Tinnitus Seems Linked with Sleep
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Basically cover your ears with your palms and snap your index fingers loudly on the back of your skull. 40 or 50 times and when I remove my hands, it is blessed silence for at least a few minutes and often long enough to fall asleep.
https://lifehacker.com/this-weird-trick-might-give-you-brief...
I think it has to do with how quiet is the environment, as the finger snaps are very loud and drown the tinnitus, but putting on my noise-cancelling headphones without music make it feel louder. Maybe a fan/rain/white noise generator would help people who have trouble sleeping because of tinnitus.
The flick might be a simulation of an impulse signal which covers all frequencies and tricks the brain into thinking that the absent frequencies were also included in the heard impulse.
I’ve also noticed my tinnitus is inversely proportional to the last night’s sleep quality for me, so the article bears out on an anecdotal standpoint.
It’s a weird motion so practice with you hand in front of you.
- Hold your right hand in front of you.
- Cross your index finger over your middle finger
- Press your index finger and your middle finger together pretty hard
- Let your index finger slip off the middle finger (You will notice the index finger has quite a bit of power)
- Now place the palms of your hands over their respective ears, covering them completely. Pointing your finger back around your head.
- Repeat the index/middle finger motion above but let the index finger smack the back of your skull (It should sound like a very loud thump)
- Repeat this 40-50 times (Your fingers will likely get tired)
- Remove your hands from your ears and hopefully you will have some relief from the tinnitus (The effectiveness and duration seems to be highly variable from person to person and type of tinnitus)
Good Luck
This doesn't make sense. If it can be heard by someone else, its by definition an aural stimulus event and not tinnitis.
“Objective tinnitus is a perceived sensation of sound that occurs in the absence of external acoustic stimulation, but it can also be heard by the examiner (eg, by placing a stethoscope over the patient's external auditory canal). Objective tinnitus can occur either from perception of an abnormal somatosound or abnormal perception of a normal somatosound. Objective tinnitus is much less common than subjective tinnitus, but it often has an identifiable cause and may be curable, whereas subjective tinnitus is often idiopathic and is seldom curable.”
The main function of this system is to protect the ear from loud sounds—noise canceling and/or modulate sensitivity as a function of spectrum.
Strangely I don't know that either of them interfere with falling asleep. It may very well be that I just don't even try to sleep unless tired and quiet, can't tell--I don't do it consciously. Lately I usually start something on Netflix or YouTube without autoplay so perhaps that's what I accidentally found to work.
I have some high frequency hearing loss in this ear, probably due to using noisy machinery in my 20s without proper hearing protection. Anytime I do loud things nowadays, I wear hearing protection.
I have noticed my tinnitus seems less frequent if I stay properly hydrated. I have a tendency to forget to drink water and making a point of it seems to help.
Meta lesson: just try things!
So, jaw relaxation, posture, sports does it for me.
Hearing loss can not be healed but the other two types always go away after good sleep.
If you got tinnitus it is good to figure out if there is a cause that can be taken away. Sometimes you are in luck and a good deep sleep can improve things.
It's been a few years now. I'm lucky since the noise in my ear is not too strong and often I don't think about it unless I'm alone in silence, but it somewhat sad to think of never being able to hear silence again.
In other words, it seems the other two types of tinnitus are sensitive to the amount of reactive oxygen species (ROS).
When you sleep, the ROS are suppressed by glutathione. Then, you feel fresh and rested when you wake up.
When you go through your day, the amount of ROS slowly but steadily increases until you sleep and allow glutathione to do its job again. The cycle repeats.
Given that your tinnitus seems to depend on ROS, I would suggest to experiment with NAC 600 mg and see whether it improves the symptoms. NAC is a glutathione precursor and causes the immediate suppression of ROS.
If there is a correlation then the condition can be treated and improved.
There are some public materials by people like Elliot Overton and Sten Ekberg. As far as I know, they do general practices combined with private consulting as well. You can try to reach them remotely or physically by visiting their clinics.
My friend had a tinnitus for a while and later found out it's due to hearing problems on both ears. He then got hearing aids and the tinnitus went away.
So it looks like, _some_ form of hearing loss induced tinnitus can be treated.
For example, if tinnitus gets worse while blood pressure and glucose both go up (without eating) then it may be a hint of an underlying metabolic problem.
To confirm this further, you can then eat 15 g of sugar and see what happens next. If tinnitus improves then the hypothesis of metabolic underlying problem becomes very, very probable.
If my tinnitus is bad during the day, I use these pages, and they do often help in varying degrees.
https://mynoise.net/NoiseMachines/whiteBurstsNoiseGenerator....
https://mynoise.net/NoiseMachines/neuromodulationTonesGenera...
