Hello there!!!
I must say i have read, many articles sent by the forums users, and it has helped me through many troubled times!!!
4 & half years ago i was at work, and experianced a fluttering effect in my chest area, this totally freaked me out!!
I went straight to ER and was realeased 1 hour later, the doctors said it was anxiety, i am a smoker so you can imagine when i got in the car, through the packet out and stopped
smokingQuitting smoking
Smoking - tips on how to quit
Smoking and copd (chronic obstructive pulmonary disorder)
Smoking and smokeless tobacco
Smoking hazards for 10 weeks, but picked the habbit up again, for about 6 months i could not figure out what was going on, i went to numerous doctors, but they said
panicPanic disorder
Panic disorder with agoraphobia attacks, obvisously this didn't help me enough, i was getting this weird feelings in my chest, i finally went to a Cardiologist who is very renowed in the country, he did numerous tests eg.. stress,
ekgAtrioventricular block, ekg tracing
Ecg
Exercise stress test, ultrasound,
thalliumThallium and sestamibi stress tests and
holterHolter monitor (24h) tests, he could only find that i was having pvc's and pacs, with bigemy and trigemny , but my problem here is that i get another feeling which is not a pvc or pac, but what i noticed the other day was when i get this strange feeling is that my rythym would speeden up slightly for a few seconds, and go away , my doctor says unless he can catch it on the
ecgEcg
Electrocardiogram (ecg)
Exercise stress test
Post myocardial infarction ecg wave tracings he can't pin point it, i have been on 50mg atenonol and 150 mg of avapro for 8 months now, i can't notice any pvc or pacs but still get this quicken beat which i can't figure it out what it is, i am 35 mildly over weight smoke half a pack of ciggarettes a day , non drinker use to have hypertension , overwise in very good shape, my question is would you have any idea what it could be???
and thank you!!!!!!!
Wow quick response!!!
actually i get a feeling in my throat area, i can feel the feeling creeping on!!!
my question is does this sound like something serious or life threatning to you????
mine are so unpredictable i get the feeling like i'm gonna die!!!
Its forums like this that give me some comfort, atleast i know i'm not alone, the thing for me is, i do alot of traveling and i always worry something catastrophic is going to happen like my heart will give in!!!
I have spent alot of time digging my head in books and on the net, I'm no doctor but i am starting to see that many of us who suffer these ill affects, nine times out of ten, have some sort of gastric trouble, there is alot of corillation between the stomach and the heart, espeacilly that they run of the same nerve system (vagal) i notice that after heavy meals and when i am tired, i am more prone to getting this weird feeling, the bad part of all this is, when i get these episodes my natural instinct kicks in ands starts to panic, its only the last few months , that i am conditioning myself not to freak out, probably you's guys would know, no matter how many doctors we visit, we are never content with there opinions, they look at me like a retard!!!!!
i hope that they will find a breakthrough for all of us, cheers!!!
Finally with the help of a very compassionate EP, I learned to manage the pvcs (not entirely, but to some degree). Last year, during an annual exam, the doctors picked up on a cardiomyopathy and determined it was a result of very frequent pvcs. To get the CM under control, my options were 1) try flecainide in the hospital; 2) try other anti-arrythmics; 3) ablation. I could no longer "live with it." Tried the flecainide and it really helped the pvcs, but the side effects were nasty. Tried rhythmol, and finally decided to give the ablation a try. For me, it worked miracles. If your doctor has determined that flecainide is safe for you, try to set aside your fears (I really do know that is easier said than done) and take "baby steps" to getting your life back. Does the flecainide help? If you trust your doctor and feel safe under his, talk with him about your anxiety. Over the years, I heard it a million times..."It won't hurt you," "They're benign," "Don't worry" and so on. I'm sure you can relate. It wasn't until I started seeing my current EP that I really, really trusted what I was hearing. It's not that she said anything differently, it's just that she let me know she understood and cared. If you feel comfortable with your physician, you will be more likely able to relax (even if it's just a little). Take care! Connie
Cardiomyopathy is a type of heart disease in which the heart is abnormally enlarged, thickened and/or stiffened. As a result, the heart muscle's ability to pump blood is usually weakened. The damage to the heart walls inhibits the ability of the heart to function effectively, which commonly results in heart failure.
