Pulsatile Tinnitus, TMJ Dysfunction And Echoing Of Noise In My Head


Mar 26, 2014

I would be interested if anyone else has this. I've had what I think is Pulsatile tinnitus for a year or so. I only hear it when it's very quiet, when I'm lying in bed or reading quietly. I believe it can be associated with temporomandibular joint dysfunction. In addition I get episodes for one to three days when any external speaking be it face to face, TV, radio echoes round in my head and is amplified. I suspect the sinuses are involved too.

The GP isn't that interested but he did prescribe a nasal irrigation which can help along with inhalation of peppermint oil in hot water, that really gets up the passages! I can't seem to work out what causes the attacks of the echoing, tho twice it's happened when the weather has been v windy or cold.

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Pulsatile Tinnitus In My Left Ear

I've had tinnitus in my right ear since I was about 10 or 11, my brother has it too and so it seems genetic, anyways, this has never really bothered me. What's been bothering me is this pulsatile tinnitus in my left ear. I developed this in June last year, at first I had crazy anxiety about it, but eventually I got used to it. It tends to be louder at night, happens when I bend down quickly, and the noise stops when I press on the vein in my neck. I had gone to an ENT in September, did a hearing test, that was fine, and he quickly examined me. He took a look down my throat, up my nose, and in my ear, he couldn't see anything wrong and told me that this happens sometimes and will go away on its own, but if it doesn't within 6 or 9 months (can't remember which) then I should come back.

Well, it's coming up to that time and although the noise doesn't bother me too much anymore it is still there. I also have anxiety in regards to my health and it can be pretty bad, I guess I'm just really worried as to whether or not there could be a serious underlying cause for this.

I'm assuming a scan of some sorts will be done but at the same time I guess I'm scared to get this.

I was wondering if anyone has had this type of tinnitus, and if so was the underlying cause found, did it go away on its own, or is it still being coped with?

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So, I bit the bullet and had the same surgeon who operated successfully on my left ear operate on the right ear yesterday. I had a much harder time with nausea and recovering from the general anesthesia than the first operation. The first time, I threw up once and that was it. Yesterday, I was throwing up a lot, and then they give me a phenergan injection, which just made me so weak and tired that the nurses had to get me dressed. And they were insistent that my friends take me home at noon, because they were getting the people for the 2 pm operations ready. My poor friend was driving with me in the back throwin up into a plastic bag.

Right now, I'm having a lot of pulsatile tinnitus in the right ear, which was not the case with the left ear operation. It's very loud because it's not masked by any external sound and is very distracting. I had pulsatile tinnitus in that ear before, and now it's even louder, unfortunately. As tired as I was last night, it kept on waking me up. Because I had some mild nasal congestion, the surgeon has me on oral antibiotics and nasal spray for a few days. I have very little discharge on the cotton balls so far, but it looks like a piece of the gelfoam packing came out on one of the cotton balls (at least I hope that it's gelfoam and not my eardrum!).

When I had the first operation, the right ear "popped" and I began to hear low frequencies sounds 8 days after the operation. Can't wait to get some relief from the tinnitus with external sounds.

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I recently had a brain MRI and there is nothing wrong with my brain. However these symptoms are changing my daily life and making my depression and anxiety far worse than they have ever been before. I'll give you a quick run through of the symptoms that have appeared and worsened during the last year.

Pulsatile tinnitus in left ear plus slight hearing loss.

Migraines more often to the point where I cannot speak or lay down or walk.

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A few months ago I suddenly couldn't write of hold my fork to feed myself, my hand just wouldn't work. I though of it as a one off. It's worse now, it happens more often and the shaking happens quite bad and in both arms and hands, sometimes I have spasms and often wake myself up by punching, kneeing or headbutting the wall next to my bed.

I have told the doctor all of this but have been told if the mri is clear than there is nothing they can do.. I am changing doctors (my current surgery is known for messing patients around and misdiagnosing). But any input on what's happening? The tremors have kinda threw me off guard, it's very uncomfortable and like I said I can't hold things, feed myself or anything when it happens.

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