Hanna teaches future doctors about CMN
Hi everyone, my name is Hanna. I am the youngest doctor in my hospital – or at least that’s what my paediatrician and her team say!
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Hi everyone, my name is Hanna. I am the youngest doctor in my hospital – or at least that’s what my paediatrician and her team say!
My name is Isla and I was born with Congenital Melanocytic Naevi on the 12th December 2016, making me 8 years old at the time of writing this. Today I had my transitioning day at school where I met the teacher who will be teaching me when I go into year 4.
After 12 years of service, Val Unsworth, co-founder of Caring Matters Now, is stepping down from her role as Chair of Trustees. After an impressive tenure, Val will be handing over the reins to Tracy Traverse Burley, who has been appointed by the Board as the new Chair of Trustees.
In a heartfelt celebration of bravery, compassion, and determination, Doug Newman has been named the winner of the prestigious 2024 Jessica Ma Award (JMA).
Ada was born with CMN in 2020, and just a few weeks later I spoke to another parent of a child with CMN and they told me about Caring Matters Now. We have been involved ever since. In 2022 I took on being one of the regional contacts for the charity and I am so proud to help many over the East Anglia region.
In 1999, we had a daughter, Holly, born with CMN. Very sadly for us all, complications related to her condition proved to be terminal and she passed away aged 10 months. 25 years on, we are still very much in touch with the charity and who’d have thought that the seeds sown all those years ago would have grown into such a strong and beneficial entity.
My connection to Caring Matters Now began when my daughter, Alicia, was born with Congenital Melanocytic Naevus (CMN). From the very start, the charity was there for us, offering support, guidance, and a sense of community that meant so much.
Are you a new member at Caring Matters Now? Join us on Sunday 23rd March at 8pm for our Annual New Members Event online. You’ll find out who we are, what we do and why we do it, as well as meeting some of our team and having an opportunity to ask any questions that you may have also!…
My name is Maja. I am a 16-year-old girl living in London. I was born with CMN covering the majority of my left leg and lower parts of my waist. Due to its size, it was not possible to remove it, but I underwent major surgery when I was just a few hours old to…
