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How to find good TRT providers

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Dr. Nagler,

I posted a question about finding a provider and not sure if it made it up to you and I apologize if you've seen it before and chose not to comment.

I am not successful in finding a TRT provider who follows Dr. Jastreboff methods in NJ. I believe TRT providers are a small community and I'm hoping you can give me some direction.

I did find audiologist Susan Adams in NYC.

Are you aware of any providers in NJ and or can you make a recommendation on Susan Adams.

I know it's important to use the best and if I was in your area the choice would obviously be to see you.

Thanks in advance.

Category: Questions and Answers


SSHL with TInnitus - post Vasectomy/Ketorolac

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Hello Dr Nagler - thank you for taking the time to answer people's questions. 

About 5 weeks ago - I had a vasectomy - 1 dose of Xanax prior, lidocaine during (of course) and then post operation I took 40 mg of Ketorolac (Toradol) over 24 hour period - then stopped and just dealt with the pain. A day later i noticed ringing in my ear, a couple days after that some hearing loss in my left ear with feeling of fullness/pressure. 

Saw ENT, was put on Prednisone very quickly, had moderate hearing loss - mostly at high frequencies. Subsequently and had 4 dexamethasone injections, and am on Day 20 of Hyperbaric Oxygen treatment. 

MRI of brain/IAC and CT were all unremarkable. 

I'm glad to say that my hearing is almost back to normal - only a 5dB difference in the affected ear vs my normal ear. The pressure fullness sometimes has gone away completely and sometimes returns but is very mild. However my tinnitus still is present. The frequency has become much more high pitched thankfully and i'm habituating. 

Have you heard any cases where Toradol (or Xanax) could cause damage to ears (permanent or temporary? Is trauma to the body (surgery - in my case a vasectomy) been known to cause autoimmune responses that result in SSHL/tinnitus? 

Are people with SSHL who recover say all of their hearing more likely to have their tinnitus go away completely? 

Thanks again

Category: Questions and Answers

Your experience with habituation of reaction and perception?

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Hello again Dr Nagler,



Trying to find patient post-TRT accounts is not easy. The only ones I could find dealt mostly the success and not with the actual mechanics if you will. I of course have spoken with my doctor about it but I'd love to hear from someone who has actually done it and experiences the results of habituation every day.



Prior to January I was completely and totally habituated to my tinnitus. I haven't a clue how long I have had it and I didn't know it was an actual thing until a year and a half before. I always thought of it simply as normal brain sounds and ironically, that's really what it is! Then, at the end of January everything changed.



Now, part of my problem in trying to understand what habituation of reaction and habituation of perception actually is is that I can no longer remember what it was like myself. I think I forgot what normal was. So, what do you experience? Do you always hear yours but it mostly doesn't bother you? Or, is it not there except in passing or when looking for it?



Thank you much,

Joel

Category: Questions and Answers

Neomycin

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Hi Dr. Nagler,



Almost 3 months ago I sustained a traumatic eardrum perforation when I fell onto a long, skinny toy. A few hours after the accident my ear began to bleed a bit so I went to the ER where the perforation was confirmed and I also found out I had a bleeding cut in my ear canal from the toy. I was prescribed neomycin/polymyxin B otic suspension. I used the drops one time only (3 drops) and then read in the pamphlet they should not be used in place of a perforation. Of course this made me nervous so I googled all night and read horror stories of people suffering severe tinnitus from these drops and read about how ototoxic neomycin is systemically.

The following day, I developed a faint ringing in my head. By morning is was much louder and high pitched. Since that day it is 24/7 and can be heard over the tv and other everyday noises.



This caused incredible anxiety as I read tinnitus is the first sign of ototoxicity from neomycin and from there can progress over weeks to months to complete deafness.



Since then, I've developed some sensitivity to noise, including thumping eardrums in response to certain sounds such as the scratchy sound of buttering toast or zesting a lemon, and recently to my children's raised voices. I also have some ear fullness and occasional sharp, shooting pains in both ears. I've been to the ENT several times and my perforation is healed and everything looks good aside from some dried blood/scabbing in my ear canal from the cut.



My question is, can 3 drops of neomycin eardrops cause ototoxicity via absorption into a bleeding wound in the ear canal? I've already read all I can read about the possibility of the drops entering my inner ear but that worries me less as it would affect only the one ear in that case.

