Thank you all. Genuinely.
I've just had lunch and probably won't be out of here until 6pm, lol. Seriously, the wait for the discharge letter and the medication is eternal in a hospital - don't understand why it
always has to take this long.
At any rate the home visits have been sorted. I'll temporarily register with my mum's GP surgery and they can send a nurse round to change dressings, remove staples, etc.
Clo - The stoma is working quite well. Sometimes get a bit of pain behind there, but nothing which walking around and very gently massaging the stoma area doesn't solve. It does feel like a massive advantage having been through all this before, so even though I'm still quite slow with changing the bag, it's still far easier compared to last time. Emptying the bag is even simpler: I just sit as far back as I can and let the bag drain between my legs. Works much better than bending over the front of the toilet and hoping you don't get splashback. Took me a long time to learn that the first time.
No name for my stoma yet! Need to get a better feel for its "personality" first. Though one thing I want to do which I never did last time is buy some ostomy bag covers with cute or interesting designs. A skull, maybe
I've been quite zonked out today, so no walking so far. Whatever little bit of energy I have seems to come to me in the evenings.
Quincy - I know my mum is looking forward to seeing me again. She was only able to visit me once (with the help of my brother) and that was last Thursday, where I was not at my sparkling best. To put it mildly. Hugs back.