I have had type one diabetes now for almost fifty years and have some autonomic neuropathy as a consequence. I have had tinnitus now for several years and I can safely say that it isn’t related to any medication as I have only had insulin injections as I always have had. It is variable and at times is harder to cope with. For me it is a high pitched whistle at about 5kHz frequency and it never goes away. Following a hearing test recently which showed my hearing dramatically reducing from about 2-3kHz I was persuaded to trial hearing aids. These certainly helped me to hear higher frequencies better but I didn’t like the tone of the sound or the extraneous noise they picked up. Wha was worse though was that the tinnitus changed frequency and was about 9kHz when I used the hearing aids. I was told that the tinnitus was probably because the brain was not receiving signals for higher frequencies and it was inventing what wasn’t there. When higher frequencies were there because of the hearing aids the invented noise just moved up to a new frequency range that was absent. I didn’t continue with the hearing aids and the tinnitus has settled back to its previous frequency. The audiologist said that damage from exposure to prolonged loud noise is of a cause of tinnitus but any nerve damage could trigger it too. Diabetes of course is a major culprit there!Hi everyone. Can you help me please?
About 4 weeks ago I developed what doctors think is peripheral neuropathy. That's still being investigated, I'm a type 1 diabetic (although quite well controlled so it's a bit of a mystery).
The doctor has subsequently put me on duloxetine (anti-depressent meds) to manage pain. About 2 weeks in, and I've developed tinnitus which has got progressively worse. I've had it for about 2 weeks now. It's tolerable in the daytimes when I'm in noiser environments, but is interrupting my sleep at night.
So I'm trying to work out which of these things has caused the tinnitus - diabetes, neuropathy or duloxetine/cymbalta? Has anyone else had an experneience with either of these?
I feel as though it may be the duloxetine/cymbalta, but also confused because doctors actually prescribe it to treat tinnitus. That would certainly be the easiest to fix, as I can speak to the doctor about changing the tablets. I've not really been able to find any threads from anyone who has had tinnitus from peripheral neuropathy.
Any ideas?
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I persevered with the hearing aids for a month and things didn’t improve at all in that time. The increased pitch of the tinnitus and the greatly amplified background noises that I could hear were far from pleasant. The grandfather clock ticking sounded like someone hammering in a nail and the tone of a historic keyboard instrument that I like to play was awful. Thank you for your suggestion and I am sure it will help other people but not for me at the moment. Maybe in the future if or when my hearing deteriorates further I will try again and bear your advice in mind.I too have tinnitus from prolonged exposure to loud noise in the work environment in the days before 'Elf 'n Safety. It is much easier to live with since I got my hearing aids, but I was warned that it would take at least 2 weeks of daily use before my brain adjusted to the new noise levels. This proved to be the case, and it was mildly unpleasant before this happened. Might it be the case for you? I appreciate we are all different, but it did take a while for me to benefit from the enhanced hearing and reduction in tinnitus, and maybe it is similar for you.
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