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
2026 Lou Gehrig Community Impact Team nominations are now open
Live Like Lou Honors Diana Buckroyd at Rangers ALS Awareness Game
Ashley's Hero Beyond the Uniform: A Daughter’s Caregiving Journey
Faith Like the Vicks
Juan Reyes’ Journey with ALS
Stuck Behind the Window: A Daughter’s Reflection on ALS Caregiving
Request for Applications - Career Development Award
The Impact of the Live Like Lou Connect & Serve Program
Tennessee Invests $1 Million in Vanderbilt ALS Research Center
Live Like Lou Announces Inaugural Graduate Fellows: He Gao and Thao Nguyen
Request for Applications - Postdoctoral Fellowship
Live Like Lou Foundation Becomes Title Sponsor of the Jax and Las Vegas College Baseball Classics
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.