泰国代孕价格,泰国代孕生男生女-泰国义诚代孕中心(合法正规) Thailand surrogacy center: legal sex selection, surrogate, for eggs. The next generation of PGD screening health quality  

泰国代孕帮助解决地中海贫血论坛

    Imagine that every time you are planning to have
a child, you ALWAYS run a risk of one in four that
your child will have a disease causing it to pass away
around age 20. Imagine that these 20 years will be filled
with hospital visits and sleepless nights of pain, drugs
injected, and tubes attached. No boy- or girlfriends
stunted growth, no play dates or sleep away nights.
No parties, no festivities at home, no trips away from
home! Always ready to go back to the hospital. Then,
you try for a second one; you think, maybe that child
w川 be healthy! This time you know better, you have
already tested and found that both yourself and
your partner are "carriers" of Thalassemia. Inherited
genetic diseases also called "single gene disorders"
are conditions where "faulty" genes confer a lOO%
susceptibility to the disease, meaning that if you have
two copies of the 'faulty' gene (our genes are always
present in two copies) then you will develop that disease.
If only one of the two copies is 'faulty" then you are a
"carrier" and since the second copy of the gene works
 perfectly well you will not get sick but may "carry" the genetic change
further to your children. Your doctor told you that you would need an
 'amniocentesis'i during the pregnancy to find out if the child is affected .
 How would you feel during these four months of unbearable wait?
Normally, a pregnant couple is fullof expectations, dreams, planning, joy,
preparations for the little one that would soon arrive. You are thinking of
names, wondering if it is a boy or a girl. Then you say it is not important,
hope it is a healthy child. Grandparents share this joy, also plan for the
beloved child about to arrive_But, no, this time you do not dare to be
happy, you know there is a cruel risk of one in four that this pregnancy
will not end as you expect. In moments of despair, you blame yourself
you even tried for this second child, but you did it because you also
heard that there is a tiny-tiny chance that nature may compensate you
for the first child's torment. That this second one could be a full match
for the first one and when you keep this second one's cord blood stem
cells, you could save the first one that has suffered so much, has had
 so many needles inserted for blood transfusions_oh, you dream, you
hope, that luck would be on your side this time and everything will be
ok againl You know that because you have been trying to find matched
stem cells for a bone marrow transplantation that is what is needed to
get rid of Thalassemia in your first child. Five years have passed and no
match has been found, while the liver and the spleen of your first borne are
increasing in size while his height stays stunted. This is why you wanted
to give it a chance. Then the day comes forthe amniocentesis and some
days later the results are in an envelope in front of you. Your doctor tells
you that the second child has Thalassemia too. You need to consider
termination of pregnancy, or having a second child with the same condition
as the first one. How would you feel?Wem this is the reality of 40% of
the Thai population that are carriers of Thalassemia. Having a child for
them is not as easy as people think it is. The grim reality is that 7 0ut
of 10 with Thalassemia will never find stem cells to rid the disease and
if they do, most will not be able to afford these donated stem cells and
succumb. Those that find stem cells in more than 80% of the cases,

