High Frequencies and Dizziness

I wonder did u sleep every night if not, then how many day u didn't sleep?

hi lavender,

i no longer have any problems with sleep because my psychiatrist gave me two doses i'm supposed to take. one is a lower dose i'm supposed to take when i feel "level" (or "normal") and the other is a higher dosage that i'm supposed to take when i'm manic (or in other words, feeling extremely happy, as if i have tons of energy, anxious, restless -- these symptoms are all related to my bipolar).

ever since starting on the higer dosage when i need it, i've been sleeping on a consistent basis.
 
I am worried about you too, I hope it's just bog standard cold. Or something so Simple that anti bios would do the trick.

I hate leaving ci off! I was happy to leave HA's off but CI, No way!

Look after yourself, wait on foot and hand by your bloke! Good luck tomorrow.


Charlotte xxxx
 
Hear Again,

Sorry to sound like the resident expert. I have no technical knowledge about a CI can affect other areas, I just believe in how the CI works is that it sends an electrical current to each of the 22 electrodes and the electrical path is through the cochlea nerves at the right position to make you "hear" the frequency. The path then goes to the ground electrodes. It is where the electrical path goes is the number one question.

Based on what I heard during both my activations. Higher pitch voices and over time, they shifted to what I remember as being normal tells me the electrical path changes slightly over time. I guess I never really thought this could change to make voices no longer sound right but I guess it is possible. I also know that during my second activation, I heard a ring at the same time when I was hearing the tones and during my second mapping, when setting the max levels, I heard a hissing sound that would taper off seconds after the tones stopped. I think the electrical path has not been established or I have not become use to it makes me believe the electrical path can travel other places just for me makes logical sense. I also know that if my max levels are set to high on certain electrodes, I can feel them in my neck, hence an alternate ground path through the muscle is logical.

I know for me that my chemical make up seamed to change ever so slightly based on when I would be dizzy with Menieres or not but it seamed to be triggered by something I ate, typically salt and caffeine. Fortunately I never had the dizzyness aspect of Menieres to bad and seamed to be able to control it with head position if I felt it coming on.

I just try to keep my thoughts open on how the CI works and how it may affect my body but also how my body may affect the CI.

It sounds like you may have an idea with the sneezing several days ago and that it is now being aggravated by the CI. Maybe letting the nerves calm down, maybe things will return to normal soon and your congestion will go away also. You may want to keep one of your programs on your current setting in case they make any drastic changes to your maps.

It must be something in the air because over the weekend, I started getting a terribly stuffed up nose and am having an awful time being able to breath. "I'm in Michigan"

Steve
 
steve,

thanks again for your comments!

by the way, when i said that i considered you ad's resident expert, i meant that as a compliment. i really do admire your knowledge when it comes to the technicalities of how ci's work. :)

several people around the midwest have told me that everyone they know has or is sick with an upper respiratory tract infection. i really hope that isn't what i have because i had a URI a month or so ago and was ill for 2 weeks. i also had a dry cough that wouldn't let up until a month after my other symptoms disappeared.

a friend of mine gave me a great idea. she suggested that i ask my landlord if she can help me decrease the sensitivity on my processors so i can at least hear some environmental sounds. i plan to see her later this morning. i'd adjust the sensitivity myself, but can't due to the severe cts in my left hand and mild cts in my right hand.

stay tuned for an update tomorrow concerning my audi appointment.
 
hi everyone,

well, i think i discovered the reason behind my dizziness. it appears that i have a cold. i don't know if it's a URI, but when i listen to my voice, i can definitely hear congestion. this is the first time i've been able to hear that in so many years, but i recognize it because when i say words with the letter "m" or "n" my voice sounds very congested.

i'm still sneezing quite a bit too, but so far, i do not have any kind of a cough. i feel really hot (and my skin feels clammy to the touch) as well, but i don't know if i'm running a fever because i do not have a thermometer.

now i'm wondering if i should even see my audi tomorrow. my former audi always told me not to come in for a mapping whenever i'm ill since the map will need to be readjusted anyways once i'm feeling better.

in another hour or so i'm going to speak to my landlord to see if she can adjust the sensitivity control on my processors so i can at least hear some environmental sounds. perhaps if i use my comtek fm system as well, i will be able to understand some, if not all parts of today's inauguration.
 
i took off both processors about 10 minutes ago, but the silence is driving me crazy. *sigh*

That is why, I am very against cochlear implants. I heard, there are so much problem in the medical issues. Hearing aid is more safety than CI.
 
That is why, I am very against cochlear implants. I heard, there are so much problem in the medical issues. Hearing aid is more safety than CI.

kalista,

the problems i'm having right now aren't due to my ci's. they're due to the fact that i'm sick with a cold. my implants have nothing to do with it.

by the way, one can experience medical problems with hearing aids just as easily as they can with ci's. please do not make generalizations such as the one you made above about ci's because it gives people the wrong impression about what medical symptom is caused by what.
 
That is why, I am very against cochlear implants. I heard, there are so much problem in the medical issues. Hearing aid is more safety than CI.


:slap: Read the post properly, think more before you post something.

It's nothing do with CI's. It's do with something that is AFFECTING the usage of CI's Just like ear infection affects the usage of HA's.
 
hi everyone,

i just heard from my audi and ci surgeon's receptionist. i was told that my ci surgeon would like me to see someone he works with who specializes in treating dizziness. if she cannot help, he would like to see me for further evaluation. i will see the dizziness specialist and my audi tomorrow.
 
