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Exactly on the driving bit. I had an implant 2 plus yrs ago and have been

driving ever since. I must say when I drove over the Washington Bridge

the first time, I thought what if .... will I end up in the mighty

Hudson? As long as you don't black out it is ok. Beyond that I don't know.

Ted

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I think the level of shock the thing is set for the first firing makes a big

difference. On my original settings, the first one hurt and gave you quite a

kick, but I still felt under control. Since then I have had a few fatal

rythems that didnt respond to a milder jolt so now the thing fires on 100%

first time. I have never blacked out, but I also cant say which direction the

steering wheel would go if it were to fire while driving. I would venture to

say I would be pulling a hard right or left for two to three seconds. Scarry

thought I hope to never experiance (had a MI and went down for the count while

driving, luckily hit a Chicken joint rather than a person)

Steve

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Dear Jon, Although I'm not much of a participant here, I just wanted you to

know that I read all of the postings and am very grateful for your kind

interest in this project. You said, I believe, that you were a journalist.

I am a writer .. Wrote a lot for the NY Times travel k, garden and long island

sections. No hard news though. Feature stuff. Have had 16 books published

and hundreds of articles. These days mostly on gardening. The latest " Seaside

Gardening " published by Harry Abrams in NY. We've just finished a companion

book " Country Gardening " to be published this coming fall. Anyway, thank you

again for your kind interest in this project. It is a great service to all of

us.

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  • 2 weeks later...

Hi Anita,

Thank you o very much for he info. I am trying to find out all I can

about the meds my step dad is taking, since is open heart surgery

1-22-99. He is still in the hospital(Heart Valve replacement) he is

having many problems with the meds not working for him, They already

zapped him once & aretalking about doing it again, if you no anyone who

has had this type of operation , please tell them to get in touch with

me. I have had no luck with this group in locating anyone that has gone

thew ths. Thank again, I really do aprreciate you taking the time to

respond to my question. Vic

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Hi Anita,

Thank you o very much for he info. I am trying to find out all I can

about the meds my step dad is taking, since is open heart surgery

1-22-99. He is still in the hospital(Heart Valve replacement) he is

having many problems with the meds not working for him, They already

zapped him once & aretalking about doing it again, if you no anyone who

has had this type of operation , please tell them to get in touch with

me. I have had no luck with this group in locating anyone that has gone

thew ths. Thank again, I really do aprreciate you taking the time to

respond to my question. Vic

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Vic -- I'm probably not going to be of much help to you in trying to

understand what is going on with your step-dad. My father-in-law had

heart valve replacement surgery a few years ago, but he never had to

cardioverted (zapped). The only trouble I remember him having with meds

was the Coumadin (blood thinner). He's still on that med but has to

have his blood checked every week or so--it's a pain. As far as the

surgery, he's doing great now.

I gather your step-dad has not been implanted with an ICD yet--that may

happen if they continue to have to zap him.

Maybe someone will read your note and have more input for you.

Meantime, hang in there-- I'll be thinking about you (and your family).

Anita from NC

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Vic -- I'm probably not going to be of much help to you in trying to

understand what is going on with your step-dad. My father-in-law had

heart valve replacement surgery a few years ago, but he never had to

cardioverted (zapped). The only trouble I remember him having with meds

was the Coumadin (blood thinner). He's still on that med but has to

have his blood checked every week or so--it's a pain. As far as the

surgery, he's doing great now.

I gather your step-dad has not been implanted with an ICD yet--that may

happen if they continue to have to zap him.

Maybe someone will read your note and have more input for you.

Meantime, hang in there-- I'll be thinking about you (and your family).

Anita from NC

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Hi Anita, Thank you for your response. My step dad is on Coumadin

already & they did tell him he would have to have his blood checked

twice a week when he does go home. He is taking all inds of medicine

right now, but they cant sem to get his Blood pressure ajusted or his

breathing, I think he is worse off for havig this operation, but that is

only my opinion. Thank you for your kind words. Vic

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Hi Anita, Thank you for your response. My step dad is on Coumadin

already & they did tell him he would have to have his blood checked

twice a week when he does go home. He is taking all inds of medicine

right now, but they cant sem to get his Blood pressure ajusted or his

breathing, I think he is worse off for havig this operation, but that is

only my opinion. Thank you for your kind words. Vic

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My cardiologist switched me from Cordarone to Pacerone which he says is the

same thing. I have been on Pacerone now for about 6 months and feel fine.

