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
Published Research by 2023 Postdoctoral Fellow
Third Annual All 4 Lou Showdown
Request for Applications - Graduate Fellowship
Neurodegenerative Disease Research Funded in Indiana
2024 ALS Research Symposium | Ann Arbor
2024 Postdoctoral Fellowships awarded
ALS Awareness Game with the Cleveland Guardians
Triple Crown awarded to 29 Phi Delta Theta chapters
2024 MLB Games in Review
Lou Gehrig Day 2024 with the Minnesota Twins
Lou Gehrig Day 2024 with the Pittsburgh Pirates
Lou Gehrig Day 2024 with the St. Louis Cardinals
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
2022-23 Iron Phi Program Successes
Sam Selley's 100-Mile Iron Phi Journey
Bob Biggs Joins LiveLikeLou Foundation Board of Trustees
Brothers, Friends, Iron Phis
The LiveLikeLou Foundation Conducts First Board Meeting, Establishes Funding Priorities
Supporting young Phis who have been personally affected by ALS
An inside look at how we support ALS families, volunteers, researchers and the legacy of Lou Gehrig.