Page results
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Among the many cancer clinical trials opening each year at UCLH, this year will see a focus on trials of personalised cancer treatments based on precision immunotherapies.
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The NHS has become the first healthcare system in the world to provide a new blood group genotyping test which is set to transform care for patients living with sickle cell disorder and thalassaemia.
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People with the acquired communication disorder aphasia – which involves problems with the understanding or production of speech –have benefitted greatly from a two-year programme of therapy at the National Hospital for Neurology and Neurosurgery at UCLH.
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This page has been written by the team in the mitochondrial clinic for patients who are seen at the National Hospital for Neurology and Neurosurgery, who have a diagnosis of mitochondrial disease.
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UCLH is continuing to scale up the number of services that offer Advice & Guidance, as well as identifying various improvements within the existing Advice & Guidance service. Over the last few months, UCLH has introduced 5 new specialties to the service, with additional specialties due to go live shortly.
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Our staff have rated UCLH as the top trust in England, improving on our ranking from last year when we were third best in England and top in London.
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UCLH is the first NHS trust to pilot a personalised educational package for patients living with stroke.
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The Adult Acute speech and language therapist (SLTs) work across a range of acute hospital specialities.
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RNOH are pleased to launch a series of regular Health and Wellbeing Information and Support Sessions to support patients following a cancer diagnosis and also during/after treatment. Theseā¦
File results
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FOI/2023/0589 - International nurse recruitment
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FOI/2023/0566 - Structure chart for IM &T, Business Intelligence, Informatics
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FOI/2023/0559 - Patients admitted to hospital with dental distress
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FOI/2023/0560 - Digital maternity training platform
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FOI/2023/0561 - Birthrate Plus
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FOI/2023/0563 - Treatment for Haemophilia B and Von Willebrand disease
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FOI/2023/0565 - Rare diseases - diagnosis/ treatment for Fabry/ Gaucher/ Pompe
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FOI/2023/0578 - Spinal Muscular Atrophy (SMA) patients
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FOI/2023/0581 - Treatment of Haemophilia
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FOI/2023/0579 - Procurement for specialist seating for patients