Archive for December, 2008

December 31, 2008: 1:36 pm: Dr. NeilAssistive Devices, Coping Strategies

by Neil Bauman, Ph.D.

A man wrote:

I thought there was a cordless phone out there that could do all the things that a regular phone could do, but could also amplify my voice as well as the voice of the person I am talking to?

I’m not aware of any voice amplified cordless (or cell) phone currently available. There are special desktop phones that give up to 26 dB of outgoing voice amplification if needed.

These phones are for people who have had throat operations, damaged vocal cords, or otherwise have exceptionally weak voices.

If you are also hard of hearing, you can get a phone that also has up to 35 dB of incoming amplification. That way you can hear the person at the other end, and they will be able to hear you.

There are also special portable devices that will amplify a person’s voice. Again, these are for people with exceptionally weak voices, or those with damaged vocal cords. The extra 12 or 15 dB these devices produce makes it possible for those around them with normal hearing to hear them.

If you are interested in a portable voice amplifier, or voice amplified phone, email me at neil@hearinglosshelp.com and I’ll help you find the best device for your needs.

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December 28, 2008: 1:34 pm: Dr. NeilOtotoxic Drugs, Tinnitus

by Neil Bauman, Ph.D.

A man wrote:

I have a question regarding alcohol. I recently visited an audiologist about my tinnitus after it got worse from a clubbing experience (first time it happened due to a club). I wore ear plugs and figured I’d be safe. She seemed convinced it was due the copious amounts of alcohol I consumed. She said that alcohol is very bad for my ears and that I should limit my drinks.

Like an idiot, I ignored her advice the next week and my tinnitus did get worse despite wearing some new, more powerful ear plugs (32 db of protection)! According to her, it was the combination of loud music + daily, noisy city life + alcohol that did it.

However, after reading your web log link to the Norway study of pre-school teachers having hearing damage from loud kids, I figured that may be why. I’m a newly-minted elementary teacher. I was hired to focus on the conversation aspect of English education here, so day in and out it’s 30 kids speaking loudly and screaming for at least 3+ hours a day. So now I’m wearing 10 dB ear protection!

Nevertheless, I wonder if the audiologist was still right. I’m gonna lay off the drinks anyway. I would like to know if alcohol can lower the threshold for hearing damage or lead to permanent damage. Is the fact that I’m drinking in a club that much more dangerous and could possibly lead to more tinnitus?

Just so you know, alcohol alone can cause tinnitus. Noise alone can cause tinnitus. So can many other factors. You were wise in wearing ear protection. However, I don’t know the sound levels in the clubs you visited. Ear protectors can only help about 30 dB or so. After that, the sound travels through your skull via bone conduction and assaults your inner ears in spite of any ear protection you may be wearing.

Thus for example, if the sound level in the club was way up there at 120 dB. Your inner ears were still being exposed to around 90 dB of sound. In this case the ear protectors were bringing it down 30 dB, but 90 dB is still too loud and can cause damage given enough time.

You would not expect 90 dB to cause much damage in just one long evening at a club. However, there were other less known factors coming into play too. For example, I’m assuming that the club was also filled with smoke, right? Breathing in that second hand smoke (or first hand if you were smoking too) exposes you to significant amounts of nicotine.

One of nicotine’s nefarious characteristics is that it works together with loud noise in a synergistic fashion to cause more damage to your ears than you would expect from noise alone or nicotine alone. Thus, even with wearing ear protectors, the presence of smoke could make your ears more sensitive to noise damage at the reduced level of noise that you thought wouldn’t damage your ears.

Carbon monoxide has the same nefarious characteristic, and in smoke filled rooms, there is more carbon monoxide than normal too.

In addition, for example, maybe you get headaches from all the noise at the club so you take a couple of aspirin. Guess what? Aspirin lowers the noise tolerance that your ears can stand before damage, just like nicotine and carbon monoxide do.

