Join us for an evening of fun, friendship, trivia, and philanthropy as we go all in for our friend Laurie Roselle at the second annual All In for Laurie Trivia Night!

Presented in partnership with Laurie’s Delta Gamma friends and Lou Gehrig’s fraternity, Phi Delta Theta, tickets include heavy appetizers, dessert, access to a curated silent auction, and memories to last forever! A cash bar will be available. Trivia "mulligans" will be available for purchase at the event (one mulligan per team per round).

All proceeds benefit the Live Like Lou Foundation and its mission to support families affected by Lou Gehrig's disease, fund ALS research, and create awareness for ALS. 

Sponsor Opportunities
If you or a business you know is interested in sponsoring the second annual All in for Laurie Trivia Night, please contact Wendy Faust with the Live Like Lou Foundation. 

TICKET SALES BEGIN SEPTEMBER 1 and we expect another sold-out crowd, so sponsor today to guarantee your table!

About Laurie Roselle
In September of 2021, Laurie Petrucce Roselle of Fishers was diagnosed with ALS. After years of giving tirelessly of herself to benefit others, those who know and love her are going All In for Laurie to fund research for Lou Gehrig’s disease through the Live Like Lou Foundation.

Laurie is a graduate of Purdue University where she was a member of Delta Gamma. She spent her career in the legal community while serving her beloved Delta Gamma as a dedicated volunteer. From serving collegiate chapters as a regional resource to serving on the international council for eight years, Laurie has been honored with a number of awards for her lifetime of commitment. She was elected and served as Delta Gamma’s international president from 2012-2014. Purdue Delta Gammas, if you're unable to attend Trivia Night but wish to donate, click here!

With more than $122,000 raised to date from the Roselles and their community of friends, family, and fans, John and Laurie Roselle have established an endowment with the Live Like Lou Foundation to fund undergraduate neurodegenerative disease research at the University of Notre Dame. The first research grant was made to a Notre Dame student in May of 2023. Read more here.

Laurie’s husband John is a graduate of the University of Notre Dame and an active member of the Notre Dame Club of Indianapolis, including eight years of service as a member of its board.

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 470 ALS families through Live Like Lou. Learn more about the Live Like Lou Foundation on our website at livelikelou.org.