Alternatively, can a perforation cause high-pitched tinnitus that is perceived in the head/both ears? And then stick around after the perforation has healed?



One ENT told me I probably already had tinnitus but didn't realize it until attention was brought to my ears. Is that possible? It's hard to believe I wouldn't have noticed this before. Another ENT says the tinnitus is from the perforation but it has healed and he's not sure why the ringing hasn't gone.



I look forward to hearing from you and really appreciate your insight!



Thank you,

Stephanie

Category: Questions and Answers

Shingles vaccine

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I was wondering if it is ok to get a shingles vaccine since the shot has neomycin in it? And that is on your list of meds to avoid, I think.



Cindy

Category: Questions and Answers

Seashell Distortion - Ear Infection?

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Dr Nagler,

Let me start by thanking you for creating this site. When I first developed idiopathic high-pitched tinnitus last year, I felt like I was trapped in a prison in my own head. Stories on certain other online communities (that may well help others) terrified me further. My road to recovery began when I read your story and started reading you replies on this community. It helped me look at it not as a life sentence, rather as a small distraction from real-life that I could either fuel or (slowly but surely) disable through focusing on everything else in life; the things I had loved long before it came along.

Now, on to my question. I'm not sure if its your area of interest but any light you could shed is much appreciated:
A week and a half a go I began feeling mildly dizzy and got one 2-3 second burst of vertigo. The mild dizziness persisted and 2 days later I began hearing a seashell-like distortion of certain low frequency sounds, like the wind in both ears (depending on which head was facing the sound and how it was turned). The seashell sound was/is not present when I'm in a quiet environment, hence my calling it a distortion. At times my ear would vibrate so its possible that it was objective. I also have been feeling a blocking/airplane-like pressure in both ears at different times. I went to my MD and he said it was likely an ear infection and gave me some drops.

I am taking them and hoping he is right but, is there a chance its Menieres starting in both ears simultaneously? Almost all the literature I've read says that it typically starts in one ear but the seashell distortion seems to be the same as is, obviously, the dizziness. Is this seashell distortion also common with ear infections?

Apologies for all the text. I've highlighted the important bits.

Thanks,
Des

Category: Questions and Answers

Ototoxic meds

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Do you know of any safe antibiotics I can take with a sinus staph infection Not MRSA they told me they tried to give me augmentin but refused it center for hearing loss has it listed as ototoxic now they given me regular amoxicillin 500 mg is this safe and do know of any safe antidepressants there suggesting I take one but Zoloft n Zannax are out to ototoxic and never new everything was ototoxic do you is this ototoxicity rare or very rare side effect or does it happen all the time. Thank you for your opinion and help

Category: Questions and Answers

Dr expertise needed

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Hi I'm 60 years old have high blood pressure diabetes high cholesterol hi Eye pressure I take Travatan drops for him I recently had a staff infection like three weeks ago but it was not M RSA but was a staff infection in my sinuses I was prescribed amoxicillin 500 mg twice a day And nasal ointment there goes your nose in and it's been three weeks since then I, i went back tho to and urgent care doctor to have a checked out make sure was gone he looked in my ears and said it looked finelooked down my throat felt around my throat felt around my ears and he told me he thought I had a eustachian tube problem because I told him my ears always felt plugged so he prescribed Ceftdinir 400 mg tablets-twice a day and Rhinocort allergy nasal spray once a day and methyl prednisolone METHYLPREDisolone however you spell it can you tell me if this is ototoxic and will cause you to lose your hearing And make you deaf I read on some sites about all these being all ototoxic medicines and I'm scared to take them now since I've gotten tinnitus I hardly function anymoreI don't want to go deaf so I don't know If I should e these medicines almost every medicine I take is listed as being ototoxic for my diabetes my high blood pressure medicine everything as little as listed as ototoxic my sleeping pill is listed as well ototoxic so can you tell me about the three new medicines are the ototoxic cause I don't want to take anything that causes deafness are hard of hearing or hearing loss I need your help thank

Category: Questions and Answers


Inconsistency and the path to habitation and healing

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Dr. Nagler,

Hope you are doing well. I've have read/searched through much of your forum history, FAQ materials, and worked through the PDF book. The resources you've provided are very helpful, thanks for providing such open access to your expertise. I'm analytical, so apologies in advance for the amount of detail below.

