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.
DetailsMy 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.
DetailsAre 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!…
DetailsMy 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…
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