Page results
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Patient information for patients undergoing Image Rehearsal Therapy (IRT).
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This page is for patients who are receiving radiotherapy to the bladder. It explains what the treatment involves, describes side-effects you may experience during and after treatment, and how best to cope with them.
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This page, written by the Physiotherapy Services at the Royal London Hospital for Integrated Medicine, is intended for patients (or their family or carers) who have been referred to the clinic.
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Information about the musculoskeletal medicine service at the Royal London Hospital for Integrated Medicine.
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Information about the nutrition and dietetics service at the Royal London Hospital for Integrated Medicine
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The Neurogenetics Unit offers a fully integrated service encompassing clinical assessment, diagnosis, molecular genetic testing and counselling for neurogenetic conditions.
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This clinic is for asymptomatic travellers (individuals with no current symptoms) who have travelled to a tropical destination and are worried about certain infections.
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This phlebotomy service is appointment based only (persons who are solely requiring a blood test), including GP patients (Camden & Islington)
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Diagnostic cytology is a specialist discipline that provides the examination of samples taken by non-invasive or minimally invasive procedures.
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Preparations for the festive season are in full swing in the UCLH Charity fundraising team.
File results
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FOI/2023/0182 - Data privacy compliance tools
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FOI/2023/0083 - Software systems/ suppliers used at Trust
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FOI/2023/0069 - Operations waits for under-18s
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FOI/2023/0073 - Telephony and UC/ collaboration, Microsoft 365 licence and on-premise or cloud storage
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FOI/2023/0075 - Attrition rates for staff working in advanced practice roles
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FOI/2023/0080 - Treatment for Myeloid leukaemia (AML) and chronic lymphocytic leukaemia
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FOI/2023/0081 - Biometric technology wearables/ data collection
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FOI/2023/0082 - Organisation structure for Performance and Planning department
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FOI/2023/0099 - Number of autoclaves used at Trust
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FOI/2023/0103 - Genetic Haemochromatosis patients