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but two years ago, they knew nothing about. Their children called Ye Ye, on April 9, 2009 at noon was born in Guangzhou, Zhongshan Hospital attached to a hospital. Born Ye Ye let family are immersed in the joy, but this joy lasted only half a day. "The next morning the doctor told me that the baby's blood platelet examination revealed only 39,000 (normal is between 100,outlet moncler,000 to 300,escarpin louboutin,000),abercrombie e fitch, worry about the risk of intracranial hemorrhage, and then go to ICU, a stay on two months,basket louboutin femme, the hospital has been unable to find the cause. "Ye Ye's resistance is very weak, the family was very careful to look after him,hollister outlet, could make him a little touch of skin bruising, a little crying can lead to blood in the urine, and less than 3-year-old Ye Ye on and it was "abnormal" wound, but has been difficult to determine the reason. Children experienced numerous blood tests,abercrombie paris, blood disorders who can think of are all investigation. "Every time I looked at the cold thick long needle inserted into the child's body emaciated, me and his mother's heart is broken!"When accidents happen, "from birth to now, because of immune deficiency, often fever cough, eczema covered his head and face, often bleeding."WAS diagnosed with SARS in Hong Kong,doudoune moncler, the global incidence of 1/5000000'Cause is struggling to find six months after Queen Mary Hospital in Hong Kong confirmed that six months, Ye Ye do not know how many times to check, how many times the blood pumping. "- Excerpt from Wei Guan Xing microblogging"When Ye Ye six months old,barbour paris, his head covered cause of thrombocytopenia due to bleeding, see people sad." At that time, Wei Guan Xing every day to search the Internet for any clues to similar diseases.
but six months,christian louboutin sale, has been the cause of Ye Ye is a mystery!Something of a turnaround after six months. Wei Guan Xing in line to see the message,abercrombie france, Chongqing, a hospital for an immune deficiency successful bone marrow transplant genetic child. Thrombocytopenia, eczema,barbour pas cher, anemia and other symptoms of the disease are very consistent with Ye Ye features. However, all of the hospitals in Guangdong are unable to make a diagnosis of the disease, because not previously found a case, the mainland is also only a dozen cases. Under the advice of experts,nike france, Wei Guan Xing Ye Ye couple decided to take to Queen Mary Hospital in Hong Kong for treatment.A total of 3 times they went to Queen Mary Hospital. Small Ye Ye finally diagnosed disease.
he is suffering from an extremely rare genetic recessive genetic disease --WAS syndrome - thrombocytopenia with eczema,parajumpers, the global incidence rate of 1/5000000! Children with this disease, usually before the age of 3 due to thrombocytopenia resulting in intracranial hemorrhage or gastrointestinal bleeding and mortality, or due to immune deficiency leads to cancer, lung infections and mortality! Bone marrow transplant is the only cure for WAS, and Guangdong for the first diagnosed case of mainland cure success rate.Find matching bone marrow microblogging collect 10,abercrombie online,000 units blessing"Ye Ye, my parents will be recorded through the microblogging each day before your surgery, along with a challenge to fate! You will also collect more people the blessing."- Excerpt from Wei Guan Xing microblogging"Ye Ye liked to go to Hong Kong, each to Queen Mary Hospital where professors received us very kindly.
he also re-planted a few acres of grapefruit, "at home with his wife, constitutes a family. I worked hard to make money, there is also something to look forward. "Shun-only said that now days,chaussure zanotti, the contentment.(Reporter Li Lizhi photo coverage), "My wish is for Ye Ye microblogging before surgery collect ten thousand blessings, another wish is our common concern genetic congenital immune deficiency diseases,red bottoms for women, help more this disease Poor baby and parents,escarpins louboutin, called for a solution to diagnose the disease as soon as possible gaps, no 'blood doubt'. "A few days ago, a two and a half parents microblogging attracted the attention of netizens.Microblogging behind a pair of young parents of the child selfless love and devotion. This little boy named Ye Ye date of birth from it with a strange illness struggle,barbour homme, he experienced numerous blood tests, six months ago had finally been diagnosed with a rare genetic recessive genetic disease in Hong Kong. His disease was first discovered in Guangdong, Mainland cured cases so far, only one case. Luckily, they found a matching bone marrow.Child and surgery, face unforeseen risks, young parents want to leave a heavy gift Ye Ye successful surgery to pray!Just enjoy the joy of discovery for a long time baby suffering from a strange disease"I have been accustomed to think of the past ... insomnia for a long time just to enjoy the taste of the joy of a father!"- Excerpt from Wei Guan Xing microbloggingWAS, these three letters of the alphabet now Wei Guan Xing couples unforgettable.
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