find them within their family, siblings, and relatives.
     This was the reality of a Thai family from the southern island of Koh Samu
until they met with knowledgeable doctors at Superior ART that offered
a viable alternative. The doctors said that it was possible to test whether
the future child would have the 'faulty' genes of Thalassemia well in
advance before this child would become a pregnancyl The family did
not believe their ears! The doctors explained that using the technique
of in vitro fertilization (IVF), the mother's ovaries would be stimulated to
produce many eggs (oocytes) at once instead of only one ortwo every month.
Then these eggs would be collected and put together with the father's
sperm in the laboratory to fertilize and produce many future, prospective
embryos. The scientists would then test each and every one of these
embryos and see which ones had the "faulty" genes and which not. This
process is a highly specialized technique only available at Superior ART
called Preimplantation Genetic Diagnosis (PGD). Then the ones without
the disease would be selected for further examination because the mother
wanted to find a way to save her first born from the agonizing prospect
of demise in Thalassemia. That would require that this future child would
be a belated twin for the first one and a full genetic match so that cord
blood stem cells would be collected and used in a life saving bone mar-
row transplantationl The whole process is called Preimplantation Genetic
Diagnosis (PGD) witti HLA matcriing and Superior ART made it possible.
An embryo that was disease free and a match was found in the first round
and could be transferred to the mother's womb. A month later, she knew
she was pregnant. She did not have to worry if this gift in her womb would
be affected; she knew already this child was the prefect match, the savior,
and the harbinger of happiness in the family. She had to take good care
of herself and her husband made that possible. Nine months later little
Joy arrived and THAI StemLife skillfully collected and processed the cord
blood stem cells that would be required to save an already tormented
little life. The second child was of course as expected not affected and
after further tests, the cord blood stem cells were a PERFECT match
for the tirst-born! A dream was slowly coming true. A specialist from a
renowned Bangkok Hospital was involved that would now take over
and using the cord blood stem cells collected and preseNed in -1960C
 by THAI Stemlife, would perform a bone marrow transplantation in the
first-born and change the course of events. Success! A few short months
later it was confirmed that the cord blood stem cells obtained through
Preimplantation Genetic Diagnosis (PGD) with HLA matching successfully
engrafted and made Thalassemia in the first-born a thing of the past, a
bad memory a nightmare to forget. Both children in the embrace of their
mother and father are disease free and happy. Indeed, a happy ending.
This is the true story of three Thai families. Another three are expecting.
    Thaiassemia is not the only disease amenable to Preimplantation
Genetic Diagnosis (PGD) with or wrthout HLA matching. Almost all single
gene disorders known, where one "faulty" gene causes the disease, can be
diagnosed via Predictive Genetic Testing and avoided via Preimplantation
Genetic Diagnosis (PGD). Furthermore, HLA matching can ensure that
the cord blood stem cells of that sibling can be used to treat affected elder
siblings! The only thing you need to do is KNOW! In more than 80% of
the cases when a child is bom with an inherited condition, it happens in
families where there has not been knowledge of that condition in advance!
These parents are faced with the "Angelina Dilemma". Find out if you are
a carrier and let the rest to the doctors and scientists. More genes are
gradually added and can be deselected, like certain genes for cancer
and debilitating diseases.


想象一下,每次你计划的时间有
小时候,你总是在四个运行一个危险的
你的孩子将有一个疾病导致它废去
20岁左右。试想一下,这20年将充满
与医院探访及疼痛,药物不眠之夜
注入和管连接。没有男孩或女友
发育不良,不玩耍日期或睡觉去晚。
没有政党,没有任何庆祝活动在家里,没有车次远离
回家!随时准备好回到医院。然后,
你尝试了第二个,你想,也许那个孩子
瓦特川是健康的!这一次,你知道更好,你有
已经测试,发现自己和
你的伴侣是地中海贫血的“携带者” 。遗传
遗传性疾病也被称为“单基因遗传病”
是这里的“缺陷”基因赋予一个厕所%的条件
患上此病的机会,也就是说,如果你有
在“故障”基因(我们的基因的两个副本总是
目前一式两份),那么你将开发这种疾病。
如果只有两个副本中的一个是“错误的”,那么你是一个
“载体”和由于基因工程的第二拷贝
 非常清楚,你不会生病,但可能“扛”的基因变化
进一步给你的孩子。你的医生告诉你,你需要一个
 怀孕找出如果孩子受到影响时“ amniocentesis'i 。
 你怎么会在这四个月难以忍受的等待感觉?
通常情况下,怀孕的夫妇是fullof的期望,梦想,计划,喜悦,
筹备小家伙很快就会到来。你是想
名字,想知道如果是男孩还是女孩。那你说这并不重要,
希望这是一个健康的孩子。爷爷奶奶分享这份喜悦,还计划为
即将arrive_But心爱的孩子,不,这个时候你不敢要
快乐,你知道有四分之一的残酷风险,这怀孕
如您预期不会结束。在绝望的时刻,你只能怪你自己
你甚至尝试了第二个孩子,但是你做到了,因为你也
听说有一个微小的,微小的机会,自然会补偿你
第一个孩子的折磨。这第二个可能是全场比赛
第一个,当你保持这个第二个脐带血干
细胞,可以保存第一个已经遭受了这么多,已经有
 插入血transfusions_oh这么多针,你的梦想,你
希望,运气会站在你这一边这个时候,一切都会
OK againl你知道,因为你一直试图找到匹配的
干细胞进行骨髓移植是什么是需要
得到你的第一个孩子摆脱地中海贫血。五年过去了,没有
比赛已经找到了,而你的第一得紧的肝脏和脾脏
在尺寸增加,而他的身高保持发育不良。这就是为什么你想要的
给它一个机会。然后有一天,满心欢喜羊膜穿刺术和一些
天后的结果是在你面前的信封。你的医生告诉
你的第二个孩子有地中海贫血了。你需要考虑
终止妊娠,或有第二个孩子用相同的条件
作为第一个。你会感觉如何? WEM这是40 %的现实
泰国人口是地中海贫血的携带者。有一个孩子
他们是不容易,因为人们认为它是。严峻的现实是, 7 0UT
10个地中海贫血将永远找不到干细胞彻底摆脱了疾病和
如果他们这样做,最不能够买得起这些捐献干细胞和
屈从。那些发现干细胞在80%以上的情况下,

