|Is your unborn baby less than perfect?|
Find out and kill it so it will not
make your life inconvenient in any way
Now we are told that scientists have developed a way to test unborn babies for 3500 genetic faults. Our world today cannot and will not deal with any imperfection or anything that might make us uncomfortable or inconveniences us in any way. It's ironic that our society has made laws that will supposedly help all of those who have physical handicaps, yet at the same time, we want to make it as easy as possible for their parents to detect "flawed" babies and then kill them so that neither they nor any of us will ever have to deal with physically imperfect people.
Here is the story from The Telegraph with all the Orwellian and gruesome details.
Unborn babies could be tested for 3,500 genetic faults
Scientists could soon be able to routinely screen unborn babies for thousands of genetic conditions, raising concerns the breakthrough could lead to more abortions.
A team has been able to predict the whole genetic code of a foetus by taking a blood sample from a woman who was 18 weeks pregnant, and a swab of saliva from the father.
18 Week Old Fetus
[Description of 18 week old fetus:
The fetus is now 6 inches long and weighs 7 ounces.
The fetus measures about 15cm and weighs almost 200 grams.
They can hear sounds and may be startled by loud noises.
Recognizable active and rest periods.
The skin is building a protective wax layer (vernix).]
They believe that, in time, the test will become widely available, enabling doctors to screen unborn babies for some 3,500 genetic disorders.
At the moment the only genetic disorder routinely tested for on the NHS is Down’s syndrome.
Other such faults are sometimes tested for, but usually only when there is a risk of inheriting them from a parent.
By contrast, the scientists say their new test would identify far more conditions, caused by genetic errors. [And thus give parents even more reasons to kill their babies]
[What other reason would there be for parents to test their unborn children?]
The American scientists were able to map the baby’s genetic code principally from tiny traces free-floating DNA, which makes its way into the mother’s blood. Blood sample DNA from the mother was also studied as well as DNA extracted from the father's saliva. Fitting pieces of the genetic jigsaw together, scientists in the US were able to reconstruct the entire genetic code of an unborn baby boy.
They were then able to see what spontaneous genetic mutations had arisen. Such natural mutations - called ‘de novo’ mutations - are responsible for the majority of genetic defects. By checking their prediction of the baby’s genetic code with actual DNA taken after the birth, the team from the University of Washington in Seattle, found they were able to identify 39 of 44 such mutations in the child. De novo mutations are thought to play a role in a number of complex conditions such as autism and schizophrenia.
The team also tested their approach on a woman who was earlier in her pregnancy than 18 weeks, and found it still worked.
Six Week Old Fetus
Dr Jay Shendure, the lead scientist, said: "This work opens up the possibility that we will be able to scan the whole genome of the foetus for more than 3,000 single-gene disorders through a single, non-invasive test."
Jacob Kitzman, who worked on the project, added: “The improved resolution is like going from being able to see that two books are stuck together to being able to notice one word mis-spelled on a page.”
In future, a more refined and less costly version of the procedure could make pre-natal genetic testing far more comprehensive than it is now, the scientists say. [Isn't that nice? They're going to make this test less expensive and more available to parents who wish to dispose of any baby who is less than perfect. Planned Parenthood, who make the vast amount of their money on killing babies, is rejoicing.]
The research is reported in the journal Science Translational Medicine.
The scientists said the test would be a considerable improvement on current techniques, which involve inserting a probe into the womb to take fluid from the foetal sac or placental samples. This can be dangerous for both mother and child. [Oh, but we're told by such websites as webmd.com that "amniocentesis presents a small risk for both the mother and her baby". So which is it - "dangerous" or "small risk"? The medical community lies to us all the time, especially when it comes to abortion.]
|Amniocentesis - see how dangerously close |
the needle is to the baby
Such existing methods only enable doctors to check for a relatively small number of genetic disorders. These include Down's syndrome and cystic fibrosis - which are both large-scale genetic defects - as well as muscular dystrophy and spina bifada, which can have hereditary elements.
However, they warned: “The less tangible implication of incorporating this level of information into pre-natal decision-making raises many ethical questions that must be considered carefully within the scientific community and on a societal level.
“As in other areas of clinical genetics, our capacity to generate data is outstripping our ability to interpret it in ways that are useful to physicians and patients.” [Pope Benedict XVI gave an excellent talk on what happens when science is divorced from God, as I have posted here. As the Holy Father said in this speech: "Without love, science also loses its nobility. Love alone guarantees the humanity of research."]
22 Week Old Fetus
Josephine Quintavalle, founder of the Pro-Life Alliance, put it more baldly. She said: “One always hopes, vainly, that in utero testing will be for the benefit of the unborn child. But, whilst this new test may not itself be invasive, given our past track record, it is difficult to imagine that this new test will not lead to more abortions.”