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Haemochromatosis Society

Hollybush House
Hadley Green
Barnet
EN5 5PR

Tel: 020 8449 1363
Fax: 020 8449 1363
Web: www.haemochromatosis.org.uk
Best time to telephone: Monday - Friday, 9am - 5pm

The aims and activities of the Haemochromatosis Society include the following.

  • To support people with haemochromatosis by providing help with their problems.
  • To ensure brothers, sisters and children are tested in due time.
  • A quarterly newsletter is published giving news and views from members in the UK and from around the world. A handbook is provided for members.
  • Opportunities to meet other members living nearby are arranged if they wish.
  • To promote awareness among the health professions, patients and their families, the general public and policy makers so that the condition may be diagnosed and treated in time.
  • There is also a need to overcome the misconceptions that haemochromatosis is rare, that only middle-aged men are at risk, and that women are seldom affected until their menopause.
  • To provide resource material for the allied medical professions and encourage research.
  • The Society keeps up to date on the latest studies of cause, diagnosis and treatment. The Society belongs to the umbrella organisations the Genetic Interest Group and Contact a Family, and is affiliated to the British Liver Trust and has contact with support groups in many countries.
Checked: 25 Feb 2008

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PS - Health and Poverty

Perhaps the biggest cause of ill health in the world is poverty. Help to Make Poverty History. For example, why not lend some of your money to disadvantaged communities to enable them to trade their way out of poverty through schemes such as Shared Interest.

See also MAKEPOVERTYHISTORY North East for details and links to campaigns against poverty.

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