I developed tinnitus after a corona infection. My ears were clogged, dysfunction of the eustachian tube and a weird clicking in my ears when I swallowed. I was sick for 3 weeks, but the ear dysfunctions remained. The worst 3 months of my life for sure. This video helped me sleep, but luckily my tinnitus is gone now. For anyone who is panicking right now and searching shit on the internet: don't do it, you'll only stress more about it and your tinnitus will get worse. Stress is your worst enemy. It CAN go away, it takes time (it can still go away after 6-12 months.) Believe me, I know it's hard I've been there too. Go for a walk, listen to music (not too loud), do the things you normally do. You can do this.
I got the same thing , it started over a sensation of one of my ears getting clogged then a few days later i started to hear this pitch sound ear or brain then i started getting sick , i got the flue troat pain and body aches, now i cant even sleep bc of it, i now too feel like worry or fear like sensation and cant seem to concentrate my sleep at all like since i got it, and sometimes when i try to sleep i feel tense and warm i hate this new years bc ive been with this just like 2 weeks and im already feeling stress or enxity, i hear well in both ears , doc told me could be bc my estachian tubes are either inflammated or block hopefully it will go away once this unblocks
@@brolyassasin8354 Hi, I'm sorry you have this shit. If I were you I would go to a specialist. I live in Belgium and went to a ear-nose-throat specialist and got Prednison (Medrol is the name). If you react quickly, you'll have more chance to recover from tinnitus.
@@Someonelol999 Hi, I'm sorry this happened. Did you go to a specialist? Ears are very sensitive so I can't tell you if it will go away or not. There is a big chance yes, but you have to go to a specialist if you didn't already they can give you cortisone if needed. My advice would be to try and pick up your old life and try to ignore it, there is a correlation with your brain. If your brain thinks the sound is dangerous because of your anxiety about it it will only get worse. It's hard but you have to train your brain that the sound is neutral, some behavior therapy could help!
You have missed out on what is probably the main cause of tinnitus which is stretched muscle nerves in the neck and shoulders or somatosensory tinnitus. I have this form of tinnitus linked to a head forward position over a computer keyboard over a long period of time but it also refers to the current generation's use of mobile phones. Brazilian researchers found that unlike animals we have to turn our heads to pinpoint sounds. This results in a signal sent to the somatosensory nucleus where the signal is integrated before being passed to the cochlear sensory nucleus and onto the hearing center in the brain. When the neck muscles are overstretched the signal waveform is distorted and so that passed on to the cochlea is too causing the tinnitus sounds. In this form of tinnitus, habituation is difficult because, as I find, the sound changes frequently depending on which muscle(s) are affected and this often depends on exercise or sleep position such that in my case the tinnitus signal can either go away completely or become very loud. Typical I "hear" several sounds at once with one becoming dominant depending on which muscle nerve dominates. I have found a chiropractor is more useful than and ENT specialist.
I would like to thank you for this information. If you have time, it would be helpful if you could share where people my learn about this further. Please feel free to share any links or resources that may be helpful.
Great video, when I was in college 15 years ago, I woke up and it started to ring in my ears and I couldn't even sleep, and now I found relief for tinnitus on Shirlest and I'm so happy I can live a life without ringing in my ears!
I get tinnitus in my ear every once in awhile usually my left ear what I do is I just sit still and close my eyes and I just imagine that the sound is coming from a volume knob and I start in my mind slowly turning it down until it's all the way down and I swear to God it's worked for me for at least twenty years. It start slowly getting quieter and then shuts off as I do that.
I get brief intermittent tinnitus like that. Usually in my right ear, but once in awhile in my left. It goes away usually within 30 seconds. Hasn't lasted longer than that, at least not yet. And I'm doing my damnedest to keep it that way.
Have persistent and continuous tinnitus for many years. Mainly a hissing / high frequency noise, but sometimes hums and noises like an engine running at idle. No issues on blood analyses. No hearing loss, but if sound frequency matches with tinnitus, I miss very low level high frequency sounds during audio tests. No healing over time. Went to ENT once, years ago. They did audio test, nothing revealed and he did not request further assessments. Thankfully, I am not obsessed / disturbed with the existence of tinnitus.
I recently started taking thyroid hormone after tests showed my TSH levels were low. Surprisingly the moderate tinnitus I've had for years was reduced significantly and even completely goes away for part of the day. This means that I needed it even when I tested at normal thyroid hormone levels.
@@Itsjennaaaay I am guessing since I had tinnitus for about 13 years and had my TSH levels checked many times during that period and tested normal. My tinnitus tapered off immediately after starting the prescription for Levothyroxine. It also immediately helped me with constipation, thinning hair and brittle nails all of which I had when my tests came out in the normal range.
I had my thyroid radiated, so basically it is dead. I don’t recommend getting your thyroid radiated. No thyroid causes hypothyroidism I have to be on medicine for the rest of my life. My tinnitus will probably never go away.
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.
Im depressed because of this. About 7 months ago i got a sinus implant for time in my 22 years of life… after it eventually cleared up it left an annoying ringing in one ear with the other sometimes ring. My right ear (the one that rings) first went muffled then after I want to say a few days/ a week it went from being muffled to ringing, at that point i gave up on life. I had mental breakdown where all i could do was cry, then after 5 months after that it went lower to where it is now, but my ear hurts randomly fir a few seconds
This says nothing about structural damage i.e. neck or spine positional alteration or soft tissue injury similar to whiplash which can be determined by the lessening or complete absence of the tinnitus "noise" during various head or neck movements.
I worked in a noisy factory for 28 years, ear protection was not a safety law till the late 80s back then, So I got Tinnitus! I am now a pensioner/carer and the Tinnitus is still with me! It used to be permanent 24/7, but since becoming a carer and keeping myself busy, I get days/weeks when it disappears, or low pitch! My hearing is bad, has been for most of my life! I got hearing aids, but don't use them much as they hurt my ears more times than not! So glad I watched your blog! Many thanks!
I get loud tinnitus if I smoke weed. THC can temporarily cause it. If any other smokers are experiencing bad tinnitus, try having a break for some days and see if it stops. It starts as soon as I smoke and goes away by the next day if I don’t smoke again. My theory is the weed increases blood pressure in the head, causing the high pitch sound for many hours/rest of the day. I was thinking it’s a permanent lifetime issue until it went away when I had a break from smoking. It sucks to get it from smoking but I’m glad it’s not there if I’m not high. My concern now is if I smoke a lot it could become permanent.
@@malekdavid132 I quit recently for a couple weeks and it totally stopped. Now I smoke daily again due to stress and am putting up with it but the tinnitus is a real bitch. It stops if I quit for a couple days so I don't think it's permanent but I don't know.
Got tinnitus after brain injury almost 4 years ago some days is more intense than others but just to be alive is a blessing I could’ve died that moment but God had a greater purpose for me is what I think every single time tinnitus get too intense 😔🙏🏼 God bless everyone that goes thru difficult situations in life ♥️
I have had this ringing in my ears, seriously I'm not exaggerating, all my life. It wasn't until I hit my 50's that I found it had a name and it's not normal, I'm 62.
Caffine was a cause for me. Reduced tea drinking and went to decaff,and the noise has gone after thirty years .Never thought of it as a cause before......
What is true about tinnitus? 1) Hearing loss due to exposure to noise is a risk factor for tinnitus 2) Tinnitus can be diagnosed with an audiometry test 3) Appears only in young people 4) It can usually be treated with medication
Mennier's Disease¬¬ Vestibular disorder of the inner ear. I have Tinnitus all day everyday,and Betahistine helps. pls educate yourself on this as well,it could be a factor!
