Loss of hearing clarity: Solutions or strategies anyone?
I have in the last couple of years lost hearing clarity. Apparently, somewhere between my auditory nerves and my brain, there is something like a disconnect. The decibels at which I hear has not changed. This clarity loss can be age-related, and I have read that it can also possibly be related to having had cirrhosis, or to taking immunosuppressants - that all seems pretty unclear though. I have been wearing hearing aids since around 2004.
Has anyone else had this type of problem and if so how do you compensate for it? I get emails from CHC -- Center for Hearing and Communications which is NYC and Florida and a book was mentioned recently that can be purchased on Amazon, "Smart Hearing: Strategies, Skills, and Resources for Living Better with Hearing Loss" by Katherine Bouton. I am thinking about purchasing it but wondered if any others have this problem too. I have Oticon Opn1 hearing aids and purchased the "Connect Clip" which helps in some situations.
Thanks for any responses.
JK
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@bookysue
Hi,
Absolutely right...wearing 2 aids is safer...sort of like surround sound for us and may help somewhat in determining the source of sound. However, when the noise is overwhelming, I need to mute or take out the left (bad) ear for comfort.
Regards from FL Mary
@judysmayo
Hi,
I have 2 aids and can get by fine with using just one in my good ear. However, wearing 2 does not help too much in determining the source of the sound. I hear it but not always sure where it is coming from. This is true mainly outdoors. You get use to familiar daily sounds but an unexpected noise can leave you guessing... not only where it is coming from but what the heck is it. My loss is profound and I have been a hearing aid user for 40 years. Like you, I rely on visual cues...it’s second nature to most of us. We’re always watching and on the alert which is why we’re so tired at the end of the day.
I can understand why single sided deafness can be a challenge. Any amplification in that ear however small would be a blessing. Others here will know more about qualifying for a CI or how the BiCros hearing aid works and if there are other options to explore for you.
Regards from FL Mary
@imallers I found that when I use my super dryer for my h.aids I can turn my T.V.down .
I wish I could take out a aid- my level of loss and quality of aids- I would lose ability to converse. I am doing less dinner outings because of this. I lost friends because of my inability - people have less patience nowadays . It’s ok books and critters are better company.
My advocacy will continue. Part of that is making sure Penn care gets praise when deserved . I had 3 tests done yesterday ( one was moved from today - same floor ) and these folks went out of their way- hearing wise and moving appts to make things easier. I joked with them on Ct scan machine not having a male voice . I thanked them and make sure management knows. It is critically important to praise as well to say something when things are off.
@lioness
The old moisture problem. My aids are in a Dry and Store nightly. This is the time of the year the humidity soars in Florida and sweaty ears lead to distorted hearing. When I am out for the day I throw a hearing aid blower in my bag. It’s a small bulb like thing. I have to twist off the tube and just blow the dry air through it a few times. You don’t want the moisture to blow back up into the aid so twisting off the tubing is a must. Moisture collects in BTEs. I re tube my own aids so I am use to doing stuff like this. I’ve tried low moisture tubing but don’t see the difference. Did you ever notice how much better you hear in cooler weather...or even cold weather? Although I have been in freezing weather when on vacation and, if out too long, that extreme cold affects the sound quality at times. But then my eyeballs are freezing too. I dunno.
My tv volume tends to be low. I guess it’s because the distance from me to the tv is not that far or maybe it’s just a good tv volume wise. Sounds loud enough for me. Other people have to turn it up.
Regards from hot hot hot ....and it’s just the start....FL
@imallers Your funny Mary eyeball freezing Mine would do that in Pa in winter .I just never new how great drying them out made a difference but it does we have the opposite here low humidity.I have 2humidifier s I use when it's dry 5-10 here Tomorrow I have to go to audiologist to have them cleaned and check my One ear plug? I need a new one.I've never took the tube of but then no humidity to speak of In 70,s this week but in 80,s end of week I feel for you but don't want to come over hate that weather now that I'm use to it here stay cool 😎
"Disco" damage? 😊 I have also thought my inability to hear clearly was due to the loud music at the discotechs (standing by the humongous speakers) because there was no other spaces available. "If that's what you mean by,"disco";or was it a corrector type error and you meant to write,"Disc".? 😁 But yet,my loss of clarity didn't start back in the 70's,but in late 80;s when I was in my 20's and I'm 60 yrs old now. So I don't believe my hearing impairment comes from aging.. And to boot,one audiologist told me,back in 1994,that there will never be a listening device that provides clarity. ...As if she were in disbelief that the sounds I hear are garbled and seems as if everyone were mumbling...on purpose! Ah,what the hey;I suppose I liked your post and wanted to share a bit of my history as well. Thanks for reading. My name is Irene.
Hi Irene. It sounds as if we have had similar experiences with progressive hearing loss. Diagnosed as a 21 year old college student, I was told by some of the best medical experts in the field that I would be 'deaf' by age 40. They could give me no reason for this happening to me. Today, after doing a lot of personal research on hearing loss, and meeting so many others like me through HLAA, I'm quite certain I had a genetic predisposition to sensorineural hearing loss, and that noise I was exposed to exacerbated it. I was told that there would be nothing available in my lifetime that would change that, and that hearing aids would not help me. That diagnosis was in 1962. Because my loss was mild at that time I didn't take it too seriously. It progressed significantly over the next 10 years.
Because I had been given no hope for anything to improve, I resisted getting help. It cost me my career, and turned an outgoing person into a semi recluse. Thankfully, I had supportive family. A turning point happened when a regional university communication disorders department gave me the opportunity to be retested. I was fitted with hearing aids that helped somewhat in quiet settings. A second turning point was when I learned about HLAA and became involved. Meeting other people who were going through this same thing let me know I was not alone. That truly gave me my life back, as I watched how people were able to cope with hearing loss by using technology and by truly understanding what was going on. I might add, that that add on technology can make a huge difference for most of us in many situations. Try it if you can
Today, I have a cochlear implant, which I use with a hearing aid. It has done wonders for me. I only wish I might have had the CI opportunity earlier. In my 40s, I returned to school for a graduate degree. In my 50s, I resumed my career, and worked past retirement age. I doubt I'd have had these successes without the support and education that HLAA made available to me.
Prior to the 80s, very little research was done on hearing loss, especially on the potential for cures and solutions. It was more about 'what should we do with these deaf people?', and deaf and hard of hearing people were all lumped together in research. Today there is a great deal of research being done, and the word 'cure' is mentioned in much of it.
Our experience is similar. Noise was a big piece of my life before anyone knew that noise damaged hearing. No ear plugs then. Sensorineural hearing loss leads us to believe that we have 'nerve damage'. Cochlear implants work because they bypass the inner ear where the damage really occurs, and stimulate the auditory nerve, which is just waiting to stimulated so it can send sound to the brain. It's pretty amazing stuff.
I hope you find the support you are looking for. Living WELL with hearing loss is possible. You just need to find the coping mechanisms that work best for you, along with the technology that makes a difference.
Keep us posted on your experiences.
Recently, I found sites on line for student audiologists to practice on. They have tones at the different test frequencies used by audiologists. Wearing my hearing aids, I set the computer volume at what seems to be a normal and comfortable level for the 2000 frequency (test middle value) then I compare either side (1000 and 3000) to the volume level of the 2000 and record whether it seems louder of softer of about the same. ...
Stephen, what is the online site you've used?
My spouse has the same problem. I am seeking answers for improved quality of life