More Than a Caregiver: The Story of Meg Reyes
The Impact of the Live Like Lou Connect & Serve Program
Katie Pier | Running for Her Dad and the ALS Community
Carrying Their Names Forward: A Veteran’s Daughter Honors Her Stepdad and the ALS Community
Live Like Lou partners with Talk to Me, Goose! to offer free AI communication support for registered ALS families
Dr. Claire Le Pichon Joins Live Like Lou’s Scientific Advisory Board
Live Like Lou Honors Diana Buckroyd at Rangers ALS Awareness Game
Tennessee Invests $1 Million in Vanderbilt ALS Research Center
Live Like Lou Foundation Becomes Title Sponsor of the Jax and Las Vegas College Baseball Classics
In the Dugout | April 2025
Request for Applications - Career Development Award
Career Development Award Research Published
VandyBoys Game for ALS Research
Request for Applications - Postdoctoral Fellowship
2024 ALS Research Symposium
Evangelos Kiskinis selected as Scientific Director
2023 Career Development Award
Blue4Lou 2025
Remembering Neil Alexander
Lou Gehrig Community Impact Team 2025
Iron Horse Scholarships Application Open for 2025
Nominate Players for College Baseball Community Impact Team
ALS Awareness Game with the Colorado Rockies
2026 Lou Gehrig Community Impact Team nominations are now open
Triple Crown awarded to 36 Phi Delta Theta chapters
Lou Gehrig Day 2025: Together, We’re Lou(d) Against ALS
Milwaukee Events Raise Awareness and Funds!
Gehrig Impact Team Presentation
Live Like Lou - Phi Delta Theta is committed to the fight against Lou Gehrig's disease
An inside look at how we support ALS families, volunteers, researchers and the legacy of Lou Gehrig.