About a year before I developed the CM, I was very short of breath and tired easily. Had a bunch of tests, and everything was fine. Kindof accepted it as a matter of fact. Still have thousands of pvcs....A year later, I was still tired and dragging a bit, but not NEARLY as short of breath. This time, my echo showed a drop in my ejection fraction (heart's pumping capability). That's when the CM showed up....So, because of the CM, my EP opted to treat the pvcs aggressively. I'm told that it is very rare for pvcs to lead to this condition. But, in my case...MANY docs and technicians concurred that is indeed what happened. The EP said I would have to be on antiarrythmics for life unless I wanted to give the ablation(s) a try. I was pretty chicken, so I opted to take the meds. Stayed on them for awhile and got up the courage to have the ablation(s)...and I'm so glad I did. Subsequent echos have shown steady improvement.
PS Thanks for Hank's email address. I'm going to give it a try. I don't know what happened to those threads but if you look back thru you will notice several of his last entries are gone. I for one miss his opinions. Thanks again!
i used get into the scenario as you, i couldnt go anywhere, when i first got these feelings, i had a world vaction organized with my gf, one stop we were supposed to go to was to climb Mt kilamanjaro, well as you all guessed that was "Totally" abandoned, and i only went to Europe instead, i tell you it was a "Nightmare" i had skipped beats, anxiety you name it, i was in places that if something happened they wouldnt find me for weeks, so you can imagine what was going through my head, i also still toady take Zoloft, i find it really helps me, but it takes time for the body to get used to, but it takes the edge off things, also i found that gaining knowledge about the problem, helps to deal with the situations, it gives me reasurance that i know i mostly over react, i was the same i could not go anyway unless there was paramedics near by, i now look at skipped beats and all over feelings like kind of a hiccup and when its done it will go away, i have had so tests, with some of the best doctors in this country, and they all comment that not to worry, i guess you really have to take the bull by its horns, or it will ruin you, you have to condition yourself, that you have nothing that is life threatning , and not to let instinct take over, i know this is easier said than done, but just remember there are people who are so sick on this planet that, they would "swap" places with you in a "HEARTBEAT" lol, so the point i am trying to make is, do you waste your life at home, or do you enjoy it?
I know you know the answer to that question!!!!
jobob52ford: Thanks for Hank's correct email address. I couldn't remember the "89" in the middle...
Has anyone talked to Hank? How is he doing? Please let him know he is missed on the boards. Notice the disclaimer that pops up now. Maybe that will quiet things down. Here's hoping.
I had 2 successful pvc ablations (one to right side, and one to the left side). I get an occasional pvc, but no runs, etc. Did the doctor mention why he felt they could not pinpoint the trigger spot (foci)? I remember just before the 2nd ablation my pvcs quieted way down (nerves, maybe). The doctor checked with the "ablator" (a different doctor) and she said that as long as I was having "some" pvcs they should be able to find the irritable foci. I was very fortunate in that the procedures worked! Are you near Cleveland? Hope you are getting some relief today. Connie
so my question is, how much of our issues are caused, not by our hearts, but our brains? it sounds like we are all going crazy with this, so maybe we were going crazy first and the palpitations just followed? like i said, when i am on the paxil 20mg, i feel fine. how do other people feel on anti anxiety drugs?
Anyway in answer to your question about anti anxiety drugs, I was prescribed valium and told not to worry so much! I took valium over a 7 year period popping a 5mg pill most days. Then I was hospitalized for a medical condition (not related to my heart) and didn't have access to my valium. I was waking up each morning feeling very nauseous and trembling and agitated feeling as if I was about to die, it was horrible. when I got home and was able to take a valium again I felt much better. I put the connection together myself and realised I was addicted physically to them. I stopped taking them and suffered the worst withdrawal symptoms for nearly 12 months, much worse than the PVC's which I still had anyway.
I strongly advise anyone against using anti-anxiety drugs for any length of time for PVC's, sure it helps your perception of them but its not a cure for them and the risk of addiction is always a worry. My PVC's actually settled down somewhat after I had gone through withdrawal and they are not nearly so frequent now. How wonderful is that blissfull feeling when the heart is quiet and beating normally? something most people take for granted and we desperately long for.