Benign Hematology and Sickle Cell Disease Programs at the ʼһ
Benign Hematology Program
Benign hematologic disorders are non-malignant disorders of the blood, including abnormalities of counts, bleeding, blood clots, and inherited conditions such as von Willebrand disease and sickle cell disease (see below). Patients with hemophilia or other severe inherited bleeding disorders are taken care of by the Comprehensive Center for Bleeding Disorders at Children's Wisconsin.
Kaitlin Annunzio, DO, MS
Assistant Professor
Lisa M. Baumann Kreuziger, MD, MS
Professor
Elinor J. Bruders, APNP, MSN
APP Outpatient
Kristen Corrao, MD
Assistant Professor
Amy Detzner, APNP
APP Hybrid
Joshua J. Field, MD, MS
Professor
Patrick C. Foy, MD
Associate Professor
Lynn M. Malec, MD, MSc
Associate Professor
Katrina M. Shay, APNP
APP Outpatient
Roy Silverstein, MD
Professor and Chair Emeritus, Department of Medicine; Associate Director, Medical Scientist Training Program; Senior Investigator, Versiti Blood Research Institute; Professor of Cell Biology and Physiology
Robert Taylor, MD
Assistant Professor
Sickle Cell Disease
Sickle cell disease (SCD) is a genetic disease that primarily affects African Americans. It creates red blood cells that have an abnormal "sickle" shape instead of a normal disc shape. The Sickle Cell Disease Program works closely with the pediatric sickle cell program at Children's Wisconsin and provides care for most adults with SCD in the state of Wisconsin. The clinic provides comprehensive care including disease-modifying therapies, pain management, and urgent evaluations.