More Than a Caregiver: The Story of Meg Reyes
Stuck Behind the Window: A Daughter’s Reflection on ALS Caregiving
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
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
Request for Applications - Career Development Award
LiveLikeLou Announces Major Grant for ALS Research at Mayo and MIT
Iron Phi funds to support the LiveLikeLou Emerging ALS Investigators Forum at the University of Pittsburgh Brain Institute
The LiveLikeLou Center for ALS Research announces a Major Breakthrough in the Study of ALS
Inaugural Live Like Lou Emerging ALS Investigators Forum at the University of Pittsburgh Brain Institute
The LiveLikeLou Foundation Conducts First Board Meeting, Establishes Funding Priorities
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.
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