Hi! I was born deaf – no idea what’s exactly behind it (nerve intact, no evident malformations, unknown genetic). For many reasons I got diagnosed with neurosensorial hearing loss only at 7yo and since then I use . My “original” hearing loss resembles a sharp ski-slope hearing loss focused on high frequencies, with a massive drop at 1500 Hz. That has been my “hearing situation” for years (now I’m 24). Back in 2021, I realized I couldn’t follow video lessons as I used to and I’ve lost some sounds (microwave, traffic, and so on).
Some showed a consistent loss at “low-central frequencies”. Like, prior at 250Hz I had 35dB loss, now it’s 55/60dB loss over 2 years and a similar loss at 500 and 1000 Hz; high frequencies remain between 110 loss and no response at 4000Hz and 8000Hz. My audiologist doctor suggested it all depends on cochlear hydrops. They were really confident I’d recover from my recent loss (prescribed me betahistine) and that this could be episodic - the same way Meniere’s disease does. In reality, 1) in my everyday life I don’t experience such a varibaility – to me, it seems like it’s only getting slowly worse 2) my last audiogram showed some uniform worsening and it’s almost impossible to follow speech from any minor distance and in noisy situations. My left ear has tons of tinnitus, while my right ear is more stable. So, my question is: what should I expect? Like, I’ve done the prescribed cure for months with no effect (the same doctor took me off that and suggested a follow-up visit in Autumn), I keep myself healthy and on a low salt diet and stuff. Can cochlear hydrops affect someone like me who already had some kind of hearing loss? It was all stable for years and now every 2-3 weeks I see more difficulties. Does anyone else experiencied something similar?
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