A SCHOOLBOY with the lung disease cystic fibrosis has signed a contract with Bradford City Academy and hopes to defy the odds to become a professional footballer.

Eight-year-old Robbie Murray, from Addingham, recently signed a two-year contract with the academy despite having a condition that progressively damages the lungs and digestive system, and means a lifetime of treatment and medication.

His dad, Andrew, said: "Robbie may have been born with cystic fibrosis but he was also born with football in his blood and that’s his life – he loves it.

"We think the reason he is so well is because he spends so much of his time chasing a ball. Exercise is essential for people with cystic fibrosis to help keep their lungs clear of sticky mucus, and Robbie has managed to avoid going into hospital for the past 24 months.

"That’s why the contract is so important for him; apart from learning football skills, he will be getting specialised and rigorous exercise, which is part and parcel of the academy’s training."

Mr Murray described his son's attitude as "absolutely amazing".

"Robbie has taken it all in his stride – I was the one who was shaking when he was initially signed up," he added.

"When he was born and we found out about the cystic fibrosis, we expected to have to care for an ill child, but Robbie is absolutely amazing. H deals with it really well and is extremely disciplined. We are dedicated to making sure he achieves as much as he can."

Robbie is determined that condition won't stop him becoming a professional one day.

He saidL: "I love playing for the team I support and I want to be a professional footballer when I grow up. Cystic fibrosis will not stop me doing that."

Robbie, who lives with his dad, mum Kathie and 12-year-old sister Charlie, was spotted by club scouts whilst playing at his school, Addingham Primary.

He has already spent a full season working with the academy’s U9s team prior to signing a formal contract last month at the club’s home, Valley Parade.

Robbie was diagnosed with cystic fibrosis a week after his birth following a routine screening.

Dr Janet Allen, director of research and care at the Cystic Fibrosis Trust, said: "Children with cystic fibrosis should be encouraged to take part in as much physical activity as possible, ideally types of exercise that leave you out of breath. Football is a great sport for Robbie to do to keep well."