Did Researchers just Cure Tinnitus? | Lenire by Neuromod
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- čas přidán 16. 03. 2023
- Did Researchers just Cure Tinnitus? Doctor Cliff Olson, Audiologist and founder of Applied Hearing Solutions in Phoenix Arizona, discusses the recent news about the Lenire tinnitus treatment from Neuromod that got FDA NeNovo Approval, by using bimodal neuromodulation to significantly reduce tinnitus symptoms.
Learn more about tinnitus features in hearing aids at hearingup.com/features/tinnitus
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Great video, I had problems with tinnitus since college, but thankfully to Shirlest I found a way out of this !
Hey what did you do
I reduce my tinnitus by running more. After few days of running my tinnitus decreased. I also start eating more fruit and veggies. Less meat. I do meditation every other day. and my tinnitus is gone. Keeping your mind busy in different activities helps too. Hope this can work for some of you.
Keeping your mind buddy???
how long time that u have tinnitus before it's gone ?
@@niku7236 I start working on my tinnitus for 6 months. I start by making different ear exercises that I saw in you tube. Then I start jogging and exercising. Drinking fruit and veggies juices. I stop drinking coffee.
@@steamboxtamales7325 please how can I message you
Your tinnitus might be simple tinnitus. Some people have permanent. I got one with 4 years.
I hear the ringing no matter what. No amount of noise (or lack thereof) changes it in any way. It also varies wildly in "volume" and tone, and seems to be tied more to my stress levels than anything else. Sometimes it's a tinny high-pitched squeal, sometimes it sounds like one of those hearing-test tones, and sometimes it's barely noticeable and other times it almost drowns out everything briefly.
And ever hearing test I've ever had demonstrates that I have no hearing loss at all.
Same
Same. I have problems with anxiety, and I notice that when my anxiety level rises, so does the tinnitus - which causes my anxiety level to rise even higher - which causes more tinnitus ... which causes ... **sigh**
Same. I describe it to others as having a constant emergency broadcast test tones 24/7, but it definitely ebbs and flows with intensity, along with the occasional whooshing sound that I never realize is happening until the second it stops. So weird. Sucks too.
Same☹️
your symptoms are similar to mine except my hearing is just about gone. I think I mite have Meniere's disease. I bought the Neosensory buzz band system and it does nothing for me. $1,000.00 up in smoke.
This video gave me new hope. I've been dealing with severe tinnitus for 4 years now and it's been gradually getting worse. 😢 I've tried EVERYTHING and nothing seems to help. This video literally lifted my spirit because honestly, lately I've been feeling like checking out. I can't handle it anymore. But as a single father of 5, my duties here aren't done yet so I have to find the strength. Thank you! 🙏
Prayers to you. May Lord Jesus relieve your suffering and eliminate the source of your tinnitus. May God bless you and keep you always.
@@blokeontheend Thank you! That meant a lot to me. 🙏 God bless you. 🙌
I suffer now I lost hope I give up to join military I hate myself because it's my fault.
I have tinnitus for 26 years now. I can’t take it anymore. I want to sleep in silence… just for once 😢
Tinnitus is crippling sometimes. Prayerfully this will aid everyone who has posted here and provide much needed relief. Thank you Doc!
Thanks for sharing this video doctor Aud, I've been suffering with tinnitus for 15 years unfortunately in my left ear. It's affected so many things and even slowed me down a little bit with my time management, because of how distracting it is.
I just want this bad dream to come to an end, and be able to get my life back on track with peace of mind 🙏✝️
I'm only two weeks into having tinnitus in my left ear. The first week or so was suicidal inducing, so loud and constant anxiety. I have since noticed some lowering in the volume and it is even forgettable at times. Luckily this occurred as a result of an assault and brain injury by a adolescent psych patient where I work. So it's being covered under workers compensation, my doctor upon learning I have ADHD prescribed me Ritalin, and despite my initial fear of using it I found that it does indeed help with the perception of the loudness. I've also been prescribed gabapentin and thus far it's been able to help lower both the perception and loudness. I'm hopeful that this device is capable of being able to eliminate this issue. Though I fear that I'm going to just have to try my best to habituate, if I may ask, have you been able to habituate after having it so long.?
@@colinkillian9265 I've had it for over 25 years. You kind of forget about it unless you intentionally pay attention. Quiet rooms are murder so I always fall asleep watching mindless CZcams videos.
I hear ya only 7 years for me & my right ear. Hate it…
@@brianbagnall3029 Man, yeah, I have this since, idk, I never really remember not having this so I'm used to it, it is not even problem in quiet rooms, I can sleep or learn with that, still I kinda don't like it
Ok
What upsets me are all the people cashing in on our suffering.
Praying this truly works 🙏
Right, I have tinnitus and its a high pitch ear eeeeeee noise constantly, drives me up the wall some days and try not to think about it.
Instead of them actually trying to find a way to fix this problem, they try to make all these devices and gadgets and claim they work for profit.
Sure its nice that they are trying but if it doesn't work and they know it and have people lie on video and pay them to push the product in order to make a quick buck off the issue, like you said, its a scum bag move.
I highly doubt it! non refundable...
@@Zanforce I downloaded 2 noises from youtube. And run them together because so it wont worse tinnitus and it is really help. 1. White Noise Black Screen Sleep Study Focus 10 Hours 2. Ten Hours of Violet Noise - Ambient Sound - High Frequency
@@HS-vr7cq Actually violet noise does kind of bring the pitch down for a bit thanks.
Other one makes it get worse but violet helps thanks.
Running the TV or a radio at low volume all night relieves my tinnitus greatly.
Just wanted to say thank you Dr. Cliff for sharing this information. There are so many people out here that are suffering from this debilitating mental torture. I have had this high pitched eeeeeeeeeee for over a year now and you are exactly right it is not in the ears. It is in the brain. I have learned to habituate to this to the best of my ability . Masking sounds and distractions to keep me busy has been the best remedy so far. Winding down and getting a good night's rest and sleep has been the most challenging thing so far. Anyways, so glad to hear of there being a possible cure. This is exciting! Thanks again for sharing. All the best to you and yours.
Oui
@@elvinomachado2404oui oui può I gotta oui oui oui ouououiyoyoyiypuoyoyoi
"high pitched eeeeeeeee" XDD sounds very funny and relatable. glad i saw your comment
As a tinnitus "victim" for the over 50 years with relentless aggression lately, I so look forward to trying this!!! YEAH!
Have you tried this
No, no yet. Lenire is not available in Canada right now.@@nipinraj1
Any update?
No. The jury id out on this after several months in the field. Failures seem to outnumber successes so I'm waiting.@@justsomeguy6336
Did this work?
