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Article

Talking to Somebody Who is Deaf in One Ear

Unilateral hearing affects a significant percentage of the population. How would you welcome a client or guest with this kind of deafness?

How would you speak to someone partially deaf? This is the next question considered by anyone who has just learned that someone is deaf in one ear. It's not a well publicized sphere; and it encompasses a whole different set of issues from either the fully hearing or the fully deaf. I've been profoundly deaf in my right ear since childhood. This article will explain what is it like to be deaf in one ear; and what you should factor in, when communicating with those with SSD.

How Does the World Sound to Someone with Unilateral Hearing?

Let me walk you through a worst case scenario. Though fictitious, it contains elements with which I am more than familiar!

"Jo!"

I'm out in the street, so it's a wonder that I heard my name being called at all. But there's a lull in the traffic and I'm away from the main pedestrian hubs.

The urgency in the tone alerts me to the fact that this probably isn't the first time that she's called me. There's psychological pressure on me to find her fast. I don't want to appear impolite.

Single-sided deafness means that I have no direction of sound, but I do have eyes. I quickly scan the road ahead of me to no avail. Then I turn around, looking until I spot the source. It's my friend and she's waving from the doorstep of her house. "Finally, you deaf cow! Come and have a cuppa. I've got news!"

I wander across the road, taking care to look for traffic. I can hear vehicles, but have no way of knowing if they're approaching or moving away. The only way to gauge their distance is to see them.

Once through the front door, I'm engulfed in a cacophony of noise. There's no depth to it, just a flat wall of sound seeming all to derive from my left side. (I'm deaf in my right ear.) The television is on. A soap opera blares out a constant stream of words, which clash and merge with those spoken by the other two people in the room.

My friend has possibly said something. I don't know. She's gestured towards the settee and that subconscious bit of body language has provided me with a clue. I'm being invited to sit down, while she disappears into the kitchen. This is a British home. She will be making a cup of tea to demonstrate how welcome I am in her home.

I feel disorientated, because it's hard to think with that white noise distracting me. My instinct is to switch the television off and yell at everyone to shut up. But etiquette demands the opposite reaction.

I'm to be on red alert. I'm to watch every person present, in case their attention or moving lips indicates that they have spoken. Unfortunately, that focus often prompts people into conversation. I'm now lip-reading and watching their non-verbal communication.

All the time, the noise feels like something physical to be warded away. It comes and goes. Just one source of sound is fine. I can hear it. As soon as there are two, it's like I've been slapped. The television and conversation over the top is the most common situation in which I have to suffer this.

Her husband has a beard and mustache. I cannot see his lips moving, though his gaze and the laughter of his teenage son tell me that I'm ignoring him. I feel like a stuck record, repeating this every time I'm here, but out it comes again, "I'm sorry. I'm deaf in one ear. What did you say?"

Whatever the response was, it must have been funny. It was probably a light-hearted joke about deafness. People are full of those. It breaks the tension, which so many seem to feel at the prospect of silence. He reaches forward for the remote control and I catch his broad smile. He wants to be helpful. He switches on the subtitles, so I can watch the television too.

And the noise goes on. Too much of it and I feel silently dizzy. I'm getting a headache from having to concentrate so hard. I start sentences with an apology, because I missed the thread of the conversation. It's not just the volume. It's not just the sound. It's the sheer scale of it all, like an assault, when they're all trying to be so welcoming.

Unilateral Hearing Loss on Wikipedia

Unilateral hearing loss or single-sided deafness is a type of hearing impairment where there is normal hearing in one ear and impaired hearing in the other ear.

Books about how the World is for the Hearing Impaired

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How the Ear Works

This YouTube video describes precisely how we hear. In my case, the cochlea is broken, so cannot pass the information into my brain.

Human Hearing

Making Life Easier for Those with Single-Sided Deafness

It's not volume that you need to watch, it's multiple sources of sound.

Being profoundly deaf in one ear is a totally different circumstance to total deafness, or even other types of partial hearing impairment.

It is stereo hearing that provides depth and direction to sound. Both of your ears will pick up the audio and then your brain will triangulate the location.

The slight variances in volume will position the source closer or further away. In this way, they work together to allow background noise to stay in the background, or your attention to lift one sound from the mass of it. Even someone with reduced hearing in one ear will be able to deduce audio information in the same way.

