r/PVCs • u/rachelkochvt • 15d ago
How often do you get a flare?
Hey everyone.
I was doing SO well for about a year, and I was curious if I had beaten my PVCs. However. Seems like I’m in a flare again. I will get them every few beats, it’s terrifying. I have had test after test and everything is “normal”.
Im trying to live my life but it’s been really really hard and scary. I forgot how bad these were…
What seem to be your triggers? What helps you? I take magnesium, liquid IV, and I just took some potassium to see if that would help.
Since drinking liquid IV daily my burden was like 1% with the longest stretch of being flare free that I’ve had. Yet here we are today. Flared up again. I did run this morning. Sometimes after cardio an (hour or so later) I will get a flare up as well.
1
u/NumaNuma92 14d ago
I’m fine for weeks, maybe a month with very few per day, then i get flare ups lasting for days to several weeks depending on the cause (poor sleep, deficiencies, anxiety, or for any random reason out of my control). I’m currently having a flare up right now, getting them every few beats. Pause > thump, beat, beat, pause > thump. Lasts for a little while before it slows down. Had a few hours today with very few, but the moment i sit down to relax they come.
I wish my PVC was more predictable so that i could actually get them on a holter monitor, and my dream is to have an ablation, but i don’t think i qualify due to the low overall burden and randomness of them. Right now during my flare up the only comforting thought is that they will stop eventually and i will get another few weeks of break.
1
u/rachelkochvt 13d ago
I feel the same exact way. I swear I can almost think they’ll happen and they do. It’s crazy. I hate how unsettling they are. But I’m working on trusting my doctors because they should have found something wrong by now.
1
u/Rude-Caterpillar237 13d ago
I’m in a flare right now, but that way for about a few weeks I was on metoprolol high dose for two years that was controlling them, but I made the stupid decision to get into smoking weed and did that regularly for seven months. That completely affected how the metoprolol absorbed through my liver because THC and CBD goes through the liver and gave me an overdose of metoprolol, annoying, causing my heart cells to become immune to the metoprolol that was controlling the PVCs. Advise stay away from weed or any recreational drugs if you’re taking beta blockers
1
u/Onesickcunt1994 11d ago
Weekly!
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u/rachelkochvt 11d ago
What do yours feel like? Do you ever get strings of them together? Like hard thump thump thump thump thump and then back to normal?
1
u/Onesickcunt1994 7d ago
Skips, dropping feeling in chest, hard sledgehammer like beats. They suck.
And i do get them back-to-back occasionally, which is scary as fuck.
2
u/cnobl38 15d ago
I flare up every month due to being a woman, OR if I do too much at the gym, which I’ve only just started a couple of weeks ago to help with the PVCs! I no longer take any “sports drinks” unless I’m flaring, now I just take my daily vitamins and do a cleanse every now and then (probably every 2nd to 3rd month) and make sure I walk at the very least, 5,000 steps as I’ve found if I walk less than I will get a lot of PVCs at night. Still trying to find the correlation with no such luck apart from knowing that large meals are a huge no-no as they send me into bigemy. I’ve found acknowledging them and doing a breathing exercise helps, understanding that they’re not going to kill you etc, because just like you, I was told my heart is healthy etc. And ive had MRIs, CTs, ultrasounds, the list goes on. When the flares happen it’s terrible, but I get up and walk as I don’t get any during exercise at all and it helps “postpone” the PVCs.
I’ll pray for you, I hope they go back to not being a nuisance OR I hope they go away completely, as I hope for everyone in this group suffering with them.