Haemochromatosis Society


Our Society is here to support people affected by genetic haemochromatosis and their families.  We also encourage research into the condition and its management and educated the medical profession, policy makers, patients and others, to improve the rates and ages of diagnosis.

The charity was founded in 1991 by people affected by genetic haemochromatosis, is run by people affected by genetic haemochromatosis, and exists to provide benefits for people affected by genetic haemochromatosis

Haemochromatosis, or GH (Genetic Haemochromatosis), is a genetic disorder causing the body to absorb an excessive amount of iron from the diet. The iron is then deposited in various organs, mainly the liver, but also the pancreas, heart, endocrine glands, and joints.

If identified early, Haemochromatis can be readily treated and patients can enjoy a normal lifespan and good quality of life.

Service Details

The Haemochromatosis Society, Hollybush House, Hadley Green Road, Barnet, EN5 5PR (directions displayed on map)
Haemochromatosis Society
Service Type:
Associations and National Organisations

Time and Date Information

Opening Times:

We are open:

Monday to Friday 9:00am to 5:00pm

Our Helpline operates Monday to Friday between 9am - 9pm

Opening Days:
  • Monday
  • Tuesday
  • Wednesday
  • Thursday
  • Friday

Cost Information


If you or a family member are affected by genetic haemochromatosis (GH), please join us. 

We also welcome membership from people with a professional or academic interest in the condition.  Please see our website for what you will receive as a member.

Individual membership currently costs just £24 a year. This is reduced by a third to £18 for those relying on state pension or unemployment benefits

Additional Information

Areas Served:
  • National
Other areas covered:

This page was last updated on 18 April 2019

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This page was last updated on 18 April 2019


Contact Details

Contact Name:
Free Helpline
0303 401102


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