Welcome to the CGD Society website

Welcome...We are a charity based in the UK whose mission is to support individuals and families affected by chronic granulomatous disorder. We aim to be the world’s leading source of information on this genetic disorder for patients and medical professionals.

Newly diagnosed

Welcome...We are a charity based in the UK whose mission is to support individuals and families affected by chronic granulomatous disorder. We aim to be the world’s leading source of information on this genetic disorder for patients and medical professionals.

Individuals and families

Welcome...We are a charity based in the UK whose mission is to support individuals and families affected by chronic granulomatous disorder. We aim to be the world’s leading source of information on this genetic disorder for patients and medical professionals.

Medical professionals

Welcome...We are a charity based in the UK whose mission is to support individuals and families affected by chronic granulomatous disorder. We aim to be the world’s leading source of information on this genetic disorder for patients and medical professionals.

Research

For those who have just received a diagnosis of CGD and need immediate help and information

For those who have just received a diagnosis of CGD and need immediate help and information

For parents of children affected by CGD, affected young people and adults

For parents of children affected by CGD, affected young people and adults

For specialist information on CGD, resources and diagnostic tools for medical professionals

For specialist information on CGD, resources and diagnostic tools for medical professionals

Welcome to the CGD Society

Before leaving our website today, please take a few minutes to register as a member of the CGD Society. It is absolutely free! The more member families we support throughout the world who are affected by chronic granulomatous disorder, the better chance we have of securing funds to develop and maintain this website, and provide you with the latest information on the management of CGD, treatments and research towards a cure.

» Yes, I would like to become a member

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Find out the basics, get the views of experts and hear from patients who have undergone bone marrow transplants

Find out the basics, get the views of experts and hear from patients who have undergone bone marrow transplants

Find out about the research we fund and the results that have been achieved through our support

Find out about the research we fund and the results that have been achieved through our support

We need your support to fundraise whether it's through running, holding your own event or organising a Jeans for Genes Day

We need your support to fundraise whether it's through running, holding your own event or organising a Jeans for Genes Day

IMPORTANT NOTE: The information contained on this website is intended only as a guideline, not as a substitute for medical advice. Always consult your doctor if you or your child has any CGD symptoms or concerns.

© 2012 The Chronic Granulomatous Disorder Society is a charitable company limited by guarantee and registered in England (registered charity number 1143049 and registered company number 07607593). The registered address is Genetic Disorders UK, 199A Victoria Street, London SW1E 5NE.