Good afternoon all. I went in and had another stent fitted on the 5th of February after a bit of a wait and 3 ambulance call outs, the third one they kept me in as they said I was a high risk. I am feeling much better and not getting so out of breath. The consultant thinks my problem is genetic and I have evidence of furring in the smaller branches which cannot be stented and the other 2 arteries that have been stented have some furring but not enough to restent, they are hoping to control it all with medication. My Cholesterol is low at 3 but they have doubled my statins hopefully that will help. I am going to start rehab soon as I’m sure that will help after 2 ½ years of not being able to do much exercise at all. The Drs and nurses were wonderful while I was in the hospital and kept a very close eye on me. Hopefully, that is it now as I would like a rest from Angiograms / Angioplasty for a while. I’m hoping I don’t get the problems with unstable angina but still have to use the GTN spray when and if needed. I am still taking the same pills except for Isosorbide mononitrate so not much has changed there. I’m feeling more positive about having CHD than I have in a long time as I have now understood all that is happening to me so it was definitely the right decision to move back from Spain last march. Thank you all for listening to me rambling on
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Joan