以下内容引用自好男妈妈的大作：【育网牵手】帮助贝贝吧！【3月3日更新，有最近采访贝贝的视频！】
又来看贝贝了，不知道电台播出后，贝贝有没有受到关注，有没有人捐款？
干细胞的事情，又进展怎样了?
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为你祈祷，可爱的贝贝！祈祷早点手术成功！不要再受这样的痛
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贝贝我们为你的进步而高兴，贝贝，你是最棒的！
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又来看贝贝了，不知道电台播出后，贝贝有没有受到关注，有没有人捐款？ 干细胞的事情，又进展怎样了? |
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贝贝要加油哦~ 希望就在前方! |
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看得哭了，不知怎样去帮助这个可怜的贝贝，希望他能好起来吧！ |
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今天下班的时候给贝贝汇了200元，可能扣了手续费还有199元。也给贝爸发了信息，小小心意！希望贝贝能奇迹般快点好起来，祝福我们可爱的贝贝！！！  |
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我都要哭了.......好可怜的宝宝......乞求上天不要夺走那个可爱的小生命,给予他新的生命吧!!!!!!!!! |
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以下内容引用貝爸寫的:
應該是好消息~~~ |
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希望小贝贝能快点好起来. http://foot.ci123.com" target="_blank" >
http://tree.ci123.com/tree.php?treeid=169243" target="_blank" >
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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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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~ |
