Oh dear- I replied to a post instead of typing a new post so here we go again! Good start!
Your posts and replies really do help me through days when my PAF rears it's ugly head and I'm not quite as frightened by each episode as I used to be. Over the past twelve months my episodes have crept up to approximately seven a month - very irregular heart beat with ' jumping frogs' but never very fast. I am on medication but am reluctant to take up the offer of ablation as many of you describe your post ablation 'angry' heart symptoms as worse than mine are now. I don't really want to make it worse before it gets better, if you see what I mean!
I'm paying to see my EP privately in Leicester next week as several of you have said this was worth it's weight in gold. I've only seen members of his team in Outpatients and the lady I saw in December was useless-total waste of the four hour round trip.
So, should I opt for ablation and cope with the consequences or hope the EP will take an interest in my medication and maybe make a few changes ? I would appreciate your comments.