This organisation provides information and educates the public about hemochromatosis. They publish a newsletter and have an online support group.

Information about the symptoms, diagnosis and treatment of hemochromatosis.

The US Centers for Disease Control and Prevention provide reviewed information on hemochromatosis, including screening, information for patients, FAQ and resources.

Voluntary organisation for patients in England, Wales, Scotland and Northern Ireland.

Light hearted and simple terms in explaining the serious disease of haemochromatosis.

Provides education, information and resources for health care providers, patients, and relatives of people with hereditary hemochromatosis.

Offers information about the symptoms and treatment of hereditary hemochromatosis.

The website of a family whose members have hemochromatosis, with a description of how they are affected, and links to hemochromatosis sites.

Resources and information about Idiopathic Pulmonary Hemosiderosis, a very rare lung disorder affecting children and adults.

Irish volunteer organisation to support people with haemochromatosis and promote the disease.

Non-profit National Voluntary Health Agency that provides information about disorders of iron such as hemochromatosis.

Information on hemochromatosis. Covered are the accepted protocols for diagnosis, treatment, maintenance and diet.

Support group for those affected by hemochromatosis

A supplement to the Annals of Internal Medicine with articles about hemochromatosis.

Merck Manual looks at this disorder, its signs and symptoms, diagnosis and treatment.

A collection of links to sites, including scientific articles, related to the genetic iron overload disease.

Detailed up-to-date scientific information on hemochromatosis.

A laymans non-technical account of living with hemochromatosis by Alan Mannering.

Multimedia guide where you can learn what it is, what causes it, what it is like to have it, and how it is inherited, diagnosed, and treated.