The Trust's relationship with medical professionals is vital and we welcome your ideas for tailoring the site to your needs. This is why we have a button just for you. Please be supportive if a patient or family dealing with CGD asks you to refer to this site! It is such a rare condition that you are quite likely never to have come across it before.
CGD is serious and the alertness of the general medical community to it saves lives, especially with early diagnosis and intervention. GPs, nurses and hospital staff in many countries will turn first to this site to understand CGD, and the available treatments. Please refer to the Care section of the site, which contains valuable information that has been carefully reviewed, in some cases authored, by top medical experts on CGD. You may also like to explore the Medical Research.
Some information is appropriate for you but not for the general visitor and forums for medics only will also be set up.
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.
© 2001-2005 The Chronic Granulomatous Disorder (CGD) Research Trust
Registered Charity No. 1003425 email:cgd@cgdrt.co.uk
The CGD Research Trust is a member of the Association of Medical Research Charities (AMRC), the Genetic Interest Group (GiG) and an associate member of the International Patient Organisation of Primary Immunodeficiencies (IPOPI)
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