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
Interested in more discussions like this? Go to the Hearing Loss Support Group.
@joyces. One of your helpful posts on VRT...I'll send the second most recent one next. You are one busy lady! Thanks for everything you're doing! Nancy
@joyces I was so focused on clarifying, I forgot that I wanted to comment on your activities! You have an unbelievable story about you and what you are doing! I hope you can snag a reporter because it should be written up!
@joyces. Another recent post on VTR. Hope you won't have to rewrite them. Thanks for sharing your knowledge and experience with this! Nancy
Nancy (nla4625): Thanks for posting some of my previous posts! Saved me from thinking and rewriting. I've saved them to my health directory and will be able to simply copy them if needed in the future. Shoot...I even went back and corrected my misspelling in one! Editors should never create anything with a misspelled or misused word! Forty whacks with that limp noodle!
Barb B, in response to your VRT not assigning you balance exercises at home: Personally, I think some PT and VRT folks don't want to overburden anyone with difficult things. However, it's often necessary to do difficult things to improve. You might ask about simply standing on a 2" thick or thicker chunk of foam (like an old camp mat or a chunk bought at a fabric store, even a pillow filling) at home, when there's something solid on both sides of you in case you begin to wobble. Do it first eyes open, then eyes closed. That's a pretty safe exercise to do by yourself. Another is to walk with eyes closed in a hallway with nothing to trip you up (no throw rugs). They may be called "throw" rugs because they can throw you! A good practice is to walk in low light situations, inside at first where you have checked for anything that could trip you, then, after lots of practice, outside...if you live where there's not lots of ambient light. Here, in the spruce woods, the nearest street lights are a very long distance away, and there are no other houses to provide light, so I walk our rough gravel road or even over the very uneven "lawn" (not grass, just whatever is there to be mowed, with frequent gopher mounds). It's crazy that VRT people avoid having you do anything "too dangerous" at home...because your everyday movements are dangerous if your balance isn't good! I know that, after I went to the specialist and got some additional ideas of things to do, I quit nearly falling every time one of the pets suddenly walked behind me in the kitchen. Before working on balance, I had been coming close to falling multiple times every day, but, after working on balance, I'm much more stable and stepping back onto the cat's tail doesn't make me come close to falling. You can walk in the dark or with your eyes closed safely in a hallway...if you're really, really unstable you can lightly touch the wall on one side to orient yourself. Even with that, you're learning to rely on proprioception instead of vision.
@joyces I really appreciate all your detailed comments. I do plenty of difficult things when I'm with my VRT but that is only 2/week. The foam cushion exercise I do with my VRT but that I could do at home, in only 1 place which is in my kitchen, with a counter top on either side. Walking down the hallway with eyes closed without touching the wall is absolutely not possible at this point. Doing so while touching the wall, I don't know if I would feel safe enough at this time. I will see. You are certainly a reminder of what cats can do to you! LOL. Fortunately, the one cat I have now is pretty good at not challenging me! I do think of my feet a lot, following your long ago suggestion. However, when I do that, it tends to be about the foot in the shoe or boot and also about how the sock feels! (Don't know if that counts towards proprioception!) Your support is precious! Thank you.
Barb, try walking a few steps without shoes (so that your feet can feel the floor) in the hall, then see if you can do the same thing with your eyes closed. It's okay if you only take 2-3 steps to start, without shoes (easier than wearing shoes). Then see if you can walk a couple more steps with your eyes closed. Always do it with your eyes open first, because that will give you confidence that it's not a great distance, that you CAN do it. Even standing on foam with something beside you, like the two counters in your kitchen, will help you learn to use proprioception. Isn't that a godawful word??? Hard to say, hard to spell, but magic when you learn to use it!
Joyces and Barbb..... Thank you for your ongoing discussion of balance issues. I am still looking for a VRT. Most seem to focus on the increased strength as in the exercises you do at home Barb. I think I need to take another look and see if they do the balance exercises in the office. My balance sees to get worse every day and with that the nausea also increases. I don't eat much since food has no appeal and have lost 35 lbs in the last two years. Also have an autoimmune disease, Takahusus Arteritis. Treatment for that caused a NTM lung infection. Antibiotics for the lung infection caused the hearing loss and the balance and dizziness issues. Had to give up the antibiotics, was stable for 3 years but now the lung disease is suddenly getting worse. I have to decide if I want to do antibiotics again. I am completely dea f now so antibiotics can't affect hearing. But they can cause balance to get even worse and loss of color vision. It's a real merry-go-round and I feel like I am losing bits of myself every day. Very depressing.
That was just some background. I do some of the Vestibular Rehab exercises every day but have seen no change yet. I looked online for different exercises but all that came up was referrals to physical therapists. Does anyone know if there is a book that spells out different exercises for vesticular rehab or proprioception? Joyce, you should write one! If anyone has any ideas for me, I'd appreciate it. Thanks....Judy
@judyca7 I empathize with your balance issues, though I've been fortunate to not experience them in spite of having bilateral progressive sensorineural hearing loss. Through involvement in HLAA I have met many who have struggled with Meniere's Disease along with hearing loss. Change in diet has helped some people, mostly related to sodium or sugar. It is not consistent among those with the problem. Thank you to Barbb and Joyces for their insight into this issue. NOTE: One of my friends with MD and resulting hearing loss has had great success with a cochlear implant.
It seems like the posts re balance, training, vertigo and VRT would be more helpful under another a Subject titled Balance not Single Sided Deafness. If people are looking for balance related problems they’re not likely to look here.