Hi everyone. I have just to LGI to see the arythmia nurse again and had the ECG before he saw me and as my heart is now permanently out of rhythm, tho no longer AF, it's now ectopic beats every couple of heart beats, he has said that I now need to see an EP.
It's been a long time getting here but at last I can talk to someone who does the ablation and lay all my fears before him.
I'm still scared but hopefully once I've talked to him I will feel more reassured. And as I'm going to the conference on Oct 4th, I will be able to talk to some of you who have it done and that will help.
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Nannadee
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Actually you've just reminded me that I need to ring Tamsin as I've paid for the day but haven't received any written confirmation or proof of payment. Have you?
I have you booked in for supper. 7 for 7.30 in reception. I usually bring a dozen Pink Carnations so dont worry
Bob
I'm the same. Not much if any AF but constant ectopics, so much so you can't take my pulse. Anyhow, my EP has found drugs that work for me and been doing fine for the last 2-3 years. Hope you get a similar result. I had to be quite definite/almost pushy about my drugs. I was started on one, told them it didn't work, then another, didn't work well enough, then a third which was/is great.
Good luck getting it sorted, and great you're seeing an EP.
I'm on Bisoporol 2.5mg twice daily and Flecainide 100mg twice daily.
The AF nurse suggested trying Amioderone but I said no as my pharmacist had told me that this is not a very pleasant drug and can have severe side effects.
I'm always put on rhythm control drugs because beta-blockers do nothing for me except make me feel very old. But what works for me is not really relevant as we're all different. Flecainide which works for most believe, doesn't work on me; Propafenone works but not too well and affects my mind; Disopyramide is what I'm on at the moment and it's working well but doesn't for others as is evident from this forum.
Your remark about Amiodarone is interesting. It is rather an aggressive drug. Certainly got me going and turned me yellow and put me on the loo for a few days (there are better places!). Rang Ward 20 at LGI and resorted to Daltiazem a much softer approach.
Had my second ablation on Wednesday morning just at LGI and recovering quietly here at home. The team at the LGI are just marvellous. You are in good hands in both the Ward and in the Catheter Laboratory (Cath. Lab.). There is no need to, in any way feel, unnerved. They are very patient, will answer any questions, are friendly and when you get your ablation, well organised and relaxed. They cannot do enough for you. If there is anything you need just ask (I had forgotten my towel!!)
It is strange going into any operating room (theatre) and the cath. lab. is more like a computer room so you do feel you are in another kind of world. Please do not worry. When the experience comes, that's what it is, another of life's experiences and a good one to relates to relations and friends. Get well.
Hi! Sorry about this - just picked up your remark. I had a local anaesthetic or I suppose that would be sedation and I am wondering whether they just relied on the dash of morphine when they went through the septum. Anyway it was all fairly painless although I could feel the catheters moving about inside and it was enough to make you hold your breath when they were ablating.
The TOE was done 3/4 days earlier. That wasn't so bad either and once the anaesthetic spray had been carried out down the throat I seem to drift away so there must have been some anaesthetic put into my arm.
Good result to be seeing EP! On to the next stage!!!
There is a load of information and experience around on this site and I am sure that you will ask!!! You aren't alone. Glad that someone said below what LGI stands for!
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