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I worried about my annual oncology checkup coming up, & I am relieved all is

well. I worry also when I go to the CI audie with unusual problems too

because it is mighty scary when I cannot see & the CI may not be fixable, as

in deteriorating auditory nerves. Ted, you are lucky you have your sight to

fall back on.

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Thank you for saying that, . Ted DOES have his sight to rely on and as my

audi said, it's very scary when you're totally blind (or visually impaired) and

can't hear. I've lived with deafblindness (i.e. being unable to see or hear) for

10 years prior to receiving my CIs, but that doesn't change the fact that I've

become attached to my CI hearing.

---- <wdywms@...> wrote:

> I worried about my annual oncology checkup coming up, & I am relieved all is

> well. I worry also when I go to the CI audie with unusual problems too

> because it is mighty scary when I cannot see & the CI may not be fixable, as

> in deteriorating auditory nerves. Ted, you are lucky you have your sight to

> fall back on.

>

>

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and ,

What most people tend to forget is, we are blessed with the technology

that gives back some of what we lost. I will soon join you both as my

vision worsens but I am thankful to have the CI and some peace of mind. To

go bilateral would be, oh I dont need to tell you, you two know! LOL

We're human, we have emotions, we worry. And we are not worrying about

nothing. As I pointed out earlier, a healthy worrying is a productive one

for it leads to resolutions.

*---* *---* *---* *---* *---*

No matter where you go, there you are.

--Buckaroo Banzai

& Dreamer Doll ke7nwn

E-mail-

rclark0276@...

Home Page-

http://webpages.charter.net/dog_guide/

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,

I sure will let yuh know, buit dont hold your breath, ok? I am not

certain that you would look good blue. LOL I may talk to my friend and see

if she wants to combine errands in Portland and then plan a mapping at that

time.

*---* *---* *---* *---* *---*

An ounce of action is worth a ton of theory.

-- Gilbert Chesterton

& Dreamer Doll ke7nwn

E-mail-

rclark0276@...

Home Page-

http://webpages.charter.net/dog_guide/

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,

Just be glad you had enough electrodes that they could turn off 6 and

you wouldn't notice it. Audi may in the future, do something to give you

sound on those electrodes, but not in high frequencies. Not sure what it

is called, but they can do it, shift stimulus around, so you're getting

22 electrodes worth of hearing, even if not in the high frequencies.

Amazing, is it not. Strawberry mochas all around, I say. Even my

pooch would drink one of those.

Tue Feb 3, 2009 11:22 pm (PST)

,

Yep. 6 high frequency electrodes were turned off on each side. Apparently

they were what caused me to hear speech in a muddy, distorted manner and

high frequencies as being off-key. Who would have thought? What's also

interesting to me is the fact that I'm still able to hear high

frequencies despite the 6 electrodes being turned off -- they just don't

sound as loud or off-key as they did before. I'm not sure why that is,

but I'm certainly not going to complain! I think this is worth

celebrating with a strawberry mocha, don't you? LOL!

____________________________________________________________

Click here to find the low cost way to send and receive faxes by email!

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,

I took 2 and a half years of medical transcription and earned a 4.0 GPA, so I'm

also well aware of the terminology that is used. Sometimes I've been tempted to

do the same because some of the questions they ask on medical forms are so

stupid. Aside from that, why ask questions about your medical condition(s) when

they request old medical records in the first place? Isn't it their job to look

at those records to find out why you suffer from the conditions and/or illnesses

you do? LOL!

Mona

Bilateral Cochlear CIs

December 2004 and February 2006

Deafblind/Postlingual

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,

What's the point of providing sound to the 6 electrodes that have been shut off

if I won't be able to hear high frequencies? Will turning them on create a

greater clarity of sound? I'm quite happy with what I'm hearing and don't want

to change anything. I think it's best to leave well enough alone and have

already told my audi that I'd like my programming to remain the way it is. I

don't want to risk having something changed only for me to hear poorly again. As

the saying goes, " If it ain't broke, don't fix it. " LOL!

