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患心脏病被两个美国家庭收养的那对中国双胞胎姐妹,10岁重逢,如今双双获名校全奖录取
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患心脏病被两个美国家庭收养的那对中国双胞胎姐妹,10岁重逢,如今双双获名校全奖录取

gafdasd
楼主 (北美华人网)
据abc新闻5月22日报道 中国出生的双胞胎姐妹Audrey Doering和Gracie Rainsberry在婴儿时期失散,她们于2017年、她们10岁时在《早安美国》节目中重逢。本周三,这对姐妹再次回到《早安美国》演播室,共同庆祝她们人生的一个新的里程碑。

这对双胞胎姐妹被两个不同的美国家庭从中国收养。大约7年前,二人在《早安美国》节目重逢,当时她们泪流满面,情绪都非常激动。现在,18岁的Audrey和Gracie作为各自高中班级的优秀毕业生,被美国两所名校以全额奖学金录取。她们再次重新回到了《早安美国》节目的演播室,庆祝这一重要时刻。
本月早些时候,Gracie从她在华盛顿州的家来到Audrey居住的威斯康星州,观看Audrey的毕业典礼,Audrey也计划去参加Gracie的毕业典礼。
当初,两个美国家庭、她们的养父母都决定从中国领养一个婴儿。在2017年接受采访时,Audrey的妈妈Jennifer Doering说,她和家人决定收养,因为他们 “真的很想有一个女儿”。而Gracie的妈妈Nicole Rainsberry也表示,她认为“收养孩子是增加家庭成员的好主意。”
这两个家庭的收养程序始于2007年夏天,当时这对双胞胎姐妹仅有15个月大,且都患有心脏病。抵达美国后,她们二人都接受了心脏手术。

大约十年后,Jennifer对女儿的过去感到好奇,之后她发现了一张女儿和可能是她姐妹的两人坐在寄养妈妈腿上的老照片,然后她从一位中国工作人员那里得知,Audrey有一个双胞胎姐妹Gracie。
Jennifer得知Gracie也被收养并被带到了美国,并最终通过Facebook找到了Gracie的妈妈Nicole。2017年,《早安美国》节目得以让姐妹二人重逢。相认以来,尽管两姐妹的家相隔1700英里,但她们仍每年见面两次,一起过生日,甚至一起去海外旅行。

姐妹俩现在均已优异的成绩毕业,并双双获得了各自将入读大学的全额奖学金。今年秋天,Audrey将进入范德堡大学(Vanderbilt University),而Gracie将进入东俄勒冈大学(Eastern Oregon University),她还加入了大学女子足球队。

教育公司Sallie Mae在节目中为她们二人分别提供了1万美元的大学费用。旅游公司Expedia还赠予这对姐妹每人5000美元的现金卡,这样她们就可以经常去看望对方了。
Audrey和Gracie还将出席美国心脏协会举办的名为“Hearts on the Hill Fly In”的活动,以表示她们对该组织的支持。Audrey曾担任该组织2023年的全美青少年心脏大使,Gracie则通过Kid's Heart Challenge挑战赛参与其中。
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Laughaway
2 楼
挺好,祝福她们
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Harenough
3 楼
Bless
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Goldenwater
4 楼
看到脱口秀里说,用钱就能买到亚裔和黑人小孩儿。
感恩祖国给了她们光明的未来。
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魏大爷的邻居
5 楼
幸运
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brookhaven
6 楼
所以她们是小时候被弃养了吗? 还好遇到了好人收养。
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阿迪迪
7 楼
感动 祝福两个孩子和家庭!他们都戴眼镜啊 看来真的有近视基因
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shoeholic
8 楼
给了她们新生命啊
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holidaycactus
9 楼
来了美国变得好漂亮啊
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lovingmom
10 楼
Goldenwater 发表于 2024-05-24 11:02
看到脱口秀里说,用钱就能买到亚裔和黑人小孩儿。
感恩祖国给了她们光明的未来。

