I'm being intentionally ambiguous, of course. I am referring to being bound in Sunderland, rather than bound for it. Although, only a fool would contend that I would not have to, at least initially, be bound for Sunderland in order to be bound in Sunderland. Nor is it one of those generic bindings which see an entire body cocooned in deft ropes. No, my binding was to be entirely more leg-based. But more of that later, if you can bear it - and, if not, how do you think I manage?
Before I stray too far along the path of redundant flippancy, let's get to the facts.
I was an outpatient yesterday - a status which brings me a profound sense of pleasure. Non-patient would be far better, but outpatient is a great second best. Having been conveyed there by the excellent Jason, we then waited for a good two hours to be seen. As it turned out, my 2.40pm appointment was the last of the day at around 5pm. The intervening time was spent in lively and humorous conversation with Jason, to the bemusement of the other people in the excitingly named "Waiting Area 3".
The doctor who saw me was predictably unhelpful and evasive, and keen for me not to be part of his problem. Sadly, I was wise to his attempts to side-step my treatment and I cornered him into.............well...making another appointment in a fortnight. I suppose, from his standpoint, it might not be him who sees me then, so it was a problem solved. If only there were cellulitis specialists...or a clearly defined department which takes care of cellulitis patients. I really do wish I had a different sort of illness, and one for which there was a designated treatment path.
As it is, everyone says something different, tries to pass me on elsewhere or simply tells me nothing can be done. I will admit to being exhausted by this constant battle to get good treatment and advice.
So yesterday, after telling me my condition was too acute for him to treat, I was re-bound by the expert binding nurses of the Vascular department. They did a good job too. I now have some very good bandages on which provide good support. The left leg still seeps much lymphatic fluid, so will still need regular changes. The right bandage can stay on for a few days, which is nice.
I am grateful for the new bandaging system, because it offers significantly increased support, which gives me a feeling of security. A few days down the line, it may help me to be more mobile and get out to clients and other such exciting things.
I feel I have turned a corner. The cellulitis is definitely getting better, albeit slowly. Now, I must just be careful not to make things worse. The biggest battle is in my own mind.
If I can win that one, I'll be fine.
Recent Comments