Has anyone experienced problems with their heart? About 3 weeks ago I experienced severe heart palpitations, lasting 3-4 days. I was able to see a cardiologist who gave me an echocardiagram. It was normal and he said "don't worry". I thought it was because I had been taking zoloft or plaquinil, so I went off EVERYTHING. But last night it happened again. Not just a little flutter that lasts a few seconds, but continual fluttering lasting for hours. It's scary.
Any ideas on what might be causing this? Thanks for the help.
<sa...@home.com> wrote: > Andrea Barnes <sa...@home.com> wrote:
> Has anyone experienced problems with their heart? About 3 weeks ago I > experienced severe heart palpitations, lasting 3-4 days. I was able to > see a cardiologist who gave me an echocardiagram. It was normal and he > said "don't worry". I thought it was because I had been taking zoloft or > plaquinil, so I went off EVERYTHING. But last night it happened again. > Not just a little flutter that lasts a few seconds, but continual > fluttering lasting for hours. It's scary.
> Any ideas on what might be causing this? Thanks for the help.
> ~~~ andrea, i got 4 calls in a row last > week from new women i'd never > spoken with ~ all with heart problems.
> could you please compile your responses > to this?
> we do have a cardiologist here in san diego > ready to listen. (not don't faint from that > please! - lol) love, ilena ~~~
------------------------------- Hello!
"Paroxysmal atrial tachycardia" is when a slightly abnormal circuit in your heart can cause it to occassionally beat rapidly such that you can feel it (a palpitation). Some effective ways to stop it are to either strain as if you are having a bowel movement, or to splash yourself with very cold water.
I'm not sure if this is what is happening to you (it sounds like it could be though). It is quite common among women (especially those with slight prolapse of their mitral valve). It is considered relatively harmless.
What did you doctor say was the cause?
Best of luck! Paul
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Although you did have medical follow-up for your fluttering this does not mean that there's nothing wrong with you. Quite to the contrary, many people have what is known as arrhythmia's repeatedly. It's difficult to hear an arrhythmia as it has the tendency to just disappear leaving the patient feeling somewhat embarrassed. Often, it may take several attempts for a physician to document it. The end result may be a "Holter Monitor" This is merely hooked up to the patient for twenty-four hours. It's a constant EKG that monitors your heart rhythm while you document your physical activities. This will hopefully show the arrhythmia you've been experiencing. Because you're on medications ec: antidepressents, by no means should anyone dismiss your symptoms without a cardiac work-up Noreen.
> > Has anyone experienced problems with their heart? About 3 weeks ago I > > experienced severe heart palpitations, lasting 3-4 days. I was able to > > see a cardiologist who gave me an echocardiagram. It was normal and he > > said "don't worry". I thought it was because I had been taking zoloft or > > plaquinil, so I went off EVERYTHING. But last night it happened again. > > Not just a little flutter that lasts a few seconds, but continual > > fluttering lasting for hours. It's scary.
> > Any ideas on what might be causing this? Thanks for the help.
> > ~~~ andrea, i got 4 calls in a row last > > week from new women i'd never > > spoken with ~ all with heart problems.
> > could you please compile your responses > > to this?
> > we do have a cardiologist here in san diego > > ready to listen. (not don't faint from that > > please! - lol) love, ilena ~~~ > ------------------------------- > Hello!
> "Paroxysmal atrial tachycardia" is when a slightly abnormal circuit in > your heart can cause it to occassionally beat rapidly such that you can > feel it (a palpitation). Some effective ways to stop it are to either > strain as if you are having a bowel movement, or to splash yourself with > very cold water.
> I'm not sure if this is what is happening to you (it sounds like it could > be though). It is quite common among women (especially those with slight > prolapse of their mitral valve). It is considered relatively harmless.
> What did you doctor say was the cause?
> Best of luck! > Paul
> ****to send email to me, please remove the x from my email address (this
helps to get rid of most of the junk mass email - aka SPAM).
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So I'm not alone in this experience, I see: I was in ER twice in 1995 and 1996 for the same problem. My rate was about 250, and despite double doses of Cardizem and Inderal, the arrythmia did not resolve until it decided it was ready! (About 4 hours after I'd gone to ER, which was 1-2.5 hours after the episodes started.) I was having episodes of arrythmia frequently before that (for about 3 years), but that "xxx" maneuver (can't remember the name, but it's what Paul described as bearing down like you're having a bowel movement) could usually interrupt the episodes within a half-hour or so (nobody taught me to do this, I just did it instinctively, so I was surprised to learn that it actually had a name). I went to ER the times that it didn't eventually work.
I rec'd a dx of PAT, but wonder about it--seemed to be the easiest thing to call what was happening without doing any diagnostics other than EKGs, which were normal except for rate. I seem to remember reading something about an increase of apparent Mitral Valve Prolapse in SBI survivors...anybody else remember this? Paul, are you taking notes on this stuff (symptoms in common in BI women) for your paper?
