Gold Gala Auction and Dinner

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It is with great excitement that we announce the date for the 2nd Annual Gold Gala benefiting Layla’s Legacy. Please mark your calendars for a special evening on September 28, 2019. 

Tickets and sponsorships are on sale now! Click here to get yours!

Layla’s Legacy is committed to raising funds to fund innovative pediatric brain cancer research while bringing help and hope to families impacted by the disease. This year we are bringing together DFW businesses with the common goal of building a legacy of funding the research that will one day eliminate the need for parents to hear “There’s nothing more we can do,” and we believe this legacy begins with you.

Join us for an evening of dinner, dancing, and fun while learning more about how your contribution is making an impact locally and across the state. It will surely be a magical evening honoring Layla and the legacy we are all continuing in her memory. Cocktails and the silent auction will begin at 6:00 pm, followed by dinner and program at 7:30 and then a live auction. Our theme is “Circus Soirée”, so feel free to play up the attire with some fun! [cocktail attire preferred]

Sponsorship details can be found here.

Sara Stamp

Sara Stamp

Layla’s Legacy Foundation is a 501(c)(3) organization funding innovative pediatric brain cancer research while bringing hope and help to families impacted by the disease.

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Our Story

In October 2016, the Stamp family was devastated by the news that their 4-year-old daughter, Layla, had a form of pediatric brain cancer called Medulloblastoma. Even after surgery, months of chemotherapy and radiation, Layla’s cancer returned. For 14 months the family fought and tried every possible treatment available only to lose Layla on November 11, 2017, shortly after her 5th birthday.
 
During their journey, the Stamps learned just how little funding there was for pediatric cancers and also how difficult it can be for families financially. Layla’s Legacy was founded to create change in research, to be advocates of the disease and to help support families by offsetting costs where needed. In their mind, it was time to Do More for our kids!

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