Binta navigates life with sickle cell disease with strength, learning to manage her health and advocate for herself with support from Children’s Minnesota.
Jariah never lets sickle cell disease define her. With her determination and specialized care at Children’s Minnesota, she thrives in school, music, and life.
Naziere “Naz” Evans has been in and out of the hospital more times than he can remember. Each time he was admitted, it was for
It’s understandable why many African Americans don’t donate blood. At one point in our history, we were turned away. But this Juneteenth, I urge you
My daughter has sickle cell disease. This is how she has changed my life.
Children’s Minnesota is pleased to announce that Dr. Stephanie Fritch Lilla has accepted the role of medical director of the sickle cell program.
Caring for kids is about more than treating their illness or condition—it’s about also caring for the whole family. That’s why family support services for
Children’s Minnesota is partnering with more than 30 local businesses during September for the Shine Bright for Cancer Kids campaign, the health care system’s annual
Mikayla has been in the hospital more than 100 times. And she’s only 13. Born with sickle cell disease, a disease that primarily affects people
A day for our generous community to join together to ensure that even the tiniest hearts get the strongest possible start.
