Hi Again,
I am still being plagued by these new sensations and feeling quite fed up with it all!I am getting an unusual palp sensation that feels like it grips me completely,it isn't a usual palp I can ignor,it comes on STRONG and forces me to listen.I had a bad palp yesterday that afterwards felt like someone was choking me and I had alot of
pressurePressure ulcer in my
faceFace pain.My
faceFace pain was hot and very flushed as too my arms and chest.It then passed.I am fearing I am having a very bad new arrhymia of some kind.I have tested
normalNormal saline flush on
ecgEcg
Electrocardiogram (ecg)
Exercise stress test
Post myocardial infarction ecg wave tracings,
ekgAtrioventricular block, ekg tracing
Ecg
Exercise stress test,holter,bloodwork and stress test. Can I still be having a heart palp that is potientially fatal even after these good tests?Should I fear these new sensations?What should I do next?I went to the ER and had a 10 sec ekg that was good, but I also didn't feel anything unusual when it was on me.What do you infer about my situation?I am at the end of my rope and need some sort of explanation as to why I shouldn't fear dying from this.I am 23,female,normal weight & currently in councilling for my nervousness over this new sensation.I fear multiple pvcs and v-tach,since v-fib is a great rish at that point. HELP! Help me to understand my risks, what this may be(possibly,the chances that it is what I fear and why I should not fear dying from this. Thanks again for your time and I hope you can really give me some insight as to what to do next and what exactly is going on with my heart.I know you suggested anitarrhymics if pvcs effect my QOL. But if I can get past the stress, do I really need a drug like that?Wouldn't a beta-blocker be safer for me? Thanks again
I'm sorry to hear of your fears and frustrations, if it can be of any comfort I know exactly the feeling you're speaking of , getting that strong double thump followed by a redness in the face neck, arms and upper chest, occasionally your heartrate will also increase with this feeling.Sometimes a warmth feeling comes over your body, sometime it can actually cause you to shake, at least this my experience with PVCs and tachycardia. I'll be 42 in just little over a month from now, had these things for the last 25-30 years. I been on beta blockers off and on mostly on for over 20 years , first inderal, now I've been on atenolol mostly since 99. I take up to 100mg daily in divided doses. I hardly have PVCs now and no tachycardia whatsoever anymore.Beta blockers are very safe medications though not everyone can tolerate them, I'm lucky not suffer any side effects. I was advised by electrophysiologist never to take anything stronger than beta blockers for PVCs, I was also told that besides being uncomfortable and alarming,they are rarely a cause for concern. Also I know the very same arrhythmia(PVCs) can feel different, yet be the same arrhythmia, I found this out during a exercise stress test in which every PVC felt different yet it was the exact same PVC coming from the same location. Good luck and try to relax. I know its easier said than done , it me took 20-25 years to realise that worry over these things is unnnecessary though sometimes you can't help it and if you let it , it can rob you of happiness and enjoyment in life.I know it's impossible to ignore the real strong ones, but don't let the fear of them cripple you, just keep on going and you'll soon realise that in itself will probably lessen the sensation for you.
http://www.anxietypanic.com/
"The symptoms of a panic attack:
raging heartbeat
difficulty breathing, feeling as though you 'can't get enough air
terror that is almost paralyzing
nervous, shaking, stress
heart palpitation, feeling of dread
dizziness, lightheadedness or nausea
trembling, sweating, shaking
choking, chest pains, distress
fear, fright, afraid, anxious
hot flashes, or sudden chills
tingling in fingers or toes ('pins and needles')
fearful that you're going to go crazy or are about to die"
Just wondering if anyone has experienced a pac/pvc (not sure of the difference) which seemed to set off a rapid hb for a few seconds then a return to normal rhythm?? This is a new palp for me I've had pacs/pvcs and sinus tach in the past but the short run of rapid hb after skipped beat is new to me. I'm 32 y/o female, 8 months pregnant. Any info would be appreciated. Thanks. Jen
i see that others wake at night with these things too and also dream about them? that is so crazy, i really thought i was the only one!
tickertock, thanks again for posting so quickly. you all have helped me alot, i will try to stay strong!
Don't let the word scare you. It is not a med for your heart. You won't be depending on it...it just keeps it quiet.
In my case, the BB usually decreases the frequency of PVCs, not just the sensation. Maybe the BB's efficacy will also depend on the cause of our PVCs?
Good luck!
Fran
i felt as if i was going to die just now, got really hot, flushed, many breath taking palps...help...what to do
Like so many others here, I have had palps, PVC's, sinus tachycardia, and a bout of afib, at various times since 1992. The PVC's have all been since 2002. I swear I have had nearly every sensation one can imagine when these things happen...the hot flush, the icy chills (anxiety based), the choking sensation, terrible gastric distress, sob, etc. Also, my PVC's have been across the spectrum...one, bigeminy, trigeminy (at least once that I recall), and several couplets that scared the stuffing out of me. Literally left me weak, terrified, and hanging on to a chair to remain upright.
I have been tested from here to next year with about 15 EKG's, an echocardiogram, lab work, and chest x-ray. Last week, a THIRD cardiologist reviewed my records, pronounced me healthy, and wondered why I was so upset because everything was "absolutely normal."
