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-- Tinnitus for some people do subside quite a bit. I find that if I cut out

certain stuff I don't have the tinnitus as much. I do know how you feel. This

am I was bothered by a whining hum in my left ear that woke me up out of a sound

sleep. I just ignored it and it went away on its own eventually. Mine is usually

masked by the implants when the processors are on.

Snoopy

bilateral CIs

prelingual due to Rubella

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Hi Snoopy,

My surgeon told me last week that my tinnitus should disappear once my CI is

activated. What has been frustrating to me are the variations in the sounds

I hear. It continually alternates between a high pitched tone, a waterfall

and a freight train. Is there any treatment that you know of for tinnitus? I

know some people have tried using white noise generators to help mask the

sound, but do you know of anything else besides cutting down on caffeine

(and salty foods)? As I said in another message, I'm going to try drinking

white soda for awhile to see if that has any positive effect.

Implanted: 12/22/04

Activation date: 1/18/05 (20 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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Hi, ,

I'm sorry to hear you are being so bothered by tinnitus. I've always

had it, and, sorry to say it is worse since my implant.

There is no cure for it, unfortunately. Alice has the best list of

suggestions I know to try to minimize its effects. (I switched to caffeine

free

diet pepsi years ago). I know it is a running joke with me to promote

tranqualizers like xanax and prozac, but I have truely read that some people do

find relief while taking these drugs. It is, of course, a matter to discuss

with your doctor should it become intolerable. I hope it doesn't come to that

for you, and that activation puts a real crimp in this very annoying tinnitus!

Happy New Year!!

Jackie

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Hi ,

I'm sorry that your tinnitus has gotten to the point of waking you up at

night. You still are healing from the surgery although you feel well.

There is most likely some swelling in the area of the implant and it sounds

like when you lay on the implanted side, you are making the tinnitus roar by

laying against the swelling. Do you have a neck pillow? It might be

helpful when you are trying to sleep on that side.

My tinnitus is usually worse when I first get up, but as soon as I put on

the processor, it goes almost completely away and becomes unnoticeable. I

can tell which days I didn't drink enough water - and I know that sounds

strange. The next morning, the tinnitus is worse. I personally have almost

completely stopped drinking anything carbonated and have made the change to

fruit drinks, vegetable drinks and water. This was my own solution and not

something recommended.

One question - are you taking anything for pain still? Would you be taking

ibuprofen or something like that? This too can make it worse. Tylenol

seems to be the best for pain relief - even for a headache.

I hope this resolves for you easily but your doctor may be right about the

activation day being the relief.

Alice

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Hi Jackie,

I woke up this morning with the same high pitched tone. After a few hours,

it turned into a whooshing type sound that I can still hear as I type this.

I've had tinnitus before, but it certainly wasn't as loud or as persistent

as it is now. I wonder if the antibiotic I'm taking (Cefadroxil - generic -

500 mg twice a day) could be partially responsible? In the meantime, I'm

going to try cutting out all caffeinated drinks to see if that helps.

Failing that, I will have to learn how to live with it until my activation

date. I don't think it will come down to this, but if need be, I may take

your suggestion and talk to my surgeon about tranquilizers. (I've already

e-mailed my audi to see if she has any suggestions.) The reason why I think

the tinnitus is so distracting to me is because I don't have any visual

input to take my mind off of it. When I experienced tinnitus before my

surgery, it wasn't as loud or as constant as it is now -- just an occasional

high pitched ringing sound that would happen every now and then (usually at

night).

Implanted: 12/22/04

Activation date: 1/18/05 (19 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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Hi Alice,

Thanks for your reply. I'm no longer on pain meds and haven't been taking

ibuprofen. However, I have been taking Extra Strength Tylenol

(acetaminophen) just before bedtime to ease the mild soreness I feel when

sleeping on my implanted ear. I don't have a neck pillow but will consider

buying one, especially if it will help bring the tinnitus down to a low

roar. Right now I have my head propped up on two pillows. Perhaps going back

to the recliner will help in the meantime?

Implanted: 12/22/04

Activation date: 1/18/05 (19 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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,

You mentioned in another e-mail that you are still taking an antibiotic. I

bet that's the culprit in making it sound so bad. I always think that

sleeping upright helps us to heal better because we don't put any pressure

on the surgical area. This is my own theory and not one that was ever given

to me by a medical professional.

