Packard Center and Project ALS host workshop to share knowledge on culturing human neurons as an essential research tool From April 28–30, more than forty
Project ALS is concerned by proposed cuts to the National Institutes of Health (NIH).
The Kirchhoffs “Happy Holidays, Project ALS Family! We are the Kirchhoff family, and we lost our father, Tom, to ALS in 2015. Our dad taught
WATCH OUR LATEST VIRTUAL TOWN HALL Watch the Project ALS Holiday Town Hall: 2025 Research Goals, where we discussed our 2025 research goals including innovative
The Hermstads “Our family has unfortunately known the devastating reality of ALS when Alex, the first of our twin daughters, began experiencing weakness at age
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
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