Reactive Tinnitus — Removal of Reactivity. Is It Possible?

Weird. I've heard of benzos causing tinnitus if one stops them abruptly but I've never heard of it causing reactive tinnitus. Most people report it cuts their volume down. Strange but I guess meds can do all kinds of things.
I did abruptly stop them after 4 years of use.

People who have gotten reactive tinnitus from benzos (I'm not pretending to know their whole story):

@RaZaH
@Brian P
@Kristen Aber

Countless people on BenzoBuddies.
 
Yes. It's very loud. Constantly high hissing that I can even feel physically in my neck and ears. And it gets worse with noises.
The way I would describe mine is both my ears have an epileptic fit of loud fizzing when exposed to a constant sound, which only needs to be 30 dB too. I'm 11 months in.

Is your tinnitus bilateral? The only thing to help me has been Clonazepam, which I've used since April. I've used it sporadically so far (30 mg total) since acquiring it mid-April. I originally had ear pain for the first 4 months.
 
My tinnitus is loud all the time, high pitch hissing, but it gets louder with every sound and will compete with everything to be louder to a point that it won't let me hear anything else.

And then there are the distortions where songs I used to know don't sound the same anymore.

But coming back to reactive tinnitus. I can't even scratch my head without making my tinnitus increase in volume. I would be ok if my tinnitus would stay at its baseline, but it doesn't. It's just hell. I'm 3 months in with these conditions.
Everything I kept quoted above is very similar to me, 19 months in now to the reactive and hissing part, along with a rumbling hum I have had for 20 years. Joy of life ruined, music ruined, audiobooks ruined, doing hobbies I used to enjoy ruined.
 
Joy of life ruined, music ruined, audiobooks ruined, doing hobbies I used to enjoy ruined.
Music soothed my mind and calmed me better than any drug could. To have that taken away is so cruel, especially not being able to wear any type of headphones.
 
Music soothed my mind and calmed me better than any drug could. To have that taken away is so cruel, especially not being able to wear any type of headphones.
It can be worth experimenting with a few speaker types. I eventually invested in a pair of near-filed monitors like these. The sound is much less intrusive to hyperacuse-y ears than laptop speakers for example (even expensive MacBook Pro ones) that were driving me crackers.
 
It can be worth experimenting with a few speaker types. I eventually invested in a pair of near-filed monitors like these. The sound is much less intrusive to hyperacuse-y ears than laptop speakers for example (even expensive MacBook Pro ones) that were driving me crackers.
Thanks @UKBloke for the recommendation of some quality speakers :) I do still listen to music, just at a much lower level than my pre-tinnitus days. But not on my headphones anymore :( I just loved my headphones and being in my own world. It helped me destress.
 
It is the same thing with mine. My tinnitus is caused by ototoxic medication, not by an acoustic trauma. My tinnitus is loud all the time, high pitch hissing, but it gets louder with every sound and will compete with everything to be louder to a point that it won't let me hear anything else. Forget about watching TV. After a few minutes, I struggle to hear anything that is not just the actors talking and the music. And even the dialogues and scores get lost into my tinnitus after a while.

And then there are the distortions where songs I used to know don't sound the same anymore. And that the fun starts when I'm near a light bulb or any electronic devices emitting low frequencies. I hear those frequencies as popping Krispies. Then there is the microphone feedback effect I hear over running water, fans, ACs, fridges, microwaves, city traffic, etc. How do we deal with that?

But coming back to reactive tinnitus. I can't even scratch my head without making my tinnitus increase in volume. I would be ok if my tinnitus would stay at its baseline, but it doesn't. It's just hell. I'm 3 months in with these conditions.
Are things any better, @Aline Mohymont?
 
Are things any better, @Aline Mohymont?
Actually, no. My reactive tinnitus is off the roof. I went to see an otologist that specializes in hyperacusis and reactive tinnitus. I don't know what all the fuss is about the use of the "reactive" term. Doctors are using it to describe the type of tinnitus I have. Anyway, my tinnitus is a category 4, level 10. So, it's bad. The only thing that got better is my hyperacusis. I did sound therapy, though.

Yes, it's in both ears. High pitch hiss, plus a church bell in the left with occasionally Morse codes and the "eeeee" in the left.

And again, my tinnitus was not the result of a sound trauma; it was a combination of ototoxic meds (Neomycin, Azithromycin, and Methylprednisolone).

It is just hell!
 
The only thing that got better is my hyperacusis.
@Aline Mohymont, I'm almost 1 year in with tinnitus, pain hyperacusis for 5-6 months. Loudness hyperacusis almost back to normal (80-90%). Reactive tinnitus the same or slightly worse but unstable with debilitating days and bearable days. Waking up is depressing, although I sleep 6-7 hours on 30 mg Mirtazapine.
 
Actually, no. My reactive tinnitus is off the roof. I went to see an otologist that specializes in hyperacusis and reactive tinnitus. I don't know what all the fuss is about the use of the "reactive" term. Doctors are using it to describe the type of tinnitus I have. Anyway, my tinnitus is a category 4, level 10. So, it's bad. The only thing that got better is my hyperacusis. I did sound therapy, though.

Yes, it's in both ears. High pitch hiss, plus a church bell in the left with occasionally Morse codes and the "eeeee" in the left.

And again, my tinnitus was not the result of a sound trauma; it was a combination of ototoxic meds (Neomycin, Azithromycin, and Methylprednisolone).

It is just hell!
Hey @Aline Mohymont, so the sound therapy you did didn't help the reactivity at all? Others on the forum have said their reactivity improved as their hyperacusis improved.
 
Hey @Aline Mohymont, so the sound therapy you did didn't help the reactivity at all? Others on the forum have said their reactivity improved as their hyperacusis improved.
Not in my case. But then I am a really severe case.

My tinnitus loudness has been rated a 10 on a 0-10 visual analogue scale. My tinnitus functional index is a 92.1 out of 100. And I have type IV tinnitus (which ranges from I to IV) based on Jastreboff categorization. This is characterized by bothersome tinnitus which reacts to sound exposure. I have dysacusis on top of everything (noise distortion).

My case is by far the most severe on the scale. If you wanna know what hell is, imagine walking in my shoes. There is no escape from this one. I envy all the people that have regular tinnitus, even loud ones. Count your blessing. Something as severe as mine is rare. So, we can't expect to find any solution.

Fortunately, I don't have a whole life in front of me since I'm already in my 50s.
 
In my case muscle relaxants (Mydocalm) and antianxiety medication (Xanax) both at small dosage every night and under the guidance of a doctor have eliminated my reactive tinnitus by more than 90%. Today I'm enjoying a very normal life.

But they take a few weeks to fully kick in and must be under the guidance of a doctor.
 
Hey @Aline Mohymont, so the sound therapy you did didn't help the reactivity at all? Others on the forum have said their reactivity improved as their hyperacusis improved.
So yeah, audiologists keep saying if you treat the loudness hyperacusis, your reactivity will go away. That may be the case with some but not all as you see on this thread. @Brian Newman did sound therapy and improved his LDLs until he developed noxacusis. I did sound therapy and improved my LDLs but my reactivity is worsened big time.

It took me a good while to realize digital audio was messing me up. If you're in the category of constantly reacting or getting pain from any digital audio, I would stop imo. I tried better quality speakers too.
 
So yeah, audiologists keep saying if you treat the loudness hyperacusis, your reactivity will go away. That may be the case with some but not all as you see on this thread. @Brian Newman did sound therapy and improved his LDLs until he developed noxacusis. I did sound therapy and improved my LDLs but my reactivity is worsened big time.

It took me a good while to realize digital audio was messing me up. If you're in the category of constantly reacting or getting pain from any digital audio, I would stop imo. I tried better quality speakers too.
Thanks for the feedback, @Wrfortiscue. I did not dive into the TRT at this time. I told her I'd let her know if I was interested in the future.
 
My tinnitus is still reactive 13 months in. The baseline is probably higher but it's so variable (3-9/10); noise-induced tinnitus tends to be this way, it seems. I'm grateful the pain in reaction to external sound has gone away but when listening to the radio and it causing your ears to go into an epileptic fit takes the fun out of it.

I did a TFI (Tinnitus Functional Index) yesterday and got 75-80 or 190 points, depending which version you use, meaning tinnitus is a very big problem for me. The TFI would be even higher if it weren't for the fact that I fall asleep OK and sleep 6-7 hours per night.
 
In my case muscle relaxants (Mydocalm) and antianxiety medication (Xanax) both at small dosage every night and under the guidance of a doctor have eliminated my reactive tinnitus by more than 90%. Today I'm enjoying a very normal life.

But they take a few weeks to fully kick in and must be under the guidance of a doctor.
Hey @TinniGone, I am on a very small dose of Ativan in the evening which helped the reactivity more at first, now not so much. Do you feel like the muscle relaxer was a notable game changer with regards to the reactivity when taken with the Xanax?
 
Hey @TinniGone, I am on a very small dose of Ativan in the evening which helped the reactivity more at first, now not so much. Do you feel like the muscle relaxer was a notable game changer with regards to the reactivity when taken with the Xanax?
Most likely yes. It is tough to tell to what extent it helped my recovery but for sure it played a role. I took one Mydocalm pill every night (best to be taken in the evening). It must be taken under the guidance of a doctor.

My understanding is that reactive sensitivity (not to be confused with hyperacusis) is due to over excitement of the nerves/muscles around the ear and often linked to specific frequencies. Hence it should make sense that a muscle relaxant helps in addressing it.
 
I did a TFI (Tinnitus Functional Index) yesterday and got 75-80 or 190 points, depending which version you use, meaning tinnitus is a very big problem for me. The TFI would be even higher if it weren't for the fact that I fall asleep OK and sleep 6-7 hours per night.
Mine is 91.1. I don't know how many points. But it is the worst case my audiologist, who specializes in the worst cases, has seen.
 

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