Although qualitative research about couples and families is becoming increasingly widespread, the aspect of data analysis remains largely underrepresented in the literature. In this methodological paper, we outline one specific approach to data analysis in the context of multi family member interview studies. Inspired by Interpretative Phenomenological Analysis and Dyadic Interview Analysis, this approach allows for the detailed and systematic analysis of family practices and the co‐construction of shared family realities. Based on an example study in the field of medically assisted reproduction, we give a detailed explanation of the aim of this approach, the different steps in the analysis process and the output of a multi family member interview study. The findings of this example study are discussed in light of the methodological challenges and opportunities.
Practitioner points
Multi family member interview analysis allows for the systematic analysis of family practices and the co‐construction of shared family realities
The findings might approximate to the therapeutic complexities that systemic therapists often encounter better than classical quantitative or qualitative research
One specific data analysis approach in the context of multi family member interview studies is outlined as data analysis remains underrepresented in the literature
Objective: In this qualitative study, we investigate how lesbian couples experience and deal with the difference in genetic relatedness in their family. Background: Previous research showed that lesbian couples handle the difference with regard to genetic relatedness by, for instance, creating a narrative about physical resemblances or by focusing on the social bond and its influence on children. Methods: The findings are based on qualitative in-depth interviews with 10 lesbian couples who had at least one donor-conceived child aged 7-10. Results: The difference with regard to the genetic link brought up complex and context-specific experiences for these parents. Generally, the genetic link was described as irrelevant: equality between both parents was presented as a given. However, some experiences of difference due to the presence of one genetic link were found. In these accounts, the genetic link was described as a valuable extra that created an inequality between them as parents. Conclusion: The findings show that these mothers have a complex attitude towards genetic relatedness
The first birth from a donated egg was reported in Australia in 1984, ushering in a new era of possibilities for the treatment of infertility (1). Since then egg donation has undergone a number of technical, regulatory and commercial transformations. Its use by a growing and diverse range of social groups and more recently the dawn of advanced freezing technologies, have reconfigured the process. Given the transformation in its organisation and practice, there is a pressing need to map these changes in finer detail and to ask critical questions about the continued fit of existing policy and regulation in this rapidly developing landscape of fertility medicine. In this paper we present a 'critical reflection' (2) on developing practices in egg donation, which we suggest are reshaping the character of egg donation as well as raising questions regarding their implications for policy. We highlight a number of policy 'blind-spots' relating specifically to information giving and informed consent for egg providers, the emergence and entry of a range of intermediaries and a shift towards certain practices which may see eggs increasingly treated as tradable commodities. We call for a re-contextualising of the debate on egg donation and for renewed attention to the new political economy of egg donation in Europe.
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