Smith-Magenis Syndrome: See Me Shine!

Smith-Magenis Syndrome (SMS) is a rare chromosomal disorder caused by a deletion or mutation of genetic material from chromosome 17, characterised by an identifiable pattern of distinctive physical features, developmental delays, mild to moderate intellectual impairment and behavioural challenges. It is estimated that SMS occurs in as many as 1 out of 15,000-25,000 people, however it is highly under-diagnosed, with under 100 individuals documented in Australia.

Smith-Magenis Syndrome: See Me Shine introduces us to Indiana and Amélie, two young girls who have been diagnosed with the rare condition. In speaking with their parents and medical experts, we can get an understanding of the syndrome, the challenges faced by the children, the SMS support network and the abilities sufferers show as they grow older.

The short documentary features a number of speakers with various exposure to children with Smith-Magenis Syndrome.

The conclusion to Smith-Magenis Syndrome: See Me Shine is that despite being faced with a serious disability, the children that are diagnosed with SMS can achieve a variety of milestones, including participating at the Special Olympics. The strength of character displayed by children with SMS, is a testament to the work of their families, medical experts and support groups.

The main objective of this short documentary is to generate awareness about the little-known syndrome, detailing the various symptoms and problems faced by diagnosed children and their families and to show children with SMS overcoming adversity to live happy and fulfilling lives. The film also serve to promote Smith-Magenis Syndrome Australia, a charity support network for families affected by Smith-Magenis Syndrome.