I've never had mine confirmed and never had any need to, but how is it confirmed that you have it?
You tell the doctor you hear noise in your ear/ears. He says: "oh you have tinnitus." However the more complicated problem is discovering what causes your T. If you for example had a tumour growing on your hearing nerve they would see that in a scan and possibly remove it as well as hopefully curing your T. But for most people sadly no one knows what is causing their T and so no one knows how to stop it.How does the doctor check/know you have it?
No, there is no way to prove it. If there was then more of us in the West at least would probably be eligible for disability support which would cost our Governments which would, funnily enough, prove a spur to better research efforts.So if you say you have tinnitus and somebody doesn't believe you because they cant hear it or see it, how do you prove it to them? There is no way to prove it?
So if you say you have tinnitus and somebody doesn't believe you because they cant hear it or see it, how do you prove it to them? There is no way to prove it?
tinnitus patients reliably show structural brain abnormalities on very specialized tests, but they are only performed for academic research, because there's literally no clinical utility in them.
Sure, but the diagnostic criteria for tinnitus are pretty clear and don't require any fancy imaging. The imaging is really just there to:Clinics' job is not only to cure the sick people when the diagnosis is clear and the cure is possible, but to diagnose people with severe and incurable afflictions, and make that diagnosis official. So I consider identifying a severe T case, so a case of a serious affliction, a job that belongs to the clinics, part of what they have to do.
I'm sorry you've had such negative experiences with doctors; mine have been a mixed bag, but I've definitely found a lot of compassion and sympathy along the way.That is the problem, that tinnitus sufferers are treated only as interesting cases to study academically, some interesting guinea pigs with an interesting abnormal brain activitiy, not as PEOPLE which, after they served as didactic material in an academic research, go home and have to live with this terrible affliction.
Much of this comes down to affluence and luck. If you're in a metropolitan area and can afford to see out-of-network specialists, then you're more likely to find practitioners who spend more time with you and take more personal interest in your welfare. If you're in a rural area on a bad medical plan, then it's much harder to find that interest -- and this is true for anyone walking in to any doctor for any condition.
That said, this is still a poorly understood symptom, and when there isn't the unusual case with a clear diagnosis of cause and treatment plan, "live with this the best you can" is really the only advice that anyone can give you.
http://www.sciencedirect.com/science/article/pii/S0149763414001389tinnitus patients reliably show structural brain abnormalities on very specialized tests, but they are only performed for academic research, because there's literally no clinical utility in them.
tinnitus is a brain problem like nerve pain or psychological illnesses, all of these are hard to cure. The brain is the most complicated thing about us. If it could be reverse engineered so easily we could make robots like us. We cannot even begin to take apart a living brain for ethical reasons.I just can't believe that if all the medical scientists would seriously put their mind to it, they couldn't solve this mistery, that is above human intelligence to understand T, I think it's a problem of lack of interest.
The issue of proving that one has T is VERY important. One can be accused that he doesn't have it, while that person may have catastrophic, therefore disabling T. A way to prove T would be fMRI (functional magnetic resonance imaging) or qEEG (quantitative electro encephalogram). The machines are very rare in the world. In my country there is no fMRI or qEEG. About qEEG machines, if my information is correct, in Europe there are only two: one in Belgium and one in Switzerland.
There should be at least a fMRI and a qEEG in every country. I tried to get together the members of this forum (to which members of other forums can join) to make a petition to World Health Organization (I couldn't think of a better suited organization, but it may be a better one) to order to countries to buy such machines, so the T sufferers are believed, so abuse (such: "your T is only in your mind", or "you lie that you have T") is prevented, and also, in case of catastrophic T (which can be shown on these machines), the sufferers to be able to go on disability.
Catastrophic T is the worst disability I know. I can't think of a worse one.
Once one has catastrophic T, he cannot sleep. Once you cannot sleep, for many many days in a row, you become so tired that you become dysfunctional. Can't do anything. If a person with catastrophic T takes drugs in order to help him fall asleep, those drugs do not wear of at exactly 6 or 7 am the next morning, so they remain drowsy (so not functional like a normal person for more) even during the day.
The search for a cure is in it's initial stages, from what I know, as if T is a problem that occurred a short time ago, when, in fact, Hippocrates had it.
If finding a cure it's so hard, how about coming with some ways to put it in evidence, so sufferers can go on disability?
But I see that even this issue is not given decent attention.
Who is supposed to bring us help, if we do not ask for help.
Who is supposed to tap on the shoulders the people on top of medical hierarchy to ask them: "Hey, what about us?" if we, the sufferers, don't do it?
If I am wrong somewhere, please show me where I am wrong and take me out of the dark! In the meantime I just can't believe the lack of wish of the members of this forum to unite and try to make things move. Yes, we appear in statistics, but nobody is in a hurry to do anything for us.
If anybody thinks that I am repeating these thing so I can go on disability based on T, is terribly wrong.
I could go on disability based on a "psychiatric disorder" ANYTIME. The bribe I would have to pay to the doctor is not even a significant amount. It's just that I am thinking about all of us.
The only problem I would have in going on disability because of a psychiatric disorder is the humiliation. A person with severe psychiatric disorder may not consider his diagnosis something demeaning, but a person like me, who has, as the latest diagnosis just "recurrent depression", to retire based on a false diagnosis (schizophrenia, or paranoia, or something like that), I find that very demeaning, and it's a potential door for more abuse (more insults).
What if it is clicking instead of ringing? Is that still T?The Tinnitus test:
Results = You have tinnitus!
- Do your ears ring? If yes, move on to #2.
- Do you have head noise when you plug your ears? If yes, move on to #3. If no, skip to results.
- Does it annoy the Sh** out of you? If yes, move to results. If no, then you may not have tinnitus or it is mild.
Seriously though, I think, people just know when they have T. There are many types of T, but for some reason we all know we have it when we do.
It is very easy to diagnose T on a simple EEG that is then run thru a software mathematical Matlab algorithm - to quantitize it and display it on a 3D brain mapping Atlas using Brodmann areas to clearly show tinnitus hyperactivity and intensity over the left, right, or both auditory cortexes (as well as other limbic areas).
how do you know this?It is very easy to diagnose T on a simple EEG that is then run thru a software mathematical Matlab algorithm
First I researched it, then I done it.how do you know this?
Nothing impressive, I just did my homeworkVery impressive knowledge. My respect, @dan