My name is Catherine Cobden and my son Oliver was born with a rare condition called Oesophageal Atresia in July 2009. When he was born he had no oesophagus and had to spend 10 weeks "growing" in hospital before he was strong enough for the 5 hour major surgery to repair his oesophagus. He was finally allowed home on 16th October 2009 at 13 weeks old! Since leaving hospital he has grown from strength to strength and is now a cheeky little boy who is always smiling. We are holding a charity fundraising event on 15th October to raise money for tofs and the Royal Alexandra Childrens Hospital in Brighton where Oliver underwent all his treatment. There will be a quiz, raffle, Disco & live band. Tickets are £5 each and can be paid for using this justgiving page.

 

 

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