Precious Memories
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|August 03 2017
We’re making every moment count with my boy’s bucket list By Joanne Ashton, 48, from Liverpool
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At first I didn’t notice anything was wrong. My son Liam was just like any other baby.
But when he was 2, I noticed his younger cousin seemed to be strides ahead.
While he climbed the stairs, Liam still crawled up and bum-shuffled down.
Our GP referred Liam to a specialist, who noticed he walked funny.
Eventually, Liam was sent to Alder Hey Children’s Hospital.
‘We think he might have muscular dystrophy (MD),’ a doctor said.
It’s a progressive muscle weakening condition.
A blood test soon confirmed it. And a muscle biopsy revealed Liam had a type called Duchenne MD.
It’s more common in boys. And it’d affect his ability to walk and stand.
‘Most sufferers need a wheelchair by the time they’re 14,’ a doctor explained.
The cruellest blow was yet to come, though…
‘It’s life-limiting,’ he said.
यह कहानी Chat के August 03 2017 संस्करण से ली गई है।
हजारों चुनिंदा प्रीमियम कहानियों और 10,000 से अधिक पत्रिकाओं और समाचार पत्रों तक पहुंचने के लिए मैगज़्टर गोल्ड की सदस्यता लें।
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