JOIN JOEY IN SUPPORTING PROJECT ALS THIS #GIVINGTUESDAY https://vimeo.com/769026584 Today is Giving Tuesday and Joey Porrello, a dear friend of Project ALS and a passionate
https://vimeo.com/773999009 Dr. Jinsy Andrews is the director of neuromuscular clinical trials at Columbia University Irving Medical Center, leads the Clinical Unit at the Project ALS
Wondering why you should support Project ALS for Giving Tuesday? Brynley Kirchhoff, a close friend of Project ALS and a fierce young woman in her
The Project ALS Tomorrow is Tonight 24th annual gala raised close to $1 million.
ALS has been a notoriously difficult disease to address therapeutically because of its heterogeneity in the clinic. The progression and symptoms of ALS differ broadly
THIS WEEK ONLY, Gwen, Desi, and Erin—of Her ALS Story—want YOU to participate in the Project ALS online auction. Her ALS Story is a group
In order to prevent, treat, or cure diseases, scientists rely on methods for identifying consistent mechanisms behind disease, and efficiently testing potential therapies on a
Motor neurons project out to the muscles in our limbs to drive muscle contraction, allowing us to speak, breathe, and move. These cells are housed
In 2020, Cathy and Richard called Project ALS after hearing about the development of a novel antisense oligonucleotide (ASO) therapy for people living with FUS ALS. So was born NextGen ALS, a Weber family initiative in collaboration with Project ALS that is committed to raising funds for targeted research toward treatments and cures for genetic forms of ALS.
Project ALS co-founder Valerie Estess sat down with Charles River to talk about how Project ALS is disrupting the norm in order to bring the
Project ALS was lucky to join five other ALS organizations at the first in-person meeting of the ALS Collaborative Cohort to discuss issues of access and inclusion within the ALS community
Last month, Coach John Campo and Gettysburg Bullets Baseball held their annual “Take ALS Yard” event at Kirchhoff Field
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