Meet the 2026 Live Like Lou Graduate Fellows Advancing ALS Research
Honoring Angie Through The Lou Workout
The Axon Holds the Answer: Meet Live Like Lou Foundation Roselle Fellow Priya Shields
For Cooper and Claire, Birthdays Are a Chance to Give Back
2026 Live Like Lou ALS Research Symposium
Triple Crown Awarded to 42 Phi Delta Theta Chapters
Justin Ramirez: “I am still me.”
Blue 4 Lou 2026
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
In the Dugout | January 2026
Together Through It All: The Quandt Family’s Story of Strength
Iron Horse Scholarships Application Open for 2026
2026 Live Like Lou Quality-of-Life Grants Open
Juan Reyes’ Journey with ALS
Stuck Behind the Window: A Daughter’s Reflection on ALS Caregiving
The Lou Gehrig Day Recap You Have Been Waiting For
On My Father’s ALS Diagnosis, the Stoics, and Finding My Faith Again
Request for Applications - 2026 Postdoctoral Fellowship
2026 ALS Research Symposium
A Legacy That Lives On: Honoring Neil Alexander
The 2026 Lou Gehrig Community Impact Team, Recognizing Community-Minded Collegiate Baseball Players
2026 Lou Gehrig Community Impact Team nominations are now open
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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