In memory of Amelia Ridout, a darling six-year-old girl whose life was tragically cut short due to an inconsistency in the approach and guidance related to Bone Marrow Aspirations (BMAs). Amelia's passing highlights a loophole in our healthcare system which currently lacks standardised protocols for BMAs, leading to methods varying from doctor to doctor, from hospital to hospital.

We petition for the NHS, the British National Institute for Health and Care Excellence (NICE), and the British Society for Haematology to construct a comprehensive database on BMAs conducted throughout the nation. This proposed database aims not to point fingers at medical professionals but to standardise the approach for BMAs, eliminating ambiguities, enhancing communication, and curbing preventable complications or fatalities.

Furthermore, using the accumulated learnings from this database, we strongly urge for the development and implementation of universally accepted, evidence-based procedures for BMAs—dubbed "Millie’s Method".

With thousands of BMAs performed each year in the UK, the potential for complications is unfortunately significant. Establishing the BMA database and adopting a universally used "Millie’s Method" for BMAs, we could significantly reduce the risk involved for patients requiring this essential procedure.

Together, let's safeguard lives. Let's ensure that no other family has to face the loss of family member, a Child. The creation and implementation of a national database and "Millie’s Method" will enhance the safety of BMAs and serve as Amelia's lasting legacy. Please, sign this petition and support this invaluable amendment for the greater good of all patients requiring BMAs.