Hi Dave, yes have exactly the same problem. I was last diagnosed with my AF coming back earlier this year but (still) waiting for results of echocardiogram to see if I can go on to flecanade - so not sure even if I'm in AF at the moment! However, same as you, if I lie on left side (practically impossible) as feel/hear heart thumping away. Don't lie on my back anyway as find it impossible to sleep in this position. The only way I can eventually drop off to sleep is on my right side, sometimes holding a small cushion against my heart as it sort of muffles it, doesn't make the thumping so obvious. I am by myself so no-one breathing over me, unless you count the cat who ventures over sometimes! Hope this helps, you are not alone on this site. Best wishes.
I treat it like having a new baby in the house never know how many times it will wake you up or if you will sleep through the night most of the time don't have a problem sleeping can do it anywhere anytime
I can't stand being breathed on either. Somebody else I knew with this problem used to have a barrier of pillows down the centre of the bed to keep his wife's breath away.
Think it's pretty much across the board with most of us with AF
I used to be a bundle of energy but have turned very lethargic since I was diagnosed with it a couple of months ago
As a HGV driver I am not allowed to drive until my heart beats back in sinus rhythm and my doctor gives the DVLA the all okay
Awaiting Cardioversion which got cancelled for yesterday due to unforeseen circumstances ,now awaiting a new date
Hope that puts you0 a little at ease
Dene
Same here except my drugs control it. I can still feel it slightly but not much. Have you been prescribed drugs by an EP? Is it acceptable to have to put up with this at night, I don't know, guess we're all different but maybe another drug would work better????
When I had AF I had the same problem. Solution was to sleep supported with lots of pillows so was never supine. Took a little getting used to but improved sleep.
Have you been tested for sleep apnea? After successful ablation my EP referred me to Physiology for sleep study which showed sleep apnea. I now use a CPAP machine at night to support my breathing. My EP said it was the biggest culprit for AF returning after successful ablation and there have been studies which demonstrate a link between sleep apnea & AF especially at night.
I have constant AF too, I have always (pre AF) preferred to sleep on my right side, but don't have the issues you have on the left. I mainly (though much less since my first ablation) feel it in the chest and have referred to it as 'someone tap-dancing in my chest', when the AF is playing up it is worse on my back.
I have persistent AF as well (I had an ablation in March this year but reverted to AF). I have learnt to sleep on my back most of the time though sometimes on my right. I used to turn over onto left occasionally but generally woke very quickly.
Also once I get woken in night over half the time I find it is difficult o get back to sleep for at least an hour - sometimes two or more!!!
Worthwhile getting tested for sleep apnoea as it is apparently quite common in AFers. In my case only have it very mildly.
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