Patient stories

Marian Harder is no stranger to hospital stays. The Menominee, Mich. native was born in Marinette, but at 10 days old was taken to HSHS St. Vincent Hospital for a sweat chloride test – the standard test used to diagnose cystic fibrosis (CF).

While listening to Iris’ heart, Dr. Huffer heard a murmur and referred her to Prevea’s team of pediatric cardiology experts in Green Bay. 

When Natalie was diagnosed with Acute Lymphoblastic Leukemia (ALL) T-Cell in 2016, she enrolled in a clinical trial to test a new cancer drug.

Hailee was your typical baby for the first month or so, but when she started not to eat and began to vomit frequently, Shannon knew something wasn’t right.

Three in one million. Those were the chances that 2-year-old Quentin’s face rash and weak muscles were an autoimmune disease known as juvenile dermatomyositis, or JDM.

Prevea Pediatric Neurologist, Dr. Terence Edgar, diagnosed Eloise with cerebral palsy (CP) at 18 months old.

With the extent of Anthony’s bilateral cleft lip and palate known, we started planning for surgery at just a few weeks old.

The hearing aids that Amanda recommended for Aden were life-changing – from the very first moment she turned them on.