Rosemarie, I'd like to learn more about vasculitis--I read a post here last year, but it wasn't clear to me what exactly vasculitis is and does, and my web search wasn't much more helpful...indulge a layman's curiosity, would you?
In article <19990223012850.13796.00002...@ng01.aol.com>, ib2spe...@aol.com
(IB2Speedy) wrote:
I was having episodes of arrythmia frequently before that
> (for about 3 years), but that "xxx" maneuver (can't remember the name, but it's > what Paul described as bearing down like you're having a bowel movement) could > usually interrupt the episodes within a half-hour or so (nobody taught me to do > this, I just did it instinctively, so I was surprised to learn that it actually > had a name).
Called a valsalva maneuver.
> I rec'd a dx of PAT, but wonder about it--seemed to be the easiest thing to > call what was happening without doing any diagnostics other than EKGs, which > were normal except for rate.
If they have your arrythmia on file, they should be able to tell what it is without any further tests. PAT should be a relatively easy diagnosis - as far as I have seen (pretty specific EKG findings). If they didn't know what the rhythm was then they should not have told you that it was nothing to worry about, and they should have done more tests...I think the only other tests that could be done would be to try to find the abnormal circuit that is causing the problem...but to do that...you already have the diagnosis known...
> I seem to remember reading something about an > increase of apparent Mitral Valve Prolapse in SBI survivors...anybody else > remember this? Paul, are you taking notes on this stuff (symptoms in common in > BI women) for your paper?
I've added it to the list. Thanks.
Talk to you later Paul
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IB2Speedy wrote: > but that "xxx" maneuver (can't remember the name, but it's > what Paul described as bearing down like you're having a bowel movement) could > usually interrupt the episodes within a half-hour or so
It's called "valsalva's maneuver " . That always use to work pretty good for me too, or they taught me how to do carotid massage on my neck too. My worst episodes were recorded in my medical records long before I connected them to my implants. This was after each of the closed capsulotomies on 3 different occasions and was accompanied with peripheral neuropathy in both legs and arms. I have not had many episodes since explanting, and I do wonder if it was related to the chemical and metals exposure from the implants.
> I rec'd a dx of PAT, but wonder about it--seemed to be the easiest thing to > call what was happening without doing any diagnostics other than EKGs, which > were normal except for rate. I seem to remember reading something about an > increase of apparent Mitral Valve Prolapse in SBI survivors...anybody else > remember this? Paul, are you taking notes on this stuff (symptoms in common in > BI women) for your paper?
MVP is quite high in the women. I have seen many posts on it. It is also prevalent in FM and we mostly all have that bad boy. I had an echo and it did not show MVP. Sure wish we had a data bank for all these health problems. Anyone have any good ideas on how we could set something like that up. All the lung problems that we hear about too. Maybe we should start a health registry of sorts.
IB2Speedy wrote: > I'd like to learn more about vasculitis--I read a post here last > year, but it wasn't clear to me what exactly vasculitis is and does, and my web > search wasn't much more helpful...indulge a layman's curiosity, would you?
> Elisabeth
I looked it up Elisabeth and it says: Vasculitis is inflammation of blood vessels. Vasculitis usually leads to damage to the lining of vessels, with narrowing or blockage, so that the blood flow is restricted or stopped.
As a result the tissues supplied are also damaged or destroyed by ischemia. Vasculitis is thought to be caused in most cases by bodies in the circulating blood know as immune complexes.
Immune complexes consist of antigens (foreign materials, such as components of microorganisms) bound to antibodies that have been formed in response to the antigens. Normally the immune complexes are destroyed by phagocytes (types of white blood cell) but sometimes they settle in the walls of the blood vessels, where they cause severe inflammation. In some cases the causative antigens are known to be viruses.
******************** Pray tell, could it be free floating silicone oil? Will we ever know? Donna
many women have complained to me about heart and breathing. i know when i wanted to celbrate with some rum drinks i damn near died, because i couldnt breathe and rushed to the hospital.
there is nerve damage for sure most drs on our side agree, that the myelin sheaths are eaten away and we have nuerological envolvement wit silicone , i feel this is not a theory but backed by tests and anecdotes.....that is why we have word loss and lost memory and we have the staggering and falling down, and look like m.s. notice the doctor wil say looks LIKE MS... most women only see ms. i know i did,,,and i thought i was a goner,
the swallwing problem is a nerve problem says dr. campbell, to me in person, he said the nerves arent firing to the place where the valve is to let the food go down, and it was true,,,,and constipation, and allergies etc,
well in the heart, my mom felt for sure she had had heart attacks and i pooh pooh her and iknow my mom is dramatic and gets anxious and frightened but she awoke several times like someone standing on her chest, she had an ekg and heart work up and she has ABSOLUTELY NOT ONE THING WRONG WITH HER ARTERIES HIGH BLOOD PRESSURE OR HEART, HOWEVER.
i took her took her to my more sophisticated dr, that uses a computer for diagnoses and we did not put it down on the form but the dr. told my mom she had a nerve to the heart andit was not firing correctly and my mom said to me...see see i told you so,,,,,so my mom was right, but the other tests were no help, but my dr. told her about the nerve and my mom was right and it was nothing to worry about,\ happy story, my mom is a tiger at 89...still.