I'm not new to tinnitus as my ears have had a slight ring to them for as long as I can remember (at least >30 years, I'm in my 40s now), but I'm new to suffering from it. In fact, in my current state, I have to wonder if I ever really had real ringing in the first place or if I just broke 30 years of habitation and only now realize the sound at its worst level -- it'd been years since I thought about it.

About 3.5 months ago, I blew the doors off the barn with the shots of a 9mm handgun at an indoor range. I wish I'd just shot the damn tinnitus horse instead.  I was wearing in-ear foam protection, but that protection was soundly defeated with the shots and my right ear rung out hard.  I wager they did not expand enough. As someone who is not a huge gun fan to begin with, the whole experience proved to be a costly mistake. My ENT found that there was more damage to my left ear than right (even though the right rang out), and that I was still hearing within "normal range." I had a slight dip from the baseline in my most recent hearing test in a few frequencies. She put me on a couple courses of prednisone, first at 60mg for a week then a 8 day 30mg taper -- and those weeks were simply awful.  The meds put me in orbit -- never knew what true anxiety was like before that -- and I don't know if they actually helped at as my hearing recovery in my post-treatment tests was clinically insignificant. 

Since then, I've been struggling most with the inconsistent nature of the sounds that remain in both ears. Three weeks after onset I developed a Somatic Modulation nature to the tinnitus in my damaged left ear -- the sound with movement is a "trigger" for me as the sound pitches (up to 3x as loud) with most steps, every bite, and with most movements of my head -- breaking through concentration grabbing attention from what I'm doing. I am a grinder, and my jaw clicks and has some form of TMJ, so I'm sure that does not help. I do wear a night guard.

I find my life with tinnitus is on a sliding scale, on intrusive days it's hard concentering on work (or do much of anything else), though I do my best to bull through it, on non-reaction days it does not bother me much even with omnipresence and I'm able to get by (though not thrive).  Today is one of those very intrusive days, probably what prompted me to finally write you after a couple months of lurking.

There is no telling how I will be one day to the next, no rhyme or reason to it, the tinnitus just is (though stress and fatigue do seem to factor). That alone is a pain in the neck, though I have 3 main flavors of sound.

  • Days that just ring easiest to ignore - these are the days I feel closest to normal and may be nearer to what may have been my original baseline.
  • Days that are very Somatic are at risk of going south due to the trigger factor, a day where movement bothers me can go bad and turn in to a hiss day (or string of them). 
  • Days that hiss are the usually most intrusive and highest risk of reacting from the moment I wake up

 … In the interest of getting to the point (too late), my questions are basically: "Now what? And does it matter?"

How common is this intrusive inconsistency and somatic complaint, and how do folks manage? If my head just picked a sound and stuck with it, I feel I'd be further along. At my quiet desk gig there are some days where I can't help but "pick" at the noise coming from my left side and neck -- and that can send me into a spiral for the day. It reminds me of an aggravated pain response, it's aggravated, so you check it, which aggravates it more -- but "leaving it alone" is a challenge.

Should I just be patient and just give it more time? While I found the CBT.PDF book helpful and it made a difference in turning a corner (positive thinking, etc.), I want to spend less time thinking about my tinnitus, not more, so I'm not wholly sold on the philosophy. Yes, I'm tuning it out more and reacting less, but I'm still reacting far too often and it interferes with day to day. I've about given up that this might go away, though I hang on to slim hope while I await habitation. 

In your experience, does the intolerance, inconsistency, or somatic nature of tinnitus tend to fade with time and habituation? Can TRT help with this? My gut says it's still "too soon" at 3.5 months to go down the TRT path, and I have improved, but I'm growing impatient for the next s-curve.  I miss "normal" but I don’t remember what normal was except quiet enough that it never bothered me.  I've been able to string together days (up to 3) where I don't think about tinnitus as much, but that seems to be the cap before I get a hiss day snuck in. 

Should I continue to look for an additional factor (TMJ, etc) for the Somatic component or does it even matter since I have a trauma event? I guess since it came up weeks after onset, and I'm not convinced the issues are completely dependent, or if that the drug treatment made it worse.  For the most part you tell folks to move on -- but I wonder if I've left a stone unturned.