Dr. Cliff- I'll be following your story! Thank you for the investigative and research work into this condition, and possible treatments like this. Please keep us updated on your experimental journey with this device!
I have tinnitus for about 20 years now, recently I discovered that taking cold showers daily helps a lot - I'd say it at least halves the symptoms. It's might be hard to start doing this, but it might help You out too
I wouldn’t be surprised if it helps certain types of tinnitus. Cold showers release all sorts of neuroprotective chemicals and other chemicals responsible for affecting multiple parts of the brain and your nerves including circulation. I may give this a shot. I was already looking at trying them out just for the benefits.
It's because of the sound of water.
no it’s because it makes the blood rush
I found out that if I stopped taking showers for months, the tinnitus goes away completely. I haven't showered in years and it works!
@@ahndeux your tinnitus didn't go away.. your friends did.
I've had tinnitus for many years. People tell me to do things like meditation and relaxation techniques for me stress, but that's when it gets, or seems like the loudest. The only temporary fix I've had is going to the beach every week and hearing the ocean waves which is louder than my tinnitus but doesn't always cancel is out completely.
Tinnitus....SO many factors that affect when it happens and the severity! I've noticed work exposure to fan noise, HVAC or droning background noises can trigger mine. But the absolute worst and quickest way for me to have a bad episode is STRESS. I believe meditation, purposeful breathing exercises, stress relieving stretching and regular exercise is the best way to minimize tinnitus. Can't get rid of it but certainly has helped me tremendously.
Oh man the HVAC drone sends me into a spiral and I nearly pass out. May God bless you with a cure to resolve the root cause. Fasting has helped me in the past. It may be associated with inflammation in the endocrine system.
Same page exactly.
Omg I'm beyond excited! I watch the TEDtalk on tinnitus from time to time to just give me hope.
Thank you so much! I'm so pogged up!
😂 That was a refreshingly honest take on the Rumble/YT business models. I have a lot of respect for that. You do great work sir.
Clinical trials by the manufacturer should be taken with a grain of salt. Also at no point does he say he is not being compensated by the company for this pretty obvious endorsement.
If the manufacturer does not pay to prove their product works, who is going to pay? Clinical trials are very expensive. Because of patent rights the only ones who are going to profit on the device are its developers.
Thanks for keeping us informed.
my tinnitus really beats by stress- free lifestyle..when i'm starting to over think and get stress, it hits the brain to start ringing til it be like a taking off plane or cruise ship sounds to lost my hearing. Then, i discover relaxation, diversion of mind to other good things and adopt irritable sounds into calm mind. I think, when the brain got stressed it starts ringing of ears because they are connected. Thanks Doc.
Me too when I’m stresssed it gets worse I don’t really mind waking up to it when I’m happy
What a great video! I've had tinnitus since childhood. It always begins with a total lack of sound in one or both ears. Lately, it is more often, and when it stops, I still have a significantly reduced or total lack of sound. I would love to give this treatment a go. I have this hearing loss, but loud environments cause incredible ear and head pain, so hearing aids may not be the answer. I already tried them twice with Virtego as a result. Anyway, I'm looking forward to my appointment with you next month. You give me hope.
24 yrs on active duty and my tinnitus was so bad by the time I retired that I would get sudden dizzy spells or these flash migraines that would almost make me feel unbalanced but not quite vertigo. In 2022 the VA ran a number of tests on me and eventually issued me the Signia hearing aids. I wore them every single day, even when I was alone at home, and at first I felt as if everything was ‘way too’ loud and that itself annoyed me, but over time I guess my brain adopted and fast forward to today, I can’t go without them. On days I forget to put them on I do notice that my tinnitus isn’t as bad as it was before. So just a simple hearing aide is worth talking to your doctor about if you have severe or even just mild tinnitus that simply annoys you. Thankfully ya’lls tax dollars paid for my hearing aides so a BIG thanks to all tax payers :).
You're lucky. The VA denied my benefits and said I wasn't losing my hearing but I am and have been. Here we are now a year later and I think I've finally figured out why I passed the hearing test. Turns out I have this thing where I hear things like my alarm clock even after I've shut if off. It's annoying because I keep getting up to shut it off because my ears still "hear" it. I think the same thing hppened to me in that audio booth.
60% disabled with hearing loss and tinnitus, I will look into this. I tried a hearing aid but noise was so loud I would almost flitch at a car door shutting and loud places made me very uncomfortable.
I have had tinnitus since I was in college. It started when I attended rock concerts and then into the military where I had no ear protection when firing small arms and being around jet engine noise. I am now 73 years old, but it has been something that I have delt with over these years. For me, the sound is similar to a forest full of crickets. The only thing that has worked for me has been white noise. I tune a radio to and off channel FM and run it in the bedroom as I go to sleep.
I also have the cricket thing with a high level solid tone at about 10khz as well.Mine was night clubs and military service mostly.I just learned to deal with it.Had it 30+ years.Keep well.
Yep, mine is like a forest with a billion crickets going off...or a very still day with rain drops hitting a still lake... Mine came on after scuba diving for a few years... I just deal with it. It is worse when I'm really tired... Listening to it as I type. Hey ho, don't remember being without it now 🙁
Affirmative, for me it is chimes or audio books by a specific person who's voice works for me to get relaxed and sleep.
Ditto :(
Rat Lips: I have the exact history with firearms and jet engines. I am also 73; we must have been in the same squadron! White noise is a go to sleep assist for me and I have used some type of sound device for years to assist sleep. Good luck with your recovery
Thank God.
As a sound engineer I really need this.
I'm so afraid my tinnitus will get worse with work and it's pretty loud now.
Cheers
I'm a 26 year old mix engineer and get occasional tinnitus where my hearing in either ear goes out and I get a ringing in my ear for 10-30 seconds. Happens a couple times a week. Definitely scary, but it's comforting knowing there are treatments like this coming out should it ever get worse! Best of luck to you
@@andrew14145 thanks
I bit of advice I can give you is. Plug your ears, at least after the sound check. Have confidence in your sound check and you really shouldn't need the full range of your ears after that.
Cheers and good luck.
I relate with you completely. I do audio mixing in ministry and find myself questioning my mixes now and have secondary source to double chick my final mixes to ensure I'm not missing anything...or adding anything that shouldn't be there. Scary.
@@danaelston9848 hi Dana, thats sound engineering to a T.
We all question our mixes, I know I do and that was b4 the tinnitus 🤔😂
But be confident. You're obviously doing something right. Otherwise you wouldn't be a sound engineer!
