How to exercise/keep fit when you have Paroxysmal AF?

Posted , 4 users are following.

I was quite fit before being diagnosed with AF - walking, gardening, playing table tennis, using a cross trainer at home. I'm 67 and having AF has very much reduced my level of activity. Only yesterday I went for a gentle walk with a friend but after about 20mins went into AF/palpitations, had to sit on a seat while she went back for the car. So frustrating. Has anyone else got any tips how to maintain fitness when activity brings on AF/palpitations with dizziness, nausea etc Thanks Maggie

0 likes, 10 replies

10 Replies

  • Posted

    Hi Maggie, Lanky lass here, I just saw your post, I haven't got any tips, but would, like you appreciate any out there. I am newly diagnosed (a little over 2 weeks), and am in AF all the time, I can feel a little bumpiness in the daytime but not much, mostly at night where I have found it a struggle to settle. I am on bisoprolol and think that these do slow me down quite a lot, I have only to walk upstairs or go a little faster than my usual snails pace and I can feel that breathlessness in my chest. However, I have not had  AF palpitations, probably because I have them to a small degree all the time. I am not sure whether or not in my case I would go into anything more than I have already got. How long have you had AF, I found this site nearly a fortnight ago, I have found the replies really useful, and humerous too. I see my cardiologist in about 8 weeks time probably to discuss the options open to me, maybe I will stay on medication, not quite sure what the future will hold. Am going on a walk later today, about 3 miles but mostly flat, will let you know how I do. Cheers, 
    • Posted

      Hi Lanky lass, Great name by the way! It's so nice to connect with others who are going through similar things. I started having AF about 10mths ago but didn't know what it was. It's only been in the last month that it's been happening most days for about an hour and has become a problem, so I feel fairly new at all this too. My GP tells me to exercise/cycle for my arthritic knees but as any activity seems to bring on dizziness/fainting it's impossible and frustrating. Maybe they haven't found the right combination of drugs yet!

      Will be interested to know how you get on with your cardiologist. I find magnesium supplement helps me sleep better and from what I read it also helps arrhythmias - so here's hoping! Hope your walk went well.

      Stay in touch, Cheers Maggie

    • Posted

      Hi Maggie, What medication are you  on? When I went into A&E,(pretty sharpish too) I had a really erratic and fast heartbeat that seemed to come from nowhere, but in addition my Blood Pressure was through the roof, probably due more to anxiety as in my 64 years, (just), I have never really had anything wrong with me. I suppose the ECG showed the irregular heartbeat and the BP monitor showed unusually high BP. Apparently high BP can be a trigger for AF but so can alcohol, chocolate, family genes etc. I was given Bisoprolol to slow the heart and in turn lower the BP and warfarin to thin the blood and dispel any clots. The first few days were a real worry and the palpitations felt really loud, I could almost hear the 'knocking' sound in my chest. It seems to have settled quite a lot now although night time is the worst. I went for a walk today, about two and a half miles mainly on the flat, I was really pleased that I only felt breathless climbing over where the motorway bridges linked the fields, (I was not scaling the bridges!!!). My friend, (who is only 55) was diagnosed with AF last September, her GP did not put her on betablockers or warfarin, instead she has asprin and another tablet, (perhaps she did not have high BP like I did), she, like yourself, goes into AF at odd times, once she was just reading a book on a hotel balcony and it happened. Now that I am on medication I am not sure that I will get 'bouts' of AF as I seem to be 'in AF' all the time, I am keeping my fingers crossed that it can now be controlled. Some people have posted that certain things have helped, someone said that vitamin D helped them although I have read that in fact it can cause AF, others have enthused over bananas, they are high in potassium which helps the heart and you have just said that magnesium helps. I suppose that none of these can do any harm and the body is a marvellous machine which can respond to all sorts of things. Anyway, keep posting. Cheers, 
    • Posted

