Three Years Later, I'm Doing So Much Better — Tinnitus Does Not Distress Me Anymore

I am not certain of the difference, but I believe that I have ear tinnitus. What is head tinnitus?
Head tinnitus would mean you hear the tinnitus more in your head than one ear or the other. I ask because, if I recall correctly, I think the Schulman protocol is suppose to be more effective for that type of tinnitus? Sorry it's not giving you relief.
 
Hi everyone,

I've been putting this off because I wanted to wait until I was fully habituated, whatever that means, before posting. Also because this forum represents some really desperate times for me, that I wanted to leave behind me. The third reason is that tinnitus is such a non-issue for me now that I almost feel like I imagined the whole drama. It's hard to remember how bad things were and how close I came to the edge.

However, I've decided to post today because I'm going through some unrelated challenges (a chronic pain condition) and I want to reflect on how I've come through bad times before. Tinnitus really taught me how resilient we are, and how terrible times can turn to good ones, even when it seems impossible.

In the middle of the bad times I PROMISED myself and everyone else that I would come back one day and tell my positive story, so here it is.

I'm over three years in and I can truly say that tinnitus does not distress me anymore. Sometimes it pops up and irritates me, and I play rain sounds on my phone to distract myself. I also play rain sounds on a sound machine continuously in my bedroom. However that is mainly out of habit and when I travel I don't bother bringing the sound machine. It is no longer a major consideration in my life.

Yesterday I was lounging on the sofa reading and playing on my laptop in total silence, and the tinnitus was like a faint static buzz. Once upon a time it would have brought me to tears.

Tinnitus volume is a tricky thing to pin down, but I will say that I don't think mine has exactly quieted with time. It's more that my brain doesn't focus in on it anymore and it fades into the background. Back when things were bad I could hear it whilst driving on the motorway with music on and sometimes with the windows open. It's high pitched and it could cut through just about anything.

Now something simple like a computer fan or a fridge humming or someone talking is enough to distract me from it. Every now and then I'll have a spike where it intrudes a lot. I'll put on a load of white noise and some music and just keep on with my life, and eventually it passes. I am confident now that things will get easier with each year that passes.

I also want to reassure people who have been in this for a while that it can take a long time to adjust, and just because you are a few years in doesn't mean there is no hope for you.

Months 5-8 were the worst for me. I had to take time off work and I was struggling to look after myself. I didn't want to be here anymore. Weirdly, I think CBT is what saved me. The therapist convinced me, over weeks of arguing, that it was up to me to make the choice to stop listening to the sound. After that, I got tough with myself and every time I walked into a new environment, instead of looking for the sound I would flick myself hard on the face with my fingernails and say "stop". The "Back to Silence" thread by @I who love music really helped me with this idea of redirecting my focus. On bad days I would go in the kitchen, put on the radio and as many appliances as possible, and cook up a storm. The activity and all the noise were enough to keep the panic at bay.

For about the first year or so I was pretty much moving all the time. I didn't want to give myself time to panic or think or listen for the noise. I was always running, and yes it was exhausting but I promise you, it didn't last forever. Nowadays I spend a lot of time in bed thanks to my other condition, and the tinnitus is barely an issue. I never ever ever ever thought this would be possible for me, but it happened.

At the end of year one I was anxious and strung out and exhausted, but I felt like I had some measure of control over everything, and I was starting to enjoy aspects of my life again.

During year two the tinnitus became less and less of an issue for me. I still had spikes where I was quite distressed, but I got better at dealing with them and I trusted them to pass. My last bad spike was a year ago now, at the end of year two. I really felt like I was back at square one, but it did pass, and I feel like those days are behind me now.

Just remember that recovery is extremely non linear, and you will have days where you feel like you've made no progress at all, but I promise you, year on year things will get better.

It's amazing to me that a few years ago I wanted to get cancer and die, and now I have the same tinnitus but I barely think about it. We are so much stronger and more adaptable than we imagine.

I want to thank @I who love music aka Terry for telling his story and for always being here with encouragement and @billie48 for telling his incredible story, which I read over and over and over on bad days, as well as all the other people who pep talked me and offered support when I truly felt I was losing my mind.

To the people who are new to this and still struggling, I want to say I see you and I know how much it sucks, but please understand that one day this will just be a bad memory. The brain is an incredible thing, and you can and will adjust. It just takes lots and lots of time and patience.

