Ashley's Hero Beyond the Uniform: A Daughter’s Caregiving Journey
Faith Like the Vicks
Juan Reyes’ Journey with ALS
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
Share the Love with a New Subaru
All in for Laurie and ALS Research
Honoring Caregivers
Live Like Lou Newsletter | In the Dugout | October 2023
Join the Live Like Lou staff
Send Flowers and Benefit Live Like Lou!
2023 Postdoctoral Fellowships awarded
Neurodegenerative Disease Research Funded at Notre Dame
Live Like Lou sponsors TDP-43 conference in Trieste, Italy
Career Development Award Open for LOIs
Vandy Boys Games for ALS Research
Striking out Lou Gehrig's Disease
2026 Lou Gehrig Community Impact Team nominations are now open
Live Like Lou Honors Diana Buckroyd at Rangers ALS Awareness Game
Live Like Lou Foundation Becomes Title Sponsor of the Jax and Las Vegas College Baseball Classics
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.