Pulsatile Tinnitus In Left Ear Plus Slight Hearing Loss
Nov 24, 2015
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.
I now need glasses, I used to have perfect vision and now cannot see any further than about 10 feet in front of me.
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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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'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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i loss my hearing at the age of 17, doctors were shocked because this usually happens to people over 30... they said that the loss was due to stress and sadness but i couldn't figure out what exactly i was stressed about. i lost 98% of my hearing in the left ear and they send me to therapy straight away, i missed a month and a half of my senior year of high school due to this. after the therapy my ear improved drastically and now i can hear 40% and have completely lost 60%. i'm 18 now and there isn't much i can do anymore. i will soon go and get a hearing aid but i still am not so sure about it. i have coped with the loss off hearing but the ringing in my ear makes me go crazy. so my question is, do you recommend a hearing aid? will it stop of perhaps lessen the ringing in my ear?
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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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Is there anyone out there who is taking the anti-hypertensive Perindopril [ACE Inhibitor] and has developed Pulsatile Tinnitus as a side effect? I take this drug and do not have any side effects only that last February I was diagnosed with slight hearing loss for which I was given hearing aids and had Pulsatile Tinnitus which sent me rapidly to the G.P. from where I was referred to the ENT dept. at the hospital. I've had a MRI brain scan, Intercranial CT scan and Doppler scan on my neck in the Vascular Dept. where I saw a consultant. He told me there was nothing wrong in my brain or my ears but he couldn't help my problem as it is very rare and he hadn't seen a similar case for 17yrs. He said maybe my brain will eventually get fed up of listening to my heart beat swishing through my left ear. Has anyone experienced the same?
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About a week ago, I was at home at the computer (I believe I was listening to music at the time), and I noticed that the hearing in my left ear had been significantly diminished (but not completely gone). About a minute (perhaps even less than a minute) later, it returned completely to normal, and so I assumed that it was just ear wax or something, and everything was fine now. However, a few seconds to a minute later, it went back to being diminished again. I can't remember for certain if I felt anything physically when all of this happened, but there may have been something that I felt in my ear - which led me to believe it was probably just ear wax.
I have researched on-line for possible solutions to this kind of problem, and I have tried every possibility that I could - peroxide, warm olive oil, blowing as hard as I can with my nose and mouth shut, blowing as hard as I can with my nose and mouth and other (good) ear shut, nasal decongestant (which successfully clears up my nose, but doesn't have any effect on the ear), hot steam bath, Similasan Ear Relief drops that are supposed to clear up water in the ears, jumping up and down with my bad ear tilted toward the ground, jogging, and of course trying to dig out ear wax with the ear wax curette that I have. Unfortunately, nothing has worked, and my hearing has been about the same ever since a week ago when it went out (diminished) for the second time.
I have been able to remove a lot of ear wax with the curette, and sometimes it seems to make it a little better, but it never restores my hearing to normal. Sometimes I feel like I am right at the spot where it is clogged up (if indeed clogged ear wax is the problem), because the curette seems to be hitting a spot that's clogged with ear wax (judging from what it feels and sounds like), but then when I dig out a bunch of ear wax at that spot, my hearing is still the same or perhaps only slightly better. Perhaps I am actually pushing the ear wax further inside, which was mentioned as a possible negative effect of trying to remove the ear wax yourself. Also, I am wary of not poking too hard or too deep, as that was also a warning given at the sites I visited in my research.
Swallowing never seems to do anything, but it's interesting that when I have a strong belch, I can feel pressure inside that left (bad) ear, and it really feels like it's about to burst out and expel whatever is stuck (if it's the case that something is stuck), but it never does. Maybe whatever is stuck in there [ear wax, presumably] is just in so tight that nothing seems to be able to remove it. However, the odd circumstance that occurred when the problem first originated - which is the fact that it got better right after getting clogged up, and then got clogged up again - would seem to suggest that there may be another reason for this happening, other than plugged-up ear wax.
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I had my first stapedectomy for my right ear 6 years ago. it was successful. stilI I hear with my operated ear well except some ringing in my ear. but 11 days ago I had another stapedectomy for my other ear- left ear.That post op problems and results are completely different when I compare to my other ear. I don't hear properly. today is the 11th day. I have a lot of ringing and I feel as if my ear was full. the ringing is irritating.When I had the same operation 6 years ago, I had no ringing, feeling full . I just remember metallic sounds and they were really high. now no voice is high and irritating.I wonder is there anyone else experienced those ringing-mostly pulping tinnitus,not hearing properly? Because I feel really worried and nervous and as if something went wrong. my doctor said it all went well. I haven't had the hearing test yet. but I am worried.please write about your experience.
