I know some of you guys have been following my thread from the beginning and know that I’m in a wheelchair. What you don’t know is that I started SW 3 weeks after getting out of hospital. I’d spent 15 months in hospital and on Friday I had a review with my consultant about how I’m getting on now that I’m home. I’ve been thinking a bit recently about the whole experience and have started to jot some of it down. Thought one or two of you would be interested. But feel free to scroll past this entry if you get bored.
I don’t have a story. I tell myself that most days. But what I mean is I don’t have a story that can be whittled down to one sentence when passing someone I once knew in the street. When people ask me what happed I can’t respond with ‘I was in a car accident’, ‘I fell out of a tree’, ‘there was a motorbike..’ I don’t have a story that I can easily sum up. There’s nothing instantly recognisable that people can relate to and picture in their minds when bumping into them in the street and trying to catch up with ten years of your life in ten seconds.
I don’t have a story because I don’t have a start. I don’t have a start because I don’t know where to begin because I don’t actually know what happened. If I have the time and inclination (not to mention a person who’s genuinely interested), I sometimes tell people I squeezed a spot. I did. I had a spot, I squeezed it and that resulted in me being admitted to hospital. But once I get there I know that that itself isn’t the beginning of the story, that that’s just the hook. The hook the reels them in. I need to give a bit more background information but by then they’re bored. They can’t relate. It’s not a case of me falling off some scaffolding whilst out on a weekend binge.
So there was this spot. It was on the inside of my thigh, close to my groin. I squeezed it. I shouldn’t have. Because of my interference the squeezed spot developed Necrotizing Fasciitis, commonly known as flesh-eating disease. The only way to deal with it was to cut it out, that meant surgery and this is where the back story comes in.
I also have a heart condition, Dilated Cardiomyopathy, this means that essentially my heart only works at 15%. My heart specialist advised the surgeon not to operate as I’d not make it through the operation and the surgeon advised that if he didn’t operate I’d not make it through the night. I’m still here so...
I ended up on life support for 3 days and on the last day my family were called and told that I wouldn’t make it through the night. The family came; said their goodbyes. Friends were called and told to expect the worst. I wasn’t for making it. At some point when everyone was gone and my mum was in the hallway with the nurse during the night my fever broke.
This I don’t remember, but I woke to find a rather unpleasant life support tube down my throat so proceeded to remove said tube. This wasn’t a very clever idea and that in itself should have been enough to kill me, but again I managed to avoid death’s clutches. It did however, have consequences.
I was in and out of it for the next few days. Don’t remember any of it but know that when I did start to become lucid and aware of things that I was aware that I couldn’t feel my legs etc so I’ve never had that shock experience of waking up to nothing, I just knew it was all gone. Maybe that happened during that first week but I can’t remember.
It had been hoped that it was just down to the anaesthetic not wearing off or maybe some swelling at the base of the spine. Something known as Spinal Shock, but, it became apparent over the course of the next few weeks that there was no improvement so the spinal specialist was called and after a number of tests it was confirmed that damage had occurred (though it’s never been confirmed how) and that it would be unlikely that I’d ever walk again.
This meant going to rehab, the only problem there was that they took one look at me and at my size and decided they didn’t want me... but maybe that’s another story for another time...