If you, your child or someone you know has just been diagnosed with CGD,
this is where you’ll find the information you need, from coping with
the news through to advice on what to do next.
Parents and carers
Children and young people
Find out more about how we support the CGD community
Listen to the presentations and see the photos
Take on a sponsored run, organise your own event or hold 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.