Inaugural Live Like Lou Emerging ALS Investigators Forum at the University of Pittsburgh Brain Institute
The LiveLikeLou Foundation Conducts First Board Meeting, Establishes Funding Priorities
Phi Delt Volunteers Needed – Give Kids of ALS Families a Great Summer Camp Experience!
Supporting young Phis who have been personally affected by ALS
Live Like Lou - Phi Delta Theta is committed to the fight against Lou Gehrig's disease
Neil Alexander: Leaving ALS better than he found it
Live Like Lou Newsletter | In the Dugout | October 2024
Connect & Serve Volunteers Assisting ALS Families | Fall 2024
ALS Awareness Game with the Colorado Rockies
Honoring Laurie Petrucce Roselle
ALS Awareness Game with the Cleveland Guardians
Join our Lou's Crew Members
High School Baseball and Softball Challenge
Introducing the Live Like Lou Store!
Striking out Lou Gehrig's Disease
Postdoctoral Fellowship Application Open
CrossFit Community Supports Live Like Lou
Iron Horse Scholarship Application Open for 2023
Grants to ALS Families for Home Improvement Projects
Friendship Grown from Service
ALS Awareness Outing with the Los Angeles Dodgers
ALS Awareness Outing with the Chicago White Sox
Team Hilliard Foundation supports home improvement grants for ALS families in Georgia
2023 Iron Horse Scholarships Awarded
Neurodegenerative Disease Research Funded in Indiana
2024 ALS Research Symposium | Ann Arbor
2024 Postdoctoral Fellowships awarded
Career Development Award Research Published
VandyBoys Game for ALS Research
Request for Applications - Postdoctoral Fellowship
Triple Crown awarded to 29 Phi Delta Theta chapters
2024 MLB Games in Review
Lou Gehrig Day 2024 with the Pittsburgh Pirates
Lou Gehrig Day 2024 with the Minnesota Twins
Phi Delta Theta's Strike Out ALS Games
Lou Gehrig Community Impact Team
Triple Crown awarded to 24 Phi Delta Theta chapters
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
An inside look at how we support ALS families, volunteers, researchers and the legacy of Lou Gehrig.