Page results
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If ataxia runs in your family, you can get tested to see if you have the genetic mistake for it Ataxia is a health condition that causes problems with movement…
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The support and information specialists were shortlisted for a self-care innovation award. The award recognises the achievements of the team in developing and delivering a package of support for…
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November is men’s health month (Movember), we are hosting our first public Live Q&A event via MS Teams.
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Neuro-rehabilitation multidisciplinary team Neuro-rehabilitation has a multidisciplinary team approach to patient care. The MDT team has expertise in neuro-rehabilitation and work together to…
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UCLH has opened a new clinic for neurology patients with ‘long Covid’ at the National Hospital for Neurology and Neurosurgery (NHNN) with funding from the National Brain Appeal. The…
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The Respiratory outpatient physiotherapy service supports patients under the care of the respiratory medicine department and COVID-19 clinics. We take referrals directly from these services to…
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There is lots of information available online - here are some useful resources:
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Introduction Fatigue is a common and invisible symptom that is not always obvious to others such as partners, family members, friends or colleagues. As a result others may not understand the…
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“No one is invulnerable” – stark messages from patients and staff about the realities of coronavirus
The enormous pressure our staff are under was the focus of a powerful BBC News report about the surge in Covid-19 cases broadcast on Wednesday 6 January.
File results
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FOI/2023/0231 - Patients seen at A&E with symptoms of taking nitrous oxide gas
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FOI/2023/0235 - Hip and knee arthroplasty litigation
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FOI/2023/0237 - Software solution to manage patient e-consent for school vaccinations/ immunisations and waitlist validation
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FOI/2023/0244 - IT systems for digital dictation, speech recognition, outsourced transcription, video consultation and health information systems
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FOI/2023/0247 - Treatment guidelines for Idiopathic Pulmonary Fibrosis
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FOI/2023/0242 - Treatment of Haemophilia A
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FOI/2023/0249 - Treatments for clotting disorders - Haemophilia B, Von Willebrand Disease
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FOI/2023/0260 - Treatment for rare diseases: Fabry, Gaucher and Pompe disease and Hunter Syndrome
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FOI/2023/0332 - Eating disorder services and Advance Decisions/ Directives to refuse medical treatment (ADRTs)
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FOI/2023/0262 - Clinical trial participation