Those with completely unilateral hearing do not have this ability.  For us, every sound is in the same place, indivisible from the rest.

If my fictitious friend had been aware, in my opening worst case scenario, then it could have played out much differently. Firstly she would have waited until there was no background noise before calling my name. She would have included her location in the shout. "Jo! Turn around, I'm behind you!" 

No initial anxiety then. I'm not only certain that I heard first time (achievement for the win!), but she's told me from the outset that she's got my back. She knows me and she is welcoming me.

Once inside her home, the television would have been removed from the equation. It could have been switched off and muted, but that isn't really fair on those who were watching it. Better still would have been to invite me into the kitchen with her. With the door closed, we have a quiet place.

People with single-sided deafness can hear perfectly well, if there are no competing sounds. I have known a few individuals for years, without them ever learning that I am deaf in one ear. The reason is that I've only ever spoken to them, one on one, in a relaxed, quiet environment.

Finally, if we were to stay in the lounge, with the television off, then my deaf aware hostess could monitor the conversation. Everyone taking turns to talk is just fine. But if over-excitement or enthusiasm means that people start speaking over the top of each other, then my friend would intercede. "One at a time, you lot. Jo's partially deaf."  A smile, a little wink, all is well in the world again.

Baking Aids to Say I Love You in ASL

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Which is best - stereo or single-sided hearing?

Anything you can do, I can do better! But let's argue this one out for once and for all!

Stereo hearing is best because...

  • Ember

    Stereo hearing can experience this piece of magic. http://cynicallyjade.tumblr.com/post/16478440504/if-you-havent-heard-this-already-you-must-try-it

  • I like to hear depth and i like to know where sounds are coming from. I think it would be scary otherwise.

  • ... you can hear from which direction the car is coming that is about to run you over ;-)

  • mae

    I wish I knew what this was like :(

  • Kim

    I taught kindergarten and pre-k talk about being overwhelmed sometimes! I told my angels I only had one ear that worked so all of their sounds would not fit in the hole! I was surprised at how well that worked!

  • SFCkimsmith@aol.com

    I wouldn't call it "better", but single-sided deafness does come in handy when the need arises to block out noises when trying to sleep... just roll over onto the "good side"!

  • Steve

    You can keep up with conversations much better and you don't feel left out. You don't have to constantly position yourself to hear better and plan your every move based on trying to hear others.

Single-sided hearing is best because...

  • I can sleep through pneumatic drills going off outside my bedroom window.

  • I have an excuse not to have to listen to drunk people babbling on.

  • I know the value of silence.

  • Paying so much attention to non-verbal communication means I catch what you wanted to say, rather than what you think you should say.

  • I have no idea what stereo hearing actually sounds like!

  • Our acronym is also a command - Ssh!

  • Bill

    When its noisy at work I can cover my hearing ear and still type with one hand. Occasionally I do tell people at work that I am lucky to be half deaf. There are days when I don't know how people who don't have any deafness can get any work done.

Add your argument

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Comments

I would naturally like to hear from anyone who has anything to say on this issue.  Please just chat away below in the usual way.

But I would especially welcome comments from people who either are deaf in one ear, or else know somebody who is.

Have you any insights and tips on how people could be more aware of the issues surrounding unilateral hearing?  How do you cope in noisy situations?  How do you make your one-sided deaf friend feel welcome in your company? 

More of my Articles About Deafness

  • Is Your Home Safe for a Deaf Person?

    Alarms in your house warn of anything from a fire to a burglary. But what if the only person there is hearing impaired?

