Since September, Emma Lynn Kissock has been seen by 50 doctors, undergone seven surgeries, been resuscitated eight times, worn a chest-to-ankle cast and -- most recently -- had a feeding tube attached. Despite all the tests and medical examinations, doctors haven't been able to figure out what's wrong with her. Adding to the anxiety is Emma's age: the Bloomington girl turned 1 just two weeks ago. "We think it's a syndrome," said Jean Rollins, the parish nurse at St. John's Lutheran Church in Chaska, which held a fundraiser for Emma last week. "It could be so rare that no one's run into it as yet."
Dr. Nancy Mendelsohn, a geneticist at Minneapolis Children's Medical Center, has been sending information about Emma's case to colleagues around the country without success.
Mendelsohn readily admits that she hasn't been able to figure out what's ailing Emma -- and even speculates that there is a chance that doctors might never be able to say what is causing her condition.
"I feel this is a puzzle we're putting together," Mendelsohn said. "We never say 'never,' but we do sometimes say we don't have any great ideas."
Although Mendelsohn said it is too early to declare that Emma is suffering from a new type of syndrome or illness, the girl's family and some of the people treating her have given her condition a nickname.
"They call it Emma's syndrome," Rollins said, "because they can't figure it out."
Robin Kissock, Emma's mother, said the situation has strained the family emotionally and financially. She said the family was incredibly grateful for the more than $15,000 donated at last week's fundraiser at their church.
"I don't know what to make of it all," she said of her daughter's condition. "The hardest part has been not knowing what to expect."