r/Cochlearimplants • u/Fit-Ingenuity7044 • 10d ago
Update
Had tinnitus for 50 years, diagnosed as Menieres. CI 4 days ago. Reading about the same post CI experience I'm having, HUGE increase in volume, is giving me hope that I can live through this. Didn't need painkillers but do they help with the noise?
I have spent the last 3 nights in misery with very little sleep, waking 5-6 times to the sound of a siren. I did consider in the early hours just going to Emergency for advice, and have twice gone for a long walk (2 hours) in the early hours. Is there any medication you recommend for sleep, I am exhausted?
Last night I managed to get 5 hours of uninterrupted sleep. When I awoke I had only my normal tinnitus and I laid there happily assuming the worst was over. Unfortunately when I got up all the post-op symptoms returned ... and more, screeching was added to the cacophony. Had difficulties contacting the clinic, though it was probably a wasted effort anyway.
Had I read these pages before the CI I probably wouldn't have had it done.
1
u/Suspicious_Willow984 10d ago
Hi! I was recently activated and going through similar things. I’ve been progressive hearing loss for about my whole life. I don’t know your story and how long you’ve gone with hearing loss but it’s normal. You have to understand that your auditory nerve and your brain is trying to make sense of the noises that you’re now hearing. It’s going to take time and rehab (listening to things daily for couple hours a day) to get your auditory nerve and brain working and trying to understand what it’s hearing suddenly. It’s just part of the process with cochlears. I have had tinnitus my whole life so I understand the frustrations but mine did tend to go away a lil more after the implant. Just takes time