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.
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.