Brent Torres, a member of LMU's Phi Delta Theta fraternity, ran 200 miles in 10 days to raise awareness for Lou Gehrig’s ...
Hundreds gathered at SoWa in the South End for the third annual Captain’s Ball – honoring the life of Pete Frates and ...
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.
Today, Google Classroom is a powerful tool in K–12 schools around the world. It recently marked 10 years since its initial ...
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).