Also, check your blood pressure!! If it's over 130/80 and you have tinnitus (not caused by hearing loss) then it time to see your Dr for Hypertension, the silent killer. Usual suspects are obesity, alcohol, smoking and poor diet. Get those factors under control and blood pressure on target you'll notice the tinnitus fades.
ive had it for 10 years now probably, i only notice it when i deeply focus on it or i am in a very quiet area nowadays. its like white noise to me at this point
Add to this a new cause in the past decade: LED light high frequency flicker. LED lighting most frequently uses cheap power conversion circuitry to convert AC line power into low voltage DC to dry the LEDs. This causes the LEDs to vary in light output at frequencies twice the mains power frequency (120 hertz in the US, 100 hertz in much of the world). This high frequency flicker causes oscillation in visual signals sent to the lateral geniculate nuclei (LGNs) which extract edges from the visual field, and identify movement for the eyes to focus on. This all happens at speeds much faster than the flicker fusion limit for visual image formation, but is entirely neglected by most brain researchers and visual specialists who wrongly presume that all vision is visual scene formation, and who often are ignorant of the many wats the eyes, and many brain structures use and analyze information from the eyes. Other brain structures like the superior colliculus and pulvinar are directly involved. And beyond tinnitus, this also involves the trigeminal nerve and pain in the eyes, behind the eyes, in the face, and in the lower jaw and molars. For tinnitus, the high frequency flicker is "seen" by the LGNs as movement that they and the other aspects of the brain cannot localize. This then causes signals to be sent to the precuneus and on to the default mode network identifying unknown danger. What happens next is speculative, but goes like this. After failing to find the potential danger, the brain directs the Medial Geniculate Nuclei, and with the Inferior colliculi to instruct the ears to listen more closely for sounds to localize the sensed danger. Through several brain structures this results in the inner hair cells of the ear turning on previously disabled defective ('dead') outer hair cells. This is done despite the harm in order to best protect the body by maximizing the potential to localize the danger through sound. There isn't an actual danger though to be found. And the result instead is very loud subjective tonal tinnitus, as the dead outer hair cells circuits "ring". The brain keeps emphasizing the need to listen, and amps up the volume while adding more dead cells in the search. The result is an increasingly loud and climbing tinnitus. Simultaneously, the DMN and other circuits fail. That results in optical migraines that progress quickly to total or partial temporary blindness, often followed by migraine headaches. On removal of the flicker source (fleeing the LED light exposure), the body works to undo the harms it created. If the exposure was minot and brief, the tinnitus may fade into the background in an hour to days. More intense or longer exposure may require dats to weeks or even months, and may never fully resolve. The optical migraines will fade into about an hour, but the migraine may last hours to days until it resolves. Repeated insults of exposure to the flicker worsen the injury. Likelihood of impact and severity is dependent on nerve conduction speed. With IQs near 100, that results in sensitivity to ~60 hertz flicker. At High IQs, the risk moves to higher frequencies as the nerve conduction speed increases. Optical flicker injury from LEDs is most likely to be most severe and most apparent in high IQ individuals. However, the entire population is subject to a second impact where many of these same brain circuits lead to several types of headache from flicker up to about 5,000 hertz. This happens most commonly from dimmers using pulse width modulation, and all of the harmonics that generates. And no, you will not find this in any single scientific study or reference. Also - no, this is not yet a scientifically or medically recognized injury. And the related adverse impacts of intense blue light exposure from LEDs in sensitive individuals (~1-3% of the population) through at least three pathways involving most of these same structures, plus genetic differences associated primarily with Neanderthal or ancient hominim heritage from low light adaptation in the far north, also occur in many people. This too is not yet recognized by researchers or doctors other than in limited field reports and fMRI studies since 2017 elucidating the mechanisms involved in sensitive individuals. These have largely been masked due to the simultaneous wide spread on the SARS-CoV-2 pandemic causing brain injuries, and the severe impacts on health care and research. We are only now seeing the companion impacts from blue light suppression of melatonin production on circadian and hormone rhythms, and the consequent rapid and severe rise in hormone sensitive cancers. The first being the rapid linear rise in the rates of breast cancers from the 2015 baseline. Expect those to reach 175% of the 2015 baseline in the next ~5 years (seen 3-5 years later in national data). Prostate, Gi and rectal cancers will follow, along with skin cancers.
@@isabellacharlotte I would wish that anyone could. I have found ways to deal with the blue light for myself. I bought a lifetime supply of incandescent lights before they were gone. And I have all of the true blue blocking glasses ..., plus the expensive test equipment to know with certainty what i am being exposed to. I have elucidated the physiology of what is happening with flicker. Why it is happening, how it works, and where my sensitivity came from (Neanderthal visual adaptations, and why and how those developed. The problem I cannot solve is dealing with flicker. The best medicine can offer is one drug as a guess. It works by slowing down brain function. Um. No thank you. Presently, no technological solution exists. I had hopes for the Apple glasses. But no. They use intense 452 nm blue LEDs and they operate at high enough frequencies that they pass the flicker. At least that is what they tell me. I haven't verified that. My only hope there was that some augmented reality/ virtual reality system would come along that would essentially see the eorld and pass it along without the intense blue, and time smearing the flicker so that it is gone. There is no impetus to create such a thing. That left getting Federal laws changed. I learned / was reminded that politicians are morons, and are utterly useless with technology. Lawyers are equally useless. And doctors only have known and approved science / medicine to work from. In short, there is no solution beyond isolation. My world has become very small because of societies choices. There is no right to Life, Liberty, .... for me. Nor will there be on the rest of my lifetime. I can and did solve all the quandaries and puzzles to understand the problem. I just can't solve the problem itself. The incredible gifts from my fore-bearers has become my cage. Along the way I learned just how horrifically bad the Federal researchers decision making and problem analysis skills are, and hoe severely it will impact others. The result has time delays. Hormone sensitive cancers have begun to rise, and to freak out the regulatory and medical communities. They "don't know why it is happening". It has them scared. But they also cannot listen to hear why. So we are doomed to the impacts coming to full effect, then waiting fir them to figure it out on their own. Meanwhile we condemn 10 million people (or more) needlessly to die, and the economy to suffer a trillion (with a T) dollars of adverse impacts per year. Then when they do figure it out, they will try band-aid solutions first, that will fail. Another decade will pass and another 10 million plus will die. And ultimately when they do fix it, it will cost over 3 trillion to do so. They will balk at that, and another 10 million plus will be consigned to die. Etc.... Bearing that knowledge and being entirely unable to correct our course is the hardest part. Then add to that the immense number of people who will be b;inded. Sigh.
I've had mild tinnitus for several years but got used to it and had a relatively normal life. However, my ringing became worse a few weeks ago and accompanied by a sensation of fullness and pressure. Doctor has told me that I may have Deniere disease. I started taking diuretics 20 days ago with no positive results. Do you guys know anybody who had this problem before and got better? This condition is nerve-wracking 😔
I have been to doctor numerous times and have never been asked any of these questions or had any test to make any assessment. I actually have felt even more depressed by doctors not seeming to care, as the loud noise …it is quite disturbing to me at times. It has never gone away and occasionally it will stop like after or during having a shower but then it’s back again.
