Adult Support

By Jodi Whitehouse Over the past couple of years, the CMN trustees have wanted to develop our adult support for those adults affected by Congenital Melanocytic Naevi. We have made a start on developing this area by holding an annual adult gathering, which includes Dr Kinsler attending to present her work. This also provides a…

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Gemma’s Story

My name is Gemma, I’m 22, grew up in Cambridge but now living and studying in Brighton. I like travelling, music and hope to graduate as a doctor in a few year’s time. But if you meet me, you might notice something a bit different about me; I was born with CMN, in other words…

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