Educational Media Reviews Online

This is an absolutely beautiful film about hope and a family, who in the face of adversity, show such strength and determination it will be inspiring to all who watch this film. Logan Madsen is literally a one in a million person. Logan was born with Miller Syndrome, an extremely rare genetic disease also known as Postaxial Acrofacial Dysostosis, Logan has not only learned to cope with his disease but thrive within a difficult situation. Facial deformities such as cleft lip and/or palette, absence of lower eyelids, ear deformities and hearing loss are common with Miller Syndrome. Arm deformities with shortened limbs as well as absent fingers and toes are also common. In addition Logan was also diagnosed with Autism.

He is an extremely talented artist with paintings that look like photographs. His artwork is stunning filled with expression and feeling. He has learned to accept his disease through his art often painting self-portraits. Since his lower arms are short and malformed he needs customized equipment and has adapted to his life style. Little is known regarding this disease so he has learned to enjoy life as it comes and live each day to its fullest.

His older sister is also affected with the disease. His parents in particular his mother, have provided constant support and encouragement. It is truly a heartwarming story with an important lesson. Life isn’t always what we expect it to be. Special needs means a different approach to everyday tasks. Logan is full of hope and inspiration. How we approach life and what we do with this gift is what matters. Contains graphic photography of injuries and may be disturbing to some viewers.

Awards

• Best Documentary, Carmel International Film Festival, 2017