Oswaldtwistle boy, 7, receives life-saving kidney transplant from dad

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Shaemus was born with Jeune’s syndrome - a form of congenital dwarfism which causes deformities in the chest.

A seven-year-old boy with a rare condition, whose family was forced to travel up to two hours a day, seven days a week for treatment, is recovering well after receiving a life-saving kidney transplant from his father.

Shaemus Flood (pictured) was born with Jeune’s syndrome, a form of congenital dwarfism which causes deformities in the chest.Shaemus Flood (pictured) was born with Jeune’s syndrome, a form of congenital dwarfism which causes deformities in the chest.
Shaemus Flood (pictured) was born with Jeune’s syndrome, a form of congenital dwarfism which causes deformities in the chest. | Family handout/PA Wire

Shaemus Flood was born with Jeune’s syndrome, a form of congenital dwarfism which causes deformities in the chest.

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People with the condition are susceptible to liver and kidney disease, as well as respiratory symptoms.

When Shaemus developed stage five kidney disease, the family was able to perform dialysis at home, which could take up to 13 hours.

This lasted four years, until Shaemus required hemodialysis.

Shaemus pictured with his family and Alder Hey hospital staff.Shaemus pictured with his family and Alder Hey hospital staff.
Shaemus pictured with his family and Alder Hey hospital staff. | Family handout/PA Wire

During this treatment, the patient is hooked to a machine in hospital, which pumps the blood out of the body to be filtered before it is returned.

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For 10 months, the family was required to travel from their home Oswaldtwistle, Lancashire, to Alder Hey Children’s Hospital in Liverpool up to seven times a week.

The journey – more than 40 miles each way – can take up to an hour in good traffic, they said.

Join our new WhatsApp Community to get the latest news and top stories from across Lancashire directly to your phone. Get the latest headlines, straight to your inbox, with The LEP’s free emails Shaemus’ consultant, paediatric nephrologist Dr Caroline Jones, said: "Although dialysis is an incredible life-saving method it can only perform up to 10 per cent of kidney function and therefore children may often feel unwell and have restrictions to what they can eat and how much they can drink.

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“It is also not a permanent solution and can be very time consuming for children and their families."

She added: "We’ve been busy preparing Shaemus for a new kidney, we had to wait until he was big enough and strong enough.”

Shaemus’ mother and father, Sarah and Kieran Flood, were tested to see if their kidneys were compatible with their son’s.

Mr Flood was found to be a perfect match, with the procedure carried out at Manchester Children’s Hospital on January 11.

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Shaemus has since returned to Alder Hey, with him and his father now recovering well.

Mrs Flood said she is looking forward to spending more time together as a family at home.

She said: "It’s so peculiar not to be at Alder Hey every day. We’re hoping Shaemus can go back to school soon.

"The renal team have been amazing, without them and Caroline, we don’t think he’d be with us today."

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"We’re so grateful Kieran was a match, this isn’t always the case for a lot of families and this is why registering for organ donation is so important."

"Shaemus’ favourite person is his little sister Josephine who has just turned one, they’re best friends.

"We can’t wait to spend more time together at home as a family.

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