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Sickle Cell Disorder – Information and Support Links

Add these links along with the below .

Resources » Sickle Cell Society
Sickle Cell Disorder Resources for Patients | NHLBI, NIH
Sickle cell disorder – NHS
Let’s Keep Talking – Living your life with Sickle Cell Disease
Sickle Cell disorders | Contact
Patient Public Voice Group (PPV) – Haemoglobinopathy Coordinating Centre

SYSCO – South Yorkshire Sickle Cell Organisation

Introductory Paragraph Explaining the Links

This page brings together a range of trusted national and patient‑focused resources to support individuals living with sickle cell disease, their families, and carers. The links include information from established organisations such as the Sickle Cell Society, alongside patient advocacy, and support groups. These resources offer guidance on understanding sickle cell disease, managing day‑to‑day life, accessing services, and connecting with support networks and lived‑experience communities.


Disclaimer:
The external links provided on this page are for information and support purposes only. We do not control or endorse the content of external websites and are not responsible for the accuracy, completeness, or updates of the information they contain. Information found through these links should not be used as a substitute for professional medical advice, diagnosis, or treatment. Always seek advice from a qualified healthcare professional regarding any medical concerns.

Could the same disclaimer go on the below page please ?

Children and Young Person’s Archives – Haemoglobinopathy Coordinating Centre

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