I am hoping to get some help on this problem I have had for about 3 years. I get a strange feeling in my chest like I could feel each heart beat in my chest and it is very bothersome. My heart is not skiping although I do get that palpatations at times also,but this is more like energy jumping around in my chest. This is an all day thing I get for days at a time. Sometimes it gets alot worse after eating a meal. My heart will feel like it is racing but most times if I take my
pulseNeck pulse
Pulse
Pulse - bounding
Pulse - weak or absent
Radial pulse
Takayasu arteritis
Taking your carotid pulse it is 72BPM but it FEELS much faster. I have been for every heart test(
HolterHolter monitor (24h), 30 day monitor, stress test, echo) and the only thing they found was an elongated
mitralMitral regurgitation - chronic
Mitral stenosis
Mitral valve prolapse valve and trace
regurgitationAortic insufficiency
Mitral regurgitation - acute
Mitral regurgitation - chronic which they tell me both are nothing, is this true?? or could that be causing these feelings?
Also If I am sitting still watching TV my eyes seem to flicker along with each heart beat. I now this sounds wierd and I am hoping you may have heard of this before but it's like every time my heart beats my eyes
pulseNeck pulse
Pulse
Pulse - bounding
Pulse - weak or absent
Radial pulse
Takayasu arteritis
Taking your carotid pulse. My blood
pressurePressure ulcer is not high at all so I dont know why that happens. I am 31 female, not overweight, non-smoker. I also have days where I feel out of breath and a rapid pulse just from walking up a flight of stairs and the very next day I feel fine walking up the same stairs. I really need to know whats going on any ideas....thanks so much and have a Happy Thanksgiving Jean :)
I’ve suffered with PVC’s, or skipped beats, or palpitations….off and on now for a dozen years. In a good weak, I notice 1 or 2 PVC’s, in a bad week I notice 1 or 2 every hour all day. I’m recently divorced so the problem has once again reared its ugly head, worse than before, over the last two years. I don’t know exactly why I get them, but I do know that all the expected agitators make it worse; i.e., caffeine, alcohol, sugar, and most definitely stress. Whereas most of these we can control, stress has a mind and will of its own and is very difficult at times to manage; and then the PVC’s start and then the stress increases, and so on. Even without much stress, I have found there is a strong correlation between thinking and/or worrying about the skips, and there frequency. So, I try not to think about it all too much. Even when I’m in good spirits and I stop too think, “wow it’s been a good few weeks” I try to immediately think of something else. Do whatever you can to distract yourself when they occur, call a friend or family before you start to dwell on it, or do some stretching and breathing exercises, watch TV…get your mind off it. This is also recommended for your overall lifestyle, try to mitigate opportunities to sit idle and dwell on your heart and health. Keep yourself occupied and busy. An idle mind is the devils workshop. If you need to dwell on it, educate yourself on it with some good books or papers on it. Anytime spent idle, should be dedicated to some simple meditation, prayer, chanting…anything that helps but your life back in perspective. In those moments when you can’t escape, have some mild medications available (I keep some Xanax available, although I’ve had the same bottle for at least a year.) I feel a majority of my issues with the skips is related to my mental state (thinking about it, worrying, stress…). I also try to remember, as I’ve read often on this board today and have confirmed with my own medical tests, my heart is physically normal and these episodes are not likely to impact my long-term health; although if I keep worrying about it, my long-term mental health will definitely be negatively impacted. I don’t think I’ve read I single case where someone who went through all the appropriate tests and was diagnosed as having a benign arrhythmia, suddenly dropped dead after forgetting about it and going on with their life. It seems for those with an otherwise healthy heart/body, the problems relate to the nervous system, making it a mind/body issue and not something western doctors are very good at dealing with. Although it can be frustrating. So with that, I’m going to exit this site and go for a walk.
My Fraternal Grandfather died in his 40's, my dad has also had heart related medical conditions. Which he was on med's for, and just had a Cauterization to fix. Am I at risk, given the symptoms I have had and with the dull ache in my left shoulder area (between my collar bone and shoulder)?
Happy Holidays.....MrsLC
I too have many symptoms with my Mitral valve prolapse and can appreciate your fears. Many good posts replied.
Visit http://clubs.yahoo.com/clubs/mitralvalveprolapse2
We offer some support too.
Hopefuly you find comfort in reading the additional posts and continue to share.
I have had all the test too...... but I am still not satisfied that it is nothing .... if so why have I not had it before in my life....nothing has changed.....
I am new to this board.
I also seem to be suffering the same symptoms as you.
Lately, my heart has been beating faster than normal.
My resting pulse has gone from 60's to 80's.
Brisk walking will bring me up to anywhere from 100-120.
Lifting a light load up the stairs will also bring me to 120-130.
Afterwards, I become tired, and short of breath.
I've had all kinds of tests, EKG, stress, echo, CT scan, and they all come back normal.
Just yesterday, I started feeling this pulse behind (or in) my right eye.
I can induce this pulse in my eye by blinking or closing and then opening it.
