Just got home from the ENT office and what I thought was going to be a consult for putting tubes in turned into setting up a surgery date for having tonsils and adnoids removed. When I told the nurse that I wanted to be the 1st patient the morning of surgery so his BG levels stay in the 100's she looked at me like I was crazy. And I got another look from her when I said that when he went under for an MRI in Feb that they used a sugar-free saline solution and that I would want to make sure that this is available at the place we are doing the surgery at since it is not at the Children's Hospital. So what have other CWD done pre-surgery and post surgery when having their tonsils out? We are in a very strong honeymoon stage and have not had insulin shots since March and are just doing a diet type control for now.