10/18/2016
TLC’s “Two in a Million” Star Elena Schefer to speak at Chattanooga Fundraiser FACES UnMasked: Beyond the Face
12-year-old Elena Schefer has Goldenhar Syndrome, a craniofacial condition. She was recently featured on TLC’s reality hit show “Two in a Million”, where she met Austin Niehus, another child with Goldenhar. She and Austin became fast friends and launched an anti-bullying campaign together to show others the importance of being more sensitive to children with craniofacial differences and their families. You can watch it here: https://www.youtube.com/watch?v=WBwkDhGE8aY
Elena will be the guest speaker at FACES Unmasked, an evening of art, food, and fun put on by FACES, the National Craniofacial Association. FACES has been helping Elena and her family cover travel expenses for the many corrective surgeries she has endured over the past 11 years. Elena will be appearing with her service dog, Tuku, and her mom, Amy Schefer. Proceeds from the event will benefit FACES and allow them to continue to serve craniofacial families around the United States.
FACES UnMasked will take place on Thursday evening, October 27, from 5:30 p.m. until 8 p.m. at The Church on Main, the perfect place to unmask on East Main. It will be an engaging evening with beautiful and unique artwork, UnMasked artists, food and adult beverages, games for prizes, and fun! The highlight of the event will be the silent auction of some truly amazing masks and artwork created and donated by local artists.
Thursday, October 27, 2016
Chattanooga, TN
FACES UnMasked
5:30 p.m. – 8 p.m.
The Church on Main, 1601 Rossville Avenue
Tickets $50 each
Includes heavy hor d'oeuves, two adult beverage tickets, and the opportunity to bid on the masks
Business Casual
To Buy Tickets Go To: http://www.facesunmasked.org/UnMaskedTickets.html
Or call 423-266-1632
FACES: The National Craniofacial Association FACES assists 75 to 135 families each year with travel away from home to specialized craniofacial medical centers for life-changing surgeries. In many cases, this is a lifelong journey for these families, as a child born with a severe craniofacial disorde...