Phoebe

Phoebe’s Story

My name is Phoebe, I am 16 and I was born with a giant CMN on my face and satellites all over my body. The process to remove my facial nevus began when I was one week old and finished when I was six. I have a skin grafted face and over 500 satellite Nevi.…

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Katy

Katy’s Story

I’m Katy, and the last time I wrote my story for Caring Matters Now, I was 12 years old and had just started at secondary school. Since then, I’ve danced with the English Youth Ballet, competed with my university dance teams, and worked at Camp America. More recently, I’ve worked on a cruise ship and…

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Complete this quick survey and help us create a support resource for young people with CMN

Caring Matters Now have successfully secured a grant from VTCT Foundation and have teamed up with Centre for Appearance Research to create a resource to support young people with Congenital Melanocytic Naevi. This will be a freely available resource that contains important information about CMN and how to cope with common issues that young people with CMN may face.…

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Elspeth's Story

Elspeth’s Story

As a fifteen-year-old with CMN, which covers my back arms and legs, I have endured many hard times as well as amazing and inspiring experiences. Having CMN evidently makes me stand out when I don’t necessarily want to and makes people stare when (you guessed it) I don’t want people to stare. Having these special…

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