A new book, “Letters to ALS,” shares personal stories from people living with ALS, families, and professionals. ALS is a ...

ALS is life‑changing, but new treatments, specialized care, and innovative research are bringing real hope. See how advances at University of Utah Health are shaping the future of ALS care.

Every few months for the past three years, Jeff Vierstra has been receiving infusions in his spine that target and disable a ...

The new project combines clinical data with advanced analytics and artificial intelligence in an effort to create ...

A dream came true for a Utah man living with ALS and confined to a wheelchair, thanks to the determination of family and friends who helped him reach the famous Delicate Arch.

Brooke Eby, a writer, speaker, and social media creator who lives with ALS, has been named ALS Network's Advocate of the Year. Through her advocacy work, Eby has increased awareness and raised more ...

The ALS Network is proud to announce Brooke Eby has been named the recipient of the 2026 Dean and Kathleen Rasmussen Advocate of the ...

Eric Dane is publishing a memoir about living with amyotrophic lateral sclerosis, known as ALS, the Associated Press reports. The book will hit shelves in 2026. “I wake up every morning, and I’m ...

ALS advocate and founder Leah Stavenhagen has died at 33, almost five years after she launched Her ALS Story and nearly seven years after she was diagnosed with amyotrophic lateral sclerosis (ALS).

Add Yahoo as a preferred source to see more of our stories on Google. Actor Eric Dane, best known for his role on Grey's Anatomy, passed away Thursday after battling ALS. Dane was 53 years old and ...

ALS is a heterogeneous disease. While 10-15% of cases are linked to inherited mutations, nearly 85% are sporadic.

Advocate and nonprofit founder Leah Stavenhagen has died at 33, nearly seven years after she was diagnosed with amyotrophic lateral sclerosis (ALS) Her death was announced on Sunday, Feb. 22, with an ...