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Last year(2014) I started having some health issues. In March I was diagnosed with Mastoiditis. After that I began to have vision issues with pain and was diagnosed with Optic Neuritis in my left eye. I did 3 days of Solumedrol at home and followed with oral steroids. Since then I have had on and off hearing loss on left side and have lost my sense of taste 3 times for a few weeks. I recently had a mri and they found a 12mm choroidal fissure cyst on my left side. I also have tingling and numbness in my left foot and leg. I still have blurry and double vision in my left eye at times. I had previous ct scans and mris and there was no cyst present. Could this newly found cyst be causing my issues?
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25 months ago I fell on my left ear, hit my head. The blow was really strong, I was out for a few seconds. The left ear was slightly bleeding for a few days. I am having tinnitus since then. Couldn't really hear with that ear very well, but it took about 2 weeks to get back around 90%. The doctor said it's common and it will be gone, but it hasn't!!!! Now I think I have full hearing, but tinnitus is still here! It's so annoying, what can I do?
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do you know anyone who completely lost their hearing and got it back? im 22 and i lost my hearing in March this year
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Last thursday all of a sudden i heard a echo sound in my right ear trying all the normal stuff popping ears blowing nose checking for wax etc nothing worked so i went to bed and noticed i could not hear at all out of this ear so i waited til in the morning and still the same so i checked like with phone and could not hear anything so i went to see my gp and she checked and said nothing looks wrong so they referred me to a ent which i could not get into see till later this week on top of not hearing i have what i assume is tinnitus anyone else had this happen to them..
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In the spring of 2015, I noticed that there was a constant ringing in my right ear. Around June, I got in with an ENT, who referred me to an audiologist, who diagnosed me with hearing loss. Progressively, the hearing loss has gotten worse. I am a teen, so to me, this seems quite uncommon.
In the fall of 2015, I noticed a constant ringing in my left ear, as well as my right. I checked with my audiologist, and I had a mild hearing loss in my left ear, and a moderate/major hearing loss in my right.
I have also been having these dizzy spells that I like to call "flares", for the past year or so. During these "flares", I get extreme vertigo, fullness in my ear, and obnoxiously loud ringing in my ear. These attacks normally happen in only one ear at a time.
On top of all of this, I have been dealing with joint pain, fatigue, and muscle pain. My memory has gotten awful, and I like I'm in a brain fog all the time. My mom has lupus, so we are thinking it could be autoimmune.
My rhuematologist, ENT, and general doctor sent me for blood work, and my ANA was positive, along with my heat shock protein. This is all so confusing!
Does anyone advice, suggestions, or personal experiences they'd like to share? I have no idea what to do! I am on 500mg of naproxen and turmeric for my joint pain/inflammation, and a bunch of natural supplements in hopes of feeling a little bit better.
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What are the devices for hearing loss?
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I have had a long term battle (6 1/2 years) with eczema in my ears with no relief. Recently I have had Major hearing loss in both ears due to outer ear infections. I was given oral antibiotics (2x a day) and ear drops (4 drops 4x a day) to help with the infection. It has been 5 days since I started both and I still have none of my hearing back. This is affecting my Job as I work at the front desk of a Hotel! When will I start to get some hearing back?
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In Jan 2016 I experienced minor episodes of vertigo on a near daily basis, which I believed was remnant of motion sickness during a traumatic sea crossing! I noticed they continued weeks after and seemed to correlate with instances where I was feeling stressed. During this time I moved to the other side of the world and began a new job. I was previously living at 2800 m and spending my weekend’s alternating between the high Andes and the beach (involving lots of air travel). I am now living in the humidity at sea level and wonder if this could have provided sufficient trauma to initiate these attacks.
After a night of moderate drinking I had my first and only severe episode of vertigo, which left me violently vomiting and unable to walk. After which, I experienced a month or so of very mild vertigo attacks, lasting 4-5 hours at a time. I felt unable to exercise and spent a lot more time at home. Throughout this time I always felt unbalanced and even a drop of alcohol would exaggerate symptoms.
