Stories of the Season: Melissa Diaz-Viera
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
November 20, 2024
No Comments
WHAT'S HAPPENING AT PROJECT ALS
Stories of the Season: The Atfields
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
November 12, 2024
No Comments
Remembering Leigh Vierstra: Her Inspiring Words at Tables Turned on ALS in Madison
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
October 15, 2024
No Comments
ALS Super Models: The 2024 Edition
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
July 30, 2024
No Comments
STUDY REVEALS DIFFERENCES AMONG PEOPLE LIVING WITH ALS
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
June 26, 2024
No Comments
26 Years Later…
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
June 25, 2024
No Comments
BREAKING NEWS
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
November 29, 2023
No Comments
25 Years of Research Progress
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
June 7, 2023
No Comments
Joey Porrello Presented with Jenifer Estess Award
“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
June 1, 2023
No Comments
Join Brooke in the Don’t Talk-A-Thon
“ALS research is the only hope we have, so anything we can do to raise money for ALS research is crucial. It directly impacts how
May 18, 2023
No Comments
Join Brynley in the Don’t Talk-A-Thon
https://vimeo.com/825968452Brynley and the Kirchhoff family have continued to be a pillar in the ALS community. Brynley’s support for the annual Don’t Talk-A-Thon is one of
May 15, 2023
No Comments