Programs & Services
Sickle Cell Program
How we treat sickle cell disease
In addition to a complete medical history and physical examination, diagnostic procedures for sickle cell may include:
- Blood tests
- Pulmonary function testing
- Newborn hemoglobinopathy testing
- A complete family history
Treatment also includes adding preventative measures into a patient’s daily life, including drinking more water to stay hydrated, and managing the pain and symptoms at home with over-the-counter and prescription medications.
Sickle cell disease brings lifelong changes to a patient. We’re here to ease the disease’s affects and help patients and families cope — today and for years down the road.
An early diagnosis
Early diagnosis is essential to providing the best preventive treatment for complications of sickle cell disease. We can perform hemoglobin electrophoresis, a blood test that determines if a child is a carrier of a specific sickle cell trait or has any of the diseases associated with the sickle cell gene.
Finding a cure
Currently, bone marrow transplantation is the most effective treatment for sickle cell disease. But we’re committed to finding more solutions. We’re involved with the latest research and clinical trials, and we give families the opportunity to participate in trials unique to the world-class research being conducted at Phoenix Children’s. From new medications to bio-technologies — like gene therapy with genetically modified stem cells — we always make sure to match eligible patients with the best possible treatment options.