Cancer as Culture

Depending on how we look at cancer, cancer can mean different things. We might think of cancer in biological terms (e.g. as cells that divide too quickly), or in population terms (e.g. statistics about incidence), or in personal terms (e.g. our symptoms and feelings, or part of our professional work), or with a focus on fund raising campaigns and television adverts, to mention a few examples. To some anthropologists and feminist theorists, however, cancer is also culture. The American anthropologist S. Lochlann Jain, for example, understands cancer in this way. But what does it mean to say that cancer is culture? Continue reading

Cancer, Stigma and Language

Many people with cancer are living with side effects of their treatment, yet they are side effects often considered taboo by much of the public, according to a recent survey by Macmillan Cancer Support. This is worrying, Macmillan says, as many people with cancer may be too shamed to seek help with life-changing side effects, potentially putting their health and recovery at risk. The survey found that 1 in 5 people with cancer find it difficult to seek help with their side effects because of embarrassment or shame, and 1 in 4 of people with cancer said they have been reluctant to talk about issues relating to their disease because of how other people might react.

Recent research by sociologists has identified similar concerns amongst patients with gynaecological cancer and breast cancer. In a Norwegian study of young women being diagnosed with gynaecological cancer (Solbraekke and Lorem 2016), it is reported that many of the women felt disrespected during medical encounters, e.g. when they were asked about sexual partners. Due to the taboo around their cancer type, many of the women also felt they had to be discrete about their illness, and couldn’t talk openly about their worries and side effects with friends, family and colleagues. That some cancer patients often feel they have to disguise their emotions and manage their appearance towards others was also reported in a study undertaken at Nottingham University in the UK (Trusson and Pilnick 2017). Continue reading

Welcome to the Gynae Cancer Narratives Blog

This blog is intended for discussions of topics and issues relating to experiences of gynae-cancer and radiotherapy. We will be blogging regularly on relevant topics such as sexuality, language, invisibility, self-care, art, faith, stigma and gender, and many others.

We encourage readers to get involved in the discussions. You can post your comments by leaving a reply.

–  Gynae Cancer Narratives Project Team