The CGD Community is a wonderful mixture of people: those with CGD and their families and friends, medical professionals, researchers, donors, Trust staff and volunteers, partner charities and many more. It is a powerful alliance. We are all working towards common goals: better quality of life, treatments and cures for people with CGD and indirectly, other genetic conditions.
This is what members of our community have said recently:
'When we realised you were there - it made such a difference. My husband was diagnosed at the age of 17, and we have been asking for years if there is anyone who knows about this, who could help us. The CGD Research Trust gives us peace of mind. We know there is someone there who knows about the condition and that they are there for us. The feeling is worth its weight in gold.'
Rachel, whose husband has CGD
'What the CGD Research Trust does to cover everything is amazing. I'm constantly surprised by what it manages to achieve.
Professor Adrian Thrasher, Consultant in Paediatric Immunology Institute of Child Health
'The charity is a lifeline for families across the whole of the UK and beyond.'
Louise Morton, Nurse Advisory Panel
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.
© 2001-2007 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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