Funny experience, post-op, sitting at home or at work with the worst case of tinnitus ever. It's not always like that, but when it's at full strength, it's pretty debilitating. I can usual switch off from it, but this is an order of magnitude worse than 'normal' (pre-implant) tinnitus.
Will anything change on activation day (6th January for me)? Or will the tinnitus stay this way? Could go either way. Oh, and the musical hallucinations have stayed. Or got worse.
Welcome
Thanks for joining me.
I am not sure where this journey is going to take me, but I've a sense from others that it isn't going to be an easy ride. There will be setbacks, periods of slow progress, maybe even lapses into depression, and moments (I hope) of reward and elation. I can't tell what, when, how quite yet.
I'm going to be writing quickly and when I can, so don't expect great prose!
I am not sure where this journey is going to take me, but I've a sense from others that it isn't going to be an easy ride. There will be setbacks, periods of slow progress, maybe even lapses into depression, and moments (I hope) of reward and elation. I can't tell what, when, how quite yet.
I'm going to be writing quickly and when I can, so don't expect great prose!
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