All the while I suspected government or military forces bombarding us with high frequency waves that we are used to but notice at extremely rare occasions.. I still think of it this way since the ringing sound occurs very rarely and starts weak to loud before fading away; it sounds like a frequency wave just passed by.
i face tennitus by continue using ear phones ,now it is three months to use earphones ,i cured tennitus with ownself , with no sound disturb me , i am feeling silence , i advise to ignore how much you can to tennitus ,enjoy your daily life
I have pressure and a ringing in my right ear. When I first got this it was in my head and both ears. Then that went away for months and when it came back it was now only I. My right ear. I had very low D a 12. Then they finally tested my Parthyroid and it was high 135 and my Calcium is a 9.5. Does anyone else have any pressure in their head? Or ears? I’m going for a blood test in 3 weeks and a 24 hour urine test. Thanks in advance,
you can call me Desmond by name, from Nigeria.. you look so beautiful to passing through all of this.. can we be friends please... believe me... I'm real.
I think I have tinnitus, it started my freshman year and now I’m a junior and up until yesterday I’ve been searching for an answer as to why I always hear a loud click sound when I swallow or eat. It would drive me crazy because I thought people could hear it. I was in a psychosis. I think it started from getting bad panic attacks when smoking 🍃, my anxiety would spike and my heart would beat fast kinda like a fight or flight response. I would still be chilling tho because I like smoking anyways it would calm me down, it was jus random bc something changed every time I smoked now. but what was weird was I would be so high that I’d forget to swallow because I was jus so lost in my thoughts lol that I would swallow manually but when I swallowed I heard this loud click and it kinda startled me cuz that wasn’t normal and I thought everyone could hear me do it but when I would look around to see if they had a reaction (my friends) they wouldn’t. But I thought they were jus ignoring it. I felt like an elephant in the room tho. I would ask them about it and they would be confused saying they never heard anything from me. That would just bother me even more because I thought they had, so it was a different answer than i expected, leaving me more confused and lost. After that I was stuck in a negative thought loop that everyone could hear me so like in school I would try to silent each swallow I took and the more I tried to focus on it the louder the click sound would become. And after one swallow I knew there would be another one soon so the anticipation would build making my anxiety worse. That’s all I would focus on to so I was mentally preparing myself for each swallow I took. I couldn’t confidently swallow either because I would be in a panic attack so I would gulp every time I had a “normal” swallow because i was nervous. It just made me feel like a weak person because I couldn’t even handle human interaction with having a slight panic attack. So for a while I was just depressed, lost, and felt outcasted. it got to a point that I just didn’t care anymore and decided to embrace it. I learned to not stress over what people thought abt me and put myself as my top priority. And when I started doing that I’ve been able to break out of that thought loop and find moments of peace in uncomfortable situations. Like taking deep breaths or focusing on my music. And when I did that I could finally swallow normal again. It took me a couple years to learn and overcome that tho. I sorta had an ego death and had to reconstruct my entire thought process it felt like. I’m much more at peace now with a positive outlook on life regardless of whatever happens, I still get anxiety spikes tho and become overstimulated very easy and when that happens the clicking comes back but I feel less pressure now after finding out a couple days ago that it could be tinnitus and those noises u hear are only in ur head, I jus wish I learned a couple years ago lol.
I still smoke, I’ve learned how to control the panic attacks and use the 🍃 to calm me back down like how it used to. Ik everyone’s experience is different so I thought I’d share mine in hopes it can help someone who might be going thru something like this. Advice like this is exactly what I would’ve needed and was looking for couple years ago, but I could never find anything so I thought I was the only one. Regardless tho it felt good talking about it, I don’t talk abt it much bc people can’t really relate so maybe someone here will. Definitely changed me as a person making me more open minded and wise since I was constantly just searching or asking for advice from people with hopes I would hear something to help my current situation.
Bro I was thinking the same thing because that's what happened to me in January I smoke some weed that I bought but it was laced with something nearly freak mi out I couldn't breathe I thought I was about to die I had to fight hard in myself to control my head because I was panicking ever since that night that ringing sound appeared till now but I try not to think of it as much
Peoples who are face these type of hmmmm or ringing sounds,listen its not tinnitus 100% it can be other thing like sick, fever, or weakness bcuz i had also face this problem 2-3 days before i was thinking it is tinnitus but suddenly when i sleep and weak up it was nothing I caused bcuz of i was sick and then i relieved, i know many people like me think that they are suffering from tinnitus and they get in anxiety but don’t be afraid be brave 🙂 thats why i decided to inform you all 😊
Iam now experiencing this Tinnitus due to removal of Ear wax by an ENT by an instrument.. Either its a "Veee" sound or a "Hush" sound..My friend who had says it will be there for quite a long time and advises to put Oil..in the affected ear.
Muchas generalidades pero las soluciones que propone son ineficaces en la gran mayoría de lis casos. Como todos los videos de perspectiva médica, ayuda poco o nada
I don't know when this started. Maybe after i gor really sick in vacation. I have always been able to ring my ear things (where you heat distant thunder) but i highly doubt that has anything to do with tinnitus. I was hearing buzzing at school today it kept getting louder And louder and louder.
To anyone struggling with tinnitus: You can learn to habituate one day. It took me a couple years but i got here. Hang in there! Try masking to ease the anxiety and one day you might be able to lower the volume of your masking sound or even turn it off.
Understanding the cause of tinnitus and deafness? I'll go there. How about: 1.) Firing a 3"50' without ear protection because not provided by the navy. 2.) Small arms firing ( M60, M14, M2, grenades, etc,etc ) and hearing protection not provided by the navy. 3.) Operating a 16 inch gun turret.
Im pretty young, and im worried. My ears have been ringing sometimes at school, and i dont know a bunch about Tinnitus, What do i take to treat this? I would love some help
Istening to all your comments guys i wanna share my story too. I have a bad habit of listening music i always wear earphones every day. One day all of a sudden i statred hearing ringing sound at first i thought the left earphone was broken and later realize it was not i threw the earphones away and after sometime i started hearing again. Days pass by and some times it started happening again but on the right side sometines on both😅 soon i realize if i dont use earphones the ringing won't occur. And now i only use earphones for 10 min sometines i hear the ringing and sometimes i don't. Idk if this is tinnitus or not. Am i cooked guys?😢😢
my tinnitus seams to be linked to a weird design on my basement floor... i shoulda taken a picture of it before scraping up the weird voodoo drawing, but its similar to "Ravahere" thats part of the french polynesia islands in middle of south pacific.... weird but... its my story i guess....
I have permanent tinnitus I'm only 14 I've heard it for 8 years i hear 2 or 3 different everyday every night sounds i think it caused for headphones on all volume
Guys, I hear this like sound in my right hear it sounds like a motor reving but it doesn’t happen constantly. I noticed this a few days ago but I thought I was it coming from outside. It goes like this “vvvv…vvvv”, and then it goes away. I’m getting scared, anybody what this is?
I tried to go to sleep one night in my bed in November 2022 when I noticed a ringing in my ears I don’t think much of it because it happened to me before the incident and went away after a few seconds but when I paid attention to it wouldn’t go I away I would freak out and I told my mom to take me to doctor but it was late at night so she said tmr and I couldn’t stand it so I put my earbud in and listened to sounds while the volume was low because I didn’t wanna make it worse and I only put my earphones in one of my ears it mainly happens when I think of it when I get anxiety I get tinnitus
hi same thing happend to me usually it go away after seconds but when I paid attention to it and freaked out it is not going away like that now how are you now? 😮💨
Tinnitus and hyperacusis often coexist, though not always. There isn't a specific factor that causes both, but all the possible causes of tinnitus can be to blame.
