Centre for Appearance Research Project
Are you Somali and do you have CMN affecting the face? Researchers at the Centre for Appearance Research want to find out about your experiences!
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Are you Somali and do you have CMN affecting the face? Researchers at the Centre for Appearance Research want to find out about your experiences!
We are excited to announce further developments in our adult support team with the introduction of a new support contact for our older teens and young adult members.
Caring Matters Now have successfully secured a grant from VTCT Foundation and have teamed up with Centre for Appearance Research to create a resource to support young people with Congenital Melanocytic Naevi. This will be a freely available resource that contains important information about CMN and how to cope with common issues that young people with CMN may face.…
In conjunction with Rare Disease Day 2021, Caring Matters Now 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!
A huge THANK YOU and CONGRATULATIONS to all those who have completed a monthly challenge so far!
After much deliberation we are delighted to announce that the winner of the 2020 Jessica Ma Award is……..
As 2020 comes to an end, we all need something positive to focus our attention on for 2021, so why not sign up to our ‘Stepping up for CMN’ challenge? You will not only make 2021 a year to remember, but you will also be supporting the work of Caring Matters Now by raising vital funds to continue our work. It’s a win-win challenge for everyone!
We are thrilled to announce the establishment of Caring Matters Now Ireland. Over the past 24 months, the Caring Matters Now Board of Trustees have been working towards establishing a sister charity in Ireland.
We are thrilled to announce Veronica Kinsler has been awarded an NIHR Professorship to continue to research targeted therapies for CMN and melanoma.
Caring Matters Now is committed to supporting all those affected by Congenital Melanocytic Naevi. We continually review our support strategy to consider new ways of ensuring the support we offer is most helpful to all our members. Over recent months, we have been putting in place a new adult support team. This exciting development will…