Finn

Hunter syndrome, a rare genetic disease affecting fewer than 500 boys in the United States, shapes every day of young Finn's life; this intimate documentary tells his story.

An intimate, tender portrait of a boy living with a rare disease, and of the family love that surrounds him.

Hunter Syndrome is a rare genetic disease that affects less than 500 boys in the United States. These boys are missing an enzyme used to break down cellular waste. Here is the story of one.

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