5k Anyway for NF1

A year ago my daughter Nellie was diagnosed with NF1, this come as a shock to us all so we would like to help raise awareness and research in to this rare genetic disorder. Me and my family will be doing a 5k run on the 5th of May to raise money in aid of Childhood Tumour Trust and every donation will help. Thank you in advance for your contribution to this cause that means so much to me.

More information about Childhood Tumour Trust: We support children and young people with Neurofibromatosis Type 1; we offer youth camps for those aged 12-17, many of these children have never met anyone with the condition and are very isolated, camps allow them to be themselves - and feel just like everyone else. We offer online support for those affected by NF1, encourage get togethers by way of online children's parties and family days out, and give money to much needed research as well as campaigning for better care and diagnosis in the NHS.