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Tinnitus relief

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  • 07-07-2020 7:06pm
    #1
    Registered Users Posts: 4,555 ✭✭✭


    So ads have been cropping up because I've been searching.
    Seems like a lot of money (I'm not too bothered by the tinnitus yet).
    Anyone any testimonials, although I presume if it worked for you , you wouldn't be in this thread.

    Mod: the ads mentioned are for Lenire


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Comments

  • Registered Users Posts: 28,372 ✭✭✭✭AndrewJRenko


    Also interested in this


  • Registered Users Posts: 2,154 ✭✭✭PukkaStukka


    Am giving this thread a bump in case anyone has or is trying Lenire. Am plagued by constant tinnitus for 7 months now and nothing has tamed it. Am trying acupuncture at the moment but anyone who claims its worked for them all say it takes quite a while.:(


  • Registered Users Posts: 620 ✭✭✭Meeoow


    Am giving this thread a bump in case anyone has or is trying Lenire. Am plagued by constant tinnitus for 7 months now and nothing has tamed it. Am trying acupuncture at the moment but anyone who claims its worked for them all say it takes quite a while.:(

    There is a Facebook group, 1st lenire group/tinnitus. A few people on there testing it. Jury still out for me. It seems to come back to some. I don't think it's as good as first made out.


  • Registered Users Posts: 480 ✭✭CJmasgrande


    I researched it a few months ago and decided against it. The general consensus was it's expected and not much good.

    My tinnitus is in one ear and is horrendous.


  • Registered Users Posts: 4,555 ✭✭✭Treppen


    Meeoow wrote: »
    There is a Facebook group, 1st lenire group/tinnitus. A few people on there testing it. Jury still out for me. It seems to come back to some. I don't think it's as good as first made out.

    It appears to me to be a CBT service to retain your brain to ignore the sound (like white noise solutions).

    Had anyone found certain foods trigger their tinnitus or make it worse?

    I've heard of the B12 or magnesium supplements alright but reluctant to go that route.

    Maybe this is worthy of a new thread.


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  • Registered Users Posts: 620 ✭✭✭Meeoow


    Treppen wrote: »
    It appears to me to be a CBT service to retain your brain to ignore the sound (like white noise solutions).

    Had anyone found certain foods trigger their tinnitus or make it worse?

    I've heard of the B12 or magnesium supplements alright but reluctant to go that route.

    Maybe this is worthy of a new thread.

    I tried magnesium, and it spiked mine. But there are several different magnesium supplements so it might be trial and error. My tinnitus was caused by ototoxic drugs.
    Salt, sugar, aspartame, msg, stress, alcohol, dehydration spikes mine. I have been good the last few days, and it is lowish. Never goes away though. I find waking up in the morning, and eee is the worst for me.
    I've tried CBD oil, no effect.


  • Registered Users Posts: 4,555 ✭✭✭Treppen


    Meeoow wrote: »
    I tried magnesium, and it spiked mine. But there are several different magnesium supplements so it might be trial and error. My tinnitus was caused by ototoxic drugs.
    Salt, sugar, aspartame, msg, stress, alcohol, dehydration spikes mine. I have been good the last few days, and it is lowish. Never goes away though. I find waking up in the morning, and eee is the worst for me.
    I've tried CBD oil, no effect.

    Interesting, I've been taking omeprazole(for acid reflux) for the last 3 years before tinnitus/deafness took hold.

    But yes I've found too much of the following:
    caffeine, salt , sugar, mature cheeses, whiskeys/spirits, IPAs all make it go crazy loud.

    I don't know if it's connected but a good few years ago (bout 20) I was starting to get wooly in the same ear, went traveling which involved a lot of sea swimming and a week long diving course. It cleared right up and I thought nothing more of it until it came back about 7 years later. Mainly due to working a few jobs and stress etc. Went away again once I got a handle on my job and cut down on coffee.
    But back again with a vengeance 2 years ago.


    If only I could lounge around Thailand Island hopping and diving for another year again I'm sure I could cure it!

    Anyone ever tried hyperbaric chamber, think there's one in Dublin?


  • Registered Users Posts: 179 ✭✭Shtanto


    I've been working on Lenire for a while now, trying to get them to be covered by Laya. Haven't had much luck myself. As CJmasgrande points out, it is expensive. You're looking at about €2,000. The rub for laya is that this is an appliance.


    Characters in my story:
    Thomas Daly - Laya customer service, very helpful
    Lorraine Harte - Lenire customer service, also very helpful
    Dr. Brendan Conlon - ENT in the Hermitage and James's who was part of the team who came up with Neuromod.