Thus you have the effects of alcohol, noise, nicotine and carbon monoxide, and maybe some pain killers—each of them ototoxic in their own right and causing damage to your ears. Then you have the synergistic effects of noise and nicotine and the synergistic effects of noise and carbon monoxide, etc. That is just some of the things your ears are dealing with in the clubs. All these little things can add up to cause big problems for your ears.

On top of that you have all the noise and exposure to drugs and chemicals that also can damage your ears in your day to day living apart from clubs. And on top of that still is all the noise you are exposed to as a pre-school teacher. (Can’t you get the kids to pipe down? It shouldn’t be that noisy or the kids are going to have hearing problems too!)

So putting it all together, I’m not surprised that your ears have taken a beating. If you value your health and your ears, you’ll cut way down on your alcohol consumption and noisy clubbing too.

If you are interested in learning more about what you can do to help bring your tinnitus under your control, you would do well to read my book, “When Your Ears Ring! Cope With Your Tinnitus—Here’s How“.

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December 25, 2008: 1:32 pm: Dr. NeilAssistive Devices, Loop Systems

by Neil Bauman, Ph.D.

A man wrote:

With a room loop system, will I be able to understand people in the same room at the same time if I’m listening to the TV through my hearing aids telecoils?

The short answer is, “That depends”

There are two ways you can accomplish this if you so desire. One way is to have one of the memories in your hearing aids programmed to have both the microphone and t-coil on at the same time. When you want to hear both the TV and people talking in the room, simply switch to that memory.

Another way to accomplish the same thing, but leaving your hearing aids programmed to t-coil mode only is to plug in an external microphone to the microphone jack on the back of the Univox loop amplifier. Now you will hear the TV (via its audio outs and patch cord to the Univox loop amplifier the same as before, and you will hear anything that comes through that external microphone (people’s voices) as well. For best results, place the microphone close to the people talking so the TV’s sound track does not drown them out.

Personally, I’d never do either. I have so much trouble hearing that I want only one source of sound at a time. Trying to hear a person talking over the TV programming is just an exercise in futility (and vice versa). I wouldn’t be able to understand much either way.

My preference is to use the t-coil setting and listen exclusively to the TV. When people talk, I’d switch to the hearing aid’s microphones, and mute the TV so it wouldn’t interfere with my hearing their voices. (Of course, I’d also have the closed captions on—so everyone could still read what the TV is saying.)

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December 22, 2008: 1:28 pm: Dr. NeilBalance Problems

by Neil Bauman, Ph.D., with Tony

In 2005, Tony had surgery to remove a large (4.5 cm) acoustic neuroma (non-malignant tumor) growing on his left auditory nerve. In the course of removing the acoustic neuroma, the surgeon, not only had to cut the auditory nerve leaving him totally deaf in his left ear, but also sever the vestibular nerve, thus totally destroying the balance system on his left side. The result of this surgery left Tony wheelchair-bound. However, he didn’t stay there. With vestibular therapy and much hard work, Tony now can lug his golf bag around the course as he plays 36 holes of golf. Here is his story.

______________________

Three years ago I lost a balance nerve to surgery and was left in a wheelchair. I could not walk unassisted, and had to relearn how to balance myself again. This was a long process. However, given the benefits and independence I now have, it certainly was worth it!

After the surgery, my first experience with poor balance occurred when I fell out of my hospital bed—face down onto the floor with some force. Ouch! You see, the surgery had cost me my left side balance, and I didn’t realize just how “shot” my balance system was.

As the days went by, I became increasingly aware that my lack of balance was affecting me in many other ways. For example, I fell numerous times. (In self-defense, I kept an eye out for somewhere soft to land if possible. I needed an area where a fall was not going to hurt me.) I collided with people and objects. I was clumsy. I often dropped things. I found it was a good idea to stay away from work on ladders!

