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‘Cyborg’ Chinese woman with rare disorder lives on feeding tube, weighs 31kg, stays optimistic

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‘Inspiring’ 32-year-old also wears a pacemaker, enjoys the fine arts, showcases her desire to thrive despite adversity on social media

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A Chinese woman with a rare disorder, which means she lives on a feeding tube and needs constant medical treatment, says she will never give up on life. Photo: SCMP composite/Douyin/Jimu
Fran Luin Beijing

A woman in China who has to be fed through a tube because she suffers from a rare disease has remarkably retained her optimism, encouraging and impressing many people.

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Liu Kaixin was born with Ehlers-Danlos syndrome, a rare genetic connective tissue disorder. The syndrome has many subtypes, and Liu’s symptoms include possible multiple organ failure.

The 32-year-old has been living on a feeding tube for the past nine years amid fears that not doing so could have dire consequences.

While she was growing up, Liu Kaixin lived life in a state of constant pain. Photo: Douyin
While she was growing up, Liu Kaixin lived life in a state of constant pain. Photo: Douyin

She has also been using a cardiac pacemaker and chemo port around the clock for years.

She jokingly refers to herself as a “cyborg”.

Born in eastern China’s Shandong province, Liu grew up in constant pain. She stopped growing at the age of 10. Her weight was 31kg last year.

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Liu’s parents consulted many doctors, but the disease was too rare for them to offer a correct diagnosis.

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