I went back to the doctor's today, for my check up - a month after my second AF attack (no more in between, thankfully). I went armed with lots of useful information on anti-coagulants thanks to this website, and about my family history of AF. I was hoping I could persuade the doctor to put me on Rivaroxaban.
Fat chance, as it happens. As I now have recurrent AF he had in fact decided to put me on an anti-coagulant. Because I am low risk, he said, I could take aspirin. I said helpfully that people on the AFA website tend to spit on aspirin (mostly because it's not an anti-coagulant, but you would think he would know that). However, I am but a patient and he is the Doctor so aspirin it is, apparently.
Even if I were to continue to get AF attacks I would be put on warfarin, he added, not one of the new drugs. Our health board apparently doesn't do new drugs (thank you, Betsi Cadwaladr Health Board). Though the doctor did let slip that they do approve it sometimes, when the AF is not valve related (have I got that right?). As mine is a cuddly family AF, it's a possibility but a distant one I think.
But meanwhile I am on aspirin, which I presume will not be very useful in preventing stroke. I know my risks are supposedly low, but for some reason this makes me nervous...