I can’t stand the buzzing in my ears and head it’s so uncomfortable ad it’s driving me insane it’s horrible I need help doctor says it’s because of blood pressure
@@HenryCavill-e1b hi, yeah I’m taking medicine right now which kinda helps not what I expected but at least I don’t hear the buzzing anymore only when my tension is high.
My tinnitus is gone after 4 months. 2 months were hell, I was not able to sleep. Shift your focus from the noise, don't take stress, keep yourself busy and one ear exercise is there on TH-cam, do it. And check your ears with a doctor. Mine was because of ear wax and I got it removed.
I worked in noisy Factory For ovr 42 years had slight Tinnitus For few Yesrs when tested for Hearing losss Had a 42 percent hearing loss got Hearing aids Help a lot with my hearing as said had a slight ringing noise now and again about couple times a week for a minute our Two during the Covid Epidemic had all the Covid jags did not make my Tinnitus any worse , 2021,22 wellduring this time got a Shingles Jag about a week or more later 2022 this is when my Tinnitus got worse constant Humming in my ears goes from my left ear then to my right ear had it worse since then could Be the combination of both the Covid Jag of the Shingles jag , i myself believie it was the Shingles Jag as thats when this really got worse and have it ever since even with hearing aids Still get it
Stay away from loud noises or wear hearing protection when around such noises. Get hearing test (if hearing loss is present hearing aids may help) and utilize some sound therapy always played below tinnitus volume do not mask it except for sleeping if needed. Tinnitus takes time to adjust too…overtime it does improve and get easier for the majority of sufferers.
You've received excellent advice from @Andrew-pp2ql, but I'd like to emphasize the importance of protecting your ears from further damage. When there's already damage to the cells of the hearing organ, the goal should be to slow down the progression of this damage. Age-related changes will naturally occur at some point, but they can be accelerated by factors like noise damage, certain ear diseases etc. I recommend finding suitable hearing protection designed for specific situations. For example, there are special filtered earplugs for music, but you will require different earplugs (or earmuffs) when using loud tools that provide more protection.
I can never thank you enough Dr Liam Ogbebor for all your services, I am now completely cured of Tinnitus after using your medication, you're truly a man of honor and words I am so happy I came across your channel on TH-cam
I developed tinnitus after a corona infection. My ears were clogged, dysfunction of the eustachian tube and a weird clicking in my ears when I swallowed. I was sick for 3 weeks, but the ear dysfunctions remained. The worst 3 months of my life for sure. This video helped me sleep, but luckily my tinnitus is gone now. For anyone who is panicking right now and searching shit on the internet: don't do it, you'll only stress more about it and your tinnitus will get worse. Stress is your worst enemy. It CAN go away, it takes time (it can still go away after 6-12 months.) Believe me, I know it's hard I've been there too. Go for a walk, listen to music (not too loud), do the things you normally do. You can do this.
Bro I don’t have hearing loss but a cracker burst near my ear 7 weeks ago will it go away
I got the same thing , it started over a sensation of one of my ears getting clogged then a few days later i started to hear this pitch sound ear or brain then i started getting sick , i got the flue troat pain and body aches, now i cant even sleep bc of it, i now too feel like worry or fear like sensation and cant seem to concentrate my sleep at all like since i got it, and sometimes when i try to sleep i feel tense and warm i hate this new years bc ive been with this just like 2 weeks and im already feeling stress or enxity, i hear well in both ears , doc told me could be bc my estachian tubes are either inflammated or block hopefully it will go away once this unblocks
Hiw long before it went away bud
@@brolyassasin8354 Hi, I'm sorry you have this shit. If I were you I would go to a specialist. I live in Belgium and went to a ear-nose-throat specialist and got Prednison (Medrol is the name). If you react quickly, you'll have more chance to recover from tinnitus.
@@Someonelol999 Hi, I'm sorry this happened. Did you go to a specialist? Ears are very sensitive so I can't tell you if it will go away or not. There is a big chance yes, but you have to go to a specialist if you didn't already they can give you cortisone if needed. My advice would be to try and pick up your old life and try to ignore it, there is a correlation with your brain. If your brain thinks the sound is dangerous because of your anxiety about it it will only get worse. It's hard but you have to train your brain that the sound is neutral, some behavior therapy could help!
You have missed out on what is probably the main cause of tinnitus which is stretched muscle nerves in the neck and shoulders or somatosensory tinnitus. I have this form of tinnitus linked to a head forward position over a computer keyboard over a long period of time but it also refers to the current generation's use of mobile phones. Brazilian researchers found that unlike animals we have to turn our heads to pinpoint sounds. This results in a signal sent to the somatosensory nucleus where the signal is integrated before being passed to the cochlear sensory nucleus and onto the hearing center in the brain. When the neck muscles are overstretched the signal waveform is distorted and so that passed on to the cochlea is too causing the tinnitus sounds. In this form of tinnitus, habituation is difficult because, as I find, the sound changes frequently depending on which muscle(s) are affected and this often depends on exercise or sleep position such that in my case the tinnitus signal can either go away completely or become very loud. Typical I "hear" several sounds at once with one becoming dominant depending on which muscle nerve dominates. I have found a chiropractor is more useful than and ENT specialist.
Hi Peter. I have neck pain associated with Tinnitus. Have you figured out what muscles exactly (to be relaxed or strengthened?). Thanks.
@@garethyevich I hope he replies because I have neck pain and tinnitus too
Hi! Do you know what muscle it’s associated with?
I would like to thank you for this information. If you have time, it would be helpful if you could share where people my learn about this further. Please feel free to share any links or resources that may be helpful.
Is that kind of tinnitus a cause for concern?
Great video, when I was in college 15 years ago, I woke up and it started to ring in my ears and I couldn't even sleep, and now I found relief for tinnitus on Shirlest and I'm so happy I can live a life without ringing in my ears!
What is this? Where ?
How you get rid of tinnitus
Please please tell the treatment you get well
Which medicine used ?
What is your mobile number please share me.
I get tinnitus in my ear every once in awhile usually my left ear what I do is I just sit still and close my eyes and I just imagine that the sound is coming from a volume knob and I start in my mind slowly turning it down until it's all the way down and I swear to God it's worked for me for at least twenty years. It start slowly getting quieter and then shuts off as I do that.
Bro that worked
@@eeeeeeeeee10really
I don't believe you.
I get brief intermittent tinnitus like that. Usually in my right ear, but once in awhile in my left.
It goes away usually within 30 seconds. Hasn't lasted longer than that, at least not yet.
And I'm doing my damnedest to keep it that way.
This used to work for me too
Have persistent and continuous tinnitus for many years. Mainly a hissing / high frequency noise, but sometimes hums and noises like an engine running at idle. No issues on blood analyses. No hearing loss, but if sound frequency matches with tinnitus, I miss very low level high frequency sounds during audio tests. No healing over time. Went to ENT once, years ago. They did audio test, nothing revealed and he did not request further assessments. Thankfully, I am not obsessed / disturbed with the existence of tinnitus.
@@emilyratajkowski2556 what is HBD?
burning sensation b hota Ky ear me
@@urvi65 kya ap mota ho?
Reply
@@not_your_chiru no
Great no worries just pray to God for healing. Many have that problem actually goes away.nothing serious just stress anxiety.