A hearing test came back fine, to my surprise, and I was treated for vestibular neurosis and given Betaserc for almost 3 months. I had no vertigo whilst on the medication but have had two or three minor episodes since coming off it (during yoga classes, playing football but also when lying in bed). The first specialist was happy the vestibular neurosis had been treated and any imbalance etc. was a product of my body overcompensating or lasting damage. I continued to turn to the extreme right when trying the Unterberg test. Now, my symptoms are fullness in my left ear, which occasionally proves painful and some mild tinnitus. The persistent fullness led my GP to refer me to another specialist, concerned it sounded like MD. Another hearing test and a pressure test both came back fine. I would suggest my hearing is more muffled but could this just be a sensation I notice because of the fullness? I am adamant my hearing suffered immediately after the vertigo attacks (before being treated) because I remember it being relatively distressing. I have been given Vinpocetine to try and hasten recovery of what the specialist believes is just a viral infection and to help with the tinnitus but I have seen no difference. I feel largely like I am not being taken seriously. It is coming up to 6 months now and I am desperate for some resolution or diagnosis that I can work with to try manage these symptoms. I am really active and travel a lot. If I should expect vertigo symptoms to return, I feel I would need to adjust or review my lifestyle as to not take unnecessary risks. Any one else in such situation? Or know anything about altitude and ear issues? Any advice or opinions are very much welcomed. Specifically, I was searching for information on whether it is possible to have MD but without suffering hearing loss? I am only 24 and so had wondered if my hearing could have been affected but remained within the so-called ‘normal’ range?
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I've had hearing loss now for a few years but don't know whether it's down to Work, crohn's or chemotherapy, anyone else?
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I woke up and was dizzy and being sick for the whole day, I have lost 30% of hearing in my left ear.
Previous to this for a year I was getting sudden dizziness that lasted for about 30 seconds and my hearing would go funny! I guess this was do to with it because I've not had it since the big attack on New Year's Day!
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My four year old son had an infection in his ear and the drum burst. Afterwards he could not hear properly but his Doc said it would sort itself out. This was a good 5 months ago now and he's just failed his school hearing test. They have said they will test it again in three months but i'm wondering if it needs addressing sooner. Has anybody had any experience of this kind of thing ?
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So, I'm back on Mirtazapine 15MG but these past few months I have halved the pill as I discovered 15MG was causing my panic attacks and high anxiety. I also tried to stop Mirtazapine completely and it was the worst time of my life, never want to experience that again but I know I did it all wrong (stopping suddenly).
Anyway, these past few months I have been doing much better. No panic attacks. Still some anxiety there but not as bad as before. However, I have found new symptoms I have been experiencing and I am unsure if it is anxiety-related. For the two months I have been experiencing this sudden loss of hearing in one ear which lasts a few seconds and then comes back. I went to the hospital about this, had my ears checked and he said everything was fine and it could just be a sinus problem where I have congestion and it can affect my hearing sometimes as the tube in my ear opens/closes , if that makes sense? I don't know the correct medical terms so that's as best as I can describe it. He prescribed me Beacons and told me to take it for 4 weeks. Also, he told me because it only lasts a few seconds and comes and goes it's nothing to worry about. Phew.
However, my anxiety has me convinced I have a brain tumor. I had headaches for a while but then they stopped completely and I haven't had one in a few weeks. Then I had this hearing problem and my anxiety told me again, "brain tumor". I went and got an eye test done because I have one or two floaters I've recently noticed and my eyes were perfect, she said. Of course, my anxiety made me ask her about if they could tell if someone has a brain tumor and she said she's only had to do that twice in her career and if there was something wrong she would definitely be able to tell.
My symptoms have definitely improved, but why am I always worrying? Why is my anxiety making me tell myself I have a brain tumor when I have no symptoms of a brain tumor? Such as seizures, constant headaches, nausea, etc? It's so annoying.
Does anyone else suffer from this problem? Or do you suffer from the same symptoms like a sudden temporary loss of hearing?
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I lost 50% hearing in right ear after having wax removed by irrigation with syringe. Seems like the water pressure was excessive. Now, hearing is muffled, nasally and distorted. MRI of brain was OK. Must use hearing aids now to hear anything. Have not used hearing protection in drum and bugle corps. Previous violin player 7 years ago so left ear shows 35% in audio test.
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