My oncologist insisted that I had the Peg installed before my
treatment began. I did fine untill almost the end & suddenly It was as though a switch was pulled. The taste of thing's except water made me physiically ill! I am going on three month's post treatment & can hardly wait to have my tube removed. Eating is a challenge for me because of the usual lack of taste.Plus salivary gland's are not functioning. I have not lost any weight however, so I did benefit from it's use. However, I can understand that some people could become dependent on it. Hopefully I will have mine removed soon. I just wish I could enjoy food more as I have no appetite, but sure do miss the social part of eating in restaurant's etc. It all comes down to what our specialist's recommend & personal choice.