Furthermore, I had trouble coordinating my left and right hands. This was brought home to me 8 weeks later when I was trimming the hedge and nearly lost a finger to the electric cutters!

Each day as the hours went by, I became more and more tired. The result was that my coordination became progressively worse to the point where I was not able to move around safely.

Consciously keeping my balance proved to be exhausting. I experienced profound fatigue when engaged in almost any task, whether physical or mental. My lack of balance affected my speech too. The wrong words came out, or I mispronounced words.

My short-term memory dropped dramatically. You see, the effort involved in consciously maintaining balance like I now had to do affected my short-term memory. As a result, in addition to my speech problems, I easily forgot simple things, and was forever losing things.

For several months after my surgery, I needed a midday nap. Unfortunately, napping messed up my night-time sleep patterns, and I would be awake in the early morning hours. The result was that I invariably awoke exhausted before the day had even started! All these balance-related problems reduced my self-confidence. I became both frustrated and depressed.

While I was still in the hospital rehabilitation unit, I was determined to get well. I requested assistance in using the gymnasium, but was told no one was available to help me. Next day, while still in my wheelchair, I broke into the gym and began using the equipment by myself. They were not too impressed with my actions (I was spotted on the security cameras), but I made my point. The following day suddenly staff were available to assist me. I made rapid progress. My stay was just 32 days, not the expected average of 82 days.

To get my balance back I needed to exercise. To some degree it almost doesn’t matter what the exercise will be. The real key is to do something that you really enjoy and be able to stick at over a long period of time. For me that was playing golf!

Hospital rehabilitation got me walking again, but my first golf experience showed me just how weak and frail I had become. For example, when playing my first golf game (four months post operation), I could only manage four holes before becoming completely exhausted.

Therefore, I set out on a course to rebuild both my balance and my stamina. Fortunately I was (and still am) a keen golfer, so I did not consider time devoted to playing golf as a big issue.

Golf involves a combination of balance, movement, and eye/hand coordination. In this respect, golfing was an ideal therapy for me. Throughout all the days, whether sunny or rainy, I don’t ever recall thinking “this is a chore”. Rather, my feelings were, “I am getting better” (both my balance and my golf game)!

Throughout all this rehabilitation I felt so tired—close to complete collapse was more like it. However, I discovered that if I simply stopped, sat down somewhere quiet, and shut my eyes for 10 or 15 minutes, something quite miraculous happened. These short breaks were equivalent to about four hours sleep in terms of my body’s recovery. They had the added advantage that they did not disrupt my night-time sleep patterns.

I really pushed myself. However, there is a fine line between pushing yourself and overdoing it. When I really did overdo things, my coordination became increasingly erratic. At this point, drills, power tools and hammers were simply too dangerous for me to use—best kept safe for another day.

Over time, my strength and stamina slowly returned. I was now able to take on increasingly longer and more demanding exercises. My average golf practice now consisted of 140-160 long-range shots, considerably more than in a full game of golf.

As my balance improved, I also noticed that my thinking and coordination improved as well. I could now get through a day without a nap.

Just how much I have improved really came home to me when I moved 300 sidewalk slabs (over three and a half tons) from the front of my house to the back garden. It took me four hours. Yes, I was smashed afterwards, and hurt just about everywhere, but I did it!

My balance will never be perfect. My new balance system requires a visual point of reference. In other words, if it is completely dark, even simple movements are difficult. Thus, in the dark I find it wise to carry a flashlight. At home, I use low-wattage nightlights in the hall. This makes a big difference when I am moving around in the early hours.

When walking up and down stairs I usually extend both elbows out as additional stabilizers. I’d rather have a bruised elbow than a bruised head! Uneven ground almost always presents a challenge for me. I’ve found it best not to try and carry stuff in such circumstances.

I am not anti-alcohol, but my new balance system does not cope as well with the effects of alcohol as my old one did. My tolerance to alcohol is now reduced. These days I only drink at home when there is no possibility of any further travel or driving that day.

