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COVID-19 Advisory: If you have a fever or cold like symptoms, call us before visiting our clinics or emergency department. Only one primary caregiver may accompany a patient at all locations. No other visitors allowed. For more information visit our COVID-19 Resource Center.

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
  • Echocardiogram
  • Ultrasound
  • X-rays
  • 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, there is no cure for sickle cell disease. But we’re committed to finding one. 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. We always make sure to match eligible patients with the best possible treatment and the most up-to-date medications.

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