Welcome to the CGD Society website

Welcome...This website has been newly launched in March 2012. It is our aim to make it the world's leading source of information for patients and medical professionals on chronic granulomatous disorder. Please click here to give us your input and feedback.

Newly diagnosed

Welcome...This website has been newly launched in March 2012. It is our aim to make it the world's leading source of information for patients and medical professionals on chronic granulomatous disorder. Please click here to give us your input and feedback.

Individuals and families

Welcome...This website has been newly launched in March 2012. It is our aim to make it the world's leading source of information for patients and medical professionals on chronic granulomatous disorder. Please click here to give us your input and feedback.

Medical professionals

Welcome...This website has been newly launched in March 2012. It is our aim to make it the world's leading source of information for patients and medical professionals on chronic granulomatous disorder. Please click here to give us your input and feedback.

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

For schools, employers, social services or other professionals seeking information on CGD

For schools, employers, social services or other professionals seeking information on CGD

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, whether it's through holding a fundraising event, participating in Jeans for Genes Day or making a donation

We need your support, whether it's through holding a fundraising event, participating in Jeans for Genes Day or making a donation

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 1st Floor Macmillan House, Paddington Station, London W2 1FT.