Photos: Sad Story Of How 7-Year Old Lost Her Skin And Now Battling To Save Her Life

    A Chinese girl has lost the skin from her entire body within
    a week of falling ill with a high fever. Blisters suddenly appeared all over 7
    year old Ma Jie’s body before large areas of skin began to peel off.

    Doctors said by the time she was admitted to the hospital in
    Hangzhou, east China, all the skin on her body had already peeled off.
    She has been diagnosed with epidermolysis bullosa (EB), a
    genetic condition that causes the skin to become very fragile.

    Those who suffer from it are often called ‘butterfly
    children’ because their skin is as delicate as butterfly wings.
    But doctors remain baffled by her condition because children
    usually get symptoms of EB shortly after birth.
    Ma Jie fell ill with a high fever on July 7 but quickly
    recovered after taking medicine.
    However, blisters suddenly appeared in her mouth and on her
    feet and palms the next day. The blisters soon spread to cover the rest of her
    body.
    Her parents initially used toilet paper to try and protect
    her skin but later decided to take her to hospital.
    Ma Jie has been given a skin graft using 930 square inches
    of pig skin, which covers approximately a third of her body.
    Doctors said the operation was successful but Ma Jie remains
    in intensive care.
    However, the skin graft only provides temporary covering and
    will be rejected by Ma Jie’s immune system within a week.
    Doctors hope this will give enough time for some of the
    wounds to heal. 
    Her parents have been warned that there could be further
    complications, and that the medical fees of 140,000 Yuan (£14,500) could rise
    even further.
    Ma Jie was adopted at a young age when her biological
    parents, who lived in a rural village and already had two children, felt that
    they could not care for another daughter.
    Her adoptive parents decided to call her biological parents
    after they became worried by the severity of the condition.
    Both sets of parents have been anxiously waiting for updates
    at the hospital.
    Yu Guanghong, Ma Jie’s adoptive mother, said: ‘Whatever
    happens, this child came to my home and I have to save her no matter what.
    ‘I thought of telling her about her biological parents when
    she is eighteen. If she wants to go back to her biological parents, we won’t
    object either. We just want her to be well.’
    EB is extremely rare, affecting just one in every 17,000
    children.
    The majority of people who suffer from EB die before the age
    of 30 because the condition can often lead to infections and means they are
    more likely to get skin cancer.
    There is no cure for EB, meaning that treatment can only
    prevent blisters becoming infected.

    Follow Us on Facebook – @LadunLiadi; Instagram – @LadunLiadi; Twitter – @LadunLiadi; Youtube – @LadunLiadiTV for updates

    LEAVE A REPLY

    Please enter your comment!
    Please enter your name here