Super Tiny, Huge Hope
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When Kenadie was born, doctors told her parents that she only had days to live. When she made it past that mark, they said she would never talk, never walk and she proved them wrong. Kenadie is the rarest of the rare, the littlest of the Little People, she has been diagnosed with a genetic condition called primordial dwarfism that is thought to affect only about 100 people worldwide. Beyond its rarity it differs from conventional dwarfism in that Kenadie, at four years old and 30 inches (76cm) tall, is perfectly proportioned for her size. Kenadie has many health issues related to her condition, so every day is a blessing.