Hannah’s Story

Hannah Bostock – by Mum Diane My daughter Hannah was born on the 26th January 2001 with multiple extensive CMN (Congenital Melanocytic Naevus) covering approx. 70 – 80% of her body with about 100 – 200 small naevi (satellites). Hannah was the most precious gift life could give to me. She was a wonderful baby…

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Leah’s Story

Leah Wigmore – by Mum Lynne Our daughter Leah was born 16th June 2005, at Frimley Park Hospital and from the very first moment we laid eyes on her, we knew she was special. It looked as though she was born with a full head of hair, but it turned out to be a CMN,…

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Teens Big Day Out

This is a great team building and social gathering for all those affected by CMN aged 11yrs – 17yrs. This event is open to teens with CMN aged 11 – 17yrs plus one accompanying adult, or friend if aged 17yrs. About: Join us for another fun, team building event at Go Ape Battersea. High Ropes,…

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