COVID-19 Advisory
If you or your child has COVID-19 symptoms (fever, cough or shortness of breath) or other COVID-19 concerns, call your child’s doctor or visit Children’s Online Urgent Care.
If you or your child has COVID-19 symptoms (fever, cough or shortness of breath) or other COVID-19 concerns, call your child’s doctor or visit Children’s Online Urgent Care.
When conventional treatments aren't working, doctors at Children's Wisconsin can turn to the future of medicine.
As challenging as they can be, remember, sleep struggles are temporary. And with some helpful tips, you and your baby will get the rest you both need.
As a neonatal nurse practitioner in the Neonatal Intensive Care Unit here at Children’s Wisconsin, I have the honor to meet so many courageous families. One of those families, Adam and Molly Van Zeeland of Appleton, recently were generous enough to share the story of their daughter Macy’s first few weeks of life, which have been eventful, to say the least. (Watch their video here)
It was known during Molly’s pregnancy that Macy would have potential kidney and heart abnormalities, but when she was born it was quickly discovered that she had other significant issues as well. After being transferred here to our Children Hospital of Wisconsin NICU in Milwaukee, Macy was diagnosed with a pair of birth defects known as TEF/EA — an esophageal atresia, which means she was born with an interruption in her esophagus (food pipe), so her food was not getting all the way to her stomach; and a tracheosophageal fistula, which is an abnormal connection of the trachea (windpipe) and the esophagus.
Molly and Adam did such a great job explaining not only what was going on with their daughter — who underwent surgery at just 3 days old — but also sharing what it’s like for families going through this experience.
I was thrilled to be able to join them to lend some medical expertise, alongside Edward Kirkpatrick, DO, who gave insight into how we treat pulmonary hypertension, which is another condition Macy is dealing with. Videos like this are a great opportunity to learn more about the amazing stories that happen every day in our NICU.
When conventional treatments aren't working, doctors at Children's Wisconsin can turn to the future of medicine.
For kids with motility disorders, a new device is providing relief and hope.
What was supposed to be the happiest time of their lives quickly came crashing down.
For Becky and Jerry Jendusa, and their five children, giving back and helping others are their family's mission.
The Gender Health Clinic is the first clinic in southeastern Wisconsin dedicated exclusively to caring for gender diverse kids.
Up until the age of 16, kids have growth plates at the end of their bones where the bone grows longer. If a break includes the growth plate, it requires pediatric expertise to treat.
As the whole world adjusts to the realities of social distancing, 20-year-old Taylor has been living with it her whole life.