People worry about the noise floor in recordings and such.I am very into good stereo home audio and have chronic tinnitus,so those worrying about the so called "noise floor" should try living with this.I still enjoy music despite this.Cheers to you too.
The beauty of this device is that it’s ACTUALLY a foot in the door. It might not cure everyone right now, but it’s something the medical field can use to improve upon that can lead to better treatments and/or cures.
You actually trust the medical or ICal establishment,ents to do the right thing vs in it to make money. Better yet they won’t do anything.
Oh my god, I would really really love this... My tinnitus has become absolutely unbelievable recently. I'm only 22 years old and I stay awake at night crying and staring at the ceiling because this high pitched ringing drives me insane. I can't sleep or hear myself think. Some nights I just want to bang my head against the wall. I really, really hope this will soon become available for everyone. It sounds like a dream to be able to perceive silence again.
omg, exactly the same for me as well. Have you found anything to help?
@@AmorilV I found that when my tinnitus gets super bad at night and I can't sleep, if I play upbeat music throughout the night in my headphones I usually wake up to it not being as bad. I can't play it very loud or else it'll hurt more but it's a temporary solution for now. I've also tried a few exercises I've found online like tapping the back of your head and tugging on your ears, but it's very temporary.
@@novadearesti got tinnitus 4 days back now i am thinking to give up on my life pls give me some hope
Hi people. I feel for you. My tinnitus came during the pandemic and I was in extreme stress when I got it. At first it was low and I was wondering what it was. But since anxiety is a disease my brain fixated on that ringing and the rest is history. I struggled for many months fighting the noise.
My recommendation is to do whatever helps. I didn’t take meds but I probably should have. Talk to your doc.
If the tinnitus is causing anxiety the anxiety has to be addressed. That’s issue number one. It’s not the tinnitus it’s the reaction to the noise. Imaging being next to a loud fan. After a couple of minutes your brain would tune it out because it doesn’t perceive it as a threat.
However if your brain thought that fan noise was a problem which is what anxiety does then it would start worrying about that fan.
There’s two different things I’ve tried.
One if masking. Finding anything that will help you sleep. For me if I didn’t sleep well it cause more anxiety. Sleep was where my battles were and continue to be. You can try going to insight timer and doing different mediations, or using their white noises or their tinnitus retaining tones with the beeping noises. Those helped me much early on. Or buy a loud fan, water foundation, run a podcast to listen to or listen to music all night. Bottom line is that once you find anything that works you’ll feel so much better and will regain some of your control.
The second option once you’re sleeping and living with it with masking is trying to lean into it. Listening to it and allowing your brain to see it’s not so dangerous so far. I worked with Dr. Gans and she helped me reminding me tinnitus is a paper tiger. It can’t harm us. It’s our interpretation of the noise that we have to deal with. So if you go to sleep with nothing in silence eventually you may be able to not need masking. I’ve done that before but I’m trying now to work my way back.
Also try to do things you enjoy. Going out and talking with other people for me helped since my brain would be engaged.
@@julesv2914did you get any of the cov*d shots by chance? They are causing an adverse event of severe tinnutis in ppl and for those who had mild tinnutis before the shots, it's made it way worse. Inflammation in the spinal cord and brain is what caused it. Stanford and mayo clinic have been studying all this. One of the cov*d manufacturers makers had it happwn to himself and has been very vocal about it. Please use a non censored search engine to research like bing. And please look into the tms treatments that are curing ppl!!
I’ve had debilitating tinnitus now for 5 years. (Tinnitus overall for many years prior). I’m really hoping this device can bring it down to a tolerable level so I and so many others who suffer have a shot at really enjoying life again. This is amazing news , especially coming on the heels of FX-322 going bust. Thank you for all you do, Doc. Stay strong everyone and take care.
What happened 5 years ago to make it debilitating? Is this the natural progression of tinnitus? Mine just started and I was hoping I would just habituate with time.
@@rz5206 mine went from noticeable to debilitating to back to pretty shitty but not terrible
@@Moon_dinosaurs Mine came on after a NBA Playoff game that was extremely loud. It has been over 20 years of head ringing. I has gotten worse because I love to play the guitar. I have not given it up, although I use ear plugs. When I go see live music use plugs. I would say it is at the shitty mode in my case. Some days it is terrible. Good luck
Read the studies dude. This is a SCAMMMM
Yes
I remember first hearing it while lying in bed when I was six years old. It went away briefly, but then came back and has been with me ever since. It's loud - bells of St. Mary's loud, and it really interferes with my ability to process speech. It's like having an obnoxious kid constantly beating pots and pans next to your head (try doing that while engaging in polite conversation, delivering a speech, trying to sleep...). I've tried all the snake oil and acupressure methods. I've spoken to specialists. They run lots of expensive tests but have no idea how to fix it. I'd try to fix it myself with ice picks, but I'm assured it won't make it go away. At 62, I'm pretty sure this is going to be with me till I die. Something to look forward to.
I'm in the same boat, 21 here and I'm almost sure it's not coming back, it's been 12 days with it and it's gonna be a long road ahead of me
Yes
Aww, I hope it gets better 😢
I've had Tinnitus since I was a little kid and growing up to work in the fire service has only served to make it worse while simultaneously increasing my hearing loss. Any treatment for Tinnitus would be amazing.
Try taking 1000mg a day of magnesium gluconate. Magnesium has shown to dramatically reduce tinnitus in some patients, including myself. It may take a few days before you notice a difference, but try it for about 2 weeks to see if it works for you. Magnesium gluconate gives the best result of all the types of magnesium.
@@RacerX888yes you need to be very careful with which type of magnesium you’re taking and really should be discussed with your doctor prior to treatment. Some magnesium supplements can cause diarrhea as some are used for constipation.
@@RacerX888
Thank you for the information. How did you get tinnitus?
🔥🔥
🔥❤️
Thanks for getting this out!
This week there are 15 US clinicians who are meeting in Dublin Ireland for training by Lenier to prepare to start fitting this unique instrument in the USA. This five day training plus an online academy has been provided to these very high level professionals who have vast experience already. I am very pleased Dr. Cliff has brought awareness to this ground breaking new program. Thanks to Ross ONeill and Hubert Lim for their outstanding science based efforts.
So today was the last day of the five day event and now these 15 conditions are headed off homeward to the United States and we are going to be able to start dispensing these units around April 23. It’s interesting because we have already been informed that there are thousands of people who have registered for Internet to receive priority in our clinics across the country and we’re spending quite a bit of time this week. Creating a plan to handle so many thousands of people who want to try this amazing new bimodal tinnitus treatment. Definitely going to be a rush of people for this new method that has been again 12 years and they make him and has definite differences from previous treatments.
