Mark Levin’s article on this site last week about eradicating the term ‘hearing impaired’ clearly struck a chord – it was viewed over 10,000 times within 24 hours and became this site’s 7th most viewed article ever (and it’s still rising).
Levin argued that “the term ‘impaired’ implies something is wrong and needs to be fixed.” His article ended by asking, when hearing people struggle to communicate with deaf people, who the ‘impaired’ people really are?
The article got dozens of comments, with many being supportive of Levin’s argument, while some, predictably, asked what the problem was – because they thought ‘impairment’ was about right. If Levin’s article drew on the cultural model of deafness and disability, you could argue that those comments came from the opposite angle – the medical model.
What was interesting were several comments that fell in between the two – from deaf people saying that they themselves use the term.
For example, one said: “I don’t have a problem with being called “hearing impaired”, I much prefer that term which is self explanatory rather than “hard of hearing” which I can’t stand.”
Another commenter added: “Interesting article – but I personally use hearing impaired myself as saying that I am deaf gives people the impression that I cannot talk or hear at all, which is wrong.”
This is a reminder that however strongly we feel about a term and the impression it might give, it’s still up to deaf people themselves to decide how they would like to be ‘deafined,’ based on their own personal experiences.
I’ve never described myself as being ‘hearing impaired,’ but I had my own brush with the term a couple of years ago, when an article I had written was published with an introductory paragraph describing me as being ‘hearing impaired.’
The first I knew of the inclusion of the term – because the introduction was written by a sub editor – was when I went on Twitter to find several angry tweets from deaf people who felt offended.
Now, I knew for a fact that the sub editor hadn’t intended any harm, so I defended the site I’d written for. I also said, in my responses to the tweeters, that I didn’t feel offended. And I didn’t. Until then, I hadn’t seen any negative connotations to the term ‘hearing impaired.’
This was mainly due to familiarity. I’d grown up around so many different terms for deafness, and this was just another one, that seemed ‘normal.’ It was only when I spent time thinking about it that I could understand why some people were against it.
Nowadays, I would not use the term to describe myself or anybody else who is deaf. Like Levin, I see it as feeling more negative than any term around deafness should be.
I also know that deaf people are not alone in moving away from the term. Indeed, an arts organisation for blind people recently started using ‘partially sighted’ instead of the term ‘visually impaired.’
However, I also believe in personal choice. If a deaf person wants to describe themselves as ‘hearing impaired,’ and it works for them, as it clearly does for those two commenters, then I respect that, because I know from my own experience how hard it is to find a term you are comfortable with to describe your deaf identity.
When I was at school, I would often describe myself (and was mostly described by the learning support department) as simply being ‘deaf.’ That worked fine in a completely hearing environment.
But when I was in my early 20s, and first mixed with deaf people of my own age, I started to be told – as a joke that drew on some element of truth in how people saw me – that I wasn’t really ‘deaf’ at all. The more I heard the ‘joke,’ the more I realised what the subtext was.
What they meant was that I wasn’t ‘deaf’ like they were deaf.
The people who said this to me were usually profoundly deaf, while I am classed as being moderate to severely deaf. They communicated in sign language all the time, but while I would use sign language, I would also use speech, lipreading and listening too.
I soon realised that describing myself as ‘deaf’ in this company caused eyebrows to be raised. So, responding to this, I started describing myself as being ‘hard of hearing.’ I found (like the commenters on Levin’s article) that people I met understood more accurately how deaf I was when I used that term.
Although this worked, I later realised that ‘hard of hearing’ wasn’t seen all that positively either, and I settled on using the term ‘partially deaf.’
‘Partially deaf’ felt much more positive, more close to being ‘me’ than anything I’d used before. It conveyed that I wasn’t completely deaf, but also said who I was, too.
I wasn’t ‘partially hearing,’ I didn’t have ‘hearing loss’. I was partially deaf. And proud of it.
Nowadays, I nearly always use that term if I’m describing my deafness in person, although now I also describe myself as being ‘deaf’ (on this site, for example) and, a few years down the line, I feel comfortable doing so.
What I’m getting at (thank you all for your patience in getting this far) is that, for many of us, finding a way of describing, or indeed ‘deafining’ your deaf identity is a tricky thing to do.
We need more debate, and more fantastic articles like Levin’s, that make an argument about what certain terms imply, and whether they are acceptable, one way or another, to help us all figure out the term or terms that best suit us.
But we need to be cautious too. As the comments on Levin’s article showed, terms are not clear cut, and not all deaf people find a given term offensive.
So while we should embrace the debate, we should be careful not to take offence too easily, or assume that the argument is cut and dried, because for many of us, there are no easy answers when it comes to deciding how to ‘deafine’ ourselves.
