A simple blood test, in conjunction with a flu diagnosis, was a blessing in disguise for 5-year-old Ethan Fisher. Fortunately, the hematologist who followed up on Ethan’s low platelet count recognized the possibility of a Fanconi anemia (FA) diagnosis and ordered tests. Sure enough, despite the rarity of this hereditary anemia, Ethan had it—meaning he would need regular blood tests and, eventually, a bone marrow transplant.
Results tagged “Children's Health”
Back in 2010, Sarah Ewald was a high school senior and alpine skier. When she noticed a bump on her foot, she assumed it was a sports injury. But at the close of ski season, she visited a physician to determine why the bump wouldn’t go away. Her doctor diagnosed alveolar rhabdomyosarcoma, a rare and aggressive sarcoma that only affects one in one million children and adolescents. Sarah began chemotherapy the week after diagnosis. That August, surgery removed her spleen and half of her pancreas, where the cancer had spread. Radiation and more chemo followed.
Most University of Minnesota pediatric patient stories have a similar start: Parents discover a medical issue and find their way to University of Minnesota Children’s Hospital. Not so with Lexi and Austin Jensen, each born with only one partially functioning kidney. First, they arrived at the U of M Children’s Hospital—one of the world’s leading kidney transplant centers—and then they found their parents.
Sameer Gupta, M.D., has a passion for tending to sick kids. A critical care physician at University of Minnesota Children's Hospital, Gupta deals with tough situations every day, fighting diseases that have brought youngsters into the hospital--the scariest of places for worried parents. But what those parents don't see is how hard Gupta works behind the scenes to prevent already sick kids from getting sicker--from what medical professionals call "hospital-acquired conditions."
Even when you've been hospitalized countless times and you're supported by a loving network like Lizzie Bell's ... even when you're as tough and brave as Lizzie herself, there's nothing easy about a blood and marrow transplant. It's a grueling and terrifying process. But thanks to several donors and the healing surroundings they've created, it's a lot less scary for some young patients at University of Minnesota Amplatz Children's Hospital.
Little Lydia Kohler's parents were horrified when a large, blood-filled sac in the back of their newborn daughter's head caused her to have a massive seizure, a result of heart failure. But thanks to an innovative treatment by a collaborative University of Minnesota team -- and a strategic use of glue -- little Lydia today is a running, talking, 2-year-old whirlwind, her parents happily report.
The right timing can make all the difference. And where children's brain development is concerned, University of Minnesota researchers are finding that particularly important. "The earlier you intervene, the bigger impact you can have," says Michael Georgieff, M.D., director of the University's Center for Neurobehavioral Development and a neonatologist at University of Minnesota Amplatz Children's Hospital. "You're laying the foundation for a healthy adult mental life."