For me it came on same time as hyperacusis. There is definitely a relation, imo.It must be some form of hyperacusis, right?
For me it came on same time as hyperacusis. There is definitely a relation, imo.It must be some form of hyperacusis, right?
That's what I have too. Since last 5 to 6 months, worser last month. The best explanation is broken speakers, along with amplified high frequencies. I sometimes hear only high frequencies end even those are not just amplified but different too, more vivid, they also vibrate, like playing on a nerve... hard to explain. I hear that more if I put music on very low level or when there is background noise like in a car.That can happen with hyperacusis, feeling like sounds are distorted or bad quality, it is like the finer sounds are dampen and the central sounds, the central frequencies, are amplified...
Yes, I had exactly all you describe and more. The distortion took around 5 to 6 months to completely go away. The hyperacusis took 8 months to leave.
For around 4 months it was constant then it become intermittent before I noticed it had gone for period of time and so far has not returned.
I hope things settle for you, I fully understand your struggle, it is really a difficult condition to cope with
I'm right there with you. I've had it over 2 months now. Its gonna settle for both of us though. I know it.
Here's my guesses.
1) loudness hyperacusis of certain frequencies coupled with dips in hearing
2) tonal remapping in the auditory cortex bringing your brain the wrong sound
3) damaged OHCs that have lost their tuning ability
4) damage to the basilar membrane or middle ear bones
Or even a wacky combination of all 4
But if anyone can point me to a definitive answer on that I would love it.
Dunno if this changes your theory at all, but mine I believe is due to damaged nerves via dental work. Also, my right ear is perfect without hearing loss, yet it still has the same symptoms of sound distortion and hyperacusis same as the left, which does have some minor hearing loss on the high end.
Probably was loud, idk. Sound did not bother me at the time though. My ENT says my audiogram isn't consistent with someone who has had noise-trauma. Current theory is something with the tooth caused damage to the auditory nerve on my left side. Either that or an acoustic neuroma, but I am too afraid of the MRI machine to rule that one out.Was the dental work quite loud? Or do you think there was actually damage to the auditory nerve itself, not just the SGN as a result from noise exposure?
Probably was loud, idk. Sound did not bother me at the time though. My ENT says my audiogram isn't consistent with someone who has had noise-trauma. Also there is very little tinnitus in my right ear. Tinnitus is primarily in left ear. I'm seeing dentist again tomorrow because the same tooth has actually been really hurting lately (upper left molar).
In that case, would that Low Level Laser Therapy (LLLT) thing help? Doesn't that target to lower inflammation?I think inflammation is right on the money. I took a week off from work, and the dysacusis got a little better. Went back to work, it got worse. We must be close.
No, work doesn't really stress me. I enjoy my job. I'm sure it's the noise of work that causes inflammation.In that case, would that Low Level Laser Therapy (LLLT) thing help? Doesn't that target to lower inflammation?
Could also be stress of going to work? Or is that part of the inflammation? My symptoms of H and Dysacusis improve by about 70% when I take 0.5 mg Ativan. I try not to take it though.
Yeah, there is a lot of noise nowadays. It is a big problem but nobody wants to talk about it at a political level and do something to fix it.No, work doesn't really stress me. I enjoy my job. I'm sure it's the noise of work that causes inflammation.
Interesting. It is a bit like reactive tinnitus or typewriter tinnitus, but with musical tones. And a bit like remembering a song, or playing it inside your head... like a musical worm.This is audio pareidolia https://hearinglosshelp.com/blog/apophenia-audio-pareidolia-and-musical-ear-syndrome/
I'm in the same boat. Sometimes it is worse, sometimes it is better. And it changes its mind what it wants to react to. Used to get it in the shower. Not anymore. A particular song by mozart used to set it off like crazy. Not anymore. But now new songs do that didn't used to. Right now sitting in bed I hear this tone coming from outside. My gf says it sounds like an idle car. So she just hears the hum, but I just hear the tone.Hey guys, anyone had any good luck with there distortions? Has anybody noticed any improvement in the overall sound and perception of the phantom noises, beeping etc?
My condition follows no pattern that I can identify, but it does seem less intense at times.
Right now I'm a little hung over and anxious and they seem to be firing on all cylinders. So I wonder if there is an element of anxiety there as cause? Anyone relate?
More importantly, has anyone's disappeared?
I'm in the same boat. Sometimes it is worse, sometimes it is better. And it changes its mind what it wants to react to. Used to get it in the shower. Not anymore. A particular song by mozart used to set it off like crazy. Not anymore. But now new songs do that didn't used to. Right now sitting in bed I hear this tone coming from outside. My gf says it sounds like an idle car. So she just hears the hum, but I just hear the tone.
Mine seems to be directly related to my hyperacusis. Both also seem to react to the weather. Colder it is the worse it is. I was in Florida for 3 days over the holidays and both my hyperacusis and distortions were very tame while I was there.
Some people get better, some get worse. No one knows why.
Distortions started almost 4 months ago. Along with hyperacusis and new tinnitus tones that are highly reactive.Thanks for the response. How long have you experienced the distortions for?
What about tinnitus, were you dealt a bad case of that along side it, or is it pretty mild or barely audible?
Distortions started almost 4 months ago. Along with hyperacusis and new tinnitus tones that are highly reactive.
I've had normal non-reactive tinnitus for 11 months now. Before 4 months ago, the non-reactive tinnitus I had had gotten pretty manageable. I miss it.
Both cases happened after getting my teeth cleaned by a hygienist.
Yes there has been improvement. It's been all over the place. First started as just one new tone (reactive). Then over the course of a week I started noticing the distortions. Then the next week I noticed sensitivity to sound. It all got worse the next week after that. Then the following week they all improved dramatically but I had made an audiologist appt. So I went to that. She did an LDL test and she let it get too loud. Next day everything came back at full force. It's been up and down ever since. Better than it was overall. But still not as good as it was before audiologist appt. And like i said before, the things that trigger the distortions have changed to other things. Many times.Wow that's horrible. So the initial cause was the dentist? It must have been loud.
Have you noticed any improvement during the 4 months?
When you say reative does the sound continue after the external noise stops?
Try massaging your neck. Getting the SCM muscles to loosen up. Get a professional massage. Multiple if you have to. Can also massage yourself. There are exercises you can look up on YouTube. Also, if you have bad posture, work on correcting that as well. I believe doing these things have been helping me. Results weren't immediate. Took 4-5 days before I started noticing an improvement. There was actually an initial worsening the first couple days. This actually encouraged me cuz it told me my neck and jaw were a factor.Dear guys do not stress a lot about this, because it can progress. I got this issue at 08.2019, stressed a lot and from 12.2019 these fucking distortions progressed / converted to music. I feel now like crazy, all sounds from ac, traffic are not just distorted with whistling, but playing music. Mentally I'm still ok, but this is horrible
I also had this scary electronic sounding sound in my left ear for a few months due to trying the sound therapy by that David Case. But I think that is mostly gone. Nvm, it's still there. It's just s little less scary sound. It's a Morse code sound that I've always had since 11 months ago. But it seemed to have changed to a higher pitch recently. And got really scary and intrusive after doing that sound therapy for one night.