In conjunction with Rare Disease Day 2021, Naevus International is partnering with CMN patient support groups across the world to raise global awareness of Congenital Melanocytic Naevus… and you can join in with us!
The Naevus International Leadership Team are very pleased to publish the Naevus International Annual Newsletter 2019-20.
Statement from Professor V Kinsler “There should be no increased risk of Covid-19 to any individual from having Congenital Melanocytic Naevus on the skin. There is no scientific evidence that there is any problem with temperatures in anyone with CMN over and above that seen in those with normal skin.” If anyone has any concerns…
In conjunction with Rare Disease Day 2020, Naevus International is partnering with CMN patient support groups across the world to raise global awareness of Congenital Melanocytic Naevus… and you can join in with us!
Naevus International Conference 2019 Programme is now available to view.
We are asking EVERYONE worldwide who has a connection with someone affected by CMN, to print out the promotional A4 poster and state on the poster the reason for raising awareness of CMN on Rare Disease Day, 28th February 2018. Follow these simple steps to join in with this fun and interactive way to raise…
ARE YOU: A professional (medical doctor, psychologist, nurse, or researcher) who has experience with patients with congenital naevi >10 cm on the body (or >1.5 cm on the face)? OR a patient (or parent of a patient) with congenital naevi >10 cm on your body (or >1.5cm on the face)? Interested in improving research and…
Naevus International (NI) is a new cross-disciplinary initiative which aims to disseminate information on Congenital Melanocytic Naevi (CMN) to a global audience of patients, families, support groups, psychologists, social teams, doctors and scientists.
We are thrilled to announce the launch of Naevus International – a new international cross-disciplinary initiative related to congenital melanocytic naevi (CMN).
