MEET THE FAMILY
Jenifer’s legacy lives on.
https://vimeo.com/546125973 When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit
Meet the Project ALS Family: Q&A with Prosetin Toxicologist Dr. Merrill Osheroff
When Project ALS decided to move prosetin to clinical trial independently, we were newcomers to drug development. Our first task: assembling a team of experts
MEET THE CORE: SUSAN BRENNER-MORTON
MEET THE CORE: SUSAN BRENNER-MORTON Susan Brenner-Morton is an antibody expert who has spent decades developing these specialized tools to help us understand how motor
Project ALS Honors Chris Combs, Who Transformed Project ALS Research to Benefit Millions
Five years ago, Raleigh, North Carolina’s own Chris Combs, a loving husband and father of three young children, was diagnosed out of nowhere with ALS.
One Family’s Passionate Fight Against Neurodegenerative Diseases
The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to
Valentine for a Pioneer
“Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother.
Tom Kirchhoff Family Continues to Support Young Leaders in ALS Research
In the medical research world, a “post-doctoral fellow” is the official title for a gifted, young scientist who works 25 hours a day in a
Team Chris Combs Galvanizes Raleigh, NC Community
Team Chris Combs hosted their third annual Hope Gala to Defeat ALS on September 28th at the Umstead Hotel in Raleigh, NC. The past three
Seven Mothers Unite in New York City to Solve Medical Mystery: ALS Geneticists at Columbia University Look to Mothers and Late Daughters for Clues to Rare Juvenile ALS
Seven teenage girls from across the country, aged 17 to 22, have died from ALS, a disease primarily affecting the middle-aged. For years, their mothers