karen millen on line Girl suffering from abnormal

School Youth League secretary, told reporters in the remote, Gu Jenny into the school in 2009, is a favorite won the teacher, the students were respectful students. Not only is she a good Communist Youth League, or the class monitor, the fourth top ten high school students.

care when the school learned of Jenny's situation, the Nineteenth Dalian school immediately launched her love activities. School teachers and students love the Fund to the initiative of calling you for the care of Jenny contributions show love. Just a week to teachers and students of the donations received ten thousand dollars, also received Qianzhi, condolence letters, cards, gifts and blessings of more than a thousand copies.

Jenny Gu Yuan Bo class where the class how the teacher can not believe, that the children have gentle and sensible suffer pain or illness. these words,designer karen millen, her heart was heavy,ferragamo mens, but to the Yuan Bo left a deep impression, so clear,nike shoxs for cheap, thorough! monitor the orderly conduct of the work, helped me a lot to reduce the burden, each in recognition of her, she just smiles shallow, but people did not think that a month later, the class that belongs to her seat, empty ... ... After writing this statement, Yuan Bo looked up at reporters, eyes with tears.




Today, Jenny Gu order to treat the family has spent three or four million, but the vision care Jenny was degraded to 0.2, but also continued to decline, and her limbs began to ache,ralph lauren top, cure Road within the foreseeable future.
endured the pain,女子连嫁3人轮流在3个家庭生活 男方均不知情, turn to comfort her,
care of Jenny's condition some of the recent increase,karen millen on line, the family forced her into a rural home Wafangdian resting, but Janet never forget learning, Zhangjun Li told reporters that she often saw her staring at the wall wall clock, said to himself, , but still at home,karren millen 茕居白叟在家中离世近一周后被发明, living in accordance with the school schedule, so staring at the clock every day to their own school, their text back.



no cure the strange disease


suffering from a rare demyelinating disease of white matter lesions still persist in studying the central nervous oppression
every morning, the 19th Dalian high school classroom will be heard recited, all of the 13-year-old girl Jenny who care, who is so sweet memories, and now is so far away. Since being diagnosed with a rare demyelinating disease of white matter, the care of Jenny was forced to drop out, went to Dalian, Beijing for treatment, but the face of this disease was only one ten thousandth of dozens of strange diseases, no medication is currently the medical profession can heal.

Affiliated Hospital of Dalian Medical University for treatment. After diagnosis, a difficult to accept the news as the bolt from the blue, down in the young girls head. Gu Jenny was diagnosed with demyelination of white matter - a few dozen parts per million incidence of the disease, and disease there are many possible reasons.


conservative treatment.
authoritative medical journals, for this disease have a more precise explanation: the white matter and spinal cord damage and to regulate autonomic disorders can not be independent self-regulation to occur Ruyang dominated zone of the diversity of pathological changes. However, little Jenny for the whole family, the doctors were even more popular interpretation of the horrors they realize the disease - in some cases,lucky jeans, bone marrow transplantation have made use of a certain effect, one year after the transcranial magnetic stimulation to improve motor conduction after two years motor function almost back to normal. But gene therapy really is too early, while others are mostly symptomatic treatment, the effect is more obvious.
recently, along with classmates 1,400 yuan donations of more than 13,000 yuan, including donations, handed Zhang Junli hands.
reporter Wang Lei
from teachers and students love

to sleep, feeling it a little stronger.
sick seeing students around 19 students in the self-organized donations for the care of Jenny, the first batch of more than 13,000 yuan has been sent to the care of his mother Jenny Zhang Junli hands. The stronger the care of Jenny is still not given up the desire for knowledge. Now she would fight back with pain every day, staring at the clock at home, according to the curriculum at school self-study.

medical treatment, the family has experienced the pain of suffering physical and psychological double.

young girls watching the clock back a day text
inexplicable headaches

care of Jenny 12 years before life is no different from other girls, a shift. According to his mother Jenny Gu Zhang Junli introduction, from the beginning of the year, 13-year-old daughter from time to time that their own headaches, but did not cause the family's attention.


with a last hope,shop ferragamo 男孩偷手机当场被抓 母亲跪求对方不要报警, Zhang Junli led her to find the Beijing Union Medical College Hospital attracted experts. In order to diagnose the specific cause, Gu Jenny received bone marrow test pumping, up to a 11 day pumping blood to the last can not get blood out both hands. Zhangjun Li told reporters, after two weeks of treatment, Jennifer's condition is still not improved, there was even multiple sclerosis, - blindness, memory loss, paralysis, coma ... ...