Thank you for the support and messages to Laurie. Together we raised over $39,000 to help leave ALS better than we found it.

Join us for an evening of fun, friendship, trivia, and philanthropy as we go all in for our friend Laurie Roselle.

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 LiveLikeLou Foundation and their mission to support ALS families, fund ALS research, and create awareness for Lou Gehrig’s disease.

Questions? Contact LiveLikeLou at info@livelikelou.org.

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 LiveLikeLou Foundation.

Laurie is a graduate of Purdue University where she was a member of Delta Gamma sorority. 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 national 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 national president from 2012-2014.

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 LiveLikeLou Foundation
The LiveLikeLou 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, LiveLikeLou 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 LiveLikeLou. Learn more about the LiveLikeLou Foundation on our website at livelikelou.org.

All in for Laurie 2022

Leaving ALS better than we found it.