The thing that I've discovered that actually makes it go away: extreme bass. Massive, 18" speaker cabinets and kilowatt amplifiers for long periods of time, the kind that makes your whole body vibrate, while wearing ear protection. I discovered my first this after DJ'ing a club with a proper bass soundsystem and have confirmed it since. The effect lasts from weeks to months.
I found a few things in the medical literature which support this as a real possibility and emailed a researchers about it who said the same thing. I am seriously considering opening up a crackpot bass-therapy clinic to help other sufferers, but need to have other people confirm it works for them first.
Btw, how long do you listen to bass sounds? And do you have thoughts/opinions on what frequencies and how much variation is needed? Just wondering if I should use a tone generator or put on some EDM, and whether I should try at home or it’ll take long enough that I should go somewhere that the neighbors won’t hear it for hours.
I've tried, I can't just listen to a low sin note on headphones to fix it (in fact maybe this makes it worse). I actually don't think the ears are important, it is being physically vibrated that does it. I tried with a SubPac transduction woofer and it maybe worked? But not to the degree I'm really talking about here. A strange phenomena. I don't even like reggae that much but I got to the monthly reggae dance here just to get vibrated.
If one is going for the first time, I'd recommend going to the qualifying rounds. It's often cheaper and usually less crowded. Make sure top fuel funny cars or dragsters are racing -- the lower classes are significantly quieter.
[0] Wearing hearing protection. I'd recommend the kind that go in the ear, covered by the kind that go over the ear.
I have tinnitus and listen to white, brown, and pink noise throughout the day. I tried notched white noise for a couple months, but didn’t notice any change compared to regular white noise. My favorite noise these days is “space ship engine noise” videos on YouTube. I get to pretend I’m working on the Enterprise. :)
I'd come in for this therapy. I think the most bothersome of my tinnitus is that it makes hearing certain speech difficult and could detract from enjoying certain parts of music.
My personal hypothesis is that the vibrations may somehow stimulate local physical interconnectivity in damaged tissues leading to their improved recovery.
Riding a car has a similar effect, especially when the road is a bit rocky.
As someone who has had chronic and constant tinnitus for nearly two decades I find this claim pretty questionable, or at least not clearly articulated (following through to the linked Lancet article didn't help much). Whenever I mention this fact in conversation people seem horrified, and in the sample "nearly everyone I have known for years" never encountered anyone who replies with "oh yea, same here".
I'm assuming that 15% of the world's population does not suffer from constant/chronic tinnitus, but I would also expect far greater than 15% has ever had tinnitus, so I'm not sure what this number means. The linked Lancet article didn't offer much help and mostly references a handbook that doesn't appear to be trivially findable online.
Curious if anyone has discovered some clarification around this?
I also had what has been called "Alice in Wonderland Syndrome" as a child where I had strange sensations of my body feeling larger or smaller when going to sleep. I never thought much of it, but eventually I heard that it happens to other people too.
“the scatter of prevalence estimates is wide, although most study results have shown rates of between 10% and 15% of the adult population. The largest and most scientifically reliable study was undertaken as part of the National Study of Hearing in England (n=48 313).3 The results of the study showed a prevalence of 10·1% among adults, with the tinnitus described as moderately annoying by 2·8% of respondents, severely annoying by 1·6%, and at a level that severely affected ability to lead a normal life by 0·5%. Results from studies in Egypt,4 Japan,5 and Nigeria,6 indicate tinnitus prevalence is broadly similar in these countries to in Europe and the USA.”
There are some treatments for both symptoms. The ones I've tried involve listening or looking at static. Neither had much effect on me.
The best way I've found to deal with it is to ignore it. focusing on treatments preversly makes me more aware of the annoyance.
In turn, that condition is commonly caused by the underlying metabolic problems, which can be caused by genetic mutations in mitochondria, toxins, episodes of hypoxia, unhealthy lifestyles, oxidative stress.
When this happens, the other symptoms may include chronic fatigue, acquired insulin resistance, T2DM, sometimes various neurological manifestations in different parts of the body, and even dementia. Personal mileage may vary, it really goes from 1 to 11.
Apparently a healthy number is 500+, most people will present with issues in the 250-300 range, and I was at 166 when critical is 144ish.
I have to take a daily pill for the rest of my life and things have improved, but the VSS is still the same.
For a long time we believed that when neurons die the condition stays forever and cannot be improved.
However the consequent observations on WW2 veterans proved the opposite - neuro tissues do recover but they do so extremely slowly.
If you had such a good response to B12 means that not all is lost.
What you can try to achieve is to provide the conditions for faster neurological recovery: speed-up the cellular ATP production to provide the energy for anabolism while slightly suppressing the immune system response so it does not get in the way. You biological machinery will do the rest.
The first part of the equation is reached with specific combinations of vitamins and coenzymes. For example, here is a combination that can serve as the basis: B1 in therapeutical doses (pills, >= 250 mg per day) + multivitamin. The second part of the equation is reached with NSAIDs.
