Partnership with 6 MLB Teams and Permobil Foundation During Lou Gehrig Day
Live Like Lou Newsletter | In the Dugout | July 2022
Collaborative Learning Advances ALS Research at Live Like Lou Emerging ALS Investigator Forum
Live Like Lou Awards 2022 Iron Horse Scholarships
Join Phi Delta Theta and Live Like Lou at PNC Park for the Pirates Lou Gehrig Day Celebration
Join Us at Kauffman Stadium on June 3 for the Lou Gehrig Memorial Award Presentation
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
Live Like Lou's 2023-2024 Impact Report
Phi Delta Theta's Strike Out ALS Games
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
Sam Selley's 100-Mile Iron Phi Journey
Phi Delta Theta, Miami University, and Live Like Lou Collaborate
Phi Delta Theta and the LiveLikeLou Foundation Present Permobil Wheelchair to Minnesota ALS Family
Now Hiring: LiveLikeLou Foundation Executive Director
ALS Research is Better Than We Found It
Ohio ALS Family Gets Helping Hands
2022-23 Iron Phi Program Successes
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.