Join us for an evening of trivia and connection with the ALS community in Ann Arbor! The Live Like Lou Foundation is hosting its biennial ALS Research Symposium for early career scientists at the University of Michigan next month, and we'd love to have YOU join us to meet them and kick off their meeting with camaraderie and fun.

All are welcome to attend this ALS community event. Teams of eight will be randomly created and include our Symposium guests. Tickets resserved together will be seated together (please email us if you have specific seating requests). Trivia will start promptly at 6:30 p.m. and last until 8 p.m.

ABOUT OUR TRIVIA HOST
Are you ready for your brain to be stretched by trivia master John Roselle? John's wife, Laurie, was diagnosed with ALS in September of 2021 and he serves as her full-time caregiver. John and Laurie host Live Like Lou's annual trivia night event in the Indianapolis area and have helped raise more than $200,000 in the last two years to fund undergraduate neurodegenerative disease research through Live Like Lou. We can't wait for you to meet him!

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 Phi Delta Theta Fraternity member, 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 505 ALS families through Live Like Lou. Learn more about the Live Like Lou Foundation on our website at livelikelou.org.

ALS Community Event

Join Live Like Lou's emerging ALS researchers in Ann Arbor