他们的家人,兄弟姐妹和亲戚中找到它们。
     这是从苏梅萨姆岛南部一个泰国家庭的现实
直到他们与提供知识渊博的医生在高级艺术会见
一个可行的选择。医生说,这是可能的,以测试是否
将来孩子会有地中海贫血的“缺陷”基因以及在
推进之前这个孩子将成为一个pregnancyl的家人做
不相信自己的耳朵!医生解释说,使用该技术
在体外受精(IVF )中,母亲的卵巢会被刺激
一次产生,而不是只有一个ortwo许多蛋(卵母细胞)每月。
那么这些鸡蛋会被收集,并与父亲的放在一起
精子在实验室中进行受精,产生许多未来,有意
胚胎。科学家会然后测试所有这些和每一个
胚胎,看看哪些有“缺陷”基因,哪些不是。这
进程是一个仅适用于高级艺术高度专业化的技术
所谓植入前遗传学诊断(PGD ) 。然后是不加的人
该病会被选中作进一步检查,因为母亲
想找到一个方法来拯救她从痛苦的前景第一个出生
消亡的地中海贫血。这得需要这个未来的孩子会
是一个迟来的双胞胎的第一个和一个完整的基因匹配,使线
造血干细胞将被收集并在生活中使用节能骨髓 -
排transplantationl整个过程被称为植入前遗传学
诊断(PGD ) witti HLA matcriing和高级艺术成为可能。
这是无病和一个匹配的胚胎中发现的第一个圆
并且可以转移到母亲的子宫里。一个月后,她知道
她怀孕了。她没有担心,如果这件礼物在她的子宫会
受到影响,她已经知道这个孩子是知府比赛,救世主,
和幸福家庭的预兆。她要照顾好
她和她的丈夫所做的可能。九个月后小
欢乐赶到,泰国StemLife巧妙地收集和处理线
将需要保存一个已经折磨造血干细胞
小生命。第二个孩子,当然是因为预期不会受到影响,
经过进一步的测试,脐带血干细胞是绝配
为tirst出生的!梦想慢慢变成现实。从一名专家
著名的曼谷医院参与,现在将接管
以及使用所收集的脐带血干细胞和preseNed在- 1960C
 由泰国Stemlife ,将执行在骨髓移植
第一个出生的,改变事件的进程。成功!短短数月
后来证实,通过获得的脐带血干细胞
植入前遗传学诊断(PGD )与HLA配对成功
在过去的第一个出生的事,栽种,并提出一个地中海贫血
记性不好的噩梦给忘了。无论是在怀抱自己的孩子
母亲和父亲是疾病的自由和快乐。事实上,一个圆满的结局。
这是三泰家庭的真实故事。另外三个期待。
    Thaiassemia不是唯一的疾病适合于植入前
遗传学诊断( PGD)或wrthout HLA配型。几乎所有的单
基因疾病已知的,其中一个“故障”基因引起的疾病,可
通过预测性基因检测确诊,并通过植入前避免
遗传学诊断( PGD ) 。此外, HLA配型可以确保
该兄弟姐妹的脐带血干细胞可用于治疗受影响老年
兄弟姐妹!你需要做的唯一事情是知道的!在超过80 %的
当孩子BOM与一种遗传性疾病,它发生在案件
家庭,没有发生过的那个条件知识在前进!
这些家长都面临着“安吉丽娜困境” 。找出如果你是
载体,让其余的医生和科学家。更多的基因是
逐渐加入,并且可以取消,就像某些基因的癌症
使人衰弱的疾病。

| 发布时间:2014.01.06    来源:    查看次数:
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