Charlie Swinbourne is the editor of Limping Chicken, as well as being a journalist and award-winning scriptwriter. He writes for the Guardian and BBC Online, and as a scriptwriter, penned the films My Song, Coming Out and Four Deaf Yorkshiremen.
The Limping Chicken is the UK’s independent deaf news and blogs website, posting the very latest in deaf opinion, commentary and news, every weekday! Don’t forget to follow the site onTwitter and Facebook, and check out our supporters here.
Andy not Mr Palmer but another one
September 27, 2013
Well, two points :
It is not an aim in life to go about not offending anyone. I notice that more and more people are claiming to be offended simply as a tool for getting their own way. The world is becoming full of things that you can’t say. I am very much against this as I see it as the “control freaks” taking over. And we all know how much deaf people get controlled by the freaks. If you have never had your speech corrected by a social worker half your age and experience then you haven’t lived.
Recently I’ve been appalled to see a duly elected Cornish councillor get literally forced out of office because he “said the wrong thing”. This was a signal for every petty bully for miles around to weigh in, and out he went. Don’t like this trend at all. If there’s bullying going on, deaf and especially Deaf people will be the victims. We always are. Don’t go there.
The other point is this : Most deaf people dislike the terms by which we are described. No matter what they call us it will be regarded as a pejorative. That is partly because people don’t appreciate that there are many, many forms of deafness each with its personal manifestations. We all like to think that, being deaf we know a lot about it.
The fact is that we know a lot about our own situation and tend to assume that everyone else is the same. Not so. It’s very misleading to think that you know a lot about the issue because you have experienced one small corner of it.
Anyone who has >studied< deafness as a subject will have a far greater understanding of the whole. It's daft to talk about the medical model and the social model. That is in fact an extreme separation of the two fundamental patterns of deafness. The truth is, it's a mixture. A lot of "deaf lore" is simply pub talk and this gives rise to further misunderstandings. People like to shout "That's medical model" as if it were some terrible offence. Well, we're all medical model. We are all social model too. You can't have one without the other. The word here is "balance".
Everything needs a label of some kind in order to describe it. People who murmur "Don't like labels" just haven't thought it through. We can't talk about it if we can't describe it and therefore if it can't be described it will never be talked about.
Or perhaps that is what they want?
Rob
September 27, 2013
I happen to think it is far more important to have a common “label” of Deafness than all these different labels. The Deaf world as far as I can make out is divisive against each other by virtue of our varying deafness which is very damaging. We all have similar problems in human communications regardless. You only have to see just how bad the subtitles are in UK, compare with USA to see that the Deaf world in UK is hopelessly weak, and unable to join up and demand better services and politics. I would say we should shut down some of the numerous charities that appear to do very little in terms of actually lobbying Government, and create a single organisation, with real connections with the UK deaf people, and fight a better battle with MPs.
Even on facebook there are so many UK deaf sites that it has become a joke.
AS for the label? Deaf sounds fine to me. Rather have better lobbying actions against Government and better laws that are enforceable.
Natalya (@barakta)
September 27, 2013
Wow, someone else who uses ‘partially deaf’ like I do to describe themselves. *does the not alone dance*
I have hardly ever seen “partially deaf” used in the deaf or hearing worlds because as you say hearing folk use hearing impaired and deaf folk use deaf/HOH – HOH is not well understood outside of deaf space in my experience. My hearing parents bought me up using the word deaf partly cos it is simple to say and partly to stress that without my hearing aids I am in practical terms completely deaf as I cannot hear speech or even most shouting.
Partially deaf as you’ve already said Charlie, it’s not about “what I don’t have” it’s linking to some level of pride although I didn’t discover deaf culture till university. My parents never let people shame me for being deaf or asking for repeats or needing to see faces. I realise I’m really lucky that my parents (mum especially) instinctively took a social model approach to “If Natalya can’t hear you, it’s because you haven’t got attention/spoken clearly/contextualised things.
I feel strongly that I do not have a hearing loss as I was born deaf and didn’t lose anything – I never had it, I don’t feel a sense of loss, I’ve never known any different and I wouldn’t want to be hearing thanks. Like deafened, hearing loss is a perfectly reasonable term which doesn’t apply to me. I wasn’t impressed when RNID went to AoHL because it felt they didn’t represent me, although that is perhaps a more accurate reflection of their aims.
Partially deaf has the additional bonus of working in my shoddy sign language as I sign half deaf and more proper signers seem to understand me and I’ve never had grief for not using HOH (which I will sometimes use).
