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Even though Hannah Ostrea died when she was 3, her family plans to make sure her name and memory live on through the Little Miss Hannah Foundation, which offers resources to families with children of life-limiting rare diseases.
Sixteen years ago, Karen Leavens gave birth prematurely to a son, Adam. Within a few weeks, she and her husband learned he couldn’t see. Without services available for the blind, the Leavens considered moving out of state. In 2006, the Nevada Blind Children’s Foundation came to fruition, and Adam began participating in its programs, which changed his life.