Sickle Cell Disease: Transitioning From Pediatric to Adult Care

About the Sickle Cell Disease Transition Program

With the only program of its kind in Metro Atlanta, Children's is leading the way in developing support for teens and young adults in their transition from pediatric to adult care.

Collaborating with the Sickle Cell Foundation of Georgia and Grady Memorial Hospital, we aim to empower patients with the skills and the knowledge pediatric sickle cell disease patients need in order to make a seamless shift into the adult healthcare system.

Why is the transition program important?

The transition from pediatric to adult sickle cell disease care is a crucial time for young adults, typically ranging from 18 to 24 years old. This period can be daunting, as these young adults face challenges that can lead them to feel lost in the healthcare system.

Developing the skills to manage their health and navigate the adult care landscape enhances their chances of staying connected to care, ultimately reducing the risk of complications and improving their overall well-being.

Our Sickle Cell Disease Transition Program is committed to elevating the level of care for those with sickle cell disease by providing structured Health Care Transition (HCT) services, aligning with standards set by Got Transition.

Participants can take full advantage of our structured program, with added support from the Sickle Cell Foundation of Georgia. Patients and their families will collaborate closely with a multidisciplinary team at both Hughes Spalding Hospital and Arthur M. Blank Hospital to create a tailored care plan that addresses their unique transition needs.

Multidisciplinary team members include:

• Clinician or physician
• Social worker
• Nurse
• Psychologist
• Child life specialists
• School teachers
• Nurse navigator

For more information about our Sickle Cell Disease Transition Program, contact aflacscdtranscoord@choa.org.

When

Coming soon

Location

Coming soon