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Born with spina bifida, Tana spent her first four months in a neonatal intensive care unit. Also diagnosed with a brain malformation, breathing disorder and MRSA—commonly known as a "super bug” because it's so hard to treat, she has suffered multiple illnesses, some of them life-threatening.
Working as a team, PHS staff, her family and Tana's other providers and caregivers make it possible to keep her at home and make fewer trips to the hospital—sometimes even when she is seriously ill.
Tana has not only exceeded expectations she would live to age five, she enjoys a remarkable quality of life. Although she is wheelchair-bound, doesn't speak and is fed through tubes, she goes to school, takes weekend trips to the cabin, swims, tubes, and goes four-wheeling. She has even taken family trips to Mexico and Disney World. People who get to know Tana, says mom Jill, look beyond all the equipment and see her for who she really is: "a girl who is full of joy, loves life, and doesn't let a moment pass her by."
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