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Clinical Information

This page is for clinical staff involved in caring for people with Sickle Cell Disease (SCD).

It brings together regional guidelines and key documents to support safe and consistent care. The page is a work in progress, and more resources will be added.

Patients and families are welcome to read this information to understand the care processes and standards used across the region.

Please note:

  • These are regional guidance documents, not replacements for local policies.
  • Clinicians must continue to follow their own trust’s protocols and governance processes.
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