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
Dr. Claire Le Pichon Joins Live Like Lou’s Scientific Advisory Board
Live Like Lou Announces Inaugural Graduate Fellows: He Gao and Thao Nguyen
Request for Applications - Postdoctoral Fellowship
2023 Lou Gehrig Day
Striking out Lou Gehrig's Disease
All 4 Lou Showdown
Iron Horse Scholarship Application Open for 2023
Leading Off in 2023... a new look!
Live Like Lou Newsletter | In the Dugout | October 2022
On Becoming a Great Man
Bob Biggs Joins LiveLikeLou Foundation Board of Trustees
DePauw and Wabash Phi's Rivalry Game Relay Race Raises Money for LiveLikeLou and ALS
The LiveLikeLou Foundation announce anonymous $100,000 donation at the 2019 Presidents Leadership Conference
Brothers, Friends, Iron Phis
The LiveLikeLou Foundation Conducts First Board Meeting, Establishes Funding Priorities
2022-23 Iron Phi Program Successes
Sam Selley's 100-Mile Iron Phi Journey
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.