
Stories of the Season: The Alfords
The Alfords “ALS has touched our family in so many ways. Our uncle, Dick Carrington, passed away from ALS at 39 and 25+ years later,

The Alfords “ALS has touched our family in so many ways. Our uncle, Dick Carrington, passed away from ALS at 39 and 25+ years later,

Shelly Stellato “I was diagnosed with ALS four years ago at the age of 32. I found Project ALS soon after and immediately saw them

Melissa Diaz-Viera “When I was diagnosed with ALS just a few weeks after my daughter’s first birthday, the fear and sadness were suffocating. In the

The Atfields “I didn’t know much about ALS until 2017 when my brother was diagnosed. Ed lived with ALS for 3 years, passing away in

Remembering Leigh Vierstra: Her Inspiring Words at Tables Turned on ALS in Madison Three weeks ago, Project ALS had the honor of hosting Tables Turned

ALS Super Models: The 2024 Edition Change is coming for ALS drug discovery. New and improved laboratory models of ALS now allow researchers and drug

STUDY OF ALS SKIN CELLS REVEALS DIFFERENCES AMONG PEOPLE LIVING WITH ALS Many doctors say it: “Every case of ALS is different.” It’s true—no two

WHY ARE WE STILL HERE 26 YEARS LATER? Dear Project ALS family, If you’d asked me 26 years ago whether I’d still be working at

Dear Friends, BREAKING NEWS: The all-new drug developed by the Project ALS Therapeutics Core for the treatment of ALS, is now moving into Phase 1

A LOOK BACK… LEARN MORE DEEPER DIVE INTO THE EARLY YEARS Project ALS Research LIVE: 25 Years of Progress The Beginning Years Hosted by Erin

“None of us would be here without Jenifer Estess. Yes, sure, there are countless other factors that brought us together today. Personally, having ALS jumps