It has been just over three years since my sudden hearing loss, which left me profoundly deaf in my left ear.
The months following this loss were spent hoping for some recovery. I was optimistic about the possibility of learning invaluable pieces of information from every specialist I met, and was hopeful concerning each new treatment or therapy I tried.
These months were also full of frustration, anger, sadness; difficult feelings that grasped at me with all their strength, making each day a duel to be fought.
Now that three years have passed, and I am confidently dealing with the practical effects of hearing loss, I can look back at this experience with clarity and more understanding about the emotional impact this loss has had on my life,
During the time immediately subsequent to losing my hearing, I didn’t allow my grief to consume my attention. In truth, I don’t think I even realised I was grieving. Instead, practical issues dominated my thoughts.
I was productive and proactive in learning how to function in my new unanticipated state. I wanted to take control of my situation. I focussed on dealing with my noise sensitivity and tinnitus.
I gradually learnt to cope more with everyday sounds. I set myself small targets to work towards and celebrated my accomplishments. I started to go outside and surround myself with difficult sounds, progressively increasing the exposure time with each day.
I discovered where the best places to sit were in a restaurant with regard to limiting background noise, and learnt how to direct my hearing ear towards sources of conversation.
I realised the power of subtitles, which enabled me to access all the dialogue when watching films and TV series. My boyfriend, and close friends and family, learnt to walk on my right-hand side so that I would be able to converse with less effort.
I began to study the movement of peoples’ lips to help me make sense of speech in noisy environments. I learnt my physical limitations. My emotional health, however, I didn’t even consider.
Hearing loss grief is something that medical professionals didn’t talk to me about. No recommendations were given for support groups or information sources. I’m not sure if the absence of emotional guidance was due to the language barrier, or if it generally isn’t offered to patients here in Spain.
Perhaps those affected by hearing loss are expected to search for the type of help they feel will be the most effective for their situation. I haven’t widely verbalised my feelings of the different stages of grief I underwent following my hearing loss.
Only those closest to me know the sadness I have felt. In fact, the impact of my hearing loss grief, and the importance of dealing with it in order to move forward in my hearing loss journey, is something that I’ve only recently started to pay much thought to.
There are so many different types of hearing loss, all that come with their own challenges and strains of grief. I wonder if having the time to prepare for the known gradual decline of hearing with age or a health condition brings any comfort.
Yet, knowing loss is imminent must also present a tremendous burden. My hearing loss was sudden. I had no time to prepare. I had very little understanding of the practical issues regarding hearing loss. I had no awareness of the mental pain hearing loss could bring,
I felt guilty for feeling sad. I was swallowing down grief in giant gulps, trying to dismiss complex emotions. The pragmatic part of my character knew there were much worse challenges that life could present to me.
Then, several months after my sudden hearing loss, I was given some advice from a stranger, who I had briefly connected with online. I was told that, as with any other loss, I would need to grieve my lost sound with the attention it deserved.
This advice proved so important in helping me address the emotional aspects of my new situation, and immediately made it feel acceptable for me to feel sad and allow myself to begin the process of grieving.
I suppose everyone with hearing loss will experience different emotions and stages of grief, and will deal with them in their own unique ways. I had periods of feeling angry. I was angry because I felt that I could no longer rely on my body; it had failed me. I contemplated the fragility of life.
I felt sadness, isolation and exhaustion from missed words in conversations, that used to be so easy to follow. I continuously questioned my feelings as to whether they were a justified measure of grief and then learned to treat myself with more kindness.
The acceptance, which took time, came ultimately when I sought a second medical opinion, and I was told bluntly by a specialist that it would be very unlikely that I would regain any hearing and that this was my new normal. I needed this closure.
I found the most help through my grief by talking to my boyfriend, who provided unfaltering support, strength, and compassion. I confided in him, explaining my feelings and new hearing sensations.
We shared the experience of loss so closely and we found our own way to deal with these new circumstances together. I also reached out to others through writing about my hearing loss journey in my blog.
I corresponded with people who were going through similar situations, and continue to encourage this communication. I now find comfort in being able to offer my advice and share experiences with others. Hearing loss grief remains one of the main topics of discussion.
I am reminded of my lost sound every day. Our senses play a significant role in how we engage with the world. For people, like me, who are accustomed to living in a ‘hearing’ world, our sense of hearing determines how we enjoy music, how we recognise the voices of our friends and family, and how we interact socially.
I don’t want to forget life before my hearing loss and I consciously hold onto memories of past experiences when having the full ability to hear made these times so special – times spent enjoying music festivals and memories of past holidays, when my hearing or noise issues didn’t even need to be considered.