外国人去中国收养一个孩子花费非常贵。祝福这两个孩子和收养她们的家庭
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Giraph
11 楼
brookhaven 发表于 2024-05-24 11:06
所以她们是小时候被弃养了吗? 还好遇到了好人收养。

显然是因为心脏病被弃养了,送福利院,然后被美国家庭收养。貌似做了手术就没事了。
每次看到这种新闻真的是五味杂陈。
美国人民让人又爱又恨。
中国人民让人又爱又恨。
不幸又万分幸运的两个女孩子,祝她们的未来健康灿烂!
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shubashuba
12 楼
祝福这俩幸运的女孩子!
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aiersha
13 楼
回复 1楼 gafdasd 的帖子
这俩女孩都是各自所在高中的年级第一。
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Texcat
14 楼
中国的医保真差,农村尤其。
现在经济上来了,什么时候也来全民健保一下
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Lisafree
15 楼
aiersha 发表于 2024-05-24 13:59
回复 1楼 gafdasd 的帖子
这俩女孩都是各自所在高中的年级第一。

太棒了!感谢好心家庭的收养和教育
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fredman
16 楼
我一个印度客户跑到中国领养了一个小女孩。这对印度人自己有三个小孩。
我听到这个真的无语。。
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Harenough
17 楼
Texcat 发表于 2024-05-24 14:04
中国的医保真差,农村尤其。
现在经济上来了,什么时候也来全民健保一下

这个美梦不要想。就是全民发点钱都被否了,要劳动致富,不要躺平懒人,还想全民医保?
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hellohey
18 楼
真好!恭喜和祝福两姐妹!
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hellohey
19 楼
lovingmom 发表于 2024-05-24 13:27
外国人去中国收养一个孩子花费非常贵。祝福这两个孩子和收养她们的家庭

是的,我同事说3-4万几年前,包含医疗检测和去中国旅行费用。她教会牧师领养了两个。
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shuma08
20 楼
感动又惭愧,作为中国人却没有这个勇气去收养弃孩
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笨笨熊
21 楼
Giraph 发表于 2024-05-24 13:42
显然是因为心脏病被弃养了,送福利院,然后被美国家庭收养。貌似做了手术就没事了。
每次看到这种新闻真的是五味杂陈。
美国人民让人又爱又恨。
中国人民让人又爱又恨。
不幸又万分幸运的两个女孩子,祝她们的未来健康灿烂!

中国好多这种被美国人收养的残障孩子都是当年在中国误诊或者耽搁了治疗导致了残障,或者因为医疗人员专业知识不够造成了不必要的截肢,美国这里有对华人夫妻这么多年一直在走访这些家庭,写的文章很感人。
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ysyyrps
22 楼
Giraph 发表于 2024-05-24 13:42
显然是因为心脏病被弃养了,送福利院,然后被美国家庭收养。貌似做了手术就没事了。
每次看到这种新闻真的是五味杂陈。
美国人民让人又爱又恨。
中国人民让人又爱又恨。
不幸又万分幸运的两个女孩子,祝她们的未来健康灿烂!

可能也不能怪她们的亲生父母 原生家庭如果比较穷,可能真负担不起两个小娃的医疗费用 因病弃养多少总有点无奈,总比因性别弃养好点
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笨笨熊
23 楼
shuma08 发表于 2024-05-24 15:04
感动又惭愧,作为中国人却没有这个勇气去收养弃孩

连身体健康的孩子都要被中国人judge基因有问题
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hellohey
24 楼
Texcat 发表于 2024-05-24 14:04
中国的医保真差,农村尤其。
现在经济上来了,什么时候也来全民健保一下