Bilateral Cochlear CIs

December 2004 and February 2006

Deafblind/Postlingual

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,

In your case the number of active electrodes did not equal greater

clarity of sound. If I understand you correctly in the past that by

turning off the six highest pitch electrodes result in the high

frequencies sounding higher pitch in addition to greater clarity?

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,

Ever since 6 high frequency electrodes have been turned off, I'm hearing *much*

*much* better (i.e. clearer) than I have before (compared to when I had all 22

electrodes activated) and am able to hear high frequencies without them sounding

off-key. Prior to having my electrodes turned off, speech sounded muddy and

distorted and high frequencies sounded off-key. In addition, I was unable to

hear extremely high frequencies.

Bilateral Cochlear CIs

December 2004 and February 2006

Deafblind/Postlingual

---- johngo57 <johngo57@...> wrote:

> ,

>

> In your case the number of active electrodes did not equal greater

> clarity of sound.

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,

I am understanding your point that turning off the six highest

frequency electrodes did not reduce your high frequency perception of

sounds in fact increased it since the high frequencies is no longer off

key. That tells me that there may be more to high frequency perception

that the electrode location in the cochlea as it seems. The reason I am

driving this is because I may have to turn off my electrode one since

it seems no longer able to do the work in simulating a tone. You gave

me courage to pursuit this and not to be overly concern about this and

I may end up in getting a bit more clarity in the process. I sure that

your audiologist is curious why this is happening but I sense no

problem in your audiologist to leave the things as they are.

> Ever since 6 high frequency electrodes have been turned off, I'm

hearing *much* *much* better (i.e. clearer) In addition, I was unable

to hear extremely high frequencies.

>

>

> Bilateral Cochlear CIs

> December 2004 and February 2006

> Deafblind/Postlingual

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,

I don't think you should experience any problems by turning off one electrode.

If I'm not having any problems with 12 of them turned off, you definitely won't

with one. I know a CI user who has only 3 functioning electrodes and yet she

hears just fine, so I wouldn't worry about this at all if I were you. I'd give

it a try to see what kind of results you receive. If this is what you decide to

do, let us know how it turns out.

Bilateral Cochlear CIs

December 2004 and February 2006

Deafblind/Postlingual

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  • 1 year later...
Guest guest

20 years ago I had surgery for a c-toma. The surgeon at the time believed he got

all of it out. This year I started having some major issues...infections that

won't go away, swelling, redness, the list goes on. I had a CT done the 25th of

May and got the results 2 days ago after being discharged from the hospital. (I

became very ill and was admitted through the ER on the 1st of June). They found

a polyp 12mm by 9mm in the right maxillary sinus and some thickening was found

in the left posterior maxillary sinus. I had a right mastoidectomy during the

first surgery 20 yrs ago. The left mastoid is perfect. They also noted the right

ossicles has some erosion along with portions of the stapes and the scutum. They

are not sure if the 2 lesions they found in the scan are c-toma's or cholesterol

granulomas. They said it was difficult to evaluate because of my mastoidectomy

changes. They are suggesting a MRI to differentiate between c-toma and

cholesterol granuloma. This sounds very scary to me. I am on high doses of

antibiotics and steroids. I am on anxiety meds and pain pills. I feel sick all

the time...I do not like the nausea feeling. I am scared but do not see the

surgeon for 3 more weeks. Does anyone else relate to these symptoms and can you

give me some advice on easing some of them. I am so scared of getting meningitis

because the scan showed the lesions right on the outer shell of the brain

lining...I am no doctor so I am not sure how concerned I should be if I should

be at all for that matter. Anyone else out there with similar results??

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  • 1 year later...

,

This may not be what you want to hear, and please check all

I say with your treating docs.

When nodes get bigger, it can be hard to tell where one

begins and the next ends, hence the term confluence. This is

somewhat dependent on the resolution of the scanner, but

can begin when then get over 3 cm or so.

I doubt they meant 11 mm, as that is nearly normal and would

not be called extensive and would not encase anything. I do

not know the " hamburger " sign.

Ask for a DVD of the scan.

Nodes this size generally need attention, but not always. It

gets harder to treat large nodes.

Stay strong

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