Updated April 28, 2015

Comments

Sherry LopezApr 29, 2017

Having normal hearing, and waking up ssd at 25, was overwhelming at first. It was a medical issue that zapped my hearing and sight on one side.I noticed vision loss, before I realized deafness. Adjusting to ssd was more frustrating, than the vision loss. I became timid and frightened easily. The full effects of ssd was an adventure in lifes lessons to say the least . Once I learned to accept it, it became easier to adapt and retrained my thought process. I quickly found myself being able to read lips. I learned situations to avoid, and what to do in unavoidable situations (safety). After 15 years of ssd, I was gifted my first set of hearing aids, in which I would I never of been able to afford. I cried just being able to hear my children play and laugh...run through the house and hear their foot steps, then to hear the birds sing, and the leaves rustle as I walked in the yard. All great sounds I missed so much. But soon it all became overwhelming. The adjustment back to hearing world I thought I so dearly missed, was causing me anxiety. I enjoy wearing them, and I enjoying not wearing them. I quickly learned having ssd I didn't fit into the deaf community, or the hearing community. Which put me in a world of my own. The people closest to me don't make it an issue. They just know to sit across or to the left of me. I am more aware of my surroundings. Particularly for safety reasons, which is huge now days. If someone approaches and tries to speak to me, Ishuffle myself around to hear them. A time or twenty I have been known to say "can you repeat that in my other good ear"..lol. Many people think they need to shout 4 inches from your face, they assume your deaf and dumb, or they talk so dang slow they forget what they were saying. So I just try to avoid the annoyance of explaining it to strangers. I've been given an opportunity, an ability to tune into hearing every little annoying sound, or tune out the world, all depending on what I chose to do. That is best thing about ssd.

JoHarringtonApr 28, 2015

Jo high-fives Bill

BillApr 28, 2015

Bill high-fives Jo

JoHarringtonApr 28, 2015

Bill speaks for me too in so much of this. I too have learned that those who don't want to include me don't deserve me attempting to include myself. They're really not worth it.

The exception being friends who ordinarily know damn well what's going on here, but are too tired/drunk/forgetful to have it registered at that moment in time. Then I just disappear into my own world, or grin at them until they remember. Getting control of the remote and pausing the TV every time they attempt to speak over it soon alerts them to their behavior.

Tom, you have hit the nail on the head there. The quiet ones on the outskirts are usually the more interesting people anyway. I hope you find your confidence to go with that wonderful compassion. It'll open up a lot of social situations for you. Then there's always online communities, where typing all responses means no need to hear a thing. You sound to me like a beautiful person and folk deserve to hear more from you.

Yes, I do get a lot of back-ache and neck cramps from turning around. But then I sit ordinarily like someone with no sense of decorum or posture, so I only have myself to blame. ;)

TomApr 26, 2015

Thanks Bill, I notice that in some situations I am carrying the conversation and in others it is just to hard for me to keep up with. I know that my hearing loss in one ear has changed my personality and it has made me a completely different person in some situations. I think that this has made me think differently about life and has made realize not to judge others so harshly. I have found myself being more of an outkast talking to people that I probably wouldn't have met if I had not had hearing loss. I find myself trying to talk to people who are not part of a big group of people and don't have much friends because I know that I can have a conversation with them with no other voices and I know what it's like to be them. Having a hearing loss has made me realize what it's like to be left out so I find myself relating to other people who don't have many friends because of other issues other than hearing loss. I am thankful that I have had the opportunity to feel what it's like to be left out. This has made me stronger and has made me be a person that I am proud of. I hope that others will learn to respect everyone no matter what because it is impossible to know what people are going through.

BillApr 25, 2015

You're welcome Tom. I think that your friends will be accommodating. Be patient. Remember they really don't know what we experience. They will probably need reminding from time-to-time.

I think that the most difficult thing for non-deaf people to comprehend is that we swing back and forth between the deaf world and the hearing world. They barely notice a little bit of background noise. It puts us in the deaf world. At times we can hear just as well as they do. From their experience it is incomprehensible that that changes. I found that after telling my friends on multiple occasions that I was having difficulty hearing, they began to recognize the noise environments that cause that to happen. Its important to let them know that because we do not have stereo hearing we cannot focus on sounds and block out background noise.

Don't be embarrassed, there is nothing wrong with you. We just hear in a different way than others do.

TomApr 25, 2015

Thanks for the advice Bill, I really appreciate it and I will educate my friends about what I am dealing with.

BillApr 24, 2015

I don't have a problem being SSD. I let people know that I'm deaf in my left ear. It doesn't take a lot to accommodate me. If they can't make the effort, why should I be embarrassed? They are obviously shallow people whom I wouldn't want to associate with anyway. I am a far better and interesting person than they are.

Most people are understanding. You need to make the effort to educate them. They cannot be expected to just know what we experience. Give them a chance. I find that people are often very interested.

