Stacey’s Story

Hi, I’m Stacey and I was born with a large bathing trunk nevus and multiple satellites all over my face and body. Despite being different to other kids I had a really good childhood and I owe so much of this to my parents. Mum and dad never treated me any different. We went on…

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CMN Conference 2019 Review

In July we held our first residential support conference at Liddington PGL Conference Centre with 112 attendees. The crammed packed 3-day programme catered for all ages, including fun outdoor pursuit activities for the children and teens, off-site activities for our adult members, psycho-social presentations and workshops for parents, adults and teens affected by CMN, plus…

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A message from Ronnie!

Hi everyone! My name is Ronnie, and I’m the new Caring Matters Now mascot! I’ve been given a mission, and I’m so excited to start! My mission has two aims; first, to raise global awareness of Congenital Melanocytic Naevus. I’m going to do this by travelling all over the world, and posting pictures of my…

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Eve’s Story

Our Warrior Princess Written by Eve’s mum – Sabrina After a perfectly normal pregnancy, Eve was born on the 8th August 2018 with a very rare skin condition called Congenital Melanocytic Naevi (CMN). This is a gene mutation that caused more than half her body to be covered in moles/birthmarks. An MRI at 6 days…

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