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!
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.
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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