What is Atrial Fibrillation AFib
Atrial fibrillation (AF or afib) is an abnormal heart rhythm (cardiac arrhythmia) which involves the two small, upper heart chambers (the atria). Heart beats in a normal heart begi...
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Atrial fibrillation (AF or afib) is an abnormal heart rhythm (cardiac arrhythmia) which involves the two small, upper heart chambers (the atria). Heart beats in a normal heart begi...

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Hi there,
I was going to reply to one post I read here....then I read another and wanted to reply....then another! So, I thought I'd just put it all in an introductory post. I have looked at a few AFib support forums but this one seems to be more practical than the others. I am in the United Kingdom and am 48 years old. I was actually first diagnosed with AFib when I was approaching 40 but Drs now accept that symptoms I have had since I was a teenager were down to AF. This included what they think might have been a TIA when I was 32 - I lost my vision whilst driving after palpitations in my chest for some time beforehand (I am grateful to still be here to tell the tale!). I did undergo significant tests at the time but it the episode remained unexplained. Since teens I have had occassional fainting - especially when getting out of bed and what I thought were palpitations. I was a sportswoman back then and although it didnt hold me back, I did notice that often I would be out of breath quicker than anyone else and it would take me longer to recover after strenuous activity. About 10 years ago I got out of bed, felt dizzy and faint and felt the 'mammal' flapping in my chest. However, I felt worse than any time before and drove myself (eek!) to the local hospital where they wired me up. The Doctor was amazed looking at my trace and refered me to specialist where I got the diagnosis of Paroxymal AFib. Since then I have tried a few meds (flecanide & sotolol) but felt so ill on them I stopped. Since diagnosis I have been sensible and never drive if I feel an episode coming on (inconvenient buy I have a supportive husband as a taxi driver!) and have made lifestyle changes to help but the meds werent for me and I have just tolerated my AFib and the restrictions it sometimes places on you. About a year ago my AFib, which I just put up with, got considerably worse - for no apparent reason. In Nov 08 it was so bad (fatigue, breathlessness, dizzy etc), with almost daily long episodes that I asked for an ablation (PVI), which I had on 14th Jan at QEH Birmingham. I had some complications (damaged an artery at groin entry site) and I had to stay in hospital for a week. However, I havent had an episode since the procedure. I hope this is a good sign but I have been off work at home doing very little since the procedure. I worry that once I go back to work this next week and return to my active life that my AFib will return as I expend more energy - my cardio said I have a 50% chance of having to have a 2nd procedure. He used a word to describe my veins but I cant for the life of me remember what it was! Another point of interest is, for reasons I wont go into here, I lost contact with my brother when I was in early twenties. I was reunited with him in 2006 where he told me that he had paroxymal Afib for some years and that he had a TIA in late 30's. I know one case doesnt make AFib automatically genetic, but it seems more than a coincidence, especially us having it so young (he's only 18 months older than me). Looking back, I have been my own worst enemy, almost in denial about sysmptoms. Had I been more open about them to medical professionals (severity, frequency & impact) then I might have been diagnosed earlier. But general practioners werent really aware of AFib then and I certainly didnt want to make a fuss. Apart from the damaged artery, my ablation procedure was fine. Although, because I was in AFib on admission and on morning of procedure, they said they would only go ahead if they pushed a camera down my throat to check not clots present. I wasnt expecting this and it was much worse than the ablation! - nasty stuff they spray in your throat before insertion!! I was told I had a lot of burns but felt absolutley no pain or discomfort in chest and still havent. Good lord, this has turned into War & Peace! Kind Regards. Posted on 02/01/09, 03:02 pm |
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Hmmm.... maybe I spoke too soon about my hopes after my PVI. I had a few skipped heartbeats Sunday night and a short period of AFib and today it started at 2pm and was still going at 6pm. It's intermittent now but still definately there :( My husband and I are really disappointed. Maybe we got our hopes to return to a normal life up too high, or maybe this is just a blip and its too early days to tell but it's disappointing nevertheless.
