Request for Applications - 2026 Postdoctoral Fellowship
Justin Ramirez: “I am still me.”
On My Father’s ALS Diagnosis, the Stoics, and Finding My Faith Again
2026 Iron Horse Scholarship Recipients Announced
Blue 4 Lou 2026
2026 ALS Research Symposium
From a Lou Gehrig Stamp to a Babe Ruth Baseball: How One Man Is Trading Up for Hope
From First Pitches to Life-Changing Moments: Inside the Las Vegas College Baseball Classic
Inaugural Live Like Lou Jax College Baseball Classic Supports Local Families and Raises ALS Awareness
The 2026 Lou Gehrig Community Impact Team, Recognizing Community-Minded Collegiate Baseball Players
Funding Opportunity - Graduate Fellowship
In the Dugout | January 2026
Together Through It All: The Quandt Family’s Story of Strength
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 Provides Free AI Communication Tool, Talk to Me, Goose!, for Registered ALS Families
Live Like Lou Honors Diana Buckroyd at Rangers ALS Awareness Game
Tennessee Invests $1 Million in Vanderbilt ALS Research Center
A Legacy That Lives On: Honoring Neil Alexander
Hebrew University Scientist Awarded Live Like Lou Career Development Award to Advance Understanding of ALS
2026 Lou Gehrig Community Impact Team nominations are now open
Triple Crown awarded to 36 Phi Delta Theta chapters
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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