I really do need to find some time and comment on the hearing impaired article because my brain is fizzing with things to say about a term I personally detest but don’t think necessarily deserves to be banned.
LJ.
September 27, 2013
Sadly society today has become a ‘play of words’. Various terms that some like and some do not like has become the battleground in our vocabulary, whatever our communication needs be.
I don’t see any harm in whatever phases are used. I am profoundly deaf and do not like describing myself as ‘deaf’ the word ‘deaf’ is too close to the words daft & dumb. I guess I’ll stick to saying I’m a bit ‘Mutton’. lol
The thing here is for us to lighten up a bit and have some humour.
Mike Gulliver
September 27, 2013
Just in case anyone’s interested in following this up in the Deaf Studies literature, from Padden and Humphries (1988: 39)
So you know, normally ‘HARD-OF-HEARING’ is understood to mean a departure from a hearing ‘norm’ – well, take a look at the way that it’s used in a discussion between Deaf people:
“The subject was whether a mutual acquaintance could use the phone… She couldn’t, our friend told us, because she was only “A-LITTLE HARD-OF-HEARING”. We understood this to mean that the woman could only hear a little, not well enough to use the phone.
On another occasion, another deaf friend brought up the name of a woman we didn’t know, and explained that she had many of the recognisable characteristics of someone who could hear well, because she was VERY HARD-OF-HEARING. Our friend added that the woman regularly used the telephone to conduct business.”
So, here are two terms used to mean the opposite of what we would assume is ‘normal’ usage – A-LITTLE HARD-OF-HEARING to mean someone who is nearly fully ‘DEAF’, and VERY HARD-OF-HEARING to mean someone who is so able to hear that they are almost not ‘DEAF’ at all.
The point that Padden and Humphries are making is that you start from where you consider to be ‘normal’ – and define away from there.
Bring politics into this, and you start to craft definitions away from a point that you think ‘should’ be normal.
Then things get very complicated…
Elisabeth McDermott
September 27, 2013
Interesting articles and comments. The thing for me is how people perceive me. I was born profoundly deaf, and speak and lipread and also sign too. Hearing people (the ones I’ve just met) often ask me “How much do you hear?” as opposed to “How deaf are you?” or “What is your hearing loss?” usually because they want to know how much of the music I can hear, or how much of what they’re saying I can hear. Their perception, despite my introduction of myself as “I’m deaf and I need to lipread you” (and I hate it when someone else steps in and says “Lizzie is deaf, she needs to lipread you”…like hello, I can do that bit myself – but that is a whole other story in itself – perhaps a blog for later?!) is that I am not profoundly deaf but partially deaf. I can never use the term “partially deaf” although it might (wrongly) get them off my back with regards to further questioning, but then it would simply mean that they would think, “she can hear some things” (which I can with my hearing aids in eg music, traffic but it still doesn’t make me “partially deaf” or able to hear words) thus leading to awkward missed conversations etc so what’s the point? The easiest thing is to explain to them my level of deafness and what it is I need from that person in order to communicate well. Did any of you see Michael McIntyre’s joke about people who spell their names…cos there are so many different ways of spelling eg Sean, Shaun, Shawn…that people spend time telling people how to spell their name (which I also do because it’s Elisabeth with an “s” not Elizabeth with a “z”!) and the point he makes about the same name with different spellings (although he was trying to say why not spell it one way so everyone understands but that’s not what I’m trying to say here) fits exactly with this whole discussion: we will always have to explain our deafness in our own way.
Robert Mandara
September 27, 2013
It seems to me that we either have to all live happily together under a broad brush term such as “Deaf” (a word which I first heard/misheard at school when other pupils asked me “Are you Death?”) or else we need to break it down into discrete and meaningful levels.
The problem with “mild”, “moderate”, “severe” and “profound” is that Joe Public can’t tell one from another. Besides that, most of us are somehow borderline between two categories. i.e. there are not enough levels and the difference is not clear enough.
It seems to me that to even begin to cover all levels, we would have to somehow be able to rapidly convey our audiograms and speech comprehension results. For example, these could be on a badge, T-shirt or tattooed on our foreheads. The latter could be really helpful in the swimming pool where too many people try to talk to me. 🙂
I don’t like Deaf/deaf because it sounds like death. Nor do I like hard of hearing because it sounds stupid; we don’t say hard of sight, hard of smell do we? Furthermore, hearing cannot be expressed as a percentage, regardless of what many people seem to think, so let’s rule that out.
Hearing impaired and partially hearing don’t offend me as such but they still don’t reveal how much hearing one has. Hence they’re not really any more useful than saying you’re deaf rather than Deaf.