    Laya review new treatments and appliances every few months to see if there's anything new coming up. Lenire published this: https://stm.sciencemag.org/content/12/564/eabb2830.full?ijkey=husCUTOHbbe0I&keytype=ref&siteid=scitransmed
    This is their published research. Laya use an old form with a filename from the days of Bupa Ireland (remember them?) called the "new benefit recognition form". It's about as lumpy and cumbersome as forms can get. 18 sections, 7 pages long. I think Lenire who give out could be forgiven for baulking at the prospect of trying to go near it. I gave it a go, but I'll be a while waiting yet to get Dr. Conlon to sign off on it. Something tells me he might not be too keen.

    Doctor Brendan Conlon (mentioned at the top of that research paper there) is a consultant ENT in the hermitage where he runs a company called audico who do hearing assessments. My own plan is to go see him privately in August. Got the GP bit done, appointment booked for the end of August. The hope is that if he prescribes it, Laya will cover it. Audico runs out of suite 24 in the Hermitage. Lenire Neuromod is suite 36, so just upstairs really.

    The goal here is to get this covered under private health insurance and then recognised by the HSE. I know, I can half hear you laughing, but when you've been fighting MS for 11 years and more, this is the type of thing you do to keep well.


    In terms of immediate relief and short term alleviation, the first thing I usually try is this: https://www.youtube.com/watch?v=2yDCox-qKbk
    Beyond that, I've got a good orthopath. The nutritional angle is a good shout, but what you're more likely looking at is something in your ethmoid bone or your TMJ.

    I've read a few paragraphs of the research paper so I'd know how it works. It's pretty clever really, though it has to be surmised that there must be a larger variety of tinnitus types and pathologies than previously thought. PM me as needed, I'd be happy to help


  • Registered Users Posts: 4,555 ✭✭✭Treppen


    What is Lenire specifically though.
    Is it a CBT to retrain your brain to ignore the tinnitus?


  • Registered Users Posts: 2,154 ✭✭✭PukkaStukka


    The Lenire product "seems" to be tuned audio into the ear(s) and some kind of electro-stimulant applied somewhere around the tongue.

    If anyone knows I'm wrong with this, please correct me.


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  • Registered Users Posts: 620 ✭✭✭Meeoow


    There was a webinar by lenire a few months ago. They emailed it to me afterwards. If you contact them, they will mail it to you. Bernard Conlon and the others explain how it works.


  • Registered Users Posts: 179 ✭✭Shtanto


    Treppen wrote: »
    What is Lenire specifically though.
    Is it a CBT to retrain your brain to ignore the tinnitus?

    Specifically, Lenire is a company that made a gadget they call the Neuromod. The Neuromod is a pair of bluetooth headphones for your ears and a trigeminal nerve stimulator that goes in your mouth. The combination of the two is supposed to help modulate you away from the tinnitus.


  • Registered Users Posts: 2,936 ✭✭✭IrishHomer


    Shtanto,

    Any updates please?

    I'm sending you a pm



  • Registered Users Posts: 2,103 ✭✭✭Living Off The Splash


    Have a look at the Tinnitus section on the website "Stuff that Works". Lots of people posting about symptoms, medications, diet and other stuff that impacts on their tinnitus.



  • Registered Users Posts: 4,555 ✭✭✭Treppen


    I regularly check in on the posts there, nothing really substantive works, diet and lifestyle changes sure do seem to alleviate it.

    The electric pulse thing isn't really a cure , it just retrains your brain to ignore the sound so it's not as loud, similar to any CBT ... and it's dam expensive.

    Others mention ototoxicity after taking other medication as a cause.

    I suppose everyone's condition is unique to them.



  • Registered Users Posts: 2,103 ✭✭✭Living Off The Splash


    I think it is about alleviating the symptoms. A low noise day is heaven compared to a high or even medium noise day. Today for me a medium noise day.....yesterday a low noise day....



  • Registered Users Posts: 4,555 ✭✭✭Treppen


    Have you identified any triggers?



  • Registered Users Posts: 2,154 ✭✭✭PukkaStukka


    I have managed to improve my own situation to a fair degree, even if there's no complete cure.

    First of all all, there's a guy called Dr Ben Thompson on YouTube who is an American audiologist and tinnitus sufferer. He discusses various things to manage and reduce tinnitus that I also found very helpful. There's also a number of YouTube channels that have various prerecordings for tinnitus sufferers and I have found listening to "Art of Zen" in the headphones to be excellent at taking tinnitus spikes down.