啥时候穷人医保也包干了,中国才是发达国家。目前还是发展中国家。你看发达国家穷人医保都是不错的,当然中产比较苦交税多,医疗上交钱也多,穷人急诊可以不付钱,等着看中国啥时候变成发达国家吧。过去这些年中国有了农保及大病保险比原来的中国强多了,还需继续努力。 也许中国有更好的办法将来,毕竟中产医疗还是出不少肉痛钱的在美国。外加医保不报销时自己也要出癌症别的方式治疗钱的,我听一个老外说他从401K里拿14万给他母亲癌症做一种治疗,医生说的,但他母亲医保没批的方式,他母亲有Medicare和medicide这两种保险还是要出不少钱的。 他是西班牙裔也是和华人一样很看重家庭,他母亲已过世现在父亲80多有点糊涂,但还算能自理,他每个月花2300多给他爸爸找个一对一护工每天白天来。剩下时间他看着。白天他上班。
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Kitty1001
25 楼
祝福她们。另外很佩服这样自己已经有3个小孩还考虑收养的。
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mtwash
26 楼
啥时候穷人医保也包干了,中国才是发达国家。目前还是发展中国家。你看发达国家穷人医保都是不错的,当然中产比较苦交税多,医疗上交钱也多,穷人急诊可以不付钱,等着看中国啥时候变成发达国家吧。过去这些年中国有了农保及大病保险比原来的中国强多了,还需继续努力。 也许中国有更好的办法将来,毕竟中产医疗还是出不少肉痛钱的在美国。外加医保不报销时自己也要出癌症别的方式治疗钱的,我听一个老外说他从401K里拿14万给他母亲癌症做一种治疗,医生说的,但他母亲医保没批的方式,他母亲有Medicare和medicide这两种保险还是要出不少钱的。 他是西班牙裔也是和华人一样很看重家庭,他母亲已过世现在父亲80多有点糊涂,但还算能自理,他每个月花2300多给他爸爸找个一对一护工每天白天来。剩下时间他看着。白天他上班。
hellohey 发表于 2024-05-24 15:16

大病医保的品质是区分一个国家发达与否最有意义的标签,这个意义上台湾真的比中国大陆强一大截
美国医疗技术发达又有钱,但医保体系太吸血;中国穷,又缺乏大病覆盖,就更差了。医保医疗对老百姓生活品质是最有感的几个方面之首,但这些所谓的超级大国的政客们假装眼瞎,倒是互相攀比造飞机大炮最舍得花钱。
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1314ll
27 楼
为什么双胞胎被分开领养,是因为单卖比打包更赚钱吗?
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hellohey
28 楼
mtwash 发表于 2024-05-24 15:22
大病医保的品质是区分一个国家发达与否最有意义的标签,这个意义上台湾真的比中国大陆强一大截
美国医疗技术发达又有钱,但医保体系太吸血;中国穷,又缺乏大病覆盖,就更差了。医保医疗对老百姓生活品质是最有感的几个方面之首,但这些所谓的超级大国的政客们假装眼瞎,倒是互相攀比造飞机大炮最舍得花钱。

国内现在也有大病医保,每年花199能保300万这种,普惠保之类的,就是在原有城镇基础医保报销外还能报销的,但有个2万5 deductible 费用,原来中国根本没有。家里有老人在国内的可以看看。每个地方叫不同名字。不过没有大病的一般用不上,因为基本医保住院已经能报销很多,医保后自付达不到deductible2万5的费用。这就属于大家都花199一年,有大病那家能用上,其他人用不上的。
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渔非凡
29 楼
fredman 发表于 2024-05-24 14:49
我一个印度客户跑到中国领养了一个小女孩。这对印度人自己有三个小孩。
我听到这个真的无语。。

你无语什么?
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mtwash
30 楼
hellohey 发表于 2024-05-24 15:29
国内现在也有大病医保,每年花199能保300万这种,普惠保之类的,就是在原有城镇基础医保报销外还能报销的,但有个2万5 deductible 费用,原来中国根本没有。家里有老人在国内的可以看看。每个地方叫不同名字。不过没有大病的一般用不上,因为基本医保住院已经能报销很多,医保后自付达不到deductible2万5的费用。这就属于大家都花199一年,有大病那家能用上,其他人用不上的。

