Eric Brunner thought his coordination issues were from exhaustion. It turns out, they were early signs of ALS. Now he's ...

Neurologist and Duke ALS Clinic Director Richard Bedlack “stitches strength” for his patients, showing the powers of hope.

For around 90% of cases of ALS, there is no known family history or a genetic mutation linked to ALS. Article continues below this ad For 5% to 10% of cases, there is a family history of the disease.

An auction to help Creston Nelson, a state Senate staffer, is open through today to help her family pay uncovered health care ...

On Tuesday, June 6, the Atlanta Braves will celebrate Lou Gehrig Day to increase awareness for amyotrophic lateral sclerosis (ALS).

'Living With ALS Is a Marathon' The couple's reality is now a far cry from that video in the summer of 2020. Living with ALS has been an immense challenge, Coultas said.

Instead, he's driving across the country, alone, interviewing people with the disease ALS along the way."It's good to think and heal and understand what's going through your head," Mauriello said.

ROANOKE, VA (WFXR) — A Roanoke man living with ALS, also known as Lou Gehrig’s Disease, is working to spread awareness and understanding about the disease, and make it livable for everyone ...

The ALS Association webpage for the Ice Bucket Challenge credits the massive trend to three men who were living with the disease: Anthony Senerchia, Pete Frates and Pat Quinn, all three of whom ...

Now his daughter, Ashley, is continuing her father’s fight to help others living with this disease. This week, Ashley met with state senators in Albany to discuss the "Dennis Crawley Genetic ...