In that regard, can chiropractic or back exercise help the somatic component since this sound doesn't seem to be originating in the ear, or do I likely just have nerve damage as part of the deal? If it were estuation tube issues my assumption is my ENT would have said something. My posture is meh as years of deskwork has taken its toll, but I've never been a real believer in chiropractic in general. I read there were some studies about exercise therapy, but found few results. 

Out of curiosity, on your barrier removal, how do you reconcile "tinnitus logs" with the "Daily Diary" reaction tracking exercises in the book? They seem to me one in the same. I'm not doing much of either any more, simply noting if something of interest happens during the day, what form of day it was, and how I reacted. In the beginning I had bullets for hours each day.

Realize this was long, so any thoughts are appreciated and will help me in working through next steps. Again, I'm a bit stuck on What Now? Hopefully some of your answers will help others as well, I know I benefited from other posts along the way (though I'm staying off boards as much as possible).

Regards,

JP

Category: Questions and Answers

What's the real truth about Clonazepam

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Dr. Nagler,

As many of us, I have been given Clonazepam .5mg as a treatment for tinnitus. I am finding it very difficult finding reliable information regarding long term use. I find it to be effective but am concerned about tolerance and eventual withdrawal issues. 

There appear to be two sides to the use of a benzo story, some say short term only and others, epilepsy patients,  I've read do well on it for years. 

Can you comment on Clonazepam as a long term treatment for tinnitus? 

Category: Questions and Answers

Update and some questions

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Hi Dr. Nagler,
Hope you are continuing to feel better following your recent illness.
Wanted to give you a quick update. I'll stop short of calling it a success story b/c I'm only half way through the program, but the CBT work I've done with Dr. Rohe is amazing. He (and you) have truly helped me.

I"m not out of the woods yet. I still react somewhat to my tinnitus when it gets louder, and sometimes even when it isn't that loud, but I am miles and miles better than I was just two months ago. It just really makes sense. You have to keep you head in the game and can't let fears rule you.

Two saturdays ago I had a very loud day, but I just followed Dr. Rohe's instructions and got on with my life. I played golf. I went to a barbecue. I had fun. I was annoyed at times by the tinnitus, but I still had a good day all things considered.


Moreover, I'm having many, many more good days. Days where I barely notice my tinnitus. I don't want to jinx myself (yes, I guess I'm superstitious) but I want to give hope to people who currently are where I was before I started CBT...you can and will get better. Have faith.


This last bit leads to my questions.

 

The first, ever since my tinnitus presented itself about six months ago, I have had days where it is completely gone. Originally, I'd have about one day like that a month. Since starting CBT, nearly every day I have long minutes or hours and sometimes whole days where it is just gone. I know I'm not supposed to go looking for it, but I can't help myself.


My question is, and I know you may not be able to answer this, but can I read anything into this? Could it go away for good some day? Does that happen? Or could I just get to the point where I'm not aware of it most of the time. Either would be fine with me. It just seems that if it can leave for an hour or two...why can't it just go? Obviously, it doesn't HAVE to be there.

My second question is, I mentioned to Dr. Rohe that my tinnitus gets louder and changes in pitch when my body is in certain positions. If I sleep on my side i wake up with it raging in my head. When I wash my face it gets louder. When I turn my head from side to side it briefly gets louder and higher in pitch. Plus my right ear feels clogged all the time.

He said it sounds as if these are somatic symptoms and he's having me see a chiropractor who specializes in tinnitus. I can't see the chiro for two weeks, but I'm trying to temper my expectations. I don't expect him to "cure" me, but could he really reduce my symptoms? Have you heard of such a thing?


Thanks for your time. This board is about the only valuable resource on the internet for people with tinnitus. Thank you so much for providing hope.

Category: Questions and Answers

Greetings.

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Hello Doctor Nagler, new to this forum. Please excuse my english if you can, im not a native speaker.

I'll give you a little backstory of my problems. A bit over two months ago I entered the worst period of my life, and that out 'nowhere'.

I've had problems with build up of earwax earlier since I tend to sleep with earplugs during in the night (very light sleeper...). My ears started to feel weird again so I did as usual, bought a do-at-home earwax removal kit where you put some oil drops in your ears over the night and then flush them next day.