The Tylenol should be fine. Try to get plenty of rest too. What makes it

bad is that when we have the horrid tinnitus, we tend to get stressed and

stress makes it worse. Vicious circle.

Alice

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Hi Alice,

Because there was some residual blood in my eardrum, my surgeon recommended

that I continue taking antibiotics for another week. I'll let you know if I

notice any difference in the tinnitus once I've stopped taking them.

As of tonight, I'm going to start sleeping in my recliner again. The implant

area has become a little sore, but like you said, sleeping in an upright

position should take care of that. Fortunately, the implant area is

starting to flatten out and doesn't protrude as much as it did last week.

Thanks for your help! <smile>

Implanted: 12/22/04

Activation date: 1/18/05 (19 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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,

I wanted to thank you for your recommendations re: tinnitus. As of now, it

appears that my tinnitus is a side effect of the antibiotics I've been

taking. If tinnitus becomes a problem for me in the future, I will

definitely ask my doctor about Valium. By the way, I was on Valium a long

time ago when my migraines were first diagnosed. A very powerful drug, but

as long as it helps, that's what counts. :) I'll see how things pan out

within the new few weeks. Hopefully after the final course of antibiotics is

finished, my tinnitus will be history. <crossing fingers>

Implanted: 12/22/04

Activation date: 1/18/05 (17 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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,

Tinnitus really is annoying, isn't it? I'm not one to complain, but I do

have to admit how annoying this has become because of how loud and

persistent it is. I've tried blocking out these sounds with the TV or radio

but because I can't understand what is said, it only adds to the noise.

Tonight I'm going to try listening to some jazz to see if that helps. Glad

to know I'm not alone. Hang in there, ...hopefully your tinnitus will

disappear once you're activated. :)

Implanted: 12/22/04

Activation date: 1/18/05 (16 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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, have you thought of taking something to hlp you sleep? Is your problem

falling asleep or staying that way. I've been having spleep problems myself

although for me I think it is just plain insomnia rearing its ugly head

which it seems to do from time to time but still anoying. I noticed last tim

I had it that if I took somethhing like tylenol pm which is not habit

forming, that it seemed to help. I'm just really tirred today been upsince 2

so jst thought of you. I know how irritating it is in many ways to not have

slept properly so you aren't feeling recharged.

Re: Re: Tinnitus

>

> ,

>

> Tinnitus really is annoying, isn't it? I'm not one to complain, but I do

> have to admit how annoying this has become because of how loud and

> persistent it is. I've tried blocking out these sounds with the TV or

radio

> but because I can't understand what is said, it only adds to the noise.

> Tonight I'm going to try listening to some jazz to see if that helps. Glad

> to know I'm not alone. Hang in there, ...hopefully your tinnitus will

> disappear once you're activated. :)

>

>

> Implanted: 12/22/04

> Activation date: 1/18/05 (16 days and counting!)

> Deafblind/Postlingual

> BTE hearing aid user 19 years

> Severe-profound hearing loss 9 1/2 years

>

>

>

>

>

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Hi everyone,

My surgeon e-mailed me this morning and said that he could put me on

steroids to help with the tinnitus I've been experiencing. Some of the side

effects I might have as a result include an upset stomach and sleeplessness.

However, I told him I'd like to give them a try -- even if they only help to

dull the sounds I'm hearing.

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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Now you will get muscles~

Pearson

sville, WA

Re: tinnitus

Hi everyone,

My surgeon e-mailed me this morning and said that he could put me on

steroids to help with the tinnitus I've been experiencing. Some of the side

effects I might have as a result include an upset stomach and sleeplessness.

However, I told him I'd like to give them a try -- even if they only help to

dull the sounds I'm hearing.

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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Hi Tina,

I have problems falling asleep. I'm also awakened by the tinnitus sometimes

but my primary complaint is not being able to get to sleep. I e-mailed my

surgeon to ask if I could take Benedryl with the steroids he is prescribing.

Hopefully both of them will help.

By the way Tina...the next time you have insomnia, try drinking warm milk.

You could also heat milk in the microwave and add Hershey's syrup. (When hot

chocolate is made with milk and Hershey's syrup, it contains no caffeine.)

Both of them have an effect that helps calm and relax you.

Hope you're able to get a better night's sleep tonight. <smile> Oh...and try

the hot chocolate as described above. It's delicious! :)

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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,

LOL! would like that. <grin>

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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,

Steroids do reduce the tinnitus. They have other side effects which are

bothersome but I do know that they make tinnitus better. You are right

about warm milk BTW and that is the reason baby's sleep so well. I'm not so

sure about the warm chocolate milk though.

