2022 Tomorrow is Tonight Auction
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
October 25, 2022
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WHAT'S HAPPENING AT PROJECT ALS
Motor Neurons in a Dish: The Scientific Breakthrough that Fundamentally Changed ALS Research
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
September 26, 2022
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Viruses for Good, Not Evil: Tools for ALS Therapy Delivery
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
July 17, 2022
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NextGen ALS: A Weber Family Initiative
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.
June 24, 2022
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Valerie the Disruptor
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
June 10, 2022
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2022 Tambourine ALS Collaborative Cohort
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
May 25, 2022
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Gettysburg Baseball’s Take ALS Yard 2022
Last month, Coach John Campo and Gettysburg Bullets Baseball held their annual “Take ALS Yard” event at Kirchhoff Field
May 10, 2022
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New Model and Gene Targeting Approach Show Promise for ALS Therapies
Researchers from the Project ALS Therapeutics Core at Columbia (the Core), in a groundbreaking collaborative effort with Ionis Pharmaceuticals, have developed a new tool for studying ALS mechanisms and therapies, as well as a novel approach for treating ALS caused by mutations…
March 10, 2022
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The McDaniel Family
“I was diagnosed with ALS in February 2020 after a frustrating year of searching for answers & even longer of progressing symptoms…”
December 22, 2021
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The Weber Family
“Our connections to ALS run deep & very personal. Our dad passed away from ALS and, of his nine children, five have been diagnosed…”
December 22, 2021
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Janet and Eileen
“My sister, Janet, was diagnosed with ALS about a year and a half ago. I was stunned…”
December 22, 2021
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December 22, 2021
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