Well it’s nine years since my first brush with Paroxysmal AF (over indulgence on my 50th birthday!). Over the years, like many of you on this forum, I’ve read just about every article online as well as contributing to occasionally to this forum. I’ve had a range of drugs prescribed and changed over the years, from Carvedilol to Bisoprorol to Fleccainide, to now Sotalol. Also been on Warfarin, now on Apixaban. I’ve had about six DC cardioversions (my god they are the best thing when you wake up).
So why am I sharing this with you? Well I’m now at that next stage of this journey, which I remember reading about when originally diagnosed nine years ago. Had my first ablation (cryo) yesterday. I say first, as I know many of you have had more than one, so I know there could be more for me on the journey. I am just hoping that it helps ease the symptoms, as my last two AF episodes were awful. I know that some people cope well with PAF, unfortunately it always knocks me for six: I really can’t function. It could be because of my size; I am well over six foot, so I suppose if my heart isn’t working 100% then there is a lot of body to keep going on reduced power! Anyway, the encouraging thing from my EP is that he called me a “prime candidate for an ablation” so here’s hoping things improve after this one. At the moment I feel fine, a bit achy and tired, and have a massive bruise on my groin due to the cardio nurses having to massage the wound area as they suspected an early growing hematoma. All healing nicely now
I just want to say that this forum certainly prepared me for what took place, so I want to thank all of you out there as sometimes you are the only ones who really understand what I am talking about, and likewise I know exactly what some of you have been through and how you all feel. This AF club is one that none of us want to be members of, but we appreciate all the members that have been forced to join and welcome their support. So thanks folks!