Megan Parrish

August 21, 2017

Young Woman Manages Rare Blood Disorder with Help of UAMS

Susan Van Dusen

Megan Parrish and Peter Emanuel

For about six years, Megan Parrish didn’t know what was happening to her own body. The teenager would miss school and outings with her friends due to bouts of extreme nausea, pain and dizziness. Her behavior also changed, although she couldn’t pinpoint any reason or pattern for the psychological and physical symptoms. “For a while…