WELCOME to our Forums. These aim to allow you to share experiences and give support to others involved with or interested in Chronic Granulomatous Disorder (CGD). As a scattered community with a rare condition, we have lots to gain by all sharing our knowledge, opinions and ideas. We hope the forums will help communication within and between various key groups including CGD patients and families, the caring professionals, the scientific community and our growing base of supporters and donors worldwide.
Please remember posts containing advertising or soliciting are not allowed and will be removed. Continual postings of these types will result in the banning of those individuals. We reserve the right to delete any thread or post that we consider to be abusive, inappropriate or out of context with the general aims of the forum as stated above.
CLICK HERE TO ENTER THE FORUMS
(You can also visit the Forums directly via www.cgd.org.uk/forum)
Who can use our forums
We welcome you all to the General Public forum. We welcome the eligible people to our special interest forums (Individuals and Families, Medical and Researchers and Youths - under 25).
If you are not registered, you may browse the General Public Forum and you'll be able to read all the messages, but not add any of your own.
Not registered? Register here (The Forums require separate registration from the CGD site registration in the grey bar above. However, you can use the same email address and password on both. Once you've registered, you will need to sign in via the login button in the forum before making posts.)
For more information on how to register, click here
What is the Code of Conduct for forum users?
Advice on using the forums
Forum FAQs (Frequently Asked Questions)
Confidentiality
Your details will be kept completely confidential and will not be shared with any other organisation.
A note on Medical Information
The forums do not aim to provide detailed medical advice as we are not able to verify the integrity of the views made through the forums. But they may help point you towards the appropriate professionals for your particular issue.
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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