Because my brain is more occupied with keeping me balanced than in remembering things, I’ve found that it is worthwhile for me to take notes during meetings and to create to-do lists rather than relying on my now faulty memory.

Without a doubt, regaining my independence definitely helped my feelings of self-esteem and self-confidence. I can now work a 12 hour day with a two-hour journey at each end. Equally, I now understand and value rest when I can take it. All of this was possible only because I took the rebuilding of my balance and my health to be a fundamental and key issue in my life. Now, I am no longer confined to a wheelchair, or to walking with a cane. Finally, and to the disgust of my golfing friends, I can now beat them at their own game! This I call “success!

______________________

To learn more about your balance system, how all the various parts work together and what happens when it gets damaged, read “Protect Your Balance System—or Else“. If your balance system has been damaged, take courage and follow Tony’s example. Never give up. Rebuild your balance system as much as is humanly possible. When you do that, you too will find your level of success!

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December 19, 2008: 1:27 pm: Dr. NeilAssistive Devices, Coping Strategies

by Neil Bauman, Ph.D.

A lady asked:

I am looking for a (small portable) device that would provide feedback when I sing to let me know if my voice is actually matching the note on the piano or the note sung by another singer. I know that there are computer programs to teach voice and pitch matching but I am more interested in something portable that I can put on my piano and carry around with me when I sing in a choir or solo to piano accompaniment. Does such a thing exist, and if so, can you point me in the right direction?

Yes, such a gizmo does exist to help you sing on pitch. The good news is that it is both portable and relatively inexpensive. The device you want is the MetroTune (MT9000). It only costs $34.95.

One source for the MetroTune is www.SingerCity.com. Click on the “Search” button across the top, then put “sabine-mt9000″ in the search box and you’ll find it, or better yet, just click on this link. Check out its specifications and see whether it is just the gizmo you are looking for.

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December 16, 2008: 1:24 pm: Dr. NeilOtotoxic Drugs

by Neil Bauman, Ph.D.

A man wrote:

I stumbled onto your web site while researching a very bizarre phenomenon that is affecting me right now. I am 56 years old with normal hearing except for perhaps a little age related high frequency loss (more so in my left ear.)

Recently my ophthalmologist wrote me a prescription for Lotemax; an eye drop that contains a steroid. I began using the drops that night and by the next day noticed pressure in my ears and very strange sensation of “distorted” sound; not from a person speaking directly at me but from reproduced sources, such as radio, TV, music, paging systems, and from overheard human voices, i.e. voices coming from another room or different part of the office at work.

The sound “wobbles” but not quite like the old “talking through a pipe” scenario in the old days of land line phones. It’s more like the pitch of the sound or music itself changes and moves. I looked on-line for side effects related to the drugs and nothing matched up. The pharmacy had no ideas either.

Typically, little is mentioned about ototoxicity, especially with the more “obscure” drugs such as Lotemax.

My drug reference books don’t list any ototoxic side effects for Lotemax either, but that doesn’t mean this drug isn’t ototoxic. For example, a bit of research turned up one lady that experienced an ear “disorder” whatever she meant by that after taking Lotemax. I also found tinnitus listed as a side effect of taking Lotemax. Therefore, even though it isn’t reported in the medical literature, it seems whatever is in Lotemax can affect the ears of some people.

The active ingredient in Lotemax is Loteprednol, and I can’t find any “official” source of ototoxic side effects for it. However, one of the “inactive” ingredients, Benzalkonium, can be ototoxic.

Thus, based on the above, it could well be that Lotemax is indeed “messing up” your ears as you describe it. Hopefully, your ears will return to normal when you stop taking the drug. However, there is not enough information available to know whether the side effects may be temporary or permanent.

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December 13, 2008: 1:22 pm: Dr. NeilWorkplace Issues

by Neil Bauman, Ph.D.