now maybe just maybe, since we all have nerve damage, if we have our hearts tested maybe it is that the nerve is damaged and god knows we had cutting in that area....
i never had heart pains but breathing, and im sure implants caused that as we have patients that were on breathing macines and when implants and then later more slicone was removed they recovered completely off machines....
the darn things, make you whole body go haywire, thats why they think were nuts.
from one nut to another....
love angie
please see my new page, updating ongoing, will add getting well, and stories.There is info on SALINE HERE, AND MANY PHOTOS. check it out, look at links and pass it on. http://www.maxpages.com/implants
>hey taught me how to do carotid massage on my neck too.
I don't think this is something that is encouraged if you are not monitored. I may be wrong, but it seems like there is a possibility of loosening plaqueor "junk" that would go to the brain. The valsalva maneuver is safer.
In message-id: <19990224233200.17554.00003...@ng113.aol.com>, boone1...@aol.com
(Boone1289) writes: >>hey taught me how to do carotid massage on my neck too. << >I don't think this is something that is encouraged if you are not monitored.
I may be wrong, but it seems like there is a possibility of loosening plaqueor "junk" that would go to the brain. The valsalva maneuver is safer.<
SusanB, I forgot until I read Donna's post, that I was instructed to do carotid massage as well as the valsalva maneuver (why do I always want to call that the "Valhalla" maneuver? ;->). Nobody bothered to tell me about the release of plaque material, or that I should be monitored if I did it, but in my case it's a moot point, because carotid massage never did anything to help anyway...
Donna, thanks for the info re: Vasculitis. I don't know what exactly what ischemia is (although I've seen the word), but the context of the rest of the post helped make things at least a *little* clearer.
Paul, I think your potential research paper could be the beginnings of a "silicone-associated symptoms" clearinghouse! Whaddya' say, buddy? <loud butt-smooching sound> ;-)
> plaque material, or that I should be monitored if I did it, but in my case it's > a moot point, because carotid massage never did anything to help anyway...
This is always a concern with carotid massage, but if your doctor listens for a carotid murmur before doing the massage and he does not hear a murmur then the massage should be ok (unless the carotid is totally occluded in which case you won't hear a murmur even though there is a plaque there). The chances of having a plaque in the carotids are increased if you are male, have high blood pressure, have diabetes, are obese, and smoke. Regardless, valsalva maneuver and dunking your head in ice water are the safer options.
> Donna, thanks for the info re: Vasculitis. I don't know what exactly what > ischemia is (although I've seen the word), but the context of the rest of the > post helped make things at least a *little* clearer.
Ischemia is when there is not enough blood flow to a particular organ, thus the organ does not get enough oxygen or other nutrients.
> Paul, I think your potential research paper could be the beginnings of a > "silicone-associated symptoms" clearinghouse! Whaddya' say, buddy? <loud > butt-smooching sound> ;-)
Hehe. Well, I'll have to wait until at least the end of March before I find out if there will be any possibility for research.
Paul
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I received implants in 1989 when I lived in Los Angeles amid all the perfect looking women that wanted to break in to the movie business. I worked in a furniture store 12 hours a day, but wanted to feel better about myself in this atmosphere I got my implants in July, by October, I could not walk through this huge (60,000 sq ft) store anymore because "my heartbeat was all screwed up" with continuous palpitations and my knees would not allow me to walk anymore. I went to my general physician, who did blood tests and called me at work at the furniture store to tell me that I had rheumatoid arthritis and told me that there was no explanation for it because no one in my large family had ever had it and that there was no cure.
I have been experiencing these erratic heartbeats for almost 10 years. Without being able to affort health insurance anymore, I have continued to LIVE. My father died of a heart attack at about the age that I received my implants. Although the erratic heartbeat persists almost daily, it is very irregular and when I have gone to the doctor, an EKG proves nothing.
Had someone told me that my implants would cost me my $75,000 a year income, that I would never be able to dance again, that I could not walk the beach, and I would feel exhausted for the rest of my life, I would never have had the surgery. At the time, I was 36.
I know that it is from my implants. I worked a 16 hour day until I got them.. Now I can't work anymore, have no energy for anything and just wish that I could turn the clock back.
I received implants in 1989 <Huge snip> Now I can't work anymore, have no energy for anything and just wish that I could turn the clock back.
***I too wish I could turn back the clock, to 1980. All of us wish this, with the years varying from woman to woman. Don't ever think that you are alone in this. We are here, well some of us are here most of the time, that is when were not losing it, or forgetting what we were doing, lol :) So many women have experienced the same problems and the doctors can't find anything. I had a good friend admitted to the hospital a couple of weeks ago, they thought she was having a heart attack, after three days in CCU, they decided that she wasn't. They kept her in the hospital for a week then let her go, because they could find nothing. It would be interesting if someone would actually study us to get some answers. What a novel idea, don't you think, wonder why they have not done this yet?