Children born with sickle cell disease (SCD) will need to start treatment a few months after birth to help prevent serious complications. Because SCD affects every organ in the body, kids with the condition need ongoing preventive care. They also need specialized care from a pediatric hematologist  (a doctor who focuses on blood disorders), as well as other types of specialists.

In our Pediatric Sickle Cell Program, our specialists provide comprehensive care for hundreds of pediatric patients and understand the specific needs of kids born with SCD. Our goal is to help children with SCD lead normal, healthy, carefree lives as much as possible.  

We partner closely with other specialists, such as pediatric pulmonologists (lung doctors) to treat conditions related to SCD, such as asthma. We’ll work with you and your child to help find any complications as early as possible, so we can begin treatment early. We also work with you to advocate for your child to get the accommodations they need to stay healthy at school, whether it’s having a water bottle at their desk, having door-to-door transportation, or wearing a jacket in the classroom to stay warm. These accommodations can make a huge difference in the quality of life for a child with SCD.

As your child approaches adulthood, at around age 21, our Transitional Care Clinic can help your child transfer their care from our Pediatric Sickle Cell Program to our Adult Sickle Cell Program.

Contact Us

850 Harrison Avenue, Boston, MA 02118
6th Floor
Yawkey Center
617.414.4841

Monday, Wednesday, Friday: 8:00 AM - 5:30PM Tuesday, Thursday 8:00 AM - 8:00 PM

Specialty Clinics

Programs and Services

Conditions We Treat

Patient Stories

Support Services

Our Team

Program Leadership

Hematologists

Pulmonologist

Robyn T Cohen, MD, MPH

Associate Medical Director of Asthma Initiatives, Population Health Services, Boston Medical Center Health System