In terms of what I actually did, well I tried everything but I think the keys for me were:

White noise/background noise. In the first year I found all the white noise type things so annoying that I thought just listening to the tinnitus would be preferable. This was a mistake. With time and patience and trying different things I finally got used to having background noise on all the time. I also had to let go of the idea that I would be able to find a noise that could completely cover the tinnitus. On bad days it can find its way through anything, so really your best bet is to just try and dilute the sound and provide something else for your brain to focus on.

Distraction and refocusing. I'm honestly grateful to tinnitus for forcing me to take on a bunch of new hobbies and social activities. Even when all I wanted to do was lie in bed and cry about tinnitus, I would force myself to do activities, and slowly slowly the interest and pleasure in other things came back.

Understanding that tinnitus is a disorder of attention, and ultimately you are the one in control. This is so hard to accept at first, but it's so so important. The more anxious attention you give to the tinnitus, the worse it will be. That's just a fact. You can make it the main focus of your life, or you can fill your life with other things and allow tinnitus to be an annoying but small nuisance in the background.

Time. Can't emphasize this enough. This shit takes time. You're essentially retraining your brain, and it's not something you can just do. It can take months and years of slowly adjusting to this new normal. But you will get there. I promise!

Love and good thoughts to everyone here.

Lizzy
Xxx
Hi Lizzy,

Why do you feel not masking was a bad idea for you? I find it annoying at night while sleeping. It seems to disturb my sleep.

You sound very positive!
 
Hi Lizzy,

Why do you feel not masking was a bad idea for you? I find it annoying at night while sleeping. It seems to disturb my sleep.

You sound very positive!
Hi there!

Sorry for the slow reply! I don't come here anymore, since I'm doing so much better, but I try to check this post from time to time.

If you can sleep okay without masking, then I say stick with what you're doing.

The reason I say not masking was a bad decision for me is I think it prolonged my suffering unnecessarily. I had very bad insomnia and I would spend a lot of time lying awake listening to the tinnitus, and going out of my mind.

For me - once I figured out the right way to mask - it took the edge off of the tinnitus and made me less panicky. When I wasn't masking I would enter my bedroom in the evenings and the quiet would hit me, and the tinnitus would hit me, and I would get super anxious, and basically it made my bedroom an unsafe space. Once I started playing rain sounds from a sound machine 24/7, I would enter the room and hear the rain sounds and it kind of reassured me that I was safe and wouldn't be left alone with the tinnitus. Hope that makes sense!

A few things that helped me with masking, in case you decide to explore that route:

1) It's worth getting a sound machine. I have an Oasis, that plays a range of different natural sounds like rain, birdsong, rivers and so on. The sound fills the room better than a phone does - it's more ambient - and you can just leave it playing all the time rather than fiddling with tracks on your phone (which just draws your attention to the whole thing).

2) I do also use my phone as backup, either for nights when I'm spiking and the Oasis isn't quite enough, or for when I'm in a different room or house. I have an app called Atmosphere, where you can pick your own sound mixes.

3) The thing I had to learn is that you probably won't find a form of masking that completely eliminates the sound of your tinnitus, and that's okay! Every now and then I would find a sound that covered it up perfectly, but eventually the tinnitus would break through and make me more miserable than before. The purpose of sound enrichment is to distract your brain, not to hide the tinnitus completely. On bad days I would play the sound machine, AND sounds on my phone, AND music, and the combination of sounds kind of jumbled my brain enough that I didn't have to focus on the tinnitus as much.

4) It's worth experimenting to find the masking sound that works for you. I went through so many until I got one that worked. Generally, sounds that closely mimic the sound of your tinnitus can work better at covering it up, but they are also more annoying! So it's about finding a balance. For me sounds like rain, crickets, or a crackling fire are close enough to take the edge off, without being unpleasant. More warm, bland sounds like quiet music or wind don't help at all, and just provide a background for the tinnitus to show up more clearly. At the other extreme, things like white noise/brown noise/pink noise are the best at covering the tinnitus, but they can be very annoying. I'll use those sounds only if I'm having a very bad day and I just want anything to distract from the tinnitus, even if it's horrible!

5) It can take a while to get used to having background noise on all the time. The point is though, it's easier to get used to that than the tinnitus! I'm so used to the sound machine now that I forget it's there. It's just part of my normal soundscape. It runs even when I'm out of the house on holiday or something, because I forget to switch it off lol. But yeah at first I really really resented having to have background noise on all the time!

