Using artificial intelligence, doctors have found a way to give people who lost their voice to ALS the ability to speak again ...
For columnist Kristin Neva, whose husband, Todd, has ALS, everyday moments like her son's football game are filled with both ...
It’s been 10 years since the ALS Ice Bucket Challenge. Since then, the CEO Soak was created to bring together community ...
Former New Orleans Saints player Steve Gleason and his wife Michel talk about how ALS has changed their lives, relive his ...
A chance encounter with an inspiring ALS patient, prompted Alon Ben-Noon to set up NeuroSense Therapeutics, a startup ...
People with rare genetic variants linked to degenerative brain disorders like Parkinson's disease are at increased risk of ...
Prince William and Kate Middleton have offered their support to Lindsey Burrow, the widow of late British rugby star Rob ...
It's gained greater awareness, thanks to grass roots initiatives. Learn about ALS based on a patient's experience and a ...
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.
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).