Alice

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Alice,

It will be interesting to see how well the steroids work. Hopefully they

will allow me to relax while I start looking ahead towards my activation.

:)

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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,

I didn't even think about Gingko Biloba. If the steroids don't work, that's

the next thing I'll try! Hmmm. Come to think of it, I could kill two birds

with one stone that way...eliminate the tinnitus while strengthening my

memory. <grin>

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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What memory?

Pearson

sville, WA

Re: Tinnitus

,

I didn't even think about Gingko Biloba. If the steroids don't work, that's

the next thing I'll try! Hmmm. Come to think of it, I could kill two birds

with one stone that way...eliminate the tinnitus while strengthening my

memory. <grin>

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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,

Gosh, I can't imagine having tinnitus for 40 years!!

I wish I could block out what I'm hearing, but I can't -- at least not now.

The high pitched tone I've been hearing has been replaced by an

ocean/whooshing sound. Just when I become used to one sound, it changes to

something else. I think that and the loudness (it's *very* loud) is what

makes this so annoying for me. Hopefully my activation will take care of

this once and for all. LOL! One thing I know for sure is that the tinnitus I

used to have before surgery was nothing compared to what I'm experiencing

now. If my tinnitus had the " courtesy " of limiting itself to only one sound,

I'd be happier and would have a much easier time concentrating on other

things. <grin>

Implanted: 12/22/04

Activation date: 1/18/05 (15 days and counting!)

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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  • 5 weeks later...

I just realise that my tinnitus has been gone since November, and I had it

for several months, and it was most annoying!! My CI implant certainly

turned the trick!! WOW!! Moses

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Hi ,

I have heard Tinnitus for many years and it especially gets annoying

when I take off my hearing aid. So, I fully expect to have it

roaring away after the surgery.

Stan (Implant scheduled for 2/24/05)

If you do experience tinnitus Stan, it will most likely

> be temporary (though there are exceptions as several people on this

list can

> testify) and only experienced when your speech processor is off.

>

>

> Implanted: 12/22/04 Activated: 1/18/05

> Deafblind/Postlingual

> BTE hearing aid user 20 years

> Severe-profound hearing loss 10 years

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Moses,

That’s a true blessing when it happens. I remember thinking that if I gained

nothing more than the silence of no tinnitus from my implant, I would be

happy. Of course, that wasn’t really the truth but I know what a relief it

is when the tinnitus fades after the activation. I wish it could happen for

everyone.

Alice

• I just realise that my tinnitus has been gone since November,  and I had

it for several months, and it was most annoying!! My CI implant certainly

turned the trick!! WOW!! Moses>

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  • 2 months later...
Guest guest

Ann

I have had the ringing since I was a teenager (45 now) I am used to it, don't

think it will ever go away. It doesn't affect hearing others though. I read

some where the Shatner has tinnitus and got a special hearing aid with

" white noise " that helped with his misery. Don't know what the device was

called.

Ann Prow <aprow@...> wrote:

With all the talk about hearing loss, I was wondering if anyone has had any

success in getting rid of tinnitus - ringing in my ears. I have had this

problem with long term undiagnosed Lyme and even with treatment the last 3

years, it only has gotten worse -louder. It is now affecting my hearing

cause I just cannot hear things people are saying.

Thank you again for your help -however you can,

Ann

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Guest guest

Hi Ann,

My husband has had tinnitus for years with late stage lyme. We did not

associate it with the lyme, we thought it was due to many years of loud

machinery. He is a contractor and always using something loud. He said

is would be non stop all the time. My husband has been using a serious

nutritional protocol with glyconutrients for 1 year, I have been using

it even longer. He said his tinnitus is only on occaison and not very

bad, so it is obviously not a permananent thing. I never had it at all.

We have never taken any abx except for the very first script right after

bullseye rash.

Ann Prow wrote:

>

>

> With all the talk about hearing loss, I was wondering if anyone has had any

> success in getting rid of tinnitus - ringing in my ears. I have had this

> problem with long term undiagnosed Lyme and even with treatment the last 3

> years, it only has gotten worse -louder. It is now affecting my hearing

> cause I just cannot hear things people are saying.

> Thank you again for your help -however you can,

> Ann

>

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