I'm seeing a cardiologist EP end of this month, and that feels a big relief, not that they'll have any magic wands! It's really worth chasing these things up. The registrar who originally referred me for the holter monitor failed to refer me to a consultant. That was weeks wasted while I waited to get the holter fitted and it was only when I chased up the cardio secretary to ask about monitor results that I learned there was no referral as such to a cardiologist EP! I had to go back to my GP to get the referral. Meanwhile I'm told the waiting time for monitor results is currently 6 weeks. So decided against all my principles and dislike of our two-tier system (not to mention financial circumstances) to take the private route to a consultation. I'm glad it's with the same consultant I'll be under with any NHS procedure. I've read here so many times how important it is to not hang around with persistent af, and I've not even been offered cardioversion or anti arrhythmia drugs yet alone been offered an opportunity to explore future options. So hopefully some further choices will open up to me, and when they do I know I'll be eternally grateful to this forum!😀
Hooray hooray got my appointment today! - Atrial Fibrillati...
Hooray hooray got my appointment today!
Hello Rainfern that is good news...
My suggestion to you would be to make a list of things to ask the consultant.
If you are newly diagnosed have you had an Echocardiogram yet , it is essential to view the condition of your heart before treatment is decided.
I wish I had seen an EP earlier (I had to pay to see one) tried Flecainide earlier and had chance to take it as a PIP , got on the list for an Ablation earlier.
I am afraid as with many conditions Covid has made things even more difficult for many AFers.
Thank you Doodle and Buffafly for your helpful suggestions. I had the echocardiogram back in early November last year. It showed Afib but the general structure of my heart to be sound. Daily reading on my Microlife Home BP/HR monitor consistently show presence of Afib and resting HR in 80s and 90s. The holter results take around 6 weeks so by the time of my appointment that will be 7 weeks and the secretary said if the results aren't in then get in touch a few days earlier and make a different appointment. As I understand it I wasn't referred to cardio because the registrar explained my condition was due to aging and that it would be dealt with at the GP practice!
🙄 A GP told me my Sinus node was wearing out. That may be true but doesn’t mean I have put up with the results and neither should you ❤️🩹
You might also consider waiting for the holter result because the more info the EP has the more valuable your consultation will be.
Rainfern I really am so pleased for you, not for the fact you’ll have had to empty the bank to see the same
Consultant consultant but that the registrar took you off radar! I hope you get the same care I have with private and you start to see light at the end of the long tunnel x
Definitely the right decision. Exploit it to the full, keep a diary of events leading up to your appointment, a list of questions (don't get pushed out of the door before you have written down the answers) for your appointment and keep a diary leading up to the next private appointment if funds allow.
A private appointment doesn't give you much extra time but sometimes that extra 10 mins yields a lot for your money 🤞😁.
Thank you secondtry for your encouragement! I've already got that diary under way, and a daily record of HR/BP and presence of AFib. I find it too easy to slip off quickly from an appointment, thinking too much about using up time and the next person waiting! So this is very helpful.
first thing on your list ask about a blood thinner please because as you probably know, that is one of the most dangerous part of a fib
You've been in afib since November & no medicines at all?? Get onto your GP as a minimum who can prescribe an anticoagulant (essential) and rate/rhythm control drugs. This will help you fel better until you see the EP.
Ah Cat, thank you for your concern. I'm sorry I didn't explain well.... Ive been on anti-coagulant from the start! But because my GP doesn't seem to have an in-depth knowledge of this condition I have not pushed him for a rhythm control prescription. I do have a beta blocker, propranolol, that I just take at night which is when things are most likely to kick off. Although I'm not comfortable with the symptoms I know from being on this forum that mine are quite mild compared with others. And I'm focused on keeping exercised, hydrated, weight control, relaxation and so forth. I'm not sure the rate/rhythm control drugs would stop me being breathless on stairs or give me my energy back in the afternoon? But it would be nice to feel normal heartbeat again!
My GP admits to not knowing about cardiology, not too reassuring is it! Sounds like you are doing all you can until you see the EP. Good luck x
By the way, where in the Southwest do you live?