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child about surgery, the face of unforeseen risks, the young parents want to leave a heavy gift Ye Ye, prayer surgery success!
only half a day to enjoy the joy of discovery baby suffering from strange diseases
Wei Xing had managed to continue looking back to Guangzhou matching bone marrow. But after about a year of waiting,ugg トール, they finally charities through Taiwan in time for the 3-year-old Ye Ye found before the match volunteer bone marrow donors. Nanfang Hospital is scheduled to visit Taiwan, November 21,tory burch 日本, collected bone marrow donors,asics nimbus, and is scheduled for November 23, a bone marrow transplant.
addition to the ten thousand blessings, is fully prepared to have surgery, Ye Ye parents a wish: I hope that caring people can type AB donor platelets. Ye Ye has now admitted to a small southern sterile hospital ward, pre-surgery preparation. Lived alone in a small isolated cabin Ye Ye very obedient, two and a half baby has learned his mouth, although from time to time by the water choke.
Doctor abnormal hard way, the baby is about to find matching bone marrow surgery.WAS, these three letters are on the tube Wei Xing couples unforgettable, but two years ago, they have a not known. Their children called Ye Ye, on April 9, 2009 at noon in Guangzhou, Zhongshan Hospital attached to a hospital birth. Ye Ye's birth for a person immersed in the joy, but joy only lasted for a long time. months, the hospital has been unable to find the cause. little blood in the urine may lead to crying, less than 3-year-old Ye Ye and it was Children experienced numerous blood tests, blood diseases, all can think of are all investigation. often fever cough, eczema covered his head and face, often bleeding. hard to find half a year after the Queen Mary Hospital in Hong Kong confirmed that six months, Ye Ye do not know how many inspections, the number of pumping blood. / p>
where Ye Ye been the cause of a mystery!
reported that so far, only the domestic Hong Kong, Shanghai, Chongqing, several hospitals had more than 20 cases found in WAS syndrome. According to Chinese Medicine Branch Immunology Section Pediatric incomplete survey, the mainland at least 30,000 and 60,000 primary immunodeficiency patients. Experts said if the children are very susceptible to early age,ugg クラシック, and simultaneously repeated pneumonia, the body often appear ecchymosis petechiae, eczema and so long the head is often the case, parents must pay attention to. More than once because of co-occurrence of several conditions, is likely to be a syndrome.
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before surgery microblogging collect ten thousand blessings, and the other wish is our common concern with congenital immune deficiency genetic disease, to help more babies with this disease and poor parents, calls for early diagnosis of the disease in the blank solution. Wei Xing said in microblogging.
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- taken from the tube Wei Xing (microblogging) microblogging
(Reporter Li Lizhi photo coverage) help more babies with this disease and poor parents, calls for early diagnosis of the disease in the blank solution, is no longer a 'blood doubt'.
find a matching bone marrow microenvironment in Taiwan, Bo collected ten thousand blessings
microblogging behind a pair of young parents and their children pay the selfless love. This little boy named Ye Ye from the date of birth on the struggle with a strange illness, he experienced numerous blood tests, six months ago and finally was diagnosed in Hong Kong had a rare genetic recessive genetic diseases. His disease was first discovered in Guangdong, the Mainland only one case so far cured cases. Fortunately, they found a matching bone marrow.
thing is a turnaround after six months. Wei Xing tube in line to see the message, the success of a hospital in Chongqing for the child for a genetic immune deficiency bone marrow transplant. Thrombocytopenia, eczema, anemia and other symptoms are very consistent with Ye Ye disease characteristics. However, not all hospitals in Guangdong this disease to diagnose because not previously found a case, the Mainland has only a dozen cases. In the expert's suggestion, the couple decided to take control Xing Wei Ye Ye, Hong Kong Queen Mary Hospital for treatment.
microblogging Recommended | today's hot microblogging (edit: SN029)three times their total to Queen Mary Hospital. Small Ye Ye finally diagnosed the disease, he is suffering from a rare genetic recessive disease - WAS syndrome - thrombocytopenia with eczema, the global incidence rate of 1 / 5000000! Children with this disease, usually before the age of 3 will lead to intracranial bleeding due to thrombocytopenia or gastrointestinal bleeding and died, or because of immune deficiency leading to cancer, lung infection and died! Bone marrow transplant is the only way to treat WAS, for the first time confirmed in Guangdong, mainland cure success rate is only one example.
Call more people will give you the blessing. professor received us very kindly, I do not know how many times the screening and matching bone marrow, in October last year also found the error one yards of cord blood, but the doctor told me to do this surgery and the Mainland to Hong Kong account the cost to prepare 1.5 million yuan , we consider the actual situation to give up in tears!
tube Wai-hing said that pre-operative platelet Ye Ye to lose, lose Type B before transplantation, bone marrow for those who are type A, type AB to lose after transplantation, and finally the bone marrow to restore hematopoiesis after the A-type ,men moncler jacket! Inform the hospital blood bank in Guangzhou, Ye Ye need the B-type platelet temporarily do without, Ye Ye's bone marrow donor is type A, 23, has not been restored after transplantation of bone marrow hematopoietic function, Ye Ye need to enter the blood type AB sustain life. In addition, Ye Ye have two or three months after surgery, recovery, hope and love people to donate platelets type AB, Ye Ye to help overcome the disease.
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