那这个还不错,199元能保300万。其实如果300万能切实落实,一年1000元保费也挺便宜
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天使美人鱼
31 楼
Sallie Mae挺小气
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hellohey
32 楼
mtwash 发表于 2024-05-24 15:32
那这个还不错,199元能保300万。其实如果300万能切实落实,一年1000元保费也挺便宜

现在国内还弄了长护保险试点,医保出99,自己家出99一年,生活不能自理的一个月能拿到30小时,也就是每天一小时上门,我觉得搭配自己家请的一对一护工一起帮老人做点事应该不错的。但目前只是在少数地区试点中。国内现在医院还有试点三甲医院医护到家服务,那个普慧保大病险也包5次陪诊还是5次到家服务我忘了,以前看过一眼。每年11月开放买。还有啥高端医疗报特需门诊之类的,特需门诊看病人少病房也是单间。高端医疗保费贵上千的https://www.zhihu.com/question/633906635?utm_id=0
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hive
33 楼
真好,两个幸运的小姑娘
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lilylily2021
34 楼
hellohey 发表于 2024-05-24 15:03
是的,我同事说3-4万几年前,包含医疗检测和去中国旅行费用。她教会牧师领养了两个。

现在双倍都不够了。中国政策也变了。很难批
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92m
35 楼
笨笨熊 发表于 2024-05-24 15:11
中国好多这种被美国人收养的残障孩子都是当年在中国误诊或者耽搁了治疗导致了残障,或者因为医疗人员专业知识不够造成了不必要的截肢,美国这里有对华人夫妻这么多年一直在走访这些家庭,写的文章很感人。

请问这对华人夫妻写的有关文章在网上哪里能看到呢?
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模拟人生
36 楼
hellohey 发表于 2024-05-24 15:29
国内现在也有大病医保,每年花199能保300万这种,普惠保之类的,就是在原有城镇基础医保报销外还能报销的,但有个2万5 deductible 费用,原来中国根本没有。家里有老人在国内的可以看看。每个地方叫不同名字。不过没有大病的一般用不上,因为基本医保住院已经能报销很多,医保后自付达不到deductible2万5的费用。这就属于大家都花199一年,有大病那家能用上,其他人用不上的。

国内的医保地域性太强了,每个省都不一样。 北上广的真是太好了,一些省做的也不错,有的地方太差了。以前治不起大病还能治小病,小县城和农村医保基本上就是个名声在外,现在大病小病都治不起了。
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hualihu
37 楼
这是又要骗国内的人杀猪了。。。
实际美国的情况是 North Augusta teen dies after double lung transplant | WJBF NORTH AUGUSTA, S.C. (WJBF) – A local high school student who underwent a lung transplant earlier this year has died. We told you about Paris Marchant back on January 5th. She was a student at Augusta Christian who had to travel to Saint Louis to receive a lung transplant.
Recipient of first pig kidney transplant dies nearly 2 months later The hospital said there was no indication the passing was due to the transplant. May 11, 2024, 6:46 PM

Lexington teacher who spent months on a machine, had two double lung transplants has died BY VALARIE HONEYCUTT SPEARS UPDATED MAY 03, 2024 11:29 AM
Read more at: https://www.kentucky.com/news/local/counties/fayette-county/article288251385.html#storylink=cpy
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hualihu
38 楼
When a Black Man’s Heart Was Transplanted Without Consent

