Scarlett is my friands daughter, she is 7 and has Cystic Fibrosis. People with CF have sticky mucus that affects their lungs and digestive system and so Scarlett needs daily physiotherapy, lots of medication and sometimes hospital treatment

Rachel ( her mum ) very cleverly sent us all a text on new years day when we were all feeling delicate and full of new years resolutions. We agreed to do the 10k run in July and as much as I have trained I am rubbish. I will do this run/walk but I will never answer my phone to her again even if I survive this torture.

In May, 1 year after her diagnosis, Scarlett and her 3 sisters took part in the Leeds mini and junior Run for All to raise money for the CF Trust. If they can do it so can I

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