchron, successfully implanted its brain-computer interface into a blood vessel on the ...

The fourth annual Walk to End ALS, sponsored by M.L. McDonald and honoring the memory of Lincoln’s Joseph Kiley, will take ...

Marshall University ALS Clinic and Marshall Health’s gastroenterology and hepatology services are now located in the new ...

It’s that time of year when ALS New Mexico brings the community together for their annual Walk n’ Wheel. This year is the 24th ALS walk and the funds raised will stay in New Mexico.

The Muscular Dystrophy Association (MDA) is proud to announce a new clinical research grant of $500,000 over three years, awarded to Sabrina Paganoni, MD, PhD, of Massachusetts General Hospital (MGH).

Hundreds gathered at SoWa in the South End for the third annual Captain’s Ball – honoring the life of Pete Frates and ...

A man with ALS became the first person to control an Amazon Alexa with his thoughts via an implanted brain-computer interface ...

The ALS Association is hosting a walk to support people with ALS on Saturday, Sept. 28, at Oakledge Park, 11 Flynn Ave., in Burlington, starting at 10 a.m.

The CEO Soak brings together community leaders to get soaked once again for ALS while raising funds and awareness for The ALS Association.