Glam for GAN Gala
![Jordan Magaziner Steinfeld Jordan Magaziner Steinfeld](https://thebuzzmagazines.com/sites/default/files/styles/140px_by_180px_user_pic_epsa_crop/public/writer-photos/Jordan%20Magaziner.jpg?itok=Gm1GHkzF)
![Go Glam for GAN co-chairs Go Glam for GAN co-chairs](https://thebuzzmagazines.com/sites/default/files/styles/large_crop/public/article-photos/2015/11/glam%20for%20gan%202.jpg?itok=22nQjHrs)
Go Glam for GAN co-chairs all glammed out. (From left) Jada Hallmark, Mindy Vondenstein, Lagenia Clark, Jessy Morgenroth and Rebekah El-Hakam. All have kids at Horn Elementary. (Photo: Kraitman Photography)
Last Saturday, about 150 people gathered to “go glam” for GAN (Giant Axonal Neuropathy). The gala, which took place at the 2727 Kirby high-rise apartments, was a huge success with over $100,000 raised for a cure for this fatal disease. Guests enjoyed dinner, dancing and libations while taking in views of the Houston night sky. Proceeds went to Hannah’s Hope Fund.
![Lisa O’Connor, Lagenia Clark and Elaine Day Lisa O’Connor, Lagenia Clark and Elaine Day](https://thebuzzmagazines.com/sites/default/files/styles/large_crop/public/article-photos/2015/11/glam%20for%20gan%2010.jpg?itok=MHThl-YK)
St. Agnes Academy juniors Meaghan O'Connor and Ally Day, owners of M & A Stones, donated 50 custom bracelets for the Heads or Tails Game. Their creations helped raise $2500 toward a cure for GAN. Although the young entrepreneurs were not in attendance at the gala, their mothers represented them well. (From left) Lisa O’Connor, Lagenia Clark and Elaine Day. (Photo: Kraitman Photography)
Highlights of the evening included a lively, live auction and a “Heads or Tails” game, where the winner took home an iWatch. Silent auction winners bid on items ranging from tickets and signed sports memorabilia from the Texans to entries into local triathlons and several kids camps.
Bellaire residents Justin Clark, age 14, and Lexi Clark, age 10, both have GAN; only 60-70 kids in the world have this rare, genetic condition. Over the last two years, the Clark family has been working to raise money for a clinical trial to cure GAN. Read this story from last year on the Clark family and learn more here.
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