I know its difficult when you are younger without the knowledge of how to deal with being half deaf. From experience, I think most of us learn how to deal with it very well. Its something to be proud of.

frankbeswickApr 24, 2015

Hopefully you will be cured! But it is always good to let people know about your problem. When I was suffering some mild hearing loss [now cured] some years ago I was open with my school students about it, and explained that sometimes I might not hear them as well as I could. I found that almost every student was co-operative and sympathetic, as most people will be with you.

TomApr 24, 2015

Being SSD sucks. Missing out on numerous conversations can have a serious impact on relationships and making friends. People assume you're just quiet and boring. Having to constantly position yourself to hear better is very tiring. If I am ever stuck in a position where I feel like I can't contribute to the conversation, I get really embarassed. This has made me shy away from going to parties or out with friends. I know it doesn't seem that tough to deal with, but the reality is that it has made my life very hard.

I used to get anxiety in the classroom because I couldn't hear my self breathe and I would get paranoid about if people thought I would breath loud or if they could hear my stomach growl which it constantly would throughout every class. I know that seems funny but it really did impact my school work. I also have problems with my spine and I walk strangely because of this. I think that this is related to how I sat in the classroom because of having to position my body to hear better. Or could it be related to a problem with my vestibular system? If anyone else has dealt with these issues let me know.

Overall being deaf in one ear has made me very depressed at times but I know that someday I will eventually be able to hear in both ears thanks to advances in technology.

JoHarringtonJan 3, 2014

Frank - This explains why my teachers never had a clue how to deal with my deafness either! Mind you, that worked out fine, because all they wanted was silence in the classroom so that they could teach. That indirectly created a good place in which I could learn.

However, I have encountered modern teaching practices, which have more focus on group discussions or pairing up with a partner to work on some project. That must be a nightmare for SSD kids in the classroom.

JoHarringtonJan 3, 2014

Thank you, Bill. You're certainly talking for me regarding the deafness being just deafness. It's not who we are. It's just a feature. I have NO idea what stereo hearing sounds like, so I'm missing absolutely nothing.

I think that if I was offered the chance to hear in my right ear again, I'd decline. I know that sounds like bravado, but I'm not sure that I'd want to give up the benefits of SSD for the vague boons of stereo. Perhaps if I could try it for an hour, just to find out what everyone has been going on about all this time, I might do it for the experience. But I really have no hankering to live like that forever.

Lori and Bill, I'd love for you both to join Wizzley and write about your hearing related experiences here too.

JoHarringtonJan 3, 2014

You are very, very welcome, Lori. You are in precisely the situation for which this article was written. Hopefully you can initiate some things in your home, which will become habit and cover those times when everyone forgets that you're deaf. They will. I recently discovered that my own mother had no idea how I actually heard the world, while my friend of 20 years admitted that he forgets about my deafness more often than I imagine. It's a hidden thing, so there are no visual clues for people to remind them. And we compensate so very well, that there's not always that side of things to prompt them either.

Good luck with it all. This isn't the end of things. In fact, we get the better deal. I've just woken from a lovely sleep to discover that my hearing friends were all disturbed earlier by a loud beeping from outside!

frankbeswickJan 1, 2014

This was an extremely useful article because, as one who has taught in classrooms I have encountered single ear deafness but have never had any training in it. This article was the training that I should have had.

BillJan 1, 2014

Lori I'm sorry you have lost hearing in one ear. It must be very difficult to loose. Jo has provided by far the best information about Single Sided Deafness that I have seen. Please understand though that those of us who have been deaf all our lives or a very long time have a different view of it. Its not something that we are going through, it is part of who we are. Sorry everyone, once again I am speaking for more than just myself.

I'm proud of being a Single Sided Deaf person. I have always been deaf in one ear. If there was suddenly a way of providing hearing to my deaf ear, I would have to seriously consider whether or not I wanted it.

The information that Jo has provided would educate someone who is not deaf as to how someone who is deaf in one ear hears sounds. It also educates us single sided deaf people as to how people who are not deaf hear sounds. Lori you are in a unique position to know both sides.

LoriDec 31, 2013

Thank you so much for posting this. I am newly diagnosed withSSNHL (as of 121/13). I gave this article to my husband to read so he has a better understanding if what I'm going through.

JoHarringtonDec 17, 2013

Wow! Go you! And yes, thank you very much for doing this for us. You certainly do speak for me too.

*hi-fives you over the internet* Thanks.

