Kasey Reamer, 14, loves snowmobiling, archery, hot pink and sleepovers with her best friend.
"She wants nothing more than to be normal, like everybody else," said her mother, Julie Reamer.
But Kasey's quest for a "normal" life has faced more challenges than most people encounter in a lifetime. Born with Goldenhar Syndrome, a rare birth defect, Kasey is deaf, blind in one eye, and has a fused spine and only partial jawbones. A doctor told her parents she'd never walk, but Kasey proved him wrong. She's undergone more than 20 surgical procedures and uses a tracheal tube to help her breathe.
"She's the toughest person I know," said her father, Paul Reamer, recalling the time Kasey was running the halls of the intensive-care unit just six hours after major surgery.
That irrepressible spirit made Kasey an immediate choice when the staff at Children's Hospitals and Clinics of Minnesota was asked to recommend a deserving child to receive a bedroom makeover via Special Spaces, a Knoxville, Tenn.-based nonprofit with a new chapter in the Twin Cities.
"Kasey is awesome. Her whole life, she's had a positive attitude, instilled by her parents," said Jeri Kayser, a child-life specialist at Children's Minneapolis campus. "A lot of kids in situations like that hit roadblocks, but Kasey is always ready to try one more thing, with that can-do attitude of hers."
Special Spaces' mission is to provide dream rooms for kids with life-threatening illnesses, to give them a comfortable, inviting place to recharge and recuperate. "Emotional state is really important when healing," said Chelsey Green, director of the Minneapolis chapter.
And families that have kids with continuing medical challenges often don't have surplus cash for decorating projects, Kayser said. "It's really hard on families financially. Any extra resources are plugged into the child's health care."