THE ORGAN THIEVES The Shocking Story of the First Heart Transplant in the Segregated South By Chip Jones In May 1968, the family and friends of Bruce Tucker, a 54-year-old African-American factory worker, became worried after he failed to come home from work. When they finally got a cryptic phone call from a friend who had seen Tucker being rushed into an operating room at the Medical College of Virginia, they made their way to the hospital, only to find out he had been taken there with a head injury and had since died. It was the funeral director, not hospital staff, who alerted Tucker’s family the following day that his heart and kidneys were missing. Tucker’s heart had been implanted into the chest of Joseph Klett, a retired 54-year-old white man, and one of the first patients to receive a heart transplant in the United States. Virginia law required that at least 24 hours elapse between determination of death and declaring the body to be abandoned by family. But in Tucker’s case, the surgeons needed to harvest the organs while they were maximally viable for transplantation and ignored this rule, instead invoking the novel concept of “brain death.”
The hospital staff insisted that they had done everything to locate Tucker’s family to obtain consent, even speculating that no one was claimed him in order to evade the cost of his care. The future Virginia governor L. Douglas Wilder, then a Richmond lawyer in private practice, represented the Tucker family in a case against the Medical College of Virginia that excluded African-Americans from the jury and ended in victory for the hospital and the researchers involved in performing the transplant. In the hands of some writers, this would have become a powerful narrative, weaving one family’s tragedy into a nuanced panorama of race, medical innovation and ethics, scientific ambition and the law. But Chip Jones’s “The Organ Thieves,” which tells the story of what happened to Bruce Tucker, disappoints, with its pedestrian language, telling omissions and hagiographic portrayals of medical actors. Image

Jones doesn’t stop to interject at key moments in the narrative. To take one example, researchers rationalized their treatment of Tucker by thinking of him as a “charity” patient, the kind charged less for substandard care in rat-infested segregated wards in exchange for being conscripted into research. Such coercion is and was unethical, and should not just be treated as another story detail.
Moreover, it should have been made abundantly clear that no amount of money could have bought an African-American a bed in a standard ward. Medicare had enforced hospital desegregation via the 1964 Title VI of the Civil Rights Act, but de facto segregation and health care bias lingered, even in the North. Image
L. Douglas Wilder in 1978.Credit...
Richmond Times-Dispatch What happened to Tucker matters for reasons far beyond the appropriation of one man’s organs. In the 19th century, Black patients received care at medical schools, clinics and hospitals by serving as “teaching material,” and the appropriation of Black tissues, organs and bodies was commonplace. In Virginia, limbs were removed solely to train medical students in amputation technique. “Bones in the Basement” by Robert Blakely and Judith M. Harrington documents post-mortem racism and Michael Sappol’s “A Traffic of Dead Bodies” discusses the theft of African-American cadavers to spare whites the indignities of serving as anatomical training. This extended to northern schools such as Harvard that contracted with Southern institutions to buy Black bodies. The author describes some of this key history of body appropriation, but fails to engage with the ethics of these practices, explaining away the moral lapses of researchers as a result of systemic racism and professional ambition. In the 1950s, “for investigational purposes,” researchers at the Medical College of Virginia deliberately inflicted third-degree burns on the skins of 100 patients a year at Dooley, a charity hospital for Black children, and at St. Philip, its sister hospital for Black adults.
Racism enabled the appropriation of Black bodies. But there is a slew of complex ethical questions that this case also demands we ask: Shouldn’t a patient or his family be entitled to informed consent, in which all implications related to surgery be shared? With Black donors having borne the brunt of the risks and benefiting least from a new technology, do we need to bring the lessons of distributive justice to our thinking about transplantation? In apartheid South Africa, transplants mirrored Virginia’s racial disparity as white patients received organs from Blacks, but Blacks received none from whites. How did the policies of both nations drive this inequitable distribution? But the book fails to engage with such questions, and Jones avoids grappling with them by claiming there were no ethical strictures governing medical practice and research at the time. “In the 1950s and 1960s,” he writes, “doctors and academic medical centers enjoyed so much prestige and authority that they often operated virtually unchecked from outside supervision. The notion of ‘informed consent’ was ‘nonexistent.’” He is not the first writer to voice this fiction, sometimes deployed by apologists to normalize the abysmal treatment of African-Americans. Far from being “nonexistent” in the 1950s and 1960s, the term “informed consent” — which describes obtaining consent that is predicated on conveying specific information about risks, benefits, known side effects, intention, design of and alternatives to medical studies and procedures — first appeared in the 1957 landmark decision in Salgo v. Leland Stanford Jr. University Board of Trustees. However, as early as 1900, the Virginia native Walter Reed observed formal procedures for obtaining the informed consent of his yellow-fever experimental subjects. In 1914, Schloendorff v. Society of New York Hospital used rights of self-determination to justify mandating consent from patients. A 1946 Atomic Energy Commission memo strictly mandated a higher degree of informed consent than even current American law requires, and that year, the Judicial Council of the American Medical Association also established widely disseminated standards for the protection of human subjects, including voluntary consent of the subject, previous animal experimentation and “proper medical protection.” Instead of engaging with questions of transplantation ethics based on documented history, the author focuses on fictional accounts, extensively invoking the fantastic Gothic writing of Edgar Allan Poe and African-American myths about “night doctors” who steal bodies. Unfortunately, he doesn’t illuminate how the myth relates to the documented bodysnatching from Black cemeteries by doctors, an elision which consigns warranted African-American fears to the realm of horror stories and folklore.
This ahistoric approach is most dismaying, especially in light of telling errors that stud the narrative. The author writes, for example, about the infamous Tuskegee syphilis study that the United States Public Health Service “recruited hundreds of African-American men and gave them the painful, fatal disease.” This claim is untrue. Although researchers have injected Americans with gonorrhea, syphilis and other venereal diseases on at least 40 occasions since 1892, the study recruited 399 African-American men who already had been diagnosed with syphilis and promised them treatment. Even a cursory look at the pertinent history, including some titles in this book’s bibliography, would have prevented Jones from making this error. “The Organ Thieves” tells an important story passably well, but its evasions and occasional missteps hobble its power to illuminate. Harriet A. Washington is the author of “Medical Apartheid: The Dark History of Medical Experimentation on Black Americans from Colonial Times to the Present” and of the forthcoming “Carte Blanche: The Erosion of Medical Consent.” THE ORGAN THIEVES The Shocking Story of the First Heart Transplant in the Segregated South
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snowpenguin
39 楼
lilylily2021 发表于 2024-05-24 18:02
现在双倍都不够了。中国政策也变了。很难批

