Hello,
I have read lots on here about the PEG tube. I assume it is for feeding. Exactly where and how is it inserted? Does it stop you from being able to use your mouth? I don't have a clue, so if someone could just pin it down just a little I would be grateful. I read somewhere that it was put down the throat, then it was surgically attached to the stomache, I am confused.
Help....
Thank you kindly
Carol

Carol if you go to the Oral Cancer Foundation main site there is a good description of the PEG tube complete with pictures and many other details of its use and care. I think you will find the information you are seeking there.

Carol,
this link explains its and has pictures.
http://www.oralcancerfoundation.org/dental/tube_feeding.htm

The idea may be creepy but it is not a big deal. I had one and although I did not used it a lot it can be a life saver! Not only can you be fed you also can administer liquids and avoid dehydration.
Even if you have it it does not mean that you have to use it. You can drink and eat normally even when you have a PEG. BUT if and when the time comes that you cannot eat and drink because your mouth hurts from radiation or other issues it will save your life. It just gives you more options and a peace of mind. Many RO require that you have one. Installation takes maybe 2-3hrs, including waking up. I my case I was working in the afternoon. Removal is a snap (literally).

Well, that explained it all, thank you all so very much. I am no longer confused and it is not as frightening a thing as I thought it was. Now I need to go on a search and learn what all of these initials and numbers mean on everyones messages.

Thank you again,
Carol

Carol
you asked and here it is. This list contains stuff such as IMRT, RO etc.

http://www.oralcancerfoundation.org...ms&topic=0&Search=true#Post38715

cut and paste the above link. If that does not work search for acronyms
OCF Main Site

Thank you Markus, I just finished printing it, looks great.
Carol