Live Auction Preview
VIEW ITEMS
Get ready for a dazzling night of glamour, games, and giving at Bollywood Blingo!
Join us on October 18, 2025, for an unforgettable evening filled with vibrant Bollywood flair, high-energy bingo rounds, delicious food, and lively entertainment-all in support of CureDuchenne's mission to find a cure for Duchenne muscular dystrophy.
DOORS OPEN AT 6:30 PM
Bollywood Blingo isn't just a fabulous night out-it's a powerful opportunity to make a difference. This event raises critical funds for CureDuchenne, fueling life-saving research, advancing care, and empowering the Duchenne community with hope and resources.
Dress Code: While its not required, we encourage all to come dressed inspired by Bollywood or in your festive best! Embrace the color, sparkle, and energy of the evening-this is your chance to shine!
Tickets: Online sales are now closed. For ticket inquiries, please email [email protected]. A few seats may still be available, but space is limited and not guaranteed.
Come dressed to dazzle, ready to play, and inspired to support the 15,000 boys and young men in the U.S. living with Duchenne. Your presence brings us one step closer to a cure.
Let's light up the night and change lives together-Bollywood style!
Sonal and Manu Gambhir stand not only as co-chairs of tonight's event but as parents with an unbreakable resolve to find a cure. Their son, Yuva, a junior at the University of Pennsylvania, faces Duchenne muscular dystrophy with courage and vision. Yuva dreams of a world where Duchenne no longer defines lives, saying, "The love I've received is overwhelming. Together, we can conquer this disease."
Yuva lost his ability to walk at 13, but he continues to live fully-pursuing studies in cognitive science, exploring DJing, and finding joy with friends. Beyond his personal battles, Yuva is driven by a mission to end Duchenne, interning in labs and healthcare firms to advance research. His father, Manu, emphasizes, "Every moment brings us closer to a cure. The support we've seen is both humbling and inspiring."
Board member Martin Lehr, who lost his brother to Duchenne, reflects: "I know Duchenne's heartbreak. Events like this are more than fundraisers; they're lifelines."
This evening isn't just a gathering; it's a rallying cry-a beacon of hope to bring an end to Duchenne for the 300,000 boys and their families worldwide.
