Thanks, JaSanne. I have an apt with this dr on Monday so I guess I will discuss it with him then. I called the office as soon as I received the prep info in the mail and was just told he doesn't use the Miralax anymore, this is safe, better etc, etc. I notice that when I try to talk to offices/nurses they tend to just go along with what the dr prescribes, say it's ok to use because it's what he uses and tell you everything will be fine. They did this to me with the phosphosoda. I remember wanting to talk to that dr and he would never get on the phone so I talked to the office manager who assured me it's a very safe prep, she has used it 5 times, etc, etc. I had a problem with it and all they wanted to know was when I wanted to reschedule. A month or so later it's pulled off the shelves and I read about
people suing their drs for their kidney failure. So, yes, I worry. And I get frustrated with the drs too because people often tell me "if you have concerns discuss them with your dr" but when I have, again, I am usually just patted on the head and told I'll be fine but after that situation its hard to trust anyone.
A huge part of me just thinks to use the Miralax and that's it no matter who says what. You feel you want to do what the dr says though especially if something does go wrong. The whole thing is very frustrating.