I am a healthy male, 23 yrs old, with no family history of major heart conditions.
Just wanted to share.
Went to my doctor about it. Response: you're just aware of it now. His only question to me was if I saw it while "day dreaming" (staring off into space) or if I saw it while I was actually involved in something. I see it only if I force my eyes out of focus. But I always feel it!
Thought it had to do with sinus pressure (terrible allergies).
Thanks.
Shawn
I was prescribed either Xanax or the equivalent then -- don't know if Xanax was around in 1977. Every step I took, I was afraid of increasing my heart rate. What got me over it then, I don't remember exactly, except I got busy doing other things in my life and before I knew it, they were "gone."
Of course, the anxiety induced ones were gone. The normal flutters would surface here and there. During times of extreme stress I didn't have any! Not sure why.
I do know that relaxation techniques and exercise help. As afraid as I was to do any exercise (for fear of falling down dead in my tracks), it has helped reduce the adrenaline in my body. I had to admit to myself that I was doing this to myself -- creating the adrenaline and thus the rapid heart beat. I would tell myself "you're okay" and work through the exercises. Sometimes I would stop to really calm down, but I never gave up.
Now, I am 44 (so I am still breathing and on this earth) and I dance 2x week with my hubby, weight lift, walk, etc. Of course, I had all the necessary tests done with my cardio to make sure I could start an exercise program. My PVCs were termed benign (like you) and I was given the go ahead to exercise to my "heart's content" which I try to do as often as possible.
You are right: the mind is a powerful being. It is amazing how quickly we can have ourselves in a tizzy. But then again, we also have the power to calm ourselves down!
Thanks for sharing,
Beth
I am also experiencing some palpitations and pounding of my heart. I notice that it is greatly related to stressors as already mentioned by many above. My concern is this; my mother died suddenly a month ago of a massive heart attach, she was only 46 and it was not expected. This had mad these heart problem so much more appearent and worriesome. My mother had extremely high blood pressure and a very unlucky family history, both parents had quadruple by pass surgeries .... I currently have no other risk factors as I am very aware...I am a medical student. Even though I have no other risk factors, could these palpitaions be an early indicator of risk? I am so worried...
Thank you!
JJ
Sorry to hear of your Mom. That's stressful enough in itself.
If I had your concerns, especially since you have heart issues in your family, I would go get checked out. If there's nothing there, you have peace of mind. If there's something there (and I doubt it from what you're saying), you can take care of it.
For me, the not knowing is worse than the knowing.
Keep on reading these posts. There's a lot of information here.
Beth
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Yes, I suspect 90 percent of the PVC and PAC's sufferers experience these rotten BUMPS while lying down; whether it is in the evening or after a (BIG) meal.
It's got to do with the nervous system.
I know the tissue surrounding the heart gets irritated by something...ie. The stomach, the lungs, the bowels,the esophaegus etc etc.
...anything down there...
You can find much more info here by looking through the posts on the archives.
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I'm not a med.person mind you! Go see your MD if you stay concerned.
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Good luck - *Ianna*
For remarks regarding my experiences and knowledge I have gained about heart murmurs and PVC's/PAC's, please refer to my comments under the category "PVC's and Murmur". Thanks. Veepster
It's getting better but I still don't feel 100%, possibly 85-95%. My pulse is back down to around 70-80, and I can breathe easier. My twitch in my right eye is also gone. But somehow I still don't feel as well as I should. It's been a few months since I've felt like a normal human being should. There's always this pressure inside my chest at certain times, and I always feel gassy inside - when I burp it out, it provides temporary relief until the gas builds up again.
I'm also afraid to do cardio exercise, or any exercise, in fear that I might drive my heart crazy and drop dead.
I also read on another forum about someone seemingly in good health (non smoker, not overweight) who didn't naturally create enough amino acid to clear cholesterol and ended up dying suddenly from a heart attack, and that scares me.
Anyway, just thought I'd share.
At the age of 65 I have started suffering missed/skipped heart beats. All tests, including ECGs (both types) and blood tests have shown no abnormality. The condition appears to be present mostly all the time - more noticeable when doing nothing or trying to get to sleep. Some discomfort in the chest. Doctors have told me not to worry! I am a verious anxious sort of person! Should I ask for further tests or wait till it gets worse? Any comments from others with similar problem.
You mentioned that you had two types of ECG's....Did you have an echocardiogram also? If you have had the "standard" tests and the doctor is not concerned, you are probably experiencing pac's or pvc's and fortunately, they are benign. But, that is not to say that they can't feel awful and make you extremely anxious. There are many of us here on the board who can relate to your anxiety. You will almost always notice them more when you are quiet (ready to go to sleep, watching T.V., etc).