But this time my ears didn't get fixed at all, they turned much worse since I stated hearing a very high pitched buzz. It was bothersome but I thought it would go away so I didnt put that much care into it. But after a few days it started messing up my sleep so I did what I 100% should not have done...went online and used google. I found so many horror stories that turned my anxity about it 10 times up.


Since then I've had the same high pitched buzz in various volumes (probably based on my anxity about it and lack of sleep). I used some benzos in the start that I got from my doctor since I hardly slept. I stopped using them a month ago since I didnt like the prospect of eating benzos for too long. I still have problems sleeping now and then. My daytime tinnitus has improved (fingers crossed...for the last week atleast).

My doctor thinks it might be ETD since I have problems equalizing one of my ears (not the ear that makes most sound tho..) and very loud crackling noises from the other ear (the one with loudest tinnitus noise) when I swallow. I have been using nasonex spray for a month now, and in my mind there has been some improvements.

But I have a few questions:

Could the ear syringing from these bulbs you get from the pharmacy have caused irrreversible damage to my ear? As far as I can tell I dont have any hearing loss (Im going to a ENT for hearing test, but the wait times in my country is extreme, atleast for me). I'm fairly confident that I didnt bust my eardrum since A) I didn't get any sudden worsening in my hearing and B) I didn't experiance any pain doing this.

Sadly I have been rather addicted to Otrivin nasal spray (kinda like the american afrin I think) for 2 year. I stopped cold turkey with this a month ago since I got the idea that this was making problem for my ETD. Can overuse of nasal decongestant cause ETD, and then in turn tinnitus?


2 weeks before my tinnitus started I was having pain in my right ear (the one that is most bothersome now) when I was swallowing and yawning. I also started hearing loud cracking/popping sounds from this ear when I swallowed at the same time. But it werent for 2 weeks later when I syringed my ears that the tinnitus started. I still have have sounds when swallowing (albeit they have gone down in volume a bit) and problems equalizing one of my ears doing the valsalva manouver.

I got my hopes that this is actually ETD and that the sounds will go down when it gets better. But if its not I hope im able to get 'used' to it after awhile. Here in norway there is very few TRT systems, if any. So I can't put my hope in that if this doesn't gets better. But in general my daytime feelings has improved a bit, instead of having anxity and depression about it 14 out of 16 waking hours I now have half of that or so. But the night time is killing me. I have tried playing white noise but it doesn't work at all since I get another sound when I listen to such, it sounds like small ziiiing sounds that plays over the white sound no matter how loud it is. Fans work better, but latey im just staying up until im so dead tired that I'll fall asleep sooner or latter no matter how much im annoyed by the sounds.

I can also give a tip if anyone else reads what I have written. Do not google your condition too much...and stay clear of forums with too much negativity (Altho alot of the people at tinnitustalk is great and supporting people) I have stopped going there because of all the negativity and horror stories. There is also some good advice there on how to cope, but also lots of weird, and perhaps dangerous stuff. Like eating potentially dangerous medecine (like trobalt and so on) and people telling you to wear earplugs 24/7. If I wanted severe H I would follow this but I dont want to.

Thanks for time doctor, wish you all the best,
Rolv.

Category: Questions and Answers

High pitch tinnitus after/during otitis media with effusion

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Dear Dr. Nagler,

I have been reading your extensive and very useful board the last few days, mostly to understand my own situation in the present, but also to learn in general. 

It has been most useful in both these respects. 

I am a relatively healthy (except from GERD) male in my mid 30s. About a week ago I got antibiotics prescribed (erythromycin, 2g per day for 10 days) for tonsillitis. Prior to this treatment, I had a blocked left ear, and a tinnitus, which accompanied the tonsillitis. 

Now, a week later, the tonsillitis is out of the picture, but my left ear is worse than before. It seems full of fluid, I have moderate hearing loss and a constant high pitch tinnitus. I have never in my life had tinnitus before. Went back to the Doctor, and he said that I have otitis media on both ears, but with effusion on the left ear. When I perform the Valsalva Maneuver, only my right ear pops, while my left ear pops sometimes after a long, warm and steamy shower. 

After taking Nasonex for the first time today, the eustachian tube in me left ear temporarily opened, and stayed opened for 10-15 seconds at a time. During this I could hear my own breathing inside my ear, in a way I have never experienced before. After about 20 minutes, this stopped, but I could still make the left ear pop with Valsalva for about an hour, then it returned to "normal". 