BillDec 17, 2013

Hi Jo. Recently I dropped my mp3 player again and consequently had to buy a new one. Other than Apple, I do not believe that there is any accommodation for us. I decided that if I am buying a product that does not meet my needs I am going to let the manufacturer know about it. My apologies if I offended anyone for speaking for all of us., but left the following on Sansa's Customer Support website:

I am a Single Sided Deaf (SSD) person. I am deaf in my left hear. Unfortunately, I have a choice of hearing either right or left channel but not both when wearing ear buds.

I am a long distance runner and I always use a Sansa Clip when I run. It would be great if I could configure it to output mono so that I could hear all of the music on my mp3's.

I frequent a couple SSD web sites. Trying to listen to stereo wearing ear buds is an irritation to all of us. I know that Apple supports mono output. I prefer your product and I would really appreciate it if you would consider this enhancement to your product.

I got a prompt response saying that they understood my issue and forwarded my feedback to their Product Developement team.

JoHarringtonNov 20, 2013

Thank you very much for being mindful of the environment around your friend. People like you are true friends and that makes you great to be around.

cazortNov 20, 2013

I think this is a really great page to draw awareness to the issues faced by people who are mostly or fully deaf in one ear.

One of my close friends also only has hearing in one ear, and she's described to me the same phenomena you talk about here--the inability to locate the source of a sound, and the problem hearing anything at all when in a loud environment, like one filled with loud chatter from a TV or other people.

I do my best to be mindful of her situation, such as by avoiding recommending or choosing a restaurant or cafe that has a loud atmosphere if she is going to be present, and also by being a bit more restrained about talking when others are speaking so as to avoid creating a confusing jumble of sound. I think not talking when others are talking is a good habit anyway, so I sometimes appreciate the direction she pushes me in! And, even though I have normal hearing, sometimes I find it anxiety-producing when there is loud chatter and background noise for my own reasons, so I think our preferences end up meshing well.

JoHarringtonOct 30, 2013

Yep. :) We have neither depth nor direction of sound, so it's all coming from precisely the same place into the same ear. We can tell quieter or louder, but that's really the only major aural clue to distance and difference. Well, different voices/accents are there.

Yay! I would be happy to visit your home, as we could converse minus the television.

jptanabeOct 29, 2013

I had no idea about the difficulties of being deaf in one ear. I never realized it would make it impossible to hear a person talking when the TV is on. Mostly I find it difficult to carry on a conversation with the TV on anyway, so there wouldn't be too much problem in my house!

JoHarringtonDec 19, 2012

I have no medical knowledge as to why this may be the case, but I can empathize. I find that I can't hear my voice, so I do have people telling me that I'm too loud or too quiet. It's so hard to find that middle ground, isn't it?

There's also the fact that all that background noise is very disorienting. I wonder if that confusion causes our brains to interrupt our speech patterns. I'm going to ask around my medical friends and see if anyone has an answer.

BillDec 18, 2012

Hi Jo, When I am in an environment with a lot of background noise I often find it difficult to control my speech. I sometimes start slurring words. I am curious if that is a result of my SSD. Do you have any insight? Thanks. Bill

JoHarringtonOct 19, 2012

*high fives* I'm deaf in the same ear! That makes us buddies from the off-set. <3

What's it like with the implants? I've never been offered them, so I don't even know if they would work for me.

And yes, so much confusion out in the hearing world over SSD. People know what to do with deafness or hearing, but not with that moveable feast in the middle.

JenOct 19, 2012

I was born completely deaf in my right ear, so I relate to this a lot! I would love to experience sound direction. It's such a foreign concept to me!
I'm now 26, but when I was 19 I got 'CROS' hearing aids for the first time. Last year I traded those in for a BAHA bone conduction implant (similar to a cochlear implant). I feel like a Borg from Star Trek haha! (or Bionic Woman). I still have days like the scenarios above, but less so since I got hearing aids. I totally agree with you, Jo Harrington when you say you've never seen SSD portrayed in media/tv before. A lot of people don't even know it exists.

JoHarringtonOct 12, 2012

Scroll up, Brenda. I've just made a badge for your daughter. *smirk* (Under the heading 'Buttons for Promoting Awareness of Single-Sided Deafness'.)

JoHarringtonOct 12, 2012

Mira - Yes! You've hit the nail on the head. That's what's so bad about being told or signaled at to lower your voice. It's like controlling a dog or something.