Can you tell me where to find the list of the 15 doctors? I’d like to add myself to the waiting list. Thank you for the information!
@@tomir2012 it will be posted soon on their site
@@tomir2012 yes me to please
Let's hope it lives up to the excitement and hype and truly helps without any symptoms or added discomfort. Optimistic but cautious. Metabolic drivers of Tinnitus are NOT easy to fix. I imagine 15 is a good start but not a lot for as many folks as there are in the USA!
I've been following this company for a few years now and I was able to get on the waiting list for when the doctor's here in the USA are trained with this treatment. I can't wait.
How can i get on this list
@@martyr4844 I was on their mailing list for updates and automatically got an email to be put on the list Try going on the website and signing up for the newsletter. There may be a spot to get on the waiting list on that.
Just looked at this in the UK £3295
@@susanmarielamphier746 What is the website or the email to reach out to get on this list? Thank you kindly.
Yes same..!!!!!
Just found your site. My tinnitus of decades has recently been getting much worse...to the point now of mild panic at what lies ahead for me. Frankly, I quit looking for resolution of the problem. Thanks for some hope!
Have you been vacc*nated w/ any of the cov*d shots by chance? They found a link between the shots & causing tinnutis. For people who already had it before the shots, the shots have made their tinnutis way worse. Doctors are studying the link/cause at Stanford, Harford, mayo clinic etc..they are pretty sure the C shots induce inflammation in the spinal cord, brain, and ears, causing the adverse event in some people. My mom is suffering severely and she never had tonnutis before the shots. Her specialists have told us it was caused by them, and for her to not get any more boosters. The more boosters you get, the worse the tinnutis can get. There's a man who was In his 60s who had the adverse event happen, causing horrible tinmutis, & he couldn't handle the mental trauma from it being so bad, and he unalived himself. I'm spreading the word bc my mom has expressed If hers doesn't get better that she can't handle this much longer. We learned that TMS treatments are helping people greatly reduce their symptoms and even cure It
That's the next step for my mom. You can research all this yourself. I suggest you do If you have gotten any of the shots. If you havnt, I'm sorry, I know tinnutis can also be caused by hearing loss and it can be genetic. But yeah, don't search on Google, make sure you use bing search engine or a search engine that is not highly Censored.
I hadn’t realized it was in the brain. My solution to deal with it has been to go away in my head. When going to sleep I get involved in an interesting daydream so I’m not focusing on the “noise” in my ears which feels deafening if I focus on it.
I was just sitting here unaware of the ringing but soon as I finished your video I can hear it pushing in again.
I worked on a flight line for 20 years. I was **religious** in my hearing protection (often doubled up) because I didn't want to spend the rest of my life with Tinnitus. Still got it. I'm hoping this device can help.
Same here. Only 8 years on the flightline.
Snake oil. Watch for Dr. Susan Shores device. Developed over 13 years.Passed all of the required studies, waiting for paper to be published and FDA approval.
Same, helicopters- 12 years 🙄
Audiologist told me you can still get even if you use ear protection as sound waves still travel down the mastoid process, great...
@@markbalancehealth "your tinnitus is not service related". . . >
I've had tinnitus for about 33 years now. for the last few years I've thought it was getitng worse but I think it's losing my hearing and as that happens the Tinnitus is getting louder. It's absolutely maddening.
Look up tms treatments! They are helping tons of ppl! Research on a search engine like bing and not one that is censored like Google.
This seems very promising. I hope to follow these developments over time to measure their effectiveness cause I've been living with this for decades. Thank you doctor Cliff for the update.
These trials were run in European countries. I wonder whether trial results would be similar for non-European people.
JPB
Tinnitus is awful - you don’t feel quite “with it” all the time. Hope this continues to be successfully as a valid treatment.
Thanks for this- I have terrible tinnitus
I’ve had tinnitus my whole life. Only recently I’ve started to get more aware of it. It’d be pretty cool if it was quieter.
Same here. Over 50 years for me, and the ringing is in my brain, not my ears.
@@thejimmy6533 Have a proper diet then , to nourish ur brain cells ..especially if ur tinnitus is in ur Brain..
Neuroplasticity
Have a good diet with Anti inflammatory things + the food rich in vitamins and proteins ..
prevent from consuming things containing sodium
Have a sound therapy for 15-20 minutes everyday
eat non veg more than veg
do exercises with high intensity
and definitely ur tinnitus will get reduced ..
Thanks
You can try the hearing Aids, even the AirPods Pro with the transparency mode can probably eliminate the problem
@@Ideal_Lightning007 you know this from experience?
@@jnorb8633 Yeah
I’ve had mine since I can remember which is 3 years old. I even asked my mom what that sound was. I thought it was the sound of my thoughts and that everyone had it. It has NEVER bothered me until I found out not everyone had it. People could actually have complete silence!
I'm the same. For the longest time, I thought it was basically just TV static for the ears.
I’ve gotten mine from the third Covid shot which is recent enough that I can still imagine what hearing silence feels like even if I cannot actually hear it anymore. It’s honestly kinda infuriating. :/
@@ThePC007 sorry to hear that. Yeah I heard thats one of the side effects of the shot. Mine might have gotten worse because of it.
Same here! Ignorance was bliss for me.
@@wonderwoman4875 Exactly!
Thank you Dr. Cliff for sharing this. I work in construction and I've had severe tinnitus for the last two years. This is really good news. I'm from Kenya and I'm hoping they can make Lenire available in my country too.
In kenya too
I used it exactly as specified and it made no difference to my Tinnitus. I would have thought Neuromod would have been more interested in contacting me and helping as much as possible to make the treatment successful. This wasn't the case either. It cost a lot of money for nothing.
Now how is that possible? it apparently is not even available yet. Do you mind elaborating? Thnx
@@recipehacker9752it’s been available in Europe for quite some time, the user experiences have not been very good contrary to the company’s claims
@@recipehacker9752 it has been available in Europe for over a year….and be warned it was not impressive in results as this video stated. Only data on its effectiveness was released by neuromod….they used the tinnitus handicap index score as their criteria for improvement so any improved score was logged as a success….however that even means if an individual improved by one or two points it was logged as a successful improvement. Of course by analogy taking a pill for a headache that moved it from a 9 to a 8.5 not very good for a cost of 3500 dollars. Please do deep dive on the actual in depth analysis that are available before spending your money. Some individuals it really did help not saying that….but many experienced no improvement or only the slightest of margin improvement for a lot of money. Bottom line it’s a gamble….no guarantee of improvement with no money back if it does not work.
