There is currently no cure for MND or any treatment which can improve symptoms for more than a few months. Newly published research led by ...

Brent Torres, a member of LMU's Phi Delta Theta fraternity, ran 200 miles in 10 days to raise awareness for Lou Gehrig’s ...

The OLE study is investigating the long-term safety, tolerability, and efficacy of its lead drug monepantel (MPL) in patients ...

Secondly, the young man, Liam Elmes, has quite a story he's sharing everywhere he goes. His best friend Luke Lawes was ...

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.

EXETER, N.H. — Exeter Hospital was set to discontinue advanced life support services in surrounding communities in just more ...

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

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 ...

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

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).

Life Time is hosting a 90-minute charity workout to benefit Augie's Quest to Cure ALS and the Life Time Foundation in Brookfield on Thursday, Sept. 28.The event aims to raise ...