JoHarringtonOct 12, 2012

Brenda - Oh! The 'lower your voice' hand sign or sushing! I can totally emphasize with her on that one. It's mortifying! You want to either crawl up into a ball or scream at them to stop setting the volume at their level.

I tend to go very, very quiet afterwards. Partially because I don't trust myself not to scream at the person telling me to lower my voice; and partially because I now know that I'm speaking too loudly.

That hand-signal or comment is a way of making us mute as well as deaf.

My advice? Tell her work-mates to take deaf awareness classes. It'll do much more good than ASL for a SSD person in hearing company. The problem is not with her.

MiraOct 12, 2012

My two cents would be for you to gently brush her upper arm. It's a softer signal, and one that makes most people feel better, too. I think the hand signal is maybe too strong and shows more power, as if you can will the other to lower their voice and they will have to obey. Again, don't take my word for all this, but maybe talk to her about finding a gesture she'd be comfortable with.

BrendaOct 12, 2012

We found out our daughter had SSD in her right ear when they tested her in kindergarten. Now she has tinnitus as well. She is now 26 years old and still has issues at her work place. She has explained to her fellow workers that she was born without her cochlea.

My daughter and I had a conversation the other day about her workplace. She was upset that her co-workers just don't get why she is so LOUD and that she can't tell how loud she is. They suggested she take ASL. Well, what good is that when they don't understand this language! I asked her if someone could use a signal such as to lower her voice with their hand. She said that infuriates her when they do this.

Does anybody have any ideas how to help my daughter with her loudness. I understand why she is loud but I don't want to offend her either with hand signals.

JoHarringtonSep 9, 2012

I would certainly get behind that suggestion!

I don't think I've ever seen unilateral hearing on a single television show. It's not really rock and roll enough for a sitcom. LOL

I wish that you were in charge of all school curriculae.

MiraSep 9, 2012

I think such information as you share on unilateral hearing should be learned in school. Maybe they should make seminars, each on a certain topic related to various conditions people experience throughout their lives. It seems to me that when it comes to illness, people have little sympathy for others because they have never learned how living through life with this condition or another can affect people and those around them. The only information most people have on people who lead different lives because of a predicament comes from watching TV, where unfortunately the info is mixed with lots of show biz . . . but maybe it's better than nothing, who knows? In any event, I think education means more than what is required in universities as general degree requirements. OK, they don't make it curricular, but make it extracurricular then for people in high school or college, who are at an age when they want to know so much about the two big L's, Love and Life.

JoHarringtonAug 21, 2012

That sounds more like you're losing your hearing, but it hasn't completely gone in either. If you were deaf in one ear completely, there would be no mumbling. It would be a wall of disorienting sound.

Good luck with your hearing test, and please do let us know how you got on. <3

TiaMariaMartiniAug 21, 2012

This reminds me to go get my hearing checked. It always seems that people are mumbling and talking low. I'm constantly saying, "what, what?" and asking people to repeat themselves. Drives my husband nuts. I must teach him to speak loud.

JoHarringtonJul 29, 2012

Wow! That is an amazing story. I didn't know any of that, nor had I heard of the university. I'm proud of their stand.

I've been musing on what you said about 'good' and 'bad' ear. I'm going to stop saying that. Thank you. :)

BillJul 29, 2012

Jo an event in the late 1980's caused me to evaluate my feelings towards my deafness and what it meant to say that I had a 'bad ear'. Until the event, I had always felt embarrassed being deaf in one ear.

Students at Gallaudet University for the deaf went on strike because the board of directors had appointed a new non-hearing impaired president to the university. Since the university had been founded in the mid-1800's it had never had a hearing impaired president. As I recall, the directors claimed that they could not find a qualified hearing impaired candidate. In protest, the students very effectively shutdown the university for days.

I watched the events every night on the nightly news. One night the university staged an event for the new president to speak to the students. She stood in front of a podium and spoke into a microphone. She was totally flustered when the students started yelling "we can't hear you". Soon afterwards the directors found a qualified hearing impaired candidate to be president.

The outrage and determination of the students made me realize that I had nothing to be embarrassed of. Later I had the epiphany that I do not have a 'bad ear'.

