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Michelle said: "In the beginning it was really hard because we didn't know Nike Roshe Run Galaxy On Feet

Nike Roshe Run Mens Custom For Sale

Nike Roshe Run Mens Custom For Sale

Nike Roshe Run Mens Custom For Sale

Nike Roshe Run Mens Custom For Sale

If you feel we have made an error in a report, or have fallen below our usual high standards, please write in the first instance to: Rob Irvine, editor, Manchester Evening News, Mitchell Henry House, Hollinwood Avenue, Chadderton, Oldham OL9 8EP.

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"His adrenal glands were removed because they were over producing so I have to give him adrenaline three times a Nike Roshe Run Pink Sole

His mum Michelle, 28, of Kenmore Grove, Cadishead, said: "He stopped growing in length but he was cushioning up like a pillow, he weighed 7lbs but he looked like he weighed 15lbs.

However he remained in hospital for more than four months and was kept on oxygen while doctors tried to diagnose his condition.

"Or we could use it to buy a wheelchair if he needed one because of his bones.

´╗┐How you can help to give Coby hope

Michelle, who is also mum to Kai, seven, Sonnie, five, and Summer, three, added: "We just want to say thanks to everyone who ran and sponsored Coby's Appeal.

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Michelle and husband Lee, 32, have now set up Coby's Appeal to raise funds for his future.

The charity kitty was kick started last weekend after Lee and friends of the couple took part in the Great Manchester Run raising 1,600.

"If he's unwell we have to double or treble the dose but if we don't realise he's ill and he falls unconscious then he could die within half an hour.

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"When they told us what he had we were upset and surprised but we knew it didn't shorten his life expectancy and mentally he is really good."

It is so rare that Michelle says only six other babies in the world have been born with it.

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what was going to happen to him and we were thinking of the worst scenarios.

"The worst thing for us would have been if he hadn't had the mental capacity to know about life.

THE parents of a toddler who needs 24 hour care after being born with an extremely Nike Roshe Run Black Sail Speckle

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Coby Hilton needs 17 different medicines a day, as well as physiotherapy and occupational therapy to help with the symptoms of Neonatal Cushings McCune Albright Syndrome.

"We don't know what the future holds for him and because of that we've started a charity appeal for him so we can set up a fund and maybe take him to America to meet the other families of children with this condition.

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Nineteen month old Coby has had to have his adrenal glands removed, his body produces no salt and he has to be fed by a tube through his nose.

Coby was taken to hospital four weeks after he was born when his parents thought he had an infection.

rare illness have set up a charity in his name.

"We were in the hospital with him for six months and the other children coped really well.

day for the rest of his life.

"It Nike Roshe Run Mens Custom For Sale affects the bones as well. If he breaks something it might not heal and he might end up needing a wheelchair."

The condition means his body produces too much cortisone, a steroid, which has led to his bones thinning out and his collar bone and spine being fractured.

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