I am proud that I carry a tiny piece of my hearing loss grief with me; an invisible scar. Like other scars on my body – shadows of scuffed knees from playground games, teenage acne, and surgical scars – I regard it with pride. My scars are evidence of victories over health issues. They are evidence of healing.
My scar of hearing loss grief is something I acknowledge every day. Yet, it’s much more than grief or sadness; it’s a little bit of strength I take with me everywhere. My hearing loss grief is part of my story.
Read more of Carly’s articles for us here.
Hi, My name is Carly. I am 35 years old and I am currently living in Spain. I am originally from a small seaside town in Yorkshire called Bridlington, and have also lived in China and Thailand. I am an Early Years primary school teacher, and have been teaching for nearly 12 years. I love spending time with my sister and her boyfriend, walking in the countryside, getting lost in Madrid, my boyfriend, traveling, going out for breakfast, my family and friends, taking photos, listening to music, storytelling podcasts, baking, running, drinking wine, and eating spicy food.
This year I experienced sudden sensorineural hearing loss in my left ear. I have started a blog as a way to inform my friends and family about my progress, for anyone else who is going through a similar experience as me, or for anybody who is interested in learning about this type of hearing loss, and the way it can affect everyday life.
Roger Hankey
December 9, 2019
Well done Carly…Please remember the Kuber-Ross Grief cycle isn’t a once and for all thing. You may return to earlier stages again. Hopefully not as deeply. Be strong.
myhearinglossstory
December 10, 2019
Hi Roger, Thank you for reading and for the comment. Yes, I have realised that I still have occasional times where I experience some of the feelings I had early on during the grieving process. I now feel more prepared for these 🙂
Best wishes.
Arlene Romoff
December 9, 2019
There’s probably a little more to this than people who have lost hearing on one side realize, and why it seems so intense. There may be a physiological reason – and the clue is when people with cochlear implants “go bilateral” – i.e. get a second cochlear implant. Most people report liking finally having two ears, but they almost always report about this feeling of happiness. In my book, “Listening Closely: A Journey to Bilateral Hearing,” I report on this happy feeling – as it feels as if the brain has been searching for that second ear and is delighted (sending happy sensations) when it finally finds it, and it’s delivering sound. So the opposite is likely the case as well – when the brain keeps searching for a second ear, but doesn’t find it sending sound signals, so keeps giving “grief, upset, negative” emotion signals to the brain. I’ve met several people with single-sided deafness, and they all seem to describe something similar. It may be comforting to know that it is real and not imagined, and may have a physiological basis – so isn’t one of those “get over it” type of situations.
myhearinglossstory
December 10, 2019
Hello Arlene, and thank you for the comment.
I find your theory very interesting. The reason I wrote this article was because I often receive messages from people who have had a sudden hearing loss which has left them with single-sided deafness. As you explained, people who have always had two hearing ears, who suddenly have to try and adjust to only having one, often describe feelings of grief.
In this article I wanted to share my experiences of grief following my hearing loss as honestly as possible, so that other people with similar feelings may find some comfort in knowing that their feelings are shared by others going through similar experiences.
I feel like I originally put a lot of pressure on myself to move forward as quickly as possible in trying to get life back to ‘normal’. Yet, what I really needed to do was to take a little time to grieve, understand my feelings, and accept my situation. I think it is comforting to know that these feelings are real and not imagined’.
Your comment has added to my curiosity in understanding the psychological effects of hearing loss, something which I will explore further. Thank you and best wishes.
Selida
January 5, 2020
Hi- this is all new to me, and my situation is quite different. I experienced SSHL two weeks ago. I am a medical professional yet I had to claw my way through the medical system to get the treatment I researched as recommended—high dose steroids. After 10 days of treatment, my hearing has returned to baseline-very good news. However, I already have hearing loss in both ears, so this was especially traumatic. I felt in danger of losing my already fragile hearing.
I can so understand the feelings that go along with this loss- I have felt the isolation, fear and a myriad of other emotions. I am grateful this was not permanent, but I wonder why the public is so uninformed.
In addition, I have noticed that although I hear, my brain doesn’t always interpret what I correctly hear. I finally had an audiologist who is recommending auditory rehab. I didn’t know it was available and plan to actively pursue this. Physical therapy for muscle weakness- why not auditory therapy for the brain/ears?
As with any illness, there is an adaptive process. There will always be challenges along the way, some more difficult than others. I plan to pursue whatever type of brain training is available. I would welcome any thoughts, etc.