Can anyone explain what their tinnitus/ringing in ears sounds likes?

Mine is like a very high pitched sound that comes on randomly and lasts no more than 10 seconds at the most. With this flare up it hasn't been happening as much. Mine is also mostly confined to my left ear.

I'm not in treatment yet so mine hasn't gone away, but detoxing has been lessening my symptoms in general so it hasn't happened as often.

Mine is a high pitched ringing but other times I've had clicking or all of sudden the volume lowers. Been in treatment almost a yr so I'm not having as often or as long.

Mine is much more like Lymesinger's, but I know mine is directly tied to having Lyme disease, as I was rid of it when I healed previously and it only came back with my reinfection.

Mine varies and can be so sudden and sharp that it makes me grab at my ear for the pain - it can be super high pitched, or low and almost not noticeable until things get quiet (how it is today), but can change in a heart beat to something much more sinister and painful. I've had buzzing, high pitches, low hums, even a clicking type of sound - that one always just about drives me totally mad!

Treatment and detoxing has always made a different for me.

I have a symphony of sounds constantly in my left ear (not as beautiful as a real orchestra, though).

Lots of different pitches...started with one higher pitch tone that got worse if I took the full dose of Singulair (Asthma drug) and would disappear when I stopped the Singulair. But I needed the drug to breathe before we discovered the cause (mold in my house).

The ringing has only gotten worse for me since it started, because I couldn't stop the Singulair for a couple years after noticing the ringing.

It is only in my left ear. Any ringing stuff I've had in my right ear has been brief, like someone struck a tuning fork, or just a few seconds of some tone or another.

Also, the volume can be painfully piercingly loud, or can be just annoyingly loud. I notice the sound in my ear more when the room is quiet.

My left ear also is much more sensitive to sounds than my right ear. From testing, the left is only 5% different from the right ear, but perceptually, it feels like 50% or more different...

Some sounds are barely audible on my right, but way too loud on the left...

I blame it all on Lyme/coinfections, as tinnitus is not listed as a known side-effect of Singulair and I've not found anyone else who has had this issue from Singulair...perhaps the ringing getting worse when I took more Singulair was coincidence, as my allergy symptoms were also worse then (which may have caused fluid in my ear, which is known to make tinnitus symptoms worse).