@@Andrew-pp2ql I appreciated your detailed response. I guess the product is too good to be true. If it were cheaper, I’d be worth a try. Stay well rested, hydrated, and otherwise healthy is all we have so far in the way of conservative treatment for this constant noise named Tinnitus.
@@recipehacker9752 perhaps at years end the American organizations offering Lenire may offer their own assessment after compiling data on its effectiveness (if Lenire would allow them to do so). Treble health is one of them and be nice if a better criterion could be established for whom this device would have a better chance to benefit vs those who would not. Unless such a thing happens it’s a buy first then see if it works shot in the dark. If your tinnitus is somatic (movement of neck or jaw muscles alter the tinnitus sound) I would certainly hold off until next year when the far more promising auricle device is released….aka Susan shores device. Take care
I suffer from tinnitus very similar to yourself high pitch ringing but in both ears. So I'm really looking forward to hearing just how effective it is, when you trial this method.
Lenire is a scam. No placebo control in the research. Susan Shore's device is what actually works.
Start saving!
@@keepingitreal618 yeah i bet it’s heaps $$$$$$
Very Diluted apple cider vinegar in water with lil salt poured in ear left in for a minute will help relax nerves
@@joeimbesi99 This is bullshit, how is this supposed to help relax nerves? Vinegar (acetic acid) is ototxic and can damage your inner ear.
Thank you. I just joined a wait list for assessment. Will let you know if I hear anything.
Hell yeah I'm signing up for this today. Thanks!
Thank you, Dr. Cliff. This was very informative.
Tinnitus impedes hearing by raising the noise floor. This is like trying to listen to a distant AM radio station in your car radio and driving under a power line that emits radio interference. In the case of tinnitus, the noise is phantom nerve noise.
I've had Tinnitus since shortly getting out of the Navy as a Radioman. I spent eight years with headphones on and under multiple speakers blaring one sound or another and sleeping under an air vent outlet. There were also many other loud noises while deployed and my ears never got any rest. And now I have hearing loss as well and the VA gave me hearing aids. I can hear better, but this whooshing, buzzing noise is in both ears and most of the time the sounds I hear are different in both ears and sometimes wakes me up and I think a truck has hit the building. I really hope the Lenire, when it comes out, will have a positive effect. Thank you.
If you have had any of the cov*d shots, please be aware they can cause tinnutis or if you already had it before the shots, they can make it much more severe. It's an adverse event. They are studying it currently at Stanford and mayo clinic. They are also finding that tms treatments are helping people reduce their symptoms greatly!
Your presentation is convincing. Thank You very much for the info. I am going to try this system.
I have a variety of tinnitus sound, I can break it down in 3 main sounds; the highest one is that high pitch iiiiii from an old television turning on, the middle is the worst, with the sound of a waterfall, and the dark tone is like a huge diesel enginge far away from you at idle rpm.
Very encouraging! Mine started a couple years ago after oral surgery. I am scheduled for hearing test and visit with ENT and will ask about this. Sign me up! Thanks to your videos I understand why it’s worse on quiet Saturdays at home-I work in an environment with white noise M-F, but that’s where I sometimes have a hard time hearing people. Tinnitus is quite a puzzle.
Can you share what your ENT says if your comfortable sharing? I also got tinnitus recently and it's very annoying
Ent are usually garbage
Mine got extremely bad after an implant operation on my jaw. I did have tinnitus before that I think from earwax & anxiety. But after the operation it was really bad & so was my anxiety. I had 3 years of hell, with the anxiety symptoms & roaring tinnitus, it brought me to tears many times. I’m kind of handling it better now, hearing aids help.. but I crave silence 😢
Mine started after surgery too! Woke up with high pitched sushing in my ears. Got worse after Covid. And now worse after a stupidly loud concert. But yes. It all started with surgery. I’ve been told it was possible the anesthesia
Ok
I suffer with tinnitus as well. It started when I was 12 years old. As a teenager and later I've accidentally had my earbuds set too high or bump a button and blast myself. Or, I work in a call center with a software that beeps 3 times to indicate the sound is working in the headphones, but the 3 beeps are obnoxiously loud and apparently no way to change it - therefore, I move my earpads away till I know it's done. But, I still sometimes forget. Or, I'll have a very quiet caller, then a very LOUD caller and get blasted. It's all made my hearing and tinnitus more prominent and annoying.
Great information thanks, hope treatment will be available, released by FDA. Thanks
I’ve watched a lot of your videos but I never knew you had tinnitus too.
I’m sorry to say that I used to think you were just like those other doctors that spoke without actually knowing the pain of the condition. Now I know you’re in it with us. Thank you for sharing research with us and for staying positive despite the challenges and disappointments with this illness seeming insurmountable.
He's full of it
@Miraak If you need to ask, no amount of explanation will help you understand.
@Miraak you're so easily triggered.
@Miraak I know more than you for sure. You're the one asking me for information. And then having a little hissy fit.
@Miraak pretty sure rockmusic is just saying stuff to get a rise out of anyone who will fall for it. If they actually had anything to prove, they would have provided some form of evidence, instead of pretending to be a pretentious snob in an attempt to avoid having to provide proof. I gotta admit, their trolling attempt was pretty low effort, but it did seem to work on you. Have a good day, and don't feed the trolls!
I worked in car audio for 10 years. I wore hearing protection all day. The only time I took it off was when I actually needed to listen to the system, and even then I kept the volume down as much as I could. My hearing was quite good until I got COVID. Now I have quite a bit of tinnitus...
I with you….long term affects never studied. Som of the videos I watch show trying to remove toxins in the body.
Interesting. I hadn’t corollated it with with Covid, but It’s been noticeable since around the time I got Covid. And I’ve only got 5% of my sense of smell nearly 1.5 years later from Covid.. … 😢
Dude, listening to your voice and what you are saying to us, reduced my tinnitus
Sweet, you're in luck...I've got over 1,000 videos.
Had it since the early 70's, going strong right now, very high pitch!
It just became available in my area and I was so excited. Sadly it is $4,000 out of pocket and not covered by insurance which puts it well out of my ability to get it 😢. I'm sure this will be the case for many people.
I predict Neuromod will eventually be sued for fraud
why aren't you using it Doc? great info god bless
Nice, but the key question is will any American medical insurance companies cover this device. Per Google the expected price in the US is between $3,000 - 3,500. No current insurance covers it. I hope this changes soon.
My personal experience is this: At first i pretended that my tinnitus was my ability ti hear special universal sounds that nobody else could hear. After that I trained myself to ignore it and not being bothered by it. That's how I live, ignoring it and never getting upset with it. Things that make it worse are: taking a daytime nap, red wine, stress.
This new device sounds promising. I will surely try it.
