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 ...
The Healthy on MSN23h
“Here’s How I Knew I Had ALS”: A Patient’s Story, with an Expert Doctor’s InsightsIt's gained greater awareness, thanks to grass roots initiatives. Learn about ALS based on a patient's experience and a ...
To be able to manage important aspects of my environment and control access to entertainment gives me back the independence ...
A New York-based neurotech startup, Synchron, successfully implanted its brain-computer interface into a blood vessel on the ...
Former New Orleans Saints player Steve Gleason and his wife Michel talk about how ALS has changed their lives, relive his ...
It’s been 10 years since the ALS Ice Bucket Challenge. Since then, the CEO Soak was created to bring together community ...
A chance encounter with an inspiring ALS patient, prompted Alon Ben-Noon to set up NeuroSense Therapeutics, a startup ...
ALS, MS, post-traumatic brain injury? This biotech company has a target choice to make for an upcoming clinical trial — and ...
People with rare genetic variants linked to degenerative brain disorders like Parkinson's disease are at increased risk of ...
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 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).
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