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BY ANNE COOPER AND BOB SWINDELL

The language used by healthcare professionals has a profoundimpact on people who live with a long-term condition, and those who care for them. It impacts how they experience their condition and feel about living with it day-to-day. It might seem like a small, inconsequential thing, and some might feel people are too sensitive, but the fact is language can have both a motivating and empowering effect or it can create burdensome feelings about health and well-being that can have a massive impact on people’s lives.

It starts right at the beginning, when someone is told they have a long-term health condition, for example, diabetes. The language used to explain what is happening, its significance and what the future might look like has an impact that will colour the way someone lives with the condition from then on. Some of the things people say are likely to stay with that person for the rest of their lives, and exert an influence over their behaviour from that day forward. But it’s not just about at the time of diagnosis. Every appointment with a healthcare professional can stick in the memory bank, drive unhelpful behaviours and reinforce unhelpful beliefs. There are some words that are used as passing language by people that can have a devastating effect on individuals, shaping the way they feel and how they are able to cope with any management of their health, from that point onwards.

The importance of careful use of language doesn’t just apply to people with diabetes; it applies to other conditions, especially those where there is a need for long-term care and management or where there might be associated stigma. Indeed, there are many examples and every experience is unique. Our exemplars here are on the experiences of people living with diabetes:

I can remember being devasted by an ophthalmologist telling me I needed to get ‘better control’ of my diabetes during a review appointment – the inference was that I was in the clinic because I was a bad patient who had ‘poor control’. I think he was just making a generalised observation, perhaps trying to give me advice, but the impact on me was massive. I felt like I was being judged and that he had no idea how hard I had tried for decades to look after myself. The irony of it was that my most recent tests had been well within target range too. He just hadn’t put any thought into what he was saying, and it was upsetting to say the least. I felt judged. The impact on me? I hate going to ophthalmology clinics. What could he have said? He could have said ‘I can see you have been trying really hard, and you are doing well. Keep up the good work, because that is also the best thing for your eyes’.

Everyone living with diabetes remembers their diagnosis, and the stories of these are as wildly varied as the people who live with their condition. However, one common feature is that no one has a “good” diagnosis. I was diagnosed with Type 2 Diabetes in Primary Care, and walked out of my appointment scared, confused and with an overwhelming sense of guilt that I had brought this upon myself. These feelings of guilt expanded to shame, embarrassment and resentment overtime, and continue to be triggered by the language used around me, and about me and to me. This language comes from those around me, the media but is most hard hitting when it comes from health care professionals; in its simplest for it can be summarised as “if only you (had) looked after yourself better…”. This feeds directly in to well established and pervasive stigma about “lifestyle” and obesity, saturated in simplistic stereotyping that represents me as being lazy, weak-willed, unsuccessful, unintelligent and lacking self-discipline. Like many people living with a long-term health condition, over time I have internalised these. Since my diagnosis this negative use of language has often been balanced by neutral or more supportive conversations, but these fade in my recollection and do little to offset the vivid negative experiences that leave me feeling like the rug has been pulled out from under me, along with the confidence and strength I need to successfully self-manage my condition.

The language used can be stigmatising and lead to the development of labels that live with the person throughout their care experience – ‘poorly controlled’, ‘non-compliant’, ‘low functioning’, ‘high functioning’ are all examples of labels that could have a lasting and detrimental impact on an individual.

For example, a label of ‘non-compliant’ can have a great effect on how an individual is perceived by the next person who might be helping them. Furthermore, the use of such prejudicial terms in medical records can continue to exhibit an influence on the care an individual receives, and will accept, long after the consultation being recorded has finished.

So, what is some of the evidence about the use of language?

In 2018 a scoping study was carried out to review existing literature in order to broaden our understanding of the role language plays during clinical encounters and inform a new Position Statement on language in diabetes care (Lloyd et al., 2018). The literature review concluded that the use of stigmatizing and discriminatory words during communication between healthcare practitioners and people with diabetes often leads to disengagement with health services. Communication was the most important factor affecting diabetes self-care and can have a significant impact on psychological wellbeing. Where social, linguistic or cultural differences exist, communication can be compromised leading to feelings of disempowerment. What little empirical evidence exists shows that training can improve language and communication skills.

In response to the importance of language in the care of people with diabetes a national group published a document with NHS England, called ‘Language Matters’. It has been copied in other languages and used as a model for other conditions like obesity, in the hope that the significance of language in care, in research, and perhaps even everyday life is given attention and that professionals reflect on their use of language.

The key recommendations of the Language Matters Position Statement • Be aware that language can have both positive and negative effects on people living with diabetes. • Become alert to the language used around you and recognize when it has a negative impact. • Seek to be more empathetic and person-centred in practice. • Aim to be culturally competent (for example explore individuals’ cultural beliefs about diabetes) and be aware of the importance of health literacy. • Support others to be aware of their language and encourage them to make changes in a non-judgemental way NHS England Language Matters Position Statement

There is no strict formula to apply or script to follow, but these documents give helpful tips to guide practitioners and encourage professional reflection on the empathetic and productive use of language.

Working with people with long-term conditions can be as professionally challenging as it is rewarding but reflecting on the language you use could be just the thing that makes a difference and stops people from feeling that they have had the rug pulled out from beneath them.

Use your language to empower and support, not to judge or label.

This post was previously published on evidentlycochrane.net and under a Creative Commons license CC BY-ND 4.0.

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The post The Impact of Language on People Living With Long-Term Conditions: Having the Rug Pulled Out From Underneath You appeared first on The Good Men Project.

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