Kate | Aaron Mavro

"Kate has Epidermolysis Bullosa, a rare and severe genetic skin disorder where the body doesn't make the protein that holds the layers of skin together. Despite her daily difficulties including constant pain and fused fingers, it doesn't stop her positive attitude and her ability to produce stunning art-work." "It doesn't matter what condition you have or what challenges have been presented, with a positive attitude, you can still pursue the things you love." I entered my film in the NOVA Focus On Ability competition and it was Runners Up in the NOVA Choice Award. For more info on Epidermolysis Bullosa, please visit DEBRA Australia(Dystrophic Epidermolysis Bullosa Research Association) at http://www.debra.org.au/ Aaron Mavrokefalos - Writer; Producer; Director; Cinematographer; Editor Special thanks to Kate Turner, Linda Turner, Laraine Frost, Alfred Engel and Matina Papas Filmed on: Sony HDR-TG1E