"Working together we can secure the best use of scarce expertise and resources, maximising the health gain for all those with rare conditions" Alastair Kent OBE, Chair of RDUK

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Motor Neurone Disease Association

dsd families

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Children's Liver Disease Foundation

Pemphigus Vulgaris Network

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Birdshot Chorioretinopathy Uveitis Society

The Arran Brown Rainbow Foundation

Purine Metabolic Patients' Association

Ataxia South Wales

George Pantziarka TP53 Trust

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RDUK News

Latest News

RDUK AGM 2011 - 12th September, London

RDUK will be having our 2011 AGM on the morning of September 12th at the NCVO near King's Cross, London. This will be an opportunity to learn more about what RDUK have been doing in the last year and what our plans are for the year ahead. We are also pleased that Dr Ed Jessop from the National Specialised Commissioning Team will be attending to update us on the development of a UK strategy for rare diseases and how RDUK can continue to contribute to this. For more information and details on how to register your attendance, please click here..

Consultation on rare disease strategy due Autumn 2011

At a recent meeting with Dr Ed Jessop from the National Specialised Commissioning Team, he again confirmed to RDUK that a consultation on the UK rare disease strategy should be launched in the Autumn. Look out for details on how we'll be helping you respond to this consultation when it is launched.

 

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