Electrical Head Buzzing Tinnitus — What Has Helped YOU?

I came off it but then had problems. Now I'm on Amitriptyline 50 mg. It has helped a bit my head tinnitus but not my ear tinnitus.
And then there are people like @Johnny Karate who has less head noise and no ear noise with higher dose Naltrexone.
I came off Nortriptyline hoping I would be ok, but the insomnia came back so my doctor appeared to put me back on it, but due to COVID-19 he did it over the phone and when I collected them from chemist it wasn't Nortriptyline he had prescribed, it was Amitriptyline, but it is helping, however not in the ears due to Meniere's disease.
I always wondered if you have ever considered the LDN (Low-Dose Naltrexone) given the speculation that Meniere's Disease may have an autoimmune component?
 
I came off it but then had problems. Now I'm on Amitriptyline 50 mg. It has helped a bit my head tinnitus but not my ear tinnitus.

Love, Glynis
So you still have tinnitus all over your brain, or maybe just a tone or two in the middle part of the head? How do you cope with it? It is hard because it can't be masked properly and is felt as well.
 
I'm only on 10 mg of Nortriptyline which is somewhat low - that helped the central pure tone "whistle" sounding tinnitus in the middle of my head but it did not seem to help the central "electrical" zzzz sound. But I am a low dose so I wouldn't say that's definitive answer on whether it helps with the electrical sound. I don't want to go up on the dose because it's a bit drying (throat, eyes) for me however some people don't have that issue with it.
 
I'm only on 10 mg of Nortriptyline which is somewhat low - that helped the central pure tone "whistle" sounding tinnitus in the middle of my head but it did not seem to help the central "electrical" zzzz sound. But I am a low dose so I wouldn't say that's definitive answer on whether it helps with the electrical sound. I don't want to go up on the dose because it's a bit drying (throat, eyes) for me however some people don't have that issue with it.
What would be the mechanism of Nortriptyline helping tinnitus?
 
What would be the mechanism of Nortriptyline helping tinnitus?
I'm mot an expert in this area and I don't want to say anything that will influence anyone's decisions to take or not take certain medications. One thing you can take away from this is that you should never want to stimulate the 5HT2A receptor as it is implicated in cause or worsening of tinnitus. This seems to be the case why some of the SSRIs make people worse (however there are some cases where people have improved tinnitus on them). This goes to show us there are still a lot of questions about medications that even the doctors dispensing them can't answer. That alone is pretty scary...
 
So you still have tinnitus all over your brain, or maybe just a tone or two in the middle part of the head? How do you cope with it? It is hard because it can't be masked properly and is felt as well.
I have dual purpose hearing aids with built in maskers.

Love,
Glynis
 
Anybody figure out their head tinnitus? Mine started in the ears and centralized to the brain after about a month after onset.
I came off Nortriptyline hoping I would be ok, but the insomnia came back so my doctor appeared to put me back on it, but due to COVID-19 he did it over the phone and when I collected them from chemist it wasn't Nortriptyline he had prescribed, it was Amitriptyline, but it is helping, however not in the ears due to Meniere's disease.

Love, Glynis
I think Amitriptyline and Nortriptyline have antihistamine effects?
 
I believe they do have antihistamine effects.
You stated that your tinnitus started in your ear/s and centralised, but still hear it in your ears from time to time.

I have always wondered what is going on with my tinnitus.

I have a centralised gas leak/hissy sound and on really bad days, it spreads to my ears so that my whole head feels encapsulated by noise. The only part of this I can modulate to some degree is the ear hissing with noise and somatic movements, but it's not a solution, as it is only a very temporary effect.

I am hopeful the gas leak in my head can be addressed by lowering histamine/inflammation and addressing my hormones. Beyond that, I don't know what to do?

Does anyone know why some days my tinnitus sits in my head all day, then it will move into my ears on other days, then my whole head including my ears?
 
Please let us know which antidepressant you switch to. I would highly advise against Celexa. If you're going to take an SSRI, Sertraline has been the one better tolerated for tinnitus from what I've read. I'm on a low dose of Nortriptyline (10 mg) but that has not helped the head buzzing although it seemed to help the central tonal tinnitus a little bit.

Mine is also very reactive but on my low days (every other day or every two days) there is little to no reactivity. For this reason, I have been thinking about trying Keppra (since it's been said on here to help with reactivity and hyperacusis) but that's a pretty hard core drug.
Have you tried Inositol?
 
