Live Like Lou Newsletter | In the Dugout | October 2022
Live Like Lou Grants Inaugural Postdoctoral Fellow
Second Annual Shootout 4 ALS
Going for the Gold: Lou's Olympics Competition Leads to Record Results
Live Like Lou Foundation Updates: Successes and Exciting Partnerships
Join Phi Delta Theta and Live Like Lou Foundation at Busch Stadium for ALS Awareness Evening
Lou Gehrig Day 2024 with the San Francisco Giants
Lou Gehrig Day 2024 with the Atlanta Braves
Lou Gehrig Day and ALS Awareness Month
Join Lou's Crew
Boston College ALS Awareness Game
Live Like Lou is now on Roon
Live Like Lou Newsletter | In the Dugout | October 2024
Live Like Lou's 2023-2024 Impact Report
Phi Delta Theta's Strike Out ALS Games
ALS Awareness Game with the Colorado Rockies
Honoring Laurie Petrucce Roselle
ALS Awareness Game with the Cleveland Guardians
Connect & Serve Volunteers Assisting ALS Families | Fall 2024
Connect & Serve Volunteers Assisting ALS Families | Summer 2024
2024 Onward Awards
2024 Iron Horse Scholarships Awarded
2024 Lou Gehrig Memorial Scholarships
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
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
Brothers, Friends, Iron Phis
The LiveLikeLou Foundation announce anonymous $100,000 donation at the 2019 Presidents Leadership Conference
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.