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9 films
Nearly 700 British Pakistani children are born with serious disabilities each year due to the high rate of first-cousin marriages in their communities.
Rebecca Medley, an 11-year-old girl with Prader-Willi syndrome, weighs 154 pounds and struggles with an uncontrollable obsession for food.
Karen, born with albinism and blindness, faces the challenges of Crohn's disease and a rare genetic disorder called Hermansky-Pudlak Syndrome.
Nineteen-year-old Stuart Wickeson, diagnosed with Duchenne muscular dystrophy, prepares to start university despite a life expectancy in the early 20s.
Children with Prader-Willi syndrome in Britain face extreme food fixation, leading families to implement strict measures to manage their unique challenges.
Eighteen-year-old Louise Wedderburn has fibrodysplasia ossificans progressiva, a rare condition that causes her muscles to turn into bone, with an average life expectancy of 41.
Alphée, a girl with a rare genetic disorder, challenges medical expectations as her father, Hugo Latulippe, dedicates a year to her education for classroom integration.
Jonny Kennedy has Dystrophic Epidermolysis Bullosa, a genetic condition that causes his skin to blister and come off with the slightest touch.
Mia suffers from a rare mitochondrial disorder that causes seizures and requires constant care, leading her family to a children's hospice in Berlin.