A hard of hearing man explained:

I have a Bachelor of Commerce degree and want to work as an accountant. However, no one will hire me as an accountant because of my hearing loss. What jobs are good for hard of hearing people to do? What do I need to do to get hired?

First, my advice is to do what you love doing in spite of your hearing loss. And if that is accounting, then go after such jobs.

You ask an excellent question, “What do I need to do to get hired since I have a hearing loss.

First, put the hearing loss issue aside for the moment. In order to get a job, you need to be the best applicant. That’s it. You get the job because you are the most qualified and have the best “fit” for the position in the company.

Therefore, although you are hard of hearing, you need to do what every other prospective employee does—get the best training, etc. you can, then apply for positions for which you are best fitted.

Second, doing the above may not be enough because your prospective boss may have reservations about hiring you since you have a hearing loss. He’s thinking of the problems your hearing loss may cause and the extra dollars it will cost him to accommodate your needs. In his mind this is a black mark against hiring you.

Therefore, what you need to do is be proactive and demonstrate to him that your hearing loss isn’t an issue because you have already worked out solutions to potential problems. Effectively, you have erased the black mark before it was even made. Now you can compete on a level playing field.

Breaking this down further, when it comes right down to it, you don’t need good hearing in order to put numbers on a piece of paper or computer—you just need training and brains, but you do need “hearing” to be an effective cog in the corporate “machine”. Therefore, think about all the places where you need “hearing”—and then think of ways you can communicate in spite of your poor hearing. Maybe it’s using amplified phones, or using email instead of phoning. If you can’t hear the boss—maybe have him email or IM you instead. In meetings know what assistive devices will help you, that kind of thing.

When a potential employer sees that you have answers already worked out to all the potential problems, and that it won’t cost him an arm and a leg, then he is going to be more inclined to give you the job (if you are the best qualified) as he sees that you are a go getter—you have already planned out how to succeed. (He figures if you are that proactive in one area, you will do the same for him with the job and that counts for some more “brownie points”.)

Employers want to know up front what it is going to “cost” them to hire you. If you show them that the benefits of hiring you outweigh the “costs”, then they are going to be happy to hire you. However, if they see your hearing loss as a “cost” with no compensating benefits, you don’t get the job.

Even little things such as “I’m not easily distracted from my work because I don’t hear all the distracting sounds and people talking around me so I’ll be more productive than hearing people.” or, “I won’t be wasting time standing around the water cooler talking with other employees since I can’t hear them. I’ll be busy working for you instead.” are benefits to the employer.

When an employer sees that your communications plan actually works (because you have successfully demonstrated that in the interview), your hearing loss ceases to be an issue. You are now well on your way to landing your dream position.

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December 10, 2008: 1:19 pm: Dr. NeilOtotoxic Drugs

by Neil Bauman, Ph.D.

A man asked:

Earlier this year I was diagnosed with reverse slope hearing loss in my right ear. I noticed the loss one day when I could barely hear the person speaking to me on the phone. I could hear with my left ear but not my right.

A hearing test revealed essentially normal hearing in my left ear. My right ear results revealed a moderately-severe to mild hearing loss up to 1000 Hz rising to normal levels beyond 1000 Hz. The loss appears to be sensorineural in nature in the right ear.

Twice in the last few months it appeared that my hearing was getting better. In the last three weeks I have stopped taking Advil and drinking coffee. Now it appears my hearing is back! I just went for a hearing test today and voila, my hearing loss has disappeared! My hearing in both my right ear and left are normal. I have continued to avoid Advil which appears to be responsible for the hearing loss I had experienced in my right ear. Can it be that Advil caused the problem and now I am cured?

You are correct. Sometimes all it takes is to stop taking an ototoxic medication and your ears return to normal. Ibuprofen (Advil) is one such drug. In some people, Ibuprofen can cause temporary hearing loss and other ear problems that return to normal when they stop taking this drug. You appear to be one of them. However, don’t bet the farm that the ototoxic side effects will always be temporary. I have heard from people who took Ibuprofen and have had tinnitus ever since as a result. Thus you still want to be careful with this drug.