Such treatment may allow you to reach some notable improvements just in few months. And those improvements will persist and accumulate.
There are various possible causes for acquiring a mitochondrial dysfunction beyond the malnutrition. The good news is that it can treated if it is not caused by a genetic defect.
The treatment is similar to treating Beriberi, regardless of the original cause. The unpleasant part is that it takes some time and patience ranging from months to years.
The MRI found absolutely nothing. My eye doctor says my eyes are extremely healthy.
My symptoms line up exactly with VSS and I had a lot of peace of mind knowing what I was experiencing and that I wasn't going blind, so I didn't pursue the proper further test (PET scan, I think).
Honestly, the peace of mind was worth it, but be armed with research on it.
I’m not sure if Covid causes it, or it’s stress that is causing it. I notice it’s worse on some days and other days I don’t notice it until I’m in a very quiet area. It’s frustrating to go to the doctor and spend money and essentially just be told I’m fucked.
Should I look for another doctor and get a second opinion? Is there any therapies I can do to help alleviate it? Any help would be greatly appreciated
I suspect that tinnitus is similar in that the lack of an external signal allows for filling in with imagined sounds. Since there's no external reset the default could be simple tones (at least that's what I hear). For the analogy to hold the pitches of the sounds imagined should match frequencies of hearing loss. I tried to match up what I imagine I hear with recorded tones and it's close to the limit, e.g. I can hear faintly up to about 16 kHz and the tone I imagine is about 15 kHz--I don't recall the exact numbers but it was relatively like that.
I suppose with practice one could imagine hearing something while awake in those frequencies to the point it's indistinguishable from actually hearing it. I don't think I'd want to learn how to induce specific sounds or voices in my head that I can't turn off at will. At least you can know that the high-pitched sounds aren't real.
Elsewhere in this thread, it's been mentioned that there are several types of tinnitus (it's apparently an umbrella term), and some tinnitus can be caused by a firm pillow and bruxism, which fits my description.
I wonder if the type of tinnitus has more or less effect on sleep than others.
I'm saying that because that was the case for me. A back then undiscovered dose of mercury led to all kinds of back then mostly ignored ("it's not that bad and it'll probably go way" - I was young) issues, and some tinnitus was just a part of it, but also some serious sleep issues.
Any such environmental factors are rarely diagnosed, because that's really hard unless it's so bad that it's severe acute poisoning. But any less than that probably won't ever be discovered and will all be attributed - by the person themselves too (in my case definitely) - to "stress" (even if there is not that much) or aging. You can't detect it with imaging, symptoms are inconclusive at best, and forget blood tests, they are only useful for said acute poisonings.
> and only dream here and there
You would not know if you dreamed, normally. Only if you wake up while still dreaming. Even then usually you quickly forget most or all of what it was about. To remember more you have to wake up right in the middle of it.
By the way, speaking about dreams, during the years when I had those issues my dreams often were nightmares, they were full of feelings of helplessness, being unable or barely able to move, and generally very unpleasant. I had more than once during those harder times dreams where parts of my body were very seriously diseased including total tissue disintegration and open holes in my body, inside the dream.
Those dreams came from "below", from the "hardware", not from my (completely unconcerned) consciousness (I hope I kind of get across what I mean, not sure how to formulate this correctly). What I mean is, at the time I had no worries about my health whatsoever. All my problems, even though something like almost-asthma allergy coming out of nowhere and suddenly, seemed normal and manageable and as if it would all go away given some time, so I just coped (for example, hyposensitization treatment) and worked around the issues but didn't think much of it.
Since the problem was actually diagnosed (university clinic, lab tests) and solved (chelators, for years) my dreams have become AMAZING, and super interesting too. I'm so glad I had to wake up during some of them (alarm was set) so that I actually remember some. I never knew what great fantasies, sophistication and city-, house- and landscapes my brain was capable of generating, it was just terrible before.
Given that experience, I think even if it's kind of useless because it's way too vague and probably very dependent on the individual, the contents of dreams might give some indications to a body's health status too.
No. 1 learning for me: it's stress. Sleep, stress, and anxiety are all wound up in a big ball that vibrates at about 13kHz inside my head, slightly biased to the left.
Beginning to hear tinnitus is one of my backstop signals for tiredness, where I can avoid sleep deprivation inertia on waking, if I go to bed within half-an-hour to 2 hours of onset.
It seems to reliably relate to changes in muscle tension I sense around my ear and upper neck, often some slow twitching as well. It's a related sensation to satisfying yawns, stretching that eustachian tube.
I do not know what exactly is that cause of it but I lean in the direction that it's one of these
1) Blood electrolyte levels
2)meat
3) carbs/sugars in large amount
One could experiment with a keto diet for start.
On support forums people often wonder why head pain is worse after laying down for awhile.
See “Idiopathic intracranial hypertension” Also called: pseudotumor cerebri