Welcome to the CGD Society website

For those who have recently received a diagnosis; for parents of children, and adults living with CGD

For those who have recently received a diagnosis; for parents of children, and adults living with CGD

For women and their daughters who are known to carry X-linked CGD

For women and their daughters who are known to carry X-linked CGD

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

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

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

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

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.