2 months in my tinnitus, a 6k frequency in my left ear, mine too wakes me up around 3am, (in fact I finish writing this at 4.30am - please mind the early morning writings) I know for sure of time as well, as I've kept a log of the T-strength. If you want to know my story keep reading.
But for those wanting immediate Tinnitus recommendations on tools that have helped me to date try these things:
1) Go to a
steam room. And meditate. I'm lucky as I found a public place that has a steam room, and a spa. If you're lucky try and find a steam room where people don't talk, so you get the nice quite place to relax. Don't try and think. Just try and relax.
2)
Ginkgo Biloba. Supplement. Helps bloodflow to the brain. Although I took one a day for the first month, not so much now. Unless my T is bad I suppose. But I'd rather not drown my T in pills. I prefer meditation. Ginkgo did help my T disappear in the day, but I still have T at night, so it is not a write-off, do try it. I heard about this by watching an interview of Chris Martin from Coldplay.
3)
Meditation, find a quite spot, like a beach, or a quite park, soak up some sun, and be around nature.
4)
SleepPhones device. A New Zealand company, where I'm from, yay kiwis:
www.sleepphones.co.nz - this has been really helpful. I go on youtube and search for "8 hours tinnitus nature", the bleeps and white noise I don't enjoy as much. I prefer water sounds, wind, or anything nature. More calming. I used to try and sleep with headphones and earphones but of course that is uncomfortable or falls out. SleepPhones is "pajamas for your ears" as it wraps around your head as a headband with speakers built in.
5)
Earplugs / further prevention - I still play music - but try and not forget my earplugs. Don't want this getting worse. Also notice that I need to bring earplugs to loud places like the cinema.
Now my story.
Do note, I am a
musician (
www.ralphe.co.nz /
www.thisflighttonight.com /
www.musicstudios.co.nz /
www.youtube.com/ralphengle) and I am a trained
audio engineer. For a long time I've been trained to hear quite noises and subtle frequencies, and have been that guy in the office who would be sensitive to radios at work, or previous to my accident I would be the guy that needed earplugs in bed as my hearing was sensitive to start with, light snores would wake me, a form of
Hyperacusis (self diagnosed of course - thanks internet forums.)
You'd think for a musician I've been known to wreck my hearing, not really as I've been cautious and trained regarding safe listening levels. I'm 33 now, and yes in my early 20s I would go to raves and have a great time listening to loud sounds all night, I used to DJ, I played in bands... but never to the point that T would give me sleepless nights, and the T wouldn't carry on in the day if I were to catch it temporarily in the past. I often wore earplugs - but if I were to get temp T in the past, it would last for a few days, not like now.
Since a work conference two months ago, my life changed.
You might say due to my 'musical' past it was like a loose branch, but since my incident the branch just snapped and fell. But I would argue and say my T was immediate, and due to a very loud sound.
So what happened two months ago?
Time of Incident: 1530pm
Date of Incident: Wednesday 26th July 2017
Hours worked before incident: 8 hours
Where did this incident happen: Work conference, offsite, well known Office stationery company, let's call them O.
At the O Supplier Expo outside of my normal office site - in Hamilton, I was with a group of people at the time - witnesses! We were heading back to the bus to go back to Auckland after a full day at the expo.
Located at the entrance between the restroom and eating area was two large PA speakers positioned in a narrow hallway, at ear level.
I was the person closest to one of the speakers, and did not see or notice the speakers as I was walking by, it was silent at the time but all of a sudden the MC started talking and I was blasted by a loud sound (twice) in my left ear which made me jump as a reaction.
I was standing at ear level to the speaker and no more than a metre distance.
That evening I noticed a loud ringing in my ear and it hasn't stopped since. I visited my doctor, some audiologists, submitted a work incident report, and finally submitted a claim with ACC.
Firstly
www.acc.co.nz is a New Zealand Government company that gets income, because everyone in NZ pays an ACC levy - through their car levies for example. Really I see them as a compulsory Government insurance company.
Overall and so far, ACC have been good, although there are a lot of initial hoops to jump and paperwork because I suppose some people take the system for a ride, but once my evidence became clear that my T was not "prior existing" due to my musical history, but an immediate change, they have just approved my claim. (I haven't seen first payment from them yet but it is early days because my claim has just been approved). I retain 80% of my income, and they pay for my GP and specialist visits. But not for any "alternative remedies" such as going to a steam room and my SleepPhones device.
Anyways my GP has just signed me off 2 weeks at work, work won't allow me to go into work as I have a medical certificate, they claim it is a legal thing in NZ, if your GP tells you you're unfit for work and you have a certificate for it, then you must not work. I tried to ask work if I can have half days as ACC only compensate 80% of my income, or work from home as all I do is sit at my desk, some managers have remote access to our system, so it would be technically possible, but they wouldn't allow me.
So now two weeks of trying to "heal myself" with alternative remedies as I wait for a specialist to see me in a week, I also signed up with University of Auckland because they carry ongoing studies on T - but they are not free, and the University is actually more expensive than GPs or specialists. For anyone in New Zealand - before you make any appointments with anyone, make sure they are ACC accredited so costs can be reimbursed by your ACC case manager, and that there are no surcharges.
My ACC claim is new so for an updated case on my story, please feel free to contact me and ask questions, I might continue to blog about it in order to get my story out there, to possibly help others, and in turn hopefully someone can reach out to me, and communicate anything that might be of help.
Thank you for this forum. (This is officially my first post at TinnitusTalk.com).
www.ralphe.co.nz