Hope that helps. I'm happy to answer any more questions :)
 
Hi there!

Sorry for the slow reply! I don't come here anymore, since I'm doing so much better, but I try to check this post from time to time.

If you can sleep okay without masking, then I say stick with what you're doing.

The reason I say not masking was a bad decision for me is I think it prolonged my suffering unnecessarily. I had very bad insomnia and I would spend a lot of time lying awake listening to the tinnitus, and going out of my mind.

For me - once I figured out the right way to mask - it took the edge off of the tinnitus and made me less panicky. When I wasn't masking I would enter my bedroom in the evenings and the quiet would hit me, and the tinnitus would hit me, and I would get super anxious, and basically it made my bedroom an unsafe space. Once I started playing rain sounds from a sound machine 24/7, I would enter the room and hear the rain sounds and it kind of reassured me that I was safe and wouldn't be left alone with the tinnitus. Hope that makes sense!

A few things that helped me with masking, in case you decide to explore that route:

1) It's worth getting a sound machine. I have an Oasis, that plays a range of different natural sounds like rain, birdsong, rivers and so on. The sound fills the room better than a phone does - it's more ambient - and you can just leave it playing all the time rather than fiddling with tracks on your phone (which just draws your attention to the whole thing).

2) I do also use my phone as backup, either for nights when I'm spiking and the Oasis isn't quite enough, or for when I'm in a different room or house. I have an app called Atmosphere, where you can pick your own sound mixes.

3) The thing I had to learn is that you probably won't find a form of masking that completely eliminates the sound of your tinnitus, and that's okay! Every now and then I would find a sound that covered it up perfectly, but eventually the tinnitus would break through and make me more miserable than before. The purpose of sound enrichment is to distract your brain, not to hide the tinnitus completely. On bad days I would play the sound machine, AND sounds on my phone, AND music, and the combination of sounds kind of jumbled my brain enough that I didn't have to focus on the tinnitus as much.

4) It's worth experimenting to find the masking sound that works for you. I went through so many until I got one that worked. Generally, sounds that closely mimic the sound of your tinnitus can work better at covering it up, but they are also more annoying! So it's about finding a balance. For me sounds like rain, crickets, or a crackling fire are close enough to take the edge off, without being unpleasant. More warm, bland sounds like quiet music or wind don't help at all, and just provide a background for the tinnitus to show up more clearly. At the other extreme, things like white noise/brown noise/pink noise are the best at covering the tinnitus, but they can be very annoying. I'll use those sounds only if I'm having a very bad day and I just want anything to distract from the tinnitus, even if it's horrible!

5) It can take a while to get used to having background noise on all the time. The point is though, it's easier to get used to that than the tinnitus! I'm so used to the sound machine now that I forget it's there. It's just part of my normal soundscape. It runs even when I'm out of the house on holiday or something, because I forget to switch it off lol. But yeah at first I really really resented having to have background noise on all the time!

Hope that helps. I'm happy to answer any more questions :)
Thank you so much for taking the time to reply! I am able to sleep without masking. Seems it is at a bearable level. I get spikes often and at 2 months am learning the triggers to avoid. I'm confident it will go away or lessen. I feel allergies are a big cause of my issues. Pollen is very high where I live.

Best wishes.
 
Thank you @Hotspur2931 for the kind words and that my story has helped you in some way towards your recovery. Yes it will take some time to get better. It took me 3 years. There is no overnight miracle in this journey. It takes patience and helpful strategies. Congratulations and thank you for willing to share your success story.
@billie48, I hope you are well, Billie. Think of you often.
 
@billie48, I hope you are well, Billie. Think of you often.
Thank you. Yes I am doing well even after losing hearing on my left ear. Life goes on and I accept the new challenge of hearing impairment. I may apply for a cochlear implant to help restore some hearing. Thank you for your kindness.
 
But the process itself is anything BUT linear, with many setbacks along the road. And days where you feel you are back to square one. We have to keep going, and not give up.
Needed to hear this as every time I'm making good progress I just stumble and worsen. Now instead of blocking it out I focus on the screeching madness.
 
I'm in month 4 and it's destroyed my life.

Desperate to find a happy medium. I'm 57 years old with chronic pain. Tinnitus follows my every step. I can't seem to ignore it.

Really desperate for positive feedback. It's driving me into a deep depression. Currently suffering from insomnia. Would love to hear positive support.