      Hi Lankylass,

      I'm on Bisoprolol 7.5mg, Digoxin 125mcg, aspirin 100mg, Atorvastatin 40mg. I think everyone's AF is so different that no two people seem to be on the same cocktail. When I have an episode of AF my BP swings wildly between say 210/100 and 85/50 over a few minutes, I think this may cause the awful symptoms I get. Yes palpitations can be very disconcerting/frightening, so I imagine your sleep is affected by yours? I wondered whether anyone had suggested cardioversion to you as they seem to use that on people with permanent AF to get them back into sinus rhythm, maybe your cardiologist will.Yes I heard about the Vitamin D and have started taking supplements of it - I'll give anything a go - well almost!! I guess you have to be sensible and not take anything to excess but most of the pills we are taking cause side effects so I feel I have nothing to lose.

      Keep well, cheers Maggie

    • Posted

      Hi Maggie, Wow, that's a cocktail and a half eh? I wonder with all that medication that you are still having episodes of AF, I was under the impression that the beta blocker would slow the heart down and keep a steady rhythm, (also regulate the BP). I am fairly new to this game, 18 days since my initial episode, I am sure that when I see my cardiologist, (a Mr Gray, who works at the Royal Oldham Hospital), he will brooch alternative procedures with me. I seem to be in permanent AF, I can fee it now as I write this, it doesn't really bother me much at the moment when I am busy, just when I am settling down to sleep, or to have a doze, then I can not only hear it but feel it. I have heard that the cardioversion where the heart is shocked back into rhythm can work for a while but quite often the heart goes back into AF. I really don't fancy the catheter ablation, (is that how you say it) a friend had that at a BUPA hospital and was on complete bed rest for weeks, it was supposed to be a 'simple' procedure but a few of us at the time think it went wrong and she ended up with an infection and loads of other problems, so no thanks. My cousin has had AF, although a slow irregular heartbeat, he is in New Zealand, and is 70. but a very 'young' 70, he drives a but to and from a residentail home to take 'the old people' to and fro, ha ha., Anyway, he has been given a pacemaker and is fine, feels great, so I suppose that is another option, wonder if you have been offered that one?? Well, I am just going for a little walk, had one yesterday, (just had a conversation with Jesse, she is also a newbie on this site) and told her that I did quite well not getting breathless. Hope you have a good day and perhaps a nice glass of Rioja later!!!
    • Posted

      Hi Lankylass,

      No a beta blocker just slows the heart rate and then your heart doesn't have to work as hard so your BP goes down too. Antiarrhythmics like Flecainide and Amiodarone control the rhythm of your heart to keep it in sinus rhythm but they generally have more side effects also. Yes from what I've heard cardioversions only seem to last a limited time for most people. Your friend had an unfortunate experience with the ablation, I think the risks are generally quite low. I've been investiagating ablations but my cardiologist said I was too old at 67 and anyway I would have to try all meds first, like antiarrhythmics.

      Very interested to hear about your cousin as I too live in New Zealand - Nelson, could I ask where he lives? Pleased he's found a solution with a pacemaker, would be interested to hear more of his story. It's nice and sunny here even tho we are in the middle of winter so may try a slow, flat walk. Cheers Maggie

    • Posted

      Hi Maggie, My cousin, (female and 71, lives in Auckland, moved from uk in 1976), she developed AF, (sporadic) a couple of years ago and is now on a beta blocker,they did put her on warfarin but she asked to come off and is now on another medication, I can find out what it is. Her husband, a little bit older, started with AF last year, in fact they found he had a very slow heartbeat, it was down to 37 bp minuts. In the end they gave him a pacemaker and he is fine, he drives the mini bus at a residential home and takes the 'old people' to their hospital appointments!! No really, they both walk miles and are great examples of being very active in later life. Neither have any repeat AF bouts now. I have been over twice and love it, up to 90 mile beach and all round North Island, would love to do South Island at some point. Just back on to the AF, I have actually been ok on my bisoprolol and warfarin, in am in AF all the time, I can feel the bumpiness especially at night. However, last night I did have a frightening episode, I thought that as I have the beta blockers my heart rate would slow down and be fine albeit bumpy. I had gone off to sleep fairly quickly at about midnight, a miracle in itself as my sleeping since this has not been good, I woke up about half one, not with a start or anything, just woke up, then my heart was really racing and banging, I must admit I was frightened and tried to calm it down by just lying still, it lasted for the best part of an hour, I  think eventually I dropped off and woke up ok but I did not really expect that because being in AF all the time I was not anticipating getting any fast heartbeat episodes. Hope that it will remain calm tonight. Been on a 3 mile walk today round Hollingworth Lake, Rochdale, not far from where the Tour de France was last week, very sunny but a bit dull now. Cheers.
  • Posted

