The changing landscape of endometriosis activism in Finland: at the crossroads of personalization and digitalization of health

In: Health Activism and Sexual Politics · 2025 · pp. 27–44 · doi:10.4324/9781003319818-4 · W7110846855
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This chapter examines how personalization and digitalization influence Finnish endometriosis activism, revealing how digital platforms allow for discussion of diverse patient experiences and concerns often overlooked by biomedical approaches.

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This chapter examines how the personalization of medicine and digitalization are reshaping endometriosis activism in Finland through interviews with patient organization members and social media advocates. It finds that digital platforms allow for the discussion of treatment experiences and highlight concerns of gender and sexual minorities often marginalized by traditional biomedical conceptualizations. The analysis emphasizes how these channels foreground patient differences relevant to care improvement while navigating tensions between individualized illness experiences and binarily gendered medical frameworks. This paper is centrally about endometriosis — specifically focusing on patient activism, digital health communication, and the sociocultural dimensions of personalized care rather than clinical pathology.

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Abstract

This chapter explores how two ongoing societal changes, personalization of medicine and increasing digitalization, are shaping endometriosis activism. The analysis draws on in-depth interviews with members of a gynaecological patient organization as well as endometriosis activists who use social media to advocate for awareness and better treatment in Finland. The chapter shows that digital channels provide outlets for discussing treatment experiences as well as addressing concerns of gender and sexual minorities affected by endometriosis but often sidelined in the medical conceptualization of endometriosis as a gynaecological condition. Digital platforms enable foregrounding differences between endometriosis patients that are highly relevant for the improvement of care but that are not captured by biomedical approaches to personalized medicine. The analysis shows the relevance of patient activism in bringing up concerns about how individualized care is realized and raises questions about what personalization ultimately means in contemporary health care. Furthermore, the chapter traces how patient activists navigate the tensions between the multiplicity of illness experiences that underpins personalization and digitalization and the conceptualization of menstruation-related pain and disorders as binarily gendered in health care.
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ABSTRACT This chapter explores how two ongoing societal changes, personalization of medicine and increasing digitalization, are shaping endometriosis activism. The analysis draws on in-depth interviews with members of a gynaecological patient organization as well as endometriosis activists who use social media to advocate for awareness and better treatment in Finland. The chapter shows that digital channels provide outlets for discussing treatment experiences as well as addressing concerns of gender and sexual minorities affected by endometriosis but often sidelined in the medical conceptualization of endometriosis as a gynaecological condition. Digital platforms enable foregrounding differences between endometriosis patients that are highly relevant for the improvement of care but that are not captured by biomedical approaches to personalized medicine. The analysis shows the relevance of patient activism in bringing up concerns about how individualized care is realized and raises questions about what personalization ultimately means in contemporary health care. Furthermore, the chapter traces how patient activists navigate the tensions between the multiplicity of illness experiences that underpins personalization and digitalization and the conceptualization of menstruation-related pain and disorders as binarily gendered in health care.

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endometriosis

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