Hannah’s Story

Hannah Bostock – by Mum Diane My daughter Hannah was born on the 26th January 2001 with multiple extensive CMN (Congenital Melanocytic Naevus) covering approx. 70 – 80% of her body with about 100 – 200 small naevi (satellites). Hannah was the most precious gift life could give to me. She was a wonderful baby…

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Leah’s Story

Leah Wigmore – by Mum Lynne Our daughter Leah was born 16th June 2005, at Frimley Park Hospital and from the very first moment we laid eyes on her, we knew she was special. It looked as though she was born with a full head of hair, but it turned out to be a CMN,…

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Teens Big Day Out

This is a great team building and social gathering for all those affected by CMN aged 11yrs – 17yrs. This event is open to teens with CMN aged 11 – 17yrs plus one accompanying adult, or friend if aged 17yrs. About: Join us for another fun, team building event at Go Ape Battersea. High Ropes,…

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Online Support

Facebook group for registered members of the Caring Matters Now Charity The charity’s primary aim for social media interaction is for Caring Matters Now members to receive up to date information about the charity, and to give a safe platform for Caring Matters Now members to interact with one another. Therefore, we have created a…

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Launching our 2016 CMN Christmas Campaign

Buy your family & friends a gift this Christmas time, which will last a lifetime! Caring Matters Now has launched a Christmas Gift/Card campaign.   You can make a lasting difference to the lives of those affected by CMN this Christmas time. Rather than spending your money on Christmas gifts or cards that don’t last,…

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20th Anniversary Celebrations!

Join in and help us to celebrate this momentous occasion. 2017 is going to be a huge year for Caring Matters Now……..We will be celebrating our 20th anniversary. Oh how things have come on in 20 years! At the age of 16 years old Jodi and her family were asked to provide support to other…

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