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
Career Development Award Research Published
2024 Lou Gehrig Day
2024 All 4 Lou Showdown
Support Live Like Lou this Valentine’s Day!
Live Like Lou Newsletter | In the Dugout | January 2024
The Lou, Year Two
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
Request for Applications - Career Development Award
Holiday Respite Grants
Live Like Lou Awards 2022 Iron Horse Scholarships
Phi Delta Theta and the LiveLikeLou Foundation Present Permobil Wheelchair to Minnesota ALS Family
LiveLikeLou Awards 2021 Iron Horse Scholarships to Children of ALS Families
Ohio ALS Family Gets Helping Hands
The LiveLikeLou Foundation Awards 2020 Iron Horse Scholarships to Children of ALS Families
Dr. Claire Le Pichon Joins Live Like Lou’s Scientific Advisory Board
Tennessee Invests $1 Million in Vanderbilt ALS Research Center
Live Like Lou Announces Inaugural Graduate Fellows: He Gao and Thao Nguyen
Request for Applications - Postdoctoral Fellowship
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.