My name is Georgia, I am 18 years old and I am a Young Ambassador with Caring Matters Now. I am excited to be a part of the team and to be able to help younger people affected by CMN and to gain new skills and confidence. I was born with bathing trunk CMN and…
On Saturday 2nd October, we were delighted to host the first in person Ireland regional gathering since the start of the pandemic. We planned the event early in the year for Dublin Zoo as it was an outside venue, optimistically hoping that any restrictions would be a thing of the past by October, but alas, it was not to be. (Another time, Dublin Zoo!)
In conjunction with Rare Disease Day 2022, Caring Matters Now is partnering with CMN patient support groups across the world to raise global awareness of Congenital Melanocytic Naevus.
Caroline Caroline – Now My name is Caroline, I am 20 years old, from Austria Vienna and was born with a giant heart shaped CMN on my lower back. I never met someone with a CMN and thought for a long time that I am the only one (until I discovered the thing called internet),…
My name is Maddie, I’m 15 and was I was born with CMN. Living with CMN, although it is very challenging at times, has also been a positive experience for me. When I was little my parents always told me that I had ‘special skin’, and this helped me with my confidence around my CMN…