If your workup was normal, as it would seem based on your comments, then I would strongly encourage you to take a serious look at what anxiety and panic can do to your health. I have struggled with these conditions for many years. At their worst, I am almost disabled. When they retreat for a while, life is dramatically better. Having said that, these conditions WILL grab you, hold you down, and have negative impact on your life. It is far too easy to become O-C about this subject.
If your doctor isn't worried, you should not be either. If you are bordering on frantic, please ask your doc about low dose beta blockers. They are not a big deal, and may well bring you considerable relief, as well as priceless peace of mind.
Take care and feel better soon.
There are several ways to deal with them. One is to do nothing, which means suffering a lot.
Two: You can try self-help books. An excellent, though old, one is Claire Weeke's excellent "Hope and Help For Your Nerves." I think there's even an audio version, and some people can talk themselves down from panic using her technique.
Three: You can try beta blockers. They may not change the frequency of your pvcs, but they may reduce your awareness of them.
Three: The simplest thing--and the hardest for many people--is to see a shrink. People often hate this suggestion, because going this route means accepting that the problem may be between the ears, and many would rather die than admit that. However, as I say, I've been there, and pooping around, hoping that a real heart problem will turn up, thereby dodging the idea of "mental illness," is pretty darn time-wasting.
thanks everyone, i will certainly be on here more and let you know what happens. thanks everyone, i will keep comin back to read about your own experiences.
I finally found peace about the palpitations when I found this wonderful forum. I too shared your fear of having some horrible potentially fatal rhythm. Even recently when I had a bad recurrence (they come in phases for many of us) I FINALLY caught the really scary stuff on Holter and it was ALL atrial, mostly singles with a couplet once. I get adrenaline-induced PSVT still, but usually fatigue, too much sugar, poor diet and lack of water play a role in that.
A couple of years back, I was so overwhelmed with a bad run of these things that it pretty much crippled me with fear. I avoided things I would have otherwise done and was just scared all the time. I was miserable. I was existing but not living. I guess I finally got to the point where I said to myself...what IS the point of existing if I am not LIVING? And I forced myself to get out of the chair, and I forced myself to start living my life again, and I forced myself to ignore the palpitations after numerous assurances that I was fine. I think you have to get tough on yourself too ;) I know, it's easier said than done, and it's easier from my side than yours right now. But believe me, you can beat the anxiety, and it's really worth it to have your life back.
A lot of us here have had these since our teens. I've never heard of anyone dying after being diagnosed with benign palpitations. Keep that in mind, hang in there, and when you're feeling doubt read the archives :)
http://209.51.172.19/forums/cardio/messages/35001.html
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I know how you feel about these damn things. I would recommend to you a program called "attacking anxiety and depression", which is a program started by a woman named Lucinda Bassett. I heard about this on the radio and checked it out. It is an EXTERMELY valuable tool in helping people deal with anxiety. She went through horrible anxiety and depression and got out of it and helps others do the same.
I've been suffering from anxiety and depression since I was a little kid, and have always been on meds. Now I'm off and I'm finding that the palpitations (especially what it seems are runs) are making it difficult for me to life to the fullest (sounds like it's affecting you similarly). I found the Attacking Anxiety program to be really helpful. It's like a 12 disc set and I've been listening to one a week. It's helping me alot, and you might wanna look into it. Don't be afraid to see a therapist - they teach many of the same coping skills that can be learned in Lucinda's program, and it's great to be able to talk to someone face to face. Also, as I've learned, it's best to make the effort to find a therapist who feels comfortable to you, and you will probably be able to determine that within a few sessions.
Good luck, and know that you are not alone in dealing with these symptoms.
I asked about this on another post, but you seem quite knowledgable about the palps. The other day (and this happened once before this bad, about a year ago) I was just sitting at my computer and out of knowhere I felt this adrenaline rush type feeling, which kind of knocked the wind out of me. It felt like a total flip flopping roller coaster feeling in my chest, and I immediately took my pulse, noticing there was nothing there (absolutely terrifying). Within a couple seconds, it was back, and my heart rate returned to normal.
Have you ever experienced this? They caught it on the event monitor and my PCP told me it was a "few beats in a row". Which is kinda vauge. I'm going to see a cardiologist finally (I can't wait, need some reassurance) and will ask him more in detail, but from your own experience or knowledge, any ideas what that could be that I was experiencing?
I took my pulse after the initial rush and didn't feel anything going on, definitely felt like a few seconds where my heart wasn't beating, then returned to normal. As it happened, it took my breath away, and I felt like I couldn't breath (actually, I was so focused on what was happening to me, I don't think I tried,lol). I felt a bit lightheaded (I think from the adrenaline sensation and accompanying anxiety) but did not feel at all like I would faint. I felt terrible the rest of the night though, because my anxiety was constant non stop through the roof.
I remember when it happened thinking "this is just like the big one I had last year", which they have on the event monitor recordings. I'm pretty confident that the type of palps were the same. The tech listening to the recording when I called it in said it was abnormal, but not dangerous. I was told that a cardiologist would read the event recordings and I would be notified.
My PCP called me in about a month after my study to look at the results and said everything looked OK, I had abnormal beats but not life threatening. I was not asked to come in by the cardiologist. I suppose this is probably a good sign, but since having another bad one, I need the reassurance that can come from speaking with a specialist.