Brian
 
Hey @Brian_ - I wanted to say I'm new to tinnitus too--I'm 2½ months in. My life too was instantly disrupted. I took short term disability from work because I couldn't concentrate. I too spiraled into depression and high anxiety. I got help in the form of medication from a psychiatrist, which is helping with my anxiety and depression and also my insomnia. I think it's really important to stabilize depression, anxiety, and sleep. Are you on any medication to help? I'm sending you positive vibes. You're not alone. I share a similar experience.
 
I'm in month 4 and it's destroyed my life.

Desperate to find a happy medium. I'm 57 years old with chronic pain. Tinnitus follows my every step. I can't seem to ignore it.

Really desperate for positive feedback. It's driving me into a deep depression. Currently suffering from insomnia. Would love to hear positive support.

Brian
4 months is very early days. Most people need at least 1.5 to 2 years to start improving. So, you need to hang in there.
 
I'm in month 4 and it's destroyed my life.

Desperate to find a happy medium. I'm 57 years old with chronic pain. Tinnitus follows my every step. I can't seem to ignore it.

Really desperate for positive feedback. It's driving me into a deep depression. Currently suffering from insomnia. Would love to hear positive support.

Brian
Hi Brian,

I'm sorry to hear that you're suffering so much. I've been exactly there and I know what it's like. The truth is that one day you will look back on this time and you won't be able to wrap your head around how you got so low because of tinnitus. You're in survival mode right now and that's ok. Please just get through the next hour, the next day, whatever. Do that over and over and over. And one day I promise you'll find yourself getting through the weeks and then the months, and then one day you'll be like me looking back three years and thinking "huh, what even was the big deal?"

It sounds crazy but I promise it's possible, and it will happen for you too.

Insomnia is the WORST, and that's what made me not want to be alive anymore, around the 5-8 month mark. I have chronic pain too, but nothing brought me as low as those months of loud screeching and no sleep. But I got through it, and you will too, and now it seems like a bad dream.

Getting your life back after tinnitus is a gradual process, with lots of tiny breakthroughs and realisations along the way. It doesn't happen overnight. But at each stage there are things you can do to support yourself and keep moving in the right direction.

Right now you sound pretty desperate, and that's when you need to reach out for help. At one point I was seeing multiple people a week - therapist one day, massage another day, acupuncture another day. It's not so much that these things fix the problem, as that when you're in such a desperate state you need to be reminded that you're not alone, and you need little checkpoints, things to look forward to throughout your week. Massage is good because it takes you out of your head and into your body a little bit.

I also took a LOT of hot baths and cold showers. The strong temperatures release endorphins, calm down your mind a bit, and ground you into your body. It won't fix anything, but it will take the edge off a little bit, and at this stage every little helps.

Exercise is also good, if your chronic pain allows. Anything to get the happy hormones pumping.

Also please reach out to friends or family if you can. Tell them what's going on, and get people to keep you company. Sometimes I just wanted to push everyone away and stay in my misery, but a bit of light socialising can help bring you back into the real world and raise your mood.

Distraction is good, and I know you'll be thinking "but I can't distract myself for the rest of my life", but trust me you won't have to. Back when things were bad my main way to distract myself was cooking with the radio on loud, the outside doors open, and sometimes some white noise playing as well. I needed the activity, smells and sounds all going on at once, just to keep the panic at bay.

If you need to rest and can't distract yourself with activity, try LOTS of sounds. So open the window, put some music on or a podcast, AND play some type of white noise or nature sounds. I know it's exhausting when you just want silence, but I found that it was a whole lot better than just listening to the tinnitus and panicking. Even visual distraction can help. If you have a garden or a balcony maybe get some colourful flowers. Or whatever it is that you're into. I know it sounds trite but it's really about giving your brain something, anything else to engage with that isn't the tinnitus. Little by little it does help, I promise.

I also played a LOT of games on my phone. It was easy enough that I could manage it even when in distress, but engaging enough to stop me spiralling. I wasn't able to read or even watch TV, so I just played these games over and over, for hours.

These days, if my tinnitus bothers me (which is rare) I can distract myself with a book, or a bit of background noise on my phone, or even just thinking about something else.

You've got this, Brian. There are millions of us who have been exactly where you are and come out the other side. You will get your life back. For now, just concentrate on getting through the days. That's all you can do at the moment. As they say, "the only way through is through".

I'm happy to answer any questions or offer any more encouragement if I can!

All my love,
Lizzy
xxx
 

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