A Bexley filmmaker who made a documentary about her Oyster Bay family is up for a national award for her work in highlighting a genetic disorder.
Nicole Molloy’s documentary explores her nephew Nash’s experiences with Angelman syndrome, a condition that primarily affects the nervous system.
It tells the story of Nash, 2, who at nine months of age was diagnosed with the rare neurological disorder.
The five-minute film ‘He Will Walk’, which she made with Matt Watt, is a finalist in the NOVA Employment 2018 Focus On Ability Short Film Festival, in the Australian open documentary category.
“This film takes an ordinary family and demonstrates extraordinary grit and will power,” Ms Molloy said.
“It intends to highlight the amazing courage of a young boy who has already come up against so many challenges and road blocks in his life.
“As filmmakers we wanted to highlight Nash’s message, which is one of hope, persistence, strength of family and one of overcoming all obstacles.
“This is a positive message for all people.”
If the film wins, Ms Molly hopes to put the prize money towards buying tailored shoes for Nash, and help make his house walk and wheelchair-friendly.
People can vote for the film until July 3 here.
Voters go in the running to win a $50 iTunes voucher.
