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UK Thalassaemia Society

19 The Broadway
Southgate Circus
London
N14 6PH

Tel: 020 8882 0011
Web: www.ukts.org

The UK Thalassaemia Society was formed in 1976 by parents of children suffering from thalassaemia. The Society is registered with the Charities Commission and most of the work is carried out by volunteers. The Society produces information in various languages and also a quarterly news review for the members of the Society. The aims of the Society are as follows:

  • The relief of persons suffering from thalassaemia.
  • The promotion and co-ordination of research in connection with thalassaemia.
  • To educate people on the problems of thalassaemia. This includes lectures with the aid of slides and/or video films in order to explain it in simple language to any group of people who wish to learn about it.
  • To offer counselling to sufferers and carriers.
  • To bring together patients, families and well-wishers to exchange ideas and information.
  • To raise funds required for the above activities.
Checked: 18 Feb 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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