Mum sets up fund to research into daughter's rare condition

For five years Zoe Crowson has devoted her time entirely to looking after her little girl who was born with the rare genetic skin condition Recessive Dystrophic Epidermolosis Bullosa or EB. Now with Phoebe, five, at school, although not yet full time, has decided to use her skills to start her own charity - The Phoebe Research Fund - to raise money for research into her daughter's condition.

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