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 ...

Former New Orleans Saints player Steve Gleason and his wife Michel talk about how ALS has changed their lives, relive his ...

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

A simple blood test has been shown to be 98% accurate at distinguishing between patients with ALS and those without the ...

ALS, the most common form of motor neuron disease, can take a long time to diagnose, but a blood test could help doctors spot ...

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 ...

ALS and FTD, frontotemporal dementia impact millions of people each year as both may seem like two totally different diseases ...

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).

It's gained greater awareness, thanks to grass roots initiatives. Learn about ALS based on a patient's experience and a ...