Sites listed in this category provide information for patients, families, and caregivers about organizations, foundations, and groups related to Hemochromatosis.
Information includes, but is not limited to, research, support, treatment, and diagnosis.
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Sites 6
This organisation provides information and educates the public about hemochromatosis. They publish a newsletter and have an online support group.
Support group led by volunteers for people who have haemochromatosis.
Voluntary organisation for patients in England, Wales, Scotland and Northern Ireland.
Offers information about the symptoms and treatment of hereditary hemochromatosis.
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.
Irish volunteer organisation to support people with haemochromatosis and promote the disease.
Voluntary organisation for patients in England, Wales, Scotland and Northern Ireland.
Non-profit National Voluntary Health Agency that provides information about disorders of iron such as hemochromatosis.
Support group led by volunteers for people who have haemochromatosis.
Offers information about the symptoms and treatment of hereditary hemochromatosis.
This organisation provides information and educates the public about hemochromatosis. They publish a newsletter and have an online support group.