I recently started taking thyroid hormone after tests showed my TSH levels were low. Surprisingly the moderate tinnitus I've had for years was reduced significantly and even completely goes away for part of the day. This means that I needed it even when I tested at normal thyroid hormone levels.
You needed thyroid hormone even when your hormone levels showed normal?
@@Itsjennaaaay I am guessing since I had tinnitus for about 13 years and had my TSH levels checked many times during that period and tested normal. My tinnitus tapered off immediately after starting the prescription for Levothyroxine. It also immediately helped me with constipation, thinning hair and brittle nails all of which I had when my tests came out in the normal range.
@@sdnikko8960 Can you tell me what was your tsh level when you needed medication.
But on the long run, you could have hepatitis with this medication (approx after 18 successive months according to my MD)
I had my thyroid radiated, so basically it is dead.
I don’t recommend getting your thyroid radiated. No thyroid causes hypothyroidism I have to be on medicine for the rest of my life. My tinnitus will probably never go away.
Tinnitus is seriously causing me a huge depression.. I can't stand it anymore! I want the ringing to stop and just be able to sleep and work in peace
read one of the top comments; when a reader treated her low thyroid, the tinnitus stopped
Hlo ..now you ok
@@rishirajjaiswal4761 still hearing it constantly
@@DragonBlueSpirithave you tried anti inflammatory diet?
Make a diet eat healthy do exercise relax and get treatment of steroids
I have TMJ, tinnitus, visual symptoms, vertigo, muscle spasms, insomnia, back pain, neck pain, etc. I love being alive so much
Damn that sucks man. Did you get into an accident?
@@我爱猪肉 no it's all idiopathic but I'm seeing a neurologist soon and I will get tested for fibromyalgia as well
@@我爱猪肉 no its all idiopathic. I may have fibromyalgia and am getting tested for it soon
Almost same here💀 TMJ, tinnitus, back pain, insomnia.
Hello paano po mawawala and anu medications po
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.
Im depressed because of this. About 7 months ago i got a sinus implant for time in my 22 years of life… after it eventually cleared up it left an annoying ringing in one ear with the other sometimes ring. My right ear (the one that rings) first went muffled then after I want to say a few days/ a week it went from being muffled to ringing, at that point i gave up on life. I had mental breakdown where all i could do was cry, then after 5 months after that it went lower to where it is now, but my ear hurts randomly fir a few seconds
So does ear infection cause permanent tinnitus?
This says nothing about structural damage i.e. neck or spine positional alteration or soft tissue injury similar to whiplash which can be determined by the lessening or complete absence of the tinnitus "noise" during various head or neck movements.
can I be of help?
I worked in a noisy factory for 28 years, ear protection was not a safety law till the late 80s back then, So I got Tinnitus! I am now a pensioner/carer and the Tinnitus is still with me! It used to be permanent 24/7, but since becoming a carer and keeping myself busy, I get days/weeks when it disappears, or low pitch! My hearing is bad, has been for most of my life! I got hearing aids, but don't use them much as they hurt my ears more times than not! So glad I watched your blog! Many thanks!
I got tinnitus and mild hear loss bc of noisy factory i work in now im struggling.
How did you manage to reduce tinnitus if you have poor hearing?
Superb, yet again.
I dunno how you keep the quality of your videos so high.
Keep it up, please !
Thanks, will do!
@@ZeroToFinals I JUST WANT IT TO STOP, HELP
Great job listing all the causes and management of tinnitus :)
Thanks!
@aigbomianosas2716 shut up
can I be of help?
can I be of help?
I get loud tinnitus if I smoke weed. THC can temporarily cause it. If any other smokers are experiencing bad tinnitus, try having a break for some days and see if it stops. It starts as soon as I smoke and goes away by the next day if I don’t smoke again. My theory is the weed increases blood pressure in the head, causing the high pitch sound for many hours/rest of the day. I was thinking it’s a permanent lifetime issue until it went away when I had a break from smoking. It sucks to get it from smoking but I’m glad it’s not there if I’m not high. My concern now is if I smoke a lot it could become permanent.
Exact same here !
You might be right because every time I smoke weed I hear it
@@malekdavid132 I quit recently for a couple weeks and it totally stopped. Now I smoke daily again due to stress and am putting up with it but the tinnitus is a real bitch. It stops if I quit for a couple days so I don't think it's permanent but I don't know.
Can I be of help?
Thanks for building my faith that it will go away
Can hyperacidity cause tinittus? I guess i get dizziness when my acidity increases.
Got tinnitus after brain injury almost 4 years ago some days is more intense than others but just to be alive is a blessing I could’ve died that moment but God had a greater purpose for me is what I think every single time tinnitus get too intense 😔🙏🏼 God bless everyone that goes thru difficult situations in life ♥️
Generally Boxers get this Tinnitis quite often i heard.. Even a small injury or the Eaustachian tube Dysfunction could aggravate this.
EXCELLENT PRESENTATION AS ALWAYS. THANKS.
I have had this ringing in my ears, seriously I'm not exaggerating, all my life. It wasn't until I hit my 50's that I found it had a name and it's not normal, I'm 62.
Caffine was a cause for me.
Reduced tea drinking and went to decaff,and the noise has gone after thirty years .Never thought of it as a cause before......
can I be of help?
What is true about tinnitus?
1) Hearing loss due to exposure to noise is a risk factor for tinnitus
2) Tinnitus can be diagnosed with an audiometry test
3) Appears only in young people
4) It can usually be treated with medication
What type of medication could be used ?
@@thikasrmg138 nodoby know that
صحيح أن علاج البنجو ملائم للطنين
Mennier's Disease¬¬ Vestibular disorder of the inner ear. I have Tinnitus all day everyday,and Betahistine helps. pls educate yourself on this as well,it could be a factor!
can I be of help?
Also, check your blood pressure!! If it's over 130/80 and you have tinnitus (not caused by hearing loss) then it time to see your Dr for Hypertension, the silent killer. Usual suspects are obesity, alcohol, smoking and poor diet. Get those factors under control and blood pressure on target you'll notice the tinnitus fades.
So I think this is my problem, because I have high blood pressure over 130/80 I am fat, yes that might be it.
ive had it for 10 years now probably, i only notice it when i deeply focus on it or i am in a very quiet area nowadays.
its like white noise to me at this point
What you're experiencing is called V2K. It's a kind of electromagnetic torture that is conducted through radio frequencies
You should check if you're blacklisted.
It helped me.
How is it now?
How did you get it?
Add to this a new cause in the past decade: LED light high frequency flicker. LED lighting most frequently uses cheap power conversion circuitry to convert AC line power into low voltage DC to dry the LEDs. This causes the LEDs to vary in light output at frequencies twice the mains power frequency (120 hertz in the US, 100 hertz in much of the world).
This high frequency flicker causes oscillation in visual signals sent to the lateral geniculate nuclei (LGNs) which extract edges from the visual field, and identify movement for the eyes to focus on. This all happens at speeds much faster than the flicker fusion limit for visual image formation, but is entirely neglected by most brain researchers and visual specialists who wrongly presume that all vision is visual scene formation, and who often are ignorant of the many wats the eyes, and many brain structures use and analyze information from the eyes.
Other brain structures like the superior colliculus and pulvinar are directly involved. And beyond tinnitus, this also involves the trigeminal nerve and pain in the eyes, behind the eyes, in the face, and in the lower jaw and molars.