JoHarringtonJul 28, 2012

Oh Bill! I'm sorry that you've had to muddle through all this time. I was very lucky, insofar as I worked at the University of Wolverhampton for ages. That is one of the best places in Europe for Deaf Studies. I had the Dean of the faculty himself explain it to me.

Hopefully now, you'll be able to arrange the background noise to participate better in conversations. <3

I'm guilty of implying 'bad ear', though it's usually the other way around. People ask which is my 'good ear' or I tell them, 'this is my good ear'. It's not occurred to me that I'm being subtly disparaging about my own nature. Thanks for pointing that out.

BillJul 27, 2012

Jo, Thank you for providing this site. I am 58 and have always been deaf in my left ear. Visiting this site, I learned more about why I have difficulty hearing when there is background noise. I could never understand why I still had trouble hearing someone speaking when I put the source of the background noise on my left side. It of course makes it easier, but the problem does not completely go away.
Switching to another topic, I don't know if anyone else feels this way, I resent when people say 'bad ear'. When people ask me which is my bad ear, I always tell them that I don't have a bad ear. I don't ear in my left ear.

JoHarringtonFeb 27, 2012

Thank you very much. As you have partial deafness too, did all of this chime with how you hear the world?

It sounds like we have slightly difficult situations, as I'm profoundly deaf in one ear, but can hear fine with the other.

I prefer the 'different way to experience and interact' one than burden. It's a boon when we get to sleep through all of the noise!

MaiaFeb 27, 2012

Thanks for writing this! I have had significant hearing loss in my left ear since I was 5 years old from a collapsed ear drum that they finally repaired when I was 16. Even after the eardrum replacement surgery my hearing has been significantly reduced in the left side. I really appreciate you writing this article and I hope that more people read it. It is important to understand that it can be a burden, or at least it is a very different way to experience and interact with the world around you. Well written.

JoHarringtonFeb 26, 2012

You are especially welcome. <3 Hopefully your husband will be able to share some of his insights too. It's often difficult to know what to say, because we haven't the comparison of knowing what you're hearing! Thanks for sharing and take care yourself. <3

SharileeSharesFeb 26, 2012

Thank you so much for writing this. My husband is partially deaf in one ear, and this really helps me understand exactly what he is going through. We have been married for five years and I know this is hard on him. I am so glad you wrote this, and I will be sharing this on a couple of sites. Take care!

JoHarringtonFeb 10, 2012

You are very welcome. I know 'I love you' in British Sign Language, and now I know it in American Sign Language too. Always a good one to have!

JoHarringtonJan 29, 2012

Oh dear! No wonder it was so awkward. *bites lip* I'm still giggling though. <3

SamJan 29, 2012

Jo, this guy surely did, and to add a twist to the story, I am actually the 'vicar's wife' so it was even more troubling for this member of our congregation ;-)

JoHarringtonJan 29, 2012

Oh Sam! I have to admit that I laughed out loud reading that story! Poor you and poor him!

It hadn't occurred to me that people might find it disconcerting to be lip-read, nor that they might assume that we're flirting!

SamJan 29, 2012

I have a story for you, Jo:
I am not deaf, but I am increasingly hearing impaired on both ears. Speaking on the phone is a pain in the back side and having a conversation with any background noise present is nearly impossible for me.
One time I was speaking with a friend after Church and we kept moving around and I had a hard time to move in a way that I could see his lips, to do auxiliary lip reading. In the end I told him to keep still and look at me so that I could understand him.
He looked at me completely flabbergasted and asked why. So I explained to him that I needed to see his lips to help me to understand what he is saying.
Long pause.
Oh, I noticed that since time and found it rather disconcerting, now I understand better why you do it.
Gosh, I was not finding his lips attractive, I just needed to see them in order to have a conversation with him! Why do people don't ask if they don't understand why we do something the way we do it???

JoHarringtonJan 29, 2012

Thank you for commenting, Othercat, particularly in your defence above for stereo hearing. I was beginning to think bilateral hearing had nothing to recommend it! :p

One thing that I've found in common with most unilateral deaf people is how quiet we are about the issues most of the time. It might be said once or twice, then never again. It feels impolite to demand a better environment, when everyone else is having fun. Makes us look like the party poopers.

