Welcome to the Scott Ward-Schofield Memorial Fund website

The Scott Ward Schofield Memorial Fund is a newly founded charity formed in memory of Scott Ward Schofield who suffered from a rare skin disorder Epidermolysis Bullosa (EB). A genetic disorder where the sufferer's external and internal skin is so fragile that it blisters and peels off at the slightest touch, causing horrendous pain for them.

At the age of just 20, Scott lost his fight against the illness on November 2010, leaving everybody who knew him devastated. Scott's mum, Alison Ganson was determined to keep his legacy alive. With support of friends and family this charity was formed to raise awareness of the illness and pay for holidays, short breaks, and days out  for sufferers and their families. Until there is a cure for EB, we can provide lasting memories for these special families whilst there's still time for them.

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