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PUMPA - Purine Metabolic Patients' Association

Dr Bridget Bax
Child Health
Division of Clinical Sciences
3rd Floor, Lanesborough Wing
St. George's, University of London
Cranmer Terrace
Tooting
London
SW17 0RE

Tel: 020 8725 5898
web: www.pumpa.org.uk

PUMPA is a registered charity supporting patients with genetic metabolic disorders. There are 28 purine metabolic disorders with a wide range of symptoms. PUMPA's constitutional aim is to advance knowledge of purine metabolic disorders among the medical profession and the public. By so doing, it aims to improve the care of patients and the support for them and their families. The main activities include the following:

  • Supporting research - PUMPA currently helps fund research at the purine research laboratory at St Thomas' Hospital in London which provides the only diagnostic service in Britain and has an international reputation.
  • Supporting patients - although there are no cures and only some patients can be treated, others can be helped to live with their disability.
  • Spreading knowledge - the Association produces a newsletter for members and organises an annual seminar on one of the diseases; information is also made available to the press and medical profession.
  • Fundraising - in order to maintain support for the purine research laboratory and to promote it as a proposed European centre.
  • PUMPA has produced booklets on Caring for Children with Lesch Nyhan Syndrome, Caring for Children with APRT deficiency, Caring for Children with FJHN, Caring for Children with ADA deficiency.
Checked: 31 Oct 2011
For the planned review period see the Data Creation and Quality Control Process.

Comprehensive patient resources are available at www.patient.co.uk

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