I bet it would be hard to get disability because how could we explain/prove to doctor that what the tinnitus is doing to us.
However, if a person is able to chat in Internet forums and on other social media websites regularly, I think most people would agree, such a person can't then say, they have loud intrusive tinnitus that they find debilitating and prevents them from working or carrying out normal every day tasks.
@Michael Leigh your thoughts in your 2nd paragraph is all wrong. I read two or three paragraphs and I am done due to the tinnitus/concentration issues. Although I did just type this response,so I guess I am all good then
I'm not Canadian but ENT's don't seem to be much help either Ronnie, they take a very 'physical' approach, i.e. if you have nothing physically wrong, then you're sent on your way. Thankfully, my ENT referred me to the hospitals hearing therapist who is apparently the country's leading specialist in T, by sheer luck of the city I'm in. It's early days, we're still trying to figure out what's the best approach for my T (which developed a new tone yesterday; wonderful), but I would definitely look up who is your hospitals hearing therapist/T specialist, and if they don't have one, find out which hospitals nearby do.I live in Southern Ontario in the Greater Toronto Area. Short answer is no. Went to emerg. about tinnitus, was sent on my merry way saying "it usually resolves itself". Saw the very uninterested doctor for less than 5 minutes despite an 8 hour wait. Despite mentioning how debilitating it was and the extreme lack of sleep I'm getting. The depression, etc.. She saw no ear drum damage and determined my hearing was fine. I think she thiught I was overexaggerating the problem.
Also went to my family doctor who had no clue. Said he would refer me to ENT. It's been two weeks and still I have heard nothing. Frankly, I don't think it's something taken very seriously around here.
I'm sure certain circumstances, such as fully losing hearing, would say otherwise...
There is a clinic that specializes in tinnitus treatments in Mississauga, Ontario.
The disability would be down to depression, anxiety.
I'm not Canadian but ENT's don't seem to be much help either Ronnie, they take a very 'physical' approach, i.e. if you have nothing physically wrong, then you're sent on your way. Thankfully, my ENT referred me to the hospitals hearing therapist who is apparently the country's leading specialist in T, by sheer luck of the city I'm in. It's early days, we're still trying to figure out what's the best approach for my T (which developed a new tone yesterday; wonderful), but I would definitely look up who is your hospitals hearing therapist/T specialist, and if they don't have one, find out which hospitals nearby do.
3 months for me, I know how it is! Don't go the private route until you've looked into all options. I was going to go private until I realised I could get it through the health service. But yeah not all hospitals have T specialists; just Google around for hospitals in your area and 'hearing therapists', they'll be the ones who know about T management. Also - mental health services can look around and put you in touch with T specialists. Good luck!You hit the nail on the head. The doctors I have seen so far have only taken physical approaches; checking my balance, having me close my eyes and do little sounds from my ears; check my vision and perception, and check the inside of my ear. Since it all checked out, that was pretty much it in their books. I did attend a major hospital here who said they don't have a hearing/T specialist, however I have found several independent clinics that have tinnitus management on their website listed. Unfortunately it's not covered under Provincial insurance and costs a pretty penny. Ah well. I'm trying to take a more positive and less fearful/anxious approach. It's almost two months since I've had this life-destroying noise, I might as well make friends with it now.
I am so sorry to hear what you're going through. It's the same in Germany. Since ENTs, therapists, audiologists and even tinnitus associations have propagated the horrible misconception that loudness doesn't matter at all and that the type of tinnitus doesn't matter to the concept of habituation, tinnitus isn't seen as a debilitating condition in itself - it's just your reaction that makes it debilitating.I was recently denied a disability claim with the Ontario government. It took me 15 years of suffering, denial of life impact, medical professional carousel, alternative medicine spent ALL of my savings, loss of career, self doubt, psychological defeat, social isolation, dependence on family, suicide contemplation, embarrassment and countless other compensations before I finally denigrated myself to apply for disability. I have learned a lot about myself through this private and personal sonic torture box that is my skull over the last decade and a half and I am grateful for that. There is a harsh reality however which is that my social, cognitive and productive aptitude have been egregiously diminished as a result of my SSIHL and associated wicked, chronic and pronounced tinnitus. It beat me. It broke me like a POW malnourished and caged. I tried for 8 years to get it fixed. I consulted every doctor here and in the USA...all tests MRI etc were fruitless, I paid for alternative therapy like LL laser, acupuncture, changed diets, fasted, prayed...every modality left me either broke or with the "learn to live with it" diagnosis.
So
I recently applied for disability with the Ontario government. I am embarrassed to do so. But I am fucked up. They said I have psychological problems not physical. They have no idea how loud it is. If I could "blutooth" my skull into theirs they would shit their pants in 15 mins and beg it to stop.
Try 15 years.
I will reapply...I need help. Its in my head but its not psychological.
Maybe these articles will help
There are so, so many cases of people in Germany trying to apply for disability benefits due to tinnitus being literally told that their condition can't be debilitating and that it's a psychological issue instead. We need to stand up against this, we need to speak out against this, we need to make it clear that tinnitus can be debilitating in itself.
Why do you say that?USA - including our military veterans.
The VA standards for disability for hearing loss are determined by the test results of speech recognition; pure tone threshold average; and/or combinations of both. Various levels of rating percentages can be issued based on the results of the testing. However, for tinnitus, there is specific ways to prove your case with the VA.Why do you say that?
This is a DISGRACE.
Should we start a petition, maybe with the WHO?
How do we go about it?
1. Petition to get disability.
2. Petition around noise levels, don't get me started (seriously I can feel blood pressure boiling - we have empty noisy bars, cafes, ambulances that are higher than police sirens, planes above half of London non-stop). It's a health crisis.
We need a Tinnitus Talk manifesto.
@Candy I said it before but people on the boards hate to hear it.Should we start a petition, maybe with the WHO?
That is billions a year.
It is called public money opposed to private money.It's interesting that tinnitus disability is accepted by military clinicians, yet generally dismissed or downplayed by civilian ones.