Hi Tracy,
If you don't fear most side-effects from anti-depressants, then why fear an exacerbation of your T? It's most unlikely to occur. I was in your position from Feb-May: in fact, I spent nearly three months in bed terrified to move, interrupted my post-doc, and had my partner watching me due to feeling suicidal. I had, after years of the normal high-pitched ringing I don't care about, a sudden onset of low frequency sounds: all over head rumbling, whooshing, electronic beeping, droning sounds, hums, zapping, roaring, static, songs, musical tones, and it goes on. None of this was maskable, and indeed, was exacerbated by external sounds.
Today, I am sitting in the sunshine in my garden and back to work. So what happened?
Well, I was prescribed Sertraline (Zoloft), and if I had listened to some of the stories here I would have been terrified of taking it. I was also given Diazepam (Valium) as needed and referred for tinnitus counselling within weeks (unusual in the U.K, but as I have a cochlear implant any hearing things are treated quickly due to needing to know if it is malfunctioning). The Sertraline got my anxiety mainly under control and when that happened the T BEGAN TO SUBSIDE. That is no coincidence: yes, there is a physical cause in my case (deafness), but my mental reaction made a massive difference. Since mid-May it has gotten lower and lower until I began experiencing intermittent periods of silence in July. When it returns, it is now a faint hum and the reactivity has largely faded. I occasionally get a 24 hour spike which I take Diazepam for as it seems to bring it down to a tolerable level (my T seems a bit like Michael Leigh's in this respect). I sometimes take PharamaGaba, but supplements are a personal thing. Anti-anxiety medications are proven, and you are prolonging your stress out of fear. But fear of what? It surely can't get much worse! But you do have an opportunity to try getting better.
I now surround myself with noise as much as possible: white noise when working, and I have the Sound Oasis 650 machine on at night (I sleep with my implant on for a bit and then take it out). This has made a massive difference as my T now blends in with external sounds instead of being the dominant sound I hear. I am not habituated, but on my way, and that only began to happen once I decided to play an active part in my recovery rather than pacing around having daily panic attacks about what had invaded my head.
This is my progress five months in. I am not 'cured' and doubt I ever will be, but even extreme T like I developed turns out to be manageable. You may read stories of how it is permanent and will get worse, but try to keep in mind that such people will naturally gravitate to forums for help. I am an example of how it can improve, and of how silence can gradually return.
All the best,
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