i am a 26 yr old man who has just recently started having pvc's and pac's and
tachycardiaArrhythmias
Multifocal atrial tachycardia
Paroxysmal supraventricular tachycardia (psvt)
Sick sinus syndrome
Ventricular tachycardia. i haven't exercised because i get nervous when the palpatations start coming. it's been 5 mths since i have exercised well or regularly. i had
normalNormal saline flush echo, stress test (tredmill),
holterHolter monitor (24h) and blood work. i have a mother and sister who also have my situation with their hearts. there are days when they go mad, happening all the time and i feel them in my chest, that makes me feel like i will die. i saw my cardiologist recently for a talk and she said that i had nothin to worry about and that i should live a
normalNormal saline flush life.
1-when i drink they happen constantly...should i stop (only have 3 or 4 maybe)
2-i played softball this weekend for the
firstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 100
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First-testosterone
First-testosterone mc time in 2 years (tring to overcome my
fearsFears and phobias) and whenever i ran from 1st to home i got pains in my chest all across the front buy they stoped pretty soon after i stoped running (should this concern me?)
3-last night i got freaked cause on every hicciup i had i got a pvc, i felt in my chest and i could also feel a very long pause in my pulse...is there a risk my heart could stop on these long pulses?
4-i want a normal life, i want to exercise and be happy again. please help me to understnad why i shouldn't fear dying from this. i feel the doctor has meissed all of the palpiatations i have that are the ones that are dangerous. i think they missed something on my tests tat is important.
5-i am new to all of this and i don't understnad why i shouldn't worry about them, it feels really BAD and SCARY and my palps are very unassuring.
HELP
I also have pvcs with hiccups. strange.
Mine are symptomatic and somedays i cant even figure out where am.
If it means anything, I have had these darn things for 25 years now, and I'm still here.
Somedays I have thousands, others just a handful. I've also gone years with only very occasional PVC's, followed by months of daily (thousands) of them. Just Saturday night, I was in the ER again. I had bad sinus tachy (161 bpm)coupled with PVC's, and as always, I was assured that they are not dangerous at any point. The Cardiologist did however start me on a full month of Xanax therapy to see if that will get my system calmed down.
For me, stressful times brings them on, which in turn triggers an extreme adrenaline sensitivity. Right now, I can't even clean the house without getting them in the dozens to hundreds daily.
People with constant anxiety (a given with PVC's) can become adrenaline sensitive; their bodies experience unpleasant symptoms when their bodies produce any bursts of adrenaline. These symptoms often include heart palpitations, tingling, chest pain, choking sensations, etc.
Hang in there, I hope you get the answers you seek.
As you can see here at this forum, there are thousands of people just like you.
Relax. It's the trick when fighting off an adrenaline mediated arrhythmia. It works for me, and I play competitive soccer (where's there is definitely a call for at least some adrenaline).
-Arthur
I wanted to drop this linked it is very informative arryhtmia's, knowledge is power.
http://cvcheart.org/Arrhythmia%20%20booklet.htm
Brief history…
In Jan/Feb of 2006 first felt the sensation of PAC and went to see cardiologist. They did an EKG and general exam…said my heart was in great shape and that many people jus live with these. Mine seemed/seem not triggered by anything, but lying down, bending over seem to exaggerate them.
In March I had a complete workup (EKG, sonogram, stress sonogram, stress EKG, blood work, etc.)…everything came back great. And at that point I was no longer feeling the PACs.
Felt good through April…but then in May started feeling some tightness in my chest (left side only) and in my back. I started thinking the worst, but then talked with my cardiologist and they said, I was fine because exercise actually made the feeling go away. They were not worried about anything heart related.
Then in mid July (without having felt PACs for a long time) I rolled over in bed one night and went into A-Fib. I was not woozy or dizzy, but could tell that my heart was all over the place. I was admitted and they tried to medicate it, but after 12 hours they decided to electro-cardio vert me. They did a sonogram again and an endoscopy? (thing where they go in to look at the back of your heart) to make sure there were no clots. Cardioversion was successful and I have been back in sinus for almost a month. They had me on coumadin for a while (ended yesterday) and a calcium blocker. My symptoms now are off and on tightness in my chest and back, 5-50 PACs a day. I have been going on 2 mile runs for the last three weeks without incident…my heart feels great after a run…but these symptoms scare me…and I am scared of going back into A-Fib.
Then, last night I talked with my mom about it for the first time and got really scared b/c of this info. My grandfather died in 1992 from complications related to lung cancer. He was treated (misdiagnosed) for infectious disease for six months and then went into cardiac arrest because the cancer had wrapped around his heart. About three months after he got sick, they had to cardiovert him b/c his rhythym got out of wack. Ofcourse this scared me and made me think I might have a tumor growing around my heart that they have not scene or diagnosed. I don’t see how they would not have seen it after the endoscopy and electrocardiograms…but I still worry, especially since he was misdiagnosed for so long.
I called my cardiologist today to check that they had looked for that…but wanted to get everyone’s opinion…
Also, does anyone else notice PACs when they bend over, lie down, or just a general weird sensation in their chest?
thanks in advance.
According to him everyone gets them also, we PVCers are just overly sensitive to them. I guess I'm actually blessed in alot of ways as I have a Cardiologist that has hundreds of noticable PVC's himself, and therefore he has always been really sympathetic of my fears, but...he is also very firm and reassuring that they are totally benign in a heart without disease or structural damage.
BTW, he knew of this site and forum and actually complimented it's support factor. :)
thanks
thanks for the encouraging words. how similar is psvt to non-sustained vt?
last night was a rough one for me...felt like I was having a full on panic attack. I even had to call my cardiologist's PA (a friend of our family) at his home. He did a pretty good job of talking me down off the ledge...but it has been pretty scary. Going from a March diagnosis of "we don't see anything wrong, you are 100% fine"...to A-Fib episode in July...to them seeing PVCs and one instance of vt on my last holter monitor. The PA said it is nothing to worry about and that I don't need to worry about SCD...but so much of what I found on the web about it was really scary.
Just for the record...are there folks out there who have been diagnosed with non-sustained vent. tach. and just learned to live with it???
My palps seem to come and go...and while there were times when I had the monitor on that they felt like they were coming 5-10 times a minute, I never thought they were 3-5 in row...but like I said...they are not really worried, but want me to go see the EP so he can figure out a possible cause...I think I am just scared by it all...I have a wife and a young son and they mean eveything to me...maybe that increases my anxiety.
Another weird thing is mine don't seem to be anxiety induced...I have not been as panicky as I was last night in a long time...and I didn't have any that I noticed.
non-sustained v-tach is basically 3+ pvc's in a row, sequencial, with no normal beats in between. that sure can be scary i have never had that that i know of and i hope i don't. trust your doctor though, ok? he/she has studied for many years and if there was something bad about your holter readings they will surely tell you ok?
It's pretty obvious most of us if not all are on the same page with the same symptoms and same concerns.
I've been battling PVCs nearly my entire adult life, I'm 46...first noticed one rounding third base in a softball game in 1979.
I've decided to pack it in and get some more serious help beyond my generalized anxiety disorder med (buspirone not effective for me, really) and perhaps consider a beta blocker while getting another thorough checkup.
My doctor told me he suspects adrenaline...today has been a hell on earth, the worst day of my life with nearly constant PVCs.
I'm going to do WHATEVER it takes to knock this bugaboo out once and for all. Wish me luck, I'm goin' in!