{"id":1822,"date":"2024-07-20T12:00:58","date_gmt":"2024-07-20T12:00:58","guid":{"rendered":"https:\/\/tradetrovex.com\/index.php\/2024\/07\/20\/boy-5-diagnosed-with-deadly-rare-condition-has-life-transformed-after-stem-cell-transplant-from-umbilical-cord-blood\/"},"modified":"2024-07-20T12:00:58","modified_gmt":"2024-07-20T12:00:58","slug":"boy-5-diagnosed-with-deadly-rare-condition-has-life-transformed-after-stem-cell-transplant-from-umbilical-cord-blood","status":"publish","type":"post","link":"https:\/\/tradetrovex.com\/index.php\/2024\/07\/20\/boy-5-diagnosed-with-deadly-rare-condition-has-life-transformed-after-stem-cell-transplant-from-umbilical-cord-blood\/","title":{"rendered":"Boy, 5, diagnosed with deadly rare condition has life transformed after stem cell transplant from umbilical cord blood"},"content":{"rendered":"
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A five-year-old boy has been able to leave his home for the first time in six months after he received a stem cell transplant made from a baby\u2019s umbilical cord blood which was donated in 2008.<\/p>\n

Gunner Lewis-Vale, from Shropshire, was diagnosed with a rare genetic disorder in March 2021, when he was about 17 months old.<\/p>\n

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At the time, his parents Holly and Jamie Lewis-Vale, both 34, were told that without a transplant, the toddler would only live for a year or two.<\/p>\n

But after a previous transplant from a donor in Germany failed, Gunner found a match with stem cells that were donated to NHS Blood and Transplant in 2008 and frozen with liquid nitrogen vapour at -150C.<\/p>\n

He underwent the surgery in January and then had to isolate for six months to give his immune system time to produce enough white blood cells to fight infection.<\/p>\n

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But now Gunner\u2019s life has transformed as he enjoys the summer with his seven-year-old sister Daisy.<\/p>\n

Mrs Lewis-Vale said: \u201cSo far, we have ventured to the park, skate park, dog walking, school runs for his big sister and out to feed the ducks.<\/p>\n

\u201cGunner\u2019s cheeky personality is coming right back. He\u2019s a clever boy with an amazing bond with his big sister.\u201d<\/p>\n

Gunner has mucopolysaccharidosis type I hurler syndrome, a rare inherited condition that prevents the breakdown of certain sugars in the body.<\/p>\n

The build-up of sugars can cause problems with physical and mental development.<\/p>\n

The first symptom Gunner showed was a pushed-out belly button, which was due to sugars building up in his liver and spleen.<\/p>\n

\u201cWe are eternally grateful to the incredible mother who donated their baby\u2019s umbilical cord,\u201d Mrs Lewis-Vale added.<\/p>\n

\u201cThe new white blood cells from the donor will hopefully make the enzyme he lacked which breaks down sugar.\u201d<\/p>\n

Gunner\u2019s family are now encouraging more people to register as stem cell donors.<\/p>\n

Guy Parkes, head of stem cell donation and transplant at NHS Blood and Transplant, said: \u201cWe\u2019re delighted to see Gunner playing outside for the first time since he received his stem cell transplant from a cord blood unit donated to our NHS cord blood bank.<\/p>\n

\u201cStem cell transplants are only possible thanks to the generosity of donors and we thank the mother who chose to donate her baby\u2019s umbilical cord more than 10 years ago. We wish Gunner and his family all the best.\u201d<\/p>\n<\/p>\n

This post appeared first on sky.com<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

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