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thanks, charlotte. i'm fine as long as my ci's are off. when i put them back on though, the dizziness starts all over again. i'm dying to watch the inauguration on tv right now, but i can't raise the sensitivity high enough to understand speech. if i try to, it just causes more dizziness.
 
kalista,

the problems i'm having right now aren't due to my ci's. they're due to the fact that i'm sick with a cold. my implants have nothing to do with it.

by the way, one can experience medical problems with hearing aids just as easily as they can with ci's. please do not make generalizations such as the one you made above about ci's because it gives people the wrong impression about what medical symptom is caused by what.

Deaf girl had her CI about four years ago, her mother was very upset because her ear fluid kept dripping during overnight. She was complained headache and dizzy. The health insurance would not coverage to removal her CI, she faught with health insurance for two years to explain about medical symptom. Finally, she had her third surgery to removal CI. It was horrible for her and her mother.

A man who worked with me, he had his CI about ten years ago. He always had dizzy and headache from CI, he turned it off but inner the ears are bothering him a lot. He is processing lawsuit against the doctor.

You need to not be jump into the wrong conclusion. :) I am still very against CI for infant babies !!
 
kalista,

that is not the subject of this thread. if you'd like to debate ci's vs. hearing aids, please start your own thread. if you don't, i will have no choice but to ask the mods to close this thread which is completely unfair to those who are benefitting from the information being shared. thank you.
 
Back to the topic of this thread.

Hear Again,
Sorry to hear the sensitivity and volume didn't help much.
Hope your cold goes away quickly and you can return to normal.

As far as the technical expert, I wish I had more information technically about how the CI's really interact with the body and how they function. More so, how salt and fluid fluctuation can affect the battery consumption and ability to hear with the electrical path changes. About the only thing I keep forgetting when I start having trouble hearing is to change the filter. This normally happens after I've been stuck out in the rain and took a direct hit on the processor which saturates the filter and creates a microphone muffler.

I like technical stuff and am really trying to push my implants and programs and am by no means afraid to try something different. There are times I forget I can not hear because there are few occasions when I really can't hear someone. I remember having so much more trouble hearing with hearing aids. I will always remember the day they turned on my CI and the relief I felt in that it worked beyond my dreams. These implants have really stabilized by ability to hear and given me back my "security" in communicating.

Well, for me, the stuffed up nose has turned into a full blown mess with drainage, feeling, well, not to great, head pressure all that on top of not sleeping worth a darn last night. So I'm doing pretty well, at least I have not been hit by a truck. Took two Motrin and two Sudafed when I got home from work and that is some really good stuff. Pain is almost gone and the Sudafed is starting to help. I'm probably not suppose to take both at once but O-Well.

I mentioned the static noise during my second mapping and some ringing during my first. Well, I can hear both with louder noises right now but because of how I feel, I'm not alarmed. I'm thinking the chemical balance in my body is a little off right now and hopefully in a few days, I'll shake the cold and get back to normal. Friday is mapping session #3. Might be interesting to see how the maps go with a cold. I'd like to see how the min and max levels change.

On a more less positive note in getting use to my new Right side implant, more of the lower frequencies are sounding better, my voice sounds more like I hear it in my Left ear. I'm able to pick up more and more of the words to songs I know so the healing and adjustment process is still happening. My right processor is louder than my left which I have set that way so I make sure my brain picks up on that first to help in training/learning.

I am really happy with how things are progressing. With everyday that goes by things are getting better and better.

Hope your dizziness calms down. Maybe your Dr will give you some antivert. I had Messlezzne (sp) when I was having dizzy feelings years ago. It never really worked how I had hoped so I didn't take them very often.

Steve
 
hi everyone,

i just heard from my audi and ci surgeon's receptionist. i was told that my ci surgeon would like me to see someone he works with who specializes in treating dizziness. if she cannot help, he would like to see me for further evaluation. i will see the dizziness specialist and my audi tomorrow.

How are you feeling today? I hope this gets sorted out ok? That you are not finding the silence too hard to cope with?

How are your hands?
 
hi dreama,

my landlord was able to increase the sensitivity level on my processors to the point where i am able to hear environmental sounds, so i am no longer in complete silence.

i'm still experiencing dizziness, but not to the same extent that i would if i were wearing my processors at full volume (i.e. numerical value of 12).

my left hand is still in a great deal of pain, but my physical therapist told me that she noticed an increased range of motion in it yesterday which is definitely a good sign. while this doesn't mean my severe cts will ever go away without the help of surgery, it does mean there has been some improvement and if truth be told, i will gladly take "some improvement" over "no improvement" at all.
 
Hearing you have a cold, it all makes sense. Glad you have that part figured out. Now if they can find a way for you to cope better while you have that cold, now that will be progress. In the meantime, glad you figured out a way on your own to calm things down a bit.
 
Hi Hear Again,

Oh, no wonder u get sick have a cold flu. A while ago, I was sick too and also, dizzy a very brief time. Hope u feel better asap with lots of rest and drink lots of fluid.
 
Hearing you have a cold, it all makes sense. Glad you have that part figured out. Now if they can find a way for you to cope better while you have that cold, now that will be progress. In the meantime, glad you figured out a way on your own to calm things down a bit.

tomorrow after i see my audi and the dizziness specialist i'm going to walgreen's to pick up some dayquil and nightquil for my cold. i also plan to purchase a humidifier to help with my congestion. my nose is so stuffed up i can hardly breathe right now. the good news though is that i don't have a dry cough, so i don't think i have an upper respiratory tract infection.
 
Hi Hear Again,

Oh, no wonder u get sick have a cold flu. A while ago, I was sick too and also, dizzy a very brief time. Hope u feel better asap with lots of rest and drink lots of fluid.

thanks, lavender. <hugs>

today i've been drinking lots of orange juice. i also had chicken soup tonight for dinner.
 
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