Hey ho, snow permitting, I return to work tomorow. I decided the best thing I can do is to keep a note in my filofax of episodes but other than that, just to forget about it for the time being. Then, when I see cardio I can recall to him precisely what's been happening (rather than the old me who would minimise everything and just say "oh just a couple" and "I'm fine" when in fact it was every other day leaving me feeling like cr*p). Regards to all.
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Are you on an event monitor? I was put on an event monitor when I was released from the hospital after my a-fib & flutter ablation for a month. I also had two episodes about 2-3 weeks after my ablation. My EP told me this was common because your heart has to heal. My episodes were recorded on the monitor I was wearing. It has been a year since my ablation (I had mine done on 1/23/08) and I am now enjoying wonderful NSR. I did have alot of pvc's and pac's for a couple of months after the ablation put that has calmed down also. So be patient and give your heart time to heal. Have you told your EP about the episodes you are having?
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Hi Jbtwin,
thanks for your encouraging reply. No I am not on an event monitor. I was on a full cardio monitor for a week after ablation whilst I was in hospital and all was quiet. I have made appt with Dr on Monday where I can discuss these episodes. I have had this bout of arythmia since 2pm yesterday and its still with me at 7pm the next day, although its not quite like it was before the ablation - not so noticeable (small fish flapping in my chest as opposed to a dolphin!) and heartbeat not quite so rapid, but I felt dizzy getting out of bed this morning and although I went to work, I kinda wish I hadn't. I may sound like an idiot here (given how long I have had this condition!) but what do PVCs and PACs feel like? Did yours go on for long periods? I promise to be more patient! I guess it took me so long to give in and have this procedure, I maybe am expecting too much too quick. Thanks again :)
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It took me over 2 years to finally have my ablation. I was too scared to have one so I tried every med before I had mine. PVC'S or PAC'S feel like skipped beats. I did have them a couple of days all day long. Now I get them every once in awhile (I will go for weeks without any) and they usually only last minutes.
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A update - life has been so busy but AF is a constant niggle. I have been booked in for a 2nd ablation on 12/08/09. Since the first one (PVI) on 3/01/09 I have remained on Cardicor (Bisoprolol) and warfarin and am still having the odd episode. At the time of the first ablation the consultant told me that I would probably have to have a second as the success rate for my condtion (lone paroxymal AF) was only 50% at the first attempt, but was 75% on a 2nd. I agreed to the 2nd abaltion beause I want to get off the medication but I was surprised at how matter of fact my consultant was about it and am wondering if I should have thought more carefully about it. I am so much better now than I was but I can't help but want to be free of it completely - but at the same time I do not want to create other problems later on in life.
Life is never easy!!
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Hi Yqueque,
great that you are off the meds, that's what I am aiming for - well done and hope things continue positvely for you :) My upper leg and groin area went purple after the first one as they nicked the artery causing an aneurism but the chances of that happening again are remote. I was in hospital for a week because of the bleed but am hoping for the usual overnight stay this time. I am heaps better after the ablation than I was before it but I want to be rid of the medication regime. I shouldnt complain because in the big scheme of things it isnt really a biggee but I do sometimes feel it all dominates my life - taking the drugs, having the INR tests etc. Hope you continue to do good! :)
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Thanks Jbtwin, i'll post how I get on :) It's funny, when I first researched AFib quite a few years ago when first diagnosed, ablations (I think we all referred to them as Maze procedures then) were cutting edge new technology and I was far too scared to have one even privately. Within a few years I am getting a second on the NHS in England within 6 months!
Health and happiness to all :)
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Hi Lesley:
Our circumstances sound similar. I did have to have the second ablation and they said the atrial fibrillation had "broken through" around two of the pulmonary veins. I think they meant that the scar tissue had not held back the wrong electrical impulses. My father had atrial fibrillation in an identical course, starting at the same age that I started mine. I am sure it must have a huge genetic component. I was a ballet dancer and they do say a lot of athletes have this but I wonder if it isn't that they notice it more. I don't know. Anyway, good luck with ablation #2. So far, so good for me, I see my doctor on July 9 and he wants to start taking me off of Sotalol. This will be less than three months from ablation #2. Does anyone know, is that too soon?
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