- Anything you try and do after surgery hurts more than you think it will, takes longer to complete and generally exhausts you. Well, I’m sure you wouldn’t think that washing could take an hour and make you feel like you’ve run a marathon – but it does!
- Learn hospital routines – when they get you up and when lunch comes etc. Hey, when you know how long ‘til the next exciting thing to happen, the day will go faster (well that’s what I found anyway!).
- Take all the drugs they offer you – don’t be brave. The best thing you can do for yourself is get moving as soon as you are allowed – you can’t do this is you are in agony.
- Take an interest in your drugs – why you are getting what you are getting and when. This will help when you get home as you will already be in a routine.
- If you have a chest drain and you need to turn, try not to roll on top of it. It will hurt (oh boy will it!). Be brave when they take it out – and don’t worry too much about that either as it’s all over pretty fast!
- Drink lots – you don’t want an infection down there to add to all your other woes – besides which, it will help keep your blood pressure stable (yes really!)
- Eat as soon as you can, your body needs calories to heal.
- When you wake up from your operation you will be all puffy and feel like the Michelin man – this will pass in a few days but makes you look and feel pretty weird.
- Wet wipes are nice when you are stuck in bed – yes, I know there are bed baths but still….
Thinks that’s all the odd stuff I wanted to tell you apart from the fact that if you want a Chippendale in hospital with you, take your own – none of the male nurses quite hit the mark there!
3 comments:
Hi, Pips.
Congrats on your successful surgery -- and I love your blog!
My old pal Titch tells me you might be willing to tell me a little about diastematomyelia.
I'm a 47-year-old with congenital scoliosis and spina bifida occulta, and I had a scoliosis fusion at age 13. I was really lucky as a kid and suffered no neurological deficit from the spina bifida, but my legs have always been tight and my left foot turns in a bit. As an adult I've developed some problems, partly because of the fusion, but the spina bifida may have become an issue as well. A recent MRI reveals a tethered cord, which appears to be split from the T9 level.
The surgeon I am consulting has talked in terms of de-tethering surgery, as well as correcting the forward lean I have developed courtesy of the Harrington Rod in my back. I sort of freaked when I read about the split cord, in the MRI report. I've read that the split is sometimes a source of tethering, and that surgical correction can sometimes improve function.
I understand your recent surgery was just to correct the scoliosis curves, but do you have a history of neurosurgery for the spina bifida? How much of an issue is the diastematomyelia (impressive word!) in your case?
I'd love to hear from you at sharon.green18@verizon.net
Thanks, and take it easy!
Sharon
Hey, I had one really hot male nurse named Bill. Too bad he saw me at my absolute worst and ugly....lol
kat
Hey-I want a hot male nurse-where do ya get one?? maybe pips & kat can chip in & send me one after surgery... http:/lynnebackattack.blogspot.com
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