In conjunction with Rare Disease Day 2022, Naevus International is partnering with CMN patient support groups across the world to raise global awareness of Congenital Melanocytic Naevus.
Our #shareyourstory campaign invites those affected by CMN to share their story of living with CMN to family and friends and the wider public through social media.
Plans are underway to host a webinar for all Naevus International members, partners and supporters on 1st March 2022. Please save this date. More details to follow.
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.
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.
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.
