my mom just had her peg tube inserted about 3 weeks ago now and was told at the time that it probably would have to be changed in 6 months or so perhaps sooner if it clogs etc....

how are you making out on your food - mom is only pumping at 40ml/hr and seems to vomit once a day or so.. having trouble digesting have you had a similar experience?

mom just dianosised with sequamous cell CA hypopharynx - would be cured with radiation -however she does not qualify as she already had radiation in same area years ago.... now has feeding tube