'Every face deserves a place': Coast boy lives acting dream
FOLLOW the cheerful voice singing through the walls of his family home and you'll always find Edward "Eddy" Meskanen.
The eight-year-old Sunshine Coast boy has a unique zest for life that his mum Anna said puts him in the spotlight wherever he goes.
Eddy is using this spotlight to his advantage by breaking down barriers surrounding deformities in the acting world, and his own facial deformity, Goldenhar Syndrome.
The craniofacial syndrome affects the bones in Eddy's face, leaving him deaf in his left ear and with a number of clefts.
It's because of these unique differences that Eddy was pioneering for change in the movie industry, believing every face deserves a place on the screen.
The budding actor was spurred to start this movement after watching film Wonder and learning the main character wore a mask to create the illusion he had similar deformities to Eddy.
"Instead of being inspired by the film, Eddy was really confused and upset as to why a person like him wasn't chosen," Anna said.
"Now he just wants to break down that barrier and open doors for people with any kind of differences, because they matter."
Eddy looked up to some famous faces with similar deformities, including Stranger Things actor Gaten Matarazzo.
Is it time to break down the barriers in the acting world?
The "outgoing" boy leaped into his first acting role this year in Acute Misfortune, and was immediately hooked.
Anna and Eddy hoped negative connotations surrounding deformities would shed if they were depicted on the silver screen.
"I had never heard of the syndrome until my son was born," Anna said.
"There are so many negative perceptions injected into people's brain surrounding facial deformities.
"But learning that we all have differences is the only way to knock these down."
Through Eddy's acting, his ultimate goal was to encourage other kids to pursue their dreams.
The massive Doctor Who fan hoped to one day be the first child to play 'The Doctor'.
"He always dresses up in bow ties, and why not regenerate the character into a child?," Anna said.
"We have a lot of work to do in changing people's perceptions, but it's just the beginning."
Anna has recently started a Sunshine Coast Facial Difference Community Facebook page for families to connect and support.