In addition to hearing loss Ibuprofen (Advil) can cause tinnitus, dizziness, nystagmus and vertigo. A lot of people don’t realize that Ibuprofen is quite so ototoxic.

Note that as in your case, drug-induced hearing losses sometimes are asymmetrical, i.e. they only affect one ear, rather than both ears as is more common.

Ibuprofen may also affect people with cochlear implants. Recently a man explained, “I’ve had recurring back problems and take NSAIDS [including Ibuprofen] to get it under control. I’ve noticed from time to time that the sound from my cochlear implant seems a little fuzzy or muddy and now realize that it may be during the times when I’m taking those drugs that it happens.” A lady with a cochlear implant also commented, “I have been taking Advil [Ibuprofen] for the past ten days. In that time I have not been able to understand on the phone as well as I usually do. It might be the Advil.” Four days after completing her 10-day course of Advil, this lady exclaimed, “Today I can hear fine on the phone again! I never associated my hearing loss with taking Advil.”

Thus, if you have a cochlear implant and are taking Ibuprofen (or other non-steroidal anti-inflammatory drugs [NSAIDs]) and your hearing seems worse or “fuzzy”, it could be the drugs that are causing this. If anyone else with a cochlear implant has had similar experiences, I’d love to hear from you.

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December 7, 2008: 1:17 pm: Dr. NeilCell Phones

by Neil Bauman, Ph.D.

Until now, captioned telephone service has been restricted to landline phones (CapTel), or to phones (landline or cell) used in conjunction with a computer (WebCapTel). Now, if you have Apple’s iPhone (cell phone) with 3G service, you can have CapTel captioned conversations where ever you are by just using your cell phone.

If you don’t have Apple’s iPhone with 3G service, you can use any cell phone for the speaking part, but you’ll need another web device in order to read the captions. This could be any portable computer with web access, one of the following smartphones—Apple iPhone, Motorola Q9C, HTC Mogul or the Treo800w or a mobile device that uses Windows Mobile 6 or Apple Mobile Safari.

Once this service becomes widely available on most cell phones, hard of hearing people will be able to “hear” on their cell phones, just like people with normal hearing. But for now, the Apple iPhone with 3G service is a viable option, and points the way to what will hopefully become commonplace in the future.

You can read about it in the CapTel News from Ultratec—Fall 2008 edition.

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December 4, 2008: 1:12 pm: Dr. NeilCoping Strategies, Hearing Aids

by Neil Bauman, Ph.D.

A concerned (and frustrated) daughter wrote

I’m hoping that you can help me. My mother is 63 and has significant hearing loss which was diagnosed about 20 years ago. She bought hearing aids about 2 years ago and has never, ever used them.

She is not in denial about her hearing loss. Her excuse is simply, ‘If I wear my hearing aids, I’ll hear all of the things that I don’t normally hear and it will drive me crazy.’ The worst part is that when my mother doesn’t hear everything someone says she will simply fill in her own blanks—which creates arguments and disagreements amongst her family and friends. She will always interpret what she missed in the most negative way, and then gets her feelings hurt over something no one said to her. This is unbelievably frustrating. I am tired of repeating myself and talking too loud, and also being the arbitrator in arguments that I know stem 99% of the time because my mother didn’t hear what she thought she heard.

How can I convince her that hearing the good things in life is far more important that being bothered by occasional noise?

Some people just aren’t ready to wear hearing aids when someone pressures them to get them. Actually, this happens a lot! The time to get hearing aids is when you are ready to wear them, not when someone says you need them. (Yes, the person does need them—but it is just wasted money if they then never wear them.)

Your mother has a valid point when she says, “If I wear the hearing aids, I will be able to hear all of the things that I don’t normally hear and it will drive me crazy.”