LOL I told myself the same thing!!! Too funny :)
Same here. You have to tell yourself this or you will go insane, but it overpowers my mind at times. Especially when I'm sleep deprived and stressed out. Hoping this really can help. I'd be happy with just half the level of ringing I experience. It started at age 16 and I'll be forty in August
@@NellyEIEI try to sleep well, very important ! Also learn to meditate, it seems to help if you do it every day. And avoid junk food. Best wishes.
@@NellyEIEI mine began after a nasty JAB in the AF in 1990. If I had it before then, IDK but only recall it after that shot and it's gotten progressively worse as my hearing has diminished. Seems they are directly improportional as far as I can tell. Right now, as I type this it's maddeningly loud in my head. I can distinguish 3 different types of noise within the umbrella of Tinnitus and that doesn't include the common random occurence of popping and cracking that has an electrical sound, like a static charge does when you zap yourself in the winter.
Yes same.
Dr. Cliff, I am extremely excited to hear this. I have very bad tinnitus and have been very depressed over no treatment for it. I know that some people have tinnitus as a result of natural hearing loss. However, I suffered physical damage from a diving accident do you know how many of the people treated successfully had physical damage? Just curious.
I’m going to chime in here in the hopes of helping you have hope. The physical damage has long since healed so the only reason the tinnitus continues is because the brain has created neural pathways and those pathways can be changed bc of brain plasticity which is what Lanier is doing. Also Look into the biopsychosocial cause and treatment of tinnitus.
Ok
This tinnitus is horrible especially for those of us who have good hearing, therefore for me its not related to hearing loss (checked recently with no hearing loss at 65)It is really annoying because I happen to be one of those people who cannot tolerate noise such as vacuum cleaners, fans, even a car idling can be annoying, but when you have this thing in your head and cannot get rid of it. I do however, find that I am worse when I am stressed. I will be off to the audiologist shortly to see if there is anything that will help (as I run out of time at my last appointment. I meant to add that I am very sensitive to noise.
I’ll wait for the reviews
Something to watch! I wonder if the company who made the device is the same one doing the studies. That would concern me greatly. Without outside studies, I wouldn't trust it.
Unfortunately it was….in addition this video left me a little disturbed….the vast majority reported improvement but once one takes a deeper dive under the hood
it gets little less positive. The amount of improvement was assessed by the tinnitus handicap score…the vast majority of scores did improve (why the high success rate) but the amount of improvement in the scores was minor improvement that is one’s tinnitus was slightly less bothersome. For a 3000 dollar expense I would like to see more not to mention many reported zero improvement with the device culminating in a large capital loss. I plan to hold off until I see more results within the states showing this device is justified by the results. 3000 cost is not cheap for something for many resulted in no change or slight improvement
@@Andrew-pp2qlvery well put I have tried the device and many have the same poor affect :( there is a forum called tinnitus talk where lots of people tried it when it first came out and the results where disappointing for these people I just hope Susan shores device is better and America will get that first :)
My tinnitus came on about twenty years ago when I was put on a beta blocker for tachycardia. I had an operation to improve it but the tablets left me with a ringing, hissing noise that has gradually got louder over the years. I now have some hearing loss too. I hope this new technology will help along with any others that are being developed but I fear they will be very expensive and stop many people from being able to benefit. I do find exercise helps as others have mentioned, and de stressing, and eating a low sugar diet. If I don’t do these things it gets worse. But going to the gym has helped, and I’ve learnt to live with it and accept it which I think you have to do, don’t fight it just try to stay calm. I’m in the UK so it probably won’t come here for ages yet as we seem to be behind the US on new medical procedures.
I wonder if that’s what caused mine. I was on a beta blocker for years for tachycardia. I now have pulsatile tinnitus.
@@HERbotanicaboutique when I read the side effects of the tablets I was on it said consult your doctor if you get ringing in the ears. I mentioned this to my doctor and she looked at me blankly and didn’t seem to know about it. Most doctors don’t seem to be that interested in the side effect that drugs can cause you. I’m pretty sure that’s what caused mine, as it only started after I’d been on the tablets for several years. I find paracetamol and any pain killers make it worse, and if I’m not well with a bad cold or virus it gets worse. I’ve read pulsatile tinnitus can be caused by lack of iron, but you probably already know this. Also B12 can help as it’s beneficial to the nervous system. I have tried B12, but didn’t notice an improvement, but I might try it again. Hope you find something that helps.
Oh, ❤I really hope this is a treatment that comes to all countries, including Australia. I will be putting my hand up for sure
Thank you for pronouncing it properly! It's not an "inflammation of", and therefore, it's not an "eye-ti s", (itis). Thanks for the info. I'm wondering about the $$ I will call about it. I have at least 2, very strong ringing pitches in my ears.
This sounds promising! I've had tinnitus for 25 years and its getting worse. I'm desperately looking for relief.
Keep me posted if you get this treatment
Do you have problems whit your temporolmanbular joint?
I’m not an Audiologist, but as a Hearing Instrument Specialist I am intrigued about the prospective effectiveness of this new technology. I have a mild hearing loss that is not considered treatable with hearing aids nor it it enough loss to cause communication issues yet I have moderate tinnitus constantly. Admittedly I have tried all the “snake oil” treatments out of desperation to no avail even though I knew better beforehand.
Appreciate you. This is something I need to look into as soon as it is available. For me it sounds like crickets, non stop crickets, and its annoying af.
im looking forward for it. ive been diagnosed with tinnitus way back 2021.
Given that the measurement had to be based on self-report, do you think part of the positive result is placebo effect? Or were they able to create a double-blind study with a control group that didn't actually get the therapy?
There was no placebo control. The study and device is a sham.
Placebo effect always plays a part in every health related study. Always.
@@Swearengen1980 That may be true, but properly designed clinical tests will sort out how much of an effect can be attributed to the placebo.
Ok
Cool
I have no hearing loss, but the opposite hearing sensitivity some noses are painful. Would this treatment be an option for me? Going on 5yrs tinnitus seems to be getting louder, sound therapy does help. Are there any negative reactions to this treatment?
I'm so keen on this. My youth was all motor racing and loud music. I can always hear ringing.
I'm an engineer, and even for me this had way more jargon than necessary. It needs to be re done with a quick brief overview and what it is, and how to get it.
Meditation and listening to Ajahn Brahm or Yongey Mingyur Rinpoche helped me so much.
I think meditation helps getting in that “let it be” mentality and being able to focus more on what I’m doing at the moment. Also noticing my breath throughout the day gives me another thing to relax and something to have some awareness or the current moment.