Am I broken or defective? I don’t know. But I do know that, if I could choose, I’d prefer to be skint and hearing rather than rich and deaf. If it becomes possible to give people like me “normal” hearing, you’ll find me at the front of the queue. 🙂
Vicky
September 28, 2013
Hi we are a hearing family with a 6 year old deaf/HI son. A few weeks ago after attending a Genie event he asked me ‘Mum what does deaf mean?’ I couldn’t believe we’d got so far without him knowing the word and I think it just goes to show how much we do tiptoe around language even within our own families !
Diane
September 28, 2013
I prefer to describe myself as partially deaf too. I’m not completely deaf, hard of hearing makes me think of old people and, like Natalya, I’ve never actually lost anything, so having a hearing loss doesn’t apply.
Whilst shopping the other day I noticed someone working on the checkout wearing a badge saying ‘I am deaf’. Then on entering a certain more upmarket store one of their employees was wearing a badge saying ‘Hearing Impaired’, maybe they thought it sounded posher!
Interesting too that hospitals are now becoming more politically correct. The audiology department in Brum, I’ve been attending for years, was once called ‘Centre for the Hearing Impaired’, now it’s known as ‘Hearing Services Centre’!
Susan Dohne
September 29, 2013
I like ‘hearing difference’ instead of ‘hard of hearing’, just as I prefer ‘learning difference’ as opposed to learning disability.
Linda Richards
October 1, 2013
I have resisted the term ‘hearing impaired’ for many years telling students and colleagues I am not an impaired hearing person. I have also resisted terms like Deaf people have “special needs”. I say in response, “No, we have specific needs, not special needs” and I go on to list them generally as well as my own specific needs. I changed the name of the Communication Support Unit I once managed to ‘Communication Services Unit’ as a more accurate term of our work and to drag the hearing (and largely unaware) community into understanding that we did not ‘support’ (thus perpetuating the dependency model) but rather, that we provided (communication) services. Services that were used by both parties – hearing and Deaf. I changed my job title too. If we are not careful with the terms we use, we risk misrepresentation and misunderstanding, even being devalued. Think about it, some of the recent news coverage in the UK has referred to Martin Luther King’s astonishing speech (with the first ever reference to ‘Black people’rather than the label of ‘negro’ that had been so often used), and now the issue of the term ‘Yid’ in relation to football chants. It is also okay to learn, evolve and modify language. This comes from greater understanding and awareness. We can influence people in the way we would like or we can perpetuate our lowly status. Remember, the term ‘hearing impaired’ was not ours. It was ascribed to us …. By a hearing person. And therein lies the imbalance as well as the dismissal of our status. Hitler considered deaf people imperfect. We, in his eyes, were impaired. And we all know what happened there….. I’m with you on this one Mark Levin.
maxiaidsblog
October 1, 2013
Reblogged this on MaxiAids.
gargly
October 2, 2013
…bit late thinking of something other than whats been said, but I found myself tweeting yesterday ” I was HI when I was 5, but socially I am deaf.. impaired is the medical factor not a cultural/social aspect “
Tim
October 2, 2013
I used to think it was fair enough if anybody wants to refer to themselves as ‘hearing impaired,’ now I’m not so sure, as I discuss at my blog:
http://tim-theregency.blogspot.co.uk/2013/09/some-more-thoughts-on-medical-model.html
It’s tricky when the right to self-determine clashes with the interests of others.
Editor
October 2, 2013
I thought that was an interesting blog Tim and it’s good to see you adding to the debate.
In my blog I mentioned that I feel we should be “slow to take offence.” When I wrote that, I was thinking about how things work in practice, when we meet (or interact online) with someone who describes themselves as being ‘hearing impaired’ for example.
Personally I wouldn’t make that a topic of discussion if I met someone who called themselves that, I would only discuss it if it came up in conversation or if they brought it up. I’d talk about whatever we were meeting to talk about.
That’s my question really – if you don’t believe in people’s right to self determine, then how does that work in practice?
I’d be interested in discussing this.
Tim
October 2, 2013
Thanks, Charlie. Yes, I think you’re right. I wouldn’t challenge anybody who chose to use the description, I would just hope that it was thoroughly debated separately and then people can make their own minds up once all the facts and opinions are in. Besides, people tend to react to being bossed about by stubbornly continuing to use their preferred words – It would likely backfire!
Another thought I’ve just had is whether people really are ‘self-determining’ when they just copy oppressive influences – that could be more accurately described as other people deciding for us. Complicated!
Editor
October 2, 2013
Good points! Definitely complicated. C
Kate 8787
November 22, 2016
Wow. So relatable. Marry me 😀