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Fundraising : A-Z of ideas

A-Z fundraising ideas for all! Would you like to fundraise for CGD Society so we can continue our services for families living with CGD? First of all – thank you!  Your support, donations and fundraising enable us to continue our vital work. We’ve got the tool for you! We have pulled together an A-Z of…

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Living with CGD – Shannon and Wendy’s story

Shannon and Wendy’s story (March 2024) Shannon and her mum, Wendy, each share their perspective on their family’s journey with CGD and bone marrow transplant (BMT) Shannon’s story:  How to live with and scold CGD in your late teens!   Having a chronic illness during your late teens is never easy. Particularly an immunodeficiency disorder,…

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Our Trustees

Our Trustees If you would like to find out about becoming a trustee of the CGD Society, please email us. Geoff Creamer, Secretary Geoff has been a Trustee for over 30 years with two periods as Chair and has seen this charity change from a small patient support group to an international resource for those affected…

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Telephone and email helpline

Contact Us Telephone and email contact details If you have a query about CGD and you cannot find the answer on our website or need help, then don’t hesitate to contact us. We will do our best to get an answer to you or to put you in touch with someone who can help. *Please…

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Our Team

Our Team In order to keep its overheads to a minimum, the CGD Society does not employ any staff directly. Instead it collaborates with Genetic Disorders UK to ensure that the charity is run professionally and at a low cost base. Claire Liddle (Jeffries), Executive Director Claire has personal family experience of CGD and so…

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COVID-19 Resource & Information

The current outbreak of the Coronavirus (COVID-19) creates an uncertain time for us all, particularly if you are living with a chronic illness such as CGD. We have created, compiled and collated as much information as we can to help you navigate these unsettling times – from the latest advice to tools and resources designed…

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Living with CGD – Bobby’s story

Bobby’s story (January-February 2024) Bonnie shares her family’s journey as Bobby undergoes his bone marrow transplant (BMT) 27th February 2024   BOB IS HOME!!!! Bob managed to do really well through transplant and he was discharged last week. Though it’s very early days and I am actually writing this from a hospital room in Stoke…

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Our Mission

You are here > Search > Latest AD0-E327 Dumps Free ✌ AD0-E327 Latest Torrent 📭 Reliable… > Our Vision Our vision is to enable families and individuals affected by CGD to live life to the full Our Mission To be the leading source of information and support for families and individuals affected by CGD in…

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For General Practitioners

For General Practitioners If a CGD-diagnosed patient presents to you, please listen to them or their parents as they are very familiar with their condition and the health problems associated with it. We are aware that you, or your colleagues, see and treat a patient/patients with CGD and we hope that this information will be…

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What is CGD?

What is CGD? Thank you for visiting the CGD Society website. This page has been superceded by the one below. Please update any links to go to our new page, CGD – The Basics   More information Read more about the different types of CGD Learn about how CGD is inherited Read more FAQs regarding…

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