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@dloos

I’m going through something similar. It started after Covid, and I am quite sure it’s all related. I wear hearing aids....not much help. They are pretty fancy Signia with the tinnitus and blue tooth features. I really don’t like Bluetooth myself because it blocks out everything else. I have hyperacusis too, so I have to balance some hearing, but not loud enough that background noises make me jump out of my skin. It’s tough to balance. It all sucks.
I have gone the Integrated Medicine route because I couldn’t get in to see an ENT early enough for the steroid treatments to be valuable.
So now, we fight the inflammation. I have no idea what the outcome may be. I hope I don’t go totally deaf.
Worse than the hearing loss for me is the “full” feeling and pressure, along with tinnitus and hyperacusis.
Feels like my head may explode.
ENTs all suggest SSRIs. I have not found one that I tolerate.
And, really have not had a definitive diagnosis either.

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Replies to "I’m going through something similar. It started after Covid, and I am quite sure it’s all..."

Interesting about Covid..I had the Omacron varient followed by “long Covid”.
They really don’t know enough about Covid because people ended up with different symptoms. My Doctor told me to take Super B with folate and in a week I was back to normal.
I saw a rheumatologist for my current ear problem and he wants me to try a drug they use for Rheumatoid Arthritis that will suppress my immune system if I can tolerate the drug there’s an 80% chance of my hearing returning. After seeing my therapist I’ve decided to give myself some time before I jump into a strong drug with side effects.
Good luck on your journey!
Lynne