The twins were born three months premature with their patent ductus arteriosus’ (PDA) still open. The Kid Experts at Children’s Minnesota developed a standard guideline and protocol for preterm babies requiring transcatheter closure of their PDA, meaning Madison and Peyton were in the best hands possible.
Four out of the six members of the Jahnz family have a blood clotting disorder called protein S deficiency. Staying positive has been a huge part of how they’ve moved forward as a family.
During the event, children battling cancer participated in Hyundai Hope On Wheels’ signature Handprint Ceremony, in which they dipped their hands in paint and placed their handprints on a white 2023 Hyundai Tucson.
Brianna Albrecht talks about being physical therapist at Children's Minnesota for National Rehabilitation Awareness Week.
Children’s Minnesota psychologists share tips for how to prepare for the conversation about suicide, have the conversation and to be prepared with outside resources.
In honor of Hispanic Heritage Month, we spoke with Wendy Zúñiga, pharmacy coordinator and co-chair of the Voces employee resource group (ERG) at Children’s Minnesota, to learn more about her role, involvement with Voces and what Hispanic Heritage Month means to her.
Some of our kid experts for the cancer and blood disorders program have joined Team Superstars and will be raising funds for the Cancer Kids Fund while running the Medtronic Twin Cities 10 Mile race on Sunday, Oct. 1, 2023.
From the outside, Matty looks like your typical 14-year-old who loves sports, especially hockey. But all his activities had to come to an abrupt stop when he was first diagnosed with ITP, a platelet disorder that can make bleeding from a cut or injury hard to stop.
The Franklin family of five lives on a small lake in Chanhassen, Minnesota where they love to play outside on the lake swimming and boating. But, their lives changed when the baby of the family, Levi, was diagnosed with acute lymphoblastic leukemia (ALL) at just 21 months old.
For 10-year-old Riley and his family, the summer was not the break they were hoping for. In early June, Kacy and Cody got the news that their son had a rare form of Hodgkin’s lymphoma. They were understandably sad and hoping it was all a bad dream. But from the beginning, the family decided they were going to face cancer head on and focus on staying positive.