    Hi Maggie in answer to your question about how fo you maintain fitness with AF - everyone is different and needs to find their limit with exercise, by that I mean, try and do your usual exercise and see how you feel, if you feel as rough as you do sitting on the sofa, then go out for a walk - that was my mantra but I can be very bloody minded about exercise as I know it is good for me and it makes me feel good... so, for me, I can walk for miles with no hills during an AF episode, hills are a bit of a pain and will hurt my chest and back a bit but sometimes that can't be helped - depends where I am on a walk of course!

    Over the years I assume that I can do what I want to do and if it doesn't work out then I return home.. I had too long of not doing stuff just IN CASE I had an AF episode, it doesn't rule of life anymore, I have had it on and off since 1994 (I am 53 now) and am two ablations down the line and each one has given me much improvement, so much so I am having a 3rd next month as my consultant believes that he can get rid of it for me - the success rate increases with each ablation because of the nature of the procedure.. next month's ablation is called 'top up' ablation so only a little bit of work should be done and I think it is worth the risks to rid myself of this embuggerance in my life once and for all..   I notice you say that you get dizzy, is that when your heart goes really really fast?  I get that very very occasionally where I do feel I am going to pass out but a big clonk of the heart and it goes back in to normal rhythm and I have never ever passed out, which was a factor in encouraging me to get on with my life.. I never feel nauseas either, I wonder if that is the medley of drugs that you are on?

    I am on nothing at the moment, but about to start one of the alternatives to warfarin 5 weeks before my ablation.  I wish you well in your quest to refind your fitness and to enjoy it.

    • Posted

      Hi Susan I know that you were speaking to Maggie not me, I have spoken to Maggie about her AF and her treatment, I was asking her about her medication, I think that she wanted to know about excercise. I am interested to hear about the ablation you were given. A friend of mine had one ablation treatment at a BUPA hospital last year, I think the treatment went ok but she got an infection and was on complete bedrest for weeks. I didn't realize at the time that I too would be diagnosed with AF, (18 days ago) too. I am 64, (only just). You mention that thes ablation treatments seem to run concurrently and that they work 'a bit at a time', I am seeing my cardiologist for the first time since hospital discharge in about 7 weeks so perhaps I will be offered this treatment, or maybe the one where they 'kickstart' your heart rhythm, or indeed a pacemaker. You sound like you are taking the proverbial bull by the horns excersice wise, good for you. I missed my walk today due to a family BBQ, rats!! Everyone was having a drink in the sun, except me, I was driving!! I am going to have a beer later when the footy is on. Thanks for your help, as Jesse said in her post, all these postings are really helpful, they are not full of 'doom and gloom' as some blogs but full of useful advice like yours. Thank you.
    • Posted

      Thanks Susan for giving time to answer my message. I am gradually realising that I can't let AF rule my life but I think for me the nausea and feeling that I'll faint are a combination of the medications and the palpitations - hard to separate the two. My heart rate doesn't go hugely fast but I think that's the rate control meds I'm on which therefore cause fatigue and breathlessness. It seems somewhat of a vicious circle! I've been refused an ablation due to my age (67!) despite being quite fit but am thinking of getting a second opinion. Sounds like ablation has helped you? I'm off for a walk now I think and will remember your words - I live in New Zealand by the way in case you think I go walking in the middle of the night!

Report or request deletion

Thanks for your help!

We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.