Living with Single-Sided Deafness

I lost the hearing in my left ear through sudden hearing loss in August 2016. There wasn’t a known cause for my hearing loss, I wasn’t feeling ill and I didn’t have an infection. One day the world to the left of me just fell into silence. The hearing loss was profound which means I have no functional hearing in my left ear, and for just over two and a half years I have been living my life with single-sided deafness (SSD).

People with SSD are able to hear through their ‘good’ ear, yet have a profound hearing loss in their other. I am thankful that I am able to hear with my right ear, yet living with SSD comes with its challenges.

Sound localisation is a skill enabled by having two working ears, and so with only one hearing ear, I have no idea where sound is coming from. I might hear some music or a noise, but I don’t know which way to look to see what has produced the sound. Trying to find a mobile phone that is ringing results in me wandering hopelessly around my apartment with my ‘good’ ear leading the way and looking to see if I can spot it, usually ending up back where I started and realising the phone had been next to me all along. Locating a music source is also a challenge. There was one occasion where I was walking in the centre of Madrid, where I live, and I could hear a busker playing the guitar and singing a Bob Marley song. Whilst gazing around to see if I could find the owner of the interesting staccato-type singing I stopped in my tracks with a jump as I almost fell over the person responsible; who was positioned in my path, undetected by my gazing view and lack of directional hearing.

Thinking that all sounds are coming from my right has resulted in some scary instances when crossing roads when I haven’t realised traffic is approaching from my deaf side. It has also resulted in some, in hindsight, comical moments. One day, I was sitting on a seat at the end of a row of seats, on the metro train. I thought that I could hear someone playing the accordion somewhere far down to the right of the train. I was feeling relaxed, and as I tried to focus on the tune that was being played, I saw the woman opposite looking at something next to me. I turned to my left, to where she was looking, only for me to jump up in my seat as I let out a little yelp; startled to see the accordion player was actually standing right next to me, on my deaf side.

My boyfriend automatically walks on my right-hand ‘good’ side where he knows I will hear him. This prevents me from having to continuously turn to face him with my ‘good’ ear, in attempts to catch some snippets of conversation. With friends, who often forget which is my hearing side, or for those who don’t consider it, I place myself on their left. When they inadvertently change sides whilst crossing a road or when they stop to look at something in a shop window, I find myself dancing around them; trying to position myself as quickly as possible back on their left side.

When I’m on my own in everyday places and situations I sometimes feel vulnerable. I worry about crossing the road, and not knowing which direction to move out of the way when I hear the siren of an emergency vehicle. I worry about strangers talking to me, and not being able to hear them, or even worse failing to acknowledge them; if they have addressed me on my deaf side. I unwittingly ignore people to the left of me and often notice a frown on a stranger’s face, presumably because I have failed to respond to them or to move out of their way. I find myself constantly scanning my surroundings; checking people’s faces to see if they show any sign or clue that they are speaking to me.

With single-sided deafness, I find it difficult to hear when there are other noises present. Our brains are responsible for selective listening, which is more challenging without the help of a second ear. In a noisy environment, it is difficult to focus on a single person’s voice. Socialising can be demanding amongst background noise. In restaurants and bars I have learnt to sit in a corner, or with my deaf ear against a wall and my hearing ear facing the person I am speaking to, in order to have some chance at hearing them in conversation. I have learnt that it is only possible to concentrate on listening to one person at a time.

With my single-sided deafness has come tiredness, frustration, loneliness within groups of friends in conversation, and super-sensitivity and hyper-reactivity; meaning I am startled easily by unpredictable or sudden noises. I also have difficulty multitasking and find it hard to perform another task while listening.

Yet, I have found that being able to see some humour and positives, however small, in some of the situations I find myself in, can help me stay positive. For instance, with single-sided deafness, I can block out sound during the night or when having a nap, just by putting my ‘good’ ear to the pillow. I only need to use one earphone when listening to music, and if there is someone I don’t want to listen to, I can make sure they are sitting on my deaf side.

If you or someone you know is also living with SSD, I’d love to hear from you. Please feel free to leave a comment and share some of your experiences.

 


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64 comments

  1. I had the same exact thing happen to me in March 2015. I was 45. I’m a high school teacher and with COVID, I’m finding it hard to function. Just found your blog today. I could have written this post.

