妈妈们好！
我已经把贝贝的片子录制下来，暂时算弄好，已经可以先看着了，挺清楚的。就在我的宝宝主页http://baobao.ci123.com/anitababy上。
因为时间的关系，前面有一小部分还没来得及剪辑掉，妈妈们可以先看着，大概也就一分半左右的时间。等晚上我会把新剪辑好的片子再重新传上来！
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以下内容引用自anitababy的大作：【育网牵手】帮助贝贝吧！【2月29日更新，捐款名单今又更新！】
支持一下 |
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看了真的很心痛!!!祈求上天起快让小贝贝快点好起来吧!!!! |
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祝福贝贝早日康复,能像别的宝宝一样健康.快乐的成长! 祝福所有好心人,一生平安^^^ |
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看了真的很心痛!!!祈求上天起快让小贝贝快点好起来吧!!!!
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支付了200.21到树杰的支付宝,祝愿小宝贝快点好起来 |
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希望育网能用公告的形式呼吁更多的人来帮助小贝贝，我还是无意间才知道这件事的，太多的好心人对此事不知情了，所以广泛求助，才能更好的帮助贝贝！
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提议大家把贝贝的主页继续下去，让大家都来关心帮助这个苦命的宝宝！
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对啊，不要放弃，我在努力给他“散播”消息~ 希望能够得到更多的回应~ |
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我之前跟贝爸联系，他有这么一封英文的信件，我希望贴上来，让楼主放在最前，让那些国外的都可以看到英文版，希望能够得到最到的帮助。 Letters of Asking for HelpDear Friends, We are a young couple from China .We feel so soory to disturb you at the beginning of this year.Today we write this letter for you is to ask for your help. We know that Britisher are very warm-hearted. So we hope that you can help our little child and rescue his life. Two months ago,our little child named Yuan Ye (CHINESE :袁野) had a terrible disease which is called Methylmalonic Acidmia MMA.His nickname is Beibei .Beibei was born in 2007’s Christmas Day and he was only 11 months old when he got this illness.We have already cost more than 100,000 yuan(RMB) for curing his disease and we borrowed a lot of money form. our friends and relatives.But we are both from the county,we still don’t have our own house two years after we get married. Only Beibei’s father have a job in two of us.His wage is only about 2,000 yuan per month,so we don’t have so much money to rescue our son. But we really don’t want to give up because we love our little baby,we need him. We had seen doctors in many hospitals but they couldn’t rescue Beibei’s life. Now we are curing Beibei in Beijing University NO.1 Hospital(CHINESE:北京大学第一医院).We live in a basement which is next to the hospital temporarily so that we can go to the hospital conveniently.We bring our son to see the doctor everyday but the trueth let us become hopeless and disapointed slowly. Beibei cries loudly every day and night.We know his body hurt heavily,but we don’t kown what to do.He seems have forgotten how to swallow and we had to feed him food by force. In these several months we cost our all money but Beibei didn’t get better.He had been in a coma many times.We also had made emergency rescue many times.We don’t kown when he would come to himself each time.We are worried about him and hope the society could help our little son. We kown that many other children who have this disease have already died,but we still believe in miracles will be up on him.Our son is only 13 months old,he is a so lovely little boy.How we wish that he could call us dad and mum!How we wish he could have a happy childhood like other children!Fate is so unfair to him. Many kind chinese people donated money to Beibei,but it is not enough to pay for his expensive medical expenses. Many web sites also give us a hand to report Beibei’s story in order to find more people to help him.Today we want to ask you for help.And we hope all the children who have got this disease would get well and live a healthy life. If you want to know more information about Beibei ,you can visit these Chinese Web Sites(I am so sorry there is no English version) 1.http://bbs./read.php?tid-64161.html 2.http://bbs.ci123.com/post/2597322.html 3.http://blog./blog.php?uid-11328.html(This is Beibei’s blog which is whote by his mother.) Beibei is waitting for the Stem-cell transplant operation now. As a famous Professor in China said, he is the best time to take an opertaion, but the mainliy difficulty is money. So we are looking for any groups or peoples to help him. Can you give a hand? Thanks a lot！ |
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希望小贝贝能快点好起来. http://foot.ci123.com" target="_blank" >
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以下内容引用貝爸寫的:
應該是好消息~~~ |
