As a musician and amateur sound engineer, the higher tinnitus was fairly manageable, but developing the lower tinnitus was pretty devastating and has largely ruined my ability to hear and mix properly. I've needed to read lips for several years now, as a double-check against what I'm hearing. Phone calls are very difficult, but the increase in video calling has helped.

Don't be me. Take care of your ears. Also, remember that noise-cancelling is NOT hearing protection. Buy some musician-quality earplugs (you still hear everything, it's just quieter) and have them with you at all times. Use them even when you think it makes you look dorky at the club or concert or sporting event. It's not worth the psychological torture that is tinnitus, I assure you.

So I’ll share my positive anecdote.

I’ve dealt with it for over 10 years, and while I can’t imagine how happy I would be to find an effective treatment, I’ve learned to cope, and do what I can to protect hearing going forward.

And once you realize you can cope with it, it makes future coping easier. I have bad days, but by knowing they’re just bad days and that I have mostly good days helps the bad days also not so bad.

Try to focus on the other good parts/distractions about life.

Hope that helps someone.

I do hope there is a cure on the horizon.

But as this is HN I wanted to share a technical detail: The device used for the stimulation is pretty new and, as all medical devices are, pricey. It is connected to a laptop through USB-C but not only for data, it‘s completely powered through it. Sounds neat, right. But what happens if either by accident or not knowing any better you unplug the cable? Then it dumps all the stored charge through the electrodes into whoever has them on their scalp at the moment. It‘s VERY uncomfortable and I am shocked (hahaha) that a device like this has such a failure mode and that this is even allowed.

YMMV but always worth a try!

Have ~10KHz very weak tinitus in left ear, and ~70Hz stronger but still "weak" tinitus in right ear. That combined with feet/legs/hands parasthesia (vibrations mostly, aka mostly no pain). It gets seriously worse during hot summers (reached tinglings and cramps). Ruled "idiopathic" by the docs (MRI scans show nothing "significant") but back and neck seem to be the culprit. Found only one med effective on it, and that only for the first months once the med concentration in the body is "enough": Amitriptyline (dangerous stuff, 2 times I tought it was about to kill me, because it seems my current biology is very sensitive to it). Did stop taking it because of the side effects and worn out effectiveness over time (and like 0 effective during hot summers). Impact, silence is the enemy: Falling asleep happens only when exausted, and intellectual focus is challenging. Usually, I am looking for locations with some some sort of "blank noise". When the parasthesia is too strong, I walk. Basically, only activities which are strong attention attractors are ok. Mindset: Accepted my disability for the rest of my life after years of looking for the causes, and still monitoring any news about it.

I have the equivalent of two jet engines in my ears, including the characteristic phase shifting. Managing it is basically mentally "locking it out", which has the side effect of becoming insensitive to real-world audio stimuli.

So when my SO talks to me when I'm off guard, I only realise that mid-sentence before I "unlock" my perception. The first few words are usually the essence which are lost, so I need to ask her to repeat the first few words.

But as a non-Tinnitus she does not understand, gets annoyed, and starts shouting the whole sentence exaggerated articulated which kinda hurts both my ears an feelings, gets me annoyed because I explained why hundreds of times. Basically ruining the the moment for both of us, especially in public.

Fighting over it isn't worth it, so now I'm more into nodding friendly and hope she doesn't notice that I didn't get what she said, which creates a whole new bunch of problems.

That was the one and only day I heard silence and it drove me crazy. I constantly made noises to make sure I wasn't completely deaf. The one thing I remember vividly actively hearing was the turning of a door knob. I could hear all the little individual metallic sounds instead of a single generic crunch.

The next day, the ringing was back and has never left despite further ear cleanings. I am 49 now.

There was no treatment then and there is no widely available treatment now. AFAIK the cause of it is poorly understood and there can hardly be an answer is we don't know what questions to ask.

Do I wish this study leads to one? Absolutely. I would pay an equivalent of a used car to get rid of my tinnitus. Probably not more than that since my case is thankfully rather mild.

I think getting used to it is unfortunately the only way out. For the first few years, I've had occasional panic attacks. Nowadays, I am aware of it in the morning when I wake up, and later only when I stop to check if it's still there (it is).

Circling back to treatments, I do wish that one eventually comes out. My tinnitus has not become worse over the years but I suspect it might once I exit the middle age.

Does anyone else have tinnitus in specific locations?

For me, I swear I am constantly hearing high-pitched screeching, but only in apartments or offices. If I’m outside it goes away — even if it’s very quiet.

Now that I've read that noise cancelling doesn't protect from sound, I'll only use this for sleeping and use actual earplugs in other situations.

https://pubmed.ncbi.nlm.nih.gov/?term=tinnitus&filter=pubt.c...

Got tinnitus due to injury to auditory nerve.

Those who are just starting with overcoming Tinnitus - Make sure to give time. Human brain is amazing at latent inhibition, ie capability to ignore things that it learns to be irrelevant.

That is your largest medicine. In my country, there are sugar cane refineries/factories that emit very pungent small that is very strong and spans across miles in radius. People who live around in that vicinity develop ignorance to the smell in a matter of months.

All I can say is - whether it is a decision to try some experimental medication or surgery, or otherwise - give it 9-12 months time after you acquired Tinnitus. There will be bad days, but there is a good chance that you will realize you could live with it. With an inconvenience (for comparison) as severe as your car's "check engine" warning beeping every 10 seconds.

Tinnitus was keeping me awake at night, and like others said it made it hard for me to follow conversations in pubs/bars/busy places..