I am sure you are already guessing my rather unoriginal question(s): is tinnitus a normal symptom for a condition such as this? will the tinnitus disappear once the ear gets unblocked and drained of fluids/mucus (either by itself or with surgery), or later, or perhaps never? 

Very best,

Peter

Category: Questions and Answers

Don't know what to do anymore

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Hello Dr. Nagler,

I hope you are doing fine. This story with tinnitus is getting harder and harder. As time passes i don't feel myself getting in a better place. In the beginning i had hopes that things would improve in a way but unfortunately they don't. Nothing in life has the same taste. I cannot be my real self anymore. Is it normal that this thing progresses in a negative way? My doctors cannot help me unfortunately. They also claim that worsening of tinnitus is in my mind and i trigger it due to negative emotions, but Dr. Nagler i would swear that what i hear is more intrusive compared to what my tinnitus was during the onset. On top of that three days before, i experienced for the first time a major spike. In a second someone decided to turn the volume up. It was like a fire alarm turned on instantly! I've been quite brave that moment. Tried to stay calm. Managed to get some sleep for a couple of hours with great difficulty. Thank God it subsided on my wake up. There was no reason for that spike. Is it a warning sign for the next level? I felt sorry for myself.

I would love to ignore this thing and keep doing my things BUT my things have to do with music. I'm having a really hard time to keep up with what i do for a living. Teaching dance. Maybe my worsening have to do with music from the speakers? I use musician earplugs and i try to keep the volume in a rational level. Teaching time used to be fun. Even now i tend to forget my tinnitus when i teach but as soon as i finish classes, a high pitch part of my tinnitus seems quite irritated. Then i get back to depression. I'm so tired of crying everyday. Therapy doesn't seem to help. I can't hold my tears. In my most creative period of my life everything is falling apart. Will this thing ever stop worsening and get a chance to habituate? How am i supposed to make my living and develop my career? And what about joy? I loved playing the piano and going to dance/music performances. Going out with friends. It feels like everyone around me keeps on with their life and my clock stopped here. It's like a jail. Why my brain reacts in this way? And why my tinnitus isn't stable and threats me? Have i missed medical tests? ENT and Neurologist couldn't find a reason. Hearing is good. Brain scans are good.

Was your tinnitus the same all these time Dr? I'm sorry for the long post. I didn't have anyone to talk. Family tries to support me. Few friends also. But nobody seems to understand this condition. They don't believe me when i say to them that this is for life and there is no actual cure. I've never ever been under this kind of disappointment, fear and sadness. I was a normal young man with dreams. I'm in despair. How can i help myself?

Category: Questions and Answers

Acoustic trauma and ear fullness -- TTTS?

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Hi Dr. Nagler,

I play jazz guitar semi-professionally.  Last September for a performance in an organ/guitar/drums trio, I hired a different drummer than I usually do, which turned out to be a mistake.  He was significantly louder and harder-hitting than my usual drummer, and I wasn’t wearing plugs, assuming the volume level would be the same as it usually is.  The next morning, I noticed diminished hearing and a sense of fullness in my right ear, the side where the drummer was.  Initially, I chalked it up to allergies, but after it didn’t go away, I saw an ENT.

He said that everything looked OK with my eardrums / Eustachian tubes / tympanogram and that I probably had an acoustic trauma and experienced some noise-induced hearing loss.  I now have a very mild noise notch in my right ear — 15 dB threshold as opposed to 5 dB threshold on my left.  (I had an audiogram a year or two before the event, and they used to be equal.) 

The problem is that six months after this event, I still feel fullness and tension in my right ear, and with it comes a perception of decreased loudness.  The feeling comes and goes — if I get a good night’s rest, I’ll often have good hearing in the morning, but by the end of the day, I’ll have tension in my right ear all the way down to my right shoulder.  Additionally, when I hear bright sounds or sibilance sounds that fall in the range that was damaged, it feels like my right ear will "seize up".  This is very frustrating to me, since I’ve always had a very fine-tuned sense of hearing, and I feel like I can’t trust my ears to locate sounds any more.  As a result, listening to music is often frustrating rather than pleasurable.

Does this sound like tonic tensor tympani syndrome?  If so, what’s the treatment?  If not, what else might it be?

Thanks!

Category: Questions and Answers


Hyperacusis or what?

