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| Home > Education > Beginning of life > Embryo experimentation > PGD | |||||||||||||||||||||||||
Pre-implantation genetic diagnosis (PGD) |
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One of the key objections to PGD is that when cells are separated from an embryo in these very early stages each separated cell has the capacity to develop and grow. Each is actually an embryo in its own right. This is similar to how identical twins occur naturally. In PGD, one of each pair of ‘twins’ is destroyed in order to test its genes. If a disability is found in the genes, the twin of that embryo is also discarded. Where no disability is found, the twin of the test embryo is transferred to the womb. Less than 15 percent of embryos implanted by this method survive2 and it has been found that only 25 percent of embryos screened for chromosomal disabilities have "entirely normal cells"3. PGD is most widely used for people who have a family history of genetic disabilities, including cystic fibrosis, Huntington’s disease and Tay-Sach’s disease. PGD also made the headlines when it was performed to select an embryo who did not have the Fanconi’s anaemia genetic disability and who, once born, would be a good source of transplant cells for a sister who did have it4. SPUC acknowledges the scientific fact that each individual human life normally5 begins at the moment of fertilisation. From the beginning of their lives, human beings, whether or not they have a disability, are entitled to the respect proper to their human nature, to protection from harm, and to rights appropriate to their stage of development – the most fundamental of which is the right to life. PGD is completely incompatible with a respect for the right to life, because it entails creating and destroying "test embryos", and also destroying any "twins" who do not measure up to an arbitrary measure of desirability. PGD is dependent on the availability of IVF technology, without which it would not be possible. In addition to the thousands of embryos destroyed during the process of developing IVF, hundreds of thousands of human embryos continue to be destroyed as a result of IVF technology6. In view of this cavalier attitude towards the destruction of very young human beings, it is perhaps not surprising that the destruction of those found to have a disabling condition has become widely accepted. It is, of course, both natural and right that parents should hope that their children will not have to contend with illness or disability, and that they should take ethical steps to try to give their children the best possible start in life. There are ways of protecting unborn children from disability which are not destructive, such as refraining from smoking or drinking alcohol, and taking supplements, such as folic acid which can prevent the disability spina bifida from occurring. Such measures cannot prevent every disabling condition, but it must be recognised that parents do not have a right to a non-disabled baby. Children are gifts, not commodities. Pro-abortion medical academic David Paintin7 has posed the question: "Does the availability of abortion to prevent the birth of a seriously abnormal fetus imply discrimination against people who have a congenital disability?"8 The answer is clear. It is impossible for a society to value a group of individuals whilst simultaneously advocating their systematic destruction. We acknowledge the equal value and dignity of every human being by wholeheartedly welcoming into our society every child, disabled or not. 1 Human Fertilisation and Embryology Authority, Eighth
Annual Report and Accounts, 1999 'A Way of Life' The Society for the Preotection of Unborn Children March 2002
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