Then one day I read about the massive artery next to your ear, which you cannot hear (OK sometime you can when you are running or have a pounding headache) but the realisation that this sound was always there but you don't hear it, was amazing for me.

Within a week I'd largely tuned it out. It is still there and if I think about it I can always hear it. But it no longer upsets me and is just a thing and not an issue for me.

One of the things I've noticed people struggle with regarding any chronic illness is constantly feeling like they are "supposed" to be feeling fine and have more distress worrying about some perceived gap between their actual life and how they imagine life should be then the ailment itself(this obviously carrier over to things other than chronic illness).

Letting go of this imagined alternative life is the biggest first step towards accepting and dealing with tinnitus. I have tinnitus the same way I have all my other features, positive and negative. That's just the life I have and there is no alternate life out there.

I do still get a kick out of the look of horror on people's faces when I tell them I've had constant, changing frequency, ringing in my ear for two decades.

I also have tinnitus, mostly in one ear. It's difficult to have a conversation in a noisy place. My partner's voice frequency seems to resonate with the tinnitus ringing, so it's difficult to hear her sometimes!! I've had it for years but five years ago the ringing wound me up so much I went to the doctor. They did various scans but couldn't find any discernable cause. The doctor suggested I just try and live with it. Not really what I wanted but with no other options I took his advice.

I put in a fair bit of effort to try and cope with it and actually, now, most of the time I don't realise it's there. Only when 1) Someone is talking to me in a busy pub or restaurant or, 2) watching the TV on low volume in the evening, do I really notice it.

Getting to sleep used to be a nightmare but I genuinely don't have any problems now.

My advice would be to chillout and forget it's even there, and when you do notice it, just accept it and carry on. It could always be worse. Good luck to all tinnitonians.

It's easy to wind yourself up about, so I think most of what I've done to cope is just learn not to wind myself up about it.

I got rid of my tinnitus - which was not even the goal, it was not too bad compared to all the many other issues I increasingly had and which forced my hand - after removing the remaining amalgam fillings in my teeth and starting chelation treatment against mercury poisoning. The diagnosis was lab-supported (fortunately, there is no guarantee to get significantly elevated blood levels for low-level long-term chronic exposure) at a university clinic by a doctor not interested in making money from me, and not making any promises, always referring to this or that study for anything he suggested, and who also did not believe all my issues could be explained by the tested low-middlish mercury levels. With the last one he gave up after not finding anything else and the unexpected overwhelming success of chelation. For example, a nodule in the enlarged thyroid that I had had for two decades disappeared within weeks after i felt a lot of strange activity in exactly that area after the fourth DMPS chelation treatment, which made me go to see an endocrinologist to check again. That endocrinologist did not believe what he found - which was nothing - and had me lie down again and repeated the ultrasound, while consulting and comparing with his old printouts to make sure he checked the right area.

With my albeit limited bio-chem background I am well aware that there's thousands of ways for things to go wrong, so I'm definitely trying to advocate everybody with tinnitus has the same problem.

A list of conditions that I had, increasingly over the years, that all went away completely through chelation, is below.

Note that I thought of myself as "healthy" all those years (I would run a half-marathon without any effort and without pushing myself, just for fun), because I considered all my issues as normal part of life and had a brain-block preventing me from thinking about it.

- Jaw bone structure and integrity damaged in four sections - all of them where there had been amalgam fillings. Discovered when a doctor tried to inject something into the mucosa with insignificant pressure he ended up deep inside the jaw bone. He then tested and found the four sections.

- Tinnitus: I had a mild one, I only really noticed it at night. I didn't like it but I thought I could live with it. Well, turns out I won't have to: it is gone.

- Warts on the soles of my feet and on fingers. Their number steadily increased until I started chelating

- From year to year catching the cold was a worse and worse experience. The last 2-3 years (before chelating) when I got a cold in November I'd not get completely rid of it until April/May the next year!!! Needless to say, I don't care about colds any more. If I get one it lasts a day. - More and more times of being tired and needing sleep despite having had enough (sleep). I did LOTS of sports, still not enough. Completely gone, I'm never tired now except for the night!

- Phases of depression, esp. in winter: I seriously considered moving far south because I could not take winter any more. I remembered that as a child I had no issues and enjoyed winter, now I had gotten one of those daylight spectrum lamps to help. Completely gone! I have anxiety attacks, but decreasing in frequency and severity, and that's very different from depression.

- Occasional nose bleeds.

- Cramps. Legs, back, head.

- Digestion. HUGE improvement.

- Candida. A doctor even gave me a systemic anti-fungal medicine (I looked pretty yellow afterwards).

- Skin issues, especially on the head.

- Halitosis.

- BIG veins on my lower arms, ALWAYS.

- Lower urinary system/prostate effects.

- Significant brain improvements, which is subjective and I could elaborate but comment space.

- Speech issues: Occasionally (actually quite often, not a rare event) I'd use completely random words, realizing it only too late. People thought it was quite funny. I don't do that any more, and during the worst parts of my chelation (which I had started with some serious mistakes so that it was quite bad at the beginning) I had even more severe issues, and now also with writing (any text that I wrote, when I read it the next day I saw that often I wrote barely comprehensible sentences that made hardly any sense, but I felt 100% sure about them when I wrote them). All gone (or mostly gone? Well, you see what I'm writing here :-) ).

- Sleep. Both finding it and quality - and dreams, they are so very interesting now! - improved significantly.

- Computer worker issues: "mouse arm" and vision problems.

EDIT: You know guys, based on what exactly do you downvote this report of my clinical experience??? My tinnitus gone and the jaw bone structure damage a lie or what? Or that it healed by itself or was "psychological"?