“You could never tell this little girl has three tubes in her."

Natasha Fuller is just 8 years old, but her grandmother, Chris Burleton, told the Fond du Lac Reporter that she doesn't let her medical condition faze her. “She is happy and sassy, and she just wants to lead a normal life, and do things like go swimming.”

Natasha was born with a rare abdominal muscle condition called Eagle-Barrett Syndrome, or "prune belly syndrome." Among other things, this means that her eight years of life so far have been plagued by urinary tract complications. She lives with her grandparents in Oakfield, Wisconsin — some 400 miles away from her parents and twin sister in Oklahoma — where it's easier to see the doctor, including thrice-weekly trips to the hospital for kidney dialysis.

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