Naava

Naava’s Story

My Journey to Self-Acceptance: Embracing My Uniqueness By Naava Agnes, age 23 Growing up in a small village in Kampala, Uganda, I was born with a congenital melanocytic nevus (CMN) on my face. It was a constant reminder that I was different, and it seemed like the world was always staring back at me. People…

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Caring Matters Now

Engaging your community

Living with CMN or parenting a child with CMN can feel quite overwhelming and stir up a whole range of emotions such as fear, anxiety, and worry. As a charity, we want to support our members to reach their full potential and help them to develop key social and emotional life skills.

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Caring Matters Now

Experiences of CMN

Experiences of CMN Living with Congenital Melanocytic Naevi (CMN), as a rare disease, is different for everyone and therefore how we can best provide support depends on these variable experiences. CMN has many different types leading to differing experiences for those affected. For some, CMN is found solely on the skin as a dark brown…

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Online Gaming Community

Online Gaming Community

A total of 10 online Community events were hosted between October 2023 and March 2024, including 3 Gaming events! This group was attended by a group of young people with CMN and siblings, between the ages of 9-13 years, getting together for an hour of gaming each month! The group are well accustomed to Fortnite,…

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Mia

Mia is the second Young Ambassador to complete the Dale Carnegie course, Level TWO of our Young Ambassador Programme!

Level 2 of the programme offers the unique opportunity to complete the prestigious Dale Carnegie Course. Designed to equip you with the communication and human relation skills required to be successful in any setting, this world famous programme of self-development helps the leaders of tomorrow leverage their skills so they can strengthen relationships between colleagues,…

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