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Proceeding contribution from Lord Jenkin of Roding (Conservative) in the House of Lords on Monday, 28 January 2008. It occurred during Debate on bill on Human Fertilisation and Embryology Bill [HL].


Human Fertilisation and Embryology Bill [HL]

moved Amendment No. 146: 146: Schedule 6, page 72, line 12, at end insert— ““(1) The Authority shall from time to time carry out a review of the law and practice concerning the inclusion in the birth certificates of donor conceived persons the fact of such conception. (2) If the Authority, after any such review, and after consulting bodies representing the parents of donor conceived persons, and bodies representing donor conceived persons, recommends that the law and practice should be changed to provide for the inclusion of the fact of donor conception on the birth certificates of donor conceived persons, the Secretary of State may by order implement any such recommendation with such amendments as he shall think fit, and a draft of any such order shall be laid before each House of Parliament and shall only take effect if both Houses approve the draft.”” The noble Lord said: My Lords, we return to donor-conceived children and the kind of issue that might be advocated by the committee that the noble Baroness, Lady Williams of Crosby, would like to see. We have already discussed the desirability of donor-conceived children being told at the earliest possible opportunity of their biological origins. This amendment is concerned with whether the fact of donor conception should appear on the child’s birth certificate. Telling the child is, of course, widely supported, but there is far less agreement about recording the fact on birth certificates. Indeed, the organisations primarily representing donor-conceived people differ: the International Donor Offspring Alliance takes a quite different view from the Donor Conception Network, a self-help group that primarily represents families. The former group, the IDOA, describes itself as, "““an international alliance of people conceived by ‘donor’ gametes, together with people with a personal or professional interest in the issues associated with the use of third party gametes””." It is an international body with members not only in this country but in France, Canada, the United States, Australia, New Zealand and Japan. It goes on to describe itself as, "““an organisation which acts as the voice of the donor-conceived as opposed to promoting the interests of would-be donee parents and donors””." The Donor Conception Network describes itself as a self-help support group and registered charity of more than 1,100 member families throughout the UK. It says: "““We are a parent-led, child-centred organisation, focusing on how best the fact of donor conception can be integrated into the lives of our children””." It goes on, at length, to describe the range of people whom it represents, including single mothers, lesbian couples, divorced people, separated people, and so on. These two bodies, as I have indicated, take very different views. The IDOA, the international body, feels strongly that the fact of donor conception should be recorded on the birth certificate. The network takes the opposite view. It warmly welcomes the objective and believes that donor-conceived children should be told, but believes that recording the fact of donor conception on the birth certificate is not the right way to achieve that and, indeed, would not be an effective way of doing so. One has to bear in mind—I suggested this when the noble Baroness, Lady Royall, replied to the previous debate—the fact that while the treatment is recorded by the HFEA at the time, if it is successful and a pregnancy is achieved, that may well be the last that either the authority or the clinic hears about the case. There is no obligation on either the parents or the clinic where the treatment took place to report the birth to the authority. I would be grateful if the noble Baroness could, as she promised, confirm this. Indeed, as the noble Lord, Lord Winston, confirmed, even the clinic may not be told that a successful birth followed IVF treatment. Why do the two representative bodies take such opposing views? The argument of the IDOA, which represents donor-conceived people, that the genetic and biological parents, as well as social parents, should be recorded, is based on six propositions. First, genetic heritage has existence. It is a fact, and has meaning and value in itself. Secondly, everyone has a moral right to know. While it cannot be universally enforced, the state should not connive in abrogating that right. Thirdly, because the state intervenes in assisted reproduction, it has a duty to give legal protection to that moral right and should not deceive the child or withhold information about its genetic parents. The genetic regulations give the donor-conceived child the right to find a donor’s identity, but this is meaningless if many parents continue to conceal the fact of donor conception. Fourthly, the truth must be put in the hands of the offspring for reasons of avoiding consanguinity or even incest. Fifthly, and this is an important fact, falsifying a birth certificate is illegal, so it is discriminatory if the state connives at concealing the fact of donor conception. Finally, only