Luke is now 12 years old and was born with a facial and head Congenital Melanocytic Naevus. In September 2011 he faced the next journey of his life in starting secondary school. Luke was to attend Magnus School in Newark. The school were made aware of CMN before Luke started and his new form teacher [...]
Due to popular demand we are making plans for another activity weekend to be held in 2012. Dates are Friday 21st to Sunday 23rd September 2012 at Boreatton Park situated in 240 acres of Shropshire countryside. Back in July we held our first ever activity weekend and it really was a superb weekend. Click here [...]
I am VERY pleased to announce that Mount Kilimanjaro is done and dusted! How amazing the experience was! It is very difficult to summarize this incredible journey, so instead I have decided to include the daily blog updates in the newsletter, along with some photographs. I do hope you enjoy reading all about our adventure! [...]
*** NEW DATE – The date for the Liverpool Family Day has changed from 10 Nov’ 12 to 24 Nov’ 12 *** The CMN support group hold family days across the UK throughout the year. The aims of the family days are to: Give one-to-one support to CMN sufferers and their families Give medical advice [...]
The CMN support group hold family days across the UK throughout the year. The aims of the family days are to: Give one-to-one support to CMN sufferers and their families Give medical advice to CMN sufferers and their families Give an opportunity for CMN members to meet and develop friendships The family days are very [...]
The CMN support group hold family days across the UK throughout the year. The aims of the family days are to: Give one-to-one support to CMN sufferers and their families Give medical advice to CMN sufferers and their families Give an opportunity for CMN members to meet and develop friendships The family days are very [...]
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