This is my last weekly post, I will provide monthly posts until the end of my blanking period or if any significant changes appear.
Improvement continues but much slower than I thought, doing a little more, over 4000 steps a day and 20 floors. Pulse rate has continued to increase now at 71BPM but it does appear to be levelling out, hopefully it will not go higher than 74. BP now a reasonable 127/75 at rest. There are long periods throughout the day when I forget I have a problem (long may it continue). Symptoms now are having the odd mild ectopic 4 or 5 times a day and pulse rate can increase to 85 when just sitting and up to 115 when just going up stairs, then other times BP will remain constant at rest and just go to 80 when going up stairs, I put this down to heart still recovering. I have 4 weeks before I see the Cardiologist and will be pushing myself to get back to "normal activity" during this time and that will give him some information to base his assessment on. Still drug free except for rivaroxiban.
Being very sedate since Cardioversion in December, then ablation in February, I have been doing some thinking (not wise I know but just cannot help it). When my symptoms started 23 years ago it was after a period when I drank 3 bottles of wine a week and had been relying on strong coffee during the day. They started some 3 hours after a few cups of very strong coffee. I have been on Omeprizole 20mg and Bisoprolol increasing from 2.5, 5 to 7.5. In January 2017 (after a bad bout), cut down wine and coffee by half, then in January 2018 (after another bad bout) cut out all together and started Mg occasionally at first then regularly from January 2019. I have also cut the omeprizole down to 10mg every 3rd day. The question I am asking myself and anyone than has an opinion is could the initial problem have been electrolyte imbalance, then when the Mg improved my electrolyte balance, the medication made my symptoms worst. The reason I jumped to this question is that after being drug free for 3 weeks I feel good with potentially only the normal ablation recovery symptoms. Unfortunately I am brought down the earth when I remember what my EP said, he had done some ablation (at least 3 places that I was aware of), told me I no longer had AFlutter but I was left with MAT (I know electrolyte imbalance can be the cause of MAT) which he could not fully ablate and would have to be treated with drugs. Has anyone had a similar experience?