honest and accurate birth certificates would be consistent with the rest of UK law, the UN Convention on the Rights of the Child and case law under the European Convention on Human Rights. The Joint Committee found these to be strong and persuasive moral and legal arguments. There are also practical arguments. As I mentioned a moment ago, how are children to find out if they were donor conceived if no one tells them? How can they find out about the medical history of a biological parent? We had the discussion earlier about how that might include grandparents. How can these children be sure of avoiding the risk of consanguinity, or even incest, if they do not have the knowledge that would prompt them to seek assurances from the HFEA? Therefore, the international association argues that that fact must appear on the birth certificate, and the law should be amended to require this. Let us look at the arguments of the DC network, which conducted a snap survey of network members, all of whom said that they had already told, or would be telling, their children. It showed that the overwhelming majority of respondents were against the birth certification proposal. Many said that they would be prepared to lie to the registrar to protect the privacy of their children or would consider going abroad for a further child in order to avoid appearing on the HFEA register. The network argues: "““The proposal might even be counter-productive. Parents who had originally decided not to tell (and didn’t tell the registrar) might feel it more difficult to change their minds about telling if they had originally committed an offence in failing to inform the registrar””." They also point out that the law on assisted reproduction, which we have had discussions about in this House, requires absolute confidentiality, on the part of both the clinic and the HFEA. Putting a note or, as was suggested at one point, some sort of code on a baby’s birth certificate would be a complete break with this protection of a family’s privacy and would broadcast to the world how the parents had set about securing the birth of their child. There are two deeply opposed and strongly held views. I spent most of one Sunday a couple of weeks ago on the telephone to both organisations. Indeed, it was an interesting and revealing day. How are we to find a way through this impasse? What emerged from those discussions is that the opposition to putting the fact on birth certificates stems from a fear that public prejudice may damage the child’s chances in life. To many among the general public, donor conception is seen as a novel, perhaps even bizarre, procedure, interfering with nature. However irrational that may appear, it could rub off on to the child and its chances in life. However, even the network says—I pressed it a bit on this—that attitudes may well change with the passage of time and that, as the public become more familiar with the concept and the practice of donor conception, that prejudice could well subside. There needs to be more public discussion. I read with great interest the article by Libby Purves in the Times a couple of weeks ago, in which she spelt out—in the way that only that competent journalist can do—the argument for putting the fact on the birth certificate. The view from both bodies suggested to me that perhaps a way forward would be to require the HFEA to keep the position under review. That is precisely what subsection (1) in my amendment suggests. I have gone on to argue that if the HFEA decides to recommend a change in the law and the practice so as to require that the fact of donor conception is recorded on the birth certificate, it should not have to wait for primary legislation; therefore, subsection (2) would give the Secretary of State a power to implement the recommendation by order subject to the affirmative procedure. This would require wide consultation and allow Ministers to amend the recommendation if they thought fit. I cannot claim that this proposal would completely satisfy both camps—indeed, it would be fair to say that they would both regard it as second best—but I think that they would both see it as a reasonable way forward. From the point of view of the Donor Conception Network it does not require the immediate change in the law that it and most of its members would oppose, while from the point of view of the IDOA it offers a possible way forward to achieving its eventual objective. There has been much talk about the Joint Committee. It is worth looking at the report. We rehearsed all these issues. In paragraph 276 we recommended that as a matter of urgency the Government should give this further consideration. I look forward to the debate and I beg to move.


Secondary information

Type
Proceeding contribution
Reference
698 c501-4 
Session
2007-08
Chamber / Committee
House of Lords chamber
Subjects
Disability Disclosure of information Codes of practice Death Abortion Congenital abnormalities Civil partners Fertility Licensing Human embryo experiments Donors Ethics IVF Northern Ireland Parents Registration Registration of births, deaths, marriages and civil partnerships Research Surrogacy Stem cells Human-animal hybrid embryos
Legislation
Human Fertilisation and Embryology Bill (HL) 2007-08
Link
View this Proceeding contribution on www.publications.parliament.uk