Our trustees

If you would like to find out about becoming a trustee of the CGD Society, please email us.

Ocean Numan - Honorary President

Ocean Numan
Honorary President

Ocean Numan founded the CGD Society (formerly the CGD Research Trust) in 1991 with the aim of finding a cure for the disorder that affected his son. Ocean was Chair of the Board for 12 years. Today, he lives in New Zealand and works as a marketing consultant. His son passed away in 2009 aged 29.

Claire Bonner

Claire Bonner

Claire's son Max was diagnosed with X-linked CGD in 2009. Claire and her family gained information and support from the charity in the lead up to Max having a successful bone marrow transplant in 2012. Claire joined as a trustee in 2015. She works as a GP and has recently relocated from Buckinghamshire to Yorkshire.

Geoff Creamer

Geoff Creamer
Chair

Geoff’s two sons were born with X-linked CGD and one has had a successful bone marrow transplant. Geoff became a trustee in 1992, and since that time has seen the charity change from a small parent support group to being a leading source of information for those affected by CGD. He is currently the technical director of a manufacturing company.

Jane Docherty

Jane Docherty

Jane first became aware of CGD in 2008 due to her friends son, Lake, being affected by X-linked CGD. Lake underwent successful gene therapy treatment in July 2016.

Jane became a trustee in 2018 and is a trained accountant. Jane currently owns a restaurant in Cornwall.

Davina Gray

Davina Gray

Davina's son Josh was diagnosed with X-linked CGD in 1993.  He is now 27 years old.  Davina became a trustee in 2018 and is currently working as a Bid Manager.  She has a Patient Advocate position on the NHS England’s Policy Working Group developing an All Ages policy on HSCT (BMT) for Primary Immunodeficiencies.

Ning He

Ning He

Ning's son, Johnathan, was diagnosed with X-linked CGD in 2006 and had a successful bone marrow transplant in 2013. His family received a lot of information and support from the CGD Society over the years. Ning became a trustee in 2015. He currently works as an accountant.

Jackie Irvine

Jackie Irvine

Jackie’s son was born with autosomal recessive CGD and had a successful bone marrow transplant in 2011 at the age of 17. Jackie joined the charity as a trustee  and lay member of the research advisory panel in 2015. She currently works in her family’s business.

Andrew Orchard

Andrew Orchard

Andrew established the first UK CGD support group in 1986 and is a founder member of the charity and a lay panel member on the research advisory panel. He has a son affected by X-linked CGD and has a nephew who had a successful bone marrow transplant in 2002. Andrew is an IT consultant and data analyst.