Echocardiograms and monitors (holter, event, loop) are great tools to assess what is going on. Has your doctor been able to "see" or "hear" the activitiy that you are concerned about? If so, and you are still getting a "benign" report, then you may ask about a beta blocker. Sometimes they help to stop or slow down the frequency of the extra beats.. Good luck
connie
Thx
wasser
SAID PERHAPS IT IS STRESS SHE PUT ME ON ZOLOFT AND FOR 2WEEKS NO THUMPS BUT WAM!!! THEY CAME BACK, I JUST WANT TO FEEL LIKE MYSELF AGAIN. YOU KNOW WHEN YOUVE BEEN SUCH AN ACTIVITE PERSON GARDENING, BRICK LANDSCAPING, SPORTS AND BUSY TAKENING CARE OF THE KIDS I JUST FEEL LIKE A STRANGER IN MY OWN BODY, COULD THE TESTS NOT SEE WHAT THEY SHOULD BE CATCHING, SOMETIMES I FEEL LIKE I AM LOSING MY MIND, ANYONE-PLEASE HELP-THANKYOU
DAVE
I am new with the Forum. I have what one EP doctor called 'idiopathic ventricular tachycardia', which started a few days before my 35th B-day (March 20). I always knew that I have a irregular heart beat, but this one Saturday while were at work, my heart was pounding away in my left ear. The condition persisted, but was too late to see my doctor. I waited until the following Monday. After my doctor saw my EKG, he called the ambulance. On the way to the ER, the paramedics gave me some Lidocaine, which worked almost immediately. All sorts of machines were alternately used on me while in ER, including X-Ray, and ultrasound. Only a minor heart murmur found. I was admitted into Garden Grove Hospital, while an EP doctor (Kelly Tucker) prepared more paperwork for me to be transferred to St. Joseph Hospital. I did not remember how viles of blood were drawn, and how many tests were done on me at GG hospital. All come back excellent.
I were transferred to St Joseph after 1.5 days at GG hospital. Dr. Tucker explained to me the EP study procedure, as well as the ablation, which he fully expected to perform following the study. Another cardiologist was there with Dr. Tucker, and performed the aniogram, which again yieled excellent result. The EP study went well with my condition being an inducible one. However, Dr. Tucker could not find the culprit and decided to withdraw without an ablation.
The next morning, Dr. Tucker informed I and my wife about an ICD or perhaps some beta blocker. He set an appointment for my visit after 2 weeks. Upon which, my 'idiopathic venticular tachy' was confirmed. Furthermore, Dr. Tucker prescribed some beta blocker and asked to see me every 6 months (I think out of curiosity). He informed me that he see thousands of patients every year, and my case is extremely rare, which he encountered less than 1 every 3 to 5 years.
Idiopathic just simply means 'unknown cause'. I seeked council from another EP doctor from UCI, Dr. Broadski, and a Cardilogist Dr. Vinh-Khiem Nguyen. Both Doctors did not seem to give much credit to Dr. Tucker EP study. Both recommended their own EP study. I requested my medical files to be sent to both Doctors prior to my visit. However, Dr. Broadski did not care to review any finding from Dr. Tucker, while Dr. Khiem Nguyen did not receive my record.
Since then, these episodes returned around my birthday once in 2000, 2002 and last night (March 18, 2004). I drove myself to the ER in 2000 and checked myself in. The ER doctor did not believe me that it is VT and not SVT. He insisted to try Adeavocard 6 mg, then 12 mg without any affect. I informed him that Lidocaine worked the first time (1999). 75 mg of Lidocaine did the trick within less than a minute. The episode in 2002 seemed to be triggered by mild dehydration. I continue to drink water for 1.5 hours upon confirmation of my tachy, using my heart monitor (ECG). By the time I got myself outside the ER, my heart rate had converged back to normal. I hang around the parking lot for 15 minutes, before drove home.
Yesterday was totally new for me. I exercised during lunch, with 10 minutes on the elliptical machine, 10 minutes on the stationary bike, some light sit ups and weight excersise, followed by 10 minutes jogging. Everything went well and I felt great. I got back to my desk at 1:00 and around 2:00 I noticed the onset. I drove myself to Garden Grove Hospital ER and were confirmed a 200+ tachy condition (3:00). Dr. Sun took my advice with the Lidocaine and I was administered with 100 mg. Thing did not work as expected. I requested for another dose of Lidocaine in less half an hour apart. The second dose seemed to stay in my system 5 times longer with a much more hard hitting side affect (heavy headed, short breathness). Adevocard 6 mg then 12 mg were administered shortly there after without any affect. A cardiologist was contacted and Amerodione 150 mg was given, which brought my HR down to 150. Sometime in the next 2 hours, ASA 162 mg was given, but my HR steadily climbed back up to 190. Dr Luc Nguyen, an EP doctor finally showed up, and prepared to shock me. I signed the consent and all the nurse and doctors standing by for the procedure. As the last ditch effort, Dr. Luc Nguyen ordered 5 mg of Virapomil, which promtly converged my HR down to 100. I was spared from the shock treatment with this last drug.
I am in the process to request for my medical record from St. Joseph (my EP study) and hopefully find some recommendation from Dr. Luc Nguyen. Is there anyone out there with 'Idiopathic VT'?
Thanks for reading my story and look forward to hear some respond.
Thai