Your mom hasn’t heard many of these background sounds for a number of years, and thus hearing them all at once is nerve-wracking to say the least.

The solution to this is that your mom has to slowly learn to wear her hearing aids—first in quiet surroundings so there are no other noises to blast her ears. In such quiet surroundings, she should converse with one person. When she is comfortable doing that, then she can slowly graduate to noisier places and do the same. Over time her brain will adjust to the extra noise, but this takes up to 3 months—so don’t hurry the process.

Like your mom, I don’t hear everything someone says—whether I wear my hearing aids or not. You see, hearing aids aren’t perfect. Thus, if your expectation is that she will hear everything, you and she will be sadly disappointed. If both of you go with the expectation that in quiet surroundings she will hear quite a bit more than she does now, then you have the right expectations. In noisy situations, all bets are off unless she also uses assistive listening devices.

You explain how your mom, when she misses something, “simply fills in her own blanks—which creates arguments and disagreements among her family and friends.”

Don’t be too hard on your mom. When we (hard of hearing people) miss words, we naturally try to fill in the blanks—sometimes we fill them in with the right words, and sometimes with the wrong words. Unfortunately, if we miss a key word, what we think we hear is likely totally “off the wall”. Problems arise when we insist that what we thought we heard is what you said. Part of adjusting to being hard of hearing is realizing that what we think we hear is often not what was actually said. Thus, we need to be flexible to others telling us what really was said when they realize we are off track.

I understand your frustration about repeating yourself. However, look at it this way. If you have to repeat yourself, this just shows that you are not doing the right things so that your mom can hear and understand you the first time.

Use me for an example. If you are going to talk to me and I don’t have my hearing aids on, you are going to have to get close (and by close I mean almost nose to nose, not talking to me from across a room). Furthermore, you need to have adequate light on your face and you must be facing me so I can speechread you. Also, you need to speak clearly and maybe a bit more slowly. If you don’t do these things every time, you will just have to repeat yourself (and get frustrated in the process).

Thus, when talking to a hard of hearing person, you need to meet their communication needs before you start talking.

You ask, “How can I convince my mom that hearing the good things in life is far more important that being bothered by occasional noise?”

I think you have the wrong idea about what you call “occasional noise”. To you, there are foreground sounds (like the person you are talking to) and background sounds (environmental sounds, etc. that you ignore).

When you are hard of hearing, there is no such thing as foreground and background sounds—they are all in the foreground so are annoying and loud—and trying to hear someone through them at times is nigh to being impossible.

That is why wearing hearing aids in quiet places with one person talking and being no more than 6 or so feet apart is the ideal. Under those conditions, wearing hearing aids really helps. However, when you add in noise and distance, hearing aids rapidly become less and less helpful. When it is too noisy, wearing hearing aids can actually make things worse, not better.

This is why hearing aids are not the whole answer. In order to successfully live with a hearing loss, you need to do four things (after you have accepted and adjusted emotionally and psychologically to your hearing loss). These four things are not optional—they are all equally important.

They are:

  1. Get and wear (when appropriate) properly fitted hearing aids.
     
  2. Supplement the hearing aids with assistive listening devices when noise and distance interfere.
     
  3. Learn to speechread (lip reading was the older term).
     
  4. Learn and practice the myriads of proper hearing loss coping skills such as get close, face the person, have adequate light on your face, cut out background noise, etc, etc.

If your mom will do all four of these things, she will understand ever so much more (and you will not be so frustrated either).

However, you need to remember that communication is a two-way street, thus both you and your mom have to do your respective parts. Your mom has to do the above 4 things, and you have to accommodate her hearing needs (basically point 4 above). When you both do this, you’ll both be much happier and communication will be ever so much easier!

For more information on communicating with hard of hearing people get the short easy-to-read book “Talking With Hard of Hearing People—Here’s How to Do It Right!“.

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