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• Meet Matthew and Lillyanne

  Matthew Fielden and Lillyanne Tran volunteer in the cognitive disorders outpatients’ clinic at the National Hospital for Neurology and Neurosurgery.

• UCLH welcomes its 1,000th NHS proton beam therapy patient – meet Seren

  UCLH has welcomed its 1000th patient to our proton beam therapy department, which opened in December 2021.

• Prime Minister visits UCLH vaccination centre

  Prime Minister Boris Johnson visited the vaccination centre at the Islington Business Design Centre yesterday. 

• App detecting neonatal jaundice from the eye successful in first major clinical trial

  A smartphone app that identifies severe neonatal jaundice could provide a cheaper alternative to expensive screening procedures, according to a study by UCLH, UCL and the University of Ghana.

• Hydrogen / methane breath test for fructose / lactose malabsorption – Face-to-face testing

  This page is for patients who are doing a face-to-face breath test in the hospital to test for either fructose or lactose malabsorption.

• Hydrogen / methane breath test for fructose / lactose malabsorption – Testing at home

  This page is for patients who are doing a breath test at home for either fructose or lactose malabsorption.

• Hydrogen / methane breath test for bacterial overgrowth – Testing at home

  This information is for patients who are doing a breath test at home.

• UCLH to lead data initiative to improve care for myeloma patients

  UCLH is to lead an initiative to improve care for myeloma patients alongside Oxford University Hospitals NHS Foundation Trust (OUH) and University Hospital Southampton NHS Foundation Trust (UHS).

• Hydrogen / methane breath test for bacterial overgrowth – Face-to-face testing

  This page is for patients who are doing a face-to-face breath test in the hospital. Please read it carefully before you arrive for your test.

• Publications and Reading Material

  The Sickle Cell Society (SCS) and the UK Thalassaemia Society (UKTS) have worked in partnership with the NHS sickle cell and thalassaemia (SCT) screening programme to engage with communities less likely to access health information through usual NHS channels. The societies provide feedback from people that share the same population background or have experience of the condition and to feed into the programme updates and improvements.