Organisation

Jane Coultrup

CMN Support

I live in East Anglia with my husband and two children, a son (born in 2000) and a daughter (born in 2002), who was born with a large CMN, she was diagnosed at the maternity hospital and we were immediately referred to Gt Ormond Street Hospital for plastic surgery. 8 months later while at my local hospital one of the nurses gave me a copy of the Birthmark Support Group Newsletter.

I soon joined as a member of the Group and started to attend the Family days in Ipswich + London. It was while we were at the London Family Day in 2003, I heard that the Committee were looking for a volunteer to take over the role of Treasurer, which I undertook from 2004 until early 2008 when I handed over to Karen Barter and changed my role to CMN Support

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