Alana Daykin, who has a rare genetic condition called Börjeson-Forssman-Lehman Syndrome, is 'really affectionate' and 'loves people'
A mother has organised a fundraising day and raffle in another appeal to raise money for her seven-year-old daughter who doctors say won't live to see her twenties. Alana Daykin, from Stanley, Derbyshire, was born at the Queen's Medical Centre with a rare genetic condition called Börjeson-Forssman-Lehman Syndrome which kept her in and out of hospital for the first two years of her life.
"She's very affectionate and she loves people. She would give hugs and hold hands every day if she could and everyone that meets her says she's left an impression on them. Megan, who is a big fan of This Country, said: "Paul donated to our fundraiser and he's been sharing everything for us. He even said he's gonna get us a signed T-shirt from Daisy.
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