And a big plus, Pacerone is much much cheaper than Cordarone, if that is an

issue.

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  • 3 weeks later...
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My cardiologist switched me from Cordarone to Pacerone, which is a generic for

Cordarone, as I understand it. The price is about 1/4, should that be of any

concern. I have a dual chamber ICD, Guidant, installed in 1996. Mercifully,

it has never fired, and I am feeling just fine. I don't have that thumping

you talk about and I have been on Cordarone 200 MG a day since my " incident "

( I love that don't you? Sort of like the incident when the North Koreans

shot down a 747 back in 1987) ... Theodore , Jr.

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  • 2 months later...
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Dear Sue, what is long q t syndrome. Some of my friends seem to think I ave

fatigue syndrome, because my energy level is often low, but only in the

spring. My doc thinks it's hayfever! Ted.

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<a7363fb1.2469747-@...> wrote:

Original Article: list//?start=604

> Dear Sue, what is long q t syndrome. Some of my friends seem to think I ave

> fatigue syndrome, because my energy level is often low, but only in the

> spring. My doc thinks it's hayfever! Ted.

>

Hi Ted,

LQTS is an abnormality of the heart's electrical system. It has to do with

heart muscle cell structure and causes a fast arrythmia called Toursade de

Pointes. The Q-T interval is a measurement of time required for repolarization

and when longer than normal presents a problem. I was able to find good

information on this subject by contacting askjeeves.com and asking " What is long

q-t symdrome? " Jeeves' site is a great place for finding good reference

material. Are you now on any heart meds, Ted? LQTS is not like chronic fatigue

syndrome. Hope you are doing OK.

Regards,

Sue

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  • 4 weeks later...
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I wonder if any of you have had similar experience. I had my implant in Nov

97. Never had a firing. Cardiologist very happy. I take 1 1/2 pacerone a

day and two blood pressure pills along with one aspirin. Last year I had

shortness of breath a lot. Went through all tests and all was in ship shape,

but shortness persisted. Then it went away around this time of year. Back in

March, I began to huff and puff again. Although I am not having shortness of

breath, If I work out in the garden, particularly getting up and down on my

knees, I huff and puff and have to catch my breath for a minute. This seems

to be persisting. My primary phys. thinks it may be an allergy or it may be

that I need to walk a half an hour a day. Anyone else have this fatigue and

Huffing and puffing? They don't seem to be concerned, but I don't have the

stamina. Is this a normal thing? Any input would be appreciated. Many

thanks.

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Hi -- I " huff & puff " when I do any activity it seems, but I can tell

you from experience that the advice about walking half an hour each

morning does help me tremendously. I feel better physically and

emotionally. I have congestive heart failure which causes shortness of

breath all the time. Of course I'm on a number of meds including

Cordarone for arrhythmia and Coreg for my CHF. But, do try the

walking--it sure helped me. Here's hoping you begin to feel better

soon. Anita in NC

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I wonder if any of you have had similar experience. I had my implant in Nov

97. Never had a firing. Cardiologist very happy. I take 1 1/2 pacerone a

day and two blood pressure pills along with one aspirin. Last year I had

shortness of breath a lot. Went through all tests and all was in ship shape,

but shortness persisted. Then it went away around this time of year. Back in

March, I began to huff and puff again. Although I am not having shortness of

breath, If I work out in the garden, particularly getting up and down on my

knees, I huff and puff and have to catch my breath for a minute. This seems

to be persisting. My primary phys. thinks it may be an allergy or it may be

that I need to walk a half an hour a day. Anyone else have this fatigue and

Huffing and puffing? They don't seem to be concerned, but I don't have the

stamina. Is this a normal thing? Any input would be appreciated. Many

thanks.

