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
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
Salvador Perez of the Kansas City Royals Wins Phi Delta Theta Fraternity's Lou Gehrig Memorial Award
Live Like Lou Newsletter | In the Dugout | January 2022
LiveLikeLou Awards 2021 Iron Horse Scholarships to Children of ALS Families
Wendy Faust Joins the LiveLikeLou Foundation as Executive Director
On Becoming a Great Man
Bob Biggs Joins LiveLikeLou Foundation Board of Trustees
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
2022-23 Iron Phi Program Successes
Sam Selley's 100-Mile Iron Phi Journey
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.