Live Like Lou Newsletter | In the Dugout | October 2024
Neurodegenerative Disease Research Funded in Indiana
Live Like Lou's 2023-2024 Impact Report
Connect & Serve Volunteers Assisting ALS Families | Fall 2024
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
Join our Lou's Crew Members
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
Serve an ALS Family in your Community through LiveLikeLou's Great Outdoor Clean Up
ALS Research is Better Than We Found It
Second ALS Research Grant for Emerging Scientist Awarded to Thomas Jefferson University
LiveLikeLou Announces Major Grant for ALS Research at Mayo and MIT
Iron Phi funds to support the LiveLikeLou Emerging ALS Investigators Forum at the University of Pittsburgh Brain Institute
The LiveLikeLou Center for ALS Research announces a Major Breakthrough in the Study of ALS
Inaugural Live Like Lou Emerging ALS Investigators Forum at the University of Pittsburgh Brain Institute
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 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
Live Like Lou
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
An inside look at how we support ALS families, volunteers, researchers and the legacy of Lou Gehrig.