Abby

Abby’s Story

My name is Abby, I am 29 and from Liverpool. I have CMN covering my back and slightly onto my abdomen with multiple birthmarks and moles across my body. I spent majority of my childhood and teenage years in hospital having multiple laser surgeries, dermabrasions and naevus removal to reduce the appearance of my CMN.…

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Diane’s Story

Diane’s Story

29 years ago, my beautiful daughter, Katy, was born. A second child for Rob & I to complete our family alongside her brother, Danny. She was born with a large CMN on her leg. 29 years ago, less than 10% of the population had internet access to be able to research these conditions on, so…

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Charlotte

Charlotte’s Story

My name is Charlotte. I am from Surrey and I was born with a large scalp CMN that also covers my right ear, as well as smaller satellites across my body. When I was born, the operating room was filled with confusion. I was healthy enough to go home; however, the head paediatrician who could…

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Laura’s Story

My name is Laura, and I am from County Derry (Northern Ireland). I am 28 years old and living with CMN. I was born with CMN covering 98% of my body. From birth I have undergone numerous surgeries to reduce the appearance of my CMN; however, it is still very visible and a part of…

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Maddie

Maddie’s Story

Hi, my name is Maddie, I am 20 years old, and I have bathing trunk CMN. I live in South East London with my parents, Sandra and Kuhan, and my two younger siblings, Reuben and Zara. I am currently in my second year of Archaeology (the study of ancient civilisations) at the University of Nottingham.…

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Luis's Story

Luis’ Story

Luis Mojica Rodriguez: The Empowerment Model Redefining Beauty Early Life and Childhood Challenges I was born in Puerto Rico in the 1980s with Congenital Melanocytic Naevus, a rare condition that doctors feared could turn cancerous. With limited treatment options on the island, my mother moved us to New York when I was ten months old.…

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Red Book Insert

Red Book Insert

In recent years, Caring Matters Now has built a strong partnership with the Childhood Tumour Trust (CTT). CTT is a charity that supports children and young people diagnosed with NF1. NF1 is characterized by café au lait birthmarks on the skin and, like CMN, is considered ‘more than a birthmark’, with potential implications beyond the…

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Tegan’s Story

Tegan’s Story

Hello, I’m Tegan, and I have been Callum’s Big Sister for nearly 25 years. I was initially quite put out when he arrived, having lived the first five years of my life as an only child! Callum was born with a large birthmark on his arm, running from his shoulder to his fingertips. I remember…

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