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Gamete donation, information sharing and the best interests of the child: an overview of the psychosocial evidence

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Abstract

This paper overviews key empirical findings from social science research regarding the impact of gamete donation on child wellbeing. In particular, the paper addresses current regulatory debates concerning information sharing and the best interests of the child by considering psychosocial aspects of telling—or not telling—children about their donor conception and the identity of their donor. The paper identifies three core sets of empirical, ethical and policy concerns underpinning these debates relating to (i) the psychosocial impact of gamete donation per se on child wellbeing, (ii) the psychosocial impact of parental disclosure decisions on child wellbeing, and (iii) the psychosocial implications of donor identification for donor-conceived offspring. The paper illustrates how these concerns are framed by ideas about the significance—or not—of ‘genetic relatedness’; ideas which have come to the fore in contemporary discussions about the potential consequences of donor-conceived individuals gaining access to their donor’s identity. By drawing together research findings that may be pertinent to the regulation of gamete donation and information sharing, a further aim of this paper is to explore the potential use and misuse of empirical ‘evidence’ in ethical and policy debates. Whilst this paper starts from the premise that psychosocial data has a vital role in grounding normative discussions, it seeks to contribute to this dialogue by highlighting both the value and limitations of social science research. In particular, the paper argues for a cautious approach to applying psychosocial evidence to ethical issues that is sensitive to the caveats and nuances of research findings and the changing cultural and regulatory context.

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Notes

  1. I have restricted the primary focus of this article to the UK because regulatory and cultural perspectives on gamete donation vary widely across countries. However, the empirical and ethical issues raised are of broader relevance and furthermore, even within a given national setting, there may be a diversity of views.

  2. This paradigm develops the foundational work on parenting of Baumrind (1991).

  3. Further discussion of these measures can be found in Golombok (2000, 2015), as well as in the published reports of individual studies which contain detailed descriptions of the measures, including their reliability.

  4. It is noteworthy that the majority of this research has been conducted by one research team. As well as meaning there are relatively few studies in this area, there is also a need for studies to be replicated by other research teams.

  5. A smaller sample of egg donation families was also recruited from the UK and yielded similar findings concerning the lack of association between egg donation and difficulties in child adjustment (Murray et al. 2006).

  6. Parents in the UK sample were also seen at age 18 years and similar observations were made concerning positive aspects of parent–child relationships in sperm donation families (Owen and Golombok 2009).

  7. There are some studies that compare child psychological adjustment in non-disclosing and disclosing families in different family types. See for example Chan et al. (1998)’s study which includes lesbian couple and single mother families.

  8. For further discussion of the limitations of these studies, see Golombok (2015).

  9. By ‘donor relations’, I am referring to anyone who may be ‘genetically’ connected via donor conception. Typically interest has focused on the relationship between a donor-conceived individual and their donor, and between donor-conceived individuals in different families who share the same donor (commonly referred to as ‘donor siblings’). However, in recent years there has been increasing consideration of the wider network of ‘genetic’ and ‘social’ kin relationships that may be created through gamete donation.

  10. Note that this section refers to contact with previously unknown sperm donors who donated via a sperm bank or clinic, rather than the increasing number of donors who may be known to recipients from the outset, whether as friends, family members or through connection websites facilitating private arrangements between donors and recipients.

  11. The DSR was founded in 2000 by Wendy Kramer and her donor-conceived son to facilitate contact between donor offspring and their donors and donor siblings. It is the largest global network of this kind and currently has approximately 45,000 members, including donors, parents and donor-conceived people.

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Acknowledgments

The empirical research presented in this paper is largely based on studies conducted at the Centre for Family Research, University of Cambridge, UK, and funded by grants awarded to Susan Golombok by the Wellcome Trust and the Nuffield Foundation. I would like to thank Susan Golombok and Vasanti Jadva for our frequent discussions of the issues covered in this paper and for their comments on the draft. I would also like to thank the two anonymous reviewers for their feedback. As ever, we are extremely grateful to all the families who have taken part in these studies.

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Freeman, T. Gamete donation, information sharing and the best interests of the child: an overview of the psychosocial evidence. Monash Bioeth. Rev. 33, 45–63 (2015). https://doi.org/10.1007/s40592-015-0018-y

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