Single Sided Hearing Loss
I'm amazed how many posts there have been lately about single sided hearing loss and think having our own thread might be beneficial. I'm missing something really important about this issue and hope someone will please help me understand it. I used to explain my hearing issue to people who asked as follows: when you have two good ears, sound comes in from both sides and your brain can select what it wants to "hear". When you have only one good ear, sound comes in on one side and your brain can't separate out what it wants to "hear." It's all noise. Is that right or am I totally wrong? If it is right and I get the cros hearing aid, how will moving sound from my deaf ear over to my good ear make any difference in my ability to hear? Sound is still going in one side and will still be noise. I understand that if I need the bicros hearing aid, it will pick up the sound from my deaf ear, move it to my good ear and enhance the ability to hear in my good ear. This is really complex. I'm rooting for the new technology in the article Ken sent out about growing new tiny hairs in the ears of hard of hearing people to help them hear more clearly. Thanks for helping me understand this. Nancy
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Once they release the AI for language translation, I will be first in line. I use my iPhone now which really helps.
I refer you to Linkedin.com.
Thank you, Barbb. I am only trying to help and you my knowledge to find answers if I have access to them. It is appreciated! Gina
@dwi Starkey's new Livio AI hearing aid translates 27 languages in real-time and also doubles as a hands-free earpiece. Today, Starkey Hearing Technologies unveiled an AI-powered hearing aid that fits snugly into your ear, automatically translates foreign languages, and tracks both your physical and mental health. Aug 27, 2018
Amazing what technology can do today. Next thing we know they'll be called 'big brother'.
How profound a loss does it work with
My ENT is a surgeon and runs the CI program at a major hospital. He wouldn’t recommend my participating in the CI evaluation because my word recognition is above 50%.
@joyces Hi Joyce, I've been meaning to write you ever since you described in long, wonderful detail all that you went through to master your balance issues. First I should say, I have you to thank for getting myself to VRT. After reading what you had to say, I called my internist and asked her to write me a prescription and then I found a VRT - so I consider myself not really doctor-referred to VRT but self referred - or I could say, "Joyce-referred"! (:-) )! So my note here is a response to that and my own experience with doing VRT, which is notably different from yours. I have been going, on average 2/week for my VRT! I have been religious about doing the exercises my VRT has prescribed which are geared to developing muscles in the hip area (and perhaps more, I'm not sure). So I do clamshells, hydrants, leg lifts for 1/2 hour every day. The kind of exercises you mention I do with my VRT. They are very challenging for me. My head gets tired - and maybe a little dizzy doing them. (I hope that makes some sense to you.) After weeks of seemingly no progress, I asked my VRT about his expectations. Bottom line: (if I understood correctly, he doesn't expect noticeable improvement but rather sees the exercises as preventative of further balance issues! At this point I have had 60 sessions with him and until last week, I was aware of no sign of improvement at all when walking about town (big city). Also, when I asked him about what could be the cause of my very bad balance, in addition to a damaged balance nerve because of benign tumor removal from acoustic nerve, he simply said he couldn't know because there are so many possibilities. As for one day last week when I seemingly, suddenly, had a significantly improved experience, I am wondering whether that was a onetime thing or whether, after so much time has elapsed, there actually is improvement! The winter snow storm has made it difficult to test that out and I had to cancel my VRT app'ts since I cannot risk a fall. I wanted to believe your insistence that exercises will make a difference but until last week, had come to think that progress partially depends on the nature of the cause of the balance problem and thus your optimism could not be valid for all but now, after the one good experience, I'm in a wait and see mode, to see if what I experienced last week was not a fluke!
I ain't no doc or expert, but it doesn't sound as though you're learning to use your third balance system (proprioception), which is what makes all the difference. Ever since the forest fire here, I've occasionally gotten so busy providing meals for those who lost everything and are working on clearing their lots so they can move back onto their own land, that I slack off on exercises...and really pay for it! Cooking for dozens of people, sometimes over a hundred, is all new, and it's made more "interesting" because the so-called mobile kitchen has no electricity or water and is seven miles from my house, which has a totally inadequate little kitchen for this kind of serious cooking. At any rate, the exercises you specifically mentioned, like leg lifts, are not really for balance, so I'm concerned that you're not being shown how to do exercises to increase your ability to balance...without using your eyes at all.
@barbb Perhaps I did not make not make myself clear enough. When I see the VRT 2/week I do nothing that relates to muscle strength, as I do at home. I am guessing that the reason why I am not doing "balance exercises" at home is because my balance is bad enough to make it unsafe for me to do it without any protection of somebody being available to "catch me" if I should fall or start to fall. When I do the balance exercises with the VRT he is always standing close or walking close to me to catch me as I do them. However, our dialogue about this is helpful because I will seek clarity with the VRT when I see him next about doing balance exercises at home.