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Dr. Nagler,



I have another question. Why does it cause me to wince when I open up a pill bottle or flip a piece of paper or anything like that but a second later I can do the same thing and it doesn't make me wince? Would that still be hyperacusis or just a startle response or anxiety? Could I be worsening my hyperacusis by not wearing earplugs around too many people. Even with earplugs sometimes it's still loud. It had gone away a little bit but is increasing again.



Cindy

Category: Questions and Answers

Ophthalmic Suspensions

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Hello Dr. Nagler:

Just a quick question for you this time....over the past couple of months my optometrist has prescribed Lotemax, Vigamox and Besivance eye drops for chronic Blepharitis. Should I have any concerns about hearing loss or tinnitus from using these drops? Two of the three also contain minute amounts of Bezalkonium Chloride as a preservative and I've read that it can pose some threat to hearing.

Thanks and regards,

Denis Schreiber

Category: Questions and Answers

Habituation without TRT?

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Hello Dr. Nagler, 
  Thank you for taking the time to help me with my question.
  I have had very intrusive, troublesome tinnitus for more than 2 years.  I am now to the point where my symptoms are quite manageable for 2 or 3 days in a row, but the next 2 days are often awful.   
  I have maskers, but have not used them as one should due to the "tactile" sensations that accompany my tinnitus, which my doctors feel are my nervous system in overload.  The white noise of the maskers make these sensations seem that much more severe under the noise.  
  My question is -- should I suffer through the bad days and force myself to use the maskers daily so I can someday soon habituate?  On the good days, the last thing I want is more noise in my ears ... but on the bad days I want to jump out of my skin, the noise is so harsh and unbearable.  I don't know that I can endure this cycle forever.  I miss the old me terribly.
   Your guidance would be very appreciated.  Two years is long enough to suffer.
   Thank you.
   

Category: Questions and Answers

Success story with some questions

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Greetings from Arizona!!

First off I want to thank you for all of your support and for being the voice of hope and possibities for people with tinnitus. Mine started in Jan. 2016 at 32 weeks pregnant and it sent me to a very dark, scary, and lonely place. I found tinnitus talk and become obsessed with reading all the stories, most of them horror stories it got so bad that my husband blocked me from the site. It was the best thing he could have done for me. I reached out to a few people who had written success stories on a couple sites and have found the most amazing support. I have also started CBT with Dr. Rohe here in AZ.

These days I am learning to live with tinnitus, the less I talk about, think about, or google the better I get. I still have a long way to go but I have to say that I am so much better and I finally understand that for the vast majority of people time really does make it better. I remember people telling me in the beginning that the noise wasn't the problem....my reaction to it was and I wanted to slap them. Lol

They were 100% correct. I am starting to see that I have an amazing life, family that I love and love me...amazing kids...everyday is a blessing and the noise in the background is just that. I still have challenging days...those days are like today were I think about a little more, hear it a little more...but my reaction is more this is annoying rather then the panic, how can I live like this reaction.

So if you are new to tinnitus and reading this it does get better!!!! If you want your life back and are committed to finding happiness again you will get better.

Here are my questions:

When tinnitus is not connected to hearing loss is the chance of it fading over time greater?

I have read about many women who's tinnitus started during pregnancy, what are your thoughts on tinnitus and hormones vs stress and anxiety. I was having panic attacks when mine came on but I also notice a spike during my period. It seems there is a correlation between tinnitus and estrogen but there isn't a ton of information out there that I can find.



Once again thank you for your logical approach to support. It so nice to have a voice of reason out there! Xo

Category: Questions and Answers

(Neuro-)Otologist in Europe

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Hello Dr. Nagler,

I have a small question in response to this topic:

http://drnagler.supporttopics.com/post/hearing-echo-nonototoxic-antibiotics-8370560

I suffer from the very same echo/distortion symptoms described in conjunction with ear fullness and ear pain. 
You've mentioned that these symptoms fall within the realm of (neuro)otology.
I live in Germany and as far as my research goes this medical profession doesn't really exist here or runs under a name that I'm not aware of. I've seen many ENT's and a Neurologist, none of which really adressed my symptoms ("It's simply tinnitus"). I guess my question is wether it's actually the case that there just are no qualified professionals who could treat me in my region or wether I'm missing something?

Best,
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Category: Questions and Answers

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