A tweet from a colleague affected me this week. The subject was stigma in substance use disorders and he related how, at the funeral of a relative who had died very young from a heroin overdose, a family member callously slandered the dead man and skillfully ‘othered’ him. The message was ‘he was not at all like us’.
This technique of labelling, blaming, applying stereotypes and stripping those with substance use disorders of their humanity – their sameness to everyone else – might be an temporarily effective way of distancing oneself from the horror and pain of addiction and loss, but it is harmful to those struggling with substances, their families and, if truth be told, to the person using stigmatising language.
As a person with lived experience of substance use disorder and recovery, I’ve had my own share of stigmatisation. I’ve just written a book chapter about it. It diminishes you, discredits you and the discrimination that accompanies it has real-life effects. Often adding to self-stigmatisation, external forms of stigmatisation are pernicious and paralysing.
Two bits of research on stigma caught my eye recently. In the first, researchers compared public stigmatisation of those with alcohol use disorder with other mental health conditions.
They defined stigma ‘as a process in which people are firstly labelled and hereby assigned to an out-group, secondly subjected to stereotypes and prejudices, and thirdly exposed to discrimination and social distance.’
They found that ‘stigmatizing beliefs and behaviours toward people with alcohol use disorder were pervasive in the general population and usually more pronounced than toward persons with depression or schizophrenia.
More specifically, people with AUD tend to be perceived as more dangerous and more responsible for their condition, as well as being faced with a greater desire for social distance and a higher degree of acceptance of structural discrimination than people with substance-unrelated disorders.’
The findings threw up some challenges, as it’s all more complex than it seems. Framing alcohol use disorder as a mental illness seems to reduce the expression of anger in others, but increase the expression of fear.
The authors say: ‘If regarded as a stable and trait-like condition, related to assumptions on “bad character,” blame and feelings of anger might be less pronounced but fear and social exclusion nevertheless high.
Conversely, if regarded as a “bad behaviour”—that is, a state that needs to be overcome—moral judgments and blame of people with alcohol use disorder could be harsher, possibly leading to more discrimination and social exclusion.’
These dilemmas and seeming contradictions need more research, but what is clear is that those with alcohol use disorder are seen as more dangerous, more responsible for their condition and are more likely to experience distancing and discrimination than those with other mental health conditions.
The Norwegian research paper titled ‘Nothing to mourn, He was just a drug addict” – stigma towards people bereaved by drug-related death’ provoked the Twitter exchange I referred to above. If the first study appeals to the mind, then this is a study that goes straight to the heart and emotions. I felt angry and sad on reading it, but I’m glad I did. There are shared themes between the two.
Norway is producing a lot of impactful research at the moment. In this study, the researchers recruited 255 people who had lost a someone close to a drug-related death. Using both standardised and open-ended questions, they analysed person to person communications experienced by participants following bereavement.
Almost half of the participants ‘reported experiencing derogatory remarks from close/extended family and friends, work colleagues, neighbours, media/social media and professionals’. That’s right, when they were grieving, those closest to them made cruel, harsh comments when what they needed most was love, comfort and support.
The content of these remarks identified in the data was grouped into four themes:
- Dehumanising labelling
- Unspoken and implicit stigma
- Blaming the deceased
- The only and best outcome
I was told she was a fucking junky and a fucking whore who had not deserved to live. She should have been taken on the day she was born; she had no right to a life, and she used others’ tax money to get drugs, tricked men into giving her money by selling herself. Girls like that should dieSaid about a woman’s 20 year-old daughter
It was a choice he made, so it was all his own fault
You are lucky to have been spared more anguish when he died
The death could not be such a big deal as he had never wanted to help himself.
One of the things that works best to tackle these kinds of attitudes is for those of us with lived experience to share our stories. Contact with those with lived experience has been shown to tackle stigma. The more that it can be seen that we are ordinary (actually, in terms of recovery – extraordinary) human beings, ‘the same as’ rather than ‘other’, the more we dissolve stigma, shame and discrimination. This is not always without risk though.
The researchers’ bottom line
Such communications were disgraceful and harsh, and contributed to marginalizing a group of grieving individuals who required support rather than being ostracised. Making people aware that stigma exists, increasing knowledge as to why it occurs and how it is transmitted in society can help remove the stigma
Continue the discussion on Twitter @DocDavidM
 Kilian, C., Manthey, J., Carr, S., Hanschmidt, F., Rehm, J., Speerforck, S. and Schomerus, G. (2021), Stigmatization of people with alcohol use disorders: An updated systematic review of population studies. Alcohol Clin Exp Res, 45: 899-911. https://doi.org/10.1111/acer.1459
 Kari Dyregrov & Lillian Bruland Selseng (2021) “Nothing to mourn, He was just a drug addict” – stigma towards people bereaved by drug-related death, Addiction Research & Theory, DOI: 10.1080/16066359.2021.1912327
One thought on “Top ten of 2021 #1 – Nothing to mourn; just a drug addict”
Great article. I got into recovery in May of 1977 and I am saddened over how pervasive stigma is with our disorder. It’s a constant work to enlighten others that we are all just people and deserving of being treated as such, with love, dignity, and respect.
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