    Liked by 1 person

    1. Hello Lori,
      Thank you for your comment. I am sorry you are finding it hard to function. With everyone wearing masks, communication can be really difficult.
      I run a small Facebook support group for people with all types of hearing loss. Many of the members have experienced sudden hearing loss or have SSD. The group is a space to share your story, to ask questions and to support others going through similar things. If you are interested in connecting with other people with hearing loss, here is a link to join the group: https://www.facebook.com/groups/1422427341250724/
      Best wishes,
      Carly.

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  2. Hello, Carly! I am delighted to find your work! I have been Hard of Hearing (and single-sided Deaf) since early childhood. I’m quite embarrassed to say that it’s taken me decades to find the Hard of Hearing community (in the words of Brene Brown, “I thought it was just me”). I’m currently learning as much as I can — I’m librarian to our College’s American Sign Language Department where I’ve begun taking ASL classes myself — and hoping to become an advocate and ally to the Deaf and Hard of Hearing community. Thank you for all your work!

    Liked by 1 person

  3. Hi Carly,

    Just found your site while looking for hearing aid replacement parts for my Oticon. I have a similar story as yours. Way back in 2009 I had a liver transplant due to liver cancer that developed because of a Hepatitis C virus I contracted probably in the 1960’s through a blood transfusion. One of my first outings after this surgery was that my husband and I went to Laughlin NV for a weekend (think maybe 50’s Las Vegas) and while there just relaxing seeing the sites, doing a little gambling, eating, resting, and just plain relaxing, I woke up early the morning we were to start the drive home to CA and I felt funny, like kind of unsure of walking and a little bit dizzy. After going to the bathroom, my husband told me to go back to sleep and I would feel better when I woke up again. He told me if we had to stay another day we would, just relax. I was afraid I was having some sort of allergy reaction and was fearful of driving through the desert in this condition. When I woke up again, it didn’t seem as bad as before so we proceded to go home. I had a doctor’s appointment the next day and decided to mention it to her as I still was feeling unsure of my balance. She had an audiologist in the office and this woman checked me out and I found out then that I had lost hearing in my right ear. The audiologist recommended that I go see a Hearing specialist so an appointment was made. I went home relaxed and napped and thought everything would be okay. The next morning I got up and promptly fell into a dresser, was sick to my stomach and felt like I was going to throw up all at the same time. I went to this new appointment and was told there was nothing they could do for me and that hearing aids wouldn’t help me at all. I was very discouraged. I lived many years just with no help at all and with no hearing in my right ear and with constant tinnitis, I finally found some info somewhere where they recommended a hearing aid to help with tinnitis and started to look into for myself. Now it’s 2021 when I’m doing this and getting someone to explain what a hearing aid can and can’t do is an impossible thing. I spent so much time just trying to find info on what could be possible for me and what I have to learn to live with. I feel like the hearing aid business as a whole does not want anyone to really understand it and there are so many different options and they keep coming out with a lot more new hearing aids and when you have a problem it seems like that answer is to always be buying a new product instead of trying to keep the original one working after a rather large investment of money to buy that origin one.

    Liked by 1 person

    1. Hi Pat,

      Thank you for your comment and for sharing your story. I’m sorry to read that you were told that there was nothing you could do to help your hearing loss or tinnitus.

      For help making more informed decisions around hearing technology, I recommend the website https://www.hearingtracker.com/, which I write for occasionally. They compare hearing aids and highlight their various features. I hope you find the website helpful.

      Wishing you all the best,
      Carly

      Like

  4. I lost the hearing in my right ear when I was 9 after having a Mastoidectomy due to Cholesteatoma. Although I knew I was deaf, I spent the next 30 years of my life confused as to why I was that weird guy who just wasn’t into socializing. I’m glad we now have a greater understanding of unilateral hearing loss and understand the potential psychological affects it can have on a persons life.

    Liked by 1 person

  5. i was born with SSD and i have been living with it for my entire life. I am now 20 years old and i have mostly learned to live with it. Even though it can be tough sometimes when in large crowds. I try to make the best of it. It does become easier and easier to focus on hearing others, you just have to get used to it. I usually try to avoid going to loud events like concerts.

    Sadly there isnt anything doctors can do(yet) since the problem lies deep within my left ear. The doctors say that the connection between my ear and my brain just isnt there. Hopefully there will be something in the future to fix it.

    I have never been part of a deaf/hearing loss community and im embarassed to say that i didnt even think about the fact that they would exist

    Liked by 1 person

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