Please let us know what insights your son gave. It might be that the 50% hearing in his right ear does help him locate sounds. That would negate some of the issues highlighted in this article. <3

OthercatJan 29, 2012

My son was born with Townes-Brocks Syndrome which resulted in an ear deformity and 50% loss of his hearing in his right ear. He hears most voices and sounds, but noises over a certain pitch are lost on him. Because he was born like this, we've never actually sat down and discussed it. He's never let on that it might affect him this way. I can't even imagine it. I'm definitely going to have a talk with him now. Thank you for this eye opening article!

JoHarringtonJan 27, 2012

Oh wow! I've learned something too here. I thought that the other 65% of your hearing in that ear would have compensated, allowing you to still triangulate sound. Thanks for putting me right on that.

I was told that a hearing aid would do no good for me. It's the cochlear that's gone, so there's nothing to transfer sound.

BrendaReevesJan 27, 2012

Jo, This is so informative. I lost 35% of my hearing in one ear when I was 34 years old. When my cell phone rings, I don't know what direction its coming from. This is something that's happened recently. I do have a hearing aid, but don't always have it in. Without my hearing aid, I have to blast the TV or I can't make out every word. It's about time I go for another hearing check-up.

JoHarringtonJan 27, 2012

i recall that journey, with utter gratitude too! On the way to Vegas, I had basically relied upon the kindness of strangers. Airports are great echoing masses of noise. There's no way I could hear flights being called. It was quite stressful making that journey alone.

Then, on the way back, life was so much easier. Thank you so much for arranging the special provision. Waving those pieces of paper at airline staff got me escorted exactly where I needed to be each time. <3

ShonnaJan 27, 2012

I remember when you flew back to the UK from Vegas and I'd told the airline people that you were partially deaf and their response was pretty great - being open can make life easier when you're in a situation you're not 100% comfortable with. Flying on your own is an example, no-one to let you know properly when it's time to get on the plane, etc. I was really pleased with what you'd said when you got home - that they really made sure you knew what was going on.

JoHarringtonJan 26, 2012

I can so empathise with your friend! The thing is that without background noise, we can hear perfectly. As soon as there's a similar sound over the top, we're not only deafened but disorientated too. The rules change constantly.

I'm glad that I've written this now though, because it is raising awareness. You will know more about what she's experiencing now. It's difficult to describe, as I discovered in writing this, because there's no comparison. I have no idea what you're hearing, in order to tell you how different it is.

I know it can't be the same, because those with stereo hearing seem obsessed with having the television on AND talking over the top. It doesn't appear to bother them at all.

Yes, so much more is said non-verbally than verbally. That's a perfect example.

EmberJan 26, 2012

I have a friend who has trouble hearing in one ear, though not completely deaf. When I was reading your story, I cringed remembering all the times she'd say something like 'What did you say? I have trouble hearing in one ear.' (Or even better 'I've told you before I have trouble hearing in this ear.' I'm not a bad friend I swear!) And other little subtle things like that, such as a night this past December we were in a town we didn't usually visit, and we saw a friend we haven't seen in ages. She had me stop the car and she called out to him. She yelled his full name, 'turn around.' The things you learn.

"Paying so much attention to non-verbal communication means I catch what you wanted to say, rather than what you think you should say."

I know I don't pay as much attention to body language, even though linguist say something like conversation/language is 80% unspoken, ie tone and body language. I think...? Anyways, I recall a time I was asking a boss a question, but I knew based on a professional level she'd say yes no matter what. But I wasn't asking because I knew she'd help me, I also knew she was insanely busy and wanted her actual answer. So I watched for any nonverbal clues that it might not be a good time, and it was so funny to me because as, 'Yes! Of course!' came out of her mouth, she was shaking her head 'no.' Which just tells me I really do need to watch body language more, because to me that was an absolutely fascinating moment to experience.

JoHarringtonJan 26, 2012

Hi Sionnach!

You and I would either have perfect hearing, or be completely deaf between us. We have unilateral hearing in opposite ears.

Yes, that is the culprit. Did I describe the busy environment noise how you hear it too?

Thanks for commenting.

SionnachJan 26, 2012

Oh yes - also, I very much agree with "Paying so much attention to non-verbal communication means I catch what you wanted to say, rather than what you think you should say."

SionnachJan 26, 2012

Thanks so much for posting this!! I have substantial hearing loss in my left ear - due to a severe infection when I was in grade school - but never really connected it to the difficulty I have in sorting out sounds in busy environments.
JoHarrington
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