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 gained greater awareness, thanks to grass roots initiatives. Learn about ALS based on a patient's experience and a ...
Former New Orleans Saints player Steve Gleason and his wife Michel talk about how ALS has changed their lives, relive his ...
The patient could make video calls, play music, stream shows, control smart home devices, shop online, and read books by ...
It’s been 10 years since the ALS Ice Bucket Challenge. Since then, the CEO Soak was created to bring together community ...
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, MS, post-traumatic brain injury? This biotech company has a target choice to make for an upcoming clinical trial — and ...
ALS, the most common form of motor neuron disease, can take a long time to diagnose, but a blood test could help doctors spot ...
People with rare genetic variants linked to degenerative brain disorders like Parkinson's disease are at increased risk of ...
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).