For tinnitus, the high frequency flicker is "seen" by the LGNs as movement that they and the other aspects of the brain cannot localize. This then causes signals to be sent to the precuneus and on to the default mode network identifying unknown danger.
What happens next is speculative, but goes like this.
After failing to find the potential danger, the brain directs the Medial Geniculate Nuclei, and with the Inferior colliculi to instruct the ears to listen more closely for sounds to localize the sensed danger. Through several brain structures this results in the inner hair cells of the ear turning on previously disabled defective ('dead') outer hair cells. This is done despite the harm in order to best protect the body by maximizing the potential to localize the danger through sound.
There isn't an actual danger though to be found. And the result instead is very loud subjective tonal tinnitus, as the dead outer hair cells circuits "ring".
The brain keeps emphasizing the need to listen, and amps up the volume while adding more dead cells in the search. The result is an increasingly loud and climbing tinnitus.
Simultaneously, the DMN and other circuits fail. That results in optical migraines that progress quickly to total or partial temporary blindness, often followed by migraine headaches.
On removal of the flicker source (fleeing the LED light exposure), the body works to undo the harms it created. If the exposure was minot and brief, the tinnitus may fade into the background in an hour to days. More intense or longer exposure may require dats to weeks or even months, and may never fully resolve. The optical migraines will fade into about an hour, but the migraine may last hours to days until it resolves.
Repeated insults of exposure to the flicker worsen the injury.
Likelihood of impact and severity is dependent on nerve conduction speed. With IQs near 100, that results in sensitivity to ~60 hertz flicker. At High IQs, the risk moves to higher frequencies as the nerve conduction speed increases.
Optical flicker injury from LEDs is most likely to be most severe and most apparent in high IQ individuals.
However, the entire population is subject to a second impact where many of these same brain circuits lead to several types of headache from flicker up to about 5,000 hertz. This happens most commonly from dimmers using pulse width modulation, and all of the harmonics that generates.
And no, you will not find this in any single scientific study or reference. Also - no, this is not yet a scientifically or medically recognized injury.
And the related adverse impacts of intense blue light exposure from LEDs in sensitive individuals (~1-3% of the population) through at least three pathways involving most of these same structures, plus genetic differences associated primarily with Neanderthal or ancient hominim heritage from low light adaptation in the far north, also occur in many people. This too is not yet recognized by researchers or doctors other than in limited field reports and fMRI studies since 2017 elucidating the mechanisms involved in sensitive individuals.
These have largely been masked due to the simultaneous wide spread on the SARS-CoV-2 pandemic causing brain injuries, and the severe impacts on health care and research.
We are only now seeing the companion impacts from blue light suppression of melatonin production on circadian and hormone rhythms, and the consequent rapid and severe rise in hormone sensitive cancers. The first being the rapid linear rise in the rates of breast cancers from the 2015 baseline. Expect those to reach 175% of the 2015 baseline in the next ~5 years (seen 3-5 years later in national data). Prostate, Gi and rectal cancers will follow, along with skin cancers.
can I be of help?
@@isabellacharlotte I would wish that anyone could. I have found ways to deal with the blue light for myself. I bought a lifetime supply of incandescent lights before they were gone. And I have all of the true blue blocking glasses ..., plus the expensive test equipment to know with certainty what i am being exposed to.
I have elucidated the physiology of what is happening with flicker. Why it is happening, how it works, and where my sensitivity came from (Neanderthal visual adaptations, and why and how those developed.
The problem I cannot solve is dealing with flicker. The best medicine can offer is one drug as a guess. It works by slowing down brain function. Um. No thank you.
Presently, no technological solution exists. I had hopes for the Apple glasses. But no. They use intense 452 nm blue LEDs and they operate at high enough frequencies that they pass the flicker. At least that is what they tell me. I haven't verified that. My only hope there was that some augmented reality/ virtual reality system would come along that would essentially see the eorld and pass it along without the intense blue, and time smearing the flicker so that it is gone.
There is no impetus to create such a thing.
That left getting Federal laws changed. I learned / was reminded that politicians are morons, and are utterly useless with technology. Lawyers are equally useless. And doctors only have known and approved science / medicine to work from.
In short, there is no solution beyond isolation. My world has become very small because of societies choices. There is no right to Life, Liberty, .... for me. Nor will there be on the rest of my lifetime.
I can and did solve all the quandaries and puzzles to understand the problem. I just can't solve the problem itself. The incredible gifts from my fore-bearers has become my cage.
Along the way I learned just how horrifically bad the Federal researchers decision making and problem analysis skills are, and hoe severely it will impact others. The result has time delays. Hormone sensitive cancers have begun to rise, and to freak out the regulatory and medical communities. They "don't know why it is happening". It has them scared. But they also cannot listen to hear why. So we are doomed to the impacts coming to full effect, then waiting fir them to figure it out on their own. Meanwhile we condemn 10 million people (or more) needlessly to die, and the economy to suffer a trillion (with a T) dollars of adverse impacts per year. Then when they do figure it out, they will try band-aid solutions first, that will fail. Another decade will pass and another 10 million plus will die. And ultimately when they do fix it, it will cost over 3 trillion to do so. They will balk at that, and another 10 million plus will be consigned to die. Etc....
Bearing that knowledge and being entirely unable to correct our course is the hardest part.
Then add to that the immense number of people who will be b;inded. Sigh.
THANK YOU!! feel like this video saved my life.
can I be of help?
I have this condition and it's horrible
I've just recently found out that a build up of Scar Tissue along a hole in my left ear and in my right it 65% deaf.
How are you doing now?
@@jannettejarvishow are u now
can I be of help?
I've had mild tinnitus for several years but got used to it and had a relatively normal life. However, my ringing became worse a few weeks ago and accompanied by a sensation of fullness and pressure. Doctor has told me that I may have Deniere disease. I started taking diuretics 20 days ago with no positive results. Do you guys know anybody who had this problem before and got better? This condition is nerve-wracking 😔
Stop taking drugs, it's waste of time. What you're experiencing is called V2K. You need to check if you're blacklisted.
I experienced this same thing
@@janice_bbwhat's v2k
How Ru doing now?
I have been to doctor numerous times and have never been asked any of these questions or had any test to make any assessment. I actually have felt even more depressed by doctors not seeming to care, as the loud noise …it is quite disturbing to me at times. It has never gone away and occasionally it will stop like after or during having a shower but then it’s back again.
All the while I suspected government or military forces bombarding us with high frequency waves that we are used to but notice at extremely rare occasions.. I still think of it this way since the ringing sound occurs very rarely and starts weak to loud before fading away; it sounds like a frequency wave just passed by.
This a greet video thank you i have 20 yr ear tinnitus so I like tinnitus video
can I be of help?
Great video, as always
Thanks!
i face tennitus by continue using ear phones ,now it is three months to use earphones ,i cured tennitus with ownself , with no sound disturb me , i am feeling silence , i advise to ignore how much you can to tennitus ,enjoy your daily life
You stopped using ear phones and its gone or you still use ear phones and its gone?
u r soo lucky dear
Yr mujhe bhi h
I’ve had it for 2 years,but now it’s bothering me more than before,I don’t know how much more i can tolerate this!
How did U get it?
It’s my 2nd day with it. Started after getting my MRI which I think I got it from there. I also have cerivcal DDD.
Do you still have it
can I be of help?
can I be of help?
