Our Warrior Princess Written by Eve’s mum – Sabrina After a perfectly normal pregnancy, Eve was born on the 8th August 2018 with a very rare skin condition called Congenital Melanocytic Naevi (CMN). This is a gene mutation that caused more than half her body to be covered in moles/birthmarks. An MRI at 6 days…
DetailsSign up now to take part in our 2020 Coffee & Cake Morning and receive a free fundraising pack full of goodies. This is a fun and easy way for everyone to get involved and help raise funds for Caring Matters Now. You can organise your coffee and cake morning at home, school, or your…
DetailsVeronica Kinsler is now the Professor of Paediatric Dermatology and Dermatogenetics at Great Ormond St Hospital for Children and the UCL Institute of Child Health. This is great recognition for the CMN research and will continue to raise awareness of CMN worldwide. Some other very exciting news about CMN research at GOSH is that the…
DetailsBe the first to get your hands on our brand new ‘how do you C Me Now™’ tees! To celebrate the huge success of our global awareness campaign #howdoyouCMeNow, we have produced branded clothing for all ages. We want to continue raising positive awareness of CMN, giving a clear message to the world; to love…
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