The 3rd Annual Hallie Grace Memorial Butterfly Ball for EB

Heroes for Hallie Grace Inc. presents the 3rd Annual Hallie Grace Memorial Butterfly Ball for EB, taking place at Savannah Station [601 Cohen St] on June 7, 2024 from 6-10PM, featuring delicious dinner and dessert, live music, DJ/dancing the night away, a fun photo booth, a live butterfly release, a silent auction and more!

The event takes place around what would have been Hallie Grace Davis’s 3rd birthday and every dollar raised goes towards fighting the condition that took her life, Epidermolysis Bullosa (EB). Adult tickets start at just $65 for General Admission; $100 for VIP [includes 2 free drinks, a reserved seat during the event, and a VIP Swag Bag]. You can also purchase a butterfly to release in memory of Hallie Grace Davis or anyone in your own life that you would like to honor, whether or not you are able to attend. All names will be read aloud as the butterflies are released. Tickets and butterflies can be purchased here: https://onecau.se/halliegrace

There will be a full dinner service generously provided by the Metro Diner in Pooler along with several delicious dessert options. Cash bar will feature a signature drink, The Halliefly, which changes color in front of your eyes! Enjoy a live performance by an incredible band, Hooked Like Helen (www.hookedlikehelen.com) sent to us by IHeartMedia! Savannah’s Best DJs of 2023, All About You Entertainment, will provide a fun photo booth as well as a couple hours of dancing fun! The community has truly come together to provide amazing donations for the Silent Auction as well as several items you must attend to bid on. You do not want to miss out! There may be several more surprises to come!

“What a fun night for a great cause! I’ll be back next year and I’m bringing 10 friends with me! – Guest from the previous year

Heroes for Hallie Grace Inc. was created in loving memory of forever 3-month-old Hallie Grace Davis, who was born with the rarest and most terminal type of Epidermolysis Bullosa (EB). Epidermolysis Bullosa is a single mutation genetic condition that stops the body from producing a needed protein to hold the skin together, so it blisters and tears with any friction. It is known as “the worst disease you’ve never heard of” and there is currently no treatment or cure. Our mission is to ultimately change that! The nonprofit specifically focuses on raising awareness, funding important research, and improving quality of life for individuals and their families impacted by EB, and 100% of the money raised during this event goes directly to that cause.

Please join us for an amazing night full of fun, education, and fundraising! We would be honored if you would help us build Hallie’s legacy and join her fight! Don’t miss it!!!