Extreme Tinnitus/Distorted Hearing Episodes for Days at a Time

Ringing2019

Member
Author
Aug 5, 2019
6
Tinnitus Since
2000
Cause of Tinnitus
Unknown
Hi everyone,

I would like to share this with you and seek advice and ask if there is anything that can be done to help me.
I am severely deaf since birth and wear BTE hearing aids.

I have always had low tinnitus when I take my hearing aid, out all my life, never once bothered me. But in the last couple of years I have been getting a massive increase of tinnitus and now I get these weird attack episodes that come at complete random and last for days at a time (usually 3 days before my hearing is reset back to normal and the ringing has subsided). I call them tinnitus attacks. When I get one of these episodes, It is a weird sensation in my head (Similar to a head rush but an auditory seizure) and then it a extremely loud ringing starts in my head and is so loud that all my hearing becomes muffled and distorted. Everything is high pitched, like the ringing.

It is like someone has turned down my hearing and turned up the ringing. It is so loud, I mean really loud, it is all I can hear, and affects my concentration, due to my head being overwhelmed by this ringing. My general speech understanding and hearing becomes distorted and messed up and I really have to focus on what the person is saying as everything is a mess of sounds that my brain cannot process properly. It makes no difference if I have my hearing aid in or out. My ears become so sensitive to sound and it goes right through my head.

I have to ride it out and wait for it to go. So that means I suffer from that one episode all day, from the time it happened and then I go to bed and wake up the next day, and I am still suffering so I have to put up with it another whole day and hope that the next day it has reset. One episode lasts an average of 3 -4 days before I wake up and check my hearing and it is back to normal.

I have no warning or cause anything to trigger them. I have had an episode when having a bath, an episode when driving my car, sitting at home resting on the sofa, talking to a friend, walking down the street, etc.... It so random and it hits me out of nowhere.

It really is getting me down.

I can go months (first time I started getting these was in 2015 and I only had 2 episodes that year but now they are getting more frequent and I am getting them every other month now, sometimes 3-4 times in a month.

My general hearing on good days has changed. Some days, voices sound robotic and weird and I can get certain sounds that really cause my hearing to react to it. A bit like my brain has tensed up to that sound, like the sound has caused my brain's processing of sounds to flinch/react momentarily. My low background tinnitus is a lot different now and 24/7, I get a droning sound that is really noticeable and sometimes clicking sound that happen in really fast bursts. In general my tinnitus is a lot more noisy and different mix of sounds now come with it.

Not sure if this is related but sometimes I have pressure in my ears sometimes and when wearing hearing aid, it is noticeable that I have pressure in my ears. but I can never seem to pop my left eardrum, when pinching my nose and swallowing. The right eardrum always pops every time. Some days my neck and upper back feels so stiff and tense, It is really noticeable especially the back of my neck can be warm to the touch. Sometimes there is a shooting nerve sensation near my lower neck/upper back.

I am worried that there is something going wrong in my brain where it processes sounds and I have had this since 2015.
 
There are no medical treatments to repair a damaged cochlea. Hearing aids do help some forms of sensori-neural hearing damage but they are limited. Audiologists pretend hearing aids are miracle devices.
 
There are no medical treatments to repair a damaged cochlea. Hearing aids do help some forms of sensori-neural hearing damage but they are limited. Audiologists pretend hearing aids are miracle devices.

Your post is confusing. I am deaf and wear hearing aids. I am not asking about that. I am asking about these episodes I have been getting. Hearing aids to a deaf person are life savers, anybody would agree with that.
 
g. My general speech understanding and hearing becomes distorted and messed up and I really have to focus on what the person is saying as everything is a mess of sounds that my brain cannot process properly. It makes no difference if I have my hearing aid in or out. My ears become so sensitive to sound and it goes right through my head.
You just stated hearing aids failed to help your hearing disability. I am confused as well. No one understands anything about the inner ear. Doctors can't repair a damaged ear therefore these "episodes" are medical mysteries that stay unresolved.
 
Muffled and distorted hearing are entirely separate forms of hearing loss. Unlike trouble hearing low volume noises.
 
You just stated hearing aids failed to help your hearing disability. I am confused as well. No one understands anything about the inner ear. Doctors can't repair a damaged ear therefore these "episodes" are medical mysteries that stay unresolved.

