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 ...
To be able to manage important aspects of my environment and control access to entertainment gives me back the independence ...
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 ...
ALS, MS, post-traumatic brain injury? This biotech company has a target choice to make for an upcoming clinical trial — and ...
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 Middleton and Kate Middleton shared their support on X for a new book written by late rugby star and ALS advocate Rob ...
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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“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 ...
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