Fanconi Anaemia

The Government is committed to improving the lives of those living with rare diseases, including Fanconi Anaemia. Where possible, the National Health Service offers reproductive options for carrier couples wishing to have a baby, including prenatal counselling prior to conception, testing in early pregnancy, and preimplantation genetic testing. The UK Rare Diseases Framework also sets out four priorities collaboratively developed with the rare disease community, which include: getting a final diagnosis faster; increasing awareness of rare diseases among healthcare professionals; better coordination of care; and improving access to specialist care, treatments, and drugs. We published the annual England action plan in February 2025, where we report on the steps we have taken to advance these priorities. The Government will be working with the devolved administrations this year to review what comes next, following the expiry of the UK Rare Diseases Framework in 2026, to support all those diagnosed with a rare diseases, including Fanconi Anaemia.