You wouldn’t know it with the amount that I probably bang on about it, but I genuinely didn’t want having a pacemaker to define me. Still, I write about it, think about it constantly, find myself telling people things about it and frequently catch myself looking at my scar in the mirror or prodding away at the bit at the top of my chest where my wires are sticking up, right at the surface.
That said, a quick search of my posts tells me that the last time I wrote a ‘Pacemaker Diary’ was actually in November 2023, a whole year after it was fitted. So, even though it’s been mentioned in some pieces I’ve written since, maybe I’m not banging on about it quite as much as I imagine. Anyone I speak to regularly can feel free to correct me on that though!
I was prompted to write this post because of Facebook memories of all things. In the lead up to Christmas and New Year just gone it felt like every few days there’d be something popping up where I was thanking people for their support or updating friends on my progress. They reminded me of both how poorly I’d been and also how far I’d come and they made me do a lot of thinking about the little machine that sits in my chest.
It’s been over 2 years since I had the pacemaker fitted. I didn’t pay much attention to the anniversary this time around. Sometimes there’s just too much going on in life for you to pause and have a think about stuff. But those Facebook memories changed all that and made me want to write something down about what life’s like these days. Self indulgent? I don’t know really, but I guess if you think that way you have the option of clicking that little x in the corner of your screen and not reading on.
I think writing about it simply helps me get on with life, which might be a bit more understandable when I tell you what it’s all like.
The pacemaker makes me feel a lot more comfortable about life, that’s for sure. I hardly ever worry about my heart. But paradoxically, it is always there to remind of just how poorly I was and the long, long time that it took me to get better. On top of that it’s a constant reminder of how low it all made me feel and the worryingly negative effects it had on my mental health.
There are both positives and negatives when it comes to having this device though and those reminders on social media made me think about a few of them. The first is just a bit of a change, I suppose, although does feel slightly negative. These days, my heart literally thumps when there’s not really been a great deal of effort. I’ve noticed it when climbing stairs and also that when getting into bed and straightening out the duvet, once I settle down my heart will be thumping! As someone who had an unnaturally low heart rate prior to all this – one of the reasons for the pacemaker – that takes a bit of getting used to!
Having the pacemaker has really made me focus on my health and fitness to the point where I’m really quite obsessive and possibly even a little evangelical about running! Silly really, but it genuinely makes me feel strong being able to run, especially in actual races. I couldn’t recommend it enough, even though I’m aware it’s not everybody’s cup of tea!
Another negative is that I live with a heart monitor by the side of my bed. This makes me feel really, really old! The monitor doesn’t do much, but I’m aware it’s feeding data back to the hospital which still feels a little bit weird. As I mentioned earlier as well, I have another scar as well as a strange bit on my chest where my wires just stick upwards. It’s a neat little scar, but those wires spoil things and coupled with the big scar that I have on my chest from a childhood heart operation, it’s not a great look!
My condition means that I still get heart palpitations, albeit nowhere near as regularly as I was having them for large parts of 2022 before my operation. However now, when they come I can rest assured that the pacemaker will kick in after about 5 seconds and stop them. It’s still quite a frightening thing, especially when it feels like the pacemaker isn’t going to react. The thought of having them for untold hours and just trying to get on with my day while wondering if I was about to pass out is a memory that still lingers! Still, that pacemaker is reassuring though.
Another drawback is that my left arm and shoulder don’t seem to work very well anymore. My scarring is really close to my left shoulder and I assume that it’s affected things as I haven’t got full movement and my left arm isn’t as ‘strong’ as it used to be. I mean, it wasn’t strong anyway, but it’s just a bit pathetic nowadays!
The final gripe I have is with my aftercare. I’ve only had one follow up appointment with a cardiologist since it all happened. Even that wasn’t actually scheduled. It was an appointment about a 24 hour monitor I’d worn, but in between times I’d had to have my pacemaker fitted, so the appointment was made later because the cardiologist didn’t realise and had to spend a load of time reading my notes before actually seeing me! Since then – January 2023 – there have been a couple of scans done but no meeting with actual doctors, which feels wrong.
I have had a letter from my hospital saying that a planned appointment had been rescheduled for later in the year, but I hadn’t even been informed about the planned appointment, so it’s all a bit of a mystery really! Luckily, I feel fit and healthy but it is concerning not to be speaking to someone when we’re almost 2 years on from the last appointment.
All in all, it’s been a bit of a whirlwind. Two years of major change that, just when you think you’ve almost forgotten about it and are living pretty normally, comes back to haunt you via bloody Facebook of all things! Clearly, while this pacemaker doesn’t really define me, it’s never going to leave me either!










