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
Juan Reyes’ Journey with ALS
Stuck Behind the Window: A Daughter’s Reflection on ALS Caregiving
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 Honors Diana Buckroyd at Rangers ALS Awareness Game
Tennessee Invests $1 Million in Vanderbilt ALS Research Center
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
Funding Opportunity - Graduate Fellowship
In the Dugout | January 2026
Together Through It All: The Quandt Family’s Story of Strength
From a Lou Gehrig Stamp to a Babe Ruth Baseball: How One Man Is Trading Up for Hope
A Legacy That Lives On: Honoring Neil Alexander
Hebrew University Scientist Awarded Live Like Lou Career Development Award to Advance Understanding of ALS
The 2026 Lou Gehrig Community Impact Team, Recognizing Community-Minded Collegiate Baseball Players
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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