Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps he is taking to raise awareness of sickle cell disease amongst the Latin American and Latinx community.

The Government is committed to improving the lives of those living with rare diseases such as sickle cell disease. Increasing awareness of rare diseases in healthcare professionals is one of the four priorities of the UK Rare Diseases Framework. We published the annual England action plan in February 2025, where we report on the steps we have taken to advance this priority.

In England, there are approximately 17,000 people living with sickle cell disease, an inherited blood disorder with approximately 250 new cases a year. It is the fastest growing genetic condition in the country. It is generally more common in people of black African and black Caribbean heritage, 77% of patients, however, we recognise that the condition is not unique to this community and NHS England remains committed to delivering quality improvement to all patients living with sickle cell.

Our national Can You Tell its Sickle Cell campaign launched in 2022, to boost public awareness of sickle cell disease, including in the Latin American and Latinx community, and help staff better understand the condition, crises, and how to care for patients during their greatest hour of need. Co-developed with NHS England’s patient advisory group, clinical experts, and the Sickle Cell Society, the campaign included staff resources as well as hand-held patient cards distributed via haemoglobinopathy coordinating centres. The campaign was relaunched as part of Sickle Cell Awareness Month in 2025, and an information toolkit remains available on the national Campaign Resource Centre.