No, please read my post again carefully, I have worn hearing aids most of my life (Worn for about 28 years) and never had one issue until I started getting these hearing seizures around 2015 so I am seeking help as something is wrong. Hearing aid in or hearing out makes no difference when I am getting the extreme ringing and distortion. I can hear without my hearing aids like listening to music with in ear headphones and when I am having one of those episodes my hearing things like music is a mess.

Like I said, I can go months without an episode and my hearing is fine and then I get an episode and I have messed up hearing for a few days which is now getting more frequent.

Something is going wrong in my brain, where it processes sounds. I want to know if this is something like menieres etc..
 
No, please read my post again carefully, I have worn hearing aids most of my life (Worn for about 28 years) and never had one issue until I started getting these hearing seizures around 2015 so I am seeking help as something is wrong. Hearing aid in or hearing out makes no difference when I am getting the extreme ringing and distortion. I can hear without my hearing aids like listening to music with in ear headphones and when I am having one of those episodes my hearing things like music is a mess.

Like I said, I can go months without an episode and my hearing is fine and then I get an episode and I have messed up hearing for a few days which is now getting more frequent.

Something is going wrong in my brain, where it processes sounds. I want to know if this is something like menieres etc..
Yes, I was aware the episodes were on and off and not chronic. However.

There are some really unfortunate people that have the distortion you describe but it's chronic. Whatever these episodes are there is still you can do but seek a ENT. Sorry about the distortion and massive tinnitus spikes you are experiencing. I hope they resolve.
 
I'm sorry that you're dealing with that. I think it's hard to determine because it could be a bunch of different things. Muscle related, ear related, brain related, etc. I mean Meniere's is a possibility, but it do you get vertigo? It could be anxiety causing muscle or brain problems. I have Celiac disease and when I ingest gluten, it affects my brain and my T.

Seeing an ENT would be a good start. I have found that they aren't always helpful, but since you have hearing aids, they may listen. Hopefully they can take note your of symptoms, do the proper tests and/or send you to other types of doctors to figure things out. I'm sure the symptoms are not fun, but not knowing what the cause is is super frustrating as well. I hope you get some answers!
 
The way I see it you have two different types of hearing damage. One benefits from the hearing aid, the other doesn't.

However what is interesting is that the problem is intermediate on and off. Once again I hope it goes away.
 
I'm sorry that you're dealing with that. I think it's hard to determine because it could be a bunch of different things. Muscle related, ear related, brain related, etc. I mean Meniere's is a possibility, but it do you get vertigo? It could be anxiety causing muscle or brain problems. I have Celiac disease and when I ingest gluten, it affects my brain and my T.

Seeing an ENT would be a good start. I have found that they aren't always helpful, but since you have hearing aids, they may listen. Hopefully they can take note your of symptoms, do the proper tests and/or send you to other types of doctors to figure things out. I'm sure the symptoms are not fun, but not knowing what the cause is is super frustrating as well. I hope you get some answers!


Thanks for that. No, when I get these episodes, I get no vertigo or sickness issues at all. I have written down all my symptoms and will print them off to to take to a doctor. Hopefully they get to the bottom of it.
 
@Ringing2019 I am sorry you are dealing with such distressing symptoms. Can you get an appointment with an otoneurologist to see about these problems. They specialize in the areas of the ear and brain... Maybe they could arrange for you to have an MRI just to rule out any other issues...

Your doctor could probably organise this for you, that would be the best starting point. Make sure you detail all your symptoms and time frame this has been occurring. This may help determine the best way forward to see if any solution can be found....

Hopefully it resolves for you quickly,

Take care.
 
It's hard to say. It sounds like intermittent tinnitus (the main tinnitus sound as opposed to the hum of which many get on top of the hiss) and as your hearing is damaged it stands to reason everything sounds distorted in these situations.

Look into your jaw as pressure and fullness with tinnitus coming and going can be associated with TMJ. There's a group on Facebook (Meniere's No More) for people who believe they have TMJ but we're diagnosed with Meniere's. They all have a variety of symptoms... but be cautious over TMJ treatment and do research as it doesn't benefit everyone...

Finally if it becomes more frequent I guess you've thought of cochlear implants?
 

Log in or register to get the full forum benefits!

Register

Register on Tinnitus Talk for free!

Register Now