Quote:
Originally Posted by dmplaura
From what I saw during the show, those having the surgery were awake during it. It wouldn't be minor, no surgery is, but it put me at ease to see the patients awake for the procedure. I've been put 'under' for 2 other surgeries so far in my life, and I think that's scarier than the surgery itself (anesthesia).
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My dad is a nurse anesthetist (the guy responsible for making sure you dont feel any pain and that you're breathing) I have anesthesia phobias because he's told me a couple of horror stories, but he's also told me about something called a
BIS monitor. that can be used to monitor what level of wakefulness you have when under anesthesia.
I've already told him that if I ever need surgery for anything, and they want to put me out, that I want him to talk to the anesthetist putting me under and make sure they use a BIS monitor.
As for being awake during a surgery, I've done that once...till the anesthetist put me out because I was driving him nuts talking. (well, gee, shoot me up with a bit of Versed to relax me and what do you expect?) I was having carpal tunnel surgery, (I'd had a
bier block because of my anesthesia phobia) and I was awake for a good part of it till I drove the anesthetist nuts (and probably the doctors too). At least they didnt have to put a mask over my face for it. That's part of my phobia. I'm claustrophobic and anything over my face freaks me out. He just pushed more Versed until I was asleep.
At least having an anesthetist parent has given me a bit of an idea of what to expect if I ever have a surgery, and that it's important to talk to the guy (or girl) giving the anesthesia to see if they can do anything to keep me from being scared of the anesthesia.
I just cant wait to talk to my regular doctor about the CCSVI and see what he thinks about it. I would love to at least be evaluated and maybe see if there's something they can do or give me and see if the MS improves or slows down.
I think if I call my doctor tomorrow morning, I'll just tell him that I read something about the CCSVI, and I was wondering if he could research it and tell me what he thinks about it. He wont give me LDN because he thinks it's a placebo and plus he cant get any neuros in Omaha to back him up on it. I just dont want him to have the same reaction that he had when I asked him for the LDN. (I think he thinks that I'm nuts or totally desperate. Probably true, but I dont want him to think that)