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The first time that happened to me my cardiologist told me my lungs were filling

up with fluid. He put me on Lasix and the problem cleared up almost over night.

That's just a water pill to put it simply. I couldn't even get in and out of bed

without having to rest and catch my breath. I thought it was going to be the

end,

but it wasn't. I'm still on it and it still happens every once in awhile. But

never as bad as before. I'm not saying that's what is wrong with you. I am not a

doctor. But please at least talk to him or your family doctor. None of us should

have to live with this discomfort.

Tom Denny

Theo1415@... wrote:

> I wonder if any of you have had similar experience. I had my implant in Nov

> 97. Never had a firing. Cardiologist very happy. I take 1 1/2 pacerone a

> day and two blood pressure pills along with one aspirin. Last year I had

> shortness of breath a lot. Went through all tests and all was in ship shape,

> but shortness persisted. Then it went away around this time of year. Back in

> March, I began to huff and puff again. Although I am not having shortness of

> breath, If I work out in the garden, particularly getting up and down on my

> knees, I huff and puff and have to catch my breath for a minute. This seems

> to be persisting. My primary phys. thinks it may be an allergy or it may be

> that I need to walk a half an hour a day. Anyone else have this fatigue and

> Huffing and puffing? They don't seem to be concerned, but I don't have the

> stamina. Is this a normal thing? Any input would be appreciated. Many

> thanks.

>

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Theo,

Stick to that low sodium diet also. You need to keep the fluid off of your

lungs. Duff has a link on his site to a low sodium food store. Check it

out and say hi to me.

Pete E

Re: digest

I wonder if any of you have had similar experience. I had my implant in Nov

97. Never had a firing. Cardiologist very happy. I take 1 1/2 pacerone a

day and two blood pressure pills along with one aspirin. Last year I had

shortness of breath a lot. Went through all tests and all was in ship

shape,

but shortness persisted. Then it went away around this time of year. Back

in

March, I began to huff and puff again. Although I am not having shortness

of

breath, If I work out in the garden, particularly getting up and down on my

knees, I huff and puff and have to catch my breath for a minute. This seems

to be persisting. My primary phys. thinks it may be an allergy or it may be

that I need to walk a half an hour a day. Anyone else have this fatigue and

Huffing and puffing? They don't seem to be concerned, but I don't have the

stamina. Is this a normal thing? Any input would be appreciated. Many

thanks.

------------------------------------------------------------------------

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eGroups.com home:

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I feel walking has done more for me then any other single facet of my

treatment. I have a similar profile to Anita. Another patient convinced me

that I could walk further then I did a couple years ago, and I think it has

kept me going. My EF is staying at the same level, but my Vo2 is increasing

a little, and the Huffing and Puffing is gone.

Walk everyone.

Pete E

Re: digest

<< Message: Re: digest (2.00 KB) >> Hi -- I " huff & puff "

when I do any activity it seems, but I can tell

you from experience that the advice about walking half an hour each

morning does help me tremendously. I feel better physically and

emotionally. I have congestive heart failure which causes shortness of

breath all the time. Of course I'm on a number of meds including

Cordarone for arrhythmia and Coreg for my CHF. But, do try the

walking--it sure helped me. Here's hoping you begin to feel better

soon. Anita in NC

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Guest guest

I rarely ever huff and puff but I am always fatigued. I know it is caused by

the propranolol and I wonder if other drugs may cause it too. Whenever I try

to run or walk up stairs or walk up a hill I get this dead feeling in my

extremeties and my legs have completely given out on me a few times. My

understanding is that without the adrenalin (which the propranolol blocks)

the O2 cannot be moved from the blood to the muscles at the rate that it is

needed. Without O2 the muscles switch to anaerobic respiration which only

produces 1/19 of the energy aerobic respiration does. It also produces

lactic acid which causes pain and muscle cramps. A good site to look up

information about drugs is rxlist.com. You can find out the mechanism of

action of cordarone. (Interesting fact: Plants and many fungi and bacteria

have a slightly different metabolic pathway for anaerobic respiration. They

produce alcohol rather than lactic acid. Isn't it a good thing we aren't

like that? We would get drunk every time we exercised!)

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