Tickets include heavy appetizers, dessert, access to curated auction items, and an open bar.
Thursday, November 6
6:00 pm EST
Undergraduate and Graduate Research Grants: Proceeds support neurodegenerative disease research at top Indiana institutions, notably Notre Dame and Purdue. These grants empower students and early-career scholars to pursue breakthrough scientific projects in ALS and related neurological disorders.
For example, students like Margaret Rakonick have worked in laboratories studying neurodegeneration and drug discovery chemistry. Previous grants have also supported clinical research exploring how neurological diseases manifest, aiming to uncover new avenues for treatment.
Thanks to this event and its supporters, Live Like Lou is making real strides: expanding vital research, fostering young scientific talent, and building a community around ALS advocacy, all in Laurie’s name.
Founded in honor of Laurie Petrucce Roselle after her ALS diagnosis in 2021, the event brings together Laurie's family, friends, Delta Gamma sisters, Lou Gehrig’s fraternity brothers, and supporters across the community for an evening of fun, friendship, and philanthropy.
Held in partnership with the Live Like Lou Foundation, this signature night features trivia, heavy appetizers, dessert, and vibrant silent auctions, all set in premier local venues like Woodland Country Club and Ritz Charles in Carmel. The event has rapidly grown, attracting hundreds of participants and surpassing $300,000 raised within the first three years.
This gathering has not only become a social highlight but also a powerful movement, channeling Laurie's commitment to service into tangible advances for ALS research
A proud graduate of Purdue University, where she joined Delta Gamma, Laurie built a distinguished legal career in both Indianapolis and New York, ultimately serving as Director of Legal Services – North America for Clifford Chance LLP. Her loyalty and warmth inspired deep connections within her family, her sorority, and the countless communities she served.
Throughout her life, Laurie took on leadership roles in Delta Gamma, earning every major award the sorority offers and leaving a lasting mark through her philanthropic efforts. Friends and colleagues describe her as tireless—someone who “simply shows up whenever there is a need for anyone anywhere”. Laurie’s impact extended far beyond her professional networks: she was known for her generosity, handwritten notes of gratitude, and infectious smile.
Laurie’s life took a profound turn in September 2021 when she was diagnosed with ALS, a progressive and incurable neurodegenerative disease also known as Lou Gehrig’s disease.
True to her character, Laurie chose to face her diagnosis publicly, sharing her journey with candor and hope across social media. Despite the rapid progression of ALS, she continued to connect, encourage, and inspire, communicating through assisted technology and always signing her messages with, “It’s a Wonderful Life”.
Together with her husband, John, Laurie turned her fight into action by partnering with the Live Like Lou Foundation. Their philanthropy has established endowments for undergraduate research on neurodegenerative diseases at Notre Dame and Purdue, expanding opportunities for new scientists to pursue cures for ALS and bringing hope to future families facing the same devastating diagnosis.
Laurie’s legacy is defined by her enduring spirit and drive to “Do Good,” which inspires her friends, family, and everyone touched by her story to go All in for Laurie and for ALS research.
