The dad and motorcycle racer thought his lack of coordination was from being tired. It was an early ALS symptom. Now, he's ...

Answer ALS, in collaboration with ALS Therapy Development Institute (ALS TDI) and Augie's Quest, today announced plans to ...

Employees from Dixie Fish Company recently volunteered at the Harry Chapin Food Bank, spending a three-hour shift filling ...

Brooke Eby posted a "dying diary" to describe the feeling of her ALS and progressing paralysis. The 36-year-old TikToker ...

Brooke Eby, who is 35 and has ALS, is teaching us what it means to live when you know your time of death is coming sooner ...

During "Connections" on 08/11/25, Racquel Stephen is back to talk about summer camps focusing on the environment. Then, a ...

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

For many people living with Amyotrophic Lateral Sclerosis (ALS), saying ‘I love you' to a partner or child is impossible. ALS is a progressive neurological disease that leads to complete paralysis.

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.

'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.

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 ...

Over a decade after the viral "ALS Ice Bucket Challenge," these college students sparked a new trend in support of mental health. Reactions are mixed.