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

New in 2024, a new location with additional seating, enhanced dining options, and more opportunities to go all in for ALS research and our friend Laurie! We'll be at the Ritz Charles in Carmel!

Presented in partnership with Laurie’s incredible community of family and friends, 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.

Thank you to our sponsors!

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

TICKET/TABLE SALES BEGIN AUGUST 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 knew and loved her are going All In for Laurie to fund research for Lou Gehrig’s disease through the Live Like Lou Foundation. With heavy hearts, we share that ALS took our friend Laurie Roselle just shy of three years after her diagnosis with Lou Gehrig's disease.

Laurie graduated from 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 many awards for her lifetime of commitment. She was elected and served as Delta Gamma’s international president from 2012-2014.

With more than $225,000 raised to date from the Roselles and their community of friends, family, Delta Gamma sisters, 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 2023. Read more here. A second research grant was made in 2024, and we will share updates as we learn about them.

Laurie’s husband, John, is a University of Notre Dame graduate and an active member of the Notre Dame Club of Indianapolis, having served on its board for eight years.

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.

All in for Laurie

Leaving ALS better than we found it