When I was diagnosed with ALS in June 2022, I didn't know what to do first. One thing I needed was a 1st floor bathroom. With help from family but also Live Like Lou, I got a first floor accessible bathroom. This organization was the first to help me. The mission of Live Like Lou is one that resonates with me. I proudly display a #4 sticker on my car. Hoping for everyone we can Live Like Lou.

About the Live Like Lou Foundation

The Live Like Lou Foundation was established in 2017 as a national nonprofit with a vision to leave ALS better than we found it. Named in honor of MLB Hall of Famer Lou Gehrig, a member of Phi Delta Theta Fraternity, Live Like Lou supports ALS families, funds emerging researchers seeking meaningful treatments and cures for ALS, and helps generate awareness of Lou Gehrig’s disease. In the face of his ALS diagnosis, Lou Gehrig continued to live his life with courage, determination, and gratitude... this is what we mean when we say Live Like Lou.

In Lou’s memory, Phi Delta Theta Fraternity members have served more than 300 ALS families through Live Like Lou. Learn more about the Live Like Lou Foundation on our website at livelikelou.org.

Sarah's Birthday Fundraiser

By Live Like Lou Foundation

Sarah's Birthday Fundraiser