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Is it right to create a tissue-donor baby?

Thursday 16 October 2003
The Guardian Newsroom
Farringdon Road, London

This event was supported by a grant from the UK Department of Health

Mohammed Taranissi
Director, Assisted Reproduction and Gynaecology Centre


My talk is going to be rather brief because my take on the issue of 'saviour siblings' is very simple. I have always believed that in modern society, medicine has got an important role. And that role, as I see it, is to try to help people who have got illnesses and to find a cure for those illnesses and, even better, to prevent those illnesses from occurring in the first place. Therefore, any procedure which seeks to treat or prevent illness is not an ethical problem.

This is the approach that we took when we were faced with the Whitaker case. Effectively, the Whitakers were asking us to try and help them complete their family by having another child. This fact is often forgotten in the debate: the child was always wanted by his parents, he was always on the cards. The child was not created just to serve a particular purpose. It is also worth remembering, however, that every child that is brought into this world for a number of reasons. We often have children for reasons like strengthening a marriage or maybe providing an existing child with a brother or a sister. There is always a reason why children are brought into this world, but that doesn't mean it is the only reason.

What we have done through PGD and tissue typing is not something that nature would have not been able to do. The Whitakers did try to conceive a tissue-matched baby naturally and they could have tried again. Maybe, four or five years down the line and perhaps three babies later, they might have had the baby that was the exact match. All that we did was to just to increase the odds. Instead of having a one in five chance of having a baby that is an exact tissue match, we have made this roughly a 98 percent chance.

Some of the criticisms that have been levelled against PGD and tissue typing is based on wrong assumptions. Some assume that there are risks associated with PGD. No-one has ever told us what those risks are. ItŐs not good enough to say that we donŐt know the risks, therefore we shouldnŐt really do this. ThatŐs a scare tactic and it confuses the issue in the minds of the public. There is no evidence of risks associated with developmental problems in babies that are born through PGD. To say, as the HFEA does, that PGD and tissue typing should only be available when we are providing a technique that will benefit the embryos, is also based on the wrong assumption. Embryos do not benefit from PGD. What PGD tells us is whether or not the embryo is normal. If it is abnormal, there is nothing that PGD can do to change that. If the embryo is normal, isnŐt not normal because of the PGD. It already was normal. PGD is simply about selecting embryos on the basis of existing characteristics.

In the case of the Hashmis, it was a two-step procedure. They checked that the embryo was normal and then they did the HLA matching. With the Whitakers, we started with an embryo that we already knew was normal. The HFEA says that the two-step procedure is fine, but the one-step one is not because PGD is too risky to warrant it being used on a normal embryo. But if you are using the two-step procedure (trying to check for the HLA matching and for genetic normality) you may occasionally end up removing more than one cell which could double the risks.

This issue is very simple in my mind. We are only trying to help people. I would suggest that any one of you, if you had a child that is suffering every day (who needs injections every day and hospital admissions every two weeks for lengthy blood transfusions) and you knew that there is a treatment out there that can help relieve that suffering, what would you do? I think every one of us knows the answer to that.


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