For Dr Judith Parsons, this became clear during her doctoral research. While her PhD interviews and focus groups were not initially designed to study stigma, women’s accounts repeatedly returned to feelings of blame and judgement.
“Many women believed their diagnosis was their fault, sometimes because of their own internal narratives, but often because of comments from others, media messages or interactions with healthcare professionals,” Judith explains.
She recalls that weight-related stigma featured heavily in women’s experiences of care. “Crucially, the emotional effects did not end when pregnancy did. For some women, what they experienced during pregnancy stayed with them long afterwards, becoming a lasting source of distress or trauma.”
Funding from Diabetes UK provided the opportunity to address these issues directly, not simply by documenting stigma, but by finding ways to challenge it.
How stigma shapes care
GDM is typically diagnosed around the end of the first trimester, at approximately 12 weeks. For many women, Angus explains, this marks a sudden disruption to what they expected pregnancy to be: “From that point on, their care becomes more intensive: regular blood glucose testing, dietary guidance and lifestyle advice designed to keep sugar levels within a safe range.”
This monitoring is important for medical reasons. High blood sugar levels can affect how a baby grows, increasing the likelihood of babies being larger than expected for their stage of pregnancy. This can raise the risk of complications such as caesarean sections, admission to neonatal intensive care and birth trauma, including shoulder dystocia. However, for many women, this level of monitoring can feel judgemental, contributing to feelings of self-blame and guilt.
Alongside the physical risks associated with GDM, there are broader and less visible consequences for both mother and baby. In this context, stigma begins to shape how women experience and engage with their care.