I have pressure and a ringing in my right ear. When I first got this it was in my head and both ears. Then that went away for months and when it came back it was now only I. My right ear. I had very low D a 12. Then they finally tested my Parthyroid and it was high 135 and my Calcium is a 9.5. Does anyone else have any pressure in their head? Or ears? I’m going for a blood test in 3 weeks and a 24 hour urine test. Thanks in advance,
Update ?
VERY NICE INFORMATION THANKS ❤❤❤❤❤❤❤
I have IIH, and when my ICP is high due to increased CFS, I get pulsatile tinitus, particularly when laying down (no relation to my heart).
I have the same
you can call me Desmond by name, from Nigeria.. you look so beautiful to passing through all of this.. can we be friends please... believe me... I'm real.
thank you for sharing the knowledge. It is true that treatment might bring tinnitus back.
I think I have tinnitus, it started my freshman year and now I’m a junior and up until yesterday I’ve been searching for an answer as to why I always hear a loud click sound when I swallow or eat. It would drive me crazy because I thought people could hear it. I was in a psychosis. I think it started from getting bad panic attacks when smoking 🍃, my anxiety would spike and my heart would beat fast kinda like a fight or flight response. I would still be chilling tho because I like smoking anyways it would calm me down, it was jus random bc something changed every time I smoked now. but what was weird was I would be so high that I’d forget to swallow because I was jus so lost in my thoughts lol that I would swallow manually but when I swallowed I heard this loud click and it kinda startled me cuz that wasn’t normal and I thought everyone could hear me do it but when I would look around to see if they had a reaction (my friends) they wouldn’t. But I thought they were jus ignoring it. I felt like an elephant in the room tho. I would ask them about it and they would be confused saying they never heard anything from me. That would just bother me even more because I thought they had, so it was a different answer than i expected, leaving me more confused and lost. After that I was stuck in a negative thought loop that everyone could hear me so like in school I would try to silent each swallow I took and the more I tried to focus on it the louder the click sound would become. And after one swallow I knew there would be another one soon so the anticipation would build making my anxiety worse. That’s all I would focus on to so I was mentally preparing myself for each swallow I took. I couldn’t confidently swallow either because I would be in a panic attack so I would gulp every time I had a “normal” swallow because i was nervous. It just made me feel like a weak person because I couldn’t even handle human interaction with having a slight panic attack. So for a while I was just depressed, lost, and felt outcasted. it got to a point that I just didn’t care anymore and decided to embrace it. I learned to not stress over what people thought abt me and put myself as my top priority. And when I started doing that I’ve been able to break out of that thought loop and find moments of peace in uncomfortable situations. Like taking deep breaths or focusing on my music. And when I did that I could finally swallow normal again. It took me a couple years to learn and overcome that tho. I sorta had an ego death and had to reconstruct my entire thought process it felt like. I’m much more at peace now with a positive outlook on life regardless of whatever happens, I still get anxiety spikes tho and become overstimulated very easy and when that happens the clicking comes back but I feel less pressure now after finding out a couple days ago that it could be tinnitus and those noises u hear are only in ur head, I jus wish I learned a couple years ago lol.
I still smoke, I’ve learned how to control the panic attacks and use the 🍃 to calm me back down like how it used to. Ik everyone’s experience is different so I thought I’d share mine in hopes it can help someone who might be going thru something like this. Advice like this is exactly what I would’ve needed and was looking for couple years ago, but I could never find anything so I thought I was the only one. Regardless tho it felt good talking about it, I don’t talk abt it much bc people can’t really relate so maybe someone here will. Definitely changed me as a person making me more open minded and wise since I was constantly just searching or asking for advice from people with hopes I would hear something to help my current situation.
Bro I was thinking the same thing because that's what happened to me in January I smoke some weed that I bought but it was laced with something nearly freak mi out I couldn't breathe I thought I was about to die I had to fight hard in myself to control my head because I was panicking ever since that night that ringing sound appeared till now but I try not to think of it as much
What if you got loud 'noise' in your ears, not so much ringing, and crackling when swallowing, is this more to do with congestion
@@emilyratajkowski2556 another scam
had it since fuckass september 2023. im mad asfk its not gone yet and it just gets fucking worse.
Bro same 😭, I hope you've at least habituated by now, what makes yours worse btw?
Thank you so much 🎩🙏🤗
Peoples who are face these type of hmmmm or ringing sounds,listen its not tinnitus 100% it can be other thing like sick, fever, or weakness bcuz i had also face this problem 2-3 days before i was thinking it is tinnitus but suddenly when i sleep and weak up it was nothing I caused bcuz of i was sick and then i relieved, i know many people like me think that they are suffering from tinnitus and they get in anxiety but don’t be afraid be brave 🙂 thats why i decided to inform you all 😊
Impacted wax in ears I had this for a long time then I had started regular ablution wudoo 5 times a day it helps
Iam now experiencing this Tinnitus due to removal of Ear wax by an ENT by an instrument.. Either its a "Veee" sound or a "Hush" sound..My friend who had says it will be there for quite a long time and advises to put Oil..in the affected ear.
Very informative ❤
I STOPPED TAKING AMLODIPINE AND MY TINNITUS WENT AWAY .
What did you use as an alternative, I began to hear the sounds a, week after taking amlodipin
Is tinnitus physical or can it be in your head like how you can think of sounds maybe your just thinking of tinnitus
BEST VIDEO THIS! THANKS.
can I be of help?
Muchas generalidades pero las soluciones que propone son ineficaces en la gran mayoría de lis casos. Como todos los videos de perspectiva médica, ayuda poco o nada
I don't know when this started. Maybe after i gor really sick in vacation. I have always been able to ring my ear things (where you heat distant thunder) but i highly doubt that has anything to do with tinnitus. I was hearing buzzing at school today it kept getting louder And louder and louder.
My tinnitus was caused by an explosion at a gold mine in the year 2000.
You didht include Somatic Tinnits occuring fron TMJ disorder, whiplash or other neck and cervocal causes
I've had it for years thought it was due to medications, but have noticed that It could be due to hypothyroid issues, which I've had all my life.
To anyone struggling with tinnitus: You can learn to habituate one day. It took me a couple years but i got here. Hang in there! Try masking to ease the anxiety and one day you might be able to lower the volume of your masking sound or even turn it off.
Do you know if the Frey Effect can be picked up by around the ear EEG?
Ok so uh its currently 2 am and i cant sleep because a new tinnitus just hitted in by the past 30 mins, im gonna test to see the comments tomorrow
Do you still have it
@@nicklopez8279 nope, the comments actually Works!
@@Lorenzokkkk741what worked?
@@nekonesto3125 the method
so not give an attention?? like hearing it and move on to seeing?
Good information
Understanding the cause of tinnitus and deafness? I'll go there. How about:
1.) Firing a 3"50' without ear protection because not provided by the navy.
2.) Small arms firing ( M60, M14, M2, grenades, etc,etc ) and hearing protection not provided by the navy.
3.) Operating a 16 inch gun turret.
Im pretty young, and im worried.
My ears have been ringing sometimes at school, and i dont know a bunch about Tinnitus,
What do i take to treat this?
I would love some help
Thank you❤
can a herniated neck disc cause Tinnitus?
I need these slides 😢
Istening to all your comments guys i wanna share my story too.
I have a bad habit of listening music i always wear earphones every day. One day all of a sudden i statred hearing ringing sound at first i thought the left earphone was broken and later realize it was not i threw the earphones away and after sometime i started hearing again. Days pass by and some times it started happening again but on the right side sometines on both😅 soon i realize if i dont use earphones the ringing won't occur. And now i only use earphones for 10 min sometines i hear the ringing and sometimes i don't. Idk if this is tinnitus or not. Am i cooked guys?😢😢
How is it going now?