80-90% of individuals naturally habituate to tinnitus without the use of any device costing thousands of dollars. That usually happens within 12-18 months naturally. So when Lenire says that the vast majority of people experience benefit of using this device 12 months later, how many of them would have habituated regardless of the device? How does Lenire measure "improvement"? How much of it is placebo? The Lenire device has been available in Ireland, Germany and other European countries for years now. Funny I haven't heard that Tinnitus has been eradicated in these countries. Many audiologists are excited about this because it is a new mode of income...I guess it is buyer beware.
The skepticism is appreciated. However, the cynicism called the authenticity of your skepticism into question. I think we should alway question if something is legit or not, but always assuming a profit motive over a noble motive is rather cynical. Audiologists have had access to limited tinnitus treatment options for our patients, and many of us just want a solution that helps them. Time will tell if this treatment moves the needle, but to many people are killing themselves for us not to try.
How much does the Lenire device cost and have you heard of any positive long term results?
The Tinnitus Club.. 30+ years dealing with this agonizing sound/tone.. wishing the best outcome/cure for all in the near future..
I was an Audio Engineer. I used to have extraordinary hearing with a range up to 22Khz and extreme sesitivity, I could hear better than dogs. I could hear sounds nobody else could and it amazed my frends many times. This was until I was in my mid thirties when my tinnnitus started. My older sibling warned me that I might get it since she already had it. It started intermittantly in both ears. It drove me crazy and with time became more cnas more constant.. Now in My fifties It is constant. I have good hearing but not the extraordinary hearing I had.
I was not aware that that the medical community was aware of the true cause.
ThisLenire system is worth investigating as you have nothing but time to lose. What concerns me this seems like a paid as since he uses the phrase "Lenire by Neuromod" many times,
Hey, have you already tried the GABA treatment? I've heard from another neuro-specialized doctor that it helps in many cases.
Lenire was approved the FDA , it’s true I am waiting until my audiologists start offering the device
My tinnitus gets triggered when I work on kick drums for a long period of time. I used to spend hours layering and processing kick drums (as well as other sounds).
So the Lenire system is free?
@@hemtet5500 I don’t believe is free
I developed classical 8000Hz tinnitus about two years ago. Hoping my local otologist office will offer the Lenire tinnitus treatment from Neuromod and that it will significantly reduce tinnitus symptoms without the use of hearing aids. I'm 64 and have normal high end hearing loss (I hear well to about 12KHz), so I'm more interested in relieving the constant 8000Hz ringing than using hearing aids at this point in my life. If this helps it would be a godsend until maybe one day this condition can be better understood.
You're the only person beside me I heard that from .. most people never investigate volume and khz .. making me think theirs isn't super high as mine
@@Lrasm13sadly my local otologist isn't participating in any trials of this methodology. The nearest one is too far from me. I still hope that if it does work and has a good benefit that more will adopt it.
This was done 6 months ago, and I'm wondering what you might have to say about this treatment now? Have you had a chance to see it work?
I finally got my information sent to a provider to get the device! I'm so excited :) Now I have to wait for scheduling due to high demand.
Hey..How did it go, did it work for you??
@@rafiikimuziki I haven’t tried it yet. Waiting to see reported results. I’m fine waiting for it and also Susan Shore’s device.
I've had tinnitus for over 40 years but now it's so loud it's keeping me awake. It's almost unbearable at times! I hope I can find and be able to afford this type of treatment! 😭🙏
Heard about linocane injections helping. Also apple cider vinegar diluted in water 20 :1 poured in ear left in a minute lie on side can reduce sound dramatically.tapping finger behind ear helps
Yes
Have exactly the same for last 16 years😢😢😢 nothing helps so far. Hopefully one day it will go away.
@@kristskanavins1921 🙏🙏🙏
I'm having a bout of tinnitus right now in the right ear so add me to your list. My tinnitus seems to get much worse when I am under extreme stress, such as today when workers are installing solar panels on the roof and my golden retriever is freaking out.
Visit a professional first. Unilateral tinnitus might need to be investigate. 🙌🏼
@@rampagealex mine is only ever present in my left ear, after an assault and head trauma from a psychiatric patient where I work. I've yet to see a ENT but the workers compensation Doctor says he has seen this type of injury thousands of times, and the VAST majority see major improvement over the course of a few months. Thus far it's been a bit over two weeks, and I've seen some mild improvement in loudness. I was prescribed gabapentin and it also seems to help, along with him also prescribing me Ritalin for my long untreated ADHD. The Ritalin doesn't make it less loud but it seems that I'm less focused on it constantly. He said that if it doesn't improve in a week, that I'll be sent to an ENT..This is truly a nightmare, but hearing other people give their accounts I feel lucky as it truly seems to hell on earth for them..God bless us all..
Mine comes from my neck as well. If your a side sleeper try thr other side for clues. Wish you remission.
I have suffered tinnitus since I was a teenager I am currently 57 years old. It has gotten worse since I’ve gained some weight it seems to go away when I lose weight. I mean it doesn’t go completely away my case of tinnitus is much more severe than the average person. I would love to be able to participate or take advantage of this program it would definitely say my sanity
Hopefully, this will be an option for veterans such as myself and VA will offer it as a treatment option.
Would love to learn more about your experience with Lenire if you decide to proceed... keep us posted. However, I am somewhat confused about Lenire's efficacy. I had read that their data wasn't all that great. Some patients also reported that their tinnitus got worse from using the Lenire device as well... maybe it was a very small number of patients reporting this?
What about Dr. Susan Shore's auricle device? Is that something you would consider waiting for and trying? Seems like there's more solid data behind her research and clinical trials, no? Also sounds like her device is going through FDA approval and could be coming out in the near future as well.
I'm also curious about Xen1101 which is apparently a much-improved version of Retigabine, which was taken off the market due to severe side effects. There seems to be optimism about Xen1101 potentially treating tinnitus for some patients since it targets the same potassium channels in the brain that impact tinnitus, as it does with epilepsy.
The 15 new providers in the United States will begin to provide the Lenier system for tinnitus therapy starting at the last week of April
I also am concerned about worsening, if the effect is related to the benefit hearing aids are supposed to offer. For me, hearing aids just made my tinnitus louder and more intrusive.
@@roxyiconoclast yep has not improved mine at all in fact with hearing aids in worse
@@gbdchannel2252 interesting. I was not aware of this. It did not come up in my research, but that's several years back--when I had a concussion in 2014 and realized that we really weren't taught much about them in my schooling, just contraindications to any treatment of client/patient and to refer out for TBI related symptoms because it's outside of the professional scope of practice (for my field). I'd love to dive deeper into this, as I'm a sponge for information and love to truly grasp the functional considerations of anything in the body. (Also, I suffered severe brain/nervous system & systemic inflammation and damage from mercury poisoning again (3rd highly symptomatic episode) since 2018, and suffered another head trauma May 2022 when a kid crashed me on a bike trail and launched me off my bike, landing hard on my hands then face. In addition, my mother suffered a series of concussions winter to spring of 2022 and now another toxic mold exposure, and I'd really like to see her fully recover.) Any links you can share to specific information and/or remediation would be greatly appreciated! Thanks so much!
