Watching Bundaberg boy Grayson Little rolling around in the mud, you’d think he was just like any other 3-year-old. But behind his playful, cheeky grin, Grayson is battling a heartbreaking rare illness that affects just one in a million.
Diagnosed at birth with a rare premature-aging disorder known as dyskeratosis congenita (DC), it means Grayson’s cells don’t regenerate and his organs progressively deteriorate, leaving his body like that of an old man.
“His prognosis was so grim that doctors didn’t expect he would make it this far, so every day is a bonus for us,” says his mum Rachel.
And despite the odds stacked against him, Grayson from day one constantly stunned and surprised everyone.
“Doctors didn’t even know if he’d be able to crawl, climb or walk,” Rachel adds. “But he’s achieved all of that and walks with a frame.”
هذه القصة مأخوذة من طبعة November 30, 2020 من New Idea.
ابدأ النسخة التجريبية المجانية من Magzter GOLD لمدة 7 أيام للوصول إلى آلاف القصص المتميزة المنسقة وأكثر من 9,000 مجلة وصحيفة.
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هذه القصة مأخوذة من طبعة November 30, 2020 من New Idea.
ابدأ النسخة التجريبية المجانية من Magzter GOLD لمدة 7 أيام للوصول إلى آلاف القصص المتميزة المنسقة وأكثر من 9,000 مجلة وصحيفة.
بالفعل مشترك? تسجيل الدخول
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