Actually earphones when not loud is good for curing tinnitis..ithink.
I have it and it sucks bad
my tinnitus seams to be linked to a weird design on my basement floor... i shoulda taken a picture of it before scraping up the weird voodoo drawing, but its similar to "Ravahere" thats part of the french polynesia islands in middle of south pacific.... weird but... its my story i guess....
What could be the cause of short-term tinnitus? about 10 seconds
I have permanent tinnitus I'm only 14 I've heard it for 8 years i hear 2 or 3 different everyday every night sounds i think it caused for headphones on all volume
Guys just to let you know you have tinnitus because your is full of ear wax this has happened to me just need ear drops or hot oil
Did that give you instant relief or ringing or gradually went away after clean
No I had impacted ear wax used otex ear drops and that caused my ringing it's been 2 months and still going 🤦🏻♀️
@@elishawright2456I also used Otex ear drops and ended up afterwards with tinnitus which I’ve had for 4 & half months. Wish I’d never used the drops.
@@elishawright2456Здравствуйте!Я с Украини!У меня такая самая история,звон у меня продолжаеться пол года,сильний звон.У вас прошол?
@@elishawright2456 Did it stop if yes. how??
Guys, I hear this like sound in my right hear it sounds like a motor reving but it doesn’t happen constantly. I noticed this a few days ago but I thought I was it coming from outside. It goes like this “vvvv…vvvv”, and then it goes away. I’m getting scared, anybody what this is?
What you're experiencing is called V2K. It's a kind of electromagnetic torture that is conducted through radio frequencies
You should check if you're blacklisted.
It helped me stopped it.
@@janice_bbcould You explain more about this kind of tinnitus,please?
I tried to go to sleep one night in my bed in November 2022 when I noticed a ringing in my ears I don’t think much of it because it happened to me before the incident and went away after a few seconds but when I paid attention to it wouldn’t go I away I would freak out and I told my mom to take me to doctor but it was late at night so she said tmr and I couldn’t stand it so I put my earbud in and listened to sounds while the volume was low because I didn’t wanna make it worse and I only put my earphones in one of my ears it mainly happens when I think of it when I get anxiety I get tinnitus
i think my buds is the cause of my tinnitus i hear it 1/2mos ago.
thats why i stop using buds
can I be of help?
hi same thing happend to me usually it go away after seconds but when I paid attention to it and freaked out it is not going away like that now how are you now? 😮💨
Shoulder muscle pain
High bp is one of reason
movement three 🗣️🔥🔥
What is the root cause of tinnitus when i also have hyperacusis?
Tinnitus and hyperacusis often coexist, though not always. There isn't a specific factor that causes both, but all the possible causes of tinnitus can be to blame.
@@hearproofI'm looking for help how to threat tinnitus and hyperacusis. My ENT's can't do nothing. Can you help me please?
Hi I am suffering of tinnitus
Anyone dealing with pulsating tinnitus?
are u oki now?
My tinnitus goes louder if I open my jaw wide
What you're experiencing is called V2K. It's a kind of electromagnetic torture that is conducted through radio frequencies
You should check if you're blacklisted.
It helped me stopped it.
@@janice_bbWhat if the tinnitus caused by prolonged loud noise (prolonged earphones)anyone suffering with this or anyone overcome this please help me
Beautiful content. I have Tinnitus. Nothing is found by ENT. No SNHL and no Tumor but still have Tinnitus.
Same here .. no SNHL no Conducive hearing loss
My ent said go to neurologist
I didn’t yet
@@ahmiad1 burning sensation b hota Ky ear me
I can’t stand the buzzing in my ears and head it’s so uncomfortable ad it’s driving me insane it’s horrible I need help doctor says it’s because of blood pressure
Have you been taking any medication?
@@HenryCavill-e1b hi, yeah I’m taking medicine right now which kinda helps not what I expected but at least I don’t hear the buzzing anymore only when my tension is high.
And all this time i thought it was caused by frequencies from superior beings. ;)
My tinnitus is gone after 4 months. 2 months were hell, I was not able to sleep.
Shift your focus from the noise, don't take stress, keep yourself busy and one ear exercise is there on TH-cam, do it.
And check your ears with a doctor. Mine was because of ear wax and I got it removed.
What ear exercise
I got this tinnitus when i remove the deep gone wax from my left ear..
I worked in noisy Factory For ovr 42 years had slight Tinnitus For few Yesrs when tested for Hearing losss Had a 42 percent hearing loss got Hearing aids Help a lot with my hearing as said had a slight ringing noise now and again about couple times a week for a minute our Two during the Covid Epidemic had all the Covid jags did not make my Tinnitus any worse , 2021,22 wellduring this time got a Shingles Jag about a week or more later 2022 this is when my Tinnitus got worse constant Humming in my ears goes from my left ear then to my right ear had it worse since then could Be the combination of both the Covid Jag of the Shingles jag , i myself believie it was the Shingles Jag as thats when this really got worse and have it ever since even with hearing aids Still get it
My tinnitus is like an MRI noise with migraines😢
Pov : ypu tried to look for tinnitus by txt but you're watching this rn
I am tinnitus please help me 👂🏿
Tinnitus caused by prolonged loud noise anyone suffering with this or anyone overcome this please help me
Stay away from loud noises or wear hearing protection when around such noises. Get hearing test (if hearing loss is present hearing aids may help) and utilize some sound therapy always played below tinnitus volume do not mask it except for sleeping if needed. Tinnitus takes time to adjust too…overtime it does improve and get easier for the majority of sufferers.
@@Andrew-pp2ql thank you
You've received excellent advice from @Andrew-pp2ql, but I'd like to emphasize the importance of protecting your ears from further damage. When there's already damage to the cells of the hearing organ, the goal should be to slow down the progression of this damage. Age-related changes will naturally occur at some point, but they can be accelerated by factors like noise damage, certain ear diseases etc. I recommend finding suitable hearing protection designed for specific situations. For example, there are special filtered earplugs for music, but you will require different earplugs (or earmuffs) when using loud tools that provide more protection.
The pausing between the words in this video is really slow...
I hear people's talk badly about me in my head
Wow it’s so crazy I can’t stand it
Since last night I have this sound ringing on my left ear
How are you now bro
@@Thunder_921 im totally fine now
@@kevinzu9039 How many days did it take you to recover, and how did you treat yourself?
@@Thunder_921 it went away itself... so don't panic nothing serious
Yeah I want it want it want it want it want it want it yeah
I can never thank you enough Dr Liam Ogbebor for all your services, I am now completely cured of Tinnitus after using your medication, you're truly a man of honor and words I am so happy I came across your channel on TH-cam
Scam
Scammer
My tinnitus finally gone after two years of suffering.
can I be of help?
@@isabellacharlotte I'm cured already.
@@HenryCavill-e1b Okay congrats, pls do help others.
Did u follow any treatment
Does you face hearing loss? Aswell
y
Dr
Please eye and hear pbm
Care one meter okay
Night eye dark
The buzzing sound on my hear almost got me Crazzzzzzzzzy, all thanks to Dr. Adebayo Ighalo who finally cured me.
My tinnitus cause is vascular loop 😢
Hi, what is vascular loop?
@@Itsjennaaaay I would like to know what that is too.