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MISSION
The Live Like Lou Foundation's mission is to create and connect communities to stimulate emerging ALS research and uniquely support families affected by Lou Gehrig’s disease. We do this in honor of MLB Hall of Famer Lou Gehrig and the 30,000 individuals in North America living with ALS.
About the lou
The Lou, named in honor of Lou Gehrig and inspired by his Yankees' jersey number, 4, is a partner workout featuring 44 rounds of 4 reps each of wallballs, pull-ups, burpees, and dumbbell snatches.
Partners split the work, pushing through strength and endurance to honor Lou's legacy and support the fight against ALS
*all activities can be modified if needed
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About Live Like Lou
All funds raised through The Lou workout supports families affected by ALS, funds early-career scientists studying ALS to find treatments or cures for Lou Gehrig’s disease, and honors Lou Gehrig’s legacy through events and creating awareness for the ALS community.
ALS Family Support
Through hands-on support by volunteers in and around the home, grants for respite and home improvement projects, and scholarship support for children in ALS families, we are meaningfully supporting families affected by Lou Gehrig's disease.
ALS Research
By supporting early-career scientists studying ALS, we aim to identify discoveries that will produce tomorrow’s trials, treatments, and cures for Lou Gehrig’s disease.
ALS Awareness
We seek to amplify Lou Gehrig’s story, his legacy, and what it means to live like Lou in the face of a 100 percent fatal ALS diagnosis. We create moments of impact for ALS families and the broader ALS community through events, strategic partnerships, and raising critical funds to power our mission.
The lou in action
Follow The Lou on Instagram @thelouworkout
share your story
At Live Like Lou, we believe in the power of community and shared experiences. Lou Gehrig's disease touches millions, bringing challenges that can feel insurmountable. We want to hear your stories—how ALS has impacted your life or how you've navigated these obstacles. Together, we can create a supportive environment that not only honors those affected but also drives innovative research. Share your journey with us, and let's inspire hope and change together!
Contact Us
Newsletter Signup
Stay in the loop with Live Like Lou! Join our newsletter to receive the latest updates on upcoming events and exciting new initiatives dedicated to stimulating ALS research. Together, we can support families affected by Lou Gehrig’s disease and create a vibrant community focused on hope and change.
Contact Us
2 South Campus Avenue, Oxford, Ohio 45056, United States
thelou@livelikelou.org
The Live Like Lou Foundation's mission is to create and connect communities to stimulate emerging ALS research and uniquely support families affected by Lou Gehrig’s disease. We do this in honor of MLB Hall of Famer Lou Gehrig and the 30,000 individuals in North America living with ALS.
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