    Without a doubt, the single best thing I did was double the amount of water I drink and reduce salt intake as much as possible. Within a few days the tinnitus difference was very noticeable and sustained to moderate degree, and is now nowhere near as bad since.

    Perhaps the biggest nugget to crack is the impact of stress on tinnitus. Most people I spoke to with it say their jobs or lives are stressful, and t there is little they can do to reduce that. But they do notice a clear correlation between being under pressure and the intensity of tinnitus. I'd be curious to see if others here are in the same situation?



  • Registered Users Posts: 4,555 ✭✭✭Treppen


    I notice the stuffthatworks have published the insights from data received yesterday.

    Seems like stress/high blood pressure are factors alright.

    I'm surprised they didn't show which ear people find most effected.

    Some of the 'relatively' best treatments people have found are through medication . But the drug listed was a treatment for anxiety which maybe reduced stress.... or made you care less about the noise🤣.



  • Registered Users Posts: 28,372 ✭✭✭✭AndrewJRenko




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  • Registered Users Posts: 1,061 ✭✭✭Quitelife


    I got very severe tinnitus as a result of an incident with an alarm about 15 years ago- for the first year i nearly mad with it before i ended up buying 2 hearing aid type pieces that i slot in my ears that play white noise . i wore them for about 6 months and it brought my tinnitus from a 9/10 problem to a 2 or 3/10.

    I occasionally pop them in for a few days here and there to suppress the tinnitus if ever i get a flare up, they weren't cheap ie 3K but they've brought my life back to normal and its great to have them mentally if ever the tinnitus starts to become an issue.

    I gave up smoking which also was a big help, anxiety is the other thing i try to avoid in so far as possible which makes it worse.



  • Registered Users Posts: 4,555 ✭✭✭Treppen


    Stress, coffee, sugar, alcohol, cheese, nuts for me. It's only in one ear though.



  • Registered Users Posts: 28,051 ✭✭✭✭looksee


    I normally have loud tinnitus, in spite of hearing aids. I just noticed when I saw this thread that it is very quiet today. I wonder what the difference is?



  • Registered Users Posts: 53,846 ✭✭✭✭Headshot


    My poor old father is a big sufferer of Tinnitus

    Has it for around 10 years at this point

    I'm currently looking at going down the Lenire route with him, has anyone tried it?

    Alot of money but if it helps him it'd be a small price to pay



  • Registered Users Posts: 2,103 ✭✭✭Living Off The Splash


    The left side of my head has the hiss. This can be low, medium or high. On the right side it is more in my ear....sound like a jar full of bees. This is always at the same pitch.



  • Registered Users Posts: 325 ✭✭Dingaan


    Did you go to an audiologist specialising in tinnitus for the hearing aid?

    I have tinnitus about a year now. It's mild. I'm still very cautious around loud noises. I'm getting fitted with custom ear plugs next week. Some bars, and restaurants blast music to an uncomfortable level.

    Do you guys take the precautions around noise?



  • Registered Users Posts: 28,051 ✭✭✭✭looksee


    Seeing this thread again I have just realised my tinnitus has gone - for the moment. I didn't notice when it happened as I can ignore it a lot of the time, then I realise it is loud again. Always previously if it is mentioned I am aware that it is there, but not at the moment. I haven't made any recent lifestyle changes, though I have not had caffeine in over 6 months.



  • Registered Users Posts: 4,555 ✭✭✭Treppen


    Restaurants and gatherings are hell for me. I work in a school too so both staff room , corridors, assemblies and classrooms can be unbearable at times.

    I don't really take any precautions, just try and avoid conversations or say "what?" a lot 😭



  • Registered Users Posts: 325 ✭✭Dingaan


    Any idea what caused yours?

    I'm sure mine was caused by headphone use.

    For relief, I play some nature sounds while sleeping. Mine is easy to ignore if I'm in a room with background noise. I also keep hydrated and try to eat reasonably well.



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  • Registered Users Posts: 4,555 ✭✭✭Treppen


    I think it was a combination of many things and tied up with hearing loss. Its weird though as about 20 years ago my hearing was going in the same ear after a cold, I did a week long diving course and a lot of swimming whilst traveling around beaches abroad. Cleared up completely and I forgot all about it until about 10 years ago it returned and gradually got worse.

    I probably had excellent diet and exercise during traveling too.

    TL;Dr I need at least 6 months in Thailand swimming and diving every day.

    Read somewhere also that it can be a side effect of some medications, I'm on omeprazole so I wonder has that caused it (or aggregated it).

    Has anyone ever tried hyperbaric chambers?



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