现在早就收养不到中国的健康孩子了,基本都是有残疾的。
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abh
40 楼
fredman 发表于 2024-05-24 14:49
我一个印度客户跑到中国领养了一个小女孩。这对印度人自己有三个小孩。
我听到这个真的无语。。

无语啥 很多美国家庭也是自己有小孩 又领养
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abh
41 楼
我采访过十几个这样的家庭 美国白人家庭领养中国女孩。我的样本里三分之一是自己未婚未育,三分之一已婚有自己小孩,三分之一已婚没有自己小孩。不过样本量有限 不代表普遍情况。
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大喜妞
42 楼
两个伟大的家庭。祝他们永远幸福!
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shuma08
43 楼
渔非凡 发表于 2024-05-24 15:32
你无语什么?

可能无语连印度人都能帮中国人扶贫了,无论是物质上还是精神上都超越咱们了
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笨笨熊
44 楼
92m 发表于 2024-05-24 18:06
请问这对华人夫妻写的有关文章在网上哪里能看到呢?

我有段时间没看了,似乎微信公众号叫七彩娘娘,你放狗搜一下应该能搜到。
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笨笨熊
45 楼
snowpenguin 发表于 2024-05-24 20:00
现在早就收养不到中国的健康孩子了,基本都是有残疾的。

好像是有点这样,以前都是刚出生的女婴,现在好多都是挺大的还有十几岁的,基本都有一些健康问题,有点不敢想这些孩子在福利院这么多年过的什么样的生活。
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luypluyp
46 楼
这才是真正的Adopt!收+养!赞!
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hongxx
47 楼
感觉变得阳光自信了
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明媚如期
48 楼
Kitty1001 发表于 2024-05-24 15:18
祝福她们。另外很佩服这样自己已经有3个小孩还考虑收养的。

而且养母非常爱她们,想知道她更是小时候的消息才发现了老照片,才知道是双胞胎,才有了后来的重逢
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