Yes same.
Skeptical. I’ve had since my first chemo treatment. 17 years later, severity up and down. Until one morning, heard 2 seconds of imagined tea kettle whistle, stopped tinnitus in left ear ALL DAY. Woke up next morning, it was back. I believe there is a physical component.
I bet it also how your Brain processes stuff.
I’m going on 15 years of tinnitus. Had a similar experience one night sitting on my couch about two years ago but mine was more of a popping noise and then silence. Woke up the next day and my ears were ringing again and have been since. Weird
@@joshuawileczek6215was it scary when it went silent? I think I would actually be nervous at first if my tinnitus went away for at least a while although I pray one one day it does.
I wasn’t nervous, I was actually thrilled because I thought it went away which would have been life changing, but it returned very shortly after. Pretty surreal experience after so many years of constant ringing tho
@@jaysquared9638 on the positive if it’s possible for it to stop for even a short period then it is possible to go away.
Few years back through the local hearing clinic, I tried hearing aids that added a background tone, the theory being it would cancel out the high pitched ring I had it in both ears (different pitch tones). After a few days I heard people better with the aids, but the tinnitus was not only worse, horribly, I now had two tones going in each ear with aids removed. The tones are so loud sometimes, I can't hear much else. Its been going on for so many years I honestly don't think anything will ever help.
Ive had tinnitus for 5 years in both ears due to ear infection and noise exposure and my advice is don't let it get worse with the biggest offender being ototoxic medication which in my three experiences has made my tinnitus sharper, louder and rawer/ more piercing and, although after 2 - 3 months it subsided to a base/ manageable level, each time it failed to settle back down to what it was before taking the medication.
Second offender is sudden sharp loud noises which I have had quite a few of but never lasting damage/ always settled back down to what it was previously after 2 - 3 weeks, sometimes its only lasted hours then settled back down (I carry foam ear plugs to go out and if I'm going somewhere I suspect could be loud I also take ear defenders).
Second bit of advice is make sure that you don't have wax in your ears or near or on you eardrum as in my experience multiple times after getting wax out my tinnitus has become almost inaudible (wax removed via an ENT using manual extraction as apparently microsuction is too loud near the eardrum which can aggravate tinnitus). As well using distilled water ear drops put in a glass pipette bottle helps to remove ear wax.
I have experienced severe tinnitus in both ears for extended periods but as for my tinnitus now my left ear is pretty inaudible its only when I lay on the pillow is when it becomes louder and bothersome but I can sleep through it, however my right ear is mild/ moderate and when I lay on the pillow it becomes quite severe, although I can still sleep through it depending on how tired I am (I sleep with 9000Hz white noise and a fan).
The best way I can describe the tinnitus in my right ear when not laying down is by using audionotch's tuner on 9550Hz at 1% volume and computer volume at 24 although the tinnitus doesn't sound quite like that and its not as pronounced as the pure tone/ the tinnitus has more of a dispersed effect.
I am 43 years old, and have always had this as far as I can remember.. and it does sound exactly like a forest of cicadas. Sometimes it gets extremely loud, sometimes it will ring very strongly in only one ear for a moment then gradually fade back to both ears. I do not know what it must be like for others who do not hear this as well…it is what I am use to. If there isn’t a fan or something running as I am trying to fall asleep, I just focus on the ringing in my ears and soon fall fast to sleep..
omg that is exactly what I hear too, a forest of cicadas..most of the time I thought of it as soothing until it started to be a little louder and now I can notice that only I can hear it :(
In 2017 outside of Chicago upon starting a new job, I was held at gunpoint, an AK-47 by 3 co-workers in a basement after a trip to a bar after work. They blasted 160 decibel deafening music and I lost my hearing. Was denied disability twice. Now I wear the Phonak Lyric 4 with some success. This Lenire tinnitus treatment could be life-changing.
😱
Many have tried it, I have also tried it and it’s not life changing what it is, is very expensive :(
@@DrCliffAuD bruh this dude said he was held hostage at gunpoint and you responded with an emoji? Hahahahahaha😂
For reference, a commercial jet engine is 120db and a gunshot is 140db. 160db music is a laugh out loud fabrication
@@Tanktanium Fr like did the dude whip out something to measure the sound while he was held hostage?
Hola Phil, soy Walter Piquinela de Uruguay y estoy expectante a tu resultado con Lenire.
Gracias
My tinnitus is a constant whooshing noise / constant white noise and it all came about since contracting covid 19 . I've been given hearing aids - they haven't helped - I can't wait to see if the treatment worked for you🤞🙏❤ 🇬🇧
This sounds like the same sort of treatment (device) used on a woman with vertigo in the book "The Brain that Changes Itself" by Norman Doidge M.D. It was invented by Paul Bach-y-Rita.
Very interesting. I am 100% deaf in my left ear. 50% deaf in my right ear. Also I’m tone deaf as well. I cannot hear high pitch sounds at all. I’ve had tinnitus for as long as I can remember. Constant buzzing sound. I’ve just become immune to it in my daily activities. It’s only when I stop or find myself in a quiet place that it is noticeable. All of that being said. I would defiantly like to not have it at all. Unfortunately I’d probably fall into the category of the folks who can’t be helped. I appreciate the video and I hope this is legit so people can get the help they need. Thank you!
Can't you receive a cochlear implant?
😢🙏
was initially excited to hear about this. having found out that the device will cost £2300, which is insanely high and brings me back to square one
i've had this as long as i can remember. i told my parents it sounded like the whine the high whine the tv made, which i later learned was the high voltage system on the old crt screen tv's. it's persisted my entire life, and i scarcely notice it anymore. i've always had very good results on military and other hearing tests, but that still remains since i was a toddler. i might give this a go if it's accessible.
i just developped it 2 weeks agp really scary
I got tinnitus like 3 years ago on right ear. Over time it did get slightly better but it is still there. I got it while being on anti-biotics. Yes anti-biotics, I wish I knew that before taking them for like a week with like 1000 mg daily dosages. Anyways, hopefully this can trick the brain from letting go of the fantom noise, i.e. what the anti-biotics did of course is kill the hairs in the cochlea especially the once that stimulate high pitch sounds
May i ask how it is now?