I'm only on 10 mg of Nortriptyline which is somewhat low - that helped the central pure tone "whistle" sounding tinnitus in the middle of my head but it did not seem to help the central "electrical" zzzz sound. But I am a low dose so I wouldn't say that's definitive answer on whether it helps with the electrical sound. I don't want to go up on the dose because it's a bit drying (throat, eyes) for me however some people don't have that issue with it.
Hi. I have read a bunch of your posts. Can you tell me how you are doing? Did you have issues with TMJ at all also with the head tinnitus? What do you think has helped the most?
 
I'm mot an expert in this area and I don't want to say anything that will influence anyone's decisions to take or not take certain medications. One thing you can take away from this is that you should never want to stimulate the 5HT2A receptor as it is implicated in cause or worsening of tinnitus. This seems to be the case why some of the SSRIs make people worse (however there are some cases where people have improved tinnitus on them). This goes to show us there are still a lot of questions about medications that even the doctors dispensing them can't answer. That alone is pretty scary...
Hi Cal,

I was wondering if you are still taking any benzos, or if you ever tapered off.

Thanks.
 
I cannot determine if my tinnitus is coming from my ears, as it feels more central, almost behind my head. It's easily masked by low-volume cicada-like sounds. My tinnitus started in 2020 without any clear reason (though I suspect it could be related to neck problems—I have a protrusion and experienced brain fog and nausea at the time). However, after a few months, those symptoms disappeared, and my tinnitus reduced to about 0.1%.

Unfortunately, it's bothering me again after a sound trauma I experienced two months ago.

Would you define this as brain-based tinnitus, or could it just be bilateral? Does the fact that it feels centered rather than in the ears affect the likelihood of it fading over time, as many cases do? Or does it make no significant difference?

Thanks.
 
Does the fact that it feels centered rather than in the ears affect the likelihood of it fading over time, or does it make no significant difference?
Hi @Furetto.

I don't think what you're experiencing will significantly affect your tinnitus fading over time. As you go through the habituation process, the tinnitus should gradually recede into the background. You mentioned in a post from 2020 that this happened to you, where you were able to forget about the tinnitus most of the time.

I'm sorry to hear you're now having difficulty managing it again. I've read some of your previous posts and would like to offer you some advice, which I hope you don't mind. Please keep in mind these are just my opinions and not medical advice.

The onset of your tinnitus in 2020 may not have been noise-induced, as you were experiencing episodes of vomiting and dizziness, which could indicate an underlying medical issue within your auditory system. I noticed you had tests with an ENT specialist. Your symptoms improved for a while, but unfortunately, they returned later with additional issues, such as feeling slightly drunk and having trouble concentrating.

In some of your later posts, you mentioned being oversensitive to sound, which could indicate hyperacusis. This is interesting, as hyperacusis often (but not always) accompanies noise-induced tinnitus. You've also seen several specialists, including two vertebrologists.

Moving forward, you noticed an increase in your tinnitus after playing the drums. I advise against playing them again. If you're still playing computer games, I suggest not using headphones or a headset. In fact, it might be best to avoid listening to audio through headphones, earbuds, or headsets altogether, even at low volumes.

Try not to stay in quiet rooms or environments, especially at night. Placing a sound machine by your bedside for low-level sound enrichment can help. Using your laptop is fine, as long as it doesn't have an internal fan or spinning hard drive that could add unwanted noise.

I hope you start to feel better soon.

Michael
 
Hi @Furetto.

I don't think what you're experiencing will significantly affect your tinnitus fading over time. As you go through the habituation process, the tinnitus should gradually recede into the background. You mentioned in a post from 2020 that this happened to you, where you were able to forget about the tinnitus most of the time.

Moving forward, you noticed an increase in your tinnitus after playing the drums. I advise against playing them again.

Try not to stay in quiet rooms or environments, especially at night. Placing a sound machine by your bedside for low-level sound enrichment can help. Using your laptop is fine, as long as it doesn't have an internal fan or spinning hard drive that could add unwanted noise.
Hello Michael,

Thank you so much for taking the time and effort to go through my old posts to help me. I really appreciate it.

I believe my first experience with tinnitus was due to cervical problems (I have a protrusion), which would explain all the symptoms I had at the time. My ENT mentioned that the body would go through an adaptation process and everything would eventually disappear, which it did. I never experienced those feelings again.

That first episode of tinnitus eventually faded to almost zero, and I considered myself cured. This is likely why I was reckless with drums, especially since I didn't associate my initial tinnitus with noise trauma. I had been in noisy places before without any problems, but perhaps that particular rehearsal was just a bit too much.

I now believe that noise trauma triggered a resurgence of my latent tinnitus. Lately, I've been feeling overly anxious because, by the end of August, it seemed like I had turned a corner, but since September, I've taken one or two steps back.

On a positive note, I no longer feel the "feverish" sensation inside my ears, so I see that as a step toward recovery.

I am following your advice about avoiding quiet rooms. I've started wearing headphones around my neck (not on my ears) with low-volume crickets playing as sound enrichment, so it follows me wherever I go. This method has helped me not notice the tinnitus as much around the house. However, the moment I take them off, the tinnitus becomes noticeable again. It's strange because the crickets at the lowest volume hide it so well, yet when I ride my scooter to the gym, I always hear it. Maybe it's because the helmet traps the sounds in my head?

I am only entering month two of this, and I know it's early. Since my tinnitus is not severe, I will most likely return to where I was in a few months, but for some reason, I still feel scared and anxious. I am practicing mindfulness twice a day and taking 0.25 mg of Alprazolam (the minimum dosage). I am also following a supplement regimen that I posted in another comment.

Since you are one of the best experts in the group, any feedback from you would be greatly appreciated.

Thank you again.
 
Since you are one of the best experts in the group, any feedback from you would be greatly appreciated.

Thank you again.
Hi @Furetto.

Thank you for your kind comments and for sharing additional information about your tinnitus. I agree that the noise trauma likely triggered a resurgence of your symptoms, and I hope that, in time, the tinnitus will subside.

You are making a good choice by avoiding quiet rooms, but I don't think wearing headphones around your neck for sound enrichment is the best approach. The issue is that it masks your tinnitus, which is something you should avoid. As you've noticed, the moment you remove the headphones, the tinnitus becomes noticeable again. This is similar to using white noise generators at a volume that masks the tinnitus. Once the white noise stops, the brain quickly fixates on the tinnitus again, and this can lead to it becoming louder and more intrusive if not handled carefully.

The proper way to use sound enrichment is to play it softly in the background without drawing attention to it. If the brain can't detect the tinnitus at all, habituation becomes more difficult or may not occur. Therefore, I suggest keeping low-level music or nature sounds playing during the day. I personally prefer classical or opera, but you should choose what you enjoy. You can use sounds from your laptop or a table-top sound machine. The key is to ensure that the volume remains low enough not to mask or completely cover your tinnitus, allowing it to be heard faintly in the background.

Please also be mindful of the noise from your scooter. Even with a helmet, if the engine is loud enough, the sound could reach your inner ear through bone conduction and aggravate your tinnitus. If you don't notice any increase in your symptoms, that's a good sign. However, it's important to be cautious about noise exposure, including at the gym, especially if you're lifting weights, as these activities can be noisy.

Running on a treadmill or hard surfaces can cause a spike in some people's tinnitus as well. I don't want to discourage you from enjoying your life, but it's important to be aware of activities that could unintentionally delay or prevent habituation to your tinnitus.

Take care, and I wish you all the best.

Michael
 
The proper way to use sound enrichment is to play it softly in the background without drawing attention to it. If the brain can't detect the tinnitus at all, habituation becomes more difficult or may not occur. Therefore, I suggest keeping low-level music or nature sounds playing during the day. I personally prefer classical or opera, but you should choose what you enjoy. You can use sounds from your laptop or a table-top sound machine. The key is to ensure that the volume remains low enough not to mask or completely cover your tinnitus, allowing it to be heard faintly in the background.
If I'm completely honest with myself, I actually used sound enrichment more as a masking method during the first few months! Even quiet cricket noises are enough to stop me from hearing my tinnitus, which is similar to @Furetto's situation. However, as soon as I switch it off, the tinnitus comes back and annoys me most of the time.

Lately, I've been trying to avoid using the cricket sounds and instead create pleasant soundscapes with indoor fountains or nature sounds through a Bluetooth speaker—though I can still hear my tinnitus. As I mentioned, it annoys me greatly, but this is probably necessary for habituation to work.

I look forward to the day when I suddenly realize that I've been busy doing something, living my life—and I wasn't aware of the tinnitus for a few moments, maybe even hours or days!
 
Lately, I've been trying to avoid using the cricket sounds and instead create pleasant soundscapes with indoor fountains or nature sounds through a Bluetooth speaker—though I can still hear my tinnitus. As I mentioned, it annoys me greatly